MRC Centre for Neuropsychiatric Genetics and Genomics

Index of publications

• Articles
  • 2013
  • 2012
  • 2011
  • 2010
  • 2009
  • 2008
  • 2007
  • 2006
  • 2005
  • 2004
  • 2003
  • 2002
  • 2001
  • 2000
  • 1999
  • 1998
  • 1997
  • 1996
  • 1995
  • 1994
  • 1993
  • 1992
  • 1991
  • 1990
  • 1989
• Conference proceedings
  • 2010
  • 2000

Publications

• Articles
  • 2013
    • Genetics of bipolar disorder.
      Craddock N, Sklar P, Lancet, Volume 381, 9878 (May 2013) pp.1654-1662
    • Reproductive outcomes and risk of subsequent illness in women diagnosed with postpartum psychosis.
      Blackmore ER, Rubinow DR, O'Connor TG, Liu X, Tang W, Craddock N, Jones I, Bipolar Disord (May 2013)
    • Association at SYNE1 in both bipolar disorder and recurrent major depression.
      Green EK, Grozeva D, Forty L, Gordon-Smith K, Russell E, Farmer A, Hamshere M, Jones IR, Jones L, McGuffin P, Moran JL, Purcell S, Sklar P, Owen MJ, O'Donovan MC, Craddock N, Mol Psychiatry, Volume 18, 5 (May 2013) pp.614-617
    • Neuropsychological testing of cognitive impairment in euthymic bipolar disorder: an individual patient data meta-analysis.
      Bourne C, Aydemir O, Balanzá-Martínez V, Bora E, Brissos S, Cavanagh JT, Clark L, Cubukcuoglu Z, Dias VV, Dittmann S, Ferrier IN, Fleck DE, Frangou S, Gallagher P, Jones L, Kieseppä T, Martínez-Aran A, Melle I, Moore PB, Mur M, Pfennig A, Raust A, Senturk V, Simonsen C, Smith DJ, Bio DS, Soeiro-de-Souza MG, Stoddart SD, Sundet K, Szöke A, Thompson JM, Torrent C, Zalla T, Craddock N, Andreassen OA, Leboyer M, Vieta E, Bauer M, Worhunsky PD, Tzagarakis C, Rogers RD, Geddes JR, Goodwin GM, Acta Psychiatr Scand (April 2013)
    • The interaction between child maltreatment, adult stressful life events and the 5-HTTLPR in major depression.
      Power RA, Lecky-Thompson L, Fisher HL, Cohen-Woods S, Hosang GM, Uher R, Powell-Smith G, Keers R, Tropeano M, Korszun A, Jones L, Jones I, Owen MJ, Craddock N, Craig IW, Farmer AE, McGuffin P, J Psychiatr Res (April 2013)
    • Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
      Cross-Disorder Group of the Psychiatric Genomics Consortium None, Smoller JW, Craddock N, Kendler K, Lee PH, Neale BM, Nurnberger JI, Ripke S, Santangelo S, Sullivan PF, Lancet, Volume 381, 9875 (April 2013) pp.1371-1379
    • Novel ATP2A2 mutations in a large sample of individuals with Darier disease.
      Green EK, Gordon-Smith K, Burge SM, Grozeva D, Munro CS, Tavadia S, Jones L, Craddock N, J Dermatol, Volume 40, 4 (April 2013) pp.259-266
    • A mega-analysis of genome-wide association studies for major depressive disorder.
      Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium None, Ripke S, Wray NR, Lewis CM, Hamilton SP, Weissman MM, Breen G, Byrne EM, Blackwood DH, Boomsma DI, Cichon S, Heath AC, Holsboer F, Lucae S, Madden PA, Martin NG, McGuffin P, Muglia P, Noethen MM, Penninx BP, Pergadia ML, Potash JB, Rietschel M, Lin D, Müller-Myhsok B, Shi J, Steinberg S, Grabe HJ, Lichtenstein P, Magnusson P, Perlis RH, Preisig M, Smoller JW, Stefansson K, Uher R, Kutalik Z, Tansey KE, Teumer A, Viktorin A, Barnes MR, Bettecken T, Binder EB, Breuer R, Castro VM, Churchill SE, Coryell WH, Craddock N, Craig IW, Czamara D, De Geus EJ, Degenhardt F, Farmer AE, Fava M, Frank J, Gainer VS, Gallagher PJ, Gordon SD, Goryachev S, Gross M, Guipponi M, Henders AK, Herms S, Hickie IB, Hoefels S, Hoogendijk W, Hottenga JJ, Iosifescu DV, Ising M, Jones I, Jones L, Jung-Ying T, Knowles JA, Kohane IS, Kohli MA, Korszun A, Landen M, Lawson WB, Lewis G, Macintyre D, Maier W, Mattheisen M, McGrath PJ, McIntosh A, McLean A, Middeldorp CM, Middleton L, Montgomery GM, Murphy SN, Nauck M, Nolen WA, Nyholt DR, O'Donovan M, Oskarsson H, Pedersen N, Scheftner WA, Schulz A, Schulze TG, Shyn SI, Sigurdsson E, Slager SL, Smit JH, Stefansson H, Steffens M, Thorgeirsson T, Tozzi F, Treutlein J, Uhr M, van den Oord EJ, Van Grootheest G, Völzke H, Weilburg JB, Willemsen G, Zitman FG, Neale B, Daly M, Levinson DF, Sullivan PF, Mol Psychiatry, Volume 18, 4 (April 2013) pp.497-511
    • Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.
      Hamshere ML, Walters JT, Smith R, Richards AL, Green E, Grozeva D, Jones I, Forty L, Jones L, Gordon-Smith K, Riley B, O'Neill T, Kendler KS, Sklar P, Purcell S, Kranz J, The Schizophrenia Psychiatric Genome-wide Association Study Consortium (PGC), Wellcome Trust Case Control Consortium+ (WTCCC+), Wellcome Trust Case Control Consortium 2 (WTCCC2) None, Morris D, Gill M, Holmans P, Craddock N, Corvin A, Owen MJ, O'Donovan MC, Mol Psychiatry (March 2013)
    • Interaction between specific forms of childhood maltreatment and the serotonin transporter gene (5-HTT) in recurrent depressive disorder.
      Fisher HL, Cohen-Woods S, Hosang GM, Korszun A, Owen M, Craddock N, Craig IW, Farmer AE, McGuffin P, Uher R, J Affect Disord, Volume 145, 1 (February 2013) pp.136-141
    • A comprehensive family-based replication study of schizophrenia genes.
      Aberg KA, Liu Y, Bukszár J, McClay JL, Khachane AN, Andreassen OA, Blackwood D, Corvin A, Djurovic S, Gurling H, Ophoff R, Pato CN, Pato MT, Riley B, Webb T, Kendler K, O'Donovan M, Craddock N, Kirov G, Owen M, Rujescu D, St Clair D, Werge T, Hultman CM, Delisi LE, Sullivan P, van den Oord EJ, Jama Psychiatry, Volume 70, 2 (February 2013) pp.1-9
    • Genome-wide association analysis of copy number variation in recurrent depressive disorder.
      Rucker JJ, Breen G, Pinto D, Pedroso I, Lewis CM, Cohen-Woods S, Uher R, Schosser A, Rivera M, Aitchison KJ, Craddock N, Owen MJ, Jones L, Jones I, Korszun A, Muglia P, Barnes MR, Preisig M, Mors O, Gill M, Maier W, Rice J, Rietschel M, Holsboer F, Farmer AE, Craig IW, Scherer SW, McGuffin P, Mol Psychiatry, Volume 18, 2 (February 2013) pp.183-189
    • Perinatal episodes across the mood disorder spectrum.
      Di Florio A, Forty L, Gordon-Smith K, Heron J, Jones L, Craddock N, Jones I, Jama Psychiatry, Volume 70, 2 (February 2013) pp.168-175
    • Risk of psychopathology in adolescent offspring of mothers with psychopathology and recurrent depression.
      Sellers R, Collishaw S, Rice F, Thapar AK, Potter R, Mars B, Harold GT, Smith DJ, Owen MJ, Craddock N, Thapar A, Br J Psychiatry, Volume 202 (February 2013) pp.108-114
  • 2012
    • Estimating the heritability of reporting stressful life events captured by common genetic variants.
      Power RA, Wingenbach T, Cohen-Woods S, Uher R, Ng MY, Butler AW, Ising M, Craddock N, Owen MJ, Korszun A, Jones L, Jones I, Gill M, Rice JP, Maier W, Zobel A, Mors O, Placentino A, Rietschel M, Lucae S, Holsboer F, Binder EB, Keers R, Tozzi F, Muglia P, Breen G, Craig IW, Müller-Myhsok B, Kennedy JL, Strauss J, Vincent JB, Lewis CM, Farmer AE, McGuffin P, Psychol Med (December 2012) pp.1-7
    • Do parents know best? Parent-reported vs. child-reported depression symptoms as predictors of future child mood disorder in a high-risk sample.
      Lewis KJ, Mars B, Lewis G, Rice F, Sellers R, Thapar AK, Craddock N, Collishaw S, Thapar A, J Affect Disord, Volume 141, 2-3 (December 2012) pp.233-236
    • Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.
      Tsoi LC, Spain SL, Knight J, Ellinghaus E, Stuart PE, Capon F, Ding J, Li Y, Tejasvi T, Gudjonsson JE, Kang HM, Allen MH, McManus R, Novelli G, Samuelsson L, Schalkwijk J, Ståhle M, Burden AD, Smith CH, Cork MJ, Estivill X, Bowcock AM, Krueger GG, Weger W, Worthington J, Tazi-Ahnini R, Nestle FO, Hayday A, Hoffmann P, Winkelmann J, Wijmenga C, Langford C, Edkins S, Andrews R, Blackburn H, Strange A, Band G, Pearson RD, Vukcevic D, Spencer CC, Deloukas P, Mrowietz U, Schreiber S, Weidinger S, Koks S, Kingo K, Esko T, Metspalu A, Lim HW, Voorhees JJ, Weichenthal M, Wichmann HE, Chandran V, Rosen CF, Rahman P, Gladman DD, Griffiths CE, Reis A, Kere J, Collaborative Association Study of Psoriasis (CASP) None, Genetic Analysis of Psoriasis Consortium None, Psoriasis Association Genetics Extension None, Wellcome Trust Case Control Consortium 2 None, Nair RP, Franke A, Barker JN, Abecasis GR, Elder JT, Trembath RC, Nat Genet, Volume 44, 12 (December 2012) pp.1341-1348
    • Bayesian refinement of association signals for 14 loci in 3 common diseases.
      Wellcome Trust Case Control Consortium None, Maller JB, McVean G, Byrnes J, Vukcevic D, Palin K, Su Z, Howson JM, Auton A, Myers S, Morris A, Pirinen M, Brown MA, Burton PR, Caulfield MJ, Compston A, Farrall M, Hall AS, Hattersley AT, Hill AV, Mathew CG, Pembrey M, Satsangi J, Stratton MR, Worthington J, Craddock N, Hurles M, Ouwehand W, Parkes M, Rahman N, Duncanson A, Todd JA, Kwiatkowski DP, Samani NJ, Gough SC, McCarthy MI, Deloukas P, Donnelly P, Nat Genet, Volume 44, 12 (December 2012) pp.1294-1301
    • Common variant at 16p11.2 conferring risk of psychosis.
      Steinberg S, de Jong S, Mattheisen M, Costas J, Demontis D, Jamain S, Pietiläinen OP, Lin K, Papiol S, Huttenlocher J, Sigurdsson E, Vassos E, Giegling I, Breuer R, Fraser G, Walker N, Melle I, Djurovic S, Agartz I, Tuulio-Henriksson A, Suvisaari J, Lönnqvist J, Paunio T, Olsen L, Hansen T, Ingason A, Pirinen M, Strengman E, GROUP None, Hougaard DM, Orntoft T, Didriksen M, Hollegaard MV, Nordentoft M, Abramova L, Kaleda V, Arrojo M, Sanjuán J, Arango C, Etain B, Bellivier F, Méary A, Schürhoff F, Szoke A, Ribolsi M, Magni V, Siracusano A, Sperling S, Rossner M, Christiansen C, Kiemeney LA, Franke B, van den Berg LH, Veldink J, Curran S, Bolton P, Poot M, Staal W, Rehnstrom K, Kilpinen H, Freitag CM, Meyer J, Magnusson P, Saemundsen E, Martsenkovsky I, Bikshaieva I, Martsenkovska I, Vashchenko O, Raleva M, Paketchieva K, Stefanovski B, Durmishi N, Pejovic Milovancevic M, Lecic Tosevski D, Silagadze T, Naneishvili N, Mikeladze N, Surguladze S, Vincent JB, Farmer A, Mitchell PB, Wright A, Schofield PR, Fullerton JM, Montgomery GW, Martin NG, Rubino IA, van Winkel R, Kenis G, De Hert M, Réthelyi JM, Bitter I, Terenius L, Jönsson EG, Bakker S, van Os J, Jablensky A, Leboyer M, Bramon E, Powell J, Murray R, Corvin A, Gill M, Morris D, O'Neill FA, Kendler K, Riley B, Wellcome Trust Case Control Consortium 2 None, Craddock N, Owen MJ, O'Donovan MC, Thorsteinsdottir U, Kong A, Ehrenreich H, Carracedo A, Golimbet V, Andreassen OA, Børglum AD, Mors O, Mortensen PB, Werge T, Ophoff RA, Nöthen MM, Rietschel M, Cichon S, Ruggeri M, Tosato S, Palotie A, St Clair D, Rujescu D, Collier DA, Stefansson H, Stefansson K, Mol Psychiatry (November 2012)
    • Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample.
      Green EK, Hamshere M, Forty L, Gordon-Smith K, Fraser C, Russell E, Grozeva D, Kirov G, Holmans P, Moran JL, Purcell S, Sklar P, Owen MJ, O'Donovan MC, Jones L, WTCCC None, Jones IR, Craddock N, Mol Psychiatry (October 2012)
    • Dissecting the genetic heterogeneity of depression through age at onset.
      Power RA, Keers R, Ng MY, Butler AW, Uher R, Cohen-Woods S, Ising M, Craddock N, Owen MJ, Korszun A, Jones L, Jones I, Gill M, Rice JP, Hauser J, Henigsberg N, Maier W, Zobel A, Mors O, Placentino AS, Rietschel M, Souery D, Kozel D, Preisig M, Lucae S, Binder EB, Aitchison KJ, Tozzi F, Muglia P, Breen G, Craig IW, Farmer AE, Müller-Myhsok B, McGuffin P, Lewis CM, Am J Med Genet B Neuropsychiatr Genet, Volume 159B, 7 (October 2012) pp.859-868
    • Genetic heterogeneity according to age at onset in bipolar disorder: a combined positional cloning and candidate gene approach.
      Dizier MH, Etain B, Lajnef M, Lathrop M, Grozeva D, Craddock N, Henry C, Gard S, Jamain S, Leboyer M, Bellivier F, Mathieu F, Am J Med Genet B Neuropsychiatr Genet, Volume 159B, 6 (September 2012) pp.653-659
    • Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe.
      Rietschel M, Mattheisen M, Degenhardt F, Genetic Risk and Outcome in Psychosis (GROUP Investigators) None, Mühleisen TW, Kirsch P, Esslinger C, Herms S, Demontis D, Steffens M, Strohmaier J, Haenisch B, Breuer R, Czerski PM, Giegling I, Strengman E, Schmael C, Mors O, Mortensen PB, Hougaard DM, Ørntoft T, Kapelski P, Priebe L, Basmanav FF, Forstner AJ, Hoffman P, Meier S, Nikitopoulos J, Moebus S, Alexander M, Mössner R, Wichmann H, Schreiber S, Rivandeneira F, Hofman A, Uitterlinden AG, Wienker TF, Schumacher J, Hauser J, Maier W, Cantor RM, Erk S, Schulze TG, SGENE-plus Consortium None, Craddock N, Owen MJ, O'Donovan MC, Børglum AD, Rujescu D, Walter H, Meyer-Lindenberg A, Nöthen NM, Ophoff RA, Cichon S, Mol Psychiatry, Volume 17, 9 (September 2012) pp.906-917
    • Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis.
      Moskvina V, Schmidt KM, Vedernikov A, Owen MJ, Craddock N, Holmans P, O'Donovan MC, Eur J Hum Genet, Volume 20, 8 (August 2012) pp.890-896
    • Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms.
      Badner JA, Koller D, Foroud T, Edenberg H, Nurnberger JI, Zandi PP, Willour VL, McMahon FJ, Potash JB, Hamshere M, Grozeva D, Green E, Kirov G, Jones I, Jones L, Craddock N, Morris D, Segurado R, Gill M, Sadovnick D, Remick R, Keck P, Kelsoe J, Ayub M, MacLean A, Blackwood D, Liu CY, Gershon ES, McMahon W, Lyon GJ, Robinson R, Ross J, Byerley W, Mol Psychiatry, Volume 17, 8 (July 2012) pp.818-826
    • Missed opportunities: mental disorder in children of parents with depression.
      Potter R, Mars B, Eyre O, Legge S, Ford T, Sellers R, Craddock N, Rice F, Collishaw S, Thapar A, Thapar AK, Br J Gen Pract, Volume 62, 600 (July 2012) pp.e487-e493
    • Depressive disorder moderates the effect of the FTO gene on body mass index.
      Rivera M, Cohen-Woods S, Kapur K, Breen G, Ng MY, Butler AW, Craddock N, Gill M, Korszun A, Maier W, Mors O, Owen MJ, Preisig M, Bergmann S, Tozzi F, Rice J, Rietschel M, Rucker J, Schosser A, Aitchison KJ, Uher R, Craig IW, Lewis CM, Farmer AE, McGuffin P, Mol Psychiatry, Volume 17, 6 (June 2012) pp.604-611
    • Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disorders.
      Van Den Bossche MJ, Strazisar M, De Bruyne S, Bervoets C, Lenaerts AS, De Zutter S, Nordin A, Norrback KF, Goossens D, De Rijk P, Green EK, Grozeva D, Mendlewicz J, Craddock N, Sabbe BG, Adolfsson R, Souery D, Del-Favero J, Am J Med Genet B Neuropsychiatr Genet, Volume 159B, 4 (June 2012) pp.465-475
    • Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.
      Hamshere ML, Walters JT, Smith R, Richards AL, Green E, Grozeva D, Jones I, Forty L, Jones L, Gordon-Smith K, Riley B, O'Neill T, Kendler KS, Sklar P, Purcell S, Kranz J, The Schizophrenia Psychiatric Genome-wide Association Study Consortium (PGC), Wellcome Trust Case Control Consortium+ (WTCCC+), Wellcome Trust Case Control Consortium 2 (WTCCC2) None, Morris D, Gill M, Holmans P, Craddock N, Corvin A, Owen MJ, O'Donovan MC, Mol Psychiatry (May 2012)
    • A genome-wide association study of attempted suicide.
      Willour VL, Seifuddin F, Mahon PB, Jancic D, Pirooznia M, Steele J, Schweizer B, Goes FS, Mondimore FM, Mackinnon DF, Bipolar Genome Study Consortium None, Perlis RH, Lee PH, Huang J, Kelsoe JR, Shilling PD, Rietschel M, Nöthen M, Cichon S, Gurling H, Purcell S, Smoller JW, Craddock N, DePaulo JR, Schulze TG, McMahon FJ, Zandi PP, Potash JB, Mol Psychiatry, Volume 17, 4 (April 2012) pp.433-444
    • Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia.
      Grozeva D, Conrad DF, Barnes CP, Hurles M, Owen MJ, O'Donovan MC, Craddock N, Kirov G, WTCCC None, Schizophr Res, Volume 135, 1-3 (March 2012) pp.1-7
    • The relationship between childhood depressive symptoms and problem alcohol use in early adolescence: findings from a large longitudinal population-based study.
      Saraceno L, Heron J, Munafò M, Craddock N, van den Bree MB, Addiction, Volume 107, 3 (March 2012) pp.567-577
    • A twin study of schizoaffective-mania, schizoaffective-depression, and other psychotic syndromes.
      Cardno AG, Rijsdijk FV, West RM, Gottesman II, Craddock N, Murray RM, McGuffin P, Am J Med Genet B Neuropsychiatr Genet, Volume 159B, 2 (March 2012) pp.172-182
    • One minute with ... Nick Craddock
      Else L, Craddock N, New Scientist, Volume 213, 2853 (February 2012) pp.31-31
    • Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain.
      Richards AL, Jones L, Moskvina V, Kirov G, Gejman PV, Levinson DF, Sanders AR, Molecular Genetics of Schizophrenia Collaboration (MGS) None, International Schizophrenia Consortium (ISC) None, Purcell S, Visscher PM, Craddock N, Owen MJ, Holmans P, O'Donovan MC, Mol Psychiatry, Volume 17, 2 (February 2012) pp.193-201
    • Offspring of parents with recurrent depression: which features of parent depression index risk for offspring psychopathology?
      Mars B, Collishaw S, Smith D, Thapar A, Potter R, Sellers R, Harold GT, Craddock N, Rice F, Thapar A, J Affect Disord, Volume 136, 1-2 (January 2012) pp.44-53
    • The bicentennial volume of the British Journal of Psychiatry: the winding pathway of mental science.
      Tyrer P, Craddock N, Br J Psychiatry, Volume 200, 1 (January 2012) pp.1-4
    • Stressful life events and the serotonin transporter gene (5-HTT) in recurrent clinical depression.
      Fisher HL, Cohen-Woods S, Hosang GM, Uher R, Powell-Smith G, Keers R, Tropeano M, Korszun A, Jones L, Jones I, Owen M, Craddock N, Craig IW, Farmer AE, McGuffin P, J Affect Disord, Volume 136, 1-2 (January 2012) pp.189-193
    • DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder.
      Håvik B, Degenhardt FA, Johansson S, Fernandes CP, Hinney A, Scherag A, Lybæk H, Djurovic S, Christoforou A, Ersland KM, Giddaluru S, O'Donovan MC, Owen MJ, Craddock N, Mühleisen TW, Mattheisen M, Schimmelmann BG, Renner T, Warnke A, Herpertz-Dahlmann B, Sinzig J, Albayrak Ö, Rietschel M, Nöthen MM, Bramham CR, Werge T, Hebebrand J, Haavik J, Andreassen OA, Cichon S, Steen VM, Le Hellard S, Plos One, Volume 7, 4 (2012) p. e35424
    • The health informatics cohort enhancement project (HICE): using routinely collected primary care data to identify people with a lifetime diagnosis of psychotic disorder.
      Economou A, Grey M, McGregor J, Craddock N, Lyons RA, Owen MJ, Price V, Thomson S, Walters JT, Lloyd K, Bmc Res Notes, Volume 5 (2012) p. 95
    • Genome-wide association of mood-incongruent psychotic bipolar disorder.
      Goes FS, Hamshere ML, Seifuddin F, Pirooznia M, Belmonte-Mahon P, Breuer R, Schulze T, Nöthen M, Cichon S, Rietschel M, Holmans P, Zandi PP, Bipolar Genome Study (BiGS) None, Craddock N, Potash JB, Transl Psychiatry, Volume 2 (2012) p. e180
    • Suggested merger of mental and neurological illnesses is premature.
      Bailey S, Burn W, Craddock N, Mynors-Wallis L, Tyrer P, Bmj, Volume 345 (2012) p. e4577
    • 'Sifting the significance from the data' - the impact of high-throughput genomic technologies on human genetics and health care.
      Clarke AJ, Cooper DN, Krawczak M, Tyler-Smith C, Wallace HM, Wilkie AO, Raymond FL, Chadwick R, Craddock N, John R, Gallacher J, Chiano M, Hum Genomics, Volume 6 (2012) p. 11
  • 2011
    • Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia.
      Hamshere ML, Holmans PA, McCarthy GM, Jones LA, Murphy KC, Sanders RD, Gray MY, Zammit S, Williams NM, Norton N, Williams HJ, McGuffin P, O'Donovan MC, Craddock N, Owen MJ, Cardno AG, Am J Med Genet B Neuropsychiatr Genet, Volume 156B, 8 (December 2011) pp.929-940
    • Evaluation of an approximation method for assessment of overall significance of multiple-dependent tests in a genomewide association study.
      Moskvina V, O'Dushlaine C, Purcell S, Craddock N, Holmans P, O'Donovan MC, Genet Epidemiol, Volume 35, 8 (December 2011) pp.861-866
    • GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia.
      Chen X, Lee G, Maher BS, Fanous AH, Chen J, Zhao Z, Guo A, van den Oord E, Sullivan PF, Shi J, Levinson DF, Gejman PV, Sanders A, Duan J, Owen MJ, Craddock NJ, O'Donovan MC, Blackman J, Lewis D, Kirov GK, Qin W, Schwab S, Wildenauer D, Chowdari K, Nimgaonkar V, Straub RE, Weinberger DR, O'Neill FA, Walsh D, Bronstein M, Darvasi A, Lencz T, Malhotra AK, Rujescu D, Giegling I, Werge T, Hansen T, Ingason A, Nöethen MM, Rietschel M, Cichon S, Djurovic S, Andreassen OA, Cantor RM, Ophoff R, Corvin A, Morris DW, Gill M, Pato CN, Pato MT, Macedo A, Gurling HM, McQuillin A, Pimm J, Hultman C, Lichtenstein P, Sklar P, Purcell SM, Scolnick E, St Clair D, Blackwood DH, Kendler KS, GROUP investigators None, International Schizophrenia Consortium None, Mol Psychiatry, Volume 16, 11 (November 2011) pp.1117-1129
    • Common variants at VRK2 and TCF4 conferring risk of schizophrenia.
      Steinberg S, de Jong S, Irish Schizophrenia Genomics Consortium None, Andreassen OA, Werge T, Børglum AD, Mors O, Mortensen PB, Gustafsson O, Costas J, Pietiläinen OP, Demontis D, Papiol S, Huttenlocher J, Mattheisen M, Breuer R, Vassos E, Giegling I, Fraser G, Walker N, Tuulio-Henriksson A, Suvisaari J, Lönnqvist J, Paunio T, Agartz I, Melle I, Djurovic S, Strengman E, GROUP None, Jürgens G, Glenthøj B, Terenius L, Hougaard DM, Ørntoft T, Wiuf C, Didriksen M, Hollegaard MV, Nordentoft M, van Winkel R, Kenis G, Abramova L, Kaleda V, Arrojo M, Sanjuán J, Arango C, Sperling S, Rossner M, Ribolsi M, Magni V, Siracusano A, Christiansen C, Kiemeney LA, Veldink J, van den Berg L, Ingason A, Muglia P, Murray R, Nöthen MM, Sigurdsson E, Petursson H, Thorsteinsdottir U, Kong A, Rubino IA, De Hert M, Réthelyi JM, Bitter I, Jönsson EG, Golimbet V, Carracedo A, Ehrenreich H, Craddock N, Owen MJ, O'Donovan MC, Wellcome Trust Case Control Consortium 2 None, Ruggeri M, Tosato S, Peltonen L, Ophoff RA, Collier DA, St Clair D, Rietschel M, Cichon S, Stefansson H, Rujescu D, Stefansson K, Hum Mol Genet, Volume 20, 20 (October 2011) pp.4076-4081
    • Unipolar and bipolar depression: different or the same?
      Smith DJ, Craddock N, British Journal Of Psychiatry, Volume 199, 4 (October 2011) pp.272-274
    • Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.
      Psychiatric GWAS Consortium Bipolar Disorder Working Group None, Nat Genet, Volume 43, 10 (October 2011) pp.977-983
    • Genome-wide association study identifies five new schizophrenia loci.
      Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium None, Nat Genet, Volume 43, 10 (October 2011) pp.969-976
    • Horses for courses: the need for pragmatism and realism as well as balance and caution. A commentary on Angel.
      Craddock N, Soc Sci Med, Volume 73, 5 (September 2011) pp.636-638
    • Rediscovering the Bipolar Spectrum
      Altinbas K, Smith DJ, Craddock N, Noropsikiyatri Arsivi-Archives Of Neuropsychiatry, Volume 48, 3 (September 2011) pp.167-170
    • A follow-up case-control association study of tractable (druggable) genes in recurrent major depression.
      Schosser A, Gaysina D, Cohen-Woods S, Domenici E, Perry J, Tozzi F, Korszun A, Gunasinghe C, Gray J, Jones L, Binder EB, Holsboer F, Craddock N, Owen MJ, Craig IW, Farmer AE, Muglia P, McGuffin P, Am J Med Genet B Neuropsychiatr Genet, Volume 156B, 6 (September 2011) pp.640-650
    • A genome-wide significant linkage for severe depression on chromosome 3: the depression network study.
      Breen G, Webb BT, Butler AW, van den Oord EJ, Tozzi F, Craddock N, Gill M, Korszun A, Maier W, Middleton L, Mors O, Owen MJ, Cohen-Woods S, Perry J, Galwey NW, Upmanyu R, Craig I, Lewis CM, Ng M, Brewster S, Preisig M, Rietschel M, Jones L, Knight J, Rice J, Muglia P, Farmer AE, McGuffin P, Am J Psychiatry, Volume 168, 8 (August 2011) pp.840-847
    • Investigation of rare non-synonymous variants at ABCA13 in schizophrenia and bipolar disorder.
      Dwyer S, Williams H, Jones I, Jones L, Walters J, Craddock N, Owen MJ, O'Donovan MC, Mol Psychiatry, Volume 16, 8 (August 2011) pp.790-791
    • Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.
      Evans DM, Spencer CC, Pointon JJ, Su Z, Harvey D, Kochan G, Oppermann U, Dilthey A, Pirinen M, Stone MA, Appleton L, Moutsianas L, Leslie S, Wordsworth T, Kenna TJ, Karaderi T, Thomas GP, Ward MM, Weisman MH, Farrar C, Bradbury LA, Danoy P, Inman RD, Maksymowych W, Gladman D, Rahman P, Spondyloarthritis Research Consortium of Canada (SPARCC) None, Morgan A, Marzo-Ortega H, Bowness P, Gaffney K, Gaston JS, Smith M, Bruges-Armas J, Couto AR, Sorrentino R, Paladini F, Ferreira MA, Xu H, Liu Y, Jiang L, Lopez-Larrea C, Díaz-Peña R, López-Vázquez A, Zayats T, Band G, Bellenguez C, Blackburn H, Blackwell JM, Bramon E, Bumpstead SJ, Casas JP, Corvin A, Craddock N, Deloukas P, Dronov S, Duncanson A, Edkins S, Freeman C, Gillman M, Gray E, Gwilliam R, Hammond N, Hunt SE, Jankowski J, Jayakumar A, Langford C, Liddle J, Markus HS, Mathew CG, McCann OT, McCarthy MI, Palmer CN, Peltonen L, Plomin R, Potter SC, Rautanen A, Ravindrarajah R, Ricketts M, Samani N, Sawcer SJ, Strange A, Trembath RC, Viswanathan AC, Waller M, Weston P, Whittaker P, Widaa S, Wood NW, McVean G, Reveille JD, Wordsworth BP, Brown MA, Donnelly P, Australo-Anglo-American Spondyloarthritis Consortium (TASC) None, Wellcome Trust Case Control Consortium 2 (WTCCC2) None, Nat Genet, Volume 43, 8 (August 2011) pp.761-767
    • Beating Bipolar: exploratory trial of a novel Internet-based psychoeducational treatment for bipolar disorder.
      Smith DJ, Griffiths E, Poole R, di Florio A, Barnes E, Kelly MJ, Craddock N, Hood K, Simpson S, Bipolar Disord, Volume 13, 5-6 (August 2011) pp.571-577
    • An examination of single nucleotide polymorphism selection prioritization strategies for tests of gene-gene interaction.
      Moskvina V, Craddock N, Müller-Myhsok B, Kam-Thong T, Green E, Holmans P, Owen MJ, O'Donovan MC, Biol Psychiatry, Volume 70, 2 (July 2011) pp.198-203
    • At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia.
      Hansen T, Ingason A, Djurovic S, Melle I, Fenger M, Gustafsson O, Jakobsen KD, Rasmussen HB, Tosato S, Rietschel M, Frank J, Owen M, Bonetto C, Suvisaari J, Thygesen JH, Pétursson H, Lönnqvist J, Sigurdsson E, Giegling I, Craddock N, O'Donovan MC, Ruggeri M, Cichon S, Ophoff RA, Pietiläinen O, Peltonen L, Nöthen MM, Rujescu D, St Clair D, Collier DA, Andreassen OA, Werge T, Biol Psychiatry, Volume 70, 1 (July 2011) pp.59-63
    • Unrecognised bipolar disorder in primary care patients with depression.
      Smith DJ, Griffiths E, Kelly M, Hood K, Craddock N, Simpson SA, Br J Psychiatry, Volume 199, 1 (July 2011) pp.49-56
    • Independent evidence for the selective influence of GABA(A) receptors on one component of the bipolar disorder phenotype.
      Breuer R, Hamshere ML, Strohmaier J, Mattheisen M, Degenhardt F, Meier S, Paul T, O'Donovan MC, Mühleisen TW, Schulze TG, Nöthen MM, Cichon S, Craddock N, Rietschel M, Mol Psychiatry, Volume 16, 6 (June 2011) pp.587-589
    • Polymorphism of the 5-HT transporter and response to antidepressants: randomised controlled trial.
      Lewis G, Mulligan J, Wiles N, Cowen P, Craddock N, Ikeda M, Grozeva D, Mason V, Nutt D, Sharp D, Tallon D, Thomas L, O'Donovan MC, Peters TJ, Br J Psychiatry, Volume 198, 6 (June 2011) pp.464-471
    • DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls.
      Green EK, Grozeva D, Sims R, Raybould R, Forty L, Gordon-Smith K, Russell E, St Clair D, Young AH, Ferrier IN, Kirov G, Jones I, Jones L, Owen MJ, O'Donovan MC, Craddock N, Am J Med Genet B Neuropsychiatr Genet, Volume 156B, 4 (June 2011) pp.490-492
    • Polygenic dissection of the bipolar phenotype
      Hamshere ML, O'Donovan MC, Jones IR, Jones L, Kirov G, Green EK, Moskvina V, Grozeva D, Bass N, McQuillin A, Gurling H, St Clair D, Young AH, Ferrier IN, Farmer A, McGuffin P, Sklar P, Purcell S, Holmans PA, Owen MJ, Craddock N, British Journal Of Psychiatry, Volume 198, 4 (April 2011) pp.284-288
    • Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder.
      Belmonte Mahon P, Pirooznia M, Goes FS, Seifuddin F, Steele J, Lee PH, Huang J, Hamshere ML, Bipolar Genome Study (BiGS) Consortium, The Wellcome Trust Case Control Consortium Bipolar Disorder Group None, Depaulo JR, Kelsoe JR, Rietschel M, Nöthen M, Cichon S, Gurling H, Purcell S, Smoller JW, Craddock N, Schulze TG, McMahon FJ, Potash JB, Zandi PP, Am J Med Genet B Neuropsychiatr Genet, Volume 156B, 3 (April 2011) pp.370-378
    • Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder.
      Williams HJ, Norton N, Dwyer S, Moskvina V, Nikolov I, Carroll L, Georgieva L, Williams NM, Morris DW, Quinn EM, Giegling I, Ikeda M, Wood J, Lencz T, Hultman C, Lichtenstein P, Thiselton D, Maher BS, Molecular Genetics of Schizophrenia Collaboration (MGS) International Schizophrenia Consortium (ISC), SGENE-plus, GROUP None, Malhotra AK, Riley B, Kendler KS, Gill M, Sullivan P, Sklar P, Purcell S, Nimgaonkar VL, Kirov G, Holmans P, Corvin A, Rujescu D, Craddock N, Owen MJ, O'Donovan MC, Mol Psychiatry, Volume 16, 4 (April 2011) pp.429-441
    • Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness.
      Ingason A, Kirov G, Giegling I, Hansen T, Isles AR, Jakobsen KD, Kristinsson KT, le Roux L, Gustafsson O, Craddock N, Möller HJ, McQuillin A, Muglia P, Cichon S, Rietschel M, Ophoff RA, Djurovic S, Andreassen OA, Pietiläinen OP, Peltonen L, Dempster E, Collier DA, St Clair D, Rasmussen HB, Glenthøj BY, Kiemeney LA, Franke B, Tosato S, Bonetto C, Saemundsen E, Hreidarsson SJ, GROUP Investigators None, Nöthen MM, Gurling H, O'Donovan MC, Owen MJ, Sigurdsson E, Petursson H, Stefansson H, Rujescu D, Stefansson K, Werge T, Am J Psychiatry, Volume 168, 4 (April 2011) pp.408-417
    • Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder.
      Cichon S, Mühleisen TW, Degenhardt FA, Mattheisen M, Miró X, Strohmaier J, Steffens M, Meesters C, Herms S, Weingarten M, Priebe L, Haenisch B, Alexander M, Vollmer J, Breuer R, Schmäl C, Tessmann P, Moebus S, Wichmann HE, Schreiber S, Müller-Myhsok B, Lucae S, Jamain S, Leboyer M, Bellivier F, Etain B, Henry C, Kahn JP, Heath S, Bipolar Disorder Genome Study (BiGS) Consortium None, Hamshere M, O'Donovan MC, Owen MJ, Craddock N, Schwarz M, Vedder H, Kammerer-Ciernioch J, Reif A, Sasse J, Bauer M, Hautzinger M, Wright A, Mitchell PB, Schofield PR, Montgomery GW, Medland SE, Gordon SD, Martin NG, Gustafsson O, Andreassen O, Djurovic S, Sigurdsson E, Steinberg S, Stefansson H, Stefansson K, Kapur-Pojskic L, Oruc L, Rivas F, Mayoral F, Chuchalin A, Babadjanova G, Tiganov AS, Pantelejeva G, Abramova LI, Grigoroiu-Serbanescu M, Diaconu CC, Czerski PM, Hauser J, Zimmer A, Lathrop M, Schulze TG, Wienker TF, Schumacher J, Maier W, Propping P, Rietschel M, Nöthen MM, Am J Hum Genet, Volume 88, 3 (March 2011) pp.372-381
    • Genome-wide association study of schizophrenia in a Japanese population.
      Ikeda M, Aleksic B, Kinoshita Y, Okochi T, Kawashima K, Kushima I, Ito Y, Nakamura Y, Kishi T, Okumura T, Fukuo Y, Williams HJ, Hamshere ML, Ivanov D, Inada T, Suzuki M, Hashimoto R, Ujike H, Takeda M, Craddock N, Kaibuchi K, Owen MJ, Ozaki N, O'Donovan MC, Iwata N, Biol Psychiatry, Volume 69, 5 (March 2011) pp.472-478
    • Neurodevelopmental hypothesis of schizophrenia.
      Owen MJ, O'Donovan MC, Thapar A, Craddock N, Br J Psychiatry, Volume 198, 3 (March 2011) pp.173-175
    • Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes.
      GoDARTS and UKPDS Diabetes Pharmacogenetics Study Group None, Wellcome Trust Case Control Consortium 2 None, Zhou K, Bellenguez C, Spencer CC, Bennett AJ, Coleman RL, Tavendale R, Hawley SA, Donnelly LA, Schofield C, Groves CJ, Burch L, Carr F, Strange A, Freeman C, Blackwell JM, Bramon E, Brown MA, Casas JP, Corvin A, Craddock N, Deloukas P, Dronov S, Duncanson A, Edkins S, Gray E, Hunt S, Jankowski J, Langford C, Markus HS, Mathew CG, Plomin R, Rautanen A, Sawcer SJ, Samani NJ, Trembath R, Viswanathan AC, Wood NW, MAGIC investigators None, Harries LW, Hattersley AT, Doney AS, Colhoun H, Morris AD, Sutherland C, Hardie DG, Peltonen L, McCarthy MI, Holman RR, Palmer CN, Donnelly P, Pearson ER, Nat Genet, Volume 43, 2 (February 2011) pp.117-120
    • Developing an online psychoeducation package for bipolar disorder.
      Barnes E, Simpson S, Griffiths E, Hood K, Craddock N, Smith DJ, J Ment Health, Volume 20, 1 (February 2011) pp.21-31
    • Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.
      UK Parkinson's Disease Consortium None, Wellcome Trust Case Control Consortium 2 None, Spencer CC, Plagnol V, Strange A, Gardner M, Paisan-Ruiz C, Band G, Barker RA, Bellenguez C, Bhatia K, Blackburn H, Blackwell JM, Bramon E, Brown MA, Brown MA, Burn D, Casas JP, Chinnery PF, Clarke CE, Corvin A, Craddock N, Deloukas P, Edkins S, Evans J, Freeman C, Gray E, Hardy J, Hudson G, Hunt S, Jankowski J, Langford C, Lees AJ, Markus HS, Mathew CG, McCarthy MI, Morrison KE, Palmer CN, Pearson JP, Peltonen L, Pirinen M, Plomin R, Potter S, Rautanen A, Sawcer SJ, Su Z, Trembath RC, Viswanathan AC, Williams NW, Morris HR, Donnelly P, Wood NW, Hum Mol Genet, Volume 20, 2 (January 2011) pp.345-353
    • Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries.
      Williams HJ, Craddock N, Russo G, Hamshere ML, Moskvina V, Dwyer S, Smith RL, Green E, Grozeva D, Holmans P, Owen MJ, O'Donovan MC, Hum Mol Genet, Volume 20, 2 (January 2011) pp.387-391
    • Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.
      Liu Y, Blackwood DH, Caesar S, de Geus EJ, Farmer A, Ferreira MA, Ferrier IN, Fraser C, Gordon-Smith K, Green EK, Grozeva D, Gurling HM, Hamshere ML, Heutink P, Holmans PA, Hoogendijk WJ, Hottenga JJ, Jones L, Jones IR, Kirov G, Lin D, McGuffin P, Moskvina V, Nolen WA, Perlis RH, Posthuma D, Scolnick EM, Smit AB, Smit JH, Smoller JW, St Clair D, van Dyck R, Verhage M, Willemsen G, Young AH, Zandbelt T, Boomsma DI, Craddock N, O'Donovan MC, Owen MJ, Penninx BW, Purcell S, Sklar P, Sullivan PF, Wellcome Trust Case-Control Consortium None, Mol Psychiatry, Volume 16, 1 (January 2011) pp.2-4
    • Genomewide association scan of suicidal thoughts and behaviour in major depression.
      Schosser A, Butler AW, Ising M, Perroud N, Uher R, Ng MY, Cohen-Woods S, Craddock N, Owen MJ, Korszun A, Jones L, Jones I, Gill M, Rice JP, Maier W, Mors O, Rietschel M, Lucae S, Binder EB, Preisig M, Perry J, Tozzi F, Muglia P, Aitchison KJ, Breen G, Craig IW, Farmer AE, Müller-Myhsok B, McGuffin P, Lewis CM, Plos One, Volume 6, 7 (2011) p. e20690
    • Methylenetetrahydrofolate reductase gene variant (MTHFR C677T) and migraine: a case control study and meta-analysis.
      Samaan Z, Gaysina D, Cohen-Woods S, Craddock N, Jones L, Korszun A, Owen M, Mente A, McGuffin P, Farmer A, Bmc Neurol, Volume 11 (2011) p. 66
  • 2010
    • Identification of high risk DISC1 protein structural variants in patients with bipolar spectrum disorder.
      Song W, Li W, Noltner K, Yan J, Green E, Grozeva D, Jones IR, Craddock N, Longmate J, Feng J, Sommer SS, Neurosci Lett, Volume 486, 3 (December 2010) pp.136-140
    • A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12.
      Butler AW, Breen G, Tozzi F, Craddock N, Gill M, Korszun A, Maier W, Middleton LT, Mors O, Owen MJ, Perry J, Preisig M, Rice JP, Rietschel M, Jones L, Farmer AE, Lewis CM, McGuffin P, Am J Med Genet B Neuropsychiatr Genet, Volume 153B, 8 (December 2010) pp.1465-1473
    • No evidence that rare coding variants in ZNF804A confer risk of schizophrenia.
      Dwyer S, Williams H, Holmans P, Moskvina V, Craddock N, Owen MJ, O'Donovan MC, Am J Med Genet B Neuropsychiatr Genet, Volume 153B, 8 (December 2010) pp.1411-1416
    • Genome-wide association study of suicide attempts in mood disorder patients.
      Perlis RH, Huang J, Purcell S, Fava M, Rush AJ, Sullivan PF, Hamilton SP, McMahon FJ, Schulze TG, Potash JB, Zandi PP, Willour VL, Penninx BW, Boomsma DI, Vogelzangs N, Middeldorp CM, Rietschel M, Nöthen M, Cichon S, Gurling H, Bass N, McQuillin A, Hamshere M, Wellcome Trust Case Control Consortium Bipolar Disorder Group None, Craddock N, Sklar P, Smoller JW, Am J Psychiatry, Volume 167, 12 (December 2010) pp.1499-1507
    • Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha.
      Carroll LS, Williams NM, Moskvina V, Russell E, Norton N, Williams HJ, Peirce T, Georgieva L, Dwyer S, Grozeva D, Greene E, Farmer A, McGuffin P, Morris DW, Corvin A, Gill M, Rujescu D, Sham P, Holmans P, Jones I, Kirov G, Craddock N, O'Donovan MC, Owen MJ, Mol Psychiatry, Volume 15, 11 (November 2010) pp.1101-1111
    • Genome wide association scan of co-morbid anxiety in major depressive disorder (MDD)
      Schosser A, Ng MY, Butler AW, Uher R, Cohen-Woods S, Craddock N, Owen M, Aitchison KJ, Breen G, Craig I, Farmer AE, Lewis CM, McGuffin P, International Journal Of Psychiatry In Clinical Practice, Volume 14 (November 2010) pp.37-37
    • The Bipolar Association Case-Control Study (BACCS) and meta-analysis: No association with the 5,10-Methylenetetrahydrofolate reductase gene and bipolar disorder.
      Cohen-Woods S, Craig I, Gaysina D, Gray J, Gunasinghe C, Craddock N, Elkin A, Jones L, Kennedy J, King N, Korszun A, Knight J, Owen M, Parikh S, Strauss J, Sterne A, Tozzi F, Perry J, Muglia P, Vincent J, McGuffin P, Farmer A, Am J Med Genet B Neuropsychiatr Genet, Volume 153B, 7 (October 2010) pp.1298-1304
    • Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder.
      Green EK, Grozeva D, Moskvina V, Hamshere ML, Jones IR, Jones L, Forty L, Caesar S, Gordon-Smith K, Fraser C, Russell E, St Clair D, Young AH, Ferrier N, Farmer A, McGuffin P, Holmans PA, Owen MJ, O'Donovan MC, Craddock N, Am J Med Genet B Neuropsychiatr Genet, Volume 153B, 7 (October 2010) pp.1347-1349
    • The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia.
      Green EK, Grozeva D, Jones I, Jones L, Kirov G, Caesar S, Gordon-Smith K, Fraser C, Forty L, Russell E, Hamshere ML, Moskvina V, Nikolov I, Farmer A, McGuffin P, Wellcome Trust Case Control Consortium None, Holmans PA, Owen MJ, O'Donovan MC, Craddock N, Mol Psychiatry, Volume 15, 10 (October 2010) pp.1016-1022
    • The neuropsychiatric phenotype in Darier disease
      Gordon-Smith K, Jones LA, Burge SM, Munro CS, Tavadia S, Craddock N, British Journal Of Dermatology, Volume 163, 3 (September 2010) pp.515-522
    • Data and clinical utility should be the drivers of changes to psychiatric classification.
      Craddock N, Owen MJ, Br J Psychiatry, Volume 197, 2 (August 2010) p. 158
    • Reducing the Hypomania Checklist (HCL-32) to a 16-item version.
      Forty L, Kelly M, Jones L, Jones I, Barnes E, Caesar S, Fraser C, Gordon-Smith K, Griffiths E, Craddock N, Smith DJ, J Affect Disord, Volume 124, 3 (August 2010) pp.351-356
    • Genome-wide association study of major recurrent depression in the U.K. population.
      Lewis CM, Ng MY, Butler AW, Cohen-Woods S, Uher R, Pirlo K, Weale ME, Schosser A, Paredes UM, Rivera M, Craddock N, Owen MJ, Jones L, Jones I, Korszun A, Aitchison KJ, Shi J, Quinn JP, Mackenzie A, Vollenweider P, Waeber G, Heath S, Lathrop M, Muglia P, Barnes MR, Whittaker JC, Tozzi F, Holsboer F, Preisig M, Farmer AE, Breen G, Craig IW, McGuffin P, Am J Psychiatry, Volume 167, 8 (August 2010) pp.949-957
    • Association of DISC1 and TSNAX genes and affective disorders in the depression case-control (DeCC) and bipolar affective case-control (BACCS) studies.
      Schosser A, Gaysina D, Cohen-Woods S, Chow PC, Martucci L, Craddock N, Farmer A, Korszun A, Gunasinghe C, Gray J, Jones L, Tozzi F, Perry J, Muglia P, Owen MJ, Craig IW, McGuffin P, Mol Psychiatry, Volume 15, 8 (August 2010) pp.844-849
    • Molecular genetics and the relationship between epilepsy and psychosis.
      Craddock N, Owen MJ, Br J Psychiatry, Volume 197, 1 (July 2010) pp.75-76
    • Suggestion of roles for both common and rare risk variants in genome-wide studies of schizophrenia.
      Owen MJ, Craddock N, O'Donovan MC, Arch Gen Psychiatry, Volume 67, 7 (July 2010) pp.667-673
    • Genome-wide association studies: a primer.
      Corvin A, Craddock N, Sullivan PF, Psychol Med, Volume 40, 7 (July 2010) pp.1063-1077
    • A systematic association mapping on chromosome 6q in bipolar affective disorder--evidence for the melanin-concentrating-hormone-receptor-2 gene as a risk factor for bipolar affective disorder.
      Abou Jamra R, Schulze TG, Becker T, Brockschmidt FF, Green E, Alblas MA, Wendland JR, Adli M, Grozeva D, Strohmeier J, Georgi A, Craddock N, Propping P, Rietschel M, Nöthen MM, Cichon S, Schumacher J, Am J Med Genet B Neuropsychiatr Genet, Volume 153B, 4 (June 2010) pp.878-884
    • Revisiting Bleuler: relationship between autism and schizophrenia Reply
      Craddock N, Owen MJ, British Journal Of Psychiatry, Volume 196, 6 (June 2010) pp.495-496
    • Affective temperaments across the bipolar-unipolar spectrum: examination of the TEMPS-A in 927 patients and controls.
      Di Florio A, Hamshere M, Forty L, Green EK, Grozeva D, Jones I, Caesar S, Fraser C, Gordon-Smith K, Jones L, Craddock N, Smith DJ, J Affect Disord, Volume 123, 1-3 (June 2010) pp.42-51
    • A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia.
      Ingason A, Giegling I, Cichon S, Hansen T, Rasmussen HB, Nielsen J, Jürgens G, Muglia P, Hartmann AM, Strengman E, Vasilescu C, Mühleisen TW, Djurovic S, Melle I, Lerer B, Möller HJ, Francks C, Pietiläinen OP, Lonnqvist J, Suvisaari J, Tuulio-Henriksson A, Walshe M, Vassos E, Di Forti M, Murray R, Bonetto C, Tosato S, GROUP Investigators None, Cantor RM, Rietschel M, Craddock N, Owen MJ, Peltonen L, Andreassen OA, Nöthen MM, St Clair D, Ophoff RA, O'Donovan MC, Collier DA, Werge T, Rujescu D, Hum Mol Genet, Volume 19, 7 (April 2010) pp.1379-1386
    • Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
      Craddock N, Hurles ME, Cardin N, Pearson RD, Plagnol V, Robson S, Vukcevic D, Barnes C, Conrad DF, Giannoulatou E, Holmes C, Marchini JL, Stirrups K, Tobin MD, Wain LV, Yau C, Aerts J, Ahmad T, Andrews TD, Arbury H, Attwood A, Auton A, Ball SG, Balmforth AJ, Barrett JC, Barroso I, Barton A, Bennett AJ, Bhaskar S, Blaszczyk K, Bowes J, Brand OJ, Braund PS, Bredin F, Breen G, Brown MJ, Bruce IN, Bull J, Burren OS, Burton J, Byrnes J, Caesar S, Clee CM, Coffey AJ, Connell JMC, Cooper JD, Dominiczak AF, Downes K, Drummond HE, Dudakia D, Dunham A, Ebbs B, Eccles D, Edkins S, Edwards C, Elliot A, Emery P, Evans DM, Evans G, Eyre S, Farmer A, Ferrier IN, Feuk L, Fitzgerald T, Flynn E, Forbes A, Forty L, Franklyn JA, Freathy RM, Gibbs P, Gilbert P, Gokumen O, Gordon-Smith K, Gray E, Green E, Groves CJ, Grozeva D, Gwilliam R, Hall A, Hammond N, Hardy M, Harrison P, Hassanali N, Hebaishi H, Hines S, Hinks A, Hitman GA, Hocking L, Howard E, Howard P, Howson JMM, Hughes D, Hunt S, Isaacs JD, Jain M, Jewell DP, Johnson T, Jolley JD, Jones IR, Jones LA, Kirov G, Langford CF, Lango-Allen H, Lathrop GM, Lee J, Lee KL, Lees C, Lewis K, Lindgren CM, Maisuria-Armer M, Maller J, Mansfield J, Martin P, Massey DCO, McArdle WL, McGuffin P, McLay KE, Mentzer A, Mimmack ML, Morgan AE, Morris AP, Mowat C, Myers S, Newman W, Nimmo ER, O'Donovan MC, Onipinla A, Onyiah I, Ovington NR, Owen MJ, Palin K, Parnell K, Pernet D, Perry JRB, Phillips A, Pinto D, Prescott NJ, Prokopenko I, Quail MA, Rafelt S, Rayner NW, Redon R, Reid DM, Renwick A, Ring SM, Robertson N, Russell E, St Clair D, Sambrook JG, Sanderson JD, Schuilenburg H, Scott CE, Scott R, Seal S, Shaw-Hawkins S, Shields BM, Simmonds MJ, Smyth DJ, Somaskantharajah E, Spanova K, Steer S, Stephens J, Stevens HE, Stone MA, Su Z, Symmons DPM, Thompson JR, Thomson W, Travers ME, Turnbull C, Valsesia A, Walker M, Walker NM, Wallace C, Warren-Perry M, Watkins NA, Webster J, Weedon MN, Wilson AG, Woodburn M, Wordsworth BP, Young AH, Zeggini E, Carter NP, Frayling TM, Lee C, McVean G, Munroe PB, Palotie A, Sawcer SJ, Scherer SW, Strachan DP, Tyler-Smith C, Brown MA, Burton PR, Caulfield MJ, Compston A, Farrall M, Gough SCL, Hall AS, Hattersley AT, Hill AVS, Mathew CG, Pembrey M, Satsangi J, Stratton MR, Worthington J, Deloukas P, Duncanson A, Kwiatkowski DP, McCarthy MI, Ouwehand WH, Parkes M, Rahman N, Todd JA, Samani NJ, Donnelly P, Control WTC, Nature, Volume 464, 7289 (April 2010) pp.713-U86
    • Predicting response to lithium in bipolar disorder: a critical review of pharmacogenetic studies.
      Smith DJ, Evans R, Craddock N, J Ment Health, Volume 19, 2 (April 2010) pp.142-156
    • Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.
      Grozeva D, Kirov G, Ivanov D, Jones IR, Jones L, Green EK, St Clair DM, Young AH, Ferrier N, Farmer AE, McGuffin P, Holmans PA, Owen MJ, O'Donovan MC, Craddock N, Wellcome Trust Case Control Consortium None, Arch Gen Psychiatry, Volume 67, 4 (April 2010) pp.318-327
    • Cognitive style, personality and vulnerability to postnatal depression.
      Jones L, Scott J, Cooper C, Forty L, Smith KG, Sham P, Farmer A, McGuffin P, Craddock N, Jones I, Br J Psychiatry, Volume 196, 3 (March 2010) pp.200-205
    • Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype.
      Craddock N, Jones L, Jones IR, Kirov G, Green EK, Grozeva D, Moskvina V, Nikolov I, Hamshere ML, Vukcevic D, Caesar S, Gordon-Smith K, Fraser C, Russell E, Norton N, Breen G, St Clair D, Collier DA, Young AH, Ferrier IN, Farmer A, McGuffin P, Holmans PA, Wellcome Trust Case Control Consortium (WTCCC) None, Donnelly P, Owen MJ, O'Donovan MC, Mol Psychiatry, Volume 15, 2 (February 2010) pp.146-153
    • The Kraepelinian dichotomy - going, going... but still not gone.
      Craddock N, Owen MJ, Br J Psychiatry, Volume 196, 2 (February 2010) pp.92-95
    • Molecular Genetics and the Kraepelinian Dichotomy: One Disorder, Two Disorders, or Do We Need to Start Thinking Afresh?
      Craddock N, Owen MJ, Psychiatric Annals, Volume 40, 2 (February 2010) pp.88-91
    • Patients must be able to derive maximum benefit from a psychiatrist's medical skills and broad training.
      Craddock N, Craddock B, World Psychiatry, Volume 9, 1 (February 2010) pp.30-31
    • NRG1 gene in recurrent major depression: no association in a large-scale case-control association study.
      Schosser A, Cohen-Woods S, Gaysina D, Chow PC, Martucci L, Farmer A, Korszun A, Gunashinghe C, Gray J, Jones L, Craddock N, Owen MJ, Craig IW, McGuffin P, Am J Med Genet B Neuropsychiatr Genet, Volume 153B, 1 (January 2010) pp.141-147
  • 2009
    • P2RX7: A bipolar and unipolar disorder candidate susceptibility gene?
      Green EK, Grozeva D, Raybould R, Elvidge G, Macgregor S, Craig I, Farmer A, McGuffin P, Forty L, Jones L, Jones I, O'Donovan MC, Owen MJ, Kirov G, Craddock N, Am J Med Genet B Neuropsychiatr Genet, Volume 150B, 8 (December 2009) pp.1063-1069
    • Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region
      Barrett JC, Lee JC, Lees CW, Prescott NJ, Anderson CA, Phillips A, Wesley E, Parnell K, Zhang H, Drummond H, Nimmo ER, Massey D, Blaszczyk K, Elliott T, Cotterill L, Dallal H, Lobo AJ, Mowat C, Sanderson JD, Jewell DP, Newman WG, Edwards C, Ahmad T, Mansfield JC, Satsangi J, Parkes M, Mathew CG, Donnelly P, Peltonen L, Blackwell JM, Bramon E, Brown MA, Casas JP, Corvin A, Craddock N, Deloukas P, Duncanson A, Jankowski J, Markus HS, McCarthy MI, Palmer CNA, Plomin R, Rautanen A, Sawcer SJ, Samani N, Trembath RC, Viswanathan AC, Wood N, Spencer CCA, Bellenguez C, Davison D, Freeman C, Strange A, Langford C, Hunt SE, Edkins S, Gwilliam R, Blackburn H, Bumpstead SJ, Dronov S, Gillman M, Gray E, Hammond N, Jayakumar A, McCann OT, Liddle J, Perez ML, Potter SC, Ravindrarajah R, Ricketts M, Waller M, Weston P, Widaa S, Whittaker P, Attwood AP, Stephens J, Sambrook J, Ouwehand WH, McArdle WL, Ring SM, Strachan DP, Consortium UKIBDG, Consor WTCC, Comm M, Grp DA, Informatics DNAGDQC, Comm P, Controls UKBS, Controls 1BC, Nature Genetics, Volume 41, 12 (December 2009) pp.1330-1U99
    • Microduplications of 16p11.2 are associated with schizophrenia.
      McCarthy SE, Makarov V, Kirov G, Addington AM, McClellan J, Yoon S, Perkins DO, Dickel DE, Kusenda M, Krastoshevsky O, Krause V, Kumar RA, Grozeva D, Malhotra D, Walsh T, Zackai EH, Kaplan P, Ganesh J, Krantz ID, Spinner NB, Roccanova P, Bhandari A, Pavon K, Lakshmi B, Leotta A, Kendall J, Lee YH, Vacic V, Gary S, Iakoucheva LM, Crow TJ, Christian SL, Lieberman JA, Stroup TS, Lehtimäki T, Puura K, Haldeman-Englert C, Pearl J, Goodell M, Willour VL, Derosse P, Steele J, Kassem L, Wolff J, Chitkara N, McMahon FJ, Malhotra AK, Potash JB, Schulze TG, Nöthen MM, Cichon S, Rietschel M, Leibenluft E, Kustanovich V, Lajonchere CM, Sutcliffe JS, Skuse D, Gill M, Gallagher L, Mendell NR, Wellcome Trust Case Control Consortium None, Craddock N, Owen MJ, O'Donovan MC, Shaikh TH, Susser E, Delisi LE, Sullivan PF, Deutsch CK, Rapoport J, Levy DL, King MC, Sebat J, Nat Genet, Volume 41, 11 (November 2009) pp.1223-1227
    • Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31.
      Hamshere ML, Schulze TG, Schumacher J, Corvin A, Owen MJ, Jamra RA, Propping P, Maier W, Orozco y Diaz G, Mayoral F, Rivas F, Jones I, Jones L, Kirov G, Gill M, Holmans PA, Nöthen MM, Cichon S, Rietschel M, Craddock N, Bipolar Disord, Volume 11, 6 (September 2009) pp.610-620
    • Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
      Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan PF, Sklar P, Ruderfer DM, McQuillin A, Morris DW, O'Dushlaine CT, Corvin A, Holmans PA, Macgregor S, Gurling H, Blackwood DHR, Corvin A, Craddock NJ, Gill M, Hultman CM, Kirov GK, Lichtenstein P, Muir WJ, Owen MJ, Pato CN, Scolnick EM, St Clair D, Craddock NJ, Holmans PA, Williams NM, Georgieva L, Nikolov I, Norton N, Williams H, Toncheva D, Milanova V, Hultman CM, Lichtenstein P, Thelander EF, Sullivan P, Kenny E, Quinn EM, Gill M, Corvin A, Choudhury K, Datta S, Pimm J, Thirumalai S, Puri V, Krasucki R, Lawrence J, Quested D, Bass N, Crombie C, Fraser G, Kuan SL, Walker N, Blackwood DHR, Muir WJ, McGhee KA, Pickard B, Malloy P, Maclean AW, Van Beck M, Wray NR, Macgregor S, Visscher PM, Pato MT, Medeiros H, Middleton F, Carvalho C, Morley C, Fanous A, Conti D, Knowles JA, Ferreira CP, Macedo A, Azevedo MH, Kirby AN, Ferreira MAR, Daly MJ, Chambert K, Kuruvilla F, Gabriel SB, Ardlie K, Moran JL, Daly MJ, Scolnick EM, Nature, Volume 460, 7256 (August 2009) pp.748-752
    • Dissecting the phenotype in genome-wide association studies of psychiatric illness.
      Cross-Disorder Phenotype Group of the Psychiatric GWAS Consortium None, Craddock N, Kendler K, Neale M, Nurnberger J, Purcell S, Rietschel M, Perlis R, Santangelo SL, Schulze TG, Smoller JW, Thapar A, Br J Psychiatry, Volume 195, 2 (August 2009) pp.97-99
    • Depression, migraine with aura and migraine without aura: their familiality and interrelatedness
      Ball HA, Samaan Z, Brewster S, Craddock N, Gill M, Korszun A, Maier W, Middleton L, Mors O, Owen MJ, Perry J, Preisig M, Rice J, Rietschel M, Jones L, Jones I, Farmer AE, McGuffin P, Cephalalgia, Volume 29, 8 (August 2009) pp.848-854
    • Genetics of psychosis; insights from views across the genome.
      O'Donovan MC, Craddock NJ, Owen MJ, Hum Genet, Volume 126, 1 (July 2009) pp.3-12
    • Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept.
      Hamshere ML, Green EK, Jones IR, Jones L, Moskvina V, Kirov G, Grozeva D, Nikolov I, Vukcevic D, Caesar S, Gordon-Smith K, Fraser C, Russell E, Breen G, St Clair D, Collier DA, Young AH, Ferrier IN, Farmer A, McGuffin P, Wellcome Trust Case Control Consortium None, Holmans PA, Owen MJ, O'Donovan MC, Craddock N, Br J Psychiatry, Volume 195, 1 (July 2009) pp.23-29
    • Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder.
      Holmans P, Green EK, Pahwa JS, Ferreira MA, Purcell SM, Sklar P, Wellcome Trust Case-Control Consortium None, Owen MJ, O'Donovan MC, Craddock N, Am J Hum Genet, Volume 85, 1 (July 2009) pp.13-24
    • Age-at-onset in bipolar-I disorder: mixture analysis of 1369 cases identifies three distinct clinical sub-groups.
      Hamshere ML, Gordon-Smith K, Forty L, Jones L, Caesar S, Fraser C, Hyde S, Tredget J, Kirov G, Jones I, Craddock N, Smith DJ, J Affect Disord, Volume 116, 1-2 (July 2009) pp.23-29
    • Genetic and non-genetic influences on the development of co-occurring alcohol problem use and internalizing symptomatology in adolescence: a review.
      Saraceno L, Munafó M, Heron J, Craddock N, van den Bree MB, Addiction, Volume 104, 7 (July 2009) pp.1100-1121
    • A longitudinal study of hypomania and depression symptoms in pregnancy and the postpartum period.
      Heron J, Haque S, Oyebode F, Craddock N, Jones I, Bipolar Disord, Volume 11, 4 (June 2009) pp.410-417
    • Genomewide association studies: history, rationale, and prospects for psychiatric disorders.
      Psychiatric GWAS Consortium Coordinating Committee None, Cichon S, Craddock N, Daly M, Faraone SV, Gejman PV, Kelsoe J, Lehner T, Levinson DF, Moran A, Sklar P, Sullivan PF, Am J Psychiatry, Volume 166, 5 (May 2009) pp.540-556
    • Psychosis genetics: modeling the relationship between schizophrenia, bipolar disorder, and mixed (or "schizoaffective") psychoses.
      Craddock N, O'Donovan MC, Owen MJ, Schizophr Bull, Volume 35, 3 (May 2009) pp.482-490
    • Clinical characteristics of unipolar disorder and bipolar disorder according to the lifetime presence of recurrent panic attacks.
      Forty L, Smith D, Jones L, Jones I, Caesar S, Cooper C, Fraser C, Gordon-Smith K, Hyde S, Farmer A, McGuffin P, Craddock N, Bipolar Disord, Volume 11, 3 (May 2009) pp.307-315
    • Support for the involvement of large copy number variants in the pathogenesis of schizophrenia.
      Kirov G, Grozeva D, Norton N, Ivanov D, Mantripragada KK, Holmans P, International Schizophrenia Consortium None, Wellcome Trust Case Control Consortium None, Craddock N, Owen MJ, O'Donovan MC, Hum Mol Genet, Volume 18, 8 (April 2009) pp.1497-1503
    • Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder
      Cohen-Woods S, Gaysina D, Craddock N, Farmer A, Gray J, Gunasinghe C, Hoda F, Jones L, Knight J, Korszun A, Owen MJ, Sterne A, Craig IW, McGuffin P, Human Molecular Genetics, Volume 18, 8 (April 2009) pp.1504-1509
    • Sub-threshold manic symptoms in recurrent major depressive disorder are a marker for poor outcome.
      Smith DJ, Forty L, Russell E, Caesar S, Walters J, Cooper C, Jones I, Jones L, Craddock N, Acta Psychiatr Scand, Volume 119, 4 (April 2009) pp.325-329
    • Migraine in recurrent depression: case-control study
      Samaan Z, Farmer A, Craddock N, Jones L, Korszun A, Owen M, McGuffin P, British Journal Of Psychiatry, Volume 194, 4 (April 2009) pp.350-354
    • Identifying hypomanic features in major depressive disorder using the hypomania checklist (HCL-32).
      Forty L, Smith D, Jones L, Jones I, Caesar S, Fraser C, Gordon-Smith K, Craddock N, J Affect Disord, Volume 114, 1-3 (April 2009) pp.68-73
    • Is depression severity the sole cause of psychotic symptoms during an episode of unipolar major depression? A study both between and within subjects.
      Forty L, Jones L, Jones I, Cooper C, Russell E, Farmer A, McGuffin P, Craddock N, J Affect Disord, Volume 114, 1-3 (April 2009) pp.103-109
    • Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk.
      Moskvina V, Craddock N, Holmans P, Nikolov I, Pahwa JS, Green E, Wellcome Trust Case Control Consortium None, Owen MJ, O'Donovan MC, Mol Psychiatry, Volume 14, 3 (March 2009) pp.252-260
    • Genetics of bipolar disorder: successful start to a long journey.
      Craddock N, Sklar P, Trends Genet, Volume 25, 2 (February 2009) pp.99-105
    • Polarity at illness onset in bipolar I disorder and clinical course of illness.
      Forty L, Jones L, Jones I, Smith DJ, Caesar S, Fraser C, Gordon-Smith K, Hyde S, Craddock N, Bipolar Disord, Volume 11, 1 (February 2009) pp.82-88
    • Diagnosis of functional psychoses: time to face the future.
      Owen MJ, Craddock N, Lancet, Volume 373, 9659 (January 2009) pp.190-191
    • Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.
      O'Donovan MC, Norton N, Williams H, Peirce T, Moskvina V, Nikolov I, Hamshere M, Carroll L, Georgieva L, Dwyer S, Holmans P, Marchini JL, Spencer CC, Howie B, Leung HT, Giegling I, Hartmann AM, Möller HJ, Morris DW, Shi Y, Feng G, Hoffmann P, Propping P, Vasilescu C, Maier W, Rietschel M, Zammit S, Schumacher J, Quinn EM, Schulze TG, Iwata N, Ikeda M, Darvasi A, Shifman S, He L, Duan J, Sanders AR, Levinson DF, Adolfsson R, Osby U, Terenius L, Jönsson EG, Cichon S, Nöthen MM, Gill M, Corvin AP, Rujescu D, Gejman PV, Kirov G, Craddock N, Williams NM, Owen MJ, Molecular Genetics of Schizophrenia Collaboration None, Mol Psychiatry, Volume 14, 1 (January 2009) pp.30-36
    • A framework for interpreting genome-wide association studies of psychiatric disorders The Psychiatric GWAS Consortium Steering Committee
      Cichon S, Craddock N, Daly M, Faraone SV, Gejman PV, Kelsoe J, Lehner T, Levinson DF, Moran A, Sklar P, Sullivan PF, Steeri PGWASC, Molecular Psychiatry, Volume 14, 1 (January 2009) pp.10-17
    • Strong evidence for multiple psychosis susceptibility genes - a rejoinder to Crow.
      O'Donovan MC, Craddock N, Owen MJ, Psychol Med, Volume 39, 1 (January 2009) pp.170-171
    • The Bipolar Interactive Psychoeducation (BIPED) study: trial design and protocol.
      Simpson S, Barnes E, Griffiths E, Hood K, Cohen D, Craddock N, Jones I, Smith DJ, Bmc Psychiatry, Volume 9 (2009) p. 50
  • 2008
    • Wake-up call for British psychiatry Reply
      Craddock N, Antebi D, Attenburrow M, Bailey T, Carson A, Cowen P, Ebmeier K, Farmer A, Fazel S, Ferrier N, Geddes J, Goodwin G, Harrison P, Hawton K, Hunter S, Jacoby R, Jones I, Keedwell P, Kerr M, Mackin P, McGuffin P, McIntyre D, McConville P, Mountain D, O'Donovan MC, Owen MJ, Oyebode F, Phillips M, Price J, Shah P, Smith DJ, Walters J, Woodruff P, Young A, Zammit S, British Journal Of Psychiatry, Volume 193, 6 (December 2008) pp.517-517
    • Schizophrenia: complex genetics, not fairy tales.
      O'Donovan MC, Craddock N, Owen MJ, Psychol Med, Volume 38, 12 (December 2008) pp.1697-1699
    • Symptoms do not helpfully distinguish unipolar and bipolar depression Authors' reply
      Forty L, Smith D, Jones L, Jones I, Caesar S, Cooper C, Fraser C, Gordon-Smith K, Hyde S, Farmer A, McGuffin P, Craddock N, British Journal Of Psychiatry, Volume 193, 5 (November 2008) pp.427-427
    • Rare chromosomal deletions and duplications increase risk of schizophrenia
      Stone JL, O'Donovan MC, Gurling H, Kirov GK, Blackwood DHR, Corvin A, Craddock NJ, Gill M, Hultman CM, Lichtenstein P, McQuillin A, Pato CN, Ruderfer DM, Owen MJ, St Clair D, Sullivan PF, Sklar P, Purcell SM, Scolnick EM, Holmans PA, Georgieva L, Nikolov I, Norton N, Williams H, Williams NM, Toncheva D, Milanova V, Thelander EF, Morris DW, O'Dushlaine CT, Kenny E, Waddington JL, Choudhury K, Datta S, Pimm J, Thirumalai S, Puri V, Krasucki R, Lawrence J, Quested D, Bass N, Curtis D, Crombie C, Fraser G, Kwan SL, Muir WJ, McGhee KA, Pickard B, Malloy P, Maclean AW, Van Beck M, Visscher PM, Macgregor S, Pato MT, Medeiros H, Middleton F, Carvalho C, Morley C, Fanous A, Conti D, Knowles JA, Ferreira CP, Azevedo MH, McCarroll SA, Gates C, Daly MJ, Sklar P, Consortium IS, Nature, Volume 455, 7210 (September 2008) pp.237-241
    • No association with the 5,10-methylenetetrahydrofolate reductase gene and major depressive disorder: Results of the depression case control (DeCC) study and a meta-analysis
      Gaysina D, Cohen S, Craddock N, Farmer A, Hoda F, Korszun A, Owen MJ, Craig IW, McGuffin P, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 147B, 6 (September 2008) pp.699-706
    • Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.
      Ferreira MA, O'Donovan MC, Meng YA, Jones IR, Ruderfer DM, Jones L, Fan J, Kirov G, Perlis RH, Green EK, Smoller JW, Grozeva D, Stone J, Nikolov I, Chambert K, Hamshere ML, Nimgaonkar VL, Moskvina V, Thase ME, Caesar S, Sachs GS, Franklin J, Gordon-Smith K, Ardlie KG, Gabriel SB, Fraser C, Blumenstiel B, Defelice M, Breen G, Gill M, Morris DW, Elkin A, Muir WJ, McGhee KA, Williamson R, MacIntyre DJ, MacLean AW, St CD, Robinson M, Van Beck M, Pereira AC, Kandaswamy R, McQuillin A, Collier DA, Bass NJ, Young AH, Lawrence J, Ferrier IN, Anjorin A, Farmer A, Curtis D, Scolnick EM, McGuffin P, Daly MJ, Corvin AP, Holmans PA, Blackwood DH, Gurling HM, Owen MJ, Purcell SM, Sklar P, Craddock N, Wellcome Trust Case Control Consortium None, Nat Genet, Volume 40, 9 (September 2008) pp.1056-1058
    • Identification of loci associated with schizophrenia by genome-wide association and follow-up.
      O'Donovan MC, Craddock N, Norton N, Williams H, Peirce T, Moskvina V, Nikolov I, Hamshere M, Carroll L, Georgieva L, Dwyer S, Holmans P, Marchini JL, Spencer CC, Howie B, Leung HT, Hartmann AM, Möller HJ, Morris DW, Shi Y, Feng G, Hoffmann P, Propping P, Vasilescu C, Maier W, Rietschel M, Zammit S, Schumacher J, Quinn EM, Schulze TG, Williams NM, Giegling I, Iwata N, Ikeda M, Darvasi A, Shifman S, He L, Duan J, Sanders AR, Levinson DF, Gejman PV, Cichon S, Nöthen MM, Gill M, Corvin A, Rujescu D, Kirov G, Owen MJ, Buccola NG, Mowry BJ, Freedman R, Amin F, Black DW, Silverman JM, Byerley WF, Cloninger CR, Molecular Genetics of Schizophrenia Collaboration None, Nat Genet, Volume 40, 9 (September 2008) pp.1053-1055
    • Genome-wide association studies in psychiatry: lessons from early studies of non-psychiatric and psychiatric phenotypes
      Craddock N, O'Donovan MC, Owen MJ, Molecular Psychiatry, Volume 13, 7 (July 2008) pp.649-653
    • Wake-up call for British psychiatry.
      Craddock N, Antebi D, Attenburrow MJ, Bailey A, Carson A, Cowen P, Craddock B, Eagles J, Ebmeier K, Farmer A, Fazel S, Ferrier N, Geddes J, Goodwin G, Harrison P, Hawton K, Hunter S, Jacoby R, Jones I, Keedwell P, Kerr M, Mackin P, McGuffin P, Macintyre DJ, McConville P, Mountain D, O'Donovan MC, Owen MJ, Oyebode F, Phillips M, Price J, Shah P, Smith DJ, Walters J, Woodruff P, Young A, Zammit S, Br J Psychiatry, Volume 193, 1 (July 2008) pp.6-9
    • Differences in depressive symptom profile between males and females.
      Smith DJ, Kyle S, Forty L, Cooper C, Walters J, Russell E, Caesar S, Farmer A, McGuffin P, Jones I, Jones L, Craddock N, J Affect Disord, Volume 108, 3 (June 2008) pp.279-284
    • The broad clinical spectrum of bipolar disorder: implications for research and practice.
      Smith D, Ghaemi S, Craddock N, J Psychopharmacol, Volume 22, 4 (June 2008) pp.397-400
    • Clinical differences between bipolar and unipolar depression.
      Forty L, Smith D, Jones L, Jones I, Caesar S, Cooper C, Fraser C, Gordon-Smith K, Hyde S, Farmer A, McGuffin P, Craddock N, Br J Psychiatry, Volume 192, 5 (May 2008) pp.388-389
    • Meta-analysis of two genome-wide association studies of bipolar disorder reveals important points of agreement.
      Baum AE, Hamshere M, Green E, Cichon S, Rietschel M, Noethen MM, Craddock N, McMahon FJ, Mol Psychiatry, Volume 13, 5 (May 2008) pp.466-467
    • Medical disorders in people with recurrent depression
      Farmer A, Korszun A, Owen MJ, Craddock N, Jones L, Jones I, Gray J, Williamson RJ, McGuffin P, British Journal Of Psychiatry, Volume 192, 5 (May 2008) pp.351-355
    • Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1.
      Bray NJ, Holmans PA, van den Bree MB, Jones L, Elliston LA, Hughes G, Richards AL, Williams NM, Craddock N, Owen MJ, O'Donovan MC, Hum Mol Genet, Volume 17, 8 (April 2008) pp.1169-1174
    • Incidence of hospitalization for postpartum psychotic and bipolar episodes.
      Jones I, Heron J, Blackmore ER, Craddock N, Arch Gen Psychiatry, Volume 65, 3 (March 2008) p. 356
    • Strong evidence that GNB1L is associated with schizophrenia.
      Williams NM, Glaser B, Norton N, Williams H, Pierce T, Moskvina V, Monks S, Del Favero J, Goossens D, Rujescu D, Giegling I, Kirov G, Craddock N, Murphy KC, O'Donovan MC, Owen MJ, Hum Mol Genet, Volume 17, 4 (February 2008) pp.555-566
    • Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene.
      Buxbaum JD, Georgieva L, Young JJ, Plescia C, Kajiwara Y, Jiang Y, Moskvina V, Norton N, Peirce T, Williams H, Craddock NJ, Carroll L, Corfas G, Davis KL, Owen MJ, Harroch S, Sakurai T, O'Donovan MC, Mol Psychiatry, Volume 13, 2 (February 2008) pp.162-172
    • Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women.
      Shifman S, Johannesson M, Bronstein M, Chen SX, Collier DA, Craddock NJ, Kendler KS, Li T, O'Donovan M, O'Neill FA, Owen MJ, Walsh D, Weinberger DR, Sun C, Flint J, Darvasi A, Plos Genet, Volume 4, 2 (February 2008) p. e28
    • Early postpartum symptoms in puerperal psychosis.
      Heron J, McGuinness M, Blackmore ER, Craddock N, Jones I, Bjog, Volume 115, 3 (February 2008) pp.348-353
    • Testing for gene x environment interaction effects in attention deficit hyperactivity disorder and associated antisocial behavior.
      Langley K, Turic D, Rice F, Holmans P, van den Bree MB, Craddock N, Kent L, Owen MJ, O'Donovan MC, Thapar A, Am J Med Genet B Neuropsychiatr Genet, Volume 147B, 1 (January 2008) pp.49-53
    • Is the perimenopause a time of increased risk of recurrence in women with a history of bipolar affective postpartum psychosis? A case series.
      Robertson Blackmore E, Craddock N, Walters J, Jones I, Arch Womens Ment Health, Volume 11, 1 (2008) pp.75-78
    • Sex differences in symptom patterns of recurrent major depression in siblings.
      Moskvina V, Farmer A, Jones IR, Brewster S, Ferrero F, Gill M, Jones LA, Maier W, Mors O, Owen MJ, Perry J, Preisig M, Rietschel M, McGuffin P, Craddock N, Korszun A, Depress Anxiety, Volume 25, 6 (2008) pp.527-534
  • 2007
    • Differentiation of executive and attention impairments in affective illness.
      Stoddart SD, Craddock NJ, Jones LA, Psychol Med, Volume 37, 11 (November 2007) pp.1613-1623
    • Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.
      Wellcome Trust Case Control Consortium None, Australo-Anglo-American Spondylitis Consortium (TASC) None, Burton PR, Clayton DG, Cardon LR, Craddock N, Deloukas P, Duncanson A, Kwiatkowski DP, McCarthy MI, Ouwehand WH, Samani NJ, Todd JA, Donnelly P, Barrett JC, Davison D, Easton D, Evans DM, Leung HT, Marchini JL, Morris AP, Spencer CC, Tobin MD, Attwood AP, Boorman JP, Cant B, Everson U, Hussey JM, Jolley JD, Knight AS, Koch K, Meech E, Nutland S, Prowse CV, Stevens HE, Taylor NC, Walters GR, Walker NM, Watkins NA, Winzer T, Jones RW, McArdle WL, Ring SM, Strachan DP, Pembrey M, Breen G, St Clair D, Caesar S, Gordon-Smith K, Jones L, Fraser C, Green EK, Grozeva D, Hamshere ML, Holmans PA, Jones IR, Kirov G, Moskivina V, Nikolov I, O'Donovan MC, Owen MJ, Collier DA, Elkin A, Farmer A, Williamson R, McGuffin P, Young AH, Ferrier IN, Ball SG, Balmforth AJ, Barrett JH, Bishop TD, Iles MM, Maqbool A, Yuldasheva N, Hall AS, Braund PS, Dixon RJ, Mangino M, Stevens S, Thompson JR, Bredin F, Tremelling M, Parkes M, Drummond H, Lees CW, Nimmo ER, Satsangi J, Fisher SA, Forbes A, Lewis CM, Onnie CM, Prescott NJ, Sanderson J, Matthew CG, Barbour J, Mohiuddin MK, Todhunter CE, Mansfield JC, Ahmad T, Cummings FR, Jewell DP, Webster J, Brown MJ, Lathrop MG, Connell J, Dominiczak A, Marcano CA, Burke B, Dobson R, Gungadoo J, Lee KL, Munroe PB, Newhouse SJ, Onipinla A, Wallace C, Xue M, Caulfield M, Farrall M, Barton A, Biologics in RA Genetics and Genomics Study Syndicate (BRAGGS) Steering Committee None, Bruce IN, Donovan H, Eyre S, Gilbert PD, Hilder SL, Hinks AM, John SL, Potter C, Silman AJ, Symmons DP, Thomson W, Worthington J, Dunger DB, Widmer B, Frayling TM, Freathy RM, Lango H, Perry JR, Shields BM, Weedon MN, Hattersley AT, Hitman GA, Walker M, Elliott KS, Groves CJ, Lindgren CM, Rayner NW, Timpson NJ, Zeggini E, Newport M, Sirugo G, Lyons E, Vannberg F, Hill AV, Bradbury LA, Farrar C, Pointon JJ, Wordsworth P, Brown MA, Franklyn JA, Heward JM, Simmonds MJ, Gough SC, Seal S, Breast Cancer Susceptibility Collaboration (UK) None, Stratton MR, Rahman N, Ban M, Goris A, Sawcer SJ, Compston A, Conway D, Jallow M, Newport M, Sirugo G, Rockett KA, Bumpstead SJ, Chaney A, Downes K, Ghori MJ, Gwilliam R, Hunt SE, Inouye M, Keniry A, King E, McGinnis R, Potter S, Ravindrarajah R, Whittaker P, Widden C, Withers D, Cardin NJ, Davison D, Ferreira T, Pereira-Gale J, Hallgrimsdo'ttir IB, Howie BN, Su Z, Teo YY, Vukcevic D, Bentley D, Brown MA, Compston A, Farrall M, Hall AS, Hattersley AT, Hill AV, Parkes M, Pembrey M, Stratton MR, Mitchell SL, Newby PR, Brand OJ, Carr-Smith J, Pearce SH, McGinnis R, Keniry A, Deloukas P, Reveille JD, Zhou X, Sims AM, Dowling A, Taylor J, Doan T, Davis JC, Savage L, Ward MM, Learch TL, Weisman MH, Brown M, Nat Genet, Volume 39, 11 (November 2007) pp.1329-1337
    • Clinical presentation of postnatal and non-postnatal depressive episodes
      Cooper C, Jones L, Dunn E, Forty L, Haque S, Oyebode F, Craddock N, Jones I, Psychological Medicine, Volume 37, 9 (September 2007) pp.1273-1280
    • Bipolar affective puerperal psychosis: genome-wide significant evidence for linkage to chromosome 16.
      Jones I, Hamshere M, Nangle JM, Bennett P, Green E, Heron J, Segurado R, Lambert D, Holmans P, Corvin A, Owen M, Jones L, Gill M, Craddock N, Am J Psychiatry, Volume 164, 7 (July 2007) pp.1099-1104
    • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
      Burton PR, Clayton DG, Cardon LR, Craddock N, Deloukas P, Duncanson A, Kwiatkowski DP, McCarthy MI, Ouwehand WH, Samani NJ, Todd JA, Donnelly P, Barrett JC, Davison D, Easton D, Evans D, Leung H, Marchini JL, Morris AP, Spencer CCA, Tobin MD, Attwood AP, Boorman JP, Cant B, Everson U, Hussey JM, Jolley JD, Knight AS, Koch K, Meech E, Nutland S, Prowse CV, Stevens HE, Taylor NC, Walters GR, Walker NM, Watkins NA, Winzer T, Jones RW, McArdle WL, Ring SM, Strachan DP, Pembrey M, Breen G, St Clair D, Caesar S, Gordon-Smith K, Jones L, Fraser C, Green EK, Grozeva D, Hamshere ML, Holmans PA, Jones IR, Kirov G, Moskvina V, Nikolov I, O'Donovan MC, Owen MJ, Collier DA, Elkin A, Farmer A, Williamson R, McGuffin P, Young AH, Ferrier IN, Ball SG, Balmforth AJ, Barrett JH, Bishop DT, Iles MM, Maqbool A, Yudasheve N, Hall AS, Braund PS, Dixon RJ, Mangino M, Stevens S, Thompson JR, Bredin F, Tremelling M, Parkes M, Drummond H, Lees CW, Nimmo ER, Satsangi J, Fisher SA, Forbes A, Lewis CM, Onnie CM, Prescott NJ, Sanderson J, Mathew CG, Barbour J, Mohiuddin MK, Todhunter CE, Mansfield JC, Ahmad T, Cummings FR, Jewell DP, Webster J, Brown MJ, Lathrop GM, Connell J, Dominiczak A, Marcano CAB, Burke B, Dobson R, Gungadoo J, Lee KL, Munroe PB, Newhouse SJ, Onipinla A, Wallace C, Xue M, Caulfield M, Farrall M, Barton A, Bruce IN, Donovan H, Eyre S, Gilbert PD, Hider SL, Hinks AM, John SL, Potter C, Silman AJ, Symmons DPM, Thomson W, Worthington J, Dunger DB, Widmer B, Frayling TM, Freathy RM, Lango H, Perry JRB, Shields BM, Weedon MN, Hattersley AT, Hitman GA, Walker M, Elliott KS, Groves CJ, Lindgren CM, Rayner NW, Timpson NJ, Zeggini E, Newport M, Sirugo G, Lynons E, Vannberg F, Brown MA, Franklyn JA, Heward JM, Simmonds MJ, Hill AVS, Bradbury LA, Farrar C, Pointon JJ, Wordsmith P, Gough SCL, Seal S, Stratton MR, Rahman N, Ban M, Goris A, Sawcer SJ, Compston A, Conway D, Jallow M, Bumpstead SJ, Chaney A, Downes K, Ghori MJR, Gwilliam R, Inouye M, Keniry A, King E, McGinnis R, Potter S, Ravindrarajah R, Whittaker P, Withers D, Easton D, Pereira-Gale J, Hallgrimsdottir IB, Howie BN, Su Z, Teo YY, Vukcevic D, Bentley D, Caulfield M, Mathew CG, Worthington J, Consortium WTCC, Syndicate BRAGGS, Collaborat BCS, Nature, Volume 447, 7145 (June 2007) pp.661-678
    • Rethinking psychosis: the disadvantages of a dichotomous classification now outweigh the advantages.
      Craddock N, Owen MJ, World Psychiatry, Volume 6, 2 (June 2007) pp.84-91
    • Symptom dimensions and the Kraepelinian dichotomy
      Craddock N, O'Donovan MC, Owen MJ, British Journal Of Psychiatry, Volume 190 (April 2007) pp.361-361
    • Phenotypic and genetic complexity of psychosis. Invited commentary on ... Schizophrenia: a common disease caused by multiple rare alleles.
      Craddock N, O'Donovan MC, Owen MJ, Br J Psychiatry, Volume 190 (March 2007) pp.200-203
    • Phenotypic and genetic complexity of psychosis - Invited commentary on ... Schizophrenia: a common disease caused by multiple rare alleles
      Craddock N, O'Donovan MC, Owen MJ, British Journal Of Psychiatry, Volume 190 (March 2007) pp.200-203
    • No 'latent period' in the onset of bipolar affective puerperal psychosis.
      Heron J, Robertson Blackmore E, McGuinness M, Craddock N, Jones I, Arch Womens Ment Health, Volume 10, 2 (2007) pp.79-81
    • Searching for the puerperal trigger: molecular genetic studies of bipolar affective puerperal psychosis.
      Jones I, Craddock N, Psychopharmacol Bull, Volume 40, 2 (2007) pp.115-128
    • Interrelationship of childhood trauma, neuroticism, and depressive phenotype.
      Moskvina V, Farmer A, Swainson V, O'Leary J, Gunasinghe C, Owen M, Craddock N, McGuffin P, Korszun A, Depress Anxiety, Volume 24, 3 (2007) pp.163-168
  • 2006
    • Familiality of postpartum depression in unipolar disorder: results of a family study.
      Forty L, Jones L, Macgregor S, Caesar S, Cooper C, Hough A, Dean L, Dave S, Farmer A, McGuffin P, Brewster S, Craddock N, Jones I, Am J Psychiatry, Volume 163, 9 (September 2006) pp.1549-1553
    • Evidence that a DISC1 frame-shift deletion associated with psychosis in a single family may not be a pathogenic mutation.
      Green EK, Norton N, Peirce T, Grozeva D, Kirov G, Owen MJ, O'Donovan MC, Craddock N, Mol Psychiatry, Volume 11, 9 (September 2006) pp.798-799
    • Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia.
      Georgieva L, Moskvina V, Peirce T, Norton N, Bray NJ, Jones L, Holmans P, Macgregor S, Zammit S, Wilkinson J, Williams H, Nikolov I, Williams N, Ivanov D, Davis KL, Haroutunian V, Buxbaum JD, Craddock N, Kirov G, Owen MJ, O'Donovan MC, Proc Natl Acad Sci U S A, Volume 103, 33 (August 2006) pp.12469-12474
    • Psychological factors in bipolar disorder - Reply
      Jones L, Scott J, Jones I, Craddock N, British Journal Of Psychiatry, Volume 189 (July 2006) pp.85-86
    • Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes.
      Hamshere ML, Williams NM, Norton N, Williams H, Cardno AG, Zammit S, Jones LA, Murphy KC, Sanders RD, McCarthy G, Gray MY, Jones G, Holmans P, O'Donovan MC, Owen MJ, Craddock N, J Med Genet, Volume 43, 7 (July 2006) pp.563-567
    • Genetics of affective (mood) disorders.
      Craddock N, Forty L, Eur J Hum Genet, Volume 14, 6 (June 2006) pp.660-668
    • Use of phenotypic covariates in association analysis by sequential addition of cases.
      Macgregor S, Craddock N, Holmans PA, Eur J Hum Genet, Volume 14, 5 (May 2006) pp.529-534
    • The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: evidence and lessons.
      Craddock N, Owen MJ, O'Donovan MC, Mol Psychiatry, Volume 11, 5 (May 2006) pp.446-458
    • Positional cloning, association analysis and expression studies provide convergent evidence that the cadherin gene FAT contains a bipolar disorder susceptibility allele.
      Blair IP, Chetcuti AF, Badenhop RF, Scimone A, Moses MJ, Adams LJ, Craddock N, Green E, Kirov G, Owen MJ, Kwok JB, Donald JA, Mitchell PB, Schofield PR, Mol Psychiatry, Volume 11, 4 (April 2006) pp.372-383
    • Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder.
      Williams NM, Green EK, Macgregor S, Dwyer S, Norton N, Williams H, Raybould R, Grozeva D, Hamshere M, Zammit S, Jones L, Cardno A, Kirov G, Jones I, O'Donovan MC, Owen MJ, Craddock N, Arch Gen Psychiatry, Volume 63, 4 (April 2006) pp.366-373
    • Genes for schizophrenia and bipolar disorder? Implications for psychiatric nosology.
      Craddock N, O'Donovan MC, Owen MJ, Schizophr Bull, Volume 32, 1 (January 2006) pp.9-16
    • Obstetric variables associated with bipolar affective puerperal psychosis.
      Blackmore ER, Jones I, Doshi M, Haque S, Holder R, Brockington I, Craddock N, Br J Psychiatry, Volume 188 (January 2006) pp.32-36
    • Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder: case-control study of over 3000 individuals from the UK.
      Green EK, Raybould R, Macgregor S, Hyde S, Young AH, O'Donovan MC, Owen MJ, Kirov G, Jones L, Jones I, Craddock N, Br J Psychiatry, Volume 188 (January 2006) pp.21-25
    • Effects of differential genotyping error rate on the type I error probability of case-control studies.
      Moskvina V, Craddock N, Holmans P, Owen MJ, O'Donovan MC, Hum Hered, Volume 61, 1 (2006) pp.55-64
  • 2005
    • Whole genome linkage scan of recurrent depressive disorder from the depression network study
      McGuffin P, Knight J, Breen G, Brewster S, Boyd PR, Craddock N, Gill M, Korszun A, Maier W, Middleton L, Mors O, Owen MJ, Perry J, Preisig M, Reich T, Rice J, Rietschel M, Jones L, Sham P, Farmer AE, Human Molecular Genetics, Volume 14, 22 (November 2005) pp.3337-3345
    • Kraepelinian dichotomy - Author's reply
      Craddock N, Owen MJ, British Journal Of Psychiatry, Volume 187 (November 2005) pp.485-486
    • Cognitive style in bipolar disorder
      Jones L, Scott J, Haque S, Gordon-Smith K, Heron J, Caesar S, Cooper C, Forty L, Hyde S, Lyon L, Greening J, Sham P, Farmer A, McGuffin P, Jones I, Craddock N, British Journal Of Psychiatry, Volume 187 (November 2005) pp.431-437
    • Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13.
      Hamshere ML, Bennett P, Williams N, Segurado R, Cardno A, Norton N, Lambert D, Williams H, Kirov G, Corvin A, Holmans P, Jones L, Jones I, Gill M, O'Donovan MC, Owen MJ, Craddock N, Arch Gen Psychiatry, Volume 62, 10 (October 2005) pp.1081-1088
    • Identification of a potential bipolar risk haplotype in the gene encoding the winged-helix transcription factor RFX4.
      Glaser B, Kirov G, Bray NJ, Green E, O'Donovan MC, Craddock N, Owen MJ, Mol Psychiatry, Volume 10, 10 (October 2005) pp.920-927
    • Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q.
      McQueen MB, Devlin B, Faraone SV, Nimgaonkar VL, Sklar P, Smoller JW, Abou Jamra R, Albus M, Bacanu SA, Baron M, Barrett TB, Berrettini W, Blacker D, Byerley W, Cichon S, Coryell W, Craddock N, Daly MJ, Depaulo JR, Edenberg HJ, Foroud T, Gill M, Gilliam TC, Hamshere M, Jones I, Jones L, Juo SH, Kelsoe JR, Lambert D, Lange C, Lerer B, Liu J, Maier W, Mackinnon JD, McInnis MG, McMahon FJ, Murphy DL, Nothen MM, Nurnberger JI, Pato CN, Pato MT, Potash JB, Propping P, Pulver AE, Rice JP, Rietschel M, Scheftner W, Schumacher J, Segurado R, Van Steen K, Xie W, Zandi PP, Laird NM, Am J Hum Genet, Volume 77, 4 (October 2005) pp.582-595
    • Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD.
      Kent L, Green E, Hawi Z, Kirley A, Dudbridge F, Lowe N, Raybould R, Langley K, Bray N, Fitzgerald M, Owen MJ, O'Donovan MC, Gill M, Thapar A, Craddock N, Mol Psychiatry, Volume 10, 10 (October 2005) pp.939-943
    • Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22.
      Lambert D, Middle F, Hamshere ML, Segurado R, Raybould R, Corvin A, Green E, O'Mahony E, Nikolov I, Mulcahy T, Haque S, Bort S, Bennett P, Norton N, Owen MJ, Kirov G, Lendon C, Jones L, Jones I, Holmans P, Gill M, Craddock N, Mol Psychiatry, Volume 10, 9 (September 2005) pp.831-841
    • Recurrence of post-partum and non-post-parturn psychosis - Reply
      Jones I, Robertson-Blackmore E, Craddock N, British Journal Of Psychiatry, Volume 187 (September 2005) pp.289-289
    • Design of case-controls studies with unscreened controls.
      Moskvina V, Holmans P, Schmidt KM, Craddock N, Ann Hum Genet, Volume 69, Pt 5 (September 2005) pp.566-576
    • Schizophrenia: genes at last?
      Owen MJ, Craddock N, O'Donovan MC, Trends Genet, Volume 21, 9 (September 2005) pp.518-525
    • Bipolar disorder and childbirth: the importance of recognising risk.
      Jones I, Craddock N, Br J Psychiatry, Volume 186 (June 2005) pp.453-454
    • Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder.
      Green EK, Raybould R, Macgregor S, Gordon-Smith K, Heron J, Hyde S, Grozeva D, Hamshere M, Williams N, Owen MJ, O'Donovan MC, Jones L, Jones I, Kirov G, Craddock N, Arch Gen Psychiatry, Volume 62, 6 (June 2005) pp.642-648
    • Vitamin D receptor variants in 192 patients with schizophrenia and other psychiatric diseases.
      Yan J, Feng J, Craddock N, Jones IR, Cook EH, Goldman D, Heston LL, Chen J, Burkhart P, Li W, Shibayama A, Sommer SS, Neurosci Lett, Volume 380, 1-2 (May 2005) pp.37-41
    • The beginning of the end for the Kraepelinian dichotomy
      Craddock N, Owen MJ, British Journal Of Psychiatry, Volume 186 (May 2005) pp.364-366
    • Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1).
      Raybould R, Green EK, MacGregor S, Gordon-Smith K, Heron J, Hyde S, Caesar S, Nikolov I, Williams N, Jones L, O'Donovan MC, Owen MJ, Jones I, Kirov G, Craddock N, Biol Psychiatry, Volume 57, 7 (April 2005) pp.696-701
    • Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients.
      Yan J, Oliveira G, Coutinho A, Yang C, Feng J, Katz C, Sram J, Bockholt A, Jones IR, Craddock N, Cook EH, Vicente A, Sommer SS, Mol Psychiatry, Volume 10, 4 (April 2005) pp.329-332
    • Postnatal euphoria: are 'the highs' an indicator of bipolarity?
      Heron J, Craddock N, Jones I, Bipolar Disord, Volume 7, 2 (April 2005) pp.103-110
    • Current status of molecular genetics of schizophrenia and bipolar disorder
      Craddock N, European Psychiatry, Volume 20 (March 2005) pp.S41-S42
    • Risk of puerperal and non-puerperal recurrence of illness following bipolar affective puerperal (post-partum) psychosis.
      Robertson E, Jones I, Haque S, Holder R, Craddock N, Br J Psychiatry, Volume 186 (March 2005) pp.258-259
    • The genetics of schizophrenia and bipolar disorder: dissecting psychosis.
      Craddock N, O'Donovan MC, Owen MJ, J Med Genet, Volume 42, 3 (March 2005) pp.193-204
    • Structural variants in the retinoid receptor genes in patients with schizophrenia and other psychiatric diseases.
      Feng J, Chen J, Yan J, Jones IR, Craddock N, Cook EH, Goldman D, Heston LL, Sommer SS, Am J Med Genet B Neuropsychiatr Genet, Volume 133B, 1 (February 2005) pp.50-53
    • Linkage disequilibrium mapping of bipolar affective disorder at 12q23-q24 provides evidence for association at CUX2 and FLJ32356.
      Glaser B, Kirov G, Green E, Craddock N, Owen MJ, Am J Med Genet B Neuropsychiatr Genet, Volume 132B, 1 (January 2005) pp.38-45
    • Localization of bipolar susceptibility locus by molecular genetic analysis of the chromosome 12q23-q24 region in two pedigrees with bipolar disorder and Darier's disease.
      Green E, Elvidge G, Jacobsen N, Glaser B, Jones I, O'Donovan MC, Kirov G, Owen MJ, Craddock N, Am J Psychiatry, Volume 162, 1 (January 2005) pp.35-42
  • 2004
    • Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin.
      Cichon S, Buervenich S, Kirov G, Akula N, Dimitrova A, Green E, Schumacher J, Klopp N, Becker T, Ohlraun S, Schulze TG, Tullius M, Gross MM, Jones L, Krastev S, Nikolov I, Hamshere M, Jones I, Czerski PM, Leszczynska-Rodziewicz A, Kapelski P, Bogaert AV, Illig T, Hauser J, Maier W, Berrettini W, Byerley W, Coryell W, Gershon ES, Kelsoe JR, McInnis MG, Murphy DL, Nurnberger JI, Reich T, Scheftner W, O'Donovan MC, Propping P, Owen MJ, Rietschel M, Nöthen MM, McMahon FJ, Craddock N, Nat Genet, Volume 36, 8 (August 2004) pp.783-784
    • MECP2 structural and 3'-UTR variants in schizophrenia, autism and other psychiatric diseases: a possible association with autism.
      Shibayama A, Cook EH, Feng J, Glanzmann C, Yan J, Craddock N, Jones IR, Goldman D, Heston LL, Sommer SS, Am J Med Genet B Neuropsychiatr Genet, Volume 128B, 1 (July 2004) pp.50-53
    • Familiality of symptom dimensions in depression.
      Korszun A, Moskvina V, Brewster S, Craddock N, Ferrero F, Gill M, Jones IR, Jones LA, Maier W, Mors O, Owen MJ, Preisig M, Reich T, Rietschel M, Farmer A, McGuffin P, Arch Gen Psychiatry, Volume 61, 5 (May 2004) pp.468-474
    • Current status of genetics of bipolar disorder
      Craddock N, European Psychiatry, Volume 19 (April 2004) pp.12S-12S
    • Mutation scanning of the androgen receptor gene in patients with psychiatric disorders reveals highly conserved variants in alcoholic and phobia patients.
      Yan J, Feng J, Goldman D, Cook EH, Craddock N, Jones IR, Heston LL, Sommer SS, Psychiatr Genet, Volume 14, 1 (March 2004) pp.57-60
    • Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD.
      Turic D, Langley K, Mills S, Stephens M, Lawson D, Govan C, Williams N, Van Den Bree M, Craddock N, Kent L, Owen M, O'Donovan M, Thapar A, Mol Psychiatry, Volume 9, 2 (February 2004) pp.169-173
    • The Depression Network (DeNT) Study: methodology and sociodemographic characteristics of the first 470 affected sibling pairs from a large multi-site linkage genetic study.
      Farmer A, Breen G, Brewster S, Craddock N, Gill M, Korszun A, Maier W, Middleton L, Mors O, Owen M, Perry J, Preisig M, Rietschel M, Reich T, Jones L, Jones I, McGuffin P, Bmc Psychiatry, Volume 4 (2004) p. 42
    • The Bipolar Affective Disorder Dimension Scale (BADDS)--a dimensional scale for rating lifetime psychopathology in bipolar spectrum disorders.
      Craddock N, Jones I, Kirov G, Jones L, Bmc Psychiatry, Volume 4 (2004) p. 19
  • 2003
    • Self-reported schizotypy and bipolar disorder: demonstration of a lack of specificity of the Kings Schizotypy Questionnaire
      Heron J, Jones I, Williams J, Owen MJ, Craddock N, Jones LA, Schizophrenia Research, Volume 65, 2-3 (December 2003) pp.153-158
    • Brain-derived neurotrophic factor as a potential risk locus for bipolar disorder: evidence, limitations, and implications.
      Green E, Craddock N, Curr Psychiatry Rep, Volume 5, 6 (December 2003) pp.469-476
    • Anticipation and repeat expansion in bipolar disorder.
      O'Donovan M, Jones I, Craddock N, Am J Med Genet C Semin Med Genet, Volume 123C, 1 (November 2003) pp.10-17
    • No association between two polymorphisms at the 5HT2A gene and bipolar affective puerperal psychosis.
      Robertson E, Jones I, Middle F, Moray J, Craddock N, Acta Psychiatr Scand, Volume 108, 5 (November 2003) pp.387-391
    • Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.
      Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberger JI, Craddock N, DePaulo JR, Baron M, Gershon ES, Ekholm J, Cichon S, Turecki G, Claes S, Kelsoe JR, Schofield PR, Badenhop RF, Morissette J, Coon H, Blackwood D, McInnes LA, Foroud T, Edenberg HJ, Reich T, Rice JP, Goate A, McInnis MG, McMahon FJ, Badner JA, Goldin LR, Bennett P, Willour VL, Zandi PP, Liu J, Gilliam C, Juo SH, Berrettini WH, Yoshikawa T, Peltonen L, Lönnqvist J, Nöthen MM, Schumacher J, Windemuth C, Rietschel M, Propping P, Maier W, Alda M, Grof P, Rouleau GA, Del-Favero J, Van Broeckhoven C, Mendlewicz J, Adolfsson R, Spence MA, Luebbert H, Adams LJ, Donald JA, Mitchell PB, Barden N, Shink E, Byerley W, Muir W, Visscher PM, Macgregor S, Gurling H, Kalsi G, McQuillin A, Escamilla MA, Reus VI, Leon P, Freimer NB, Ewald H, Kruse TA, Mors O, Radhakrishna U, Blouin JL, Antonarakis SE, Akarsu N, Am J Hum Genet, Volume 73, 1 (July 2003) pp.49-62
    • Mutational analysis of two positional candidate susceptibility genes for bipolar disorder on chromosome 12q23-q24: phenylalanine hydroxylase and human LIM-homeobox LHX5
      Green EK, Elvidge GP, Owen MJ, Craddock N, Psychiatric Genetics, Volume 13, 2 (June 2003) pp.97-101
    • Variation in the coding sequence and flanking splice junctions of the estrogen receptor alpha (ERalpha) gene does not play an important role in genetic susceptibility to bipolar disorder or bipolar affective puerperal psychosis.
      Middle F, Jones I, Robertson E, Morey J, Lendon C, Craddock N, Am J Med Genet B Neuropsychiatr Genet, Volume 118B, 1 (April 2003) pp.72-75
    • Is there a relationship between attention deficit hyperactivity disorder and bipolar disorder?
      Kent L, Craddock N, J Affect Disord, Volume 73, 3 (February 2003) pp.211-221
    • Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder.
      Børglum AD, Kirov G, Craddock N, Mors O, Muir W, Murray V, McKee I, Collier DA, Ewald H, Owen MJ, Blackwood D, Kruse TA, Am J Med Genet B Neuropsychiatr Genet, Volume 117B, 1 (February 2003) pp.18-22
  • 2002
    • Attitudes towards future testing for bipolar disorder susceptibility genes: a preliminary investigation.
      Jones I, Scourfield J, McCandless F, Craddock N, J Affect Disord, Volume 71, 1-3 (September 2002) pp.189-193
    • Do puerperal psychotic episodes identify a more familial subtype of bipolar disorder? Results of a family history study.
      Jones I, Craddock N, Psychiatr Genet, Volume 12, 3 (September 2002) pp.177-180
    • Triplet repeats and bipolar disorder.
      Jones I, Gordon-Smith K, Craddock N, Curr Psychiatry Rep, Volume 4, 2 (April 2002) pp.134-140
    • Association of DRD4 in children with ADHD and comorbid conduct problems.
      Holmes J, Payton A, Barrett J, Harrington R, McGuffin P, Owen M, Ollier W, Worthington J, Gill M, Kirley A, Hawi Z, Fitzgerald M, Asherson P, Curran S, Mill J, Gould A, Taylor E, Kent L, Craddock N, Thapar A, Am J Med Genet, Volume 114, 2 (March 2002) pp.150-153
    • Sibling pairs with affective disorders: resemblance of demographic and clinical features.
      O'Mahony E, Corvin A, O'Connell R, Comerford C, Larsen B, Jones R, McCandless F, Kirov G, Cardno AG, Craddock N, Gill M, Psychol Med, Volume 32, 1 (January 2002) pp.55-61
    • Evidence for familial cosegregation of major affective disorder and genetic markers flanking the gene for Darier's disease
      Jones I, Jacobsen N, Green EK, Elvidge GP, Owen MJ, Craddock N, Molecular Psychiatry, Volume 7, 4 (2002) pp.424-427
    • Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus. Brain-derived neutrophic factor.
      Sklar P, Gabriel SB, McInnis MG, Bennett P, Lim Y, Tsan G, Schaffner S, Kirov G, Jones I, Owen M, Craddock N, DePaulo JR, Lander ES, Mol Psychiatry, Volume 7, 6 (2002) pp.579-593
    • Evidence to suggest biased phenotypes in children with Attention Deficit Hyperactivity Disorder from completely ascertained trios.
      West A, Langley K, Hamshere ML, Kent L, Craddock N, Owen MJ, O'Donovan M, Thapar A, Mol Psychiatry, Volume 7, 9 (2002) pp.962-966
    • Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT(1B) receptor gene in 273 nuclear families from a multi-centre sample.
      Hawi Z, Dring M, Kirley A, Foley D, Kent L, Craddock N, Asherson P, Curran S, Gould A, Richards S, Lawson D, Pay H, Turic D, Langley K, Owen M, O'Donovan M, Thapar A, Fitzgerald M, Gill M, Mol Psychiatry, Volume 7, 7 (2002) pp.718-725
    • Evidence that variation at the serotonin transporter gene influences susceptibility to attention deficit hyperactivity disorder (ADHD): analysis and pooled analysis.
      Kent L, Doerry U, Hardy E, Parmar R, Gingell K, Hawi Z, Kirley A, Lowe N, Fitzgerald M, Gill M, Craddock N, Mol Psychiatry, Volume 7, 8 (2002) pp.908-912
    • The Wellcome trust UK-Irish bipolar affective disorder sibling-pair genome screen: first stage report.
      Bennett P, Segurado R, Jones I, Bort S, McCandless F, Lambert D, Heron J, Comerford C, Middle F, Corvin A, Pelios G, Kirov G, Larsen B, Mulcahy T, Williams N, O'Connell R, O'Mahony E, Payne A, Owen M, Holmans P, Craddock N, Gill M, Mol Psychiatry, Volume 7, 2 (2002) pp.189-200
  • 2001
    • No association between CHRNA7 microsatellite markers and attention-deficit hyperactivity disorder.
      Kent L, Green E, Holmes J, Thapar A, Gill M, Hawi Z, Fitzgerald M, Asherson P, Curran S, Mills J, Payton A, Craddock N, Am J Med Genet, Volume 105, 8 (December 2001) pp.686-689
    • Association studies of bipolar disorder.
      Craddock N, Davé S, Greening J, Bipolar Disord, Volume 3, 6 (December 2001) pp.284-298
    • A significant association of serotonin transporter polymorphism haplotypes in attention deficit hyperactivity disorder (ADHD)
      Kent L, Hardy E, Hawzi Z, Fitzgerald M, Kirley A, Gill M, Craddock N, American Journal Of Medical Genetics, Volume 105, 7 (October 2001) pp.574-575
    • Susceptibility gene(s) for Alzheimer's disease on chromosome 10.
      Lendon C, Craddock N, Trends Neurosci, Volume 24, 10 (October 2001) pp.557-559
    • Is LBP-1c/CP2/LSF a disease-modifying gene for Alzheimer's disease?
      Lendon C, Craddock N, Lancet, Volume 358, 9287 (September 2001) pp.1029-1030
    • Evidence of association between DRD4 and ADHD with conduct disturbance.
      Thapar A, Holmes J, Payton A, Barrett J, Harrington R, McGuffm P, Owen M, Ollier W, Gill M, Kirley A, Hawi Z, Fitzgerald M, Asherson P, Curran S, Mill J, Gould A, Taylor E, Kent L, Craddock N, Worthington J, Behavior Genetics, Volume 31, 5 (September 2001) pp.470-471
    • Cigarette smoking and psychotic symptoms in bipolar affective disorder.
      Corvin A, O'Mahony E, O'Regan M, Comerford C, O'Connell R, Craddock N, Gill M, Br J Psychiatry, Volume 179 (July 2001) pp.35-38
    • Familiality of the puerperal trigger in bipolar disorder: results of a family study.
      Jones I, Craddock N, Am J Psychiatry, Volume 158, 6 (June 2001) pp.913-917
    • Scanning of estrogen receptor alpha (ERalpha) and thyroid hormone receptor alpha (TRalpha) genes in patients with psychiatric diseases: four missense mutations identified in ERalpha gene.
      Feng J, Yan J, Michaud S, Craddock N, Jones IR, Cook EH, Goldman D, Heston LL, Peltonen L, Delisi LE, Sommer SS, Am J Med Genet, Volume 105, 4 (May 2001) pp.369-374
    • Allelic variation of a BalI polymorphism in the DRD3 gene does not influence susceptibility to bipolar disorder: Results of analysis and meta-analysis
      Elvidge G, Jones I, McCandless F, Asherson P, Owen MJ, Craddock N, American Journal Of Medical Genetics, Volume 105, 4 (May 2001) pp.307-311
    • Candidate gene studies of bipolar disorder.
      Jones I, Craddock N, Ann Med, Volume 33, 4 (May 2001) pp.248-256
    • CUX2, a potential regulator of NCAM expression: genomic characterization and analysis as a positional candidate susceptibility gene for bipolar disorder.
      Jacobsen NJ, Elvidge G, Franks EK, O'Donovan MC, Craddock N, Owen MJ, Am J Med Genet, Volume 105, 3 (April 2001) pp.295-300
    • Nicotinic acetylcholine receptor alpha4 subunit gene polymorphism and attention deficit hyperactivity disorder.
      Kent L, Middle F, Hawi Z, Fitzgerald M, Gill M, Feehan C, Craddock N, Psychiatr Genet, Volume 11, 1 (March 2001) pp.37-40
    • An in-frame deletion in the alpha(2C) adrenergic receptor is common in African--Americans.
      Feng J, Zheng J, Gelernter J, Kranzler H, Cook E, Goldman D, Jones IR, Craddock N, Heston LL, Delisi L, Peltonen L, Bennett WP, Sommer SS, Mol Psychiatry, Volume 6, 2 (March 2001) pp.168-172
    • Systematic screening for mutations in the glycine receptor alpha2 subunit gene (GLRA2) in patients with schizophrenia and other psychiatric diseases.
      Feng J, Craddock N, Jones IR, Cook EH, Goldman D, Heston LL, Peltonen L, DeLisi LE, Sommer SS, Psychiatr Genet, Volume 11, 1 (March 2001) pp.45-48
    • Exclusion of the Darier's disease gene, ATP2A2, as a common susceptibility gene for bipolar disorder.
      Jacobsen NJ, Franks EK, Elvidge G, Jones I, McCandless F, O'Donovan MC, Owen MJ, Craddock N, Mol Psychiatry, Volume 6, 1 (January 2001) pp.92-97
  • 2000
    • Molecular genetic studies of bipolar disorder and puerperal psychosis at two polymorphisms in the estrogen receptor alpha gene (ESR 1).
      Jones I, Middle F, McCandless F, Coyle N, Robertson E, Brockington I, Lendon C, Craddock N, Am J Med Genet, Volume 96, 6 (December 2000) pp.850-853
    • Tumour necrosis factor alpha and bipolar affective puerperal psychosis.
      Middle F, Jones I, Robertson E, Lendon C, Craddock N, Psychiatr Genet, Volume 10, 4 (December 2000) pp.195-198
    • No evidence of association from transmission disequilibrium analysis of the hKCa3 gene in bipolar disorder.
      Bowen T, Ashworth L, Kirov G, Guy CA, Jones IR, McCandless F, Craddock N, O'Donovan MC, Owen MJ, Bipolar Disord, Volume 2, 4 (December 2000) pp.328-331
    • Psychiatric genetics
      Craddock N, British Journal Of Psychiatry, Volume 177 (December 2000) pp.571-571
    • Human leucocyte antigen-A2 increases risk of Alzheimer's disease but does not affect age of onset in a Scottish population.
      Harris JM, Cumming AM, Craddock N, St Clair D, Lendon CL, Neurosci Lett, Volume 294, 1 (November 2000) pp.37-40
    • Variation at the serotonin transporter gene influences susceptibility to bipolar affective puerperal psychosis.
      Coyle N, Jones I, Robertson E, Lendon C, Craddock N, Lancet, Volume 356, 9240 (October 2000) pp.1490-1491
    • The Wellcome Trust UK-Irish Bipolar Sib-pair Genome Screen: Complete first stage data and second stage progress report.
      Bennett P, Bort S, Seguardo R, Middle F, Jones I, Heron J, Lambert D, O'Mahony E, Corvin A, Gill M, Craddock N, Grp WTB, American Journal Of Medical Genetics, Volume 96, 4 (August 2000) pp.467-467
    • Five missense variants in the amino-terminal domain of the glucocorticoid receptor: no association with puerperal psychosis or schizophrenia.
      Feng J, Zheng J, Bennett WP, Heston LL, Jones IR, Craddock N, Sommer SS, Am J Med Genet, Volume 96, 3 (June 2000) pp.412-417
    • Update on chromosomal locations for psychiatric disorders: report of the interim meeting of chromosome workshop chairpersons from the VIIth World Congress of Psychiatric Genetics, Monterey, California, October 14-18, 1999.
      DeLisi LE, Craddock NJ, Detera-Wadleigh S, Foroud T, Gejman P, Kennedy JL, Lendon C, Macciardi F, McKeon P, Mynett-Johnson L, Nurnberger JI, Paterson A, Schwab S, Van Broeckhoven C, Wildenauer D, Crow TJ, Am J Med Genet, Volume 96, 3 (June 2000) pp.434-449
    • Comparative sequencing and association studies of aromatic L-amino acid decarboxylase in schizophrenia and bipolar disorder.
      Speight G, Turic D, Austin J, Hoogendoorn B, Cardno AG, Jones L, Murphy KC, Sanders R, McCarthy G, Jones I, McCandless F, McGuffin P, Craddock N, Owen MJ, Buckland P, O'Donovan MC, Mol Psychiatry, Volume 5, 3 (May 2000) pp.327-331
    • Bipolar disorder and variation at a common polymorphism (A1832G) within exon 8 of the Wolfram gene
      Middle F, Jones I, McCandless F, Barrett T, Khanim F, Owen MJ, Lendon C, Craddock N, American Journal Of Medical Genetics, Volume 96, 2 (April 2000) pp.154-157
    • Association analysis of the proneurotensin gene and bipolar disorder.
      Austin J, Hoogendoorn B, Buckland P, Jones I, McCandless F, Williams N, Middle F, Owen MJ, Craddock N, O'Donovan MC, Psychiatr Genet, Volume 10, 1 (March 2000) pp.51-54
    • Pooled genotyping of microsatellite markers in parent-offspring trios.
      Kirov G, Williams N, Sham P, Craddock N, Owen MJ, Genome Res, Volume 10, 1 (January 2000) pp.105-115
  • 1999
    • A functional polymorphism in the promoter of monoamine oxidase A gene and bipolar affective disorder.
      Kirov G, Norton N, Jones I, McCandless F, Craddock N, Owen MJ, Int J Neuropsychopharmacol, Volume 2, 4 (December 1999) pp.293-298
    • Family-based association studies of bipolar disorder with candidate genes involved in dopamine neurotransmission: DBH, DAT1, COMT, DRD2, DRD3 and DRD5.
      Kirov G, Jones I, McCandless F, Craddock N, Owen MJ, Mol Psychiatry, Volume 4, 6 (November 1999) pp.558-565
    • Linkage studies of bipolar disorder with chromosome 18 markers.
      Bowen T, Kirov G, Gill M, Spurlock G, Vallada HP, Murray RM, McGuffin P, Collier DA, Owen MJ, Craddock N, Am J Med Genet, Volume 88, 5 (October 1999) pp.503-509
    • Puerperal psychosis: Evidence for familiality of the puerperal trigger.
      Jones I, Coyle N, Roberstson E, Middle F, Mcandless F, Lendon C, Brockington I, Craddock N, Molecular Psychiatry, Volume 4 (September 1999) pp.S26-S26
    • ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes.
      Jacobsen NJ, Lyons I, Hoogendoorn B, Burge S, Kwok PY, O'Donovan MC, Craddock N, Owen MJ, Hum Mol Genet, Volume 8, 9 (September 1999) pp.1631-1636
    • Bipolar disorder and the serotonin transporter gene: a family-based association study.
      Kirov G, Rees M, Jones I, MacCandless F, Owen MJ, Craddock N, Psychol Med, Volume 29, 5 (September 1999) pp.1249-1254
    • The Wellcome Trust UK-Irish Bipolar Sib-pair Study: First stage genome screen.
      Craddock N, Gill M, Molecular Psychiatry, Volume 4 (September 1999) pp.S21-S21
    • Further evidence of familial cosegregation of major affective disorder and Darier's disease.
      Jones I, Owen MJ, Craddock N, Molecular Psychiatry, Volume 4 (September 1999) pp.S73-S73
    • Genetics of bipolar disorder.
      Craddock N, Jones I, J Med Genet, Volume 36, 8 (August 1999) pp.585-594
    • CTG18.1 and ERDA-1 CAG/CTG repeat size in bipolar disorder.
      Guy CA, Bowen T, Jones I, McCandless F, Owen MJ, Craddock N, O'Donovan MC, Neurobiol Dis, Volume 6, 4 (August 1999) pp.302-307
    • CAG repeat length in the hKCa3 gene and symptom dimensions in schizophrenia.
      Cardno AG, Bowen T, Guy CA, Jones LA, McCarthy G, Williams NM, Murphy KC, Spurlock G, Gray M, Sanders RD, Craddock N, McGuffin P, Owen MJ, O'Donovan MC, Biol Psychiatry, Volume 45, 12 (June 1999) pp.1592-1596
    • Neurogenetic determinism and the new euphenics. Psychosocial and ethical issues in psychiatric genetics require constructive debate.
      Craddock N, Jones IR, Kent L, Bmj, Volume 318, 7196 (May 1999) p. 1488
    • Mutational analysis of phospholipase A2A: a positional candidate susceptibility gene for bipolar disorder.
      Jacobsen NJ, Franks EK, Owen MJ, Craddock NJ, Mol Psychiatry, Volume 4, 3 (May 1999) pp.274-279
    • Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease.
      Sakuntabhai A, Ruiz-Perez V, Carter S, Jacobsen N, Burge S, Monk S, Smith M, Munro CS, O'Donovan M, Craddock N, Kucherlapati R, Rees JL, Owen M, Lathrop GM, Monaco AP, Strachan T, Hovnanian A, Nat Genet, Volume 21, 3 (March 1999) pp.271-277
    • No association between a polymorphic CAG repeat in the human potassium channel gene hKCa3 and bipolar disorder.
      Guy CA, Bowen T, Williams N, Jones IR, McCandless F, McGuffin P, Owen MJ, Craddock N, O'Donovan MC, Am J Med Genet, Volume 88, 1 (February 1999) pp.57-60
    • Eleven trinucleotide repeat loci that map to chromosome 12 excluded from involvement in the pathogenesis of bipolar disorder.
      Franks E, Guy C, Jacobsen N, Bowen T, Owen MJ, O'Donovan MC, Craddock N, Am J Med Genet, Volume 88, 1 (February 1999) pp.67-70
    • Tryptophan hydroxylase gene and manic-depressive illness.
      Kirov G, Owen MJ, Jones I, McCandless F, Craddock N, Arch Gen Psychiatry, Volume 56, 1 (January 1999) pp.98-99
    • Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families.
      Nöthen MM, Cichon S, Rohleder H, Hemmer S, Franzek E, Fritze J, Albus M, Borrmann-Hassenbach M, Kreiner R, Weigelt B, Minges J, Lichtermann D, Maier W, Craddock N, Fimmers R, Höller T, Baur MP, Rietschel M, Propping P, Mol Psychiatry, Volume 4, 1 (January 1999) pp.76-84
  • 1998
    • Ethical issues in genetics of mental disorders.
      Jones I, Craddock N, Lancet, Volume 352, 9142 (November 1998) p. 1788
    • New susceptibility gene for Alzheimer's disease on chromosome 12?
      Craddock N, Lendon C, Lancet, Volume 352, 9142 (November 1998) pp.1720-1721
    • The Wellcome Trust UK-Irish Bipolar Sib-pair Study: Chromosome 21.
      Bennett P, Mulcahy T, Owen MJ, Craddock N, Gill M, Grp WTB, American Journal Of Medical Genetics, Volume 81, 6 (November 1998) pp.541-541
    • The Wellcome Trust UK-Irish bipolar sib-pair study: Sample and study design.
      Gill M, Craddock N, Grp WTB, American Journal Of Medical Genetics, Volume 81, 6 (November 1998) pp.461-461
    • Molecular genetic approaches to puerperal psychosis.
      Jones IR, McCandless F, Morey J, Benjamin J, Brockington I, Craddock N, American Journal Of Medical Genetics, Volume 81, 6 (November 1998) pp.544-544
    • A study of chromosome 4p markers and dopamine D5 receptor gene in schizophrenia and bipolar disorder.
      Asherson P, Mant R, Williams N, Cardno A, Jones L, Murphy K, Collier DA, Nanko S, Craddock N, Morris S, Muir W, Blackwood B, McGuffin P, Owen MJ, Mol Psychiatry, Volume 3, 4 (July 1998) pp.310-320
    • Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder.
      Kirov G, Murphy KC, Arranz MJ, Jones I, McCandles F, Kunugi H, Murray RM, McGuffin P, Collier DA, Owen MJ, Craddock N, Mol Psychiatry, Volume 3, 4 (July 1998) pp.342-345
    • Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22.
      Lendon CL, Lynch T, Norton J, McKeel DW, Busfield F, Craddock N, Chakraverty S, Gopalakrishnan G, Shears SD, Grimmett W, Wilhelmsen KC, Hansen L, Morris JC, Goate AM, Neurology, Volume 50, 6 (June 1998) pp.1546-1555
    • Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia.
      Bowen T, Guy CA, Craddock N, Cardno AG, Williams NM, Spurlock G, Murphy KC, Jones LA, Gray M, Sanders RD, McCarthy G, Chandy KG, Fantino E, Kalman K, Gutman GA, Gargus JJ, Williams J, McGuffin P, Owen MJ, O'Donovan MC, Mol Psychiatry, Volume 3, 3 (May 1998) pp.266-269
    • Linked polymorphisms upstream of exons 1 and 2 of the human cholecystokinin gene are not associated with schizophrenia or bipolar disorder.
      Bowen T, Norton N, Jacobsen NJ, Guy C, Daniels JK, Sanders RD, Cardno AG, Jones LA, Murphy KC, McGuffin P, Craddock N, O'Donovan MC, Owen MJ, Mol Psychiatry, Volume 3, 1 (January 1998) pp.67-71
    • Linkage analysis between bipolar affective disorder and markers on chromosome X.
      Vallada HP, Vasques L, Curtis D, Zatz M, Kirov G, Lauriano V, Gentil V, Murray RM, McGuffin P, Owen M, Gill M, Craddock N, Collier DA, Psychiatr Genet, Volume 8, 3 (1998) pp.183-186
    • Association between functional psychosis and expanded CAG/CTG repeats is not explained by health stratification.
      Cardno AG, McCandless F, Bowen T, Guy CA, Jones LA, Murphy KC, McGuffin P, Owen MJ, Craddock N, O'Donovan MC, Psychiatr Genet, Volume 8, 1 (1998) pp.29-32
    • Intrafamilial association of pericentric inversion of chromosome 9, inv (9)(p11-q21), and rapid cycling bipolar disorder.
      McCandless F, Jones I, Harper K, Craddock N, Psychiatr Genet, Volume 8, 4 (1998) pp.259-262
  • 1997
    • Linkage studies of bipolar disorder with chromosome 18 markers.
      Craddock N, Bowen T, Kirov G, Gill M, Spurlock G, Vallada H, Powell J, Murray R, McGuffin P, Collier D, Owen MJ, American Journal Of Medical Genetics, Volume 74, 6 (November 1997) pp.672-672
    • Dimensional classification for use in biological studies of bipolar disorder.
      Craddock N, Jones IR, McCandless F, Kirov G, Cardno AG, American Journal Of Medical Genetics, Volume 74, 6 (November 1997) pp.588-588
    • Expanded CAG/CTG repeats in bipolar disorder: no correlation with phenotypic measures of illness severity.
      Craddock N, McKeon P, Moorhead S, Guy C, Harrison D, Mynett-Johnson L, Claffey E, Feldman E, McGuffin P, Owen MJ, O'Donovan MC, Biol Psychiatry, Volume 42, 10 (November 1997) pp.876-881
    • No evidence for expanded polyglutamine sequences in bipolar disorder and schizophrenia.
      Jones AL, Middle F, Guy C, Spurlock G, Cairns NJ, McGuffin P, Craddock N, Owen M, O'Donovan MC, Mol Psychiatry, Volume 2, 6 (October 1997) pp.478-482
    • Association studies of bipolar disorder at the human serotonin transporter gene (hSERT; 5HTT).
      Rees M, Norton N, Jones I, McCandless F, Scourfield J, Holmans P, Moorhead S, Feldman E, Sadler S, Cole T, Redman K, Farmer A, McGuffin P, Owen MJ, Craddock N, Mol Psychiatry, Volume 2, 5 (September 1997) pp.398-402
    • Exclusion of expansion of 50 CAG/CTG trinucleotide repeats in bipolar disorder.
      Guy C, Bowen T, Daniels JK, Speight G, McKeon P, Mynett-Johnson L, Claffey E, McGuffin P, Owen MJ, Craddock N, O'Donovan MC, Am J Psychiatry, Volume 154, 8 (August 1997) pp.1146-1147
    • No association between bipolar disorder and alleles at a functional polymorphism in the COMT gene - Biomed European Bipolar Collaborative Group
      Craddock N, Spurlock G, McGuffin P, Owen MJ, NostenBertrand M, Bellivier F, Meloni R, Leboyer M, Mallet J, MynettJohnson L, Murphy V, McKeon P, Kirov G, Powell J, Kunugi H, Collier D, Larosa M, Nacmias B, Sorbi S, Schwab S, Ackenheil M, Maier W, British Journal Of Psychiatry, Volume 170 (June 1997) pp.526-528
    • The crisis in psychiatry.
      Jones I, Craddock N, Lancet, Volume 349, 9064 (May 1997) p. 1550
    • Exclusion of CAG/CTG trinucleotide repeat loci which map to chromosome 4 in bipolar disorder and schizophrenia.
      Speight G, Guy C, Bowen T, Asherson P, McGuffin P, Craddock N, Owen MJ, O'Donovan MC, Am J Med Genet, Volume 74, 2 (April 1997) pp.204-206
    • Contractures in neuroleptic malignant syndrome.
      Craddock B, Craddock N, Am J Psychiatry, Volume 154, 3 (March 1997) p. 436
    • Efficient strategies for genome scanning using maximum-likelihood affected-sib-pair analysis.
      Holmans P, Craddock N, Am J Hum Genet, Volume 60, 3 (March 1997) pp.657-666
    • Single major locus models for bipolar disorder are implausible
      Craddock N, VanEerdewegh P, Reich T, American Journal Of Medical Genetics, Volume 74, 1 (February 1997) pp.18-18
    • Genetic association studies between dementia of the Alzheimer's type and three receptors for apolipoprotein E in a Caucasian population.
      Lendon CL, Talbot CJ, Craddock NJ, Han SW, Wragg M, Morris JC, Goate AM, Neurosci Lett, Volume 222, 3 (February 1997) pp.187-190
  • 1996
    • Involvement of expanded trinucleotide repeats in common diseases
      ODonovan MC, Craddock N, Guy C, McGuffin P, Owen M, Lancet, Volume 348, 9043 (December 1996) pp.1739-1740
    • Introducing Selfcite 2.0--career enhancing software.
      Craddock N, O'Donovan MC, Owen MJ, Bmj, Volume 313, 7072 (December 1996) pp.1659-1660
    • Linkage studies in bipolar affective disorder with markers on chromosome 21.
      Vallada H, Craddock N, Vasques L, Curtis D, Kirov G, Lauriano V, Gentil V, Passos-Bueno R, Murray RM, Zatz M, McGuffin P, Powell JF, Gill M, Owen M, Collier DA, J Affect Disord, Volume 41, 3 (December 1996) pp.217-221
    • Candidate gene association studies in psychiatric genetics: A SERTain future?
      Craddock N, Owen MJ, Molecular Psychiatry, Volume 1, 6 (December 1996) pp.434-436
    • Confirmation of association between expanded CAG/CTG repeats and both schizophrenia and bipolar disorder.
      O'Donovan MC, Guy C, Craddock N, Bowen T, McKeon P, Macedo A, Maier W, Wildenauer D, Aschauer HN, Sorbi S, Feldman E, Mynett-Johnson L, Claffey E, Nacmias B, Valente J, Dourado A, Grassi E, Lenzinger E, Heiden AM, Moorhead S, Harrison D, Williams J, McGuffin P, Owen MJ, Psychol Med, Volume 26, 6 (November 1996) pp.1145-1153
    • Psychiatric genetics.
      Craddock N, Br J Psychiatry, Volume 169, 3 (September 1996) pp.386-392
    • Modern molecular genetic approaches to psychiatric disease.
      Craddock N, Owen MJ, Br Med Bull, Volume 52, 3 (July 1996) pp.434-452
    • Concurrent validity of the OPCRIT Diagnostic System - Comparison of OPCRIT diagnoses with consensus best-estimate lifetime diagnoses
      Craddock N, Asherson P, Owen MJ, Williams J, McGuffin P, Farmer AE, British Journal Of Psychiatry, Volume 169, 1 (July 1996) pp.58-63
    • Assessing the statistical power to detect linkage in a sample of 51 bipolar affective disorder pedigrees
      Lim LCC, Craddock N, Owen M, Sham P, Nothen MM, Korner J, Rietschel M, Fimmer R, Propping P, McGuffin P, Murray R, Gill M, Behavior Genetics, Volume 26, 2 (March 1996) pp.113-122
    • Modern molecular genetic approaches to complex traits: implications for psychiatric disorders.
      Owen MJ, Craddock N, Mol Psychiatry, Volume 1, 1 (March 1996) pp.21-26
    • Increasing the efficiency of genomic searches for linkage in complex disorders by DNA pooling of affected sib-pairs.
      Craddock N, Daniels J, Holmans P, Williams N, Owen MJ, Mol Psychiatry, Volume 1, 1 (March 1996) pp.59-64
    • Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's disease
      Wragg M, Hutton M, Talbot C, Busfield F, Han SW, Lendon C, Clark RF, Morris JC, Edwards D, Goate A, Pfeiffer E, Crook R, Prihar G, Phillips H, Baker M, Hardy J, Rossor M, Houlden H, Karran E, Roberts G, Craddock N, Lancet, Volume 347, 9000 (February 1996) pp.509-512
    • Polymorphism in AACT gene may lower age of onset of Alzheimer's disease.
      Talbot C, Houlden H, Craddock N, Crook R, Hutton M, Lendon C, Prihar G, Morris JC, Hardy J, Goate A, Neuroreport, Volume 7, 2 (January 1996) pp.534-536
    • Association study of bipolar disorder at the phospholipase A2 gene (PLA2A) in the Darier's disease (DAR) region of chromosome 12q23-q24.1.
      Jacobsen N, Daniels J, Moorhead S, Harrison D, Feldman E, McGuffin P, Owen MJ, Craddock N, Psychiatr Genet, Volume 6, 4 (1996) pp.195-199
  • 1995
    • Mathematical limits of multilocus models: the genetic transmission of bipolar disorder.
      Craddock N, Khodel V, Van Eerdewegh P, Reich T, Am J Hum Genet, Volume 57, 3 (September 1995) pp.690-702
    • No evidence for allelic association between bipolar disorder and monoamine oxidase A gene polymorphisms.
      Craddock N, Daniels J, Roberts E, Rees M, McGuffin P, Owen MJ, Am J Med Genet, Volume 60, 4 (August 1995) pp.322-324
    • EXPANDED CAG REPEATS IN SCHIZOPHRENIA AND BIPOLAR DISORDER
      ODONOVAN M, GUY C, CRADDOCK N, MURPHY K, CARDNO A, JONES L, OWEN M, MCGUFFIN P, Nature Genetics, Volume 10, 4 (August 1995) pp.380-381
    • LINKAGE STUDIES OF BIPOLAR DISORDER IN THE REGION OF THE DARIERS-DISEASE GENE ON CHROMOSOME 12Q23-24.1
      DAWSON E, PARFITT E, ROBERTS Q, DANIELS J, LIM L, SHAM P, NOTHEN M, PROPPING P, LANCZIK M, MAIER W, REUNER U, WEISSENBACH J, GILL M, POWELL J, MCGUFFIN P, OWEN M, CRADDOCK N, American Journal Of Medical Genetics, Volume 60, 2 (April 1995) pp.94-102
    • ASSOCIATION STUDY OF BIPOLAR DISORDER USING A FUNCTIONAL POLYMORPHISM (SER311-]CYS) IN THE DOPAMINE D2 RECEPTOR GENE
      CRADDOCK N, ROBERTS Q, WILLIAMS N, MCGUFFIN P, OWEN M, Psychiatric Genetics, Volume 5, 2 (1995) pp.63-65
    • Linkage studies on chromosome 22 in familial schizophrenia
      Vallada HP, Gill M, Sham P, Lim LC, Nanko S, Asherson P, Murray RM, McGuffin P, Owen M, Collier D, , Volume 60, 2 (1995) pp.139-46-139-46
  • 1994
    • IS THERE AN INVERSE RELATIONSHIP BETWEEN DOWNS-SYNDROME AND BIPOLAR AFFECTIVE-DISORDER - LITERATURE-REVIEW AND GENETIC-IMPLICATIONS
      CRADDOCK N, OWEN M, Journal Of Intellectual Disability Research, Volume 38 (December 1994) pp.613-620
    • DARIERS-DISEASE COSEGREGATING WITH AFFECTIVE-DISORDER
      CRADDOCK N, MCGUFFIN P, OWEN M, British Journal Of Psychiatry, Volume 165 (August 1994) pp.272-272
    • Variation at the fragile X locus does not influence susceptibility to bipolar disorder.
      Craddock N, Daniels J, McGuffin P, Owen M, Am J Med Genet, Volume 54, 2 (June 1994) pp.141-143
    • Protection against Alzheimer's disease with apoE epsilon 2.
      Talbot C, Lendon C, Craddock N, Shears S, Morris JC, Goate A, Lancet, Volume 343, 8910 (June 1994) pp.1432-1433
    • Estimates of risks in relatives of psychotic probands.
      Craddock N, Giuffra LA, Br J Psychiatry, Volume 164, 5 (May 1994) pp.706-707
    • Chromosomal aberrations and bipolar affective disorder.
      Craddock N, Owen M, Br J Psychiatry, Volume 164, 4 (April 1994) pp.507-512
    • Familial cosegregation of major affective disorder and Darier's disease (keratosis follicularis)
      Craddock N, Owen M, Burge S, Kurian B, Thomas P, McGuffin P, Br J Psychiatry, Volume 164, 3 (March 1994) pp.355-358
    • BIPOLAR AFFECTIVE PUERPERAL PSYCHOSIS ASSOCIATED WITH CONSANGUINITY
      CRADDOCK N, BROCKINGTON I, MANT R, PARFITT E, MCGUFFIN P, OWEN M, British Journal Of Psychiatry, Volume 164 (March 1994) pp.359-364
    • The gene for Darier's disease maps between D12S78 and D12S79.
      Parfitt E, Burge S, Craddock N, Roberts E, McLean WH, Weissenbach J, McGuffin P, Owen M, Hum Mol Genet, Volume 3, 1 (January 1994) pp.35-38
    • ASSOCIATION AND HAPLOTYPE ANALYSIS AT THE TYROSINE-HYDROXYLASE LOCUS IN A COMBINED GERMAN-BRITISH SAMPLE OF MANIC-DEPRESSIVE PATIENTS AND CONTROLS
      KORNER J, RIETSCHEL M, HUNT N, CASTLE D, GILL M, NOTHEN M, CRADDOCK N, DANIELS J, OWEN M, FIMMERS R, FRITZE J, MOLLER H, PROPPING P, Psychiatric Genetics, Volume 4, 3 (1994) pp.167-175
    • Partial trisomy of C11q and its effect on affective disorder segregating in a three generation family.
      Craddock N, Krishnan VH, Prasher VP, Davison V, Psychiatr Genet, Volume 4, 1 (1994) pp.67-69
  • 1993
    • THE GENE FOR DARIERS-DISEASE MAPS TO CHROMOSOME 12Q23-Q24.1 (VOL 2, PG 1941, 1993)
      CRADDOCK N, DAWSON E, BURGE S, PARFITT L, MANT R, ROBERTS Q, DANIELS J, GILL M, MCGUFFIN P, POWELL J, OWEN M, Human Molecular Genetics, Volume 2, 12 (December 1993) pp.2214-2214
    • THE GENE FOR DARIERS-DISEASE MAPS TO CHROMOSOME 12Q23-Q24.1
      CRADDOCK N, DAWSON E, BURGE S, PARFITT L, MANT B, ROBERTS Q, DANIELS J, GILL M, MCGUFFIN P, POWELL J, OWEN M, Human Molecular Genetics, Volume 2, 11 (November 1993) pp.1941-1943
    • Approaches to the genetics of affective disorders.
      Craddock N, McGuffin P, Ann Med, Volume 25, 4 (August 1993) pp.317-322
    • THE DOPAMINE-D3 RECEPTOR GENE - NO ASSOCIATION WITH BIPOLAR AFFECTIVE-DISORDER
      SHAIKH S, BALL D, CRADDOCK N, CASTLE D, HUNT N, MANT R, OWEN M, COLLIER D, GILL M, Journal Of Medical Genetics, Volume 30, 4 (April 1993) pp.308-309
    • Linkage is excluded between Darier's disease and the Duffy blood group locus in five British families.
      Craddock N, Burge S, Parfitt L, Owen M, Ann Genet, Volume 36, 4 (1993) pp.211-213
  • 1992
    • Missed neuroleptic malignant syndrome.
      Craddock B, Craddock N, Bmj, Volume 304, 6836 (May 1992) p. 1246
    • CHRISTMAS DISEASE AND MAJOR AFFECTIVE-DISORDER
      CRADDOCK N, OWEN M, British Journal Of Psychiatry, Volume 160 (May 1992) pp.715-715
  • 1991
    • CPK IN NMS
      CRADDOCK B, CRADDOCK N, MILNER G, British Journal Of Psychiatry, Volume 158 (January 1991) pp.131-131
    • CPK in NMS.
      Craddock B, Craddock N, Milner G, Br J Psychiatry, Volume 158 (January 1991) p. 130
  • 1990
    • Pseudocyesis followed by depressive psychosis.
      Craddock B, Craddock N, Liebling LI, Br J Psychiatry, Volume 157 (October 1990) pp.624-625
  • 1989
    • Psychiatric discharge summaries: differing requirements of psychiatrists and general practitioners.
      Craddock N, Craddock B, Bmj, Volume 299, 6712 (December 1989) p. 1382
    • UNITED-STATES VISAS AND INSANITY
      CRADDOCK N, CRADDOCK B, British Journal Of Psychiatry, Volume 155 (November 1989) pp.712-713
    • HOSPITAL SUICIDES
      SMYTH M, CRADDOCK N, British Journal Of Psychiatry, Volume 154 (May 1989) pp.728-728
• Conference proceedings
  • 2010
    • THE GENETIC DECONSTRUCTION OF PSYCHOSIS
      Owen MJ, Craddock N, Jablensky A, Deconstructing Psychosis: Refining The Research Agenda For Dsm-V (2010) pp.69-82
  • 2000
    • DOVAM-S: Evidence for generic scanning conditions and application to the steroid receptor gene family.
      Feng J, Buzin CH, Craddock N, Jones I, Cook E, Goldman D, Heston LL, Sommer SS, American Journal Of Human Genetics, Volume 67, 4 (October 2000) pp.352-352
    • The Bipolar Affective Disorder Dimensional Scale (BADDS): A dimensional classification for use in bipolar disorder.
      Craddock N, Jones IR, McCandless F, Kirov G, Heron J, Robertson E, Cardno A, American Journal Of Medical Genetics, Volume 96, 4 (August 2000) pp.473-473