MRC Centre for Neuropsychiatric Genetics and Genomics

Index of publications

• Articles
  • 2012
  • 2011
  • 2010
  • 2009
  • 2008
  • 2007
  • 2006
  • 2005
  • 2004
  • 2003
  • 2002
  • 2001
  • 2000
  • 1999
  • 1998
  • 1997
  • 1996
  • 1995
  • 1994
• Conference proceedings
  • 2012
  • 2010
  • 2007
  • 2006
  • 2005
  • 2004
  • 2003
  • 2002
  • 2001
  • 2000
  • 1999
  • 1998
  • 1997

Publications

• Articles
  • 2012
    • Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease.
      Keller MF, Saad M, Bras J, Bettella F, Nicolaou N, Simón-Sánchez J, Mittag F, Büchel F, Sharma M, Gibbs JR, Schulte C, Moskvina V, Durr A, Holmans P, Kilarski LL, Guerreiro R, Hernandez DG, Brice A, Ylikotila P, Stefánsson H, Majamaa K, Morris HR, Williams N, Gasser T, Heutink P, Wood NW, Hardy J, Martinez M, Singleton AB, Nalls MA, International Parkinson's Disease Genomics Consortium (IPDGC) None, Wellcome Trust Case Control Consortium 2 (WTCCC2) None, Hum Mol Genet, Volume 21, 22 (November 2012) pp.4996-5009
    • Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease.
      Kilarski LL, Pearson JP, Newsway V, Majounie E, Knipe MD, Misbahuddin A, Chinnery PF, Burn DJ, Clarke CE, Marion MH, Lewthwaite AJ, Nicholl DJ, Wood NW, Morrison KE, Williams-Gray CH, Evans JR, Sawcer SJ, Barker RA, Wickremaratchi MM, Ben-Shlomo Y, Williams NM, Morris HR, Mov Disord, Volume 27, 12 (October 2012) pp.1522-1529
    • Genome-Wide Association Study of Multiplex Schizophrenia Pedigrees
      Levinson DF, Shi J, Wang K, Oh S, Riley B, Pulver AE, Wildenauer DB, Laurent C, Mowry BJ, Gejman PV, Owen MJ, Kendler KS, Nestadt G, Schwab SG, Mallet J, Nertney D, Sanders AR, Williams NM, Wormley B, Lasseter VK, Albus M, Godard-Bauche S, Alexander M, Duan J, O'Donovan MC, Walsh D, O'Neill A, Papadimitriou GN, Dikeos D, Maier W, Lerer B, Campion D, Cohen D, Jay M, Fanous A, Eichhammer P, Silverman JM, Norton N, Zhang N, Hakonarson H, Gao C, Citri A, Hansen M, Ripke S, Dudbridge F, Holmans PA, Consor SPGWAS, American Journal Of Psychiatry, Volume 169, 9 (September 2012) pp.963-973
    • C9ORF72 expansion in amyotrophic lateral sclerosis/frontotemporal dementia also causes parkinsonism.
      O'Dowd S, Curtin D, Waite AJ, Roberts K, Pender N, Reid V, O'Connell M, Williams NM, Morris HR, Traynor BJ, Lynch T, Mov Disord, Volume 27, 8 (July 2012) pp.1072-1074
    • Recent advances in the genetics of the ALS-FTLD complex.
      Morris HR, Waite AJ, Williams NM, Neal JW, Blake DJ, Curr Neurol Neurosci Rep, Volume 12, 3 (June 2012) pp.243-250
    • Tau acts as an independent genetic risk factor in pathologically proven PD.
      Charlesworth G, Gandhi S, Bras JM, Barker RA, Burn DJ, Chinnery PF, Gentleman SM, Guerreiro R, Hardy J, Holton JL, Lees A, Morrison K, Sheerin UM, Williams N, Morris H, Revesz T, Wood NW, Neurobiol Aging, Volume 33, 4 (April 2012) pp.838.e7-838.11
    • Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.
      Majounie E, Renton AE, Mok K, Dopper EG, Waite A, Rollinson S, Chiò A, Restagno G, Nicolaou N, Simon-Sanchez J, van Swieten JC, Abramzon Y, Johnson JO, Sendtner M, Pamphlett R, Orrell RW, Mead S, Sidle KC, Houlden H, Rohrer JD, Morrison KE, Pall H, Talbot K, Ansorge O, Chromosome 9-ALS/FTD Consortium None, French research network on FTLD/FTLD/ALS None, ITALSGEN Consortium None, Hernandez DG, Arepalli S, Sabatelli M, Mora G, Corbo M, Giannini F, Calvo A, Englund E, Borghero G, Floris GL, Remes AM, Laaksovirta H, McCluskey L, Trojanowski JQ, Van Deerlin VM, Schellenberg GD, Nalls MA, Drory VE, Lu CS, Yeh TH, Ishiura H, Takahashi Y, Tsuji S, Le Ber I, Brice A, Drepper C, Williams N, Kirby J, Shaw P, Hardy J, Tienari PJ, Heutink P, Morris HR, Pickering-Brown S, Traynor BJ, Lancet Neurol, Volume 11, 4 (April 2012) pp.323-330
    • Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.
      Stergiakouli E, Hamshere M, Holmans P, Langley K, Zaharieva I, Hawi Z, Kent L, Gill M, Williams N, Owen MJ, O'Donovan M, Thapar A, Am J Psychiatry, Volume 169, 2 (February 2012) pp.186-194
    • Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.
      Williams NM, Franke B, Mick E, Anney RJ, Freitag CM, Gill M, Thapar A, O'Donovan MC, Owen MJ, Holmans P, Kent L, Middleton F, Zhang-James Y, Liu L, Meyer J, Nguyen TT, Romanos J, Romanos M, Seitz C, Renner TJ, Walitza S, Warnke A, Palmason H, Buitelaar J, Rommelse N, Vasquez AA, Hawi Z, Langley K, Sergeant J, Steinhausen HC, Roeyers H, Biederman J, Zaharieva I, Hakonarson H, Elia J, Lionel AC, Crosbie J, Marshall CR, Schachar R, Scherer SW, Todorov A, Smalley SL, Loo S, Nelson S, Shtir C, Asherson P, Reif A, Lesch KP, Faraone SV, Am J Psychiatry, Volume 169, 2 (February 2012) pp.195-204
    • Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.
      Williams NM, Franke B, Mick E, Anney RJ, Freitag CM, Gill M, Thapar A, O'Donovan MC, Owen MJ, Holmans P, Kent L, Middleton F, Zhang-James Y, Liu L, Meyer J, Nguyen TT, Romanos J, Romanos M, Seitz C, Renner TJ, Walitza S, Warnke A, Palmason H, Buitelaar J, Rommelse N, Vasquez AA, Hawi Z, Langley K, Sergeant J, Steinhausen HC, Roeyers H, Biederman J, Zaharieva I, Hakonarson H, Elia J, Lionel AC, Crosbie J, Marshall CR, Schachar R, Scherer SW, Todorov A, Smalley SL, Loo S, Nelson S, Shtir C, Asherson P, Reif A, Lesch KP, Faraone SV, Am J Psychiatry, Volume 169, 2 (February 2012) pp.195-204
    • Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.
      Stergiakouli E, Hamshere M, Holmans P, Langley K, Zaharieva I, deCODE Genetics None, Psychiatric GWAS Consortium None, Hawi Z, Kent L, Gill M, Williams N, Owen MJ, O'Donovan M, Thapar A, Am J Psychiatry, Volume 169, 2 (February 2012) pp.186-194
    • Chromosome 9 ALS and FTD locus is probably derived from a single founder.
      Mok K, Traynor BJ, Schymick J, Tienari PJ, Laaksovirta H, Peuralinna T, Myllykangas L, Chiò A, Shatunov A, Boeve BF, Boxer AL, DeJesus-Hernandez M, Mackenzie IR, Waite A, Williams N, Morris HR, Simón-Sánchez J, van Swieten JC, Heutink P, Restagno G, Mora G, Morrison KE, Shaw PJ, Rollinson PS, Al-Chalabi A, Rademakers R, Pickering-Brown S, Orrell RW, Nalls MA, Hardy J, Neurobiol Aging, Volume 33, 1 (January 2012) pp.209.e3-209.e8
    • Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder.
      Elia J, Glessner JT, Wang K, Takahashi N, Shtir CJ, Hadley D, Sleiman PM, Zhang H, Kim CE, Robison R, Lyon GJ, Flory JH, Bradfield JP, Imielinski M, Hou C, Frackelton EC, Chiavacci RM, Sakurai T, Rabin C, Middleton FA, Thomas KA, Garris M, Mentch F, Freitag CM, Steinhausen HC, Todorov AA, Reif A, Rothenberger A, Franke B, Mick EO, Roeyers H, Buitelaar J, Lesch KP, Banaschewski T, Ebstein RP, Mulas F, Oades RD, Sergeant J, Sonuga-Barke E, Renner TJ, Romanos M, Romanos J, Warnke A, Walitza S, Meyer J, Pálmason H, Seitz C, Loo SK, Smalley SL, Biederman J, Kent L, Asherson P, Anney RJ, Gaynor JW, Shaw P, Devoto M, White PS, Grant SF, Buxbaum JD, Rapoport JL, Williams NM, Nelson SF, Faraone SV, Hakonarson H, Nat Genet, Volume 44, 1 (January 2012) pp.78-84
    • Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease.
      Simón-Sánchez J, Kilarski LL, Nalls MA, Martinez M, Schulte C, Holmans P, International Parkinson's Disease Genomics Consortium None, Wellcome Trust Case Control Consortium None, Gasser T, Hardy J, Singleton AB, Wood NW, Brice A, Heutink P, Williams N, Morris HR, Plos One, Volume 7, 3 (2012) p. e28787
  • 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
    • Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants.
      Langley K, Martin J, Agha SS, Davies C, Stergiakouli E, Holmans P, Williams N, Owen M, O'Donovan M, Thapar A, Br J Psychiatry, Volume 199, 5 (November 2011) pp.398-403
    • A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
      Renton AE, Majounie E, Waite A, Simón-Sánchez J, Rollinson S, Gibbs JR, Schymick JC, Laaksovirta H, van Swieten JC, Myllykangas L, Kalimo H, Paetau A, Abramzon Y, Remes AM, Kaganovich A, Scholz SW, Duckworth J, Ding J, Harmer DW, Hernandez DG, Johnson JO, Mok K, Ryten M, Trabzuni D, Guerreiro RJ, Orrell RW, Neal J, Murray A, Pearson J, Jansen IE, Sondervan D, Seelaar H, Blake D, Young K, Halliwell N, Callister JB, Toulson G, Richardson A, Gerhard A, Snowden J, Mann D, Neary D, Nalls MA, Peuralinna T, Jansson L, Isoviita VM, Kaivorinne AL, Hölttä-Vuori M, Ikonen E, Sulkava R, Benatar M, Wuu J, Chiò A, Restagno G, Borghero G, Sabatelli M, ITALSGEN Consortium None, Heckerman D, Rogaeva E, Zinman L, Rothstein JD, Sendtner M, Drepper C, Eichler EE, Alkan C, Abdullaev Z, Pack SD, Dutra A, Pak E, Hardy J, Singleton A, Williams NM, Heutink P, Pickering-Brown S, Morris HR, Tienari PJ, Traynor BJ, Neuron, Volume 72, 2 (October 2011) pp.257-268
    • 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
    • Molecular mechanisms in 22q11 deletion syndrome.
      Williams NM, Schizophr Bull, Volume 37, 5 (September 2011) pp.882-889
    • A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease
      Plagnol V, Nalls MA, Bras JM, Hernandez DG, Sharma M, Sheerin U, Saad M, Simon-Sanchez J, Schulte C, Lesage S, Sveinbjornsdottir S, Amouyel P, Arepalli S, Band G, Barker RA, Bellinguez C, Ben-Shlomo Y, Berendse HW, Berg D, Bhatia K, de Bie RMA, Biffi A, Bloem B, Bochdanovits Z, Bonin M, Brockmann K, Brooks J, Burn DJ, Charlesworth G, Chen H, Chinnery PF, Chong S, Clarke CE, Cookson MR, Cooper JM, Corvol JC, Counsell C, Damier P, Dartigues J, Deloukas P, Deuschl G, Dexter DT, van Dijk KD, Dillman A, Durif F, Duerr A, Edkins S, Evans JR, Foltynie T, Freeman C, Gao J, Gardner M, Gibbs JR, Goate A, Gray E, Guerreiro R, Gustafsson O, Harris C, Hellenthal G, van Hilten JJ, Hofman A, Hollenbeck A, Holton J, Hu M, Huang X, Huber H, Hudson G, Hunt SE, Huttenlocher J, Illig T, Jonsson PV, Langford C, Lees A, Lichtner P, Limousin P, Lopez G, Lorenz D, McNeill A, Moorby C, Moore M, Morris H, Morrison KE, Mudanohwo E, O'Sullivan SS, Pearson J, Pearson R, Perlmutter JS, Petursson H, Pirinen M, Pollak P, Post B, Potter S, Ravina B, Revesz T, Riess O, Rivadeneira F, Rizzu P, Ryten M, Sawcer S, Schapira A, Scheffer H, Shaw K, Shoulson I, Sidransky E, de Silva R, Smith C, Spencer CCA, Stefansson H, Steinberg S, Stockton JD, Strange A, Su Z, Talbot K, Tanner CM, Tashakkori-Ghanbaria A, Tison F, Trabzuni D, Traynor BJ, Uitterlinden AG, Vandrovcova J, Velseboer D, Vidailhet M, Vukcevic D, Walker R, van de Warrenburg B, Weale ME, Wickremaratchi M, Williams N, Williams-Gray CH, Winder-Rhodes S, Stefansson K, Martinez M, Donnelly P, Singleton AB, Hardy J, Heutink P, Brice A, Gasser T, Wood NW, WTCCC2 None, Plos Genetics, Volume 7, 6 (June 2011)
    • Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p.
      Pearson JP, Williams NM, Majounie E, Waite A, Stott J, Newsway V, Murray A, Hernandez D, Guerreiro R, Singleton AB, Neal J, Morris HR, J Neurol, Volume 258, 4 (April 2011) pp.647-655
    • Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder.
      Stergiakouli E, Langley K, Williams H, Walters J, Williams NM, Suren S, Giegling I, Wilkinson LS, Owen MJ, O'Donovan MC, Rujescu D, Thapar A, Davies W, Genes Brain Behav, Volume 10, 3 (April 2011) pp.334-344
    • 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
    • Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
      Nalls MA, Plagnol V, Hernandez DG, Sharma M, Sheerin U, Saad M, Simon-Sanchez J, Schulte C, Lesage S, Sveinbjornsdottir S, Arepalli S, Barker R, Ben-Shlomo Y, Berendse HW, Berg D, Bhatia K, de Bie RMA, Biffi A, Bloem B, Bochdanovits Z, Bonin M, Bras JM, Brockmann K, Brooks J, Burn DJ, Charlesworth G, Chen H, Chinnery PF, Chong S, Clarke CE, Cookson MR, Cooper JM, Corvol JC, Counsell C, Damier P, Dartigues J, Deloukas P, Deuschl G, Dexter DT, van Dijk KD, Dillman A, Durif F, Duerr A, Edkins S, Evans JR, Foltynie T, Gao J, Gardner M, Gibbs JR, Goate A, Gray E, Guerreiro R, Gustafsson O, Harris C, van Hilten JJ, Hofman A, Hollenbeck A, Holton J, Hu M, Huang X, Huber H, Hudson G, Hunt SE, Huttenlocher J, Illig T, Jonsson PV, Lambert J, Langford C, Lees A, Lichtner P, Limousin P, Lopez G, Lorenz D, McNeill A, Moorby C, Moore M, Morris HR, Morrison KE, Mudanohwo E, O'Sullivan SS, Pearson J, Perlmutter JS, Petursson H, Pollak P, Post B, Potter S, Ravina B, Revesz T, Riess O, Rivadeneira F, Rizzu P, Ryten M, Sawcer S, Schapira A, Scheffer H, Shaw K, Shoulson I, Sidransky E, Smith C, Spencer CCA, Stefansson H, Stockton JD, Strange A, Talbot K, Tanner CM, Tashakkori-Ghanbaria A, Tison F, Trabzuni D, Traynor BJ, Uitterlinden AG, Velseboer D, Vidailhet M, Walker R, van de Warrenburg B, Wickremaratchi M, Williams N, Williams-Gray CH, Winder-Rhodes S, Stefansson K, Martinez M, Hardy J, Heutink P, Brice A, Gasser T, Singleton AB, Wood NW, Consort IPDG, Consor WTC, Lancet, Volume 377, 9766 (February 2011) pp.641-649
    • Structural variations in attention-deficit hyperactivity disorder - Authors' reply.
      Williams N, O'Donovan MC, Owen MJ, Thapar A, Lancet, Volume 377, 9763 (January 2011) pp.378-378
    • 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
    • Steroid sulfatase is a potential modifier of cognition in Attention Deficit Hyperactivity Disorder.
      Stergiakouli E, Langley K, Williams H, Walters J, Williams NM, Suren S, Giegling I, Wilkinson LS, Owen MJ, O'Donovan MC, Rujescu D, Thapar A, Davies W, Genes Brain Behav (January 2011)
  • 2010
    • 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
    • Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.
      Williams NM, Zaharieva I, Martin A, Langley K, Mantripragada K, Fossdal R, Stefansson H, Stefansson K, Magnusson P, Gudmundsson OO, Gustafsson O, Holmans P, Owen MJ, O'Donovan M, Thapar A, Lancet, Volume 376, 9750 (October 2010) pp.1401-1408
    • Prevalence of Mutations in Parkin, PINK1, and DJ-1 in Early Onset Parkinson's Disease - A Community Based and Regional Study
      Pearson JP, Kilarski LL, Newsway V, Majounie E, Perera D, Misbahuddin A, Chinnery PF, Burn DJ, Lewthwaite AJ, Clarke CE, Morrison KE, Evans JR, Sawcer SJ, Barker RA, Wickremaratchi MM, Williams NM, Morris HR, Movement Disorders, Volume 25 (September 2010) pp.S610-S610
    • Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.
      Neale BM, Medland SE, Ripke S, Asherson P, Franke B, Lesch KP, Faraone SV, Nguyen TT, Schäfer H, Holmans P, Daly M, Steinhausen HC, Freitag C, Reif A, Renner TJ, Romanos M, Romanos J, Walitza S, Warnke A, Meyer J, Palmason H, Buitelaar J, Vasquez AA, Lambregts-Rommelse N, Gill M, Anney RJ, Langely K, O'Donovan M, Williams N, Owen M, Thapar A, Kent L, Sergeant J, Roeyers H, Mick E, Biederman J, Doyle A, Smalley S, Loo S, Hakonarson H, Elia J, Todorov A, Miranda A, Mulas F, Ebstein RP, Rothenberger A, Banaschewski T, Oades RD, Sonuga-Barke E, McGough J, Nisenbaum L, Middleton F, Hu X, Nelson S, Psychiatric GWAS Consortium: ADHD Subgroup None, J Am Acad Child Adolesc Psychiatry, Volume 49, 9 (September 2010) pp.884-897
    • Failure to confirm association between PIK4CA and psychosis in 22q11.2 deletion syndrome.
      Ikeda M, Williams N, Williams HJ, Smith R, Monks S, Owen MJ, Murphy KC, O'Donovan MC, Am J Med Genet B Neuropsychiatr Genet, Volume 153B, 4 (June 2010) pp.980-982
    • Perry syndrome due to the DCTN1 G71R mutation: a distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure.
      Newsway V, Fish M, Rohrer JD, Majounie E, Williams N, Hack M, Warren JD, Morris HR, Mov Disord, Volume 25, 6 (April 2010) pp.767-770
    • Mutation screening of the DTNBP1 exonic sequence in 669 schizophrenics and 710 controls using high-resolution melting analysis.
      Dwyer S, Carroll L, Mantripragada KK, Owen MJ, O'Donovan MC, Williams NM, Am J Med Genet B Neuropsychiatr Genet, Volume 153B, 3 (April 2010) pp.766-774
    • Excessive appetitive arousal in Prader-Willi syndrome.
      Hinton EC, Isles AR, Williams NM, Parkinson JA, Appetite, Volume 54, 1 (February 2010) pp.225-228
    • Experimental approaches for identifying schizophrenia risk genes.
      Mantripragada KK, Carroll LS, Williams NM, Curr Top Behav Neurosci, Volume 4 (2010) pp.587-610
  • 2009
    • Evidence that putative ADHD low risk alleles at SNAP25 may increase the risk of schizophrenia.
      Carroll LS, Kendall K, O'Donovan MC, Owen MJ, Williams NM, Am J Med Genet B Neuropsychiatr Genet, Volume 150B, 7 (October 2009) pp.893-899
    • 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
    • Meta-analysis of 32 genome-wide linkage studies of schizophrenia.
      Ng MY, Levinson DF, Faraone SV, Suarez BK, DeLisi LE, Arinami T, Riley B, Paunio T, Pulver AE, Irmansyah None, Holmans PA, Escamilla M, Wildenauer DB, Williams NM, Laurent C, Mowry BJ, Brzustowicz LM, Maziade M, Sklar P, Garver DL, Abecasis GR, Lerer B, Fallin MD, Gurling HM, Gejman PV, Lindholm E, Moises HW, Byerley W, Wijsman EM, Forabosco P, Tsuang MT, Hwu HG, Okazaki Y, Kendler KS, Wormley B, Fanous A, Walsh D, O'Neill FA, Peltonen L, Nestadt G, Lasseter VK, Liang KY, Papadimitriou GM, Dikeos DG, Schwab SG, Owen MJ, O'Donovan MC, Norton N, Hare E, Raventos H, Nicolini H, Albus M, Maier W, Nimgaonkar VL, Terenius L, Mallet J, Jay M, Godard S, Nertney D, Alexander M, Crowe RR, Silverman JM, Bassett AS, Roy MA, Mérette C, Pato CN, Pato MT, Roos JL, Kohn Y, Amann-Zalcenstein D, Kalsi G, McQuillin A, Curtis D, Brynjolfson J, Sigmundsson T, Petursson H, Sanders AR, Duan J, Jazin E, Myles-Worsley M, Karayiorgou M, Lewis CM, Mol Psychiatry, Volume 14, 8 (August 2009) pp.774-785
    • Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms.
      Holmans PA, Riley B, Pulver AE, Owen MJ, Wildenauer DB, Gejman PV, Mowry BJ, Laurent C, Kendler KS, Nestadt G, Williams NM, Schwab SG, Sanders AR, Nertney D, Mallet J, Wormley B, Lasseter VK, O'Donovan MC, Duan J, Albus M, Alexander M, Godard S, Ribble R, Liang KY, Norton N, Maier W, Papadimitriou G, Walsh D, Jay M, O'Neill A, Lerer FB, Dikeos D, Crowe RR, Silverman JM, Levinson DF, Mol Psychiatry, Volume 14, 8 (August 2009) pp.786-795
    • The genetic aetiology of late-onset chronic progressive cerebellar ataxia. A population-based study.
      Wardle M, Majounie E, Muzaimi MB, Williams NM, Morris HR, Robertson NP, J Neurol, Volume 256, 3 (March 2009) pp.343-348
    • Parkin-related disease clinically diagnosed as a pallido-pyramidal syndrome.
      Wickremaratchi MM, Majounie E, Morris HR, Williams NM, Lewis H, Gill SS, Khan S, Heywood P, Hardy J, Wiles CM, Singleton AB, Quinn NP, Mov Disord, Volume 24, 1 (January 2009) pp.138-140
    • An examination of MUTED as a schizophrenia susceptibility gene.
      Gerrish A, Williams H, Moskvina V, Owen MJ, O'Donovan MC, Williams NM, Schizophr Res, Volume 107, 1 (January 2009) pp.110-111
    • 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
    • Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia.
      Liu Y, Chen G, Norton N, Liu W, Zhu H, Zhou P, Luan M, Yang S, Chen X, Carroll L, Williams NM, O'Donovan MC, Kirov G, Owen MJ, J Biomed Biotechnol, Volume 2009 (2009) p. 536918
  • 2008
    • Analysis of copy number variation using quantitative interspecies competitive PCR.
      Williams NM, Williams H, Majounie E, Norton N, Glaser B, Morris HR, Owen MJ, O'Donovan MC, Nucleic Acids Res, Volume 36, 17 (October 2008) p. e112
    • 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
    • Support for neuregulin 1 as a susceptibility gene for bipolar disorder and schizophrenia.
      Georgieva L, Dimitrova A, Ivanov D, Nikolov I, Williams NM, Grozeva D, Zaharieva I, Toncheva D, Owen MJ, Kirov G, O'Donovan MC, Biol Psychiatry, Volume 64, 5 (September 2008) pp.419-427
    • 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
    • Gene copy number variation in schizophrenia.
      Sutrala SR, Norton N, Williams NM, Buckland PR, Am J Med Genet B Neuropsychiatr Genet, Volume 147B, 5 (July 2008) pp.606-611
    • Dentatorubral pallidoluysian atrophy in South Wales.
      Wardle M, Majounie E, Williams NM, Rosser AE, Morris HR, Robertson NP, J Neurol Neurosurg Psychiatry, Volume 79, 7 (July 2008) pp.804-807
    • 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
    • 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
  • 2007
    • Case control analysis of repeat expansion size in ataxia.
      Majounie E, Wardle M, Muzaimi M, Cross WC, Robertson NP, Williams NM, Morris HR, Neurosci Lett, Volume 429, 1 (December 2007) pp.28-32
    • Association analysis of the glial cell line-derived neurotrophic factor (GDNF) gene in schizophrenia.
      Williams HJ, Norton N, Peirce T, Dwyer S, Williams NM, Moskvina V, Owen MJ, O'Donovan MC, Schizophr Res, Volume 97, 1-3 (December 2007) pp.271-276
    • Gene copy number variation in schizophrenia.
      Sutrala SR, Goossens D, Williams NM, Heyrman L, Adolfsson R, Norton N, Buckland PR, Del-Favero J, Schizophr Res, Volume 96, 1-3 (November 2007) pp.93-99
    • Genotype effects of CHRNA7, CNR1 and COMT in schizophrenia: interactions with tobacco and cannabis use.
      Zammit S, Spurlock G, Williams H, Norton N, Williams N, O'Donovan MC, Owen MJ, Br J Psychiatry, Volume 191 (November 2007) pp.402-407
    • Can community volunteers work to trace patients defaulting from scheduled psychiatric clinic appointments?
      Richards DA, Bradshaw TJ, Mairs H, Ricks E, Strumpher J, Williams N, Richardson R, S Afr Med J, Volume 97, 10 (October 2007) pp.946-947
    • Association analysis of AKT1 and schizophrenia in a UK case control sample.
      Norton N, Williams HJ, Dwyer S, Carroll L, Peirce T, Moskvina V, Segurado R, Nikolov I, Williams NM, Ikeda M, Iwata N, Owen MJ, O'Donovan MC, Schizophr Res, Volume 93, 1-3 (July 2007) pp.58-65
  • 2006
    • Genetic dissection of behavioural abnormalities in mouse models of DiGeorge/velocardiofacial syndrome
      Scambler PJ, Paylora R, Glaser B, Mupod A, Ataliotis P, Spencer C, Sobotka A, Sparks C, Choi C, Oghalai J, Curran S, Murphy KC, Monks S, Williams N, O'Donovan MC, Owen MJ, Lindsay E, Journal Of Intellectual Disability Research, Volume 50 (November 2006) pp.781-781
    • Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility.
      Glaser B, Moskvina V, Kirov G, Murphy KC, Williams H, Williams N, Owen MJ, O'Donovan MC, Schizophr Res, Volume 87, 1-3 (October 2006) pp.21-27
    • 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
    • Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples.
      Talkowski ME, Seltman H, Bassett AS, Brzustowicz LM, Chen X, Chowdari KV, Collier DA, Cordeiro Q, Corvin AP, Deshpande SN, Egan MF, Gill M, Kendler KS, Kirov G, Heston LL, Levitt P, Lewis DA, Li T, Mirnics K, Morris DW, Norton N, O'Donovan MC, Owen MJ, Richard C, Semwal P, Sobell JL, St Clair D, Straub RE, Thelma BK, Vallada H, Weinberger DR, Williams NM, Wood J, Zhang F, Devlin B, Nimgaonkar VL, Biol Psychiatry, Volume 60, 2 (July 2006) pp.152-162
    • 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
    • Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome
      Paylor R, Glaser B, Mupo A, Ataliotis P, Spencer C, Sobotka A, Sparks C, Choi CH, Oghalai J, Curran S, Murphy KC, Monks S, Williams N, O'Donovan MC, Owen MJ, Scambler PJ, Lindsay E, Proceedings Of The National Academy Of Sciences Of The United States Of America, Volume 103, 20 (May 2006) pp.7729-7734
    • 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
    • Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia.
      Norton N, Moskvina V, Morris DW, Bray NJ, Zammit S, Williams NM, Williams HJ, Preece AC, Dwyer S, Wilkinson JC, Spurlock G, Kirov G, Buckland P, Waddington JL, Gill M, Corvin AP, Owen MJ, O'Donovan MC, Am J Med Genet B Neuropsychiatr Genet, Volume 141B, 1 (January 2006) pp.96-101
    • Convergent evidence for 2',3'-cyclic nucleotide 3'-phosphodiesterase as a possible susceptibility gene for schizophrenia.
      Peirce TR, Bray NJ, Williams NM, Norton N, Moskvina V, Preece A, Haroutunian V, Buxbaum JD, Owen MJ, O'Donovan MC, Arch Gen Psychiatry, Volume 63, 1 (January 2006) pp.18-24
    • Chromosome 22 deletion syndrome and schizophrenia.
      Williams NM, O'Donovan MC, Owen MJ, Int Rev Neurobiol, Volume 73 (2006) pp.1-27
  • 2005
    • 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
    • Is the dysbindin gene (DTNBP1) a susceptibility gene for schizophrenia?
      Williams NM, O'Donovan MC, Owen MJ, Schizophr Bull, Volume 31, 4 (October 2005) pp.800-805
    • No association between schizophrenia and polymorphisms in COMT in two large samples.
      Williams HJ, Glaser B, Williams NM, Norton N, Zammit S, MacGregor S, Kirov GK, Owen MJ, O'Donovan MC, Am J Psychiatry, Volume 162, 9 (September 2005) pp.1736-1738
    • Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression.
      Bray NJ, Preece A, Williams NM, Moskvina V, Buckland PR, Owen MJ, O'Donovan MC, Hum Mol Genet, Volume 14, 14 (July 2005) pp.1947-1954
    • No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples.
      Glaser B, Schumacher J, Williams HJ, Jamra RA, Ianakiev N, Milev R, Ohlraun S, Schulze TG, Czerski PM, Hauser J, Jönsson EG, Sedvall GC, Klopp N, Illig T, Becker T, Propping P, Williams NM, Cichon S, Kirov G, Rietschel M, Murphy KC, O'Donovan MC, Nöthen MM, Owen MJ, Biol Psychiatry, Volume 58, 1 (July 2005) pp.78-80
    • A family based study implicates solute carrier family 1-member 3 (SLC1A3) gene in attention-deficit/hyperactivity disorder.
      Turic D, Langley K, Williams H, Norton N, Williams NM, Moskvina V, Van den Bree MB, Owen MJ, Thapar A, O'Donovan MC, Biol Psychiatry, Volume 57, 11 (June 2005) pp.1461-1466
    • 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
    • Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease.
      Holmans P, Hamshere M, Hollingworth P, Rice F, Tunstall N, Jones S, Moore P, Wavrant DeVrieze F, Myers A, Crook R, Compton D, Marshall H, Meyer D, Shears S, Booth J, Ramic D, Williams N, Norton N, Abraham R, Kehoe P, Williams H, Rudrasingham V, O'Donovan M, Jones L, Hardy J, Goate A, Lovestone S, Owen M, Williams J, Am J Med Genet B Neuropsychiatr Genet, Volume 135B, 1 (May 2005) pp.24-32
    • 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
    • Streamlined analysis of pooled genotype data in SNP-based association studies.
      Moskvina V, Norton N, Williams N, Holmans P, Owen M, O'donovan M, Genet Epidemiol, Volume 28, 3 (April 2005) pp.273-282
    • No evidence for association between polymorphisms in GRM3 and schizophrenia.
      Norton N, Williams HJ, Dwyer S, Ivanov D, Preece AC, Gerrish A, Williams NM, Yerassimou P, Zammit S, O'Donovan MC, Owen MJ, Bmc Psychiatry, Volume 5 (2005) p. 23
  • 2004
    • Association analysis of two candidate phospholipase genes that map to the chromosome 15q15.1-15.3 region associated with reading disability.
      Morris DW, Ivanov D, Robinson L, Williams N, Stevenson J, Owen MJ, Williams J, O'Donovan MC, Am J Med Genet B Neuropsychiatr Genet, Volume 129B, 1 (August 2004) pp.97-103
    • Multicenter linkage study of schizophrenia loci on chromosome 22q.
      Mowry BJ, Holmans PA, Pulver AE, Gejman PV, Riley B, Williams NM, Laurent C, Schwab SG, Wildenauer DB, Bauché S, Owen MJ, Wormley B, Sanders AR, Nestadt G, Liang KY, Duan J, Ribble R, Norton N, Soubigou S, Maier W, Ewen-White KR, DeMarchi N, Carpenter B, Walsh D, Williams H, Jay M, Albus M, Nertney DA, Papadimitriou G, O'Neill A, O'Donovan MC, Deleuze JF, Lerer FB, Dikeos D, Kendler KS, Mallet J, Silverman JM, Crowe RR, Levinson DF, Mol Psychiatry, Volume 9, 8 (August 2004) pp.784-795
    • Genetic abnormalities of chromosome 22 and the development of psychosis.
      Williams NM, Owen MJ, Curr Psychiatry Rep, Volume 6, 3 (June 2004) pp.176-182
    • Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria.
      Kirov G, Ivanov D, Williams NM, Preece A, Nikolov I, Milev R, Koleva S, Dimitrova A, Toncheva D, O'Donovan MC, Owen MJ, Biol Psychiatry, Volume 55, 10 (May 2004) pp.971-975
    • Identification and analysis of the promoter region of the human hyaluronan synthase 2 gene.
      Monslow J, Williams JD, Guy CA, Price IK, Craig KJ, Williams HJ, Williams NM, Martin J, Coleman SL, Topley N, Spicer AP, Buckland PR, Davies M, Bowen T, J Biol Chem, Volume 279, 20 (May 2004) pp.20576-20581
    • Dysbindin-1 and schizophrenia: from genetics to neuropathology.
      Owen MJ, Williams NM, O'Donovan MC, J Clin Invest, Volume 113, 9 (May 2004) pp.1255-1257
    • Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1).
      Williams NM, Preece A, Morris DW, Spurlock G, Bray NJ, Stephens M, Norton N, Williams H, Clement M, Dwyer S, Curran C, Wilkinson J, Moskvina V, Waddington JL, Gill M, Corvin AP, Zammit S, Kirov G, Owen MJ, O'Donovan MC, Arch Gen Psychiatry, Volume 61, 4 (April 2004) pp.336-344
    • 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
    • Support for RGS4 as a susceptibility gene for schizophrenia.
      Williams NM, Preece A, Spurlock G, Norton N, Williams HJ, McCreadie RG, Buckland P, Sharkey V, Chowdari KV, Zammit S, Nimgaonkar V, Kirov G, Owen MJ, O'Donovan MC, Biol Psychiatry, Volume 55, 2 (January 2004) pp.192-195
    • The molecular genetics of schizophrenia: new findings promise new insights.
      Owen MJ, Williams NM, O'Donovan MC, Mol Psychiatry, Volume 9, 1 (January 2004) pp.14-27
    • DNA pooling as a tool for large-scale association studies in complex traits.
      Norton N, Williams NM, O'Donovan MC, Owen MJ, Ann Med, Volume 36, 2 (2004) pp.146-152
  • 2003
    • A systematic genomewide linkage study in 353 sib pairs with schizophrenia.
      Williams NM, Norton N, Williams H, Ekholm B, Hamshere ML, Lindblom Y, Chowdari KV, Cardno AG, Zammit S, Jones LA, Murphy KC, Sanders RD, McCarthy G, Gray MY, Jones G, Holmans P, Nimgaonkar V, Adolfson R, Osby U, Terenius L, Sedvall G, O'Donovan MC, Owen MJ, Am J Hum Genet, Volume 73, 6 (December 2003) pp.1355-1367
    • Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis. Molecular genetic study.
      Ivanov D, Kirov G, Norton N, Williams HJ, Williams NM, Nikolov I, Tzwetkova R, Stambolova SM, Murphy KC, Toncheva D, Thapar A, O'Donovan MC, Owen MJ, Br J Psychiatry, Volume 183 (November 2003) pp.409-413
    • Recent advances in the genetics of schizophrenia.
      O'Donovan MC, Williams NM, Owen MJ, Hum Mol Genet, Volume 12 Spec No 2 (October 2003) pp.R125-R133
    • Variation in the protocadherin gamma A gene cluster.
      Kirov G, Georgieva L, Williams N, Nikolov I, Norton N, Toncheva D, O'Donovan M, Owen MJ, Genomics, Volume 82, 4 (October 2003) pp.433-440
    • Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia.
      Williams HJ, Williams N, Spurlock G, Norton N, Zammit S, Kirov G, Owen MJ, O'Donovan MC, Am J Med Genet B Neuropsychiatr Genet, Volume 120B, 1 (July 2003) pp.42-46
    • Mutation screening of the Homer gene family and association analysis in schizophrenia.
      Norton N, Williams HJ, Williams NM, Spurlock G, Zammit S, Jones G, Jones S, Owen R, O'Donovan MC, Owen MJ, Am J Med Genet B Neuropsychiatr Genet, Volume 120B, 1 (July 2003) pp.18-21
    • A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain.
      Bray NJ, Buckland PR, Williams NM, Williams HJ, Norton N, Owen MJ, O'Donovan MC, Am J Hum Genet, Volume 73, 1 (July 2003) pp.152-161
    • Association between PRODH and schizophrenia is not confirmed.
      Williams HJ, Williams N, Spurlock G, Norton N, Ivanov D, McCreadie RG, Preece A, Sharkey V, Jones S, Zammit S, Nikolov I, Kehaiov I, Thapar A, Murphy KC, Kirov G, Owen MJ, O'Donovan MC, Mol Psychiatry, Volume 8, 7 (July 2003) pp.644-645
    • Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia.
      Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I, Williams NM, Schwab SG, Pulver AE, Faraone SV, Brzustowicz LM, Kaufmann CA, Garver DL, Gurling HM, Lindholm E, Coon H, Moises HW, Byerley W, Shaw SH, Mesen A, Sherrington R, O'Neill FA, Walsh D, Kendler KS, Ekelund J, Paunio T, Lönnqvist J, Peltonen L, O'Donovan MC, Owen MJ, Wildenauer DB, Maier W, Nestadt G, Blouin JL, Antonarakis SE, Mowry BJ, Silverman JM, Crowe RR, Cloninger CR, Tsuang MT, Malaspina D, Harkavy-Friedman JM, Svrakic DM, Bassett AS, Holcomb J, Kalsi G, McQuillin A, Brynjolfson J, Sigmundsson T, Petursson H, Jazin E, Zoëga T, Helgason T, Am J Hum Genet, Volume 73, 1 (July 2003) pp.34-48
    • Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia.
      Williams NM, Preece A, Spurlock G, Norton N, Williams HJ, Zammit S, O'Donovan MC, Owen MJ, Mol Psychiatry, Volume 8, 5 (May 2003) pp.485-487
    • Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.
      Turic D, Robinson L, Duke M, Morris DW, Webb V, Hamshere M, Milham C, Hopkin E, Pound K, Fernando S, Grierson A, Easton M, Williams N, Van Den Bree M, Chowdhury R, Gruen J, Stevenson J, Krawczak M, Owen MJ, O'Donovan MC, Williams J, Mol Psychiatry, Volume 8, 2 (February 2003) pp.176-185
  • 2002
    • Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the molecule.
      Richards AJ, Morgan J, Bearcroft PW, Pickering E, Owen MJ, Holmans P, Williams N, Tysoe C, Pope FM, Snead MP, Hughes H, J Med Genet, Volume 39, 9 (September 2002) pp.661-665
    • Schizophrenia and functional polymorphisms in the MAOA and COMT genes: no evidence for association or epistasis.
      Norton N, Kirov G, Zammit S, Jones G, Jones S, Owen R, Krawczak M, Williams NM, O'Donovan MC, Owen MJ, Am J Med Genet, Volume 114, 5 (July 2002) pp.491-496
    • Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools.
      Norton N, Williams NM, Williams HJ, Spurlock G, Kirov G, Morris DW, Hoogendoorn B, Owen MJ, O'Donovan MC, Hum Genet, Volume 110, 5 (May 2002) pp.471-478
    • No major schizophrenia locus detected on chromosome 1q in a large multicenter sample.
      Levinson DF, Holmans PA, Laurent C, Riley B, Pulver AE, Gejman PV, Schwab SG, Williams NM, Owen MJ, Wildenauer DB, Sanders AR, Nestadt G, Mowry BJ, Wormley B, Bauché S, Soubigou S, Ribble R, Nertney DA, Liang KY, Martinolich L, Maier W, Norton N, Williams H, Albus M, Carpenter EB, DeMarchi N, Ewen-White KR, Walsh D, Jay M, Deleuze JF, O'Neill FA, Papadimitriou G, Weilbaecher A, Lerer B, O'Donovan MC, Dikeos D, Silverman JM, Kendler KS, Mallet J, Crowe RR, Walters M, Science, Volume 296, 5568 (April 2002) pp.739-741
    • Full genome screen for Alzheimer disease: stage II analysis.
      Myers A, Wavrant De-Vrieze F, Holmans P, Hamshere M, Crook R, Compton D, Marshall H, Meyer D, Shears S, Booth J, Ramic D, Knowles H, Morris JC, Williams N, Norton N, Abraham R, Kehoe P, Williams H, Rudrasingham V, Rice F, Giles P, Tunstall N, Jones L, Lovestone S, Williams J, Owen MJ, Hardy J, Goate A, Am J Med Genet, Volume 114, 2 (March 2002) pp.235-244
    • 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
    • Characterisation, mutation detection, and association analysis of alternative promoters and 5' UTRs of the human dopamine D3 receptor gene in schizophrenia.
      Anney RJ, Rees MI, Bryan E, Spurlock G, Williams N, Norton N, Williams H, Cardno A, Zammit S, Jones S, Jones G, Hoogendoorn B, Smith K, Hamshere ML, Coleman S, Guy C, O'Donovan MC, Owen MJ, Buckland PR, Mol Psychiatry, Volume 7, 5 (2002) pp.493-502
    • Genome scans and microarrays: converging on genes for schizophrenia?
      Williams NM, O'Donovan MC, Owen MJ, Genome Biol, Volume 3, 4 (2002) p. REVIEWS1011
    • Determination of the genomic structure and mutation screening in schizophrenic individuals for five subunits of the N-methyl-D-aspartate glutamate receptor.
      Williams NM, Bowen T, Spurlock G, Norton N, Williams HJ, Hoogendoorn B, Owen MJ, O'Donovan MC, Mol Psychiatry, Volume 7, 5 (2002) pp.508-514
    • Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach.
      Williams NM, Spurlock G, Norton N, Williams HJ, Hamshere ML, Krawczak M, Kirov G, Nikolov I, Georgieva L, Jones S, Cardno AG, O'Donovan MC, Owen MJ, Mol Psychiatry, Volume 7, 10 (2002) pp.1092-1100
  • 2001
    • A genomewide linkage study of age at onset in schizophrenia.
      Cardno AG, Holmans PA, Rees MI, Jones LA, McCarthy GM, Hamshere ML, Williams NM, Norton N, Williams HJ, Fenton I, Murphy KC, Sanders RD, Gray MY, O'Donovan MC, McGuffin P, Owen MJ, Am J Med Genet, Volume 105, 5 (July 2001) pp.439-445
    • Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls.
      Sklar P, Schwab SG, Williams NM, Daly M, Schaffner S, Maier W, Albus M, Trixler M, Eichhammer P, Lerer B, Hallmayer J, Norton N, Williams H, Zammit S, Cardno AG, Jones S, McCarthy G, Milanova V, Kirov G, O'Donovan MC, Lander ES, Owen MJ, Wildenauer DB, Nat Genet, Volume 28, 2 (June 2001) pp.126-128
    • Mutation screening of the KCNN3 gene reveals a rare frameshift mutation.
      Bowen T, Williams N, Norton N, Spurlock G, Wittekindt OH, Morris-Rosendahl DJ, Williams H, Brzustowicz L, Hoogendoorn B, Zammit S, Jones G, Sanders RD, Jones LA, McCarthy G, Jones S, Bassett A, Cardno AG, Owen MJ, O'Donovan MC, Mol Psychiatry, Volume 6, 3 (May 2001) pp.259-260
    • Chromosome 22q, velo-cardio-facial syndrome (VCFS) and schizophrenia
      Murphy KC, Williams NM, Cardno AG, Jones LA, Holmans P, McGuffin P, Owen MJ, Schizophrenia Research, Volume 49, 1-2 (April 2001) pp.76-76
  • 2000
    • Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools.
      Hoogendoorn B, Norton N, Kirov G, Williams N, Hamshere ML, Spurlock G, Austin J, Stephens MK, Buckland PR, Owen MJ, O'Donovan MC, Hum Genet, Volume 107, 5 (November 2000) pp.488-493
    • Chromosome 22q, velo-cardio-facial syndrome (VCFS) and schizophrenia
      Murphy KC, Williams NM, Cardno AG, Jones LA, Holmans P, Thompson P, Thomas N, McGuffin P, Owen MJ, Journal Of Medical Genetics, Volume 37 (September 2000) pp.S58-S58
    • Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III.
      Levinson DF, Holmans P, Straub RE, Owen MJ, Wildenauer DB, Gejman PV, Pulver AE, Laurent C, Kendler KS, Walsh D, Norton N, Williams NM, Schwab SG, Lerer B, Mowry BJ, Sanders AR, Antonarakis SE, Blouin JL, DeLeuze JF, Mallet J, Am J Hum Genet, Volume 67, 3 (September 2000) pp.652-663
    • The high affinity neurotensin receptor gene (NTSR1): comparative sequencing and association studies in schizophrenia.
      Austin J, Buckland P, Cardno AG, Williams N, Spurlock G, Hoogendoorn B, Zammit S, Jones G, Sanders R, Jones L, McCarthy G, Jones S, Bray NJ, McGuffin P, Owen MJ, O'Donovan MC, Mol Psychiatry, Volume 5, 5 (September 2000) pp.552-557
    • Identification of a polymorphism in the human NURR1 gene and investigation of an association with schizophrenia.
      Walters SE, Williams NM, Spurlock G, Sanders RD, McCarthy GM, Cardno AG, Owen MJ, American Journal Of Medical Genetics, Volume 96, 4 (August 2000) pp.535-535
    • No evidence for association between a non-synonymous polymorphism in the gene encoding human metabotropic glutamate receptor 7 and schizophrenia.
      Bray NJ, Williams NM, Bowen T, Cardno AG, Gray M, Jones LA, Murphy KC, Sanders RD, Spurlock G, Odonovan MC, Owen MJ, Psychiatr Genet, Volume 10, 2 (June 2000) pp.83-86
    • Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q.
      Morris DW, Robinson L, Turic D, Duke M, Webb V, Milham C, Hopkin E, Pound K, Fernando S, Easton M, Hamshere M, Williams N, McGuffin P, Stevenson J, Krawczak M, Owen MJ, O'Donovan MC, Williams J, Hum Mol Genet, Volume 9, 5 (March 2000) pp.843-848
    • 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
    • Comparative sequencing of the proneurotensin gene and association studies in schizophrenia.
      Austin J, Hoogendoorn B, Buckland P, Speight G, Cardno A, Bowen T, Williams N, Spurlock G, Sanders R, Jones L, Murphy K, McCarthy G, McGuffin P, Owen MJ, O'Donovan MC, Mol Psychiatry, Volume 5, 2 (March 2000) pp.208-212
    • 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
    • No evidence for association between schizophrenia and MAO-A promoter polymorphism.
      Norton N, Bray NJ, Williams NM, Cardno AC, Murphy KC, Jones LA, Sanders RD, McCarthy G, McGuffin P, Owen MJ, Molecular Psychiatry, Volume 4 (September 1999) pp.S96-S96
    • A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs.
      Williams NM, Rees MI, Holmans P, Norton N, Cardno AG, Jones LA, Murphy KC, Sanders RD, McCarthy G, Gray MY, Fenton I, McGuffin P, Owen MJ, Hum Mol Genet, Volume 8, 9 (September 1999) pp.1729-1739
    • Polymorphism screening and association studies of the Wolfram syndrome gene in schizophrenia.
      Williams NM, Bowen T, Kirov G, Williams H, Hoogendorn B, Asherson P, Owen MJ, Molecular Psychiatry, Volume 4 (September 1999) pp.S42-S42
    • Autosome search for schizophrenia susceptibility genes in multiply affected families.
      Rees MI, Fenton I, Williams NM, Holmans P, Norton N, Cardno A, Asherson P, Spurlock G, Roberts E, Parfitt E, Mant R, Vallada H, Dawson E, Li MW, Collier DA, Powell JF, Nanko S, Gill M, McGuffin P, Owen MJ, Mol Psychiatry, Volume 4, 4 (July 1999) pp.353-359
    • 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
    • DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children.
      Fisher PJ, Turic D, Williams NM, McGuffin P, Asherson P, Ball D, Craig I, Eley T, Hill L, Chorney K, Chorney MJ, Benbow CP, Lubinski D, Plomin R, Owen MJ, Hum Mol Genet, Volume 8, 5 (May 1999) pp.915-922
    • 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
    • A full genome scan for late onset Alzheimer's disease.
      Kehoe P, Wavrant-De Vrieze F, Crook R, Wu WS, Holmans P, Fenton I, Spurlock G, Norton N, Williams H, Williams N, Lovestone S, Perez-Tur J, Hutton M, Chartier-Harlin MC, Shears S, Roehl K, Booth J, Van Voorst W, Ramic D, Williams J, Goate A, Hardy J, Owen MJ, Hum Mol Genet, Volume 8, 2 (February 1999) pp.237-245
    • Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography.
      Hoogendoorn B, Owen MJ, Oefner PJ, Williams N, Austin J, O'Donovan MC, Hum Genet, Volume 104, 1 (January 1999) pp.89-93
    • Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease.
      Kehoe PG, Russ C, McIlory S, Williams H, Holmans P, Holmes C, Liolitsa D, Vahidassr D, Powell J, McGleenon B, Liddell M, Plomin R, Dynan K, Williams N, Neal J, Cairns NJ, Wilcock G, Passmore P, Lovestone S, Williams J, Owen MJ, Nat Genet, Volume 21, 1 (January 1999) pp.71-72
  • 1998
    • PsycheMap - An interactive Internet-based database of psychiatric genetics linkage, association, and genome mapping projects.
      Williams NM, Fenton I, Owen MJ, American Journal Of Medical Genetics, Volume 81, 6 (November 1998) pp.463-464
    • QTLs for general cognitive ability in children: DNA pooling for chromosome 22.
      Hill L, Asherson P, Ball D, Craig I, Daniels J, Eley T, Freeman B, Ninomiya T, Fisher P, Turic D, Williams N, Chorney M, Chorney K, Lubinski D, Benbow C, Thompson LA, Detterman DK, Owen MJ, McGuffin P, Plomin R, American Journal Of Medical Genetics, Volume 81, 6 (November 1998) pp.486-486
    • DNA pooling for genomic scanning - Application to an association study.
      Fisher PJ, Turic D, Asherson P, Ball D, Benbow C, Chorney M, Chorney K, Craig I, Eley T, Hill L, Lubinski D, Williams N, McGuffin P, Plomin R, Owen MJ, American Journal Of Medical Genetics, Volume 81, 6 (November 1998) pp.469-469
    • Polymorphism screening of the human type 1 sigma (sigma) receptor (a candidate gene for schizophrenia) using a modified dideoxy fingerprinting technique.
      Spurlock G, Williams NM, Williams HJ, Owen MJ, American Journal Of Medical Genetics, Volume 81, 6 (November 1998) pp.525-526
    • Screening the critical region on chromosome 4p with DNA pooling for association with bipolar disorder.
      Williams N, Kirov G, Craddock N, Owen MJ, American Journal Of Medical Genetics, Volume 81, 6 (November 1998) pp.486-486
    • Genetic studies on chromosome 12 in late-onset Alzheimer disease.
      Wu WS, Holmans P, Wavrant-DeVrièze F, Shears S, Kehoe P, Crook R, Booth J, Williams N, Pérez-Tur J, Roehl K, Fenton I, Chartier-Harlin MC, Lovestone S, Williams J, Hutton M, Hardy J, Owen MJ, Goate A, Jama, Volume 280, 7 (August 1998) pp.619-622
    • 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
    • A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies.
      Daniels J, Holmans P, Williams N, Turic D, McGuffin P, Plomin R, Owen MJ, Am J Hum Genet, Volume 62, 5 (May 1998) pp.1189-1197
    • 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
    • A linkage study of chromosome 22q in SIB-pairs with schizophrenia
      Murphy KC, Williams NM, Cardno AG, Jones LA, Holmans P, McGuffin P, Owen MJ, Schizophrenia Research, Volume 29, 1-2 (January 1998) pp.131-132
  • 1997
    • Association of the angiotensin I converting enzyme gene deletion polymorphism with early onset of ESRF in PKD1 adult polycystic kidney disease.
      Baboolal K, Ravine D, Daniels J, Williams N, Holmans P, Coles GA, Williams JD, Kidney Int, Volume 52, 3 (September 1997) pp.607-613
    • Linkage study of chromosome 6p in sib-pairs with schizophrenia.
      Daniels JK, Spurlock G, Williams NM, Cardno AG, Jones LA, Murphy KC, Asherson P, Holmans P, Fenton I, McGuffin P, Owen MJ, Am J Med Genet, Volume 74, 3 (May 1997) pp.319-323
    • No evidence for an allelic association between schizophrenia and markers D22S278 and D22S283.
      Williams NM, Jones LA, Murphy KC, Cardno AG, Asherson P, Williams J, McGuffin P, Owen MJ, Am J Med Genet, Volume 74, 1 (February 1997) pp.37-39
    • Association between schizophrenia and a microsatellite polymorphism at the dopamine D5 receptor gene.
      Williams NM, Cardno AG, Murphy KC, Jones LA, Asherson P, McGuffin P, Owen MJ, Psychiatr Genet, Volume 7, 2 (1997) pp.83-85
  • 1996
    • 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
    • No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity.
      Daniels JK, Williams NM, Williams J, Jones LA, Cardno AG, Murphy KC, Spurlock G, Riley B, Scambler P, Asherson P, McGuffin P, Owen MJ, Am J Psychiatry, Volume 153, 2 (February 1996) pp.268-270
    • Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1->q32
      Lin MW, Curtis D, Williams N, Arranz M, Nanko S, Collier D, McGuffin P, Murray R, Owen M, Gill M, Powell JF, Cytogenetics And Cell Genetics, Volume 75, 2-3 (1996) pp.108-108
    • Suggestive evidence for linkage of schizophrenia to markers on chromosome (vol 5, pg 117, 1995)
      Lin MW, Curtis D, Williams N, Arranz M, Nanko S, Collier D, McGuffin P, Murray R, Owen M, Gill M, Powell J, Psychiatric Genetics, Volume 6, 1 (1996) pp.U3-U3
  • 1995
    • 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 MJ, Psychiatr Genet, Volume 5, 2 (1995) pp.63-65
    • Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32.
      Lin MW, Curtis D, Williams N, Arranz M, Nanko S, Collier D, McGuffin P, Murray R, Owen M, Gill M, Psychiatr Genet, Volume 5, 3 (1995) pp.117-126
  • 1994
    • DRD2 SER311/CYS311 POLYMORPHISM IN SCHIZOPHRENIA
      ASHERSON P, WILLIAMS N, ROBERTS E, MCGUFFIN M, OWEN M, Lancet, Volume 343, 8904 (April 1994) pp.1045-1045
• Conference proceedings
  • 2012
    • PREVALENCE OF MUTATIONS IN PARKIN, PINK1, DJ-1 AND LRRK2 IN EARLY ONSET PARKINSON'S DISEASE: A UK BASED STUDY AND SYSTEMATIC REVIEW
      Morris H, Pearson JP, Kilarski LL, Wickremaratchi MM, Knipe MDW, Newsway V, Williams NM, Ben-Shlomo Y, Journal Of Neurology Neurosurgery And Psychiatry, Volume 83, 3 (March 2012)
  • 2010
    • EVIDENCE THAT PUTATIVE ADHD LOW RISK ALLELES AT SNAP25 MAY INCREASE THE RISK OF SCHIZOPHRENIA
      Carroll LS, Kendall KM, O'Donovan MC, Owen MJ, Williams NM, Schizophrenia Research, Volume 117, 2-3 (April 2010) pp.337-337
  • 2007
    • Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia
      O'Donovan M, Georgieva L, Moskvina V, Peirce T, Norton N, Bray N, Jones L, Holmans P, MacGregor S, Zammit S, Wilkinson J, Williams H, Nikolov I, Williams N, Ivanov D, Davis K, Haroutunian V, Buxbaum J, Craddock N, Kirov G, Owen M, Schizophrenia Bulletin, Volume 33, 2 (March 2007) pp.311-312
    • Mapping schizophrenia susceptibility loci
      Williams NM, Schizophrenia Bulletin, Volume 33, 2 (March 2007) pp.305-305
    • Searching for susceptibility genes of schizophrenia using microarray analysis
      Williams NM, Schizophrenia Bulletin, Volume 33, 2 (March 2007) pp.305-306
  • 2006
    • Lack of support for association between AKT1 and schizophrenia in a UK case control sample
      Norton N, Williams H, Dwyer S, Carroll L, Peirce T, Moskvina V, Segurado R, Williams N, Owen M, O'Donovan M, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 141B, 7 (October 2006) pp.797-797
    • An examination of muted as a schizophrenia susceptibility gene
      Gerrish A, Williams N, Williams H, Owen M, O'Donovan M, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 141B, 7 (October 2006) pp.803-803
    • A critical evaluation of high resolution DNA melting analysis using a lightscanner (TM)
      Dwyer S, Williams NM, Norton N, Owen MJ, O'Donovan MC, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 141B, 7 (October 2006) pp.803-803
    • Cis- and trans-acting loci influence expression of DTNBP1, a susceptibility gene for schizophrenia
      Bray N, Holmans P, van den Bree M, Williams N, Jones L, Craddock N, Owen M, O'Donovan M, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 141B, 7 (October 2006) pp.723-724
    • Association mapping of the glial cell line-derived neurotrophic factor (GDNF) gene in schizophrenia
      Williams H, Norton N, Peirce T, Dwyer S, Williams N, O'donovan M, Owen M, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 141B, 7 (October 2006) pp.796-797
    • Support for reticulon 4 (RTN4) as a potential susceptibility gene for schizophrenia
      Pierce T, Bray N, Williams N, Ivanov D, Owen M, O'Donovan M, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 141B, 7 (October 2006) pp.779-779
    • Genomewide SNP linkage scan of schizophrenia in a large multicenter sample
      Levinson D, Gejman PV, Laurent C, Owen MJ, Pulver AE, Riley B, Wildenauer DB, Kendler KS, Mallet J, Mowry BJ, Nestadt G, O'Donovan M, Sanders AR, Schwab SG, Williams N, Albus M, Bauche S, deMarchi N, Dikeos D, Duan J, Jay M, Lasseter VK, Lerer FB, Maier W, Nertney DA, Nikolov I, Norton N, O'Neill A, Papadimitriou G, Segurado R, Silverman JM, Walsh D, Williams H, Holmans PA, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 141B, 7 (October 2006) pp.697-697
    • Recent advances in the genetics of schizophrenia
      Williams NM, International Journal Of Neuropsychopharmacology, Volume 9 (July 2006) pp.S29-S29
  • 2005
    • Analysis of COMT, ProDH and ZDHHC8 risk variants does not provide evidence for a single or combined-synergistic risk effect of these genes to schizophrenia
      Glaser B, Moskvina V, Kirov G, Murphy KC, Williams HJ, Williams NM, Owen MJ, O'Donovan MC, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 138B, 1 (September 2005) pp.26-26
    • Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in patients with schizophrenia and bipolar disorder
      Williams NM, Green E, Dwyer S, Williams H, Norton N, Kirov G, Jones I, Jones L, Grozeva D, McGregor S, O'Donovan MC, Owen MJ, Craddock N, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 138B, 1 (September 2005) pp.24-25
    • Streamlined analysis of pooled genotype data in SNP-based association studies
      Moskvina V, Norton N, Williams N, Holmans P, Owen M, O'Donovan M, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 138B, 1 (September 2005) pp.6-6
    • Will whole genome amplification prove reliable FR large-scale association studies?
      Norton N, Ivanov D, Williams NM, Owen MJ, O'Donovan MC, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 138B, 1 (September 2005) pp.100-101
    • TBX1 - A VCFS candidate with relevance to autism spectrum disorder and schizophrenia?
      Glaser B, Monks S, Gerrish A, Dwyers S, Ivanov D, Norton N, Williams NM, Murphy KC, O'Donovan MC, Owen MJ, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 138B, 1 (September 2005) pp.7-7
    • No evidence for association between polymorphisms in GRM3 and schizophrenia
      Norton N, Williams HJ, Dwyer S, Ivanov D, Preece AC, Gerrish A, Williams NM, Yerassimou P, Zammit S, O'Donovan MC, Owen MJ, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 138B, 1 (September 2005) pp.89-89
    • Refinement of a schizophrenia linkage region at 17p11.2-q25.1
      Carroll LS, Williams NM, Hamshere M, Holt RA, O'Donovan MC, Owen MJ, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 138B, 1 (September 2005) pp.117-117
    • Association analyses of the BLOC-1 genes suggest the involvement of BLOC-1 in schizophrenia etiology
      Morris DW, Murphy K, Kenny N, Williams NM, McGhee KA, Schwaiger S, Nangle J, Donohoe G, Clarke S, Owen MJ, O'Donovan MC, Waddington JL, Gill M, Corvin AP, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 138B, 1 (September 2005) pp.129-129
    • Psychosis in velo-cardio-facial (22q11 deletion) syndrome
      Monks SD, Murphy KC, Owen MJ, Williams NM, Glaser B, O'Donovan MC, Murphy DG, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 138B, 1 (September 2005) pp.129-129
    • Is the RGS4 gene associated with schizophrenia? Meta-analyses of individual genotypes from 12,615 samples across 12 international sites
      Talkowski M, Bassett AS, Brzustowicz LM, Chen X, Chowdari KV, Collier DA, Cordeiro Q, Corvin A, Deshpande S, Egan MF, Gill M, Kendler KS, Kirov G, Levitt P, Lewis DA, Mirnics K, Morris DW, O'Donovan MC, Owen MJ, Seltman H, Sobell JL, Thelma BK, Weinberger DR, Williams NM, Nimgaonkar VL, Schizophrenia Bulletin, Volume 31, 2 (April 2005) pp.278-278
  • 2004
    • Genetic analysis of DARPP-32 in schizophrenia
      Carroll LS, Williams NM, O'Donovan MC, Owen MJ, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 130B, 1 (September 2004) pp.143-143
    • Interaction between neuregulin 1 and its receptor ERBB4 increases susceptibility to schizophrenia
      Norton N, Moskvina V, Morris DW, Bray NJ, Zammit S, Williams NM, Williams HJ, Preece AC, Dwyer SL, Wilkinson JC, Kirov G, Buckland P, Waddington JL, Gill M, Corvin AP, Owen MJ, O'Donovan MC, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 130B, 1 (September 2004) pp.18-18
    • Genome-wide significant linkage in schizophrenia conditioning on occurrence of depressive and manic episodes
      Hamshere ML, Williams NM, Norton N, Williams H, Zammit S, Cardno S, Jones LA, Murphy KC, Sanders RD, McCarthy MY, Jones G, Holmans P, O'Donovan MC, Owen MJ, Craddock N, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 130B, 1 (September 2004) pp.28-28
    • Evidence for linkage disequilibrium at both G72/G30 and D-amino acid oxidase with genetic risk for bipolar disorder
      Green EK, Dimitrova A, Grozeva D, McGregor S, Nikolov I, Dwyer S, Preece A, Norton N, Williams H, Williams NM, Jone L, Jones I, O'Donovan MC, Owen MJ, Kirov G, Craddock N, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 130B, 1 (September 2004) pp.26-27
    • No evidence of association between polymorphisms at the serotonin transporter gene (SLC6A4) and schizophrenia
      Preece AC, Williams NM, Norton N, Williams HJ, O'Donovan MC, Owen MJ, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 130B, 1 (September 2004) pp.83-83
    • Allelic variation in the expression of neuropsychiatric candidate genes
      Bray NJ, Preece A, Moskvina V, Williams NM, Williams HJ, Norton N, Wilkinson J, Buckland PR, Owen MJ, O'Donovan MC, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 130B, 1 (September 2004) pp.25-25
    • No evidence for association between COMT genotypes and schizophrenia in two large samples
      Williams HJ, Glaser B, Williams NM, Zammit S, Mcgregor S, Murphy KC, Kirov G, Owen MJ, O'Donovan MC, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 130B, 1 (September 2004) pp.84-84
    • An examination of the G72/G30 and DAO loci in schizophrenia
      Williams NM, Dwyer S, Norton N, Williams H, Kirov G, Green E, Dimitrova A, Grozeva D, McGregor S, Craddock N, Owen MJ, O'Donovan MC, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 130B, 1 (September 2004) pp.20-20
    • Evidence that variation at the Neuregulin gene (NRG1) influences susceptibility to Bipolar Disorder with maximal effect in individuals who experience mania and mood-incongruent psychotic features
      Green E, Raybould R, Macgregor S, Grozeva D, Williams N, Norton N, Williams H, Nikolov I, Heron H, Gordon-Smith K, Caesar S, Jones L, Jones I, Kirov G, O'Donovan MC, Owen MJ, Craddock N, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 130B, 1 (September 2004) pp.27-27
    • Evaluating an association of RGS4 polymorphisms with schizophrenia: Mega-analysis of over 12,000 individuals from 11 international sites
      Talkowski M, Bassett AS, Brzustowicz LM, Chen X, Chowdari KV, Collier DA, Cordeiro Q, Corvin AP, Deshpande S, Egan MF, Gill M, Kendler KS, Kirov G, Levitt P, Lewis DA, Li None, Mirnics K, Morris DW, O'Donovan MC, Owen MJ, Seltman H, Semwall P, Sobell JL, Thelma BK, Weinberger DR, Williams NM, Wood J, Nimgaonkar VL, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 130B, 1 (September 2004) pp.142-142
    • Evidence for linkage (LOD=3.54) at IQ42 close to DISC2 in a genome scan of functional psychosis pedigrees including at least one member with schizoaffective disorder of Bipolar type
      Hamshere ML, Williams NM, Segurado R, Lambert D, Jones LA, Holmans P, Kirov G, Corvin A, Jones I, O'Donovan MC, Gill M, Owen MJ, Craddock N, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 130B, 1 (September 2004) pp.127-127
    • Convergent functional genomics, association and linkage analysis suggests 2 ',3 '-cyclic nucleotide 3 '-phosphodiesterase (CNP) as a potential susceptibility gene for schizophrenia
      Peirce TR, Bray NJ, Williams N, Haroutunian V, Buxbaum J, Buckland P, Owen M, O'Donovan M, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, Volume 130B, 1 (September 2004) pp.81-81
    • Interaction of RGS4 polymorphisms with gender in schizophrenia and schizoaffective disorder
      Talkowski ME, Chowdari KV, Deshpande S, Thelma BK, Williams N, Owen MJ, O'Donovan MC, Prasad KM, Wood JA, Morris DW, Gill M, Cordeiro Q, Vallada H, Nimgaonkar VL, Biological Psychiatry, Volume 55 (April 2004) pp.209S-210S
  • 2003
    • Association of RGS4 polymorphisms with schizophrenia: interactions with gender.
      Talkowski ME, Chowdari KV, Wood JA, Ceilley JW, Ferrell RE, Mirnics K, Lewis DA, Levitt P, Devlin B, Williams N, Owen MJ, Kirov G, O'Donovan MC, Nimgaonkar VL, American Journal Of Human Genetics, Volume 73, 5 (November 2003) pp.484-484
  • 2002
    • Analysis of the T102C 5HT2A and the DRD3 BAL1 polymorphisms in a large case control sample of schizophrenia
      Spurlock G, Williams N, Norton N, Williams H, Zammit S, Jones S, Jones G, O'Donovan MC, Owen MJ, American Journal Of Medical Genetics, Volume 114, 7 (October 2002) pp.873-873
    • Large-scale candidate gene association analysis in psychiatric disorders
      Norton N, Williams NM, Stephens M, Williams HJ, Spurlock G, Preece A, Turic D, Grierson A, Williams J, Kirov G, Thapar A, Plomin R, Owen MJH, O'Donovan MC, American Journal Of Medical Genetics, Volume 114, 7 (October 2002) pp.723-723
    • Detection of cis-acting polymorphisms and epigenetic modification affecting gene expression
      Bray NJ, Buckland PR, Williams HJ, Norton N, Williams NM, Owen MJ, O'Donovan MC, American Journal Of Medical Genetics, Volume 114, 7 (October 2002) pp.750-750
    • Linkage disequilibrium mapping provides further evidence for a gene for reading disability on chromosome 6p21.3-22
      Williams J, Turic D, Robinson L, Duke M, Morris DW, Webb V, Hamshere M, Grierson A, Williams N, Van Den Bree M, Chowdhury R, McGuffin P, Stevenson J, Krawczak M, Owen MJ, O'Donovan MC, American Journal Of Medical Genetics, Volume 114, 7 (October 2002) pp.725-725
    • Mutation screening of the Homer gene family and association with schizophrenia
      Norton N, Williams HJ, Williams NM, Spurlock G, Preece A, Zammit S, Jones G, Jones S, Owen R, O'Donovan MC, Owen MJ, American Journal Of Medical Genetics, Volume 114, 7 (October 2002) pp.864-864
    • Analysis of PRODH in VCFS and schizophrenia
      Williams HJ, Williams NM, Norton N, Spurlock G, Preece A, Jones S, Zammit S, Murphy KC, Owen MJ, O'Donovan MC, American Journal Of Medical Genetics, Volume 114, 7 (October 2002) pp.877-877
    • Candidate gene screening of the VCFS deleted region for mutations associated with schizophrenia
      Williams NM, Norton N, Preece A, Spurlock G, Williams HJ, Zammit S, Murphy KC, O'Donovan MC, Owen MJ, American Journal Of Medical Genetics, Volume 114, 7 (October 2002) pp.877-878
    • Analysis of glutamate related genes in ADHD
      Turic D, Williams NM, Stephens M, Langley K, Lawson D, Owen MJ, Thapar A, O'Donovan MC, American Journal Of Medical Genetics, Volume 114, 7 (October 2002) pp.737-737
    • Screening of neuregulin genes for polymorphisms associated with schizophrenia
      Williams NM, Preece A, Spurlock G, Norton N, Williams HJ, Kirov G, Zammit S, Owen MJ, O'Donovan MC, American Journal Of Medical Genetics, Volume 114, 7 (October 2002) pp.878-878
    • Analysis of glutamate related genes in dyslexia
      Stephens M, Williams NM, Owen MJ, Williams J, O'Donovan MC, American Journal Of Medical Genetics, Volume 114, 7 (October 2002) pp.821-822
    • Linkage disequilibrium mapping provides further evidence for a gene for reading disability on chromosome 6P21.3-22.
      O'Donovan MC, Turic D, Robinson L, Duke M, Morris DW, Webb V, Hamshere M, Grierson A, Williams N, Van den Bree M, Chowdhury R, McGuffin R, Stevenson J, Krawczak M, Owen MJ, Williams J, American Journal Of Human Genetics, Volume 71, 4 (October 2002) pp.497-497
    • Candidate gene screening of the VCFS deleted region for mutations associated with schizophrenia.
      Williams NM, Norton N, Preece A, Spurlock G, Williams H, Zammit S, Murphy KC, O'Donovan MC, Owen MJ, American Journal Of Human Genetics, Volume 71, 4 (October 2002) pp.485-485
    • Candidate gene screening of the VCFS deleted region for mutations associated with schizophrenia
      Norton N, Williams NM, Preece A, Spurlock G, Williams HJ, Zammit S, Murphy KC, O'Donovan MC, Owen MJ, Journal Of Medical Genetics, Volume 39 (September 2002) pp.S83-S83
    • Progress toward the identification of the chromosome 10 locus for late onset Alzheimer's disease
      Goate AM, Myers A, Marshall H, Meyer D, Shears S, Booth J, Ramic D, Nowotny P, Smemo S, Morris JC, Knowles H, De Vrieze FW, Ertekin-Taner N, Ronald J, Crook R, Younkin S, Holmans P, Hamshere M, Compton D, Williams N, Norton N, Abraham R, Kehoe P, Williams H, Rudrasingham V, Rice F, Giles P, Tunstall N, Jones L, O'Donovan M, Williams J, Owen M, Tucker M, Estus S, Lovestone S, Hardy J, Neurobiology Of Aging, Volume 23, 1 (2002) pp.S11-S11
  • 2001
    • Screening of candidate genes related to myelination for mutations associated with schizophrenia
      Williams NM, Spurlock G, Williams H, Norton N, Davis KL, Buxbaum JD, Haroutunian V, Saunders R, Cardno AG, McCarthy G, O'Donovan MC, Owen MJ, American Journal Of Medical Genetics, Volume 105, 7 (October 2001) pp.589-589
    • Screening of candidate genes related to mylination for mutations associated with schizophrenia.
      Williams HJ, Williams NM, Spurlock G, Norton N, Davis KL, Buxbaum JD, Haroutunian V, Saunders R, Cardno AG, McCarthy G, Odonovan MC, Owen MJ, American Journal Of Human Genetics, Volume 69, 4 (October 2001) pp.501-501
    • Large-scale candidate gene screening and association analysis in schizophrenia.
      Norton N, Williams NM, Williams HJ, Spurlock G, Bray NJ, Jones S, McCarthy GS, Jones G, Zammit S, Cardno A, Owen R, Davis KL, Buxbaum JD, Haroutunian V, Owen MJ, O'Donovan MC, American Journal Of Human Genetics, Volume 69, 4 (October 2001) pp.533-533
  • 2000
    • Linkage disequilibrium mapping and candidate gene screening of the VCFS deleted region for mutations associated with schizophrenia.
      Williams NM, Spurlock G, Williams H, Norton N, Walters A, Saunders R, Cardno AG, McCarthy G, O'Donovan MC, Owen MJ, American Journal Of Medical Genetics, Volume 96, 4 (August 2000) pp.475-475
    • Linkage disequilibrium mapping provides evidence for a susceptibility gene for reading disability on chromosome 6p.
      Turic D, Morris DW, Robinson L, Duke M, Grierson A, Raha-Chowdhury R, Southgate L, Webb V, Hamshere M, Williams N, McGuffin P, Stevenson J, Krawczak M, Owen MJ, O'Donovan MC, Williams J, American Journal Of Medical Genetics, Volume 96, 4 (August 2000) pp.556-556
    • Suggestive evidence of linkage with reading disability in a large Norwegian family.
      Norton N, Heiervang E, Hamshere M, Williams N, Stevenson J, Owen MJ, O'Donovan MC, Williams J, American Journal Of Medical Genetics, Volume 96, 4 (August 2000) pp.556-556
    • Identification and characterisation of SNP's in candidate genes for schizophrenia.
      Williams NM, Bowen T, Spurlock G, Williams H, Norton N, Austin J, Walters A, Owen MJ, O'Donovan MC, American Journal Of Medical Genetics, Volume 96, 4 (August 2000) pp.462-462
    • Allele frequency estimation in DNA pools of single nuleotide polymorphisms by primer extension and DHPLC.
      Norton N, Hoogendoorn B, Williams N, Hamshere ML, Spurlock G, Austin J, Owen MJ, O'Donovan MC, American Journal Of Medical Genetics, Volume 96, 4 (August 2000) pp.482-482
    • Linkage disequilibrium and positional candidate gene analyses of a susceptibility locus for reading disability on chromosome 15Q.
      Morris DW, Robinson L, Turic D, Duke M, Webb V, Southgate L, Hamshere M, Williams N, McGuffin P, Rowen L, Stevenson J, Krawczak M, Owen MJ, Williams J, O'Donovan MC, American Journal Of Medical Genetics, Volume 96, 4 (August 2000) pp.471-472
    • Comparative study of family based haplotypic association methods.
      Hamshere ML, Krawczak M, Morris DW, Robinson L, Turic D, Duke M, Webb V, Southgate L, Williams N, McGuffin P, Stevenson J, Owen MJ, O'Donovan MC, Williams J, American Journal Of Medical Genetics, Volume 96, 4 (August 2000) pp.486-486
  • 1999
    • Allele frequency estimation and comparison by SNP genotyping of genomic DNA pools.
      Hoogendoorn B, Owen MJ, Williams N, Norton N, Austin J, O'Donovan MC, American Journal Of Human Genetics, Volume 65, 4 (October 1999) pp.A255-A255
    • Neurotensin and its receptor in schizophrenia and bipolar disorder.
      Austin J, Hoogendoorn B, Buckland P, Middle F, Williams N, Craddock N, McGuffin P, Owen MJ, O'Donovan MC, Molecular Psychiatry, Volume 4 (September 1999) pp.S102-S103
  • 1998
    • A systematic search for genes determining age of onset in schizophrenia.
      Cardno AG, Holmans PA, Jones LA, Rees MI, Murphy KC, Williams NM, Sanders RS, Fenton I, McGuffin P, Owen MJ, American Journal Of Medical Genetics, Volume 81, 6 (November 1998) pp.530-530
    • Comparative sequencing and association studies of proneurotensin in schizophrenia and bipolar disorder.
      Austin J, Hoogendoorn B, Buckland P, Williams N, Craddock N, McGuffin P, Owen MJ, O'Donovan MC, American Journal Of Medical Genetics, Volume 81, 6 (November 1998) pp.525-525
    • Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography.
      Hoogendoorn B, Owen MJ, Oefner PJ, Williams N, Austin J, O'Donovan MC, American Journal Of Medical Genetics, Volume 81, 6 (November 1998) pp.469-470
    • Schizophrenia, smoking and the alpha 7 nicotinic receptor gene.
      McCarthy G, Sanders RD, Gray M, Jones LA, Cardno A, Murphy K, Rees M, Williams NM, Norton N, Holmans P, Owen MJ, American Journal Of Medical Genetics, Volume 81, 6 (November 1998) pp.509-509
    • An affected sib pair study for schizophrenia on the X chromosome.
      Norton N, Williams NM, Rees MI, Holmans P, Fenton I, Cardno AC, Murphy KC, Jones LA, Sanders RD, Asherson P, McGuffin P, Owen MJ, American Journal Of Medical Genetics, Volume 81, 6 (November 1998) pp.529-529
    • A two-stage sib-pair genome scan for schizophrenia susceptibility genes.
      Williams NM, Rees MI, Norton N, Holmans P, Fenton I, Cardno AG, Murphy KC, Jones LA, McCarthy G, Sanders R, McGuffin P, Owen MJ, American Journal Of Medical Genetics, Volume 81, 6 (November 1998) pp.453-453
  • 1997
    • A linkage study of chromosome 22q in sib-pairs with schizophrenia.
      Murphy KC, Williams NM, Cardno AG, Jones LA, Asherson P, Holmans P, McGuffin P, Owen MJ, American Journal Of Medical Genetics, Volume 74, 6 (November 1997) pp.678-678
    • Genome search for schizophrenia susceptibility genes using a two-stage sib-pair approach.
      Williams NM, Rees MI, Holmans P, Daniels J, Fenton I, Cardno AG, Murphy KC, Jones LA, Asherson P, McGuffin P, Owen MJ, American Journal Of Medical Genetics, Volume 74, 6 (November 1997) pp.559-559