| Common polygenic variation contributes to risk of schizophrenia and bipolar disorder International Schizophrenia Consortium Manuscript preparation Purcell Shaun ... Nature 460 (7256), 748-752, 2009 | 4954 | 2009 |
| Genome-wide association study identifies five new schizophrenia loci Nature genetics 43 (10), 969-976, 2011 | 1928 | 2011 |
| De novo mutations in schizophrenia implicate synaptic networks M Fromer, AJ Pocklington, DH Kavanagh, HJ Williams, S Dwyer, ... Nature 506 (7487), 179-184, 2014 | 1698 | 2014 |
| Identification of loci associated with schizophrenia by genome-wide association and follow-up MC O'donovan, N Craddock, N Norton, H Williams, T Peirce, V Moskvina, ... Nature genetics 40 (9), 1053-1055, 2008 | 1288 | 2008 |
| A full genome scan for late onset Alzheimer's disease P Kehoe, FWD Vrieze, R Crook, WS Wu, P Holmans, I Fenton, G Spurlock, ... Human Molecular Genetics 8 (2), 237-245, 1999 | 450 | 1999 |
| A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain NJ Bray, PR Buckland, NM Williams, HJ Williams, N Norton, MJ Owen, ... The American Journal of Human Genetics 73 (1), 152-161, 2003 | 422 | 2003 |
| Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders T Singh, MI Kurki, D Curtis, SM Purcell, L Crooks, J McRae, J Suvisaari, ... Nature neuroscience 19 (4), 571-577, 2016 | 400 | 2016 |
| Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease PG Kehoe, C Russ, S McIlroy, H Williams, P Holmans, C Holmes, ... Nature genetics 21 (1), 71-72, 1999 | 336 | 1999 |
| Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder HJ Williams, N Norton, S Dwyer, V Moskvina, I Nikolov, L Carroll, ... Molecular psychiatry 16 (4), 429-441, 2011 | 326 | 2011 |
| Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia NM Williams, A Preece, G Spurlock, N Norton, HJ Williams, S Zammit, ... Molecular psychiatry 8 (5), 485-487, 2003 | 313 | 2003 |
| Identification in 2 Independent Samples of a Novel Schizophrenia RiskHaplotype of the Dystrobrevin Binding Protein Gene (DTNBP1) NM Williams, A Preece, DW Morris, G Spurlock, NJ Bray, M Stephens, ... Archives of general psychiatry 61 (4), 336-344, 2004 | 250 | 2004 |
| Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13 ML Hamshere, P Bennett, N Williams, R Segurado, A Cardno, N Norton, ... Archives of general psychiatry 62 (10), 1081-1088, 2005 | 249 | 2005 |
| Is COMT a Susceptibility Gene for Schizophrenia? HJ Williams, MJ Owen, MC O'Donovan Schizophrenia bulletin 33 (3), 635-641, 2007 | 243 | 2007 |
| 100,000 genomes pilot on rare-disease diagnosis in health care—preliminary report 100,000 Genomes Project Pilot Investigators New England Journal of Medicine 385 (20), 1868-1880, 2021 | 238 | 2021 |
| Genotype effects of CHRNA7, CNR1 and COMT in schizophrenia: interactions with tobacco and cannabis use S Zammit, G Spurlock, H Williams, N Norton, N Williams, MC O'Donovan, ... The British Journal of Psychiatry 191 (5), 402-407, 2007 | 234 | 2007 |
| An update on the genetics of schizophrenia N Norton, HJ Williams, MJ Owen Current opinion in psychiatry 19 (2), 158-164, 2006 | 228 | 2006 |
| Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries HJ Williams, N Craddock, G Russo, ML Hamshere, V Moskvina, S Dwyer, ... Human molecular genetics 20 (2), 387-391, 2011 | 211 | 2011 |
| Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia N Norton, V Moskvina, DW Morris, NJ Bray, S Zammit, NM Williams, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141 …, 2006 | 208 | 2006 |
| Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities S Drury, H Williams, N Trump, C Boustred, GOSGene, N Lench, RH Scott, ... Prenatal diagnosis 35 (10), 1010-1017, 2015 | 196 | 2015 |
| Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools N Norton, NM Williams, HJ Williams, G Spurlock, G Kirov, DW Morris, ... Human genetics 110, 471-478, 2002 | 190 | 2002 |
