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Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
Singh T, Kurki MI, Curtis D, Purcell SM, Crooks L, McRae J, Suvisaari J, Chheda H, Blackwood D, Breen G, Pietiläinen O, Gerety SS, Ayub M, Blyth M, Cole T, Collier D, Coomber EL, Craddock N, Daly MJ, Danesh J, DiForti M, Foster A, Freimer NB, Geschwind D, Johnstone M, Joss S, Kirov G, Körkkö J, Kuismin O, Holmans P, Hultman CM, Iyegbe C, Lönnqvist J, Männikkö M, McCarroll SA, McGuffin P, McIntosh AM, McQuillin A, Moilanen JS, Moore C, Murray RM, Newbury-Ecob R, Ouwehand W, Paunio T, Prigmore E, Rees E, Roberts D, Sambrook J, Sklar P, St Clair D, Veijola J, Walters JT, Williams H; Swedish Schizophrenia Study; INTERVAL Study; DDD Study; UK10 K Consortium; Sullivan PF, Hurles ME, O'Donovan MC, Palotie A, Owen MJ, Barrett JC. Singh T, et al. Among authors: williams h. Nat Neurosci. 2016 Apr;19(4):571-7. doi: 10.1038/nn.4267. Epub 2016 Mar 14. Nat Neurosci. 2016. PMID: 26974950 Free PMC article.
Schizophrenia genetics: advancing on two fronts.
Owen MJ, Williams HJ, O'Donovan MC. Owen MJ, et al. Curr Opin Genet Dev. 2009 Jun;19(3):266-70. doi: 10.1016/j.gde.2009.02.008. Epub 2009 Apr 1. Curr Opin Genet Dev. 2009. PMID: 19345090 Review.
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. Dwyer S, et al. Among authors: williams h. Am J Med Genet B Neuropsychiatr Genet. 2010 Dec 5;153B(8):1411-6. doi: 10.1002/ajmg.b.31117. Epub 2010 Sep 22. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20862696
Is COMT a susceptibility gene for schizophrenia?
Williams HJ, Owen MJ, O'Donovan MC. Williams HJ, et al. Schizophr Bull. 2007 May;33(3):635-41. doi: 10.1093/schbul/sbm019. Epub 2007 Apr 4. Schizophr Bull. 2007. PMID: 17412710 Free PMC article. Review.
Association between TCF4 and schizophrenia does not exert its effect by common nonsynonymous variation or by influencing cis-acting regulation of mRNA expression in adult human brain.
Williams HJ, Moskvina V, Smith RL, Dwyer S, Russo G, Owen MJ, O'Donovan MC. Williams HJ, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(7):781-4. doi: 10.1002/ajmg.b.31219. Epub 2011 Aug 2. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21812098 Free PMC article.
Genome-wide association study identifies five new schizophrenia loci.
Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium. Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium. Nat Genet. 2011 Sep 18;43(10):969-76. doi: 10.1038/ng.940. Nat Genet. 2011. PMID: 21926974 Free PMC article.
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. Hamshere ML, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(8):929-40. doi: 10.1002/ajmg.b.31240. Epub 2011 Sep 29. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21960518
Schizophrenia two-hit hypothesis in velo-cardio facial syndrome.
Williams HJ, Monks S, Murphy KC, Kirov G, O'Donovan MC, Owen MJ. Williams HJ, et al. Am J Med Genet B Neuropsychiatr Genet. 2013 Mar;162B(2):177-82. doi: 10.1002/ajmg.b.32129. Epub 2013 Jan 17. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23335482
4,671 results