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The psychiatric phenotypes of 1q21 distal deletion and duplication.
Linden SC, Watson CJ, Smith J, Chawner SJRA, Lancaster TM, Evans F, Williams N, Skuse D, Raymond FL, Hall J, Owen MJ, Linden DEJ, Green-Snyder L, Chung WK, Maillard AM, Jacquemont S, van den Bree MBM. Linden SC, et al. Among authors: williams n. Transl Psychiatry. 2021 Feb 4;11(1):105. doi: 10.1038/s41398-021-01226-9. Transl Psychiatry. 2021. PMID: 33542195 Free PMC article.
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. Kirov G, et al. Among authors: williams n. Genomics. 2003 Oct;82(4):433-40. doi: 10.1016/s0888-7543(03)00167-8. Genomics. 2003. PMID: 13679023
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. Raybould R, et al. Among authors: williams n. Biol Psychiatry. 2005 Apr 1;57(7):696-701. doi: 10.1016/j.biopsych.2005.01.018. Biol Psychiatry. 2005. PMID: 15820225
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. Green EK, et al. Among authors: williams n. Arch Gen Psychiatry. 2005 Jun;62(6):642-8. doi: 10.1001/archpsyc.62.6.642. Arch Gen Psychiatry. 2005. PMID: 15939841
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. Hamshere ML, et al. Among authors: williams n, williams h. Arch Gen Psychiatry. 2005 Oct;62(10):1081-8. doi: 10.1001/archpsyc.62.10.1081. Arch Gen Psychiatry. 2005. PMID: 16203953
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. Paylor R, et al. Among authors: williams n. Proc Natl Acad Sci U S A. 2006 May 16;103(20):7729-34. doi: 10.1073/pnas.0600206103. Epub 2006 May 9. Proc Natl Acad Sci U S A. 2006. PMID: 16684884 Free PMC article.
4,712 results