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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.
Davies RW, Fiksinski AM, Breetvelt EJ, Williams NM, Hooper SR, Monfeuga T, Bassett AS, Owen MJ, Gur RE, Morrow BE, McDonald-McGinn DM, Swillen A, Chow EWC, van den Bree M, Emanuel BS, Vermeesch JR, van Amelsvoort T, Arango C, Armando M, Campbell LE, Cubells JF, Eliez S, Garcia-Minaur S, Gothelf D, Kates WR, Murphy KC, Murphy CM, Murphy DG, Philip N, Repetto GM, Shashi V, Simon TJ, Suñer DH, Vicari S, Scherer SW; International 22q11.2 Brain and Behavior Consortium; Bearden CE, Vorstman JAS. Davies RW, et al. Among authors: owen mj. Nat Med. 2020 Dec;26(12):1912-1918. doi: 10.1038/s41591-020-1103-1. Epub 2020 Nov 9. Nat Med. 2020. PMID: 33169016 Free PMC article.
Recent advances in the genetics of schizophrenia.
O'Donovan MC, Williams NM, Owen MJ. O'Donovan MC, et al. Among authors: owen mj. Hum Mol Genet. 2003 Oct 15;12 Spec No 2:R125-33. doi: 10.1093/hmg/ddg302. Epub 2003 Sep 2. Hum Mol Genet. 2003. PMID: 12952866 Review.
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: owen mj. Genomics. 2003 Oct;82(4):433-40. doi: 10.1016/s0888-7543(03)00167-8. Genomics. 2003. PMID: 13679023
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. Glaser B, et al. Among authors: owen mj. Biol Psychiatry. 2005 Jul 1;58(1):78-80. doi: 10.1016/j.biopsych.2005.03.017. Biol Psychiatry. 2005. PMID: 15992527
1,096 results