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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. Williams NM, et al. Among authors: monks s. Hum Mol Genet. 2008 Feb 15;17(4):555-66. doi: 10.1093/hmg/ddm330. Epub 2007 Nov 13. Hum Mol Genet. 2008. PMID: 18003636
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. Among authors: monks s. 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
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: monks s. 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.
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. 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.
Practical guidelines for managing patients with 22q11.2 deletion syndrome.
Bassett AS, McDonald-McGinn DM, Devriendt K, Digilio MC, Goldenberg P, Habel A, Marino B, Oskarsdottir S, Philip N, Sullivan K, Swillen A, Vorstman J; International 22q11.2 Deletion Syndrome Consortium. Bassett AS, et al. J Pediatr. 2011 Aug;159(2):332-9.e1. doi: 10.1016/j.jpeds.2011.02.039. Epub 2011 May 12. J Pediatr. 2011. PMID: 21570089 Free PMC article. No abstract available.
115 results