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Page 1
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: murphy kc. 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.
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: murphy kc. Biol Psychiatry. 2005 Jul 1;58(1):78-80. doi: 10.1016/j.biopsych.2005.03.017. Biol Psychiatry. 2005. PMID: 15992527
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: murphy kc. 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
Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study.
Azuma R, Daly EM, Campbell LE, Stevens AF, Deeley Q, Giampietro V, Brammer MJ, Glaser B, Ambery FZ, Morris RG, Williams SC, Owen MJ, Murphy DG, Murphy KC. Azuma R, et al. Among authors: murphy kc, murphy dg. J Neurodev Disord. 2009 Mar;1(1):46-60. doi: 10.1007/s11689-009-9008-9. Epub 2009 Mar 5. J Neurodev Disord. 2009. PMID: 21547621 Free PMC article.
263 results