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Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate.
Melhem NM, Lu C, Dresbold C, Middleton FA, Klei L, Wood S, Faraone SV, Vinogradov S, Tiobech J, Yano V, Roeder K, Byerley W, Myles-Worsley M, Devlin B. Melhem NM, et al. Among authors: devlin b. Am J Med Genet B Neuropsychiatr Genet. 2014 Sep;165B(6):521-30. doi: 10.1002/ajmg.b.32255. Epub 2014 Jul 1. Am J Med Genet B Neuropsychiatr Genet. 2014. PMID: 24980794 Free PMC article.
Association and linkage analyses of RGS4 polymorphisms in schizophrenia.
Chowdari KV, Mirnics K, Semwal P, Wood J, Lawrence E, Bhatia T, Deshpande SN, B K T, Ferrell RE, Middleton FA, Devlin B, Levitt P, Lewis DA, Nimgaonkar VL. Chowdari KV, et al. Among authors: b k t, devlin b. Hum Mol Genet. 2002 Jun 1;11(12):1373-80. doi: 10.1093/hmg/11.12.1373. Hum Mol Genet. 2002. PMID: 12023979
No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.
Devlin B, Bennett P, Cook EH Jr, Dawson G, Gonen D, Grigorenko EL, McMahon W, Pauls D, Smith M, Spence MA, Schellenberg GD; Collaborative Programs of Excellence in Autism (CPEA) Genetics Network. Devlin B, et al. Am J Med Genet. 2002 Aug 8;114(6):667-72. doi: 10.1002/ajmg.10603. Am J Med Genet. 2002. PMID: 12210285 Free article.
Selection of eating-disorder phenotypes for linkage analysis.
Bulik CM, Bacanu SA, Klump KL, Fichter MM, Halmi KA, Keel P, Kaplan AS, Mitchell JE, Rotondo A, Strober M, Treasure J, Woodside DB, Sonpar VA, Xie W, Bergen AW, Berrettini WH, Kaye WH, Devlin B. Bulik CM, et al. Among authors: devlin b. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):81-7. doi: 10.1002/ajmg.b.30227. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 16152575 Free PMC article.
412 results