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Fogel, BL, Lee JY, Lane J, Wahnich A, Chan S, Huang A, Osborn GE, Klein E, Mamah C, Perlman S et al..  2012.  Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia.. Movement disorders : official journal of the Movement Disorder Society. 27(3):442-6. Abstract
Geschwind, DH.  2011.  Genetics of autism spectrum disorders.. Trends in cognitive sciences. 15(9):409-16. Abstract
Curran, S, Bolton P, Rozsnyai K, Chiocchetti A, Klauck SM, Duketis E, Poustka F, Schlitt S, Freitag CM, Lee I et al..  2011.  No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. 156B(6):633-9. Abstract
Root, TL, Szatkiewicz JP, Jonassaint CR, Thornton LM, Pinheiro AP, Strober M, Bloss C, Berrettini W, Schork NJ, Kaye WH et al..  2011.  Association of candidate genes with phenotypic traits relevant to anorexia nervosa.. European eating disorders review : the journal of the Eating Disorders Association. 19(6):487-93. Abstract
Lee, Y-S, Silva AJ.  2011.  Modeling hyperactivity: of mice and men.. Nature medicine. 17(5):541-2.
Zhang, Y, Cantor RM, MacGibbon K, Romero R, Goodwin TM, Mullin PM, Fejzo MS.  2011.  Familial aggregation of hyperemesis gravidarum.. American journal of obstetrics and gynecology. 204(3):230.e1-7. Abstract