Tiffany Vu, B.S.

"Tiffany Vu"
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Girirajan S, Dennis MY, Baker C, et al. (2013) Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder. American Journal of Human Genetics. 92: 221-37
Priest JR, Girirajan S, Vu TH, et al. (2012) Rare copy number variants in isolated sporadic and syndromic atrioventricular septal defects. American Journal of Medical Genetics. Part A. 158: 1279-84
Girirajan S, Brkanac Z, Coe BP, et al. (2011) Relative burden of large CNVs on a range of neurodevelopmental phenotypes. Plos Genetics. 7: e1002334
Cooper GM, Coe BP, Girirajan S, et al. (2011) A copy number variation morbidity map of developmental delay. Nature Genetics. 43: 838-46
Vu TH, Coccaro EF, Eichler EE, et al. (2011) Genomic architecture of aggression: rare copy number variants in intermittent explosive disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 808-16
Peter B, Raskind WH, Matsushita M, et al. (2011) Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample. Journal of Neurodevelopmental Disorders. 3: 39-49
Campbell CD, Sampas N, Tsalenko A, et al. (2011) Population-genetic properties of differentiated human copy-number polymorphisms. American Journal of Human Genetics. 88: 317-32
Chen DH, Raskind WH, Parson WW, et al. (2010) A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: phenotypic spectrum and structural study of FHL1 mutations. Journal of the Neurological Sciences. 296: 22-9
Brkanac Z, Spencer D, Shendure J, et al. (2009) IFRD1 is a candidate gene for SMNA on chromosome 7q22-q23. American Journal of Human Genetics. 84: 692-7
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