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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 |
| 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 |
| 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 |