Kristen M. West

A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism

Dan E. Arking, David J. Cutler, Camille W. Brune et al. · The American Journal of Human Genetics · 2008 · 594 citations · Full text

Life Sciences, Genetics, Neuroscience +12

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

Dan E. Arking, Arne Pfeufer, Wendy S. Post et al. · Nature Genetics · 2006 · 551 citations

Life Sciences, Cardiology, Genetics +10

Differential Contributions of Rare and Common, Coding and Noncoding Ret Mutations to Multifactorial Hirschsprung Disease Liability

E Emison, Mercè Garcia-Barceló, Elizabeth A. Grice et al. · The American Journal of Human Genetics · 2010 · 244 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Relative Contribution of Genetic and Nongenetic Modifiers to Intestinal Obstruction in Cystic Fibrosis

Scott M. Blackman, Rebecca Deering–Brose, Rita McWilliams et al. · Gastroenterology · 2006 · 157 citations · Full text

Veterinary Medicine, Genetics, Molecular Genetics +15

Functional Loss of Semaphorin 3C and/or Semaphorin 3D and Their Epistatic Interaction with Ret Are Critical to Hirschsprung Disease Liability

Qian Jiang, Stacey Arnold, Tiffany A. Heanue et al. · The American Journal of Human Genetics · 2015 · 149 citations · Full text

Life Sciences, Genetics, Molecular Biology +13