Kevin A. Strauss

Investigations of caspr2, an autoantigen of encephalitis and neuromyotonia

Eric Lancaster, Maartje G. Huijbers, Vered Bar et al. · Annals of Neurology · 2010 · 721 citations · Full text

Recessive Symptomatic Focal Epilepsy and Mutant Contactin-Associated Protein-like 2

Kevin A. Strauss, Erik G. Puffenberger, Matthew J. Huentelman et al. · New England Journal of Medicine · 2006 · 624 citations

Genetics, Neurotransmission, Social Sciences +17

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling

Lot Snijders Blok, Erik Madsen, Jane Juusola et al. · The American Journal of Human Genetics · 2015 · 324 citations · Full text

Unexplained Intellectual Disability, Gender-specific Effects, Mendelian Disorder +10

Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT

Victoria Carlton, Baruch Z. Harris, Erik G. Puffenberger et al. · Nature Genetics · 2003 · 324 citations

Genetic Disorder, Genetics, Inherited Metabolic Disease +9

Diagnosis and Treatment of Maple Syrup Disease: A Study of 36 Patients

D. Holmes Morton, Kevin A. Strauss, Erik G. Puffenberger et al. · PEDIATRICS · 2002 · 321 citations