Sumit Parikh

Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants

Santhosh Girirajan, Jill A. Rosenfeld, Bradley P. Coe et al. · New England Journal of Medicine · 2012 · 620 citations · Full text

CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development

Scott Demarest, Heather E. Olson, Angela Moss et al. · Epilepsia · 2019 · 158 citations · Full text

Efficacy of Low-Dose Buspirone for Restricted and Repetitive Behavior in Young Children with Autism Spectrum Disorder: A Randomized Trial

Diane C. Chugani, Harry T. Chugani, Max Wiznitzer et al. · The Journal of Pediatrics · 2015 · 110 citations · Full text

Implementation of Clinical Pharmacogenomics within a Large Health System: From Electronic Health Record Decision Support to Consultation Services

J. Kevin Hicks, David F. Stowe, Marc Willner et al. · Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy · 2016 · 109 citations

Pharmacotherapy, Translational Medicine, Drug-prescribing Process +21

Pathogenic mechanism of recurrent mutations of <scp><i>SCN8A</i></scp> in epileptic encephalopathy

Jacy L. Wagnon, Bryan S. Barker, James A. Hounshell et al. · Annals of Clinical and Translational Neurology · 2015 · 108 citations · Full text