Rare Genomic Variants Link Bipolar Disorder with Anxiety Disorders to CREB-Regulated Intracellular Signaling PathwaysBerit Kerner, Stanley F. Nelson, Aliz R. Rao et al.|Frontiers in Psychiatry|2013Cited by 44
Rich annotation of DNA sequencing variants by leveraging the Ensembl Variant Effect Predictor with pluginsMichael Yourshaw, Stanley F. Nelson, S. Paige Taylor et al.|Briefings in Bioinformatics|2014Cited by 40
Calculating the statistical significance of rare variants causal for Mendelian and complex disordersAliz R. Rao, Stanley F. Nelson|BMC Medical Genomics|2018Cited by 19
Exome Sequencing Identified a Splice Site Mutation in <i>FHL1</i> that Causes Uruguay Syndrome, an X-Linked Disorder With Skeletal Muscle Hypertrophy and Premature Cardiac DeathYuan Xue, William R. Wilcox, Benedikt Schoser et al.|Circulation Cardiovascular Genetics|2016Cited by 10
Calculating the statistical significance of rare variants causal for Mendelian and complex disordersAliz R. Rao, Stanley F. Nelson|bioRxiv (Cold Spring Harbor Laboratory)|2017Cited by 4