Gil Chernin

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

Saskia F. Heeringa, Gil Chernin, Moumita Chaki et al. · Journal of Clinical Investigation · 2011 · 394 citations · Full text

ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling

Heon Yung Gee, Pawaree Saisawat, Shazia Ashraf et al. · Journal of Clinical Investigation · 2013 · 226 citations · Full text

Glomerulonephritis, Renal Function, Disease Mechanism +15

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome

Jillian K. Warejko, Weizhen Tan, Ankana Daga et al. · Clinical Journal of the American Society of Nephrology · 2017 · 225 citations · Full text

A Novel TRPC6 Mutation That Causes Childhood FSGS

Saskia F. Heeringa, Clemens Möller, Jianyang Du et al. · PLoS ONE · 2009 · 170 citations · Full text

A Systematic Approach to Mapping Recessive Disease Genes in Individuals from Outbred Populations

Friedhelm Hildebrandt, Saskia F. Heeringa, Franz Rüschendorf et al. · PLoS Genetics · 2009 · 161 citations · Full text

Single Affected Individuals, Genetics, Genetic Epidemiology +19