Howard Trachtman

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

David B. Simon, Ranjit S. Bindra, Traci A. Mansfield et al. · Nature Genetics · 1997 · 863 citations

Channelopathies, Genetic Disorder, Chloride Channel Gene +7

APOL1 Genetic Variants in Focal Segmental Glomerulosclerosis and HIV-Associated Nephropathy

Jeffrey B. Kopp, George W. Nelson, Karmini Sampath et al. · Journal of the American Society of Nephrology · 2011 · 836 citations · Full text

Glomerular Disease, Trypanolytic Variants, Apol1 Variants +19

Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMK

David B. Simon, Fiona E. Karet, Juan Rodríguez‐Soriano et al. · Nature Genetics · 1996 · 820 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis

Jeffrey B. Kopp, Michael W. Smith, George W. Nelson et al. · Nature Genetics · 2008 · 700 citations · Full text

Glomerular Disease, Glomerulonephritis, Urology +8

Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities

Lynn M. Boyden, Murim Choi, Keith A. Choate et al. · Nature · 2012 · 625 citations

Molecular Physiology, Genetics, Physiology +7