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 · 870 citations

Life Sciences, Genetics, Molecular Genetics +13

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 · 859 citations · Full text

Medicine, Genetics, Nephrology +9

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 · 825 citations

Life Sciences, Genetics, Molecular Genetics +12

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 · 708 citations

Medicine, Genetics, Molecular Genetics +13

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 · 633 citations

Life Sciences, Genetics, Molecular Genetics +11