Martin R. Pollak

Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans

Giulio Genovese, David J. Friedman, Michael D. Ross et al. · Science · 2010 · 2K citations · Full text

Glomerulonephritis, Urology, Renal Function +15

Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis

Joshua M. Kaplan, Sung Hyun Kim, Kathryn N. North et al. · Nature Genetics · 2000 · 1.2K citations

Glomerulonephritis, Urology, Medicine +7

Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

Martin R. Pollak, Edward M. Brown, Yah‐Huei Wu Chou et al. · Cell · 1993 · 1K citations

Genetics, Physiology, Neonatal Severe Hyperparathyroidism +4

TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function

Jochen Reiser, Krishna R. Polu, Clemens Möller et al. · Nature Genetics · 2005 · 846 citations · Full text

Urology, Signal Transduction, Molecular Physiology +10

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