Michelle P. Winn

A Mutation in the <i>TRPC6</i> Cation Channel Causes Familial Focal Segmental Glomerulosclerosis

Michelle P. Winn, Peter J. Conlon, Kelvin L. Lynn et al. · Science · 2005 · 1.1K citations

Medicine, Molecular Genetics, Nephrology +17

Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis

Shreeram Akilesh, Hani Suleiman, Haiyang Yu et al. · Journal of Clinical Investigation · 2011 · 265 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +17

Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis

Andrew F. Malone, Paul J. Phelan, Gentzon Hall et al. · Kidney International · 2014 · 239 citations · Full text

Medicine, Genetics, Molecular Genetics +13

TRPC1 Channels Are Critical for Hypertrophic Signaling in the Heart

Malini Seth, Zhu-Shan Zhang, Lan Mao et al. · Circulation Research · 2009 · 221 citations · Full text

Life Sciences, Cardiology, Physiology +17

Parkin mutations and susceptibility alleles in late‐onset Parkinson's disease

Sofia A. Oliveira, William K. Scott, Eden R. Martin et al. · Annals of Neurology · 2003 · 214 citations

Life Sciences, Genetics, Molecular Genetics +17