Rasheed Gbadegesin

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

Bernward Hinkes, Roger C. Wiggins, Rasheed Gbadegesin et al. · Nature Genetics · 2006 · 557 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

Nephrotic Syndrome in the First Year of Life: Two Thirds of Cases Are Caused by Mutations in 4 Genes (<i>NPHS1</i>, <i>NPHS2</i>, <i>WT1</i>, and <i>LAMB2</i>)

Bernward Hinkes, Bettina E. Mucha, Christopher N. Vlangos et al. · PEDIATRICS · 2007 · 432 citations

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

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 · 259 citations · Full text

Glomerular Disease, Specialized Epithelial Cell, Pathology +21

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 · 232 citations · Full text

Glomerulonephritis, Urology, Renal Pathology +3