Bernard S. Kaplan

Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome

Véronique Frémeaux‐Bacchi, Elizabeth C. Miller, M. Kathryn Liszewski et al. · Blood · 2008 · 371 citations · Full text

Factor H Mutations in Hemolytic Uremic Syndrome Cluster in Exons 18–20, a Domain Important for Host Cell Recognition

Anna Richards, M. Buddles, Rosemary L. Donne et al. · The American Journal of Human Genetics · 2001 · 310 citations · Full text

Exons 18–20, Genetic Disorder, Factor H Mutations +9

Autosomal recessive polycystic kidney disease

Bernard S. Kaplan, Joseph W. Fay, Vanita Shah et al. · Pediatric Nephrology · 1989 · 248 citations

Glomerulonephritis, Urology, Renal Disease +7

Non-enteropathic hemolytic uremic syndrome: causes and short-term course

A. Constantinescu, Martin Bitzan, Lynne Weiss et al. · American Journal of Kidney Diseases · 2004 · 229 citations

Hemodialysis, Medicine, Kidney Failure +4

Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans

Jan Halbritter, Albane A. Bizet, Miriam Schmidts et al. · The American Journal of Human Genetics · 2013 · 225 citations · Full text