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 · 373 citations · Full text

Life Sciences, Genetics, Hematology +14

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 · 311 citations · Full text

Medicine, Genetics, Molecular Genetics +15

Autosomal recessive polycystic kidney disease

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

Medicine, Genetics, Nephrology +12

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 · 231 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

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

A. Constantinescu, Martin Bitzan, Lynne Weiss et al. · American Journal of Kidney Diseases · 2004 · 230 citations

Medicine, Internal Medicine, Nephrology +10