John W. Foreman

Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination

Edgar A. Otto, Bernhard Schermer, Tomoko Obara et al. · Nature Genetics · 2003 · 642 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities

Lynn M. Boyden, Murim Choi, Keith A. Choate et al. · Nature · 2012 · 633 citations

Life Sciences, Genetics, Molecular Genetics +11

Inhibition of calcium oxalate crystal growth in vitro by uropontin: another member of the aspartic acid-rich protein superfamily.

Hiroshi Shiraga, William J. VanDusen, Michael D. Clayman et al. · Proceedings of the National Academy of Sciences · 1992 · 398 citations

Medicine, Biochemistry, Nephrology +14

Hypercalcemia, Hypercalciuria, and Elevated Calcitriol Concentrations with Autosomal Dominant Transmission Due to<i>CYP24A1</i>Mutations: Effects of Ketoconazole Therapy

Peter J. Tebben, Dawn S. Milliner, Ronald L. Horst et al. · The Journal of Clinical Endocrinology & Metabolism · 2012 · 193 citations · Full text

Medicine, Endocrinology, Genetics +17

HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome

Rasheed Gbadegesin, Adebowale Adeyemo, Nicholas J.A. Webb et al. · Journal of the American Society of Nephrology · 2014 · 149 citations · Full text

Life Sciences, Genetics, Immunology +17