Richard Warth

Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and <i>KCNJ10</i> Mutations

Detlef Böckenhauer, Sally Feather, Horia Stanescu et al. · New England Journal of Medicine · 2009 · 580 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension

Felix Beuschlein, Sheerazed Boulkroun, Thomas Wieland et al. · Nature Genetics · 2013 · 568 citations · Full text

Medicine, Endocrinology, Genetics +15

A constitutively open potassium channel formed by KCNQ1 and KCNE3

Björn C. Schroeder, Siegfried Waldegger, Susanne Fehr et al. · Nature · 2000 · 495 citations

Natural Sciences, Biochemistry, Biophysics +11

Mineralocorticoid receptor knockout mice: Pathophysiology of Na ⁺ metabolism

Stefan Berger, Markus Bleich, Wolfgang Schmid et al. · Proceedings of the National Academy of Sciences · 1998 · 412 citations · Full text

Medicine, Pharmacology, Physiology +17

Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder

Robert Kleta, Elisa Romeo, Zorica Ristic et al. · Nature Genetics · 2004 · 309 citations · Full text

Life Sciences, Genetics, Molecular Genetics +6