Ute I. Scholl

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

Murim Choi, Ute I. Scholl, Weizhen Ji et al. · Proceedings of the National Academy of Sciences · 2009 · 1.3K citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

K ⁺ Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension

Murim Choi, Ute I. Scholl, Peng Yue et al. · Science · 2011 · 983 citations

Medicine, Endocrinology, Molecular Genetics +17

Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism

Ute I. Scholl, Gerald Goh, Gabriel Stölting et al. · Nature Genetics · 2013 · 619 citations

Medicine, Endocrinology, Molecular Genetics +16

Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in <i>KCNJ10</i>

Ute I. Scholl, Murim Choi, Tiewen Liu et al. · Proceedings of the National Academy of Sciences · 2009 · 493 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism

Ute I. Scholl, Gabriel Stölting, Carol Nelson‐Williams et al. · eLife · 2015 · 355 citations · Full text

Life Sciences, Endocrinology, Genetics +15