Erin Loring

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 · 604 citations

Primary Aldosteronism, Aldosterone-producing Adenomas, Physiology

Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation

Neil Romberg, Khatoun Al Moussawi, Carol Nelson‐Williams et al. · Nature Genetics · 2014 · 504 citations · Full text

Autoimmune Disease, Disease Mechanism, Pathogenesis +7

L-Histidine Decarboxylase and Tourette's Syndrome

A. Gulhan Ercan‐Sencicek, Althea Stillman, Ananda K. Ghosh et al. · New England Journal of Medicine · 2010 · 362 citations · Full text

Genetics, Molecular Biology, Molecular Genetics +16

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 · 345 citations · Full text

Histidine Decarboxylase Deficiency Causes Tourette Syndrome: Parallel Findings in Humans and Mice

Lissandra Castellan Baldan, Kyle A. Williams, Jean‐Dominique Gallezot et al. · Neuron · 2014 · 251 citations · Full text

Parallel Findings, Psychiatry, Syndromic Autism +5