Steven Hébert

Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

Martin R. Pollak, Edward M. Brown, Yah‐Huei Wu Chou et al. · Cell · 1993 · 1.1K citations

Life Sciences, Endocrinology, Genetics +16

Autosomal dominant hypocalcaemia caused by a Ca2+-sensing receptor gene mutation

Martin R. Pollak, Edward M. Brown, Herschel L. Estep et al. · Nature Genetics · 1994 · 599 citations

Medicine, Genetics, Molecular Genetics +14

Genetic Ancestry and Natural Selection Drive Population Differences in Immune Responses to Pathogens

Yohann Nédélec, Joaquín Sanz, Golshid Baharian et al. · Cell · 2016 · 571 citations · Full text

Veterinary Medicine, Genetics, Immunology +16

Molecular Cloning and Functional Expression of Human Parathyroid Calcium Receptor cDNAs

James E. Garrett, Irene V. Capuano, Lance G. Hammerland et al. · Journal of Biological Chemistry · 1995 · 502 citations · Full text

Life Sciences, Endocrinology, Molecular Biology +17

Reduced immunostaining for the extracellular Ca2+-sensing receptor in primary and uremic secondary hyperparathyroidism.

Olga Kifor, Francis D. Moore, P Wang et al. · The Journal of Clinical Endocrinology & Metabolism · 1996 · 479 citations · Full text

Medicine, Endocrinology, Molecular Biology +17