M. Andrew Nesbit

GATA3 haplo-insufficiency causes human HDR syndrome

Hilde Van Esch, Peter Groenen, M. Andrew Nesbit et al. · Nature · 2000 · 645 citations

Autoimmune Disease, Genetic Disorder, Genetics +5

Mutations Affecting G-Protein Subunit α₁₁in Hypercalcemia and Hypocalcemia

M. Andrew Nesbit, Fadil Hannan, Sarah Howles et al. · New England Journal of Medicine · 2013 · 389 citations · Full text

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

Jenny C. Taylor, Hilary C. Martin, Stefano Lise et al. · Nature Genetics · 2015 · 378 citations · Full text

Sequencing, Psychiatry, Clinical Genome +8

Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3

M. Andrew Nesbit, Fadil Hannan, Sarah Howles et al. · Nature Genetics · 2012 · 279 citations · Full text

Molecular Physiology, Mendelian Disorder, Genetic Disorder +4

Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites

Fadil Hannan, M. Andrew Nesbit, C. Zhang et al. · Human Molecular Genetics · 2012 · 183 citations