Caroline M. Gorvin

Whole-Exome Sequencing Studies of Nonhereditary (Sporadic) Parathyroid Adenomas

Paul Newey, M. Andrew Nesbit, Andrew J. Rimmer et al. · The Journal of Clinical Endocrinology & Metabolism · 2012 · 141 citations · Full text

Mutant Prolactin Receptor and Familial Hyperprolactinemia

Paul Newey, Caroline M. Gorvin, Stephen J. Cleland et al. · New England Journal of Medicine · 2013 · 130 citations · Full text

Human Growth, Genetics, Janus Kinase 2 +18

AP2σ Mutations Impair Calcium-Sensing Receptor Trafficking and Signaling, and Show an Endosomal Pathway to Spatially Direct G-Protein Selectivity

Caroline M. Gorvin, Angela Rogers, Benoît Hastoy et al. · Cell Reports · 2018 · 91 citations · Full text

Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype–phenotype correlations, codon bias and dominant-negative effects

Fadil Hannan, Sarah Howles, Angela Rogers et al. · Human Molecular Genetics · 2015 · 86 citations · Full text

Whole-Exome Sequencing Studies of Nonfunctioning Pituitary Adenomas

Paul Newey, M. Andrew Nesbit, Andrew J. Rimmer et al. · The Journal of Clinical Endocrinology & Metabolism · 2013 · 84 citations · Full text