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 · 142 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Mutant Prolactin Receptor and Familial Hyperprolactinemia

Paul Newey, Caroline M. Gorvin, Stephen J. Cleland et al. · New England Journal of Medicine · 2013 · 131 citations · Full text

Medicine, Endocrinology, Genetics +16

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

Life Sciences, Cell Biology, Molecular Biology +17

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 · 89 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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 · 87 citations · Full text

Medicine, Genetics, Molecular Genetics +17