Michael G. Gartside

A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

Satoru Yokoyama, Susan L. Woods, Glen M. Boyle et al. · Nature · 2011 · 466 citations · Full text

POT1 loss-of-function variants predispose to familial melanoma

Carla Daniela Robles‐Espinoza, Mark Harland, Andrew Ramsay et al. · Nature Genetics · 2014 · 378 citations · Full text

Pot1 Loss-of-function Variants, Melanoma, Pathology +4

Mice Lacking the Vascular Endothelial Growth Factor-B Gene ( <i>Vegfb</i> ) Have Smaller Hearts, Dysfunctional Coronary Vasculature, and Impaired Recovery From Cardiac Ischemia

Daniela Bellomo, John P. Headrick, Ginters Silins et al. · Circulation Research · 2000 · 326 citations · Full text

Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes

Pamela M. Pollock, Michael G. Gartside, L C Dejeza et al. · Oncogene · 2007 · 302 citations · Full text

Mendelian Disorder, Skeletal Dysplasia Syndromes, Pathology +5

Frequent somatic mutations in MAP3K5 and MAP3K9 in metastatic melanoma identified by exome sequencing

Mitchell Stark, Susan L. Woods, Michael G. Gartside et al. · Nature Genetics · 2011 · 195 citations · Full text

Somatic Variant, Exome Sequencing, Medicine +9