María Currás-Freixes

Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas

Luis Jaime Castro‐Vega, Alexandre Buffet, Aguirre A. de Cubas et al. · Human Molecular Genetics · 2013 · 391 citations

Life Sciences, Genetics, Oncology +13

SDHB/SDHA immunohistochemistry in pheochromocytomas and paragangliomas: a multicenter interobserver variation analysis using virtual microscopy: a Multinational Study of the European Network for the Study of Adrenal Tumors (ENS@T)

Thomas Papathomas, Lindsey Oudijk, Alexandre Persu et al. · Modern Pathology · 2015 · 227 citations · Full text

Medicine, Endocrinology, Pathology +17

Whole-Exome Sequencing Identifies MDH2 as a New Familial Paraganglioma Gene

Alberto Cascón, Iñaki Comino‐Méndez, María Currás-Freixes et al. · JNCI Journal of the National Cancer Institute · 2015 · 189 citations · Full text

Medicine, Genetics, Oncology +16

Prognosis of Malignant Pheochromocytoma and Paraganglioma (MAPP-Prono Study): A European Network for the Study of Adrenal Tumors Retrospective Study

S. Hescot, María Currás-Freixes, Timo Deutschbein et al. · The Journal of Clinical Endocrinology & Metabolism · 2019 · 180 citations · Full text

Medicine, Oncology, Radiology +15

Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients

María Currás-Freixes, Lucía Inglada‐Pérez, Veronika Mančíková et al. · Journal of Medical Genetics · 2015 · 127 citations · Full text

Life Sciences, Genetics, Oncology +17