María
Currás Freixes
Investigadora hasta 2022
Hôpital Européen Georges-Pompidou
París, FranciaPublicaciones en colaboración con investigadores/as de Hôpital Européen Georges-Pompidou (7)
2019
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Integrative multi-omics analysis identifies a prognostic miRNA signature and a targetable miR-21-3p/TSC2/ mTOR axis in metastatic pheochromocytoma/ paraganglioma
Theranostics, Vol. 9, Núm. 17, pp. 4946-4958
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Prognosis of malignant pheochromocytoma and paraganglioma (MAPP-PronO study): A European network for the study of adrenal tumors retrospective study
Journal of Clinical Endocrinology and Metabolism, Vol. 104, Núm. 6, pp. 2367-2374
2018
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Role of MDH2 pathogenic variant in pheochromocytoma and paraganglioma patients
Genetics in Medicine, Vol. 20, Núm. 12, pp. 1652-1662
2017
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The mTORC1 Complex Is Significantly Overactivated in SDHX -Mutated Paragangliomas
Neuroendocrinology, Vol. 105, Núm. 4, pp. 384-393
2015
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DNA methylation profiling in pheochromocytoma and paraganglioma reveals diagnostic and prognostic markers
Clinical Cancer Research, Vol. 21, Núm. 13, pp. 3020-3030
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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)
Modern Pathology, Vol. 28, Núm. 6, pp. 807-821
2014
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Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas
Human Molecular Genetics, Vol. 23, Núm. 9, pp. 2440-2446