María
Currás Freixes
Chercheuse jusqu' 2022
Hospital Universitario Puerta de Hierro
Madrid, EspañaPublications en collaboration avec des chercheurs de Hospital Universitario Puerta de Hierro (6)
2023
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Genomic and immune landscape Of metastatic pheochromocytoma and paraganglioma
Nature Communications, Vol. 14, Núm. 1
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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Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas
American Journal of Human Genetics, Vol. 104, Núm. 4, pp. 651-664
2017
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PheoSeq: A Targeted Next-Generation Sequencing Assay for Pheochromocytoma and Paraganglioma Diagnostics
Journal of Molecular Diagnostics, Vol. 19, Núm. 4, pp. 575-588
2015
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Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients
Journal of Medical Genetics, Vol. 52, Núm. 10, pp. 647-656
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Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene
Journal of the National Cancer Institute, Vol. 107, Núm. 5