María
Currás Freixes
Investigadora hasta 2022
Lucía
Inglada Pérez
Publicaciones en las que colabora con Lucía Inglada Pérez (11)
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
2018
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Gain-of-function mutations in DNMT3A in patients with paraganglioma
Genetics in Medicine, Vol. 20, Núm. 12, pp. 1644-1651
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
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Targeted sequencing reveals low-frequency variants in EPHA genes as markers of paclitaxel-induced peripheral neuropathy
Clinical Cancer Research, Vol. 23, Núm. 5, pp. 1227-1235
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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Functional and in silico assessment of MAX variants of unknown significance
Journal of Molecular Medicine, Vol. 93, Núm. 11, pp. 1247-1255
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High frequency and founder effect of the CYP3A4∗20 loss-of-function allele in the Spanish population classifies CYP3A4 as a polymorphic enzyme
Pharmacogenomics Journal, Vol. 15, Núm. 3, pp. 288-292
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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
2014
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DNA methylation profiling of well-differentiated thyroid cancer uncovers markers of recurrence free survival
International Journal of Cancer, Vol. 135, Núm. 3, pp. 598-610
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VEGF, VEGFR3, and PDGFRB protein expression is influenced by ras mutations in medullary thyroid carcinoma
Thyroid, Vol. 24, Núm. 8, pp. 1251-1255