Seguir
Lucia Inglada-Pérez
Lucia Inglada-Pérez
UCM, UNED, CNIO, CIBERER
Dirección de correo verificada de ucm.es
Título
Citado por
Citado por
Año
Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma
I Comino-Méndez, FJ Gracia-Aznárez, F Schiavi, I Landa, ...
Nature genetics 43 (7), 663-667, 2011
5362011
MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and ParagangliomaMAX Causes Pheochromocytoma and Paraganglioma
N Burnichon, A Cascón, F Schiavi, NP Morales, I Comino-Méndez, ...
Clinical cancer research 18 (10), 2828-2837, 2012
3182012
The miR-200 family controls β-tubulin III expression and is associated with paclitaxel-based treatment response and progression-free survival in ovarian cancer patients
S Leskelä, LJ Leandro-García, M Mendiola, J Barriuso, L Inglada-Pérez, ...
Endocrine-related cancer 18 (1), 85-95, 2011
2222011
Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas
L Yao, F Schiavi, A Cascon, Y Qin, L Inglada-Pérez, EE King, RA Toledo, ...
Jama 304 (23), 2611-2619, 2010
2192010
Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene
A Cascón, I Comino-Méndez, M Currás-Freixes, AA de Cubas, ...
JNCI: Journal of the National Cancer Institute 107 (5), 2015
2032015
Research resource: transcriptional profiling reveals different pseudohypoxic signatures in SDHB and VHL-related pheochromocytomas
E López-Jiménez, G Gómez-López, LJ Leandro-García, I Muñoz, ...
Molecular endocrinology 24 (12), 2382-2391, 2010
1992010
Tumor microRNA expression profiling identifies circulating microRNAs for early breast cancer detection
N Matamala, MT Vargas, R Gonzalez-Campora, R Minambres, JI Arias, ...
Clinical chemistry 61 (8), 1098-1106, 2015
1772015
The Variant rs1867277 in FOXE1 Gene Confers Thyroid Cancer Susceptibility through the Recruitment of USF1/USF2 Transcription Factors
I Landa, S Ruiz-Llorente, C Montero-Conde, L Inglada-Pérez, F Schiavi, ...
PLoS genetics 5 (9), e1000637, 2009
1732009
Tumoral EPAS1 (HIF2A) mutations explain sporadic pheochromocytoma and paraganglioma in the absence of erythrocytosis
I Comino-Méndez, AA de Cubas, C Bernal, C Álvarez-Escolá, ...
Human Molecular Genetics 22 (11), 2169-2176, 2013
1512013
Overexpression and activation of EGFR and VEGFR2 in medullary thyroid carcinomas is related to metastasis
C Rodríguez-Antona, J Pallares, C Montero-Conde, L Inglada-Pérez, ...
Endocrine-Related Cancer 17 (1), 7-16, 2010
1262010
Genetic anticipation is associated with telomere shortening in hereditary breast cancer
B Martinez-Delgado, K Yanowsky, L Inglada-Perez, S Domingo, M Urioste, ...
PLoS genetics 7 (7), e1002182, 2011
1182011
Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients
M Currás-Freixes, L Inglada-Pérez, V Mancikova, C Montero-Conde, ...
Journal of medical genetics 52 (10), 647-656, 2015
1022015
SIRT1 promotes thyroid carcinogenesis driven by PTEN deficiency
D Herranz, A Maraver, M Canamero, G Gomez-Lopez, L Inglada-Perez, ...
Oncogene 32 (34), 4052-4056, 2013
722013
DNA methylation profiling of well‐differentiated thyroid cancer uncovers markers of recurrence free survival
V Mancikova, R Buj, E Castelblanco, L Inglada‐Pérez, A Diez, ...
International Journal of cancer 135 (3), 598-610, 2014
702014
Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy
LJ Leandro-García, L Inglada-Pérez, G Pita, E Hjerpe, S Leskelä, C Jara, ...
Journal of medical genetics 50 (9), 599-605, 2013
702013
Regulatory Polymorphisms in β-Tubulin IIa Are Associated with Paclitaxel-Induced Peripheral Neuropathyβ-Tubulin IIa SNPs Associated with Paclitaxel Neuropathy
LJ Leandro-García, S Leskelä, C Jara, H Gréen, E Åvall-Lundqvist, ...
Clinical Cancer Research 18 (16), 4441-4448, 2012
702012
Gain-of-function mutations in DNMT3A in patients with paraganglioma
L Remacha, M Currás-Freixes, R Torres-Ruiz, F Schiavi, R Torres-Pérez, ...
Genetics in Medicine 20 (12), 1644-1651, 2018
632018
DNA methylation profiling in pheochromocytoma and paraganglioma reveals diagnostic and prognostic markers
AA De Cubas, E Korpershoek, L Inglada-Pérez, E Letouzé, ...
Clinical Cancer Research 21 (13), 3020-3030, 2015
602015
MicroRNA deep-sequencing reveals master regulators of follicular and papillary thyroid tumors
V Mancikova, E Castelblanco, E Pineiro-Yanez, J Perales-Paton, ...
Modern Pathology 28 (6), 748-757, 2015
582015
PheoSeq: a targeted next-generation sequencing assay for pheochromocytoma and paraganglioma diagnostics
M Currás-Freixes, E Piñeiro-Yañez, C Montero-Conde, M Apellániz-Ruiz, ...
The Journal of Molecular Diagnostics 19 (4), 575-588, 2017
542017
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
Artículos 1–20