Lucia Inglada-Pérez
Lucia Inglada-Pérez
UC3M, UNED, CNIO, CIBERER
Dirección de correo verificada de cnio.es
TítuloCitado porAño
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, 2011
4162011
MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma
N Burnichon, A Cascón, F Schiavi, NP Morales, I Comino-Méndez, ...
Clinical cancer research 18 (10), 2828-2837, 2012
2212012
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
1862011
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
1622010
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
1472010
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
1372009
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
1322015
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
992013
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
942010
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
942010
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
842011
Tumor microRNA expression profiling identifies circulating microRNAs for early breast cancer detection
N Matamala, MT Vargas, R González-Cámpora, R Miñambres, JI Arias, ...
Clinical chemistry 61 (8), 1098-1106, 2015
792015
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
602015
SIRT1 promotes thyroid carcinogenesis driven by PTEN deficiency
D Herranz, A Maraver, M Canamero, G Gomez-Lopez, L Inglada-Perez, ...
Oncogene 32 (34), 4052, 2013
572013
Regulatory polymorphisms in β-tubulin IIa are associated with paclitaxel-induced peripheral neuropathy
LJ Leandro-García, S Leskelä, C Jara, H Gréen, E Åvall-Lundqvist, ...
Clinical Cancer Research 18 (16), 4441-4448, 2012
542012
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
412013
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, 2015
362015
Shorter telomere length is associated with increased ovarian cancer risk in both familial and sporadic cases
B Martinez-Delgado, K Yanowsky, L Inglada-Perez, M de la Hoya, ...
Journal of medical genetics 49 (5), 341-344, 2012
362012
Integrative analysis of miRNA and mRNA expression profiles in pheochromocytoma and paraganglioma identifies genotype-specific markers and potentially regulated pathways
AA De Cubas, LJ Leandro-García, F Schiavi, V Mancikova, ...
Endocrine-related cancer 20 (4), 477-493, 2013
35*2013
Allelic variant at− 79 (C> T) in CDKN1B (p27Kip1) confers an increased risk of thyroid cancer and alters mRNA levels
I Landa, C Montero-Conde, D Malanga, S De Gisi, G Pita, ...
Endocrine-related cancer 17 (2), 317-328, 2010
352010
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Artículos 1–20