| 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 | 416 | 2011 |
| 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 | 221 | 2012 |
| 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 | 186 | 2011 |
| 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 | 162 | 2010 |
| 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 | 147 | 2010 |
| 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 | 137 | 2009 |
| 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 | 132 | 2015 |
| 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 | 99 | 2013 |
| 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 | 94 | 2010 |
| 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 | 94 | 2010 |
| 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 | 84 | 2011 |
| 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 | 79 | 2015 |
| 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 | 60 | 2015 |
| 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 | 57 | 2013 |
| 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 | 54 | 2012 |
| 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 | 41 | 2013 |
| 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 | 36 | 2015 |
| 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 | 36 | 2012 |
| 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 | 35 | 2010 |
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