| 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 | 474 | 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 | 283 | 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 | 212 | 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 | 193 | 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 | 180 | 2010 |
| 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 | 170 | 2015 |
| 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 Genet 5 (9), e1000637, 2009 | 161 | 2009 |
| 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 | 147 | 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 | 129 | 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 | 114 | 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 Genet 7 (7), e1002182, 2011 | 106 | 2011 |
| 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 | 81 | 2015 |
| SIRT1 promotes thyroid carcinogenesis driven by PTEN deficiency D Herranz, A Maraver, M Canamero, G Gomez-Lopez, L Inglada-Perez, ... Oncogene 32 (34), 4052-4056, 2013 | 66 | 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 | 63 | 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 | 58 | 2013 |
| 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 | 57 | 2014 |
| 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 | 50 | 2015 |
| 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 | 46 | 2015 |
| Genetics of pheochromocytoma and paraganglioma in Spanish pediatric patients A Cascón, L Inglada-Pérez, I Comino-Méndez, AA de Cubas, R Letón, ... Endocrine-related cancer 20 (3), L1-L6, 2013 | 46 | 2013 |
| 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 | 45* | 2013 |
Gonzalo Gómez-LópezComputational Biologist, CNIO - (ORCID: 0000-0002-4146-0551)Dirección de correo verificada de cnio.es
