| Role of POLE and POLD1 in familial cancer P Mur, S García-Mulero, J Del Valle, L Magraner-Pardo, A Vidal, ... Genetics in medicine 22 (12), 2089-2100, 2020 | 102 | 2020 |
| MLH1 promoter hypermethylation in the analytical algorithm of Lynch syndrome: a cost-effectiveness study M Gausachs, P Mur, J Corral, M Pineda, S González, L Benito, ... European Journal of Human Genetics 20 (7), 762-768, 2012 | 92 | 2012 |
| Evidence suggests that germline RNF43 mutations are a rare cause of serrated polyposis I Quintana, R Mejías-Luque, M Terradas, M Navarro, V Piñol, P Mur, ... Gut 67 (12), 2230-2232, 2018 | 63 | 2018 |
| Codeletion of 1p and 19q determines distinct gene methylation and expression profiles in IDH-mutated oligodendroglial tumors P Mur, M Mollejo, Y Ruano, ÁR de Lope, C Fiaño, JF García, ... Acta neuropathologica 126, 277-289, 2013 | 63 | 2013 |
| Genetic alterations associated with progression and recurrence in meningiomas E Pérez-Magán, Y Campos-Martín, P Mur, C Fiaño, T Ribalta, JF García, ... Journal of Neuropathology & Experimental Neurology 71 (10), 882-893, 2012 | 59 | 2012 |
| Impact on prognosis of the regional distribution of MGMT methylation with respect to the CpG island methylator phenotype and age in glioma patients P Mur, Á Rodríguez de Lope, FJ Díaz-Crespo, T Hernández-Iglesias, ... Journal of neuro-oncology 122, 441-450, 2015 | 58 | 2015 |
| The inherited and familial component of early-onset colorectal cancer M Daca Alvarez, I Quintana, M Terradas, P Mur, F Balaguer, L Valle Cells 10 (3), 710, 2021 | 57 | 2021 |
| Delineating the phenotypic spectrum of the NTHL1-associated polyposis S Belhadj, P Mur, M Navarro, S González, V Moreno, G Capellá, L Valle Clinical Gastroenterology and Hepatology 15 (3), 461-462, 2017 | 56 | 2017 |
| MLH1 methylation screening is effective in identifying epimutation carriers M Pineda, P Mur, MD Iniesta, E Borràs, O Campos, G Vargas, S Iglesias, ... European journal of human genetics 20 (12), 1256-1264, 2012 | 53 | 2012 |
| Molecular classification defines 4 prognostically distinct glioma groups irrespective of diagnosis and grade P Mur, M Mollejo, T Hernández-Iglesias, AR de Lope, JS Castresana, ... Journal of Neuropathology & Experimental Neurology 74 (3), 241-249, 2015 | 50 | 2015 |
| Association between germline mutations in BRF1, a subunit of the RNA polymerase III transcription complex, and hereditary colorectal cancer F Bellido, N Sowada, P Mur, C Lázaro, T Pons, R Valdés-Mas, M Pineda, ... Gastroenterology 154 (1), 181-194. e20, 2018 | 41 | 2018 |
| Gene expression changes associated with erlotinib response in glioma cell lines A García-Claver, M Lorente, P Mur, Y Campos-Martín, M Mollejo, ... European Journal of Cancer 49 (7), 1641-1653, 2013 | 40 | 2013 |
| NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas S Belhadj, I Quintana, P Mur, PM Munoz-Torres, MH Alonso, M Navarro, ... Scientific Reports 9 (1), 9020, 2019 | 34 | 2019 |
| Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposis P Mur, RM De Voer, R Olivera-Salguero, S Rodríguez-Perales, T Pons, ... Molecular Cancer 17, 1-6, 2018 | 30 | 2018 |
| miR-543 regulates the epigenetic landscape of myelofibrosis by targeting TET1 and TET2 E Fuentes-Mattei, R Bayraktar, T Manshouri, AM Silva, C Ivan, D Gulei, ... JCI insight 5 (1), 2020 | 23 | 2020 |
| Plasma viral miRNAs indicate a high prevalence of occult viral infections E Fuentes-Mattei, DE Giza, M Shimizu, C Ivan, JT Manning, S Tudor, ... EBioMedicine 20, 182-192, 2017 | 22 | 2017 |
| Germline variation in O6-methylguanine-DNA methyltransferase (MGMT) as cause of hereditary colorectal cancer S Belhadj, C Moutinho, P Mur, F Setien, P Llinàs-Arias, M Pérez-Salvia, ... Cancer Letters 447, 86-92, 2019 | 17 | 2019 |
| Copy number alterations in glioma cell lines B Meléndez, A García-Claver, Y Ruano, Y Campos-Martín, AR de Lope, ... Glioma-Exploring Its Biology and Practical Relevance, 2011 | 16 | 2011 |
| Identification of a founder EPCAM deletion in Spanish Lynch syndrome families P Mur, M Pineda, A Romero, J Del Valle, E Borras, A Canal, M Navarro, ... Clinical Genetics 85 (3), 260-266, 2014 | 15 | 2014 |
| Approaches to functionally validate candidate genetic variants involved in colorectal cancer predisposition L Bonjoch, P Mur, C Arnau-Collell, G Vargas-Parra, B Shamloo, ... Molecular Aspects of Medicine 69, 27-40, 2019 | 13 | 2019 |
