| Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer C Esteban-Jurado, M Vila-Casadesús, P Garre, JJ Lozano, ... Genetics in Medicine 17 (2), 131-142, 2015 | 112 | 2015 |
| Mutational Signatures in Cancer (MuSiCa): a web application to implement mutational signatures analysis in cancer samples M Díaz-Gay, M Vila-Casadesús, S Franch-Expósito, E Hernández-Illán, ... BMC bioinformatics 19, 1-6, 2018 | 103 | 2018 |
| Interplay between chromosomal alterations and gene mutations shapes the evolutionary trajectory of clonal hematopoiesis T Gao, R Ptashkin, KL Bolton, M Sirenko, C Fong, B Spitzer, ... Nature communications 12 (1), 338, 2021 | 79 | 2021 |
| The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer C Esteban-Jurado, S Franch-Expósito, J Muñoz, T Ocaña, S Carballal, ... European Journal of Human Genetics 24 (10), 1501-1505, 2016 | 76 | 2016 |
| The landscape of genomic copy number alterations in colorectal cancer and their consequences on gene expression levels and disease outcome T Ried, GA Meijer, DJ Harrison, G Grech, S Franch-Expósito, R Briffa, ... Molecular aspects of medicine 69, 48-61, 2019 | 54 | 2019 |
| CNApp, a tool for the quantification of copy number alterations and integrative analysis revealing clinical implications S Franch-Expósito, L Bassaganyas, M Vila-Casadesús, ... elife 9, e50267, 2020 | 53 | 2020 |
| POLE and POLD1 screening in 155 patients with multiple polyps and early-onset colorectal cancer C Esteban-Jurado, D Giménez-Zaragoza, J Muñoz, S Franch-Exposito, ... Oncotarget 8 (16), 26732, 2017 | 51 | 2017 |
| Copy-number alteration burden differentially impacts immune profiles and molecular features of hepatocellular carcinoma L Bassaganyas, R Pinyol, R Esteban-Fabró, L Torrens, S Torrecilla, ... Clinical Cancer Research 26 (23), 6350-6361, 2020 | 42 | 2020 |
| Zeb1 in Stromal Myofibroblasts Promotes Kras-Driven Development of Pancreatic Cancer I Sangrador, X Molero, F Campbell, S Franch-Expósito, M Rovira-Rigau, ... Cancer research 78 (10), 2624-2637, 2018 | 25 | 2018 |
| Germline mutations in FAF1 are associated with hereditary colorectal cancer L Bonjoch, S Franch-Expósito, P Garre, S Belhadj, J Muñoz, ... Gastroenterology 159 (1), 227-240. e7, 2020 | 21 | 2020 |
| Integrated analysis of germline and tumor DNA identifies new candidate genes involved in familial colorectal cancer M Díaz-Gay, S Franch-Exposito, C Arnau-Collell, S Park, F Supek, ... Cancers 11 (3), 362, 2019 | 20 | 2019 |
| Rare germline copy number variants in colorectal cancer predisposition characterized by exome sequencing analysis S Franch-Expósito, C Esteban-Jurado, P Garre, I Quintanilla, ... Journal of genetics and genomics= Yi chuan xue bao 45 (1), 41-45, 2018 | 18 | 2018 |
| Somatic mutational signatures in polyposis and colorectal cancer JE Grolleman, M Diaz-Gay, S Franch-Exposito, S Castellvi-Bel, ... Molecular Aspects of Medicine 69, 62-72, 2019 | 17 | 2019 |
| Germline and somatic whole-exome sequencing identifies new candidate genes involved in familial predisposition to serrated polyposis syndrome Y Soares de Lima, C Arnau-Collell, M Díaz-Gay, L Bonjoch, ... Cancers 13 (4), 929, 2021 | 15 | 2021 |
| 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 |
| Using linkage studies combined with whole‐exome sequencing to identify novel candidate genes for familial colorectal cancer C Toma, M Díaz‐Gay, S Franch‐Expósito, C Arnau‐Collell, B Overs, ... International Journal of Cancer 146 (6), 1568-1577, 2020 | 11 | 2020 |
| Comprehensive genomic characterization of fifteen early-onset Lynch-like syndrome colorectal cancers M Golubicki, M Díaz-Gay, L Bonjoch, S Franch-Expósito, J Muñoz, ... Cancers 13 (6), 1259, 2021 | 7 | 2021 |
| Identification of a novel candidate gene for serrated polyposis syndrome germline predisposition by performing linkage analysis combined with whole-exome sequencing C Toma, M Diaz-Gay, YS de Lima, C Arnau-Collell, S Franch-Exposito, ... Clinical and translational gastroenterology 10 (10), e00100, 2019 | 7 | 2019 |
| Integrated multi‐omics profiling of high‐grade estrogen receptor‐positive, HER2‐negative breast cancer K Wang, L Li, S Franch‐Expósito, X Le, J Tang, Q Li, Q Wu, ... Molecular Oncology 16 (12), 2413-2431, 2022 | 6 | 2022 |
| Associations between cancer predisposition mutations and clonal hematopoiesis in patients with solid tumors S Franch-Expósito, M Mehine, RN Ptashkin, KL Bolton, C Bandlamudi, ... JCO Precision Oncology 7, e2300070, 2023 | 4 | 2023 |
Sergi Castellví-BelInstitut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS)在 recerca.clinic.cat 的电子邮件经过验证
