Guerau Fernandez Isern
Investigador
Research group
The researcher Guerau Fernández earned a Ph.D. in Genetics and Cell Biology from the Autonomous University of Barcelona in 2005. He obtained the master's degree in Bioinformatics and Bioestadistics from the Universitat Oberta de Catalunya in 2014.
Since 2016 he has been a collaborating professor in the Master in Bioinformatics and Bio-Statistics.
Professional network profiles
Last Publications
- Domínguez-Rovira X, Arnau-Collell C, Gonfaus-Ortiz G, Llargués-Sistac G, Muñoz J, Llopis A, Soares de Lima Y, Herrera-Pariente C, Moreira L, Ocaña T, Díaz-Gay M, Cuatrecasas M, Carballal S, López-Novo A, Fernandez-Isern G, Castells A, Bujanda L, Capellà G, Cubiella J, Rodríguez-Alcalde D, Valle L, Balaguer F, Ruiz-Ponte C, Bonjoch L and Castellví-Bel S Germline pathogenic variants in HIC1 DNA binding domains are associated with familial serrated polyposis syndrome INTERNATIONAL JOURNAL OF CANCER . : .
- Vicente-Garces C, Fernandez-Isern G, Esperanza-Cebollada E, Richarte M, Crespo-Carrasco A, Montesdeoca S, Isola I, Sarrate E, Cuatrecasas E, Rives-Solà S, Dapena JL, Camós-Guijosa M and Vega-García N RNA-sequencing: A reliable tool to unveil transcriptional landscape of paediatric B-other acute lymphoblastic leukaemia. BRITISH JOURNAL OF HAEMATOLOGY . 206(5): 1355-1365.
- Llargués-Sistac G, Bonjoch L, Muñoz J, Domínguez-Rovira X, Ocaña T, Alvarez-Mora MI, Badenas C, Esteve-Codina A, Reyes-Silva C, Jaramillo-Koupermann G, Rodrigo MT, López-Prades S, Cuatrecasas M, Castells A, Balaguer F, Moreira L, Fernandez-Isern G and Castellví-Bel S Germline structural variant as the cause of Lynch Syndrome in a family from Ecuador npj Genomic Medicine . 10(1): 3-3.
Projects
- Project name:
- BETTER_Better rEal-world healTh-daTa distributEd analytics Research platform
- Leader
- Francesc Palau Martínez
- Funding entities:
- European Commission, Fundació Privada per a la Recerca i la Docència Sant Joan de Déu - FSJD, Palau Martínez, Francesc
- Code
- 101136262
- Starting - finishing date:
- 2023 - 2027
- Project name:
- Genes y Fenotipos de Síndromes Parkinsonianos: validación funcional de hallazgos genéticos - ParkGenPhen
- Leader
- Janet Hoenicka
- Funding entities:
- Instituto de Salud Carlos III (ISCIII), Fundació Privada per a la Recerca i la Docència Sant Joan de Déu - FSJD, Hoenicka, Janet
- Code
- PI22/00680
- Starting - finishing date:
- 2023 - 2025
- Project name:
- SGR 2022-2024_Precision Medicine of Genetic and Rare Diseases (PrecisionRare)
- Leader
- Francesc Palau Martínez
- Funding entities:
- Agaur - Agència de Gestió d'Ajuts Universitaris i de Recerca
- Code
- 2021 SGR 01610
- Starting - finishing date:
- 2022 - 2025