Directory

HERNÁNDEZ VIEDMA, Gonzalo

Department of Basic Areas
Hereditary Hematology and Iron metabolism
ORCID
ORCID
Section

HERNÁNDEZ VIEDMA, Gonzalo

CV

Teacher profile

Professor Investigador

Basic Areas, DEPARTMENT OF BASIC SCIENCIES. Universitat Internacional de Catalunya

Academic curriculum
  • Genetica Universitat Autónoma de Barcelona
  • Biotecnologia Universitat Autonoma de Barcelona
  • Master en Genética Universitat Autònoma de Barcelona
  • Master en Bioinformática y Bioestadística Universitat Oberta de Catalunya

Education

Doctor in Genetics, UNIVERSITAT AUTÒNOMA DE BARCELONA
Master's Degree in Advanced Genetics, UNIVERSITAT AUTÒNOMA DE BARCELONA
Master's Degree in Bioinformatics and Biostatistics, UNIVERSITAT OBERTA DE CATALUNYA
Bachelor's Degree in Biotechnology, UNIVERSITAT AUTÒNOMA DE BARCELONA

Professional experience

I am a researcher based in the field of DNA repair, candidate gene screening in human diseases. Recently interested in expanding my experience to the field of Bioinformatics. Halfway between the most classic molecular biology and computer science applied to the new challenges of biomedical research. I have combined my research with university teaching, both in bachelor's and master's degrees related to health sciences, biology...

Publications

Articles
  • Mara, M.; Venturi, V.; Ferrer, X.; Romero, L.; Hernández Viedma, G.; Leoz, P.; Ricard, M.; Morado, M.; Fernández , M.; Beneitez, D.; Ortuño, A.; Moreno, M.; Senent, L.; Perez-Valencia, A.; Pérez-Montero, S.; Tornador, C.; Sánchez, M., (2023), "New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II", International Journal of Molecular Sciences, vol. 24, No. 12, ISSN: 1422-0067.
  • Hernández Viedma, G.; Romero, L.; Ferrer, X.; Venturi, V.; Dessy, M.; Olivella, M.; Husami, A.; Pérez, C.; Morales, R.; Villegas, A.; González , F.; Morado, M.; Kalfa, T.; Quintana, O.; Pérez-Montero, S.; Tornador, C.; Segovia, J.; Sánchez, M., (2023), "Mutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III", Haematologica-the Hematology journal, vol. 108, No. 2, pp. 581-587, ISSN: 0390-6078.
  • Romero, L.; Hernández Viedma, G.; Ferrer, X.; Zalba-Jadraque, L.; Fuster, JL.; Bermúdez-Cortés, M.; Galera-Minarro, A.; Pérez-Montero, S.; Tornador, C.; Sánchez, M., (2022), "New Cases of Hypochromic Microcytic Anemia Due to Mutations in the SLC11A2 Gene and Functional Characterization of the G75R Mutation", International Journal of Molecular Sciences, vol. 23, No. 8, ISSN: 1422-0067.
  • Minguillón, J.; Ramírez, M.; Rovirosa, L.; Bustamante, P.; Camps, C.; Ruiz, G.; Shimelis, H.; Montanuy, H.; Pujol, R.; Hernández Viedma, G.; Bogliolo, M.; Castillo, P.; Soucy, P.; Martrat, G.; Gómez, A.; Cuadras, D.; García, M.; Gayarre, J.; Lázaro, C.; Benítez, J.; J Couch, F.; Pujana, M.; Surrallés, J., (2022), "CDK5RAP3, a New BRCA2 Partner That Regulates DNA Repair, Is Associated with Breast Cancer Survival", CANCERS, vol. 14, No. 2, ISSN: 2072-6694.
  • Hernández Viedma, G.; Ferrer, X.; Venturi, V.; Mara, M.; Floor, M.; Munoz-Torres, PM.; Hernández-Rodriguez, I.; Ruiz Mínguez, M.A.; Kelleher, N.J.; Pelucchi, S.; Piperno, A.; Plensa Alberca, E.; Gener Ricós, G.; Cañamero Giró, E.; Pérez-Montero, S.; Tornador, C.; Villà-Freixa, J.; Sánchez, M., (2021), "New mutations in hfe2 and tfr2 genes causing non hfe-related hereditary hemochromatosis", Genes, vol. 12, No. 12, ISSN: 2073-4425.
  • Celma, F.; Hernández Viedma, G.; Ferrer, X.; Hernández-Rodriguez, I.; Navarro-Almenzar, B.; Fuster, JL.; Bermúdez-Cortés, M.; Pérez-Montero, S.; Tornador, C.; Sánchez, M., (2021), "Hereditary hyperferritinemia cataract syndrome: Ferritin l gene and physiopathology behind the disease—report of new cases", International Journal of Molecular Sciences, vol. 22, No. 11, ISSN: 1422-0067.
  • Athie, A.; Arce-Gallego, S.; Gonzalez, M.; Morales-Barrera, R.; Suarez, C.; Casals, T.; Hernández Viedma, G.; Carles, J.; Mateo, J., (2019), "Targeting DNA Repair Defects for Precision Medicine in Prostate Cancer", Current oncology reports (Online), vol. 21, No. 5, ISSN: 1534-6269.
  • Hernández Viedma, G.; Ramírez, M.; Minguillón, J.; Quiles, P.; Ruiz, G.; Aza-Carmona, M.; Bogliolo, M.; Pujol, R.; Prados-Carvajal, R.; Fernández, J.; García, N.; López, A.; Gutiérrez-Enríquez, S.; Díez, O.; Benítez, J.; Salinas, M.; Teulé, A.; Brunet, J.; Radice, P.; Peterlongo, P.; Schindler, D.; Huertas, P.; S Puente, X.; Lázaro, C.; Pujana, M.; Surralles, J., (2018), "Decapping protein EDC4 regulates DNA repair and phenocopies BRCA1", Nature communications, vol. 9, ISSN: 2041-1723.
  • Martrat, G.; A, C.; Tominaga, E.; Porta-de-la-Riva, M.; Bonifaci, N.; Gómez-Baldó, L.; Bogliolo, M.; Lazaro, C.; Lazaro, C.; Blanco, I.; Brunet, J.; Aguilar, H.; Fernández-Rodríguez, J.; Seal, S.; Renwick, A.; Rahman, N.; Kühl, J.; Neveling, K.; Schindler, D.; J Ramírez, M.; Castellà, M.; Hernández Viedma, G.; F Easton, D.; Peock, S.; Cook, M.; T Oliver, C.; Frost, D.; Platte, R.; Evans, G.; Lalloo, F.; Eeles, R.; Izatt, L.; Chu, C.; Davidson, R.; Ong, K.; Cook, J.; Douglas, F.; Hodgson, S.; Brewer, C.; J Morrison, P.; Porteous, M.; Peterlongo, P.; Manoukian, S.; Peissel, B.; Zaffaroni, D.; Roversi, G.; Barile, M.; Viel, A.; Pasini, B.; Ottini, L.; Putignano, A.; Savarese, A.; Bernard, L.; Radice, P.; Healey, S.; Spurdle, A.; Chen, X.; Beesley, J.; A Rookus, M.; Verhoef, S.; A Tilanus-Linthorst, M.; P Vreeswijk, M.; J Asperen, C.; Bodmer, D.; Gem Ausems, M.; A van Os, T.; J Blok, M.; EJ Meijers-Heijboer, H.; BL Hogervorst, F.; E Goldgar, D.; Buys, S.; M John, E.; Miron, A.; Southey, M.; B Daly, M.; Harbst, K.; Borg, Å.; Rantala, J.; Barbany-Bustinza, G.; Ehrencrona, H.; Stenmark-Askmalm, M.; Kaufman, B.; Laitman, Y.; Milgrom, R.; Friedman, E.; M Domchek, S.; L Nathanson, K.; R Rebbeck, T.; Thor Johannsson, O.; J Couch, F.; Wang, X.; Fredericksen, Z.; Cuadras, D.; Moreno, V.; K Pientka, F.; Depping, R.; Caldés, T.; Osorio, A.; Benítez, J.; Bueren, J.; Heikkinen, T.; Nevanlinna, H.; Hamann, U.; Torres, D.; Adelaide, M.; K Godwin, A.; N Imyanitov, E.; Janavicius, R.; M Sinilnikova, O.; Stoppa-Lyonnet, D.; Mazoyer, S.; Verny-Pierre, C.; Castera, L.; de Pauw, A.; Bignon, Y.; Uhrhammer, N.; Peyrat, J.; Vennin, P.; Fert, S.; Collonge-Rame, M.; Mortemousque, I.; McGuffog, L.; Chenevix-Trench, G.; M Pereira-Smith, O.; C Antoniou, A.; Cerón, J.; Tominaga, K.; Surrallés, J.; Pujana, M., (2011), "Exploring the link between MORF4L1 and risk of breast cancer. Revista: Breast Cancer Research", BREAST CANCER RESEARCH, vol. 13, ISSN: 1465-542X.

Activities

  • Gordon Research Conference on Red Cells Ponència convidada "RACGAP1, the Gene Responsible for Congenital Dyserythropoietic Anemia Type IIIB", 2023.
  • Annual Congress of the European Hematology Association Ponència "Mutations in the RACGAP1 gene cause autosomal recessive Congenital Dyserythropoietic Anemia type III", 2022.
  • American Society of Hematology (ASH) Meeting Ponència "Autosomal Recessive Congenital Dyserythropoietic Anemia Type III Is Caused By Mutations in the Centralspindlin RACGAP1 Component", 2021.
  • Annual Congress of the European Hematology Association Ponència "IDENTIFICATION OF A NOVEL GENE CAUSING AN AUTOSOMAL RECESSIVE FORM OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE III", 2021.
  • GINBAR Ponència "Decapping protein EDC4 regulates DNA repair and phenocopies BRCA1", 2017.
  • Fanconi Anemia Research Fund Presentació de poster "A novel FANCL-interactor that modulates MMC survival", 2011.
  • EEMS Presentació de poster "Effect of diet and folate on human telomere length", 2011.
  • Sociedad Española de Mutagénesis Ambiental Ponència "Ácido Fólico y telómeros: ¿Cómo se relacionan?", 2009.
  • Annual Congress of the European Hematology Association Ponència "PPP1R1B Binds Iron Regulatory Proteins and Modulates Iron Cellular Content"
  • Fanconi Anemia Research Fund Ponència "Identification of a P-body protein with a dual role in the Fanconi anemia-BRCA DNA repair pathway"