About the VHIR
Here at the Vall d'Hebron Research Institute (VHIR) we promote biomedical research, innovation and teaching. Over 1,800 people are seeking to understand diseases today so the treatment can be improved tomorrow.
Research
We are working to understand diseases, to find out how they operate and to create better treatments for patients. Get to know about our groups and their lines of research.
People
People are the centre of the Vall d'Hebron Research Institute (VHIR). This is why we are bound by the principles of freedom of research, gender equality and professional attitudes that HRS4R promotes.
Clinical trials
Our work is not just basic or translational; we are leaders in clinical research. Enter and find about the clinical trials we are conducting and why we are a world reference in this field.
Progress
Our aim is to make the research carried out at the Vall d’Hebron Research Institute (VHIR) a driving force for transformation. How? By identifying new channels and solutions for the promotion of people's health and well-being.
Core facilities
We offer specialist support for researchers, internal and external alike, ranging from specific services to preparing complete projects. All this, from a perspective of quality and speed of response.
News
We offer you a gateway for staying up to date on everything going on at the Vall d’Hebron Research Institute (VHIR), from the latest news to future solidarity activities and initiatives that we are organising.
The Genetics Medicine group of the VHIR belongs to the Clinical and Molecular Genetic Area of the Hospital Vall d’Hebron and combines genetic diagnosis and translational research in hereditary diseases and the study of pathologies and malformations during human development.
The group actively works in different consortiums and networks for rare disorders including ERN Ithaca, Cranio, Bond and NMD.
Specific research lines and teams include:
PMID: 37503210 Journal: Year: 2023 Reference: medRxiv. 2023 Jun 10:2023.06.06.23290887. doi: 10.1101/2023.06.06.23290887. Preprint. Impact factor: Publication type: Other (letters to the editor, abstracts, corrigendum, etc.) Authors: Abdalla, Ebtesam; Abdelrazek, Ibrahim M; Aguado-Barrera, Miguel E; Alaaeldin, Khoshoua; Alizadeh, Behrooz Z; Alsner, Jan; Altabas, Manuel; Andreassen, Christian Nicolaj; Arlt, Annabelle; Artem, Borovikov et al. DOI: 10.1101/2023.06.06.23290887
PMID: 37857131 Journal: PSYCHIATRY RESEARCH Year: 2023 Reference: Psychiatry Res. 2023 Oct 11;329:115540. doi: 10.1016/j.psychres.2023.115540. Impact factor: Publication type: Paper in international publication Authors: Abdalla, Ebtesam; Abdelrazek, Ibrahim M; Alaaeldin, Khoshoua; Antoni Ramos-Quiroga, Josep; Arlt, Annabelle; Artem, Borovikov; Caro, Pilar; Daigre-Blanco, Constanza; Devriendt, Koen; Ebstein, Frederic et al. DOI: 10.1016/j.psychres.2023.115540
PMID: 38117302 Journal: HUMAN GENETICS Year: 2023 Reference: Hum Genet. 2023 Dec 20. doi: 10.1007/s00439-023-02622-5. Impact factor: Publication type: Paper in international publication Authors: Bramswig, Nuria C; Bruel, Ange-Line; Caumes, Roseline; Charles, Perrine; Chatron, Nicolas; Chrzanowska, Krystyna; Codina-Sola, Marta; Colson, Cindy; Cusco, Ivon; Denomme-Pichon, Anne-Sophie et al. DOI: 10.1007/s00439-023-02622-5
PMID: 38183850 Journal: NEUROMUSCULAR DISORDERS Year: 2023 Reference: Neuromuscul Disord. 2023 Dec 14;34:114-122. doi: 10.1016/j.nmd.2023.12.008. Impact factor: Publication type: Other (letters to the editor, abstracts, corrigendum, etc.) Authors: Abiusi, Emanuela; Bertini, Enrico Silvio; Costa-Roger, Mar; Tiziano, Francesco Danilo; Tizzano, Eduardo F et al. DOI: 10.1016/j.nmd.2023.12.008
The results show that, in some patients with mutations in the X chromosome, the healthy gene is inactivated and the mutated gene manifests itself, which favors the onset of the disease.
On January 24, a session was held to explain what these three-dimensional models are and what advantages they have, as well as to review some of their applications in research.
The research has studied the structure and function of proteins related to this degenerative disease and their interaction with SMN2 messenger RNA (mRNA), which is key to the evolution of patients.
