Daniel Raúl Grinberg Vaisman
Investigador
Research group
Research line:
Lysosomal diseases, bone diseases, intellectual disability
The researcher Daniel Grinberg graduated in Biology in 1981 from the University of Barcelona and obtained his PhD in Genetics from the University of Barcelona in 1986.
Between 1987 and 1990, he undertook a postdoctoral stay at the Imperial Cancer Reserch Fund in London where he studied the transcriptional regulation mechanisms of the int-2 gene responsible for the mouse breast tumor.
Since 1990 he has been a professor at the University of Barcelona as a professor until 2008 and as a cathedratic professor from 2008 until today. He was Director of the Department of Genetics at the University of Barcelona from 2008 to 2012 and member of the Scientific Program Committee of the European Society of Human Genetics from 2012 to 2016.
He is currently leading the research group on Human Molecular Genetics, a group recognized as a quality group by the Generalitat de Catalunya (2017 SGR 738), and a group from the CIBERER, the IBUB and the IRSJD, where he studies the genetic and molecular bases of monogenic diseases and complexes, the generation of models and new therapeutic strategies.
Last Publications
- Garcia-Giralt N, Ovejero D, Grinberg-Vaisman DR, Nogues X, Castañeda S, Balcells S and Rabionet-Janssen R Assessing the contribution of genes involved in monogenic bone disorders to the etiology of atypical femoral fractures. HUMAN GENOMICS . 18(1): 87-87.
- Centeno-Pla M, Alcaide-Consuegra E, Gibson S, Prat-Planas A, Gutiérrez-Ávila JD, Grinberg-Vaisman DR, Urreizti R, Rabionet-Janssen R and Balcells S Subcellular localisation of truncated MAGEL2 proteins: insight into the molecular pathology of Schaaf-Yang syndrome. JOURNAL OF MEDICAL GENETICS . 61(8): 780-782.
- Palma-Milla C, Prat-Planas A, Soengas-Gonda E, Centeno-Pla M, Sánchez-Pozo J, Lazaro-Rodriguez I, Quesada-Espinosa JF, Arteche-Lopez A, Olival J, Pacio-Miguez M, Palomares-Bralo M, Santos-Simarro F, Cancho-Candela R, Vázquez-López M, Seidel V, Martinez-Monseny T, Casas-Alba D, Grinberg-Vaisman DR, Balcells S, Serrano M, Rabionet-Janssen R, Martin MA and Urreizti R Expanding the Phenotypic Spectrum of TRAF7-Related Cardiac, Facial, and Digital Anomalies With Developmental Delay: Report of 11 New Cases and Literature Review PEDIATRIC NEUROLOGY . 155: 8-17.
Projects
- Project name:
- Incorporació de R. Rabionet al projecte d'anàlisi d'exomes en síndrome d'Opitz i Fractura atípica. Beneficiari: Raquel Rabionet
- Leader
- Daniel Raúl Grinberg Vaisman
- Funding entities:
- Generalitat de Catalunya
- Code
- SLT002/16/00310
- Starting - finishing date:
- 2017 - 2019
News
-
First clinical guideline on Schaaf-Yang syndrome for professionals and families
Improving knowledge of the Schaaf-Yang syndrome (SYS) -an ultrarare disease caused by mutations in the MAGEL2 gene- is the aim of the first clinical guideline aimed at healthcare professionals and families of children affected by this pathology.