Daniel Natera de Benito
Investigador post-doc
Research group
The researcher Daniel Natera graduated in Medicine from the University of Salamanca in 2009 and specialized in Paediatrics at the University Hospital of Alcorcón in Madrid in 2013. In 2015, he obtained the Master's degree in Neuropediatrics from the University of Barcelona. In 2017, he obtained the PhD from the University of Barcelona.
In 2015, he made a stay at the Muscle Center in Newcastle thanks to a grant from the Spanish Paediatric Association.
In 2017, he joined the Neuromuscular Diseases Unit of the Hospital Sant Joan de Déu in Barcelona.
He has a special interest in clinical and genetic research of neuromuscular diseases.
Professional network profiles
Last Publications
- Almici E, Chiappini V, López-Márquez A, Badosa-Gallego MC, Blázquez B, Caballero D, Montero J, Natera-de Benito D, Nascimento-Osorio A, Roldán M, Lagunas A, Jimenez-Mallebrera C and Samitier J Personalized in vitro Extracellular Matrix Models of Collagen VI-Related Muscular Dystrophies. Frontiers in Bioengineering and Biotechnology . 10: 851825-851825.
- López-Márquez A, Morín M, Fernández-Peñalver S, Badosa-Gallego MC, Hernández-Delgado A, Natera-de Benito D, Ortez-Gonzalez CI, Nascimento-Osorio A, Grinberg-Vaisman DR, Balcells S, Roldán M, Moreno-Pelayo MÁ and Jimenez-Mallebrera C CRISPR/Cas9-Mediated Allele-Specific Disruption of a Dominant COL6A1 Pathogenic Variant Improves Collagen VI Network in Patient Fibroblasts. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES . 23(8): .
- Natera-de Benito D, Jurgens JA, Yeung A, Zaharieva IT, Manzur A, DiTroia SP, Di Gioia SA, Pais L, Pini V, Barry BJ, Chan WM, Elder JE, Christodoulou J, Hay E, England EM, Munot P, Hunter DG, Feng L, Ledoux D, O'Donnell-Luria A, Phadke R, Engle EC, Sarkozy A and Muntoni F Recessive variants in COL25A1 gene as novel cause of arthrogryposis multiplex congenita with ocular congenital cranial dysinnervation disorder. HUMAN MUTATION . 43(4): 487-498.
Projects
- Project name:
- ArmTracker: A state-of-the-art wearable system to assess upper limb motor function in reallife conditions for patients with Duchenne muscular dystrophy and spinal muscular atrophy.
- Leader
- Daniel Natera de Benito
- Funding entities:
- Fundació La Marató de TV3
- Code
- 561/C/2020
- Starting - finishing date:
- 2021 - 2024