Author

María Sanchiz-Calvo

Observed name: Maria Sanchiz-Calvo

Institutions: Aligning Science Across Parkinson's, KU Leuven

Observed institutions: Centre for Human Genetics, University of Oxford, Institute for Research in Biomedicine, Barcelona Institute of Science and Technology, Aligning Science Across Parkinson's, KU Leuven

ORCID: 0000-0003-1773-8696

Observed ORCID: 0000-0003-1773-8696

OpenAlex ID: A5074178397

53BP1 cooperation with the REV7–shieldin complex underpins DNA structure-specific NHEJ

2018 · Hind Ghezraoui, Catarina Oliveira, et al. · Nature · 337

Tousled-Like Kinases Suppress Innate Immune Signaling Triggered by Alternative Lengthening of Telomeres

2020 · Sandra Segura-Bayona, Marina Villamor-Payà, et al. · Cell Reports · 43

Functional analysis of TLK2 variants and their proximal interactomes implicates impaired kinase activity and chromatin maintenance defects in their pathogenesis

2020 · Lisa Pavinato, Marina Villamor-Payà, et al. · Journal of Medical Genetics · 18

Rodent models based on endolysosomal genes involved in Parkinson's disease

2021 · María Sanchiz-Calvo, Eduard Bentea, et al. · Current Opinion in Neurobiology · 8

The G2019S LRRK2 mutation exacerbates α-synuclein and tau neuropathology through divergent pathways in Parkinson’s disease models

2025 · George Tsafaras, Diego Cabezudo, et al. · Acta Neuropathologica · 7

Loss of the lysosomal lipid flippase ATP10B leads to progressive dopaminergic neurodegeneration and parkinsonian motor deficits

2025 · María Sanchiz-Calvo, Elena Coccia, et al. · Acta Neuropathologica · 6

De novo TLK1 and MDM1 mutations in a patient with a neurodevelopmental disorder and immunodeficiency

2024 · Marina Villamor-Payà, María Sanchiz-Calvo, et al. · iScience · 4

Works count: 8

Citation count: 423

H-index: 6

I10-index: 3