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David Ros‐Pardo

Observed names: D Ros-Pardo, David Ros-Pardo, Ros Pardo, David
ORCID: 0000-0002-8934-8585
Observed ORCID: 0000-0002-8934-8585
OpenAlex ID: A5073736155
Distinct GSDMB protein isoforms and protease cleavage processes differentially control pyroptotic cell death and mitochondrial damage in cancer cells
2023 · Sara S. Oltra, Sara Colomo, et al. · Cell Death and Differentiation · 87
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Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder
2022 · Maria B. Christensen, Amanda M. Levy, et al. · Clinical Genetics · 16
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STAG2: Computational Analysis of Missense Variants Involved in Disease
2024 · David Ros-Pardo, Paulino Gómez-Puertas, et al. · International Journal of Molecular Sciences · 10
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The phenotypic and genotypic spectrum of individuals with mono‐ or biallelic ANK3 variants
2024 · Francesca Furia, Amanda M. Levy, et al. · Clinical Genetics · 8
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Biallelic loss-of-function variants in ZNF142 are associated with a robust DNA methylation signature affecting a limited number of genomic loci
2025 · Mathis Hildonen, Andrea Ciolfi, et al. · European Journal of Human Genetics · 4
Structural and functional insights into GSDMB isoforms complex roles in pathogenesis
2023 · Sara Colomo, David Ros-Pardo, et al. · Cell Cycle · 4
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A Novel Intragenic Duplication in the HDAC8 Gene Underlying a Case of Cornelia de Lange Syndrome
2022 · Cristina Lucia-Campos, Irene Valenzuela, et al. · Genes · 4
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In Silico Design of miniACE2 Decoys with In Vitro Enhanced Neutralization Activity against SARS-CoV-2, Encompassing Omicron Subvariants
2024 · Jenny Andrea Arévalo-Romero, Gina López-Cantillo, et al. · International Journal of Molecular Sciences · 2
Pathogenic effects of Leu200Pro and Arg387His VRK1 protein variants on phosphorylation targets and H4K16 acetylation in distal hereditary motor neuropathy
2024 · Aurora Campos-Díaz, Patricia Morejón-García, et al. · Journal of Molecular Medicine · 2
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HCN4 Mutation Causing Familial Inappropriate Sinus Tachycardia Leads to a Conformational Change Mimicking cAMP Binding and Induces Constitutive Channel Activity
2025 · Sara L. Bober, Qiuju Li, et al. · Circulation Arrhythmia and Electrophysiology · 1
Ligand–Enzyme Interaction Modeling of Missense Variants Implicated in Mitochondrial HMG-CoA Synthase Deficiency
2025 · María Arnedo, David Ros-Pardo, et al. · International Journal of Molecular Sciences · 1
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A novel gain-of-function HCN4 variant responsible for familial inappropriate sinus tachycardia
2025 · S L Bober, Q Li, et al. · EP Europace · 1
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STAG2-RAD21 complex: A unidirectional DNA ratchet mechanism in loop extrusion
2024 · David Ros-Pardo, Paulino Gómez-Puertas, et al. · International Journal of Biological Macromolecules · 1
Expanding the ABCA2-associated neurodevelopmental phenotype
2026 · Kaisa T. Oja, Karit Reinson, et al. · Human Genetics and Genomics Advances
ROGDI-Related Disorder Resulting from Disruption of Complex Interactive Neuro-Dental Developmental Networks: A Review and Description of the First Missense Variant
2025 · Sopio Gverdtsiteli, Trine Bjørg Hammer, et al. · Genes
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Works count: 17
Citation count: 141
H-index: 4
I10-index: 3
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