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Cristina Méndez‐Vidal

Wrap53, a Natural p53 Antisense Transcript Required for p53 Induction upon DNA Damage
2009 · Salah Mahmoudi, Sofia Henriksson, et al. · Molecular Cell · 254
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Wrap53, a Natural p53 Antisense Transcript Required for p53 Induction upon DNA Damage
2016 · Salah Mahmoudi, Sofia Henriksson, et al. · Molecular Cell · 253
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267 Spanish Exomes Reveal Population-Specific Differences in Disease-Related Genetic Variation
2016 · Joaquín Dopazo, Alicia Amadoz, et al. · Molecular Biology and Evolution · 100
Unravelling the genetic basis of simplex Retinitis Pigmentosa cases
2017 · Nereida Bravo-Gil, María González-del Pozo, et al. · Scientific Reports · 87
Human wig-1, a p53 target gene that encodes a growth inhibitory zinc finger protein
2001 · Fredrik Hellborg, Wang Qian, et al. · Oncogene · 70
The p53-induced mouse zinc finger protein wig-1 binds double-stranded RNA with high affinity
2002 · C. Mendez-Vidal · Nucleic Acids Research · 63
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Improving the management of Inherited Retinal Dystrophies by targeted sequencing of a population-specific gene panel
2016 · Nereida Bravo-Gil, Cristina Méndez-Vidal, et al. · Scientific Reports · 60
Mutational Spectrum of Semaphorin 3A and Semaphorin 3D Genes in Spanish Hirschsprung patients
2013 · Berta Luzón-Toro, Raquel M. Fernández, et al. · PLoS ONE · 36
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Proliferative potential after DNA damage and non-homologous end joining are affected by loss of securin
2007 · J A Bernal, M Roche, et al. · Cell Death and Differentiation · 36
Unmasking Retinitis Pigmentosa complex cases by a whole genome sequencing algorithm based on open-access tools: hidden recessive inheritance and potential oligogenic variants
2020 · María González-del Pozo, Elena Fernández-Suárez, et al. · Journal of Translational Medicine · 34
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A map of human microRNA variation uncovers unexpectedly high levels of variability
2012 · José Carbonell, Eva Alloza, et al. · Genome Medicine · 30
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Induction of Dlk1 by PTTG1 Inhibits Adipocyte Differentiation and Correlates with Malignant Transformation
2009 · Águeda G. Espina, Cristina Méndez-Vidal, et al. · Molecular Biology of the Cell · 28
Searching the second hit in patients with inherited retinal dystrophies and monoallelic variants in ABCA4, USH2A and CEP290 by whole-gene targeted sequencing
2018 · María González-del Pozo, Marta Martín-Sánchez, et al. · Scientific Reports · 27
A genomic strategy for precision medicine in rare diseases: integrating customized algorithms into clinical practice
2025 · Cristina Méndez-Vidal, Nereida Bravo-Gil, et al. · Journal of Translational Medicine · 24
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Re‐evaluation casts doubt on the pathogenicity of homozygous USH2A p.C759F
2015 · María González‐del Pozo, Nereida Bravo‐Gil, et al. · American Journal of Medical Genetics Part A · 22
A comprehensive WGS-based pipeline for the identification of new candidate genes in inherited retinal dystrophies
2022 · María González-del Pozo, Elena Fernández-Suárez, et al. · npj Genomic Medicine · 21
Novel RP1 mutations and a recurrent BBS1variant explain the co-existence of two distinct retinal phenotypes in the same pedigree
2014 · Cristina Méndez-Vidal, Nereida Bravo-Gil, et al. · BMC Genetics · 21
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Identification of functional p53‐binding motifs in the mouse wig‐1 promoter
2002 · Margareta T Wilhelm, Cristina Méndez-Vidal, et al. · FEBS Letters · 21
Whole-exome sequencing identifies novel compound heterozygous mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa.
2013 · Cristina Méndez-Vidal, María González-Del Pozo, et al. · Europe PMC (PubMed Central) · 20
Exome Sequencing Reveals Novel and Recurrent Mutations with Clinical Significance in Inherited Retinal Dystrophies
2014 · María González-del Pozo, Cristina Méndez-Vidal, et al. · PLoS ONE · 19
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Deciphering intrafamilial phenotypic variability by exome sequencing in a Bardet–Biedl family
2013 · María González‐del Pozo, Cristina Méndez‐Vidal, et al. · Molecular Genetics & Genomic Medicine · 18
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PTTG2 silencing results in induction of epithelial-to-mesenchymal transition and apoptosis
2013 · C Méndez-Vidal, M del Mar Gámez-Del Estal, et al. · Cell Death and Disease · 18
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Expanding the phenotype of THRB: a range of macular dystrophies as the major clinical manifestations in patients with a dominant splicing variant
2023 · Elena Fernández-Suárez, María González-del Pozo, et al. · Frontiers in Cell and Developmental Biology · 14
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Novel small RNA expression libraries uncover hsa-miR-30b and hsa-miR-30c as important factors in anoikis resistance
2013 · Miguel A. Moreno-Mateos, Verónica Barragán, et al. · RNA · 14
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Long-read sequencing improves the genetic diagnosis of retinitis pigmentosa by identifying an Alu retrotransposon insertion in the EYS gene
2024 · Elena Fernández-Suárez, María González-del Pozo, et al. · Mobile DNA · 11
Works count: 57
Citation count: 1,341
H-index: 19
I10-index: 25
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