Cristina Méndez‐Vidal

Author

Also Known As

C Méndez-Vidal, C. Mendez-Vidal, Cristina Mendez-Vidal, Cristina Méndez-Vidal, Cristina Méndez-Vidal (287453), Cristina Méndez‐Vidal, Méndez-Vidal, Cristina

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

Universidad de Sevilla Instituto de Biomedicina de Sevilla Centre for Biomedical Network Research on Rare Diseases Centro de Investigacion Principe Felipe Centro Andaluz de Biología Molecular y Medicina Regenerativa

About

Cristina Méndez‐Vidal is an author at Universidad de Sevilla specializing in medicine, genetics, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	595
2	Public Health	3	3	145
3	Engineering	2	2	30
4	Natural Sciences	2	2	286
5	Biology	1	1	16

Cristina Méndez‐Vidal

Publications

Citations

H-Index

Page 1

	Year	Citations
Wrap53, a Natural p53 Antisense Transcript Required for p53 Induction upon DNA Damage Salah Mahmoudi, Sofia Henriksson, Martin Corcoran, Molecular Cell Genome InstabilityDna DamageNatural SciencesMolecular BiologyDna Replication	2009	250
267 Spanish Exomes Reveal Population-Specific Differences in Disease-Related Genetic Variation Joaquı́n Dopazo, Alicia Amadoz, Marta Bleda, Molecular Biology and Evolution Phenotypic VariationGeneticsGenetic EpidemiologyHuman PolymorphismGenomics	2016	107
Unravelling the genetic basis of simplex Retinitis Pigmentosa cases Nereida Bravo‐Gil, María González‐del Pozo, Marta Martín-Sánchez, Scientific Reports	2017	79
Human wig-1, a p53 target gene that encodes a growth inhibitory zinc finger protein Fredrik Hellborg, Qian Wang, Cristina Méndez‐Vidal, Oncogene Developmental BiologyCell DivisionHuman Wig-1Tumor SuppressorMedicine	2001	71
The p53-induced mouse zinc finger protein wig-1 binds double-stranded RNA with high affinity Cristina Méndez‐Vidal Nucleic Acids Research	2002	59
Improving the management of Inherited Retinal Dystrophies by targeted sequencing of a population-specific gene panel Nereida Bravo‐Gil, Cristina Méndez‐Vidal, Laura Romero‐Pérez, Scientific Reports	2016	59
Mutational Spectrum of Semaphorin 3A and Semaphorin 3D Genes in Spanish Hirschsprung patients Berta Luzón‐Toro, Raquel M. Fernández, Ana Torroglosa, PLoS ONE GeneticsGene CharacterizationMolecular GeneticsDisease Gene IdentificationGenomics	2013	36
Proliferative potential after DNA damage and non-homologous end joining are affected by loss of securin Juan A. Bernal, Cristina Méndez‐Vidal, Águeda G. Espina, Cell Death and Differentiation Genome InstabilityDna DamageCell DivisionNatural SciencesGenetics	2007	36
Unmasking Retinitis Pigmentosa complex cases by a whole genome sequencing algorithm based on open-access tools: hidden recessive inheritance and potential oligogenic variants María González‐del Pozo, Elena Fernández-Suárez, Marta Martín-Sánchez, Journal of Translational Medicine	2020	34
A map of human microRNA variation uncovers unexpectedly high levels of variability José Carbonell‐Caballero, Eva Alloza, Pablo Arce, Genome Medicine	2012	33

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