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Pablo Minguez

Showing results (81-90 of 88) with videos related to

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Scientific Reports|January 16, 2021
Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implicationsIrene Perea-Romero, Gema Gordo, Ionut F Iancu, et al.
American Journal of Ophthalmology|June 16, 2023
Comprehensive Genotyping and Phenotyping Analysis of GUCY2D-Associated Rod- and Cone-Dominated DystrophiesCristina Rodilla, Inmaculada Martín-Merida, Fiona Blanco-Kelly, et al.
American Journal of Human Genetics|March 26, 2024
Detection of elusive DNA copy-number variations in hereditary disease and cancer through the use of noncoding and off-target sequencing readsMathieu Quinodoz, Karolina Kaminska, Francesca Cancellieri, et al.
International Journal of Molecular Sciences|March 13, 2024
<i>PRPH2</i>-Related Retinal Dystrophies: Mutational Spectrum in 103 Families from a Spanish CohortLidia Fernández-Caballero, Inmaculada Martín-Merida, Fiona Blanco-Kelly, et al.
Nucleic Acids Research|September 29, 2020
CSVS, a crowdsourcing database of the Spanish population genetic variabilityMaría Peña-Chilet, Gema Roldán, Javier Perez-Florido, et al.
Biomedicines|March 28, 2025
Pharmacogenomic Study of SARS-CoV-2 Treatments: Identifying Polymorphisms Associated with Treatment Response in COVID-19 PatientsAlexandre Serra-Llovich, Natalia Cullell, Olalla Maroñas, et al.
Elife|October 3, 2024
Novel risk loci for COVID-19 hospitalization among admixed American populationsSilvia Diz-de Almeida, Raquel Cruz, Andre D Luchessi, et al.
Human Molecular Genetics|June 16, 2022
Novel genes and sex differences in COVID-19 severityRaquel Cruz, Silvia Diz-de Almeida, Miguel López de Heredia, et al.
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Showing results (81-90 of 88) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 88 results.
Scientific Reports|January 16, 2021
Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implicationsIrene Perea-Romero, Gema Gordo, Ionut F Iancu, et al.
American Journal of Ophthalmology|June 16, 2023
Comprehensive Genotyping and Phenotyping Analysis of GUCY2D-Associated Rod- and Cone-Dominated DystrophiesCristina Rodilla, Inmaculada Martín-Merida, Fiona Blanco-Kelly, et al.
American Journal of Human Genetics|March 26, 2024
Detection of elusive DNA copy-number variations in hereditary disease and cancer through the use of noncoding and off-target sequencing readsMathieu Quinodoz, Karolina Kaminska, Francesca Cancellieri, et al.
International Journal of Molecular Sciences|March 13, 2024
<i>PRPH2</i>-Related Retinal Dystrophies: Mutational Spectrum in 103 Families from a Spanish CohortLidia Fernández-Caballero, Inmaculada Martín-Merida, Fiona Blanco-Kelly, et al.
Nucleic Acids Research|September 29, 2020
CSVS, a crowdsourcing database of the Spanish population genetic variabilityMaría Peña-Chilet, Gema Roldán, Javier Perez-Florido, et al.
Biomedicines|March 28, 2025
Pharmacogenomic Study of SARS-CoV-2 Treatments: Identifying Polymorphisms Associated with Treatment Response in COVID-19 PatientsAlexandre Serra-Llovich, Natalia Cullell, Olalla Maroñas, et al.
Elife|October 3, 2024
Novel risk loci for COVID-19 hospitalization among admixed American populationsSilvia Diz-de Almeida, Raquel Cruz, Andre D Luchessi, et al.
Human Molecular Genetics|June 16, 2022
Novel genes and sex differences in COVID-19 severityRaquel Cruz, Silvia Diz-de Almeida, Miguel López de Heredia, et al.
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