Author

Paz Pérez-Vázquez

Hospital Universitario De CabueñesORCID 0000-0002-4383-9151Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alvaro Gallego‐MartineziD· 1 shared Andrés Soto-VarelaiD· 1 shared Ángel Batuecas CaletríoiD· 1 shared Ismael ArániD· 1 shared Jose Antonio Lopez-EscameziD· 1 shared Juan Carlos Amor‐DoradoiD· 1 shared Juan Manuel Espinosa-SáncheziD· 1 shared M Del Carmen MoleoniD· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 36 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetics

Alvaro Gallego‐MartinezORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

Rare Variants in the OTOG Gene Are a Frequent Cause of Familial Meniere’s Disease

Pablo Román-Naranjo, Alvaro Gallego‐Martinez, Andrés Soto-Varela, Ismael Arán, M Del Carmen Moleon, Juan Manuel Espinosa-Sánchez, Juan Carlos Amor‐Dorado, Ángel Batuecas Caletrío, Paz Pérez-Vázquez, Jose Antonio Lopez-Escamez

The paper identifies rare variants in the OTOG gene as a frequent cause of familial Meniere’s disease through exome sequencing and variant analysis.

bioRxiv · Sep 21, 2019 · PreprintGenetics