Author

Ismael Arán

Complejo Hospitalario de PontevedraORCID 0000-0002-0753-6380Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2

Frequent Co-Authors

Alvaro Gallego‐MartineziD· 2 shared Andrés Soto-VarelaiD· 2 shared Jose Antonio Lopez-EscameziD· 2 shared Pablo Román-NaranjoiD· 2 shared Alba Escalera‐BalseraiD· 1 shared Alberto M. Parra‐PereziD· 1 shared Andreas H. EckhardiD· 1 shared Ángel Batuecas CaletríoiD· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 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

2 shared papersGenetic & Genomic Medicine

Alvaro Gallego‐MartinezORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Ultrarare missense and frameshift variants in the TECTA gene may involve tectorial membrane in familial Meniere disease

Pablo Román-Naranjo, Alberto M. Parra‐Perez, Alba Escalera‐Balsera, Andrés Soto-Varela, Alvaro Gallego‐Martinez, Ismael Arán, Nicolás Pérez‐Fernández, David Bächinger, Andreas H. Eckhard, Rocío González Aguado, Lidia Frejo, Jose Antonio Lopez-Escamez

The paper identifies rare variants in the TECTA gene associated with familial Meniere disease and suggests their impact on tectorial membrane stability.

Clinical and Translational Medicine · Jun 1, 2022Peer-reviewedGenetic & Genomic Medicine

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