List of works - Teresa Requena

A Systematic Review of Extreme Phenotype Strategies to Search for Rare Variants in Genetic Studies of Complex Disorders

scientific article published on 25 August 2020

A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease.

scientific article

A pipeline combining multiple strategies for prioritizing heterozygous variants for the identification of candidate genes in exome datasets

scientific article

Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere's disease.

scientific article

Bioinformatic Integration of Molecular Networks and Major Pathways Involved in Mice Cochlear and Vestibular Supporting Cells.

scientific article published on 5 April 2018

Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family.

scientific article published on 23 March 2018

Enrichment of damaging missense variants in genes related with axonal guidance signalling in sporadic Meniere's disease

scientific article published on 07 September 2019

Expanding the CRISPR Toolbox in Zebrafish for Studying Development and Disease

article

Familial clustering and genetic heterogeneity in Meniere's disease.

scientific article published on 9 April 2013

Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.

scientific article published on 21 November 2012

Genetic and clinical heterogeneity in Meniere's disease

scientific article published on 03 March 2012

Genetic susceptibility to bilateral tinnitus in a Swedish twin cohort.

scientific article published on 23 March 2017

Genetics of dizziness: cerebellar and vestibular disorders.

scientific article published on February 2014

Identification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere's disease

scientific article

Innovations in Doctoral Training and Research on Tinnitus: The European School on Interdisciplinary Tinnitus Research (ESIT) Perspective

scientific article published in January 2017

Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease

scientific article

Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease.

scientific article published on 13 April 2018

Transcriptomic Analyses of Inner Ear Sensory Epithelia in Zebrafish

scientific article published on 28 December 2019

Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease.

scientific article published on 23 November 2016

List of works by Teresa Requena

A Systematic Review of Extreme Phenotype Strategies to Search for Rare Variants in Genetic Studies of Complex Disorders

A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease.

A pipeline combining multiple strategies for prioritizing heterozygous variants for the identification of candidate genes in exome datasets

Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere's disease.

Bioinformatic Integration of Molecular Networks and Major Pathways Involved in Mice Cochlear and Vestibular Supporting Cells.

Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family.

Enrichment of damaging missense variants in genes related with axonal guidance signalling in sporadic Meniere's disease

Expanding the CRISPR Toolbox in Zebrafish for Studying Development and Disease

Familial clustering and genetic heterogeneity in Meniere's disease.

Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.

Genetic and clinical heterogeneity in Meniere's disease

Genetic susceptibility to bilateral tinnitus in a Swedish twin cohort.

Genetics of dizziness: cerebellar and vestibular disorders.

Identification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere's disease

Innovations in Doctoral Training and Research on Tinnitus: The European School on Interdisciplinary Tinnitus Research (ESIT) Perspective

Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease

Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease.

Transcriptomic Analyses of Inner Ear Sensory Epithelia in Zebrafish

Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease.