关注
Requena T
Requena T
Roslin Institute, Edinburgh University, UK
在 exseed.ed.ac.uk 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
Familial clustering and genetic heterogeneity in Meniere's disease
T Requena, JM Espinosa‐Sanchez, S Cabrera, G Trinidad, A Soto‐Varela, ...
Clinical genetics 85 (3), 245-252, 2014
1502014
Expanding the CRISPR toolbox in zebrafish for studying development and disease
K Liu, C Petree, T Requena, P Varshney, GK Varshney
Frontiers in cell and developmental biology 7, 13, 2019
1412019
Identification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere's disease
T Requena, S Cabrera, C Martín-Sierra, SD Price, A Lysakowski, ...
Human molecular genetics 24 (4), 1119-1126, 2015
1362015
Genetic susceptibility to bilateral tinnitus in a Swedish twin cohort
IL Maas, P Brüggemann, T Requena, J Bulla, NK Edvall, AJ Szczepek, ...
Genetics in Medicine 19 (9), 1007-1012, 2017
1072017
Innovations in doctoral training and research on tinnitus: The European School on Interdisciplinary Tinnitus Research (ESIT) Perspective
W Schlee, DA Hall, B Canlon, RFF Cima, E De Kleine, F Hauck, A Huber, ...
Frontiers in aging neuroscience 9, 447, 2018
882018
Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere’s disease
C Martín-Sierra, A Gallego-Martinez, T Requena, L Frejo, ...
European Journal of Human Genetics 25 (2), 200-207, 2017
842017
Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease
L Frejo, A Gallego-Martinez, T Requena, E Martin-Sanz, JC Amor-Dorado, ...
Scientific reports 8 (1), 5974, 2018
772018
A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere’s disease
C Martín-Sierra, T Requena, L Frejo, SD Price, A Gallego-Martinez, ...
Human molecular genetics 25 (16), 3407-3415, 2016
772016
Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere's disease.
LEJA Requena T, Gazquez I, Moreno A, Batuecas A, Aran I
Immunogenetics, 2013
722013
Regulation of Fn14 receptor and NF-κB underlies inflammation in Meniere’s disease
L Frejo, T Requena, S Okawa, A Gallego-Martinez, M Martinez-Bueno, ...
Frontiers in Immunology 8, 1739, 2017
622017
Genetics of dizziness: cerebellar and vestibular disorders
T Requena, JM Espinosa-Sanchez, JA Lopez-Escamez
Current opinion in neurology 27 (1), 98-104, 2014
512014
A systematic review of extreme phenotype strategies to search for rare variants in genetic studies of complex disorders
S Amanat, T Requena, JA Lopez-Escamez
Genes 11 (9), 987, 2020
502020
Excess of rare missense variants in hearing loss genes in sporadic Meniere disease
A Gallego-Martinez, T Requena, P Roman-Naranjo, JA Lopez-Escamez
Frontiers in genetics 10, 76, 2019
462019
MICA-STR A. 4 is associated with slower hearing loss progression in patients with Meniere’s disease
I Gazquez, A Moreno, I Aran, A Soto-Varela, S Santos, H Perez-Garrigues, ...
Otology & Neurotology 33 (2), 223-229, 2012
462012
Intronic Variants in the NFKB1 Gene May Influence Hearing Forecast in Patients with Unilateral Sensorineural Hearing Loss in Meniere's Disease
S Cabrera, E Sanchez, T Requena, M Martinez-Bueno, J Benitez, N Perez, ...
PloS one 9 (11), e112171, 2014
442014
Enrichment of damaging missense variants in genes related with axonal guidance signalling in sporadic Meniere’s disease
A Gallego-Martinez, T Requena, P Roman-Naranjo, P May, ...
Journal of Medical Genetics 57 (2), 82-88, 2020
322020
Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière’s disease
I Gázquez, A Moreno, T Requena, J Ohmen, S Santos-Perez, I Aran, ...
European Archives of Oto-Rhino-Laryngology 270, 1521-1529, 2013
272013
Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family
H Ahmad, T Requena, L Frejo, M Cobo, A Gallego-Martinez, F Martin, ...
Frontiers in genetics 9, 85, 2018
222018
A pipeline combining multiple strategies for prioritizing heterozygous variants for the identification of candidate genes in exome datasets
T Requena, A Gallego-Martinez, JA Lopez-Escamez
Human Genomics 11, 1-11, 2017
152017
Genetic and clinical heterogeneity in Meniere's disease
I Gazquez-Perez, MT Requena-Navarro, JM Espinosa-Sanchez, ...
Autoimmunity Reviews, 2012
132012
系统目前无法执行此操作,请稍后再试。
文章 1–20