| 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 | 150 | 2014 |
| 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 | 141 | 2019 |
| 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 | 136 | 2015 |
| 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 | 107 | 2017 |
| 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 | 88 | 2018 |
| 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 | 84 | 2017 |
| 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 | 77 | 2018 |
| 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 | 77 | 2016 |
| 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 | 72 | 2013 |
| 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 | 62 | 2017 |
| Genetics of dizziness: cerebellar and vestibular disorders T Requena, JM Espinosa-Sanchez, JA Lopez-Escamez Current opinion in neurology 27 (1), 98-104, 2014 | 51 | 2014 |
| 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 | 50 | 2020 |
| 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 | 46 | 2019 |
| 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 | 46 | 2012 |
| 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 | 44 | 2014 |
| 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 | 32 | 2020 |
| 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 | 27 | 2013 |
| 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 | 22 | 2018 |
| 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 | 15 | 2017 |
| Genetic and clinical heterogeneity in Meniere's disease I Gazquez-Perez, MT Requena-Navarro, JM Espinosa-Sanchez, ... Autoimmunity Reviews, 2012 | 13 | 2012 |
Jose Antonio Lopez-Escamez MD, PhDUniversidad de Granada, University of Sydney, GENyO, ibs.GRANADA在 go.ugr.es 的电子邮件经过验证
