| 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 | 85 | 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 | 78 | 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 |
| Differential proinflammatory signature in vestibular migraine and meniere disease M Flook, L Frejo, A Gallego-Martinez, E Martin-Sanz, M Rossi-Izquierdo, ... Frontiers in Immunology 10, 1229, 2019 | 74 | 2019 |
| Burden of rare variants in the OTOG gene in familial Meniere’s disease P Roman-Naranjo, A Gallego-Martinez, A Soto-Varela, I Aran, ... Ear and hearing 41 (6), 1598-1605, 2020 | 62 | 2020 |
| 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 |
| Genetic architecture of Meniere’s disease A Gallego-Martinez, JA Lopez-Escamez Hearing Research 397, 107872, 2020 | 54 | 2020 |
| CSVS, a crowdsourcing database of the Spanish population genetic variability M Peña-Chilet, G Roldán, J Perez-Florido, FM Ortuno, R Carmona, ... Nucleic acids research 49 (D1), D1130-D1137, 2021 | 47 | 2021 |
| 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 |
| Towards a unification of treatments and interventions for tinnitus patients: The EU research and innovation action UNITI W Schlee, S Schoisswohl, S Staudinger, A Schiller, A Lehner, B Langguth, ... Progress in brain research 260, 441-451, 2021 | 45 | 2021 |
| Genetic contribution to vestibular diseases A Gallego-Martinez, JM Espinosa-Sanchez, JA Lopez-Escamez Journal of neurology 265 (Suppl 1), 29-34, 2018 | 34 | 2018 |
| Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study S Amanat, A Gallego-Martinez, J Sollini, P Perez-Carpena, ... EBioMedicine 66, 2021 | 33 | 2021 |
| 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 |
| Genetics of vestibular syndromes P Roman-Naranjo, A Gallego-Martinez, JAL Escamez Current opinion in neurology 31 (1), 105-110, 2018 | 28 | 2018 |
| Identification of potential Meniere's disease targets in the adult stria vascularis S Gu, R Olszewski, L Nelson, A Gallego-Martinez, JA Lopez-Escamez, ... Frontiers in Neurology 12, 630561, 2021 | 26 | 2021 |
| 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 |
| Unification of Treatments and Interventions for Tinnitus Patients (UNITI): a study protocol for a multi-center randomized clinical trial S Schoisswohl, B Langguth, M Schecklmann, A Bernal-Robledano, ... Trials 22, 1-16, 2021 | 18 | 2021 |
| Defective α‐tectorin may involve tectorial membrane in familial Meniere disease P Roman‐Naranjo, AM Parra‐Perez, A Escalera‐Balsera, A Soto‐Varela, ... Clinical and Translational Medicine 12 (6), 2022 | 17 | 2022 |
| DNA methylation signature in mononuclear cells and proinflammatory cytokines may define molecular subtypes in sporadic Meniere disease M Flook, A Escalera-Balsera, A Gallego-Martinez, JM Espinosa-Sanchez, ... Biomedicines 9 (11), 1530, 2021 | 15 | 2021 |
| 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 |
Jose Antonio Lopez-Escamez MD, PhDUniversidad de Granada, University of Sydney, GENyO, ibs.GRANADADirección de correo verificada de go.ugr.es
