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2016 2
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2020 3
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31 results

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Page 1
Genetics of vestibular syndromes.
Roman-Naranjo P, Gallego-Martinez A, Lopez Escamez JA. Roman-Naranjo P, et al. Among authors: gallego martinez a. Curr Opin Neurol. 2018 Feb;31(1):105-110. doi: 10.1097/WCO.0000000000000519. Curr Opin Neurol. 2018. PMID: 29095749 Review.
Genetic contribution to vestibular diseases.
Gallego-Martinez A, Espinosa-Sanchez JM, Lopez-Escamez JA. Gallego-Martinez A, et al. J Neurol. 2018 Oct;265(Suppl 1):29-34. doi: 10.1007/s00415-018-8842-7. Epub 2018 Mar 26. J Neurol. 2018. PMID: 29582143 Review.
Genetic architecture of Meniere's disease.
Gallego-Martinez A, Lopez-Escamez JA. Gallego-Martinez A, et al. Hear Res. 2020 Nov;397:107872. doi: 10.1016/j.heares.2019.107872. Epub 2019 Dec 13. Hear Res. 2020. PMID: 31874721 Review.
Genetic Inheritance and Its Contribution to Tinnitus.
Amanat S, Gallego-Martinez A, Lopez-Escamez JA. Amanat S, et al. Among authors: gallego martinez a. Curr Top Behav Neurosci. 2021;51:29-47. doi: 10.1007/7854_2020_155. Curr Top Behav Neurosci. 2021. PMID: 32705497 Review.
A crowdsourcing database for the copy-number variation of the Spanish population.
López-López D, Roldán G, Fernández-Rueda JL, Bostelmann G, Carmona R, Aquino V, Perez-Florido J, Ortuño F, Pita G, Núñez-Torres R, González-Neira A; CSVS Crowdsourcing Group; Peña-Chilet M, Dopazo J. López-López D, et al. Hum Genomics. 2023 Mar 9;17(1):20. doi: 10.1186/s40246-023-00466-8. Hum Genomics. 2023. PMID: 36894999 Free PMC article.
A Systematic Review on the Genetic Contribution to Tinnitus.
Perez-Carpena P, Lopez-Escamez JA, Gallego-Martinez Á. Perez-Carpena P, et al. Among authors: gallego martinez a. J Assoc Res Otolaryngol. 2024 Feb;25(1):13-33. doi: 10.1007/s10162-024-00925-6. Epub 2024 Feb 9. J Assoc Res Otolaryngol. 2024. PMID: 38334885 Free PMC article.
The statistical analysis plan for the unification of treatments and interventions for tinnitus patients randomized clinical trial (UNITI-RCT).
Simoes JP, Schoisswohl S, Schlee W, Basso L, Bernal-Robledano A, Boecking B, Cima R, Denys S, Engelke M, Escalera-Balsera A, Gallego-Martinez A, Gallus S, Kikidis D, López-Escámez JA, Marcrum SC, Markatos N, Martin-Lagos J, Martinez-Martinez M, Mazurek B, Vassou E, Jarach CM, Mueller-Locatelli N, Neff P, Niemann U, Omar HK, Puga C, Schleicher M, Unnikrishnan V, Perez-Carpena P, Pryss R, Robles-Bolivar P, Rose M, Schecklmann M, Schiele T, Schobel J, Spiliopoulou M, Stark S, Vogel C, Wunder N, Zachou Z, Langguth B. Simoes JP, et al. Among authors: gallego martinez a. Trials. 2023 Jul 24;24(1):472. doi: 10.1186/s13063-023-07303-2. Trials. 2023. PMID: 37488627 Free PMC article. Clinical Trial.
Defective α-tectorin may involve tectorial membrane in familial Meniere disease.
Roman-Naranjo P, Parra-Perez AM, Escalera-Balsera A, Soto-Varela A, Gallego-Martinez A, Aran I, Perez-Fernandez N, Bächinger D, Eckhard AH, Gonzalez-Aguado R, Frejo L, Lopez-Escamez JA. Roman-Naranjo P, et al. Among authors: gallego martinez a. Clin Transl Med. 2022 Jun;12(6):e829. doi: 10.1002/ctm2.829. Clin Transl Med. 2022. PMID: 35653455 Free PMC article. No abstract available.
CSVS, a crowdsourcing database of the Spanish population genetic variability.
Peña-Chilet M, Roldán G, Perez-Florido J, Ortuño FM, Carmona R, Aquino V, Lopez-Lopez D, Loucera C, Fernandez-Rueda JL, Gallego A, García-Garcia F, González-Neira A, Pita G, Núñez-Torres R, Santoyo-López J, Ayuso C, Minguez P, Avila-Fernandez A, Corton M, Moreno-Pelayo MÁ, Morin M, Gallego-Martinez A, Lopez-Escamez JA, Borrego S, Antiñolo G, Amigo J, Salgado-Garrido J, Pasalodos-Sanchez S, Morte B; Spanish Exome Crowdsourcing Consortium; Carracedo Á, Alonso Á, Dopazo J. Peña-Chilet M, et al. Among authors: gallego martinez a. Nucleic Acids Res. 2021 Jan 8;49(D1):D1130-D1137. doi: 10.1093/nar/gkaa794. Nucleic Acids Res. 2021. PMID: 32990755 Free PMC article.
31 results