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Year | Number of Results |
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2020 | 2 |
2021 | 5 |
2024 | 0 |
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Page 1
Heritability and Genetics Contribution to Tinnitus.
Otolaryngol Clin North Am. 2020 Aug;53(4):501-513. doi: 10.1016/j.otc.2020.03.003. Epub 2020 Apr 23.
Otolaryngol Clin North Am. 2020.
PMID: 32334875
Review.
Genetic Inheritance and Its Contribution to Tinnitus.
Amanat S, Gallego-Martinez A, Lopez-Escamez JA.
Amanat S, et al.
Curr Top Behav Neurosci. 2021;51:29-47. doi: 10.1007/7854_2020_155.
Curr Top Behav Neurosci. 2021.
PMID: 32705497
Review.
Item in Clipboard
Multidisciplinary Tinnitus Research: Challenges and Future Directions From the Perspective of Early Stage Researchers.
Simoes JP, Daoud E, Shabbir M, Amanat S, Assouly K, Biswas R, Casolani C, Dode A, Enzler F, Jacquemin L, Joergensen M, Kok T, Liyanage N, Lourenco M, Makani P, Mehdi M, Ramadhani AL, Riha C, Santacruz JL, Schiller A, Schoisswohl S, Trpchevska N, Genitsaridi E.
Simoes JP, et al. Among authors: amanat s.
Front Aging Neurosci. 2021 Jun 11;13:647285. doi: 10.3389/fnagi.2021.647285. eCollection 2021.
Front Aging Neurosci. 2021.
PMID: 34177549
Free PMC article.
Review.
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Corrigendum: Multidisciplinary Tinnitus Research: Challenges and Future Directions From the Perspective of Early Stage Researchers.
Simoes JP, Daoud E, Shabbir M, Amanat S, Assouly K, Biswas R, Casolani C, Dode A, Enzler F, Jacquemin L, Joergensen M, Kok T, Liyanage N, Lourenco M, Makani P, Mehdi M, Ramadhani AL, Riha C, Santacruz JL, Schiller A, Schoisswohl S, Trpchevska N, Genitsaridi E.
Simoes JP, et al. Among authors: amanat s.
Front Aging Neurosci. 2021 Aug 9;13:730758. doi: 10.3389/fnagi.2021.730758. eCollection 2021.
Front Aging Neurosci. 2021.
PMID: 34434102
Free PMC article.
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Towards a unification of treatments and interventions for tinnitus patients: The EU research and innovation action UNITI.
Schlee W, Schoisswohl S, Staudinger S, Schiller A, Lehner A, Langguth B, Schecklmann M, Simoes J, Neff P, Marcrum SC, Spiliopoulou M, Niemann U, Schleicher M, Unnikrishnan V, Puga C, Mulansky L, Pryss R, Vogel C, Allgaier J, Giannopoulou E, Birki K, Liakou K, Cima R, Vlaeyen JWS, Verhaert N, Ranson S, Mazurek B, Brueggemann P, Boecking B, Amarjargal N, Specht S, Stege A, Hummel M, Rose M, Oppel K, Dettling-Papargyris J, Lopez-Escamez JA, Amanat S, Gallego-Martinez A, Escalera-Balsera A, Espinosa-Sanchez JM, Garcia-Valdecasas J, Mata-Ferron M, Martin-Lagos J, Martinez-Martinez M, Martinez-Martinez MJ, Müller-Locatelli N, Perez-Carpena P, Alcazar-Beltran J, Hidalgo-Lopez L, Vellidou E, Sarafidis M, Katrakazas P, Kostaridou V, Koutsouris D, Manta R, Paraskevopoulos E, Haritou M, Elgoyhen AB, Goedhart H, Koller M, Shekhawat GS, Crump H, Hannemann R, Holfelder M, Oberholzer T, Vontas A, Trochidis I, Moumtzi V, Cederroth CR, Koloutsou K, Spanoudakis G, Basdekis I, Gallus S, Lugo A, Stival C, Borroni E, Markatos N, Bibas A, Kikidis D.
Schlee W, et al. Among authors: amanat s.
Prog Brain Res. 2021;260:441-451. doi: 10.1016/bs.pbr.2020.12.005. Epub 2021 Feb 4.
Prog Brain Res. 2021.
PMID: 33637231
Clinical Trial.
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Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study.
Amanat S, Gallego-Martinez A, Sollini J, Perez-Carpena P, Espinosa-Sanchez JM, Aran I, Soto-Varela A, Batuecas-Caletrio A, Canlon B, May P, Cederroth CR, Lopez-Escamez JA.
Amanat S, et al.
EBioMedicine. 2021 Apr;66:103309. doi: 10.1016/j.ebiom.2021.103309. Epub 2021 Apr 1.
EBioMedicine. 2021.
PMID: 33813136
Free PMC article.
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A Systematic Review of Extreme Phenotype Strategies to Search for Rare Variants in Genetic Studies of Complex Disorders.
Amanat S, Requena T, Lopez-Escamez JA.
Amanat S, et al.
Genes (Basel). 2020 Aug 25;11(9):987. doi: 10.3390/genes11090987.
Genes (Basel). 2020.
PMID: 32854191
Free PMC article.
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