Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study-Reference-Cited by-同舟云学术

Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study

Published:2021-04 Issue: Volume:66 Page:103309
ISSN:2352-3964
Container-title:EBioMedicine
language:en
Short-container-title:EBioMedicine

Author:

Amanat Sana,Gallego-Martinez Alvaro^ORCID,Sollini Joseph^ORCID,Perez-Carpena Patricia,Espinosa-Sanchez Juan M.,Aran Ismael,Soto-Varela Andres,Batuecas‐Caletrio Angel,Canlon Barbara,May Patrick,Cederroth Christopher R.,Lopez-Escamez Jose A.

Funder

H2020

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference48 articles.

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3. Heritability and genetics contribution to tinnitus;Lopez-Escamez;Otolaryngol Clin,2020

4. Excess of rare missence variants in hearing loss genes in sporadic Meniere disease;Gallego-Martinez;Front Genet,2019

5. Current understanding and clinical management of Meniere ’s disease;Perez-Carpena;Semin Neurol,2020

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3. The causal relationship between anxiety and tinnitus severity: a Mendelian randomization study;Egyptian Journal of Medical Human Genetics;2024-04-08

4. Phenotypic spectrum of tinnitus patients bearing rare ANK2 gene variants;European Archives of Oto-Rhino-Laryngology;2024-03-20

5. Transcriptional-profile changes in the medial geniculate body after noise-induced tinnitus;Experimental Biology and Medicine;2024-03-18