Hearing loss and tinnitus: association studies for complex-hearing disorders in mouse and man
Author:
Funder
National Institute on Deafness and Other Communication Disorders
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
https://link.springer.com/content/pdf/10.1007/s00439-021-02317-9.pdf
Reference91 articles.
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2. Amanat S, Requena T, Lopez-Escamez JA (2020) A Systematic review of extreme phenotype strategies to search for rare variants in genetic studies of complex disorders. Genes. https://doi.org/10.3390/genes11090987
3. Amanat S, Gallego-Martinez A, Sollini J et al (2021) Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study. EBioMedicine. https://doi.org/10.1016/j.ebiom.2021.103309
4. Anwar MN, Oakes MP (2012) Data mining of audiology patient records: Factors influencing the choice of hearing aid type. BMC Med Inform Decis Mak 12:1–8. https://doi.org/10.1186/1472-6947-12-S1-S6
5. Bennett BJ, Farber CR, Orozco L et al (2010) A high-resolution association mapping panel for the dissection of complex traits in mice. Genome Res. https://doi.org/10.1101/gr.099234.109
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