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个人简介
My research focuses on the discovery and characterization of genes responsible for hereditary hearing loss. As our lab is located in Tel Aviv, Israel, we have the opportunity to study the genetic basis of deafness in families from the Middle East, from both the Israeli Jewish and Palestinian Arab populations. Given the complexity of the inner ear and of auditory transduction, many of us predicted that variants in any of many different genes would lead to hearing loss. This prediction has been confirmed many times over and is the basis of the genomic technologies I have integrated into our research.In the last decade, my work has covered the transcriptome and epigenome of the auditory and vestibular systems, in order to dissect the regulatory pathways of these systems. This work includes the microRNAs, long non-coding RNAs and whole genome methylation. My team has studied the mechanisms and pathophysiology of deafness in several mouse models, which mimic human hearing loss extremely well.
研究兴趣
论文共 218 篇作者统计合作学者相似作者
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Christina Canavati,Dana Sherill-Rofe,Lara Kamal,Idit Bloch,Fouad Zahdeh,Elad Sharon, Batel Terespolsky, Islam Abu Allan,Grace Rabie, Mariana Kawas, Hanin Kassem,Karen B. Avraham,
Genome Medicineno. 1 (2024): 1-22
Max Drabkin, Matan M Jean,Yael Noy,Daniel Halperin,Yuval Yogev,Ohad Wormser,Regina Proskorovski-Ohayon,Vadim Dolgin, Noam Levaot, Vlad Brumfeld, Shira Ovadia, Mor Kishner,
Journal of medical geneticsno. 2 (2023): 117-124
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Elizabeth L Wagner, Jun-Sub Im,Stefano Sala, Maura I Nakahata, Terence E Imbery,Sihan Li,Daniel Chen,Katherine Nimchuk,Yael Noy, David W Archer,Wenhao Xu, George Hashisaki,
eLife (2023)
HUMAN MOLECULAR GENETICSno. 14 (2023): 2265-2268
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Roni Hahn,Karen B. Avraham
AUDIOLOGY RESEARCHno. 6 (2023): 952-966
Life science allianceno. 6 (2023): e202201847-e202201847
Proceedings of the National Academy of Sciences of the United States of Americano. 35 (2022)
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