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Laboratory of
Neural & Sensory Genomics 

SMARCA4 mutation causes human otosclerosis and a similar phenotype in mice

Drabkin M, Jean MM, Noy Y, Halperin D, Yogev Y, Wormser O, Proskorovski-Ohayon R, Dolgin V, Levaot N, Brumfeld V, Ovadia S, Kishner M, Kazenell U, Avraham KB, Shelef I, Birk OS (2024). J Med Genet. 61:117-124.
Shared and organ-specific gene-expression programs during the development of the cochlea and the superior olivary complex

Bordeynik-Cohen M*, Sperber M*, Ebbers L, Messika-Gold N, Krohs C, Koffler-Brill T, Noy Y, Elkon R, Nothwang HG, Avraham, KB (2023). RNA Biol, 20:629-640.
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Using multi-scale genomics to associate poorly annotated genes with rare diseases

Canavati C, Sherill-Rofe D, Kamal L, Bloch I, Zahdeh F, Sharon E, Terespolsky B, Allan IA, Rabie G, Kawas M, Kassem H, Avraham KB, Renbaum P, Levy-Lahad E, Kanaan M, Tabach Y (2024). Genome Med. 16:4.
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A fascinating journey

We use state-of-the-art imaging tools, including advanced confocal and electron microscopy, to study the pathophysiology of hearing impairment as a result of genetic variants.

Contact us

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Prof. Karen B. Avraham
Principal Investigator, Dean, Faculty of Medical & Health Sciences
Drs. Sarah and Felix Dumont Chair for Research of Hearing Disorders

Email: karena@tauex.tau.ac.il

Telephone: +972-3-6406642

Fax: +972-3-6409360

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Ms. Helen Berman
Administrative Assistant

Email: Helenbe@tauex.tau.ac.il

Telephone: +972-3-6406642

Fax: +972-3-6409360

Address

Dept. of Human Molecular Genetics & Biochemistry, Faculty of Medical & Health Sciences

Floor 10, room 1003, Tel Aviv University
Tel Aviv 6997801 Israel

Funding 

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