top of page
.jpg){kind=logo}
25.10.23
science
25.10.23
1/5
Laboratory of
Neural & Sensory Genomics
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.
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.
Publication_anchor
A mouse model of GRIN2D developmental and epileptic encephalopathy recapitulates the human disease
Yam M*, Nassir J*, Galber D, Quinn S, Gal R, Ovadia M, Bordeynik-Cohen M, Peled E, Makinson CD, Hausman-Kedem M, Fattal-Valevski A, Frankel WN, Avraham KB, Rubinstein M (2025). Brain, awaf149.
Future events
Future conferences
Association for Research in Otolaryngology (ARO) 49th Annual Meeting
February 7-11, 2026
San Juan, Puerto Rico, USA
Contact us
Prof. Karen B. Avraham
Principal Investigator, Dean, Gray Faculty of Medical & Health Sciences
Drs. Sarah and Felix Dumont Chair for Research of Hearing Disorders
Ms. Helen Berman
Administrative Assistant
Address
Dept. of Human Molecular Genetics & Biochemistry, Gray Faculty of Medical & Health Sciences
Floor 10, room 1003, Tel Aviv University
Tel Aviv 6997801 Israel
Funding
.png){kind=small}
Klass Family
Contact Us
bottom of page