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Publications-
Reviews
Insights into the regulation of hearing regeneration
Khalaily L, Avraham KB
Gene therapy for inherited hearing loss: updates and remaining challenges
Hahn R, Avraham KB
The long and short: Non-coding RNAs in the mammalian inner ear
Koffler-Brill T, Noy Y, Avraham KB
Emerging complexities of the mouse as a model for human hearing loss
Carson RJ, Avraham KB
The genomics of auditory function and disease
Taiber S, Gwilliam K, Hertzano R, Avraham KB
The noncoding genome and hearing loss
Avraham, K.B., Khalaily, L., Noy, Y., Kamal, L., Koffler-Brill, T, Taiber, S.
Genetic therapies for hearing loss: Accomplishments and remaining challenges
Taiber, S. and Avraham, K.B.
Single cell analysis of the inner ear sensory organs
Yizhar-Barnea, O. and Avraham, K.B.
Avraham, K.B.
Doetzlhofer, A. and Avraham, K.B.
Genetics of hearing loss – syndromic
Koffler, T., Ushakov, K. and Avraham, K.B.
MicroRNAs in sensorineural diseases of the ear
Ushakov, K., Rudnicki, A., Avraham, K.B.
Rescue from hearing loss in Usher’s syndrome
Avraham, K.B.
Advances in genetic diagnostics for hereditary hearing loss
​Idan, N., Brownstein, Z., Shivatzki, S. and Avraham, K.B.
A “Tric” to tighten cell-cell junctions in the cochlea for hearing
Higashi, T., Lenz, D.R., Furuse, M. and Avraham, K.B.
Genomic advances for gene discovery in hereditary hearing loss
Avraham, K.B. and Kanaan, M.
microRNAs: the art of silencing in the ear
Rudnicki, A. and Avraham, K.B.
High-throughput sequencing to decipher the genetic heterogeneity of deafness
Brownstein, Z., Bhonker, Y., Avraham, K.B.
Integration of human and mouse genetics reveals pendrin function in hearing and deafness
Dror, A., Brownstein, Z. and Avraham, K.B.
Hereditary hearing loss: From human mutation to mechanism
Lenz, D.R. and Avraham, K.B.
Collaborative genomics for human health and cooperation in the Mediterranean region
Ozçelik, T., Kanaan, M., Avraham, K.B., Yannoukakos, D., Mégarbané, A., Tadmouri, G.O., Middleton, L., Romeo, G., King, M.C. and Levy-Lahad, E.
Hearing impairment: a panoply of genes and functions
Dror, A.A. and Avraham, K.B.
Hearing loss: a common disorder caused by many rare alleles
Raviv, D., Dror, A.A. and Avraham, K.B.
Hearing loss: Mechanisms revealed by genetics and cell biology
Dror, A.A. and Avraham, K.B.
Deafness genes in Israel: implications for diagnostics in the clinic
Brownstein, Z. and Avraham, K.B.
MicroRNAs and epigenetic regulation in the mammalian inner ear: implications for deafness
Friedman, L.M. and Avraham, K.B.
Mouse models developed to study inner ear development and hereditary hearing loss
Friedman, L., Dror, A.A. and Avraham, K.B.
Future trends and potential for treatment of sensorineural hearing loss
Brownstein, Z. and Avraham, K.B.
Connexins in hearing loss: a comprehensive overview
Sabag-Dgani, A., Dagan, O. and Avraham, K.B.
Therapeutics of hearing loss: expectations vs. reality
Atar, O. and Avraham, K.B.
Promoting Arab and Israeli cooperation: a model for peacebuilding through health initiatives
Skinner, H., Abdeen, Z., Abdeen, H., Aber, P., Al-Masri, M., Attias, J., Avraham, K.B., Carmi, R., Chalin, C., El Nasser, Z., Hijazi, M., Othman Jebara, R., Kanaan, M., Pratt, H., Raad, F., Roth, Y., Williams, A.P. and Noyek, A.
Prospects for gene therapy in hearing loss
Avraham. K.B. and Raphael, Y.
Genetics of deafness: recent advances and clinical implications
Goldfarb, A. and Avraham. K.B.
Mouse models for human deafness: Current tools for new fashions
Ahituv, N. and Avraham, K.B.
Avraham, K.B.
Auditory and vestibular mouse mutants: models for human deafness
Ahituv, N. and Avraham, K.B.
Unconventional myosins and the genetics of hearing loss
Friedman, T.B., Sellers, J.R. and Avraham, K.B.
Ben-David, O. and Avraham, K.B.
The Genetics of Deafness
Ben-David, O. and Avraham, K.B.
Avraham, K.B.
Avraham, K.B.
Motors, channels and the sounds of silence
Avraham, K.B.