Avraham KB. (2016) What's hot about otoferlin. Embo J. pii: e201695881. [Epub ahead of print] [PDF]

Koffler T, Ushakov K, Avraham KB. (2015) Genetics of Hearing Loss: Syndromic. Otolaryngol Clin North Am. pii: S0030-6665(15)00120-6. doi: 10.1016/j.otc.2015.07.007. [Epub ahead of print]

Ushakov, K., Rudnicki, A., Avraham K.B. (2013) MicroRNAs in sensorineural diseases of the ear. Front. Molec. Neurosci. 6:52. [PDF]

Brownstein, Z., Shivatzki, S. and Avraham, K.B. (2013) Molecular Etiology of Deafness and Cochlear Consequences. In: Deafness: Springer Handbook of Auditory Research. (A. Kral, A.N. Popper, R.R. Fay, eds). Springer-Verlag, NY. 47:17-39. [PDF]

Avraham, KB. (2013) Rescue from hearing loss in Usher’s Syndrome. N Engl J Med. 369:18. [PDF]

Elkan-Miller, T. and Avraham, K.B. (2013) Deafness Gene Discovery in the Genomic Era. InInner Ear Development and Hearing Loss. (Z. Ahmed, S. Riazuddin, eds). Nova Science Publishers. Chapter 8. [PDF]

Higashi T, Lenz DR, Furuse M, Avraham KB.  A “Tric” to tighten cell-cell junctions in the cochlea for hearing. J. Clin. Invest. doi:10.1172/JCI69651. [PDF]

Idan N, Brownstein Z, Shivatzki S, Avraham KB. (2013) Advances in genetic diagnostics for hereditary hearing loss. J Basic Clin Physiol Pharmacol. 24:165-170. [PDF]

Avraham KB, Kanaan M. Genomic advances for gene discovery in hereditary hearing loss. J Basic Clin Physiol Pharmacol. 2012 Sep 7;23(3):93-7. [PDF]

Rudnicki A, Avraham KB: microRNAs: the art of silencing in the ear. EMBO molecular medicine 2012. doi: 10.1002/emmm.201100922. [PDF]

Brownstein Z, Bhonker Y, Avraham KB: High-throughput sequencing to decipher the genetic heterogeneity of deafnessGenome biology 2012, 13(5):245. [PDF]

Dossena S, Nofziger C, Brownstein Z, Kanaan M, Avraham KB, Paulmichl M: Functional characterization of pendrin mutations found in the Israeli and Palestinian populationsCellular physiology and biochemistry 2011, 28(3):477-484.[PDF]

Dror AA, Brownstein Z, Avraham KB: Integration of human and mouse genetics reveals pendrin function in hearing and deafnessCellular physiology and biochemistry 2011, 28(3):535-544. [PDF]

Lenz DR, Avraham KB: Hereditary hearing loss: From human mutation to mechanismHearing Research 2011, doi:10.1016. [PDF]

Raviv D , Dror AA, Avraham KB: Hearing loss: a common disorder caused by many rare allelesAnn N Y Acad Sci 2010, 1214: 168-17. [PDF]

Dror AA, Avraham KB: Hearing impairment: a panoply of genes and functionsNeuron 2010, 68: 293-308. [PDF]

Friedman LM, Avraham KB: MicroRNAs and epigenetic regulation in the mammalian inner ear: implications for deafnessMamm Genome 2009, 20(9-10):581-603.[PDF]

Avraham KB. (2009 Noise stresses the junctions to deafEMBO Mol Med. 1:85-87. [PDF]

Dror AA, Avraham KB: Hearing loss: mechanisms revealed by genetics and cell biologyAnnu Rev Genet 2009, 43:411-437.[PDF]

Brownstein Z, Avraham KB: Deafness genes in Israel: implications for diagnostics in the clinicPediatr Res 2009, 66(2):128-134. [PDF]

Friedman LM, Dror AA, Avraham KB: Mouse models to study inner ear development and hereditary hearing lossInt J Dev Biol 2007, 51(6-7):609-631. [PDF]

Sabag AD, Dagan O, Avraham KB: Connexins in hearing loss: a comprehensive overviewJ Basic Clin Physiol Pharmacol 2005, 16(2-3):101-116. [PDF]

Skinner H, Abdeen Z, Abdeen H, Aber P, Al-Masri M, Attias J, Avraham KB, Carmi R, Chalin C, El Nasser Z, Hijazi M, Jebara RO, Kanaan M, Pratt H, Raad F, Roth Y, Williams AP, Noyek A. (2005) Promoting Arab and Israeli cooperation: peacebuilding through health initiativesThe Lancet 365:1274-1277. [PDF]

Atar O, Avraham KB: Therapeutics of hearing loss: expectations vs realityDrug Discov Today 2005, 10(19):1323-1330. [PDF]

Avraham KB: Mouse models for deafness: lessons for the human inner ear and hearing lossEar Hear 2003, 24(4):332-341. [PDF]

Avraham KB, Raphael Y: Prospects for gene therapy in hearing lossJ Basic Clin Physiol Pharmacol 2003, 14(2):77-83.[PDF]

Goldfarb A, Avraham KB: Genetics of deafness: recent advances and clinical implicationsJ Basic Clin Physiol Pharmacol 2002, 13(2):75-88. [PDF]

Avraham KB: The genetics of deafness: a model for genomic and biological complexityErnst Schering Res Found Workshop 2002, (36):71-93.

Ahituv N, Avraham KB: Mouse models for human deafness: current tools for new fashionsTrends Mol Med 2002, 8(9):447-451.[PDF]

Avraham KB: Positional-candidate cloning of genes from mouse mutants.Methods Mol Biol 2001, 158:369-379

Avraham KB: Inherited connexin mutations associated with hearing lossCell Commun Adhes 2001, 8(4-6):419-424.

Avraham KB: Modifying with mitochondriaNat Genet 2001, 27(2):136-137. [PDF]

Avraham KB: Dfna15Adv Otorhinolaryngol 2000, 56:107-115.

Ahituv N, Avraham KB: Auditory and vestibular mouse mutants: models for human deafnessJ Basic Clin Physiol Pharmacol 2000, 11(3):181-191. [PDF]

Friedman TB, Sellers JR, Avraham KB: Unconventional myosins and the genetics of hearing lossAm J Med Genet 1999, 89(3):147-157. [PDF]

Ben-David O, Avraham KB: The genetics of hearing lossJ Basic Clin Physiol Pharmacol 1999, 10(3):163-171.

Avraham KB: Hear come more genes! Nat Med 1998, 4(11):1238-1239. [PDF]

Avraham KB: Deafness. Sounds from the cochleaNature 1997, 390(6660):559-560. [PDF]

Avraham KB: Motors, channels and the sounds of silenceNat Med 1997, 3(6):608-609. [PDF]