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 deafness. Genome 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 populations. Cellular 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 deafness. Cellular physiology and biochemistry 2011, 28(3):535-544. [PDF]
Lenz DR, Avraham KB: Hereditary hearing loss: From human mutation to mechanism. Hearing Research 2011, doi:10.1016. [PDF]
Raviv D , Dror AA, Avraham KB: Hearing loss: a common disorder caused by many rare alleles. Ann N Y Acad Sci 2010, 1214: 168-17. [PDF]
Dror AA, Avraham KB: Hearing impairment: a panoply of genes and functions. Neuron 2010, 68: 293-308. [PDF]
Friedman LM, Avraham KB: MicroRNAs and epigenetic regulation in the mammalian inner ear: implications for deafness. Mamm Genome 2009, 20(9-10):581-603.[PDF]
Dror AA, Avraham KB: Hearing loss: mechanisms revealed by genetics and cell biology. Annu Rev Genet 2009, 43:411-437.[PDF]
Brownstein Z, Avraham KB: Deafness genes in Israel: implications for diagnostics in the clinic. Pediatr Res 2009, 66(2):128-134. [PDF]
Friedman LM, Dror AA, Avraham KB: Mouse models to study inner ear development and hereditary hearing loss. Int J Dev Biol 2007, 51(6-7):609-631. [PDF]
Sabag AD, Dagan O, Avraham KB: Connexins in hearing loss: a comprehensive overview. J Basic Clin Physiol Pharmacol 2005, 16(2-3):101-116. [PDF]
Atar O, Avraham KB: Therapeutics of hearing loss: expectations vs reality. Drug Discov Today 2005, 10(19):1323-1330. [PDF]
Avraham KB: Mouse models for deafness: lessons for the human inner ear and hearing loss. Ear Hear 2003, 24(4):332-341. [PDF]
Avraham KB, Raphael Y: Prospects for gene therapy in hearing loss. J Basic Clin Physiol Pharmacol 2003, 14(2):77-83.[PDF]
Goldfarb A, Avraham KB: Genetics of deafness: recent advances and clinical implications. J Basic Clin Physiol Pharmacol 2002, 13(2):75-88. [PDF]
Avraham KB: The genetics of deafness: a model for genomic and biological complexity. Ernst Schering Res Found Workshop 2002, (36):71-93.
Ahituv N, Avraham KB: Mouse models for human deafness: current tools for new fashions. Trends 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 loss. Cell Commun Adhes 2001, 8(4-6):419-424.
Avraham KB: Modifying with mitochondria. Nat Genet 2001, 27(2):136-137. [PDF]
Avraham KB: Dfna15. Adv Otorhinolaryngol 2000, 56:107-115.
Ahituv N, Avraham KB: Auditory and vestibular mouse mutants: models for human deafness. J Basic Clin Physiol Pharmacol 2000, 11(3):181-191. [PDF]
Friedman TB, Sellers JR, Avraham KB: Unconventional myosins and the genetics of hearing loss. Am J Med Genet 1999, 89(3):147-157. [PDF]
Ben-David O, Avraham KB: The genetics of hearing loss. J 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 cochlea. Nature 1997, 390(6660):559-560. [PDF]
Avraham KB: Motors, channels and the sounds of silence. Nat Med 1997, 3(6):608-609. [PDF]
