Rescue from Hearing Loss in Usher's SyndromeAVRAHAM, Karen B.The New England journal of medicine. 2013, Vol 369, Num 18, pp 1758-1760, issn 0028-4793, 3 p.Article

Deafness Genes in Israel: Implications for Diagnostics in the ClinicBROWNSTEIN, Zippora; AVRAHAM, Karen B.Pediatric research. 2009, Vol 66, Num 2, pp 128-134, issn 0031-3998, 7 p.Article

Hereditary hearing loss: From human mutation to mechanismLENZ, Danielle R; AVRAHAM, Karen B.Hearing research. 2011, Vol 281, Num 1-2, pp 3-10, issn 0378-5955, 8 p.Article

Progressive vestibular mutation leads to elevated anxietySHEFER, Shahar; GORDON, Carlos R; AVRAHAM, Karen B et al.Brain research. 2010, Vol 1317, pp 157-164, issn 0006-8993, 8 p.Article

Therapeutics of hearing loss: expectations vs realityATAR, Orna; AVRAHAM, Karen B.Drug discovery today. 2005, Vol 10, Num 19, pp 1323-1330, issn 1359-6446, 8 p.Article

Balance deficit enhances anxiety and balance training decreases anxiety in vestibular mutant miceSHEFER, Shahar; GORDON, Carlos; AVRAHAM, Karen B et al.Behavioural brain research. 2015, Vol 276, pp 76-83, issn 0166-4328, 8 p.Article

Chromosomal mapping and phenotypic characterization of hereditary otosclerosis linked to the OTSC4 locusBROWNSTEIN, Zippora; GOLDFARB, Abraham; LEVI, Haya et al.Archives of otolaryngology, head & neck surgery. 2006, Vol 132, Num 4, pp 416-424, issn 0886-4470, 9 p.Article

Genomic Duplication and Overexpression of TJP2/ZO-2 Leads to Altered Expression of Apoptosis Genes in Progressive Nonsyndromic Hearing Loss DFNA51WALSH, Tom; PIERCE, Sarah B; BEN-NERIAH, Ziva et al.American journal of human genetics. 2010, Vol 87, Num 1, pp 101-109, issn 0002-9297, 9 p.Article

A mutation in GJB3 is associated with recessive erythrokeratodermia variabilis (EKV) and leads to defective trafficking of the connexin 31 proteinGOTTFRIED, Irit; LANDAU, Marina; GLASER, Fabian et al.Human molecular genetics (Print). 2002, Vol 11, Num 11, pp 1311-1316, issn 0964-6906Article

Mice with vestibular deficiency display hyperactivity, disorientation, and signs of anxietyAVNI, Reut; ELKAN, Tal; DROR, Amiel A et al.Behavioural brain research. 2009, Vol 202, Num 2, pp 210-217, issn 0166-4328, 8 p.Article

Connexin-associated deafness and speech perception outcome of cochlear implantationTAITELBAUM-SWEAD, Riki; BROWNSTEIN, Zippora; MUCHNIK, Chava et al.Archives of otolaryngology, head & neck surgery. 2006, Vol 132, Num 5, pp 495-500, issn 0886-4470, 6 p.Article

Mutations in a novel isoform of TRIOBP that encodes a filamentous- actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing lossSHAHIN, Hashem; WALSH, Tom; SOBE, Tama et al.American journal of human genetics. 2006, Vol 78, Num 1, pp 144-152, issn 0002-9297, 9 p.Article

Transcription profiling of inner ears from Pou4f3^ddl/ddl identifies Gfi1 as a target of the Pou4f3 deafness geneHERTZANO, Ronna; MONTCOUQUIOL, Mireille; AVRAHAM, Karen B et al.Human molecular genetics (Print). 2004, Vol 13, Num 18, pp 2143-2153, issn 0964-6906, 11 p.Article

Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84SHAHIN, Hashem; RAHIL, Michael; ABU RAYAN, Amal et al.Journal of medical genetics. 2010, Vol 47, Num 9, pp 643-645, issn 0022-2593, 3 p.Article

A Novel SLC26A4 (PDS) Deafness Mutation Retained in the Endoplasmic ReticulumBROWNSTEIN, Zippora N; DROR, Amiel A; GILONY, Dror et al.Archives of otolaryngology, head & neck surgery. 2008, Vol 134, Num 4, pp 403-407, issn 0886-4470, 5 p.Article

Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereociliaKAROLYI, I. Jill; PROBST, Frank J; RAPHAEL, Yehoash et al.Human molecular genetics (Print). 2003, Vol 12, Num 21, pp 2797-2805, issn 0964-6906, 9 p.Article

Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter studyDEL CASTILLO, Ignacio; MORENO-PELAYO, Miguel A; BALLANA, Ester et al.American journal of human genetics. 2003, Vol 73, Num 6, pp 1452-1458, issn 0002-9297, 7 p.Article

Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian familiesSHAHIN, Hashem; WALSH, Tom; STRAY, Sunday et al.European journal of human genetics. 2010, Vol 18, Num 4, pp 407-413, issn 1018-4813, 7 p.Article

A mutation of PCDH15 among ashkenazi jews with the type 1 Usher syndromeBEN-YOSEF, Tamar; NESS, Seth L; ODDOUX, Carole et al.The New England journal of medicine. 2003, Vol 348, Num 17, pp 1664-1670, issn 0028-4793, 7 p.Article

Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairmentLOPEZ-BIGAS, Nuria; OLIVE, Montserrat; FERRER, Isidre et al.Human molecular genetics (Print). 2001, Vol 10, Num 9, pp 947-952, issn 0964-6906Article

MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing lossMELCHIONDA, Salvatore; AHITUV, Nadav; ZELANTE, Leopoldo et al.American journal of human genetics. 2001, Vol 69, Num 3, pp 635-640, issn 0002-9297Article

Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82WALSH, Tom; SHAHIN, Hashem; KANAAN, Moien et al.American journal of human genetics. 2010, Vol 87, Num 1, pp 90-94, issn 0002-9297, 5 p.Article

GJB2 mutations and degree of hearing loss : A multicenter studySNOECKX, Rikkert L; HUYGEN, Patrick L. M; ORZAN, Eva et al.American journal of human genetics. 2005, Vol 77, Num 6, pp 945-957, issn 0002-9297, 13 p.Article

The R245X mutation of PCDH15 in Ashkenazi Jewish children diagnosed with nonsyndromic hearing loss foreshadows retinitis pigmentosaBROWNSTEIN, Zippora; BEN-YOSEF, Tamar; FRIEDMAN, Thomas B et al.Pediatric research. 2004, Vol 55, Num 6, pp 995-1000, issn 0031-3998, 6 p.Article

Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing lossDONAUDY, Francesca; FERRARA, Antonella; ESPOSITO, Laura et al.American journal of human genetics. 2003, Vol 72, Num 6, pp 1571-1577, issn 0002-9297, 7 p.Article