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425:, and the current Dean of the Faculty of Medicine, Avraham has a laboratory in the Department of Human Molecular Genetics and Biochemistry and holds the Drs Sarah and Felix Dumont Chair for Research of Hearing Disorders. Currently resides as the President of the Israel Society for Auditory Research (ISAR), Avraham held presidency with the Federation of Israel Societies for Experimental Biology (FISEB/ILANIT, 2017) as well a former board membership of the I-CORE: Gene Regulation in Complex Human Disease. Avraham is a council member of the
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in France, council member of the Human Genome
Organization (HUGO, 2017), an elected member of the International Collegium Oto-Rhino-Laryngologicum Amicitiae Sacrum (CORLAS), and past president of the Association for Research in Otolaryngology (ARO) and the Genetic Society of Israel (GSI). She is an
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Avraham has supervised more than 130 students through their M.Sc. or Ph.D. training, students, physicians and post docs have trained in her lab. She has published extensively in peer-reviewed journals, with an H-index of 48, and written reviews and book chapters.
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Avraham's research has centered on the discovery of disease genes, focusing on hereditary hearing loss. Her team studies the molecular basis of hearing loss using genetic, developmental, biochemical, cellular and bioinformatic tools. She leads the effort in
599:, Brownstein, Zippora; Shivatzki, Shaked; Avraham, Karen B., Deafness, Kral, Andrej; Popper, Arthur N.; Fay, Richard R. (eds).Springer handbook of auditory research, 47. Springer, c2013.
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Paz, Arnon; Brownstein
Zippora; Ber Yaara; Bialik Shani; David Eyal; Sagir Dorit; Ulitsky Igor; Elkon Ran; Kimchi Adi; Avraham Karen B; Shiloh Yosef; Shamir Ron (Jan 2011).
515:. the Teva Prize for Groundbreaking Research in Field of Rare Diseases from Teva Pharmaceuticals (Israel) and the Teva Founders Prize on Breakthroughs (Israel).
586:, Gene knockout protocols, Martin J. Tymms and Ismail Kola (eds.). John M. Walker (series editor), Methods in molecular biology series 158. Humana Press, c2010.
559:, Genetics and auditory disorders. Keats, Bronya J. B.; Popper, Arthur N.; Fay, Richard R.(eds.), Springer handbook of auditory research, 14, Springer, c2002.
538:, Gene knockout protocols, Martin J. Tymms; Ismail Kola (eds.). John M. Walker (series ed.), Methods in molecular biology series, 158. Humana Press, c2001.
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385:. Born in Canada in 1962, Avraham moved to the US at a young age. Her research focuses on the discovery and characterization of genes responsible for
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for the discovery of disease genes to identify mutations that are relevant for the hearing-impaired population. Her group has demonstrated that
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in vertebrates and has characterized the first long non-coding RNAs (lncRNAs) and methylation in the auditory system.
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Avraham has been awarded the Sir
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is a database of highly curated interactions for particular human pathways. SPIKE was developed by
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Contentious material about living persons that is unsourced or poorly sourced
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Positional-Candidate
Cloning of Genes from Mouse Mutants, Karen B. Avraham
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836:"About the journal : European Journal of Human Genetics"
409:, under the supervision of Nancy Jenkins and Neal Copeland.
625:"Prof. Karen Avraham Elected Dean of TAU's Medical Faculty"
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2. Molecular
Etiology of Deafness and Cochlear Consequences
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Positional-Candidate
Cloning of Genes from Mouse Mutants
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recipient for his research in systems biology, all from
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are essential for development and function of inner ear
429:(EMBO, 2017), chair of the Scientific Committee of the
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SPIKE (Signaling
Pathways Integrated Knowledge Engine)
397:Avraham received her B.A. degree in Biology from
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650:"פרופ' קרן אברהם | הפקולטה לרפואה ע"ש סאקלר"
518:Funding in her laboratory includes from the
333:, Israeli-Palestinian Scientific Cooperation
53:Learn how and when to remove these messages
1035:Washington University in St. Louis alumni
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885:Search Results for author Avraham KB
557:Genes and mutations in hearing impairment
383:Tel Aviv University's Faculty of Medicine
255:Learn how and when to remove this message
237:Learn how and when to remove this message
124:Learn how and when to remove this message
427:European Molecular Biology Organization
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913:(Database issue). England: D793-9.
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85:it lacks sufficient corresponding
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171:must be removed immediately
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79:includes a list of general
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387:hereditary hearing loss
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271:Prof. Karen B. Avraham
165:Please help by adding
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861:"Editors & Board"
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656:(in Hebrew)
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301:Nationality
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106:introducing
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660:2022-09-07
635:2022-11-15
611:References
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565:0387985018
544:0896035727
485:Ron Shamir
466:hair cells
434:editor of
227:March 2019
197:newspapers
156:references
81:references
39:improve it
700:"Council"
679:fiseb.org
462:microRNAs
393:Education
304:US/Israel
45:talk page
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349:Genetics
331:Deafness
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