Karen Avraham

Karen B. Avraham is an Israeli-American human geneticist. Born in Canada in 1962, Avraham moved to the US at a young age. She holds the Drs Sarah and Felix Dumont Chair for Research of Hearing Disorders.

Prof. Karen B. Avraham
Born1962
Quebec, Canada
NationalityUS/Israel
Alma materWeizmann Institute
NCI-NIH
Known forHuman Genetics, Deafness, Israeli-Palestinian Scientific Cooperation
Scientific career
FieldsGenetics, Hearing Impairment
InstitutionsTel Aviv University

Education

Avraham received her B.A. degree in Biology from Washington University, St. Louis, Missouri, U.S., her Ph.D. from the Weizmann Institute of Science, Rehovot, Israel, under the supervision of Yoram Groner, and post-doctoral training at the National Cancer Institute, Frederick, Maryland, U.S., under the supervision of Nancy Jenkins and Neal Copeland.

Career

As a full professor at Tel Aviv University, and the current Vice Dean of the Sackler Faculty of Medicine, Avraham has a laboratory in the Department of Human Molecular Genetics and Biochemistry. 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)[1] as well a former board membership of the I-CORE: Gene Regulation in Complex Human Disease. Avraham is a council member of the European Molecular Biology Organization (EMBO, 2017),[2] chair of the Scientific Committee of the Fondation Pour L’Audition in France,[3] council member of the Human Genome Organization (HUGO, 2017),[4] an elected member of the International Collegium Oto-Rhino-Laryngologicum Amicitiae Sacrum (CORLAS), and past president of the Association for Research in Otolaryngology (ARO)[5] and the Genetic Society of Israel (GSI). She is an editor of Mammalian Genome (2017),[6] section editor of the European Journal of Human Genetics (2017),[7] associate editor of Human Genomics, and on the advisory editorial board of EMBO Molecular Medicine.[8]

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 exome sequencing for the discovery of disease genes to identify mutations that are relevant for the hearing-impaired population. Her group has demonstrated that microRNAs are essential for development and function of inner ear hair cells in vertebrates and has characterized the first long non-coding RNAs (lncRNAs) and methylation in the auditory system.

Avraham has supervised many 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.[9]

Awards and funding

Avraham has been awarded the Sir Bernard Katz Prize from the Alexander-von Humboldt Foundation (Germany), the Bruno Memorial Prize from the Rothschild Foundation.[10] the Teva Prize for Groundbreaking Research in Field of Rare Diseases from Teva Pharmaceuticals (Israel) and the Teva Founders Prize on Breakthroughs (Israel).

Funding in her laboratory includes from the National Institutes of Health, European Commission, Human Frontiers, I-CORE, Israel Science Foundation and the US-Israel Binational Science Foundation.

Papers
  • Positional-Candidate Cloning of Genes from Mouse Mutants, Karen B. Avraham, Gene knockout protocols, Martin J. Tymms; Ismail Kola (eds.). John M. Walker (series ed.), Methods in molecular biology series, 158. Humana Press, c2001. ISBN 0896035727LCCN 00-50603
  • Avraham, Karen B.; Hasson, Tama. Genes and mutations in hearing impairment, Genetics and auditory disorders. Keats, Bronya J. B.; Popper, Arthur N.; Fay, Richard R.(eds.), Springer handbook of auditory research, 14, Springer, c2002.ISBN 0387985018
  • Hertzano, Ronna; Avraham, Karen B. POU-Domain transcription factors, Genetic hearing loss. Patrick J. Willems (ed), Marcel Dekker, c2004. LCCN 2003-62467
  • Positional-Candidate Cloning of Genes from Mouse Mutants, Gene knockout protocols, Martin J. Tymms and Ismail Kola (eds.). John M. Walker (series editor), Methods in molecular biology series 158. Humana Press, c2010. LCCN 00-50603
  • 2. Molecular Etiology of Deafness and Cochlear Consequences, 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. LCCN 2013-944528
gollark: Most of them are just for compiling and stuff, the final client-side JS output is pretty small.
gollark: Though my project only uses 703 libraries.
gollark: I mean, I haven't run into any issues like that myself.
gollark: I just don't really care.
gollark: I'm aware of it.

References
  1. "About ILANIT". fiseb.org. Retrieved 9 July 2017.
  2. "Council". EMBO. Retrieved 9 July 2017.
  3. "Governance". Fondation Pour l'Audition. 20 July 2015. Retrieved 9 July 2017.
  4. "Human Genome Organisation (HUGO) International Ltd. - HUGO President & Council". hugo-international.org. Archived from the original on 23 July 2017. Retrieved 9 July 2017.
  5. "Past Presidents - Association for Research in Otolaryngology". www.aro.org. Retrieved 9 July 2017.
  6. "Mammalian Genome - incl. option to publish open access (Editorial Board)". springer.com. Retrieved 9 July 2017.
  7. "About the journal : European Journal of Human Genetics". www.nature.com. Retrieved 9 July 2017.
  8. "Editors & Board". embomolmed.embopress.org. Retrieved 9 July 2017.
  9. Search Results for author Avraham KB on PubMed.
  10. "Recipients". ias.huji.ac.il. Retrieved 9 July 2017.
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