Karen B Avraham

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 18

Top Venues

European journal of human genetics : EJHG

Proceedings of the National Academy of Sciences of the United States of America

RNA biology

Human genetics

Tel Aviv University

Weizmann Institute of Science (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Tel Aviv University

Israel

Vice Dean :: Dept of Human Molecular Genetics & Biochemistry, Sackler Faculty of Medicine and Sagol School of Neuroscience

Education History

Weizmann Institute of Science

Israel

PHD :: Molecular Genetics

Washington University

United States

BSC

Publications

Mor Bordeynik-Cohen, Michal Sperber, Lena Ebbers, Naama Messika-Gold, Constanze Krohs, Tal Koffler-Brill, Yael Noy, Ran Elkon, Hans Gerd Nothwang, Karen B Avraham
Shared and organ-specific gene-expression programs during the development of the cochlea and the superior olivary complex. RNA biology 20 (1) (2023)
Alexandra Frohne, Martin Koenighofer, Hakan Cetin, Michael Nieratschker, David Tianxiang Liu, Franco Laccone, Juergen Neesen, Stefan F Nemec, Ursula Schwarz-Nemec, Christian Schöfer, Karen B Avraham, Klemens Frei, Katharina Grabmeier-Pfistershammer, Bernhard Kratzer, Klaus Georg Schmetterer, Winfried F Pickl, Thomas Parzefall
A homozygous AP3D1 missense variant in patients with sensorineural hearing loss as the leading manifestation. Human genetics (2022)
Ryan J Carlson, Karen B Avraham
Emerging complexities of the mouse as a model for human hearing loss. Proceedings of the National Academy of Sciences of the United States of America 119 (35) (2022)
Yoel Hirsch, Chayada Tangshewinsirikul, Kevin T A Booth, Hela Azaiez, Devorah Yefet, Adina Quint, Tzvi Weiden, Zippora Brownstein, Michal Macarov, Bella Davidov, John G Pappas, Rachel Rabin, Margaret A Kenna, Andrea M Oza, Katherine Lafferty, Sami S Amr, Heidi L Rehm, Diana L Kolbe, Kathy Frees, Carla Nishimura, Minjie Luo, Chantal Farra, Cynthia C Morton, Sholem Y Scher, Josef Ekstein, Karen B Avraham, Richard J H Smith, Jun Shen
A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing. European journal of human genetics : EJHG 29 (6) (2021)
Karen B Avraham, Lama Khalaily, Yael Noy, Lara Kamal, Tal Koffler-Brill, Shahar Taiber
The noncoding genome and hearing loss. Human genetics (2021)
S Paridhy Vanniya, Jayasankaran Chandru, Justin Margret Jeffrey, Tom Rabinowitz, Zippora Brownstein, Mathuravalli Krishnamoorthy, Karen B Avraham, Le Cheng, Noam Shomron, C R Srikumari Srisailapathy
PNPT1, MYO15A, PTPRQ, and SLC12A2-associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern India. Annals of human genetics (2021)
Shahar Taiber, Roie Cohen, Ofer Yizhar-Barnea, David Sprinzak, Jeffrey R Holt, Karen B Avraham
Neonatal AAV gene therapy rescues hearing in a mouse model of SYNE4 deafness. EMBO molecular medicine 13 (2) (2020)
Tal Koffler-Brill, Shahar Taiber, Alejandro Anaya-Rocha, Mor Bordeynik-Cohen, Einat Rosen, Likhitha Kolla, Naama Messika-Gold, Ran Elkon, Matthew William Kelley, Igor Ulitsky, Karen B Avraham
Identification and characterization of key long non-coding RNAs in the mouse cochlea. RNA biology 18 (8) (2020)
Roie Cohen, Liat Amir-Zilberstein, Micha Hersch, Shiran Woland, Olga Loza, Shahar Taiber, Fumio Matsuzaki, Sven Bergmann, Karen B Avraham, David Sprinzak
Mechanical forces drive ordered patterning of hair cells in the mammalian inner ear. Nature communications 11 (1) (2020)
Nada Danial-Farran, Elena Chervinsky, Prathamesh T Nadar-Ponniah, Eran Cohen Barak, Shahar Taiber, Morad Khayat, Karen B Avraham, Stavit A Shalev
Homozygote loss-of-function variants in the human COCH gene underlie hearing loss. European journal of human genetics : EJHG 29 (2) (2020)
Zippora Brownstein, Suleyman Gulsuner, Tom Walsh, Fábio Tadeu Arrojo Martins, Shahar Taiber, Ofer Isakov, Ming K Lee, Mor Bordeynik-Cohen, Maria Birkan, Weise Chang, Silvia Casadei, Nada Danial-Farran, Amal AbuRayyan, Ryan J Carlson, Lara Kamal, Asgeir Ö Arnthórsson, Meirav Sokolov, Dror Gilony, Noga Lipschitz, Moshe Frydman, Bella Davidov, Michal Macarov, Michal Sagi, Chana Vinkler, Hana Poran, Reuven Sharony, Nadra Samra, Na'ama Zvi, Hagit Baris-Feldman, Amihood Singer, Ophir Handzel, Ronna Hertzano, Doaa Ali-Naffaa, Noa Ruhrman-Shahar, Ory Madgar, Efrat Sofrin-Drucker, Amir Peleg, Morad Khayat, Mordechai Shohat, Lina Basel-Salmon, Elon Pras, Dorit Lev, Michael Wolf, Eirikur Steingrimsson, Noam Shomron, Matthew William Kelley, Moien N Kanaan, Stavit Allon-Shalev, Mary-Claire King, Karen B Avraham
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1. Clinical genetics 98 (4) (2020)
Amiel A Dror, Shahar Taiber, Eyal Sela, Ophir Handzel, Karen B Avraham
A mouse model for benign paroxysmal positional vertigo with genetic predisposition for displaced otoconia. Genes, brain, and behavior 19 (5) (2020)
Amal AbuRayyan, Lara Kamal, Silvia Casadei, Zippora Brownstein, Fouad Zahdeh, Hashem Shahin, Christina Canavati, Dima Dweik, Tamara Jaraysa, Grace Rabie, Ryan J Carlson, Suleyman Gulsuner, Ming K Lee, Karen B Avraham, Tom Walsh, Mary-Claire King, Moien N Kanaan
Genomic analysis of inherited hearing loss in the Palestinian population. Proceedings of the National Academy of Sciences of the United States of America 117 (33) (2020)
Jun Shen, Andrea M Oza, Ignacio Del Castillo, Hatice Duzkale, Tatsuo Matsunaga, Arti Pandya, Hyunseok P Kang, Rebecca Mar-Heyming, Saurav Guha, Krista Moyer, Christine Lo, Margaret Kenna, John J Alexander, Yan Zhang, Yoel Hirsch, Minjie Luo, Ye Cao, Kwong-Wai Choy, Yen-Fu Cheng, Karen B Avraham, Xinhua Hu, Gema Garrido, Miguel Angel Moreno-Pelayo, John Greinwald, Kejian Zhang, Yukun Zeng, Zippora Brownstein, Lina Basel-Salmon, Bella Davidov, Moshe Frydman, Tzvi Weiden, Narasimhan Nagan, Alecia Willis, Sarah E Hemphill, Andrew R Grant, Rebecca K Siegert, Marina T DiStefano, Sami S Amr, Michael J Bamshad, Ahmad N Abou Tayoun, null null
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel. Genetics in medicine : official journal of the American College of Medical Genetics 21 (11) (2019)
Nada Danial-Farran, Zippora Brownstein, Suleyman Gulsuner, Luna Tammer, Morad Khayat, Ola Aleme, Elena Chervinsky, Olfat Aboleile Zoubi, Tom Walsh, Gil Ast, Mary-Claire King, Karen B Avraham, Stavit A Shalev
Genetics of hearing loss in the Arab population of Northern Israel. European journal of human genetics : EJHG 26 (12) (2018)
Ofer Yizhar-Barnea, Cristina Valensisi, Naresh Doni Jayavelu, Kamal Kishore, Colin Andrus, Tal Koffler-Brill, Kathy Ushakov, Kobi Perl, Yael Noy, Yoni Bhonker, Mattia Pelizzola, R David Hawkins, Karen B Avraham
DNA methylation dynamics during embryonic development and postnatal maturation of the mouse auditory sensory epithelium. Scientific reports 8 (1) (2018)
Kobi Perl, Ron Shamir, Karen B Avraham
Computational analysis of mRNA expression profiling in the inner ear reveals candidate transcription factors associated with proliferation, differentiation, and deafness. Human genomics 12 (1) (2018)
Karen B Avraham
What's hot about otoferlin. The EMBO journal 35 (23) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Karen B Avraham