Nada Danial-Farran

Publication Activity (10 Years)

Years Active: 2020-2020
Publications (10 Years): 2

Top Topics

Transcription Factor

Circulating Tumor

Top Venues

European journal of human genetics : EJHG

Clinical genetics

Emek Medical Center

Tel Aviv University (PHD)

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

Affiliation History

Emek Medical Center Feb 01 2017

Israel

Director of NGS unit :: Genetic institute

Education History

Tel Aviv University Feb 01 2014 - Dec 11 2018

Israel

PHD :: Human genetic, Karen B. Avraham laboratory

Technion Israel Institute of Technology Feb 01 2014 - Dec 11 2018

Israel

PHD :: Human genetics

Publications

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)