Fábio Tadeu Arrojo Martins (Fábio T A Martins)

Publication Activity (10 Years)

Years Active: 2018-2020
Publications (10 Years): 2

Top Topics

Circulating Tumor Cells

Transcription Factor

Genome Wide Identification

Top Venues

Genetics and molecular biology

Clinical genetics

Tampere University

State University of Campinas (MSC)

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

Affiliation History

Tampere University Nov 13 2017

Finland

Postdoctoral researcher :: Faculty of Medicine and Health Technology

Education History

State University of Campinas Mar 01 2011 - Feb 28 2013

Brazil

MSC :: Center of Molecular Biology and Genetic Engineering

University of Sorocaba Feb 02 2007

Brazil

BSC :: Biotechnology Department

Publications

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)
Fábio Tadeu Arrojo Martins, Berenice Dias Ramos, Edi Lúcia Sartorato
A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene. Genetics and molecular biology 41 (4) (2018)