Hanno J Bolz

Publication Activity (10 Years)

Years Active: 2017-2019
Publications (10 Years): 2

Top Topics

Transcription Factor

Intellectual Disability

Top Venues

Molecular genetics & genomic medicine

Journal of translational medicine

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

Publications

Dominika Oziębło, Anna Sarosiak, Marcin Ludwik Leja, Birgit S Budde, Grażyna Tacikowska, Nataliya Di Donato, Hanno J Bolz, Peter Nürnberg, Henryk Skarzynski, Monika Ołdak
First confirmatory study on PTPRQ as an autosomal dominant non-syndromic hearing loss gene. Journal of translational medicine 17 (1) (2019)
Christine Neuhaus, Tobias Eisenberger, Christian Decker, Sandra Nagl, Cornelia Blank, Markus Pfister, Ingo Kennerknecht, Cornelie Müller-Hofstede, Peter Charbel Issa, Raoul Heller, Bodo Beck, Klaus Rüther, Diana Mitter, Klaus Rohrschneider, Ute Steinhauer, Heike M Korbmacher, Dagmar Huhle, Solaf M Elsayed, Hesham M Taha, Shahid M Baig, Heidi Stöhr, Markus Preising, Susanne Markus, Fabian Moeller, Birgit Lorenz, Kerstin Nagel-Wolfrum, Arif O Khan, Hanno J Bolz
Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome. Molecular genetics & genomic medicine 5 (5) (2017)