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Botond Banfi (Botond Bánfi)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 3

Top Topics

Intellectual Disability

Duchenne Muscular Dystrophy

Top Venues

European journal of human genetics : EJHG

Life science alliance

University of Iowa

Semmelweis University (PHD)

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

Affiliation History

University of Iowa

United States

Associate Professor :: Department of Anatomy and Cell Biology

Education History

Semmelweis University

Hungary

PHD :: Department of Physiology

Publications

Yoko Nakano, Botond Banfi
The cause of Jones syndrome put to REST: a mutation in the REST gene causes gingival fibromatosis and hearing loss. European journal of human genetics : EJHG (2023)
Memoona Ramzan, Christophe Philippe, Inna A Belyantseva, Yoko Nakano, Cristina Fenollar-Ferrer, Risa Tona, Rizwan Yousaf, Rasheeda Basheer, Ayesha Imtiaz, Rabia Faridi, Zunaira Munir, Hafiza Idrees, Midhat Salman, Sophie Nambot, Antonio Vitobello, Souad Kartti, Oumaima Zarrik, P Dane Witmer, Nara Lygia de Macena Sobreira, Azeddine Ibrahimi, Botond Banfi, Sebastien Moutton, Thomas B Friedman, Sadaf Naz
Variants of human CLDN9 cause mild to profound hearing loss. Human mutation 42 (10) (2021)
Yoko Nakano, Susan Wiechert, Bernd Fritzsch, Botond Banfi
Inhibition of a transcriptional repressor rescues hearing in a splicing factor-deficient mouse. Life science alliance 3 (12) (2020)