Wim Wuyts

ResearcherID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 6

Top Topics

Mitochondrial Dna

Intellectual Disability

Top Venues

European journal of human genetics : EJHG

JMIR medical informatics

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

Publications

Thomas Clabout, Laurence Maes, Frederic R E Acke, Wim Wuyts, Kristof Van Schil, Paul Coucke, Sandra Janssens, Els De Leenheer
Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next? Genes 14 (1) (2022)
Thomas Clabout, Laurence Maes, Frederic R E Acke, Wim Wuyts, Kristof Van Schil, Paul Coucke, Sandra Janssens, Els De Leenheer
Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next? Genes 14 (1) (2022)
Thomas Clabout, Laurence Maes, Frederic R E Acke, Wim Wuyts, Kristof Van Schil, Paul Coucke, Sandra Janssens, Els De Leenheer
Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next? Genes 14 (1) (2022)
Thomas Clabout, Laurence Maes, Frederic R E Acke, Wim Wuyts, Kristof Van Schil, Paul Coucke, Sandra Janssens, Els De Leenheer
Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next? Genes 14 (1) (2022)
Joséphine Lantoine, Anne Brysse, Vinciane Dideberg, Kathleen B M Claes, Sofie Symoens, Wim Coucke, Valérie Benoit, Sonia Rombout, Martine De Rycke, Sara Seneca, Lut Van Laer, Wim Wuyts, Anniek Corveleyn, Kris Van Den Bogaert, Catherine Rydlewski, Françoise Wilkin, Marie Ravoet, Elodie Fastré, Arnaud Capron, Nathalie Monique Vandevelde
Frequency of Participation in External Quality Assessment Programs Focused on Rare Diseases: Belgian Guidelines for Human Genetics Centers. JMIR medical informatics 9 (7) (2021)
Sebastien P F JanssensdeVarebeke, Guy Van Camp, Nils Peeters, Ellen Elinck, Josine Widdershoven, Tony Cox, Kristof Deben, Katrien Ketelslagers, Tom Crins, Wim Wuyts
Bi-allelic inactivating variants in the COCH gene cause autosomal recessive prelingual hearing impairment. European journal of human genetics : EJHG 26 (4) (2018)