Brecht Guillemyn

ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 5

Top Venues

American journal of medical genetics. Part A

PLoS genetics

Human mutation

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Center for Medical Genetics Ghent

Hogeschool West-Vlaanderen (MSC)

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

Affiliation History

Center for Medical Genetics Ghent Jan 01 2018

Belgium

PhD student :: Department of Biomolecular Medicine

Education History

Hogeschool West-Vlaanderen Sep 01 2005 - Jun 01 2009

Belgium

MSC

Publications

Brecht Guillemyn, Hanna De Saffel, Jan Willem Bek, Piyanoot Tapaneeyaphan, Adelbert De Clercq, Tamara Jarayseh, Sophie Debaenst, Andy Willaert, Riet De Rycke, Peter H Byers, Toon Rosseel, Paul Coucke, Bettina Blaumeiser, Delfien Syx, Fransiska Malfait, Sofie Symoens
Syntaxin 18 defects in human and zebrafish unravel key roles in early cartilage and bone development. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research (2023)
Delfien Syx, Yoshihiro Ishikawa, Jan M Gebauer, Sergei P Boudko, Brecht Guillemyn, Tim Van Damme, Sanne D'hondt, Sofie Symoens, Sheela Nampoothiri, Douglas B Gould, Ulrich Baumann, Hans Peter Bächinger, Fransiska Malfait
Aberrant binding of mutant HSP47 affects posttranslational modification of type I collagen and leads to osteogenesis imperfecta. PLoS genetics 17 (2) (2021)
Brecht Guillemyn, Sheela Nampoothiri, Delfien Syx, Fransiska Malfait, Sofie Symoens
Loss of TANGO1 Leads to Absence of Bone Mineralization. JBMR plus 5 (3) (2021)
Giulia Ascari, Frank Peelman, Pietro Farinelli, Toon Rosseel, Nina Lambrechts, Kirsten A Wunderlich, Matias Wagner, Konstantinos Nikopoulos, Pernille Martens, Irina Balikova, Lara Derycke, Gabriële Holtappels, Olga Krysko, Thalia Van Laethem, Sarah De Jaegere, Brecht Guillemyn, Teddy Jégu, Jan De Bleecker, David Creytens, Jo Van Dorpe, Jan Gerris, Claus Bachert, Christiane M Neuhofer, Sophie Walraedt, Almut Bischoff, Lotte Bang Pedersen, Florentine Radelfahr, Carlo Rivolta, Bart Peter Leroy, Elfriede De Baere, Frauke Coppieters
Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertility. Human mutation 41 (5) (2020)
Sheela Nampoothiri, Brecht Guillemyn, Nursel Elcioglu, Sujatha Jagadeesh, Dhanya Yesodharan, Beena Suresh, Serap Turan, Sofie Symoens, Fransiska Malfait
Ptosis as a unique hallmark for autosomal recessive WNT1-associated osteogenesis imperfecta. American journal of medical genetics. Part A 179 (6) (2019)

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Publication Activity (10 Years)

Top Topics

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Brecht Guillemyn