Researcher
Brecht Guillemyn
- Disciplines:Palliative care and end-of-life care, Laboratory medicine, Other translational sciences, Clinical genetics and molecular diagnostics, Regenerative medicine, Nursing, Other clinical sciences, Other basic sciences, Other paramedical sciences, Other health sciences, Other medical and health sciences
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → 25 Sep 2022 - Department of Pediatrics and medical genetics (Department)
Member
From1 Oct 2011 → 30 Sep 2018
Publications
11 - 20 of 24
- Nucleic acids enrichment of fungal pathogens to study host-pathogen interactions(2019)
Authors: Antonio José Rodriguez Sánchez, Brecht Guillemyn, Paul Coucke, Mario Vaneechoutte
- The clinical and mutational spectrum of B3GAT3 linkeropathy : two case reports and literature review(2019)
Authors: Marlies Colman, Tim Van Damme, Elisabeth Steichen-Gersdorf, Franco Laccone, Sheela Nampoothiri, Delfien Syx, Brecht Guillemyn, Sofie Symoens, Fransiska Malfait
- Ptosis as a unique hallmark for autosomal recessive WNT1-associated osteogenesis imperfecta(2019)
Authors: Sheela Nampoothiri, Brecht Guillemyn, Nursel Elcioglu, Sujatha Jagadeesh, Dhanya Yesodharan, Beena Suresh, Serap Turan, Fransiska Malfait
Pages: 908 - 914 - A homozygous pathogenic missense variant broadens the phenotypic and mutational spectrum of CREB3L1-related osteogenesis imperfecta(2019)
Authors: Brecht Guillemyn, Hülya Kayserili, Lynn Demuynck, Fransiska Malfait
Pages: 1801 - 1809 - Biallelic B3GALT6 mutations cause spondylodysplastic Ehlers-Danlos syndrome(2018)
Authors: Tim Van Damme, Xiaomeng Pang, Brecht Guillemyn, Sandrine Gulberti, Olivier Kaye, Christine E. M. de Die-Smulders, Rolph Pfundt, Ariana Kariminejad, Sheela Nampoothiri, Genevieve Pierquin, et al.
Pages: 3475 - 3487 - Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies(2018)
Authors: Charlotte Gistelinck, Ronald Y Kwon, Fransiska Malfait, Matthew P Harris, Katrin Henke, Michael B Hawkins, Shannon Fisher, Brecht Guillemyn, Petra Vermassen, Hanna De Saffel, et al.
Pages: E8037 - E8046 - Type III collagen affects dermal and vascular collagen fibrillogenesis and tissue integrity in a mutant Col3a1 transgenic mouse model(2018)
Authors: Sanne D'hondt, Brecht Guillemyn, Leen Vanhoutte, Wendy Toussaint, Douglas R Keene, Yoshihiro Ishikawa, Hans Peter Bächinger, Mathieu Bertrand, Fransiska Malfait
Pages: 72 - 83 - Mutations in ATP6V1E1 or ATP6V1A cause autosomal-recessive cutis laxa(2017)
Authors: Tim Van Damme, Thatjana Gardeitchik, Miski Mohamed, Sergio Guerrero-Castillo, Peter Freisinger, Brecht Guillemyn, Ariana Kariminejad, Daisy Dalloyaux, Sanne van Kraaij, Dirk J Lefeber, et al.
Pages: 216 - 227 - A homozygous B3GAT3 mutation causes a multisystemic cutis laxa-like syndrome, expanding the phenotype of linkeropathies(2016)
Authors: Brecht Guillemyn, Tim Van Damme, Wouter Steyaert, Sheela Nampoothiri, Fransiska Malfait
Number of pages: 1 - Defective proteolytic processing of fibrillar procollagens and prodecorin due to biallelic BMP1 mutations results in a severe, progressive form of osteogenesis imperfecta(2015)
Authors: Brecht Guillemyn, Ana Berta Sousa, Ana Medeira, Margo Whiteford, Trinh Hermanns-Lê, Fransiska Malfait
Pages: 1445 - 1456