Onderzoeker
Sascha Vermeer
- Disciplines:Genetica, Klinische genetica en moleculaire diagnostiek
Affiliaties
- Departement Menselijke Erfelijkheid (Departement)
Lid
Vanaf19 mrt 2020 → Heden
Publicaties
1 - 10 van 15
- A Case of Chorea with Slow Saccades Caused by NKX2-1 Mutation(2024)
Auteurs: Joke Terryn, Sascha Vermeer, Wim Vandenberghe
- Whole genome sequencing delineates novel non-coding variants and candidate genes in inherited retinal diseases(2024)
Auteurs: Sascha Vermeer
Pagina's: 41 - 41 - Intrafamilial Correlation and Variability in the Clinical Evolution of Pulmonary Fibrosis(2023)
Auteurs: Tinne Goos, Marie Vermant, Stefan Gogaert, Laurens De Sadeleer, Ellen De Langhe, Birgit Weynand, Marianne Carlon, Sascha Vermeer, Wim Wuyts
Pagina's: 1476 - 1480 - Targeted sequencing using single-molecule Molecular Inversion Probes reveals severe bi-allelic ABCA4 alleles in probands diagnosed with Leber congenital amaurosis(2023)
Auteurs: Sascha Vermeer
- Whole genome sequencing delineates novel non-coding variants and candidate genes in inherited retinal diseases(2023)
Auteurs: Sascha Vermeer
- Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction(2023)
Auteurs: Sascha Vermeer
- The MUC5B Promoter Polymorphism is Not Associated With Non-ILD Chronic Respiratory Diseases or Post-transplant Outcome(2022)
Auteurs: Tinne Goos, Laurens De Sadeleer, Arno Vanstapel, Janne Kaes, Vincent Geudens, Diether Lambrechts, Sascha Vermeer, Laurens Ceulemans, Dirk Van Raemdonck, Laurent Godinas, et al.
- Case Report: An Unusual Course of Angiosarcoma After Lung Transplantation(2022)
Auteurs: Lucienne Michaux, Isabelle Vanden Bempt, Sascha Vermeer, Patrick Schöffski, Birgit Weynand, Raf Sciot, Laurens Ceulemans, Laurent Godinas, Geert Verleden, Dirk Van Raemdonck, et al.
- Genetics in primary congenital glaucoma: Implications in disease management and counseling(2022)
Auteurs: Catherine Cassiman, Sascha Vermeer, Ingele Casteels, Irina Balikova
- RNF170 mutation causes autosomal dominant sensory ataxia with variable pyramidal involvement(2022)
Auteurs: Sien Van Daele, Sascha Vermeer, Hilde Van Esch, Kristl Claeys, Philip Van Damme
Pagina's: 345 - 349