Researcher
Lynn Backers
- Disciplines:Immunogenetics, Molecular diagnostics, Genetics, Cancer biology
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → Today
Publications
1 - 10 of 11
- TIM3+ TRBV11-2 T cells and IFNγ signature in patrolling monocytes and CD16+ NK cells delineate MIS-C(2022)
Authors: Levi Hoste, Lisa Roels, Leslie Naesens, Victor Bosteels, Stijn Vanhee, Sam Dupont, Cédric Bosteels, Robin Browaeys, Niels Vandamme, Kevin Verstaen, et al.
- Integration of genomics and transcriptomics allows the identification of rare DNA damage defects in PID patients with a cancer predisposition(2021)
Authors: Lynn Backers, Bram Parton, Marieke De Bruyne, Filomeen Haerynck
Number of pages: 1 - Integration of genomics and transcriptomics to identify DNA damage defects in PID patients prone to cancer(2021)
Authors: Lynn Backers, Bram Parton, Mattias Van Heetvelde, Marieke De Bruyne, Kim De Leeneer, Anne Vral, Filomeen Haerynck, Kathleen Claes
Number of pages: 1 - Missing heritability in Bloom syndrome : First report of a deep-intronic variant leading to pseudo-exon activation in the BLM gene(2021)
Authors: Lynn Backers, Bram Parton, Marieke De Bruyne, Kris Van Den Bogaert, Filomeen Haerynck
Number of pages: 1 - Missing heritability in Bloom syndrome : first report of a deep intronic variant leading to pseudo‐exon activation in the BLM gene(2021)
Authors: Lynn Backers, Bram Parton, Marieke De Bruyne, Simon Tavernier, Kris Van Den Bogaert, Bart Lambrecht, Filomeen Haerynck, Kathleen Claes
Pages: 292 - 297 - Integration of genomics and transcriptomics to identify DNAdamage defects in PID patients with a cancer predisposition(2021)
Authors: Lynn Backers, Bram Parton, Marieke De Bruyne, Filomeen Haerynck
Number of pages: 1 - Missing heritability in Bloom syndrome : first report of a deep-intronic variant leading to pseudo-exon activation in the BLM gene(2020)
Authors: Lynn Backers, Bram Parton, Marieke De Bruyne, Simon Tavernier, Kris Van Den Bogaert, Bart Lambrecht, Filomeen Haerynck, Kathleen Claes
Number of pages: 1 - Missing heritability in Bloom syndrome : first report of a deep-intronic variant leading to pseudo-exon activation in the BLM gene(2020)
Authors: Lynn Backers, Bram Parton, Marieke De Bruyne, Kris Van Den Bogaert, Filomeen Haerynck
Number of pages: 1 - First patient with bloom syndrome caused by a deep intronic variant leading to pseudoexon activation(2020)
Authors: Lynn Backers, Bram Parton, Stephanie Vermeulen, Marieke De Bruyne, Kris Van Den Bogaert, Anne Vral, Ans Baeyens, Simon Tavernier, Filomeen Haerynck, Kathleen Claes
Number of pages: 1 - Radiosensitivity analysis in patients with a primary immunodeficiency disease(2019)
Authors: Victoria Bordon, Elien Beyls, Lynn Backers, Stephanie Vermeulen, Filomeen Haerynck
Number of pages: 1