Researcher
Nele Cosemans
- Disciplines:Public health care, Public health sciences, Public health services
Affiliations
- Laboratory for Genetic Epidemiology (Division)
Member
From1 Oct 2014 → 30 Jun 2020 - Clinical Genetics (Division)
Member
From1 Aug 2014 → 30 Sep 2014
Projects
1 - 1 of 1
- The genetics of autism spectrum disorder: family based translational research on rare variantsFrom1 Aug 2014 → 10 Sep 2018Funding: Own budget, for example: patrimony, inscription fees, gifts
Publications
1 - 10 of 12
- 8p21.3 deletions are rare causes of non-syndromic autism spectrum disorder(2021)
Authors: Nele Cosemans, Jarymke Maljaars, Annick Vogels, Koenraad Devriendt, Jean Steyaert, Kris Van Den Bogaert, Ilse Noens, Hilde Peeters
Pages: 207 - 213 - The clinical relevance of intragenic NRXN1 deletions(2020)
Authors: Nele Cosemans, Annick Vogels, Koenraad Devriendt, Hilde Van Esch, Griet Van Buggenhout, Thomy de Ravel de l'Argentière, Els Ortibus, Eric Legius, Jeroen Breckpot, Joris Vermeesch, et al.
Pages: 347 - 355 - Increased Ca2+ signaling in NRXN1a(+/-) neurons derived from ASD induced pluripotent stem cells(2019)
Authors: Nele Cosemans, Hilde Peeters
- The genetics of autism spectrum disorder: family based translational research on rare variants(2018)
Authors: Nele Cosemans, Hilde Peeters, Ilse Noens, Peter Claes
- Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next-generation sequencing(2018)
Authors: Molka Kammoun, Erika Souche, Jia Ding, Nele Cosemans, Koenraad Devriendt, Jan Deprest, Joris Vermeesch
Pages: 654 - 663 - ZNF462 and KLF12 are disrupted by a de novo translocation in a patient with syndromic intellectual disability and autism spectrum disorder(2018)
Authors: Nele Cosemans, Laura Vandenhove, Jarymke Maljaars, Hilde Van Esch, Koenraad Devriendt, Jean-Pierre Frijns, Ilse Noens, Hilde Peeters
Pages: 376 - 383 - Noise-robust assessment of SNP array based CNV calls through local noise estimation of log R ratios(2018)
Authors: Nele Cosemans, Peter Claes, Nathalie Brison, Joris Vermeesch, Hilde Peeters
- CLINICAL CHARACTERISATION OF NEUREXIN1 DELETIONS AND THEIR ROLE IN NEURODEVELOPMENTAL DISORDERS(2017)
Authors: Jacqueline Fitzgerald, Jeremy Hall, Marianne Van Den Bree, Linh Duong, Thomas Werge, Richard Delorme, Anne-Claude Tabet, Hilde Peeters, Nele Cosemans, Ilse Noens, et al.
Pages: S181 - S182 - Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator(2017)
Authors: Nele Cosemans, Jeroen Breckpot, Thomy de Ravel de l'Argentière, Griet Van Buggenhout, Hilde Peeters, Prosper Lukusa-Tshilobo, Koenraad Devriendt
Pages: 166 - 171 - Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases(2017)
Authors: Nele Cosemans, Hilde Peeters
Pages: 515 - 526