Project
GENOMED - Genomics in Medicine.
Researchers
- Frank Kooy (Co-promoter)Duration: 1 Jan 2015 → 31 Dec 2019
- Bart Loeys (Co-promoter)Duration: 1 Jan 2015 → 31 Dec 2019
- Guy Van Camp (Co-promoter)Duration: 1 Jan 2015 → 31 Dec 2019
- Wim Van Hul (Co-promoter)
Medical genetics of obesity and skeletal disorders (MGENOS)
Duration: 1 Jan 2015 → 31 Dec 2019
Project partners
- Medical Genetics (MEDGEN) (Research group)
Project owner
From1 Jan 2015 → 31 Dec 2019 - Medical genetics of obesity and skeletal disorders (MGENOS) (Research group)From1 Jan 2015 → 31 Dec 2019
- Cognitive Genetics (COGNET) (Research group)From1 Jan 2015 → 31 Dec 2019
- Human molecular genetics (Research group)From1 Jan 2015 → 31 Dec 2019
Funding
1 - 1 of 1 results
- Funding: BOF - Other initiatives(Principal funding)
Funding party: Flemish Government
Policy level funding: Flemish
Publications
- Camurati-Engelmann disease(2019)
Authors: Wim Van Hul, Eveline Boudin, Geert Mortier
- Pathogenic variants in GPC4 cause Keipert syndrome(2019)
Authors: David J. Amor, Sarah E. M. Stephenson, Mirna Mustapha, Martin A. Mensah, Charlotte W. Ockeloen, Wei Shern Lee, Rick M. Tankard, Dean G. Phelan, Marwan Shinawi, Arjan P. M. de Brouwer, et al.
- Een patiënt met dense botten(2019)
Authors: Jasper Dierckx, Geert Mortier
- Clinical, molecular genetics and therapeutic aspects of syndromic obesity(2019)
Authors: Ellen Geets, Marije Meuwissen, Wim Van Hul
- A mouse model for intellectual disability caused by mutations in the X-linked 2'-O-methyltransferase Ftsj1 gene(2019)
Authors: Lars R. Jensen, Lillian Garrett, Sabine M. Hoelter, Birgit Rathkolb, Ildiko Racz, Thure Adler, Cornelia Prehn, Wolfgang Hans, Jan Rozman, Lore Becker, et al.
- Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants(2019)
Authors: Lucilla Pizzo, Matthew Jensen, Andrew Polyak, Jill A. Rosenfeld, Katrin Mannik, Arjun Krishnan, Elizabeth McCready, Olivier Pichon, Cedric Le Caignec, Anke Van Dijck, et al.
- Association of hereditary angioedema type 1 with developmental anomalies due to a large and unusual de novo pericentromeric rearrangement of chromosome 11 spanning the entire C1 inhibitor gene (SERPING1)(2019)
Authors: Didier Ebo, Bettina Blaumeiser, Frank Kooy, Sigri Beckers, Athina Van Gasse, Michael Saerens, Maarten Spinhoven, Vito Sabato, Hélène A. Poirel
- Discovery of autism/intellectual disability somatic mutations in Alzheimer's brains(2021)
Authors: Yanina Ivashko-Pachima, Adva Hadar, Iris Grigg, Vlasta Korenková, Oxana Kapitansky, Gidon Karmon, Michael Gershovits, C. Laura Sayas, Johannes Attems, David Gurwitz, et al.
- GABAergic abnormalities in the fragile X syndrome(2020)
Authors: Nathalie Van der Aa, Frank Kooy
- The translational regulator FMRP controls lipid and glucose metabolism in mice and humans(2019)
Authors: Antoine Leboucher, Didier F. Pisani, Laura Martinez-Gili, Julien Chilloux, Patricia Bermudez-Martin, Anke Van Dijck, Tariq Ganief, Boris Macek, Jerome A. J. Becker, Julie Le Merrer, et al.