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
1 - 10 of 77
- Protein interaction network analysis reveals genetic enrichment of immune system genes in frontotemporal dementia(2022)
Authors: Cemile Kocoglu, Raffaele Ferrari, Maxime Roes, Geert Vandeweyer, Frank Kooy, Christine Van Broeckhoven, Claudia Manzoni, Julie van der Zee
Pages: 67 - 79 - Gaps in current autism research(2019)
Authors: David G. Amaral, George M. Anderson, Anthony Bailey, Raphe Bernier, Somer Bishop, Gene Blatt, Ricardo Canal‐Bedia, Tony Charman, Geraldine Dawson, Petrus J. Vries, et al.
Pages: 700 - 714 - Diagnostic implications of genetic copy number variation in epilepsy plus(2019)
Authors: Antonietta Coppola, Elena Cellini, Hannah Stamberger, Elmo Saarentaus, Valentina Cetica, Dennis Lal, Tania Djémié, Magdalena Bartnik-Glaska, Berten Ceulemans, J. Helen Cross, et al.
Pages: 689 - 706 - ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs(2019)
Authors: Marina T. DiStefano, Sarah E. Hemphill, Andrea M. Oza, Guy Van Camp, et al.
Pages: 2239 - 2247 - Arterial tortuosity novel implications for an old phenotype(2019)
Authors: Simina Ciurica, Marilucy Lopez-Sublet, Bart Loeys, Ibtissem Radhouani, Nalin Natarajan, Miikka Vikkula, Angela H. E. M. Maas, David Adlam, Alexandre Persu
Pages: 951 - 960 - Comparison of biomechanical properties in ascending aortic aneurysms of patients with congenital bicuspid aortic valve and Marfan syndrome(2019)
Authors: Junfeng Yan, Ann-Cathrin Lehsau, Benjamin Sauer, Barbara Pieper, Salah A. Mohamed, Bart Loeys, Harry C. Dietz, Lut Van Laer, Andrew S. McCallion, Per Eriksson, et al.
Pages: 65 - 69 - Clinical presentation of a complex neurodevelopmental disorder caused by mutations in ADNP(2019)
Authors: Anke Van Dijck, Anneke T. Vulto-van Silfhout, Elisa Cappuyns, Ilse van der Werf, Grazia M. Mancini, Andreas Tzschach, Raphael Bernier, Illana Gozes, Evan E. Eichler, Corrado Romano, et al.
Pages: 287 - 297 - ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm(2019)
Authors: Russell A. Gould, Hamza Aziz, Courtney E. Woods, Manuel Alejandro Seman-Senderos, Elizabeth Sparks, Christoph Preuss, Florian Wunnemann, Djahida Bedja, Cassandra R. Moats, Sarah A. McClymont, et al.
Pages: 42 - 50 - Camurati-Engelmann disease(2019)
Authors: Wim Van Hul, Eveline Boudin, Geert Mortier
Pages: 554 - 560 - 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.
Pages: 914 - 924