Céline Helsmoortel

Céline Helsmoortel

University of Antwerp - Antwerp / Belgium
Medical and Health Sciences / Medical Genetics
AD Scientific Index ID: 1389813
Universiteit Antwerpen
person_outline Céline Helsmoortel's MOST POPULAR ARTICLES
1-) A SWI/SNF-related autism syndrome caused by de novo mutations in ADNPC Helsmoortel, AT Vulto-van Silfhout, BP Coe, G Vandeweyer, L Rooms, ...Nature genetics 46 (4), 380-384, 20142812014
2-) Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt SignalingLS Blok, E Madsen, J Juusola, C Gilissen, D Baralle, MRF Reijnders, ...The American Journal of Human Genetics, 20152302015
3-) Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disordersZ Iqbal, G Vandeweyer, M van der Voet, AM Waryah, MY Zahoor, ...Human molecular genetics 22 (10), 1960-1970, 20131612013
4-) The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autismG Vandeweyer, C Helsmoortel, A Van Dijck, AT Vulto‐van Silfhout, ...American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2014932014
5-) The Compassionate Side of Neuroscience: Tony Sermone’s Undiagnosed Genetic Journey—ADNP MutationI Gozes, C Helsmoortel, G Vandeweyer, N Van der Aa, F Kooy, ...Journal of Molecular Neuroscience, 1-7, 2015422015