Stefaan Scheers

Microdeletions involving theSCN1A gene may be common inSCN1A-mutation-negative SMEI patients

Arvid Suls, Kristl G. Claeys, D. Goossens et al. · Human Mutation · 2006 · 115 citations

Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA)

Liesbeth Rooms, Edwin Reyniers, Rob van Luijk et al. · Human Mutation · 2003 · 105 citations

Cytogenetics, Neurological Disorder, Genetics +22

Multiplex ligation‐dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics

Liesbeth Rooms, Edwin Reyniers, Wim Wuyts et al. · Clinical Genetics · 2005 · 69 citations

Five patients with a chromosome 1q21.1 triplication show macrocephaly, increased weight and facial similarities

Anke Van Dijck, Ilse M. van der Werf, Edwin Reyniers et al. · European Journal of Medical Genetics · 2015 · 48 citations

Triplication Show Macrocephaly, Chromatin, Chromosome 1Q21.1 +10

TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions

Liesbeth Rooms, Edwin Reyniers, Stefaan Scheers et al. · European Journal of Human Genetics · 2006 · 40 citations · Full text

Subtelomeric 6Q, Psychiatry, Genetic Disorder +8