Zafar Iqbal

Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders

Zafar Iqbal, Geert Vandeweyer, Monique van der Voet et al. · Human Molecular Genetics · 2013 · 176 citations · Full text

Psychiatric Disorders, Genetics, Molecular Genetics +18

Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features

Valter Tucci, Tjitske Kleefstra, Andrea Hardy et al. · Journal of Clinical Investigation · 2014 · 137 citations · Full text

Brain Development, Genetics, Neurochemical Biomarkers +25

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers

Afif Hentati, Margaret A. Pericak‐Vance, Felicia Lennon et al. · Human Molecular Genetics · 1994 · 108 citations

Down Syndrome, Mendelian Disorder, Genetic Disorder +12

Disruption of the Podosome Adaptor Protein TKS4 (SH3PXD2B) Causes the Skeletal Dysplasia, Eye, and Cardiac Abnormalities of Frank-Ter Haar Syndrome

Zafar Iqbal, Pilar Cejudo-Martı́n, Arjan de Brouwer et al. · The American Journal of Human Genetics · 2010 · 101 citations · Full text

Frank-ter Haar Syndrome, Transcriptional Regulation, Genetic Disorder +7

De novo mutations in PLXND1 and REV3L cause Möbius syndrome

Laura Tomás‐Roca, Anastasia Tsaalbi‐Shtylik, Jacob G. Jansen et al. · Nature Communications · 2015 · 96 citations · Full text