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Department of Human Genetics,
Donders Institute for Brain,
Cognition and Behaviour,
Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour
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Neuroinformatic analyses of common and distinct genetic components associated with major neuropsychiatric disorders.
Frontiers in neuroscience , 2014 | Pubmed ID: 25414627
Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules.
American journal of human genetics Jan, 2016 | Pubmed ID: 26748517
De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila.
European journal of human genetics : EJHG Aug, 2016 | Pubmed ID: 26757981
Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders.
American journal of human genetics Mar, 2016 | Pubmed ID: 26942287
BOD1 Is Required for Cognitive Function in Humans and Drosophila.
PLoS genetics May, 2016 | Pubmed ID: 27166630
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.
Nature genetics Apr, 2017 | Pubmed ID: 28191889
Radboud university medical center
Ilse Eidhof*,1,
Michaela Fenckova*,1,
Dei M. Elurbe2,
Bart van de Warrenburg3,
Anna Castells Nobau*,1,
Annette Schenck*,1
1Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center,
2Centre for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center,
3Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center
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