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Herman van Engeland

Researcher at Utrecht University

Publications -  219
Citations -  22813

Herman van Engeland is an academic researcher from Utrecht University. The author has contributed to research in topics: Autism & Attention deficit hyperactivity disorder. The author has an hindex of 77, co-authored 219 publications receiving 21459 citations. Previous affiliations of Herman van Engeland include Icahn School of Medicine at Mount Sinai & University of Groningen.

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Journal ArticleDOI

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Peter Szatmari, +139 more
- 01 Mar 2007 - 
TL;DR: Linkage and copy number variation analyses implicate chromosome 11p12–p13 and neurexins, respectively, among other candidate loci, highlighting glutamate-related genes as promising candidates for contributing to ASDs.
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Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

Dalila Pinto, +131 more
TL;DR: For example, the authors analyzed 2,446 ASD-affected families and confirmed an excess of genic deletions and duplications in affected versus control groups (1.41-fold, p = 1.0 × 10(-5)) and an increase in affected subjects carrying exonic pathogenic CNVs overlapping known loci associated with dominant or X-linked ASD and intellectual disability.
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Theory of mind in schizophrenia: meta-analysis.

TL;DR: This meta-analysis showed significant and stable mentalising impairment in schizophrenia and the finding that patients in remission are also impaired favours the notion thatmentalising impairment represents a possible trait marker of schizophrenia.
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A meta-analytic review of stopping performance in attention-deficit/hyperactivity disorder: deficient inhibitory motor control?

TL;DR: Whether deficient inhibitory motor control is the core deficit of attention-deficit/hyperactivity disorder (ADHD) is discussed, and why it may be less crucial in children than in adults with ADHD.
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A genome-wide linkage and association scan reveals novel loci for autism

Lauren A. Weiss, +214 more
- 08 Oct 2009 - 
TL;DR: A linkage and association mapping study using half a million genome-wide single nucleotide polymorphisms in a common set of 1,031 multiplex autism families, implicating SEMA5A as an autism susceptibility gene.