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Kerstin Wittemeyer

Researcher at University of Birmingham

Publications -  16
Citations -  6545

Kerstin Wittemeyer is an academic researcher from University of Birmingham. The author has contributed to research in topics: Autism & Genome-wide association study. The author has an hindex of 12, co-authored 16 publications receiving 6029 citations. Previous affiliations of Kerstin Wittemeyer include University of Toulouse & University of Oxford.

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Functional impact of global rare copy number variation in autism spectrum disorders

Dalila Pinto, +181 more
- 15 Jul 2010 - 
TL;DR: The genome-wide characteristics of rare (<1% frequency) copy number variation in ASD are analysed using dense genotyping arrays to reveal many new genetic and functional targets in ASD that may lead to final connected pathways.
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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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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.
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A genome-wide scan for common alleles affecting risk for autism

Richard Anney, +170 more
TL;DR: In one of four primary association analyses, the association signal for marker rs4141463, located within MACROD2, crossed the genome-wide association significance threshold of P < 5 × 10−8 and, consistent with the winner's curse, its effect size in the replication sample was much smaller.