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Elemi J. Breetvelt

Researcher at Utrecht University

Publications -  25
Citations -  1330

Elemi J. Breetvelt is an academic researcher from Utrecht University. The author has contributed to research in topics: Population & Schizophrenia. The author has an hindex of 13, co-authored 23 publications receiving 1084 citations. Previous affiliations of Elemi J. Breetvelt include Centre for Addiction and Mental Health & University Health Network.

Papers
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Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

Gunter Schumann, +122 more
TL;DR: A genome-wide association study meta-analysis of ∼2.5 million directly genotyped or imputed SNPs with alcohol consumption among 12 population-based samples of European ancestry finds a genotype-specific expression of AUTS2 in 96 human prefrontal cortex samples and finds a regulator of alcohol consumption.

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

Gunter Schumann, +115 more
Journal ArticleDOI

Cognitive Decline Preceding the Onset of Psychosis in Patients With 22q11.2 Deletion Syndrome

TL;DR: In 22q11DS, early cognitive decline is a robust indicator of the risk of developing a psychotic illness, and these findings mirror those observed in idiopathic schizophrenia.
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Early interventions in risk groups for schizophrenia: what are we waiting for?

TL;DR: In this article, the authors investigated preventive interventions in high-risk children to mitigate or prevent the development of schizophrenia and related psychiatric disorders, and showed that the preventive interventions could improve stress resilience, optimize brain maturation, and prevent or alleviate adverse environmental circumstances.
Journal ArticleDOI

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.

Robert W. Davies, +44 more
- 09 Nov 2020 - 
TL;DR: Data show a shared genetic basis for schizophrenia and schizophrenia-related phenotypes and also highlight the future potential of polygenic scores for risk stratification among individuals with highly, but incompletely, penetrant genetic variants.