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B.W.J.H. Penninx

Researcher at VU University Medical Center

Publications -  78
Citations -  3576

B.W.J.H. Penninx is an academic researcher from VU University Medical Center. The author has contributed to research in topics: Major depressive disorder & Anxiety. The author has an hindex of 23, co-authored 65 publications receiving 2914 citations. Previous affiliations of B.W.J.H. Penninx include Public Health Research Institute.

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Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group.

Lianne Schmaal, +93 more
- 01 Jun 2017 - 
TL;DR: In this article, the authors present the largest ever worldwide study by the ENIGMA (Enhancing Neuro Imaging Genetics through Meta-Analysis) Major Depressive Disorder Working Group on cortical structural alterations in MDD.
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Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo

TL;DR: A genome-wide association study of single nucleotide polymorphisms genotyped in 1738 MDD cases and 1802 controls selected to be at low liability for MDD found 11 signals localized to a 167 kb region overlapping the gene piccolo, whose protein product localizes to the cytomatrix of the presynaptic active zone and is important in monoaminergic neurotransmission in the brain.
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Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations

Yukinori Okada, +414 more
- 01 Aug 2012 - 
TL;DR: A meta-analysis of genome-wide association studies for kidney function–related traits, including 71,149 east Asian individuals from 18 studies in 11 population-, hospital- or family-based cohorts, conducted as part of the Asian Genetic Epidemiology Network (AGEN), identified 17 loci newly associated with kidney function-related traits.
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Polygenic dissection of major depression clinical heterogeneity

TL;DR: Polygenic features of major depressive disorder and two common clinical subtypes defined by symptom profiles in a large sample of adults with established diagnoses are examined, finding that subtypes are characterized by partially distinct polygenic liabilities and may represent more homogeneous phenotypes.