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Mitochondrial genetic variants identified to be associated with BMI in adultsGenetic studies of body mass index yield new insights for obesity biologyGenome-wide association analyses identify 18 new loci associated with serum urate concentrationsGenome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levelsMutation in the ARH gene and a chromosome 13q locus influence cholesterol levels in a new form of digenic-recessive familial hypercholesterolemiaNo evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning levelLarge-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repairGenome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanismsRare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWFDirectional dominance on stature and cognition in diverse human populationsBurden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsiesSystematic identification of trans eQTLs as putative drivers of known disease associationsThe genetic architecture of type 2 diabetesGenetic loci associated with heart rate variability and their effects on cardiac disease risk.Genome-wide analysis identifies 12 loci influencing human reproductive behavior.Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.Analyzing illumina gene expression microarray data from different tissues: methodological aspects of data analysis in the metaxpress consortiumGenetic analysis of phenotypes derived from longitudinal data: Presentation Group 1 of Genetic Analysis Workshop 13.Meta-Analysis of Genome-Wide Association Studies and Network Analysis-Based Integration with Gene Expression Data Identify New Suggestive Loci and Unravel a Wnt-Centric Network Associated with Dupuytren's Disease.Genome-wide methylation data mirror ancestry information.Quantitative trait linkage analysis of longitudinal change in body weight.Linkage analysis of alcohol dependence using MOD scores.Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.Investigating the causal effect of smoking on hay fever and asthma: a Mendelian randomization meta-analysis in the CARTA consortiumBreast cancer risk assessment across the risk continuum: genetic and nongenetic risk factors contributing to differential model performance.Lipoprotein (a) concentrations, apolipoprotein (a) phenotypes, and peripheral arterial disease in three independent cohorts.52 Genetic Loci Influencing Myocardial Mass.Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes.Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index.Genome-wide association study identifies 74 loci associated with educational attainment.Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.Study protocol: Transition from localized low back pain to chronic widespread pain in general practice: identification of risk factors, preventive factors and key elements for treatment--a cohort study.A comparison of different linkage statistics in small to moderate sized pedigrees with complex diseases.Defining the role of common variation in the genomic and biological architecture of adult human height.Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility lociTobacco smoking leads to extensive genome-wide changes in DNA methylation.Novel genetic associations with serum level metabolites identified by phenotype set enrichment analyses.Genome-wide linkage analysis of congenital heart defects using MOD score analysis identifies two novel lociEvidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level.
P50
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P50
name
Konstantin Strauch
@en
Konstantin Strauch
@nl
type
label
Konstantin Strauch
@en
Konstantin Strauch
@nl
prefLabel
Konstantin Strauch
@en
Konstantin Strauch
@nl