about
Genetic studies of body mass index yield new insights for obesity biologyCharacterization of large structural genetic mosaicism in human autosomeMeta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitisDetectable clonal mosaicism from birth to old age and its relationship to cancerDirectional dominance on stature and cognition in diverse human populationsThe Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditionsGenome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroupsPlasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosisGenome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption.Maternal contributions to preterm delivery.Genetic regulation of gene expression in the epileptic human hippocampus.Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis.Genome-wide association study identifies four loci associated with eruption of permanent teeth.Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studiesGenetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremiaParent-of-origin-specific allelic associations among 106 genomic loci for age at menarcheUsing family data as a verification standard to evaluate copy number variation calling strategies for genetic association studiesThe essence of linkage-based imprinting detection: comparing power, type 1 error, and the effects of confounders in two different analysis approaches.Use of macrolides in mother and child and risk of infantile hypertrophic pyloric stenosis: nationwide cohort studyDefining the role of common variation in the genomic and biological architecture of adult human height.Common variants associated with general and MMR vaccine-related febrile seizures.The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.Genome-wide associations for birth weight and correlations with adult diseaseX-chromosomal maternal and fetal SNPs and the risk of spontaneous preterm delivery in a Danish/Norwegian genome-wide association study.Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumptionSequence variants in oxytocin pathway genes and preterm birth: a candidate gene association studyGenome partitioning of genetic variation for complex traits using common SNPsGenome-wide association study identifies sequence variants on 6q21 associated with age at menarche.Mapping quantitative trait loci by an extension of the Haley-Knott regression method using estimating equationsReplication of a genome-wide association study of birth weight in preterm neonatesA novel common variant in DCST2 is associated with length in early life and height in adulthoodGenome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypesGenetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight.Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitisNew loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolismGenetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight.Genome-wide association analysis identifies three new susceptibility loci for childhood body mass indexCommon variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis.No observed association for mitochondrial SNPs with preterm delivery and related outcomes.Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances
P50
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P50
description
researcher, ORCID id # 0000-0003-1478-649X
@en
wetenschapper
@nl
name
Bjarke Feenstra
@ast
Bjarke Feenstra
@en
Bjarke Feenstra
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Bjarke Feenstra
@nl
type
label
Bjarke Feenstra
@ast
Bjarke Feenstra
@en
Bjarke Feenstra
@es
Bjarke Feenstra
@nl
prefLabel
Bjarke Feenstra
@ast
Bjarke Feenstra
@en
Bjarke Feenstra
@es
Bjarke Feenstra
@nl
P106
P31
P496
0000-0003-1478-649X