about
Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitisSequence variants affecting eosinophil numbers associate with asthma and myocardial infarctionGenome-wide association study of blood lead shows multiple associations near ALADGenome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohortsA genome-wide association meta-analysis identifies new childhood obesity loci.Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.Common variation near ROBO2 is associated with expressive vocabulary in infancy.LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.The association of C-reactive protein and CRP genotype with coronary heart disease: findings from five studies with 4,610 cases amongst 18,637 participantsThe longitudinal association of common susceptibility variants for type 2 diabetes and obesity with fasting glucose level and BMI.Apolipoprotein E genotype is associated with serum C-reactive protein but not abdominal aortic aneurysmPhenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment.Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight.Association between common variation at the FTO locus and changes in body mass index from infancy to late childhood: the complex nature of genetic association through growth and development.Hospitalisation with infection, asthma and allergy in Kawasaki disease patients and their families: genealogical analysis using linked population data.Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studiesGenome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitizationGenome-wide association study to identify the genetic determinants of otitis media susceptibility in childhoodModelling BMI trajectories in children for genetic association studiesA comprehensive investigation of variants in genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1/R2), and their association with serum adiponectin, type 2 diabetes, insulin resistance and the metabolic syndrome.Genome-wide associations for birth weight and correlations with adult diseaseA population-based study of polymorphisms in genes related to sex hormones and abdominal aortic aneurysmAssociation of genetic Loci with glucose levels in childhood and adolescence: a meta-analysis of over 6,000 children.Genetic variants in adult bone mineral density and fracture risk genes are associated with the rate of bone mineral density acquisition in adolescenceA novel common variant in DCST2 is associated with length in early life and height in adulthoodLoci affecting gamma-glutamyl transferase in adults and adolescents show age × SNP interaction and cardiometabolic disease associations.A genome-wide association study of body mass index across early life and childhoodGenome-wide meta-analysis of common variant differences between men and women.Genetic influences on trajectories of systolic blood pressure across childhood and adolescenceNew loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolismCommon variants at 12q15 and 12q24 are associated with infant head circumference.Association of adiposity genetic variants with menarche timing in 92,105 women of European descentAssociation of a body mass index genetic risk score with growth throughout childhood and adolescence.Common variation contributes to the genetic architecture of social communication traits.Sequence variants in three loci influence monocyte counts and erythrocyte volume.Using Mendelian randomization to determine causal effects of maternal pregnancy (intrauterine) exposures on offspring outcomes: Sources of bias and methods for assessing them.Shared genetic variants suggest common pathways in allergy and autoimmune diseases.Analyses of associations with asthma in four asthma population samples from Canada and Australia.Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Nicole M Warrington
@ast
Nicole M Warrington
@en
Nicole M Warrington
@es
Nicole M Warrington
@nl
Nicole M Warrington
@sl
type
label
Nicole M Warrington
@ast
Nicole M Warrington
@en
Nicole M Warrington
@es
Nicole M Warrington
@nl
Nicole M Warrington
@sl
altLabel
Nicole Warrington
@en
prefLabel
Nicole M Warrington
@ast
Nicole M Warrington
@en
Nicole M Warrington
@es
Nicole M Warrington
@nl
Nicole M Warrington
@sl
P1053
P-4868-2014
P106
P1153
57200630008
P21
P2798
P31
P3829
P496
0000-0003-4195-775X