about
WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture riskGenome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distributionCommon variants in left/right asymmetry genes and pathways are associated with relative hand skillGenetic determinants of height growth assessed longitudinally from infancy to adulthood in the northern Finland birth cohort 1966Genetic variation associated with differential educational attainment in adults has anticipated associations with school performance in childrenGWAS of 126,559 individuals identifies genetic variants associated with educational attainmentMR-PheWAS: hypothesis prioritization among potential causal effects of body mass index on many outcomes, using Mendelian randomizationMeta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitisA common variant of HMGA2 is associated with adult and childhood height in the general populationCommon variation in the FTO gene alters diabetes-related metabolic traits to the extent expected given its effect on BMIGenome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopiaCommon variants near MC4R are associated with fat mass, weight and risk of obesitySix new loci associated with body mass index highlight a neuronal influence on body weight regulationA common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesityThe CHRNA5-A3-B4 Gene Cluster and Smoking: From Discovery to TherapeuticsNewly identified loci that influence lipid concentrations and risk of coronary artery diseaseGenome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markersNew genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes riskA genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility lociNine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive errorMosaic structural variation in children with developmental disordersGenome-wide association study of blood lead shows multiple associations near ALADInflammation, insulin resistance, and diabetes--Mendelian randomization using CRP haplotypes points upstreamGenome wide association identifies common variants at the SERPINA6/SERPINA1 locus influencing plasma cortisol and corticosteroid binding globulinAssessing causality in the association between child adiposity and physical activity levels: a Mendelian randomization analysisThe causal effect of vitamin D binding protein (DBP) levels on calcemic and cardiometabolic diseases: a Mendelian randomization studyImproved imputation of low-frequency and rare variants using the UK10K haplotype reference panelDirectional dominance on stature and cognition in diverse human populationsCommon genetic variants associated with cognitive performance identified using the proxy-phenotype methodReplication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetesThe effect of elevated body mass index on ischemic heart disease risk: causal estimates from a Mendelian randomisation approachGenome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohortsA genome-wide association search for type 2 diabetes genes in African AmericansGenetic markers of adult obesity risk are associated with greater early infancy weight gain and growthA genome-wide association meta-analysis identifies new childhood obesity loci.Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.Body mass index: Has epidemiology started to break down causal contributions to health and disease?Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
P50
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P50
description
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Nicholas J Timpson
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Nicholas J Timpson
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Nicholas J. Timpson
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Nicholas J. Timpson
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Nicholas Timpson
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Nicholas J Timpson
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Nicholas J Timpson
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Nicholas J. Timpson
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Nicholas J. Timpson
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Nicholas Timpson
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Nic Timpson
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Nicholas J Timpson
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Nicholas Timpson
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prefLabel
Nicholas J Timpson
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Nicholas J Timpson
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Nicholas J. Timpson
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Nicholas J. Timpson
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Nicholas Timpson
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P1153
P1053
O-7548-2015
P106
P1153
35355373400
57197025508
57202570731
P21
P2798
P31
P3829
P3835
nicholas-timpson
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0000-0002-7141-9189