about
Meta-analysis and imputation refines the association of 15q25 with smoking quantityGWAS of 126,559 individuals identifies genetic variants associated with educational attainmentCommon variants in SLC17A3 gene affect intra-personal variation in serum uric acid levels in longitudinal time seriesGenes predict village of origin in rural EuropeGenome-wide association analyses identify 18 new loci associated with serum urate concentrationsGenome-wide association study identifies five loci associated with lung functionGenetic variants in novel pathways influence blood pressure and cardiovascular disease riskNew loci associated with kidney function and chronic kidney diseaseHundreds of variants clustered in genomic loci and biological pathways affect human heightGenome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopiaPredictive value of 8 genetic loci for serum uric acid concentrationRuns of homozygosity in European populationsGenome-wide association study of anthropometric traits in Korcula Island, CroatiaSLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and goutLarge-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repairNew genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes riskNine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive errorMeta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levelsRare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWFThe role of host genetic factors in respiratory tract infectious diseases: systematic review, meta-analyses and field synopsisDirectional dominance on stature and cognition in diverse human populationsLow-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibilityGenome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levelsGenetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarizationGenome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular diseaseGenome-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 AmericansGenome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architectureMeta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive errorRare and low-frequency coding variants alter human adult heightCommon variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine.Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.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.The association between galactosylation of immunoglobulin G and body mass index.Employment outcomes among junior researchers in medicine in CroatiaGenome-wide association analysis identifies six new loci associated with forced vital capacityAssociation of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks
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P50
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Ozren Polasek
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Ozren Polasek
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Ozren Polasek
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Ozren Polašek
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P214
P1053
B-6002-2011
P106
P1153
8232027400
P21
P214
P31
P3829
P496
0000-0002-5765-1862
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viaf-305647554