sameAs
Genome-wide association with bone mass and geometry in the Framingham Heart StudyNRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE ConsortiumGenome-wide association with select biomarker traits in the Framingham Heart StudyA mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass traitCommon variants at 30 loci contribute to polygenic dyslipidemiaCommon genetic determinants of vitamin D insufficiency: a genome-wide association studyTwelve type 2 diabetes susceptibility loci identified through large-scale association analysisGenome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetesVariants in MTNR1B influence fasting glucose levels.Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritisMendelian randomization studies do not support a causal role for reduced circulating adiponectin levels in insulin resistance and type 2 diabetesAssociation of the ADAM33 gene with asthma and bronchial hyperresponsivenessNew genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes riskLarge-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetesGenome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary functionTrans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin.Directional dominance on stature and cognition in diverse human populationsLow-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibilityStrategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyAssociation of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyCausal relationship between obesity and vitamin D status: bi-directional Mendelian randomization analysis of multiple cohortsA genome-wide association search for type 2 diabetes genes in African AmericansAssociation of variants in RETN with plasma resistin levels and diabetes-related traits in the Framingham Offspring StudyGenetic variation in GIPR influences the glucose and insulin responses to an oral glucose challengeGenome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibilityStratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.The genetic architecture of type 2 diabetesGenome-wide association study of subclinical interstitial lung disease in MESA.Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis.Evidence for large-scale gene-by-smoking interaction effects on pulmonary function.Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent strokeIntegrative pathway genomics of lung function and airflow obstruction.Association of a 62 Variants Type 2 Diabetes Genetic Risk Score With Markers of Subclinical Atherosclerosis: A Transethnic, Multicenter Study.Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study.Genome-wide association analysis identifies six new loci associated with forced vital capacityMeta-analysis investigating associations between healthy diet and fasting glucose and insulin levels and modification by loci associated with glucose homeostasis in data from 15 cohortsTransferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource.Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstructionAssociation of exome sequences with plasma C-reactive protein levels in >9000 participants.Genome-wide gene-environment interactions on quantitative traits using family data.
P50
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