about
Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart StudyThree-dimensional architecture of the isolated yeast nuclear pore complex: functional and evolutionary implicationsLarge-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.Using family-based imputation in genome-wide association studies with large complex pedigrees: the Framingham Heart Study.Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.Description of the Framingham Heart Study data for Genetic Analysis Workshop 13.Power and type I error rate of false discovery rate approaches in genome-wide association studies.Thyroid function and lipid subparticle sizes in patients with short-term hypothyroidism and a population-based cohort.CDKN1C/p57kip2 is a candidate tumor suppressor gene in human breast cancer.Handling linkage disequilibrium in linkage analysis using dense single-nucleotide polymorphismsGWAF: an R package for genome-wide association analyses with family data.Thyroid function and left ventricular structure and function in the Framingham Heart StudyA three-stage approach for genome-wide association studies with family data for quantitative traitsPower evaluations for family-based tests of association with incomplete parental genotypes.Analyze multivariate phenotypes in genetic association studies by combining univariate association tests.Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels.A comparison of strategies for analyzing dichotomous outcomes in genome-wide association studies with general pedigrees.Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.Role of SNAREs and H+-ATPase in the targeting of proton pump-coated vesicles to collecting duct cell apical membrane.An exome array study of the plasma metabolome.A novel cellular survival factor--the B2 subunit of vacuolar H+-ATPase inhibits apoptosis.Syntaxin 1A has a specific binding site in the H3 domain that is critical for targeting of H+-ATPase to apical membrane of renal epithelial cells.A genome-wide search for genes affecting circulating fibrinogen levels in the Framingham Heart Study.Genome-wide linkage analyses and candidate gene fine mapping for HDL3 cholesterol: the Framingham Study.The -174 IL-6 GG genotype is associated with a reduced risk of type 2 diabetes mellitus in a family sample from the National Heart, Lung and Blood Institute's Framingham Heart Study.Genome-wide search for genes affecting serum uric acid levels: the Framingham Heart Study.Epigenome-wide association studies identify DNA methylation associated with kidney function.Quantitative DNA fingerprinting may distinguish new primary breast cancer from disease recurrence.Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.The Third Generation Cohort of the National Heart, Lung, and Blood Institute's Framingham Heart Study: Design, Recruitment, and Initial ExaminationMaternal influence on blood pressure suggests involvement of mitochondrial DNA in the pathogenesis of hypertension: the Framingham Heart StudyEffect of linkage disequilibrium between markers in linkage and association analysesUsing linkage and association to identify and model genetic effects: summary of GAW15 Group 4Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levelsInteraction of normal and expanded CAG repeat sizes influences age at onset of Huntington diseaseGenome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulationGenetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processingAuthor Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive functionGenome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuriaTarget genes, variants, tissues and transcriptional pathways influencing human serum urate levels
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onderzoeker
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հետազոտող
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Qiong Yang
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Qiong Yang
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Qiong Yang
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Qiong Yang
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Qiong Yang
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Qiong Yang
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Qiong Yang
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Qiong Yang
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Qiong Yang
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Qiong Yang
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Qiong Yang
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Qiong Yang
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P106
P31
P496
0000-0002-3658-1375