Pages that link to "Q37389746"
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The following pages link to Cristen J. Willer (Q37389746):
Displaying 50 items.
- Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution (Q21092459) (← links)
- Genetic studies of body mass index yield new insights for obesity biology (Q22305005) (← links)
- Common variants at 30 loci contribute to polygenic dyslipidemia (Q24598765) (← links)
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (Q24609915) (← links)
- Biological, clinical and population relevance of 95 loci for blood lipids (Q24622541) (← links)
- Hundreds of variants clustered in genomic loci and biological pathways affect human height (Q24630979) (← links)
- MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes (Q24635938) (← links)
- Common variants near MC4R are associated with fat mass, weight and risk of obesity (Q24641880) (← links)
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (Q24646434) (← links)
- Newly identified loci that influence lipid concentrations and risk of coronary artery disease (Q28264535) (← links)
- The power of meta-analysis in genome-wide association studies (Q28658972) (← links)
- Common variants associated with plasma triglycerides and risk for coronary artery disease (Q28659915) (← links)
- Discovery and refinement of loci associated with lipid levels (Q28661470) (← links)
- WikiGWA: an open platform for collecting and using genome-wide association results (Q28703576) (← links)
- A genome-wide association search for type 2 diabetes genes in African Americans (Q28740367) (← links)
- Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (Q28943288) (← links)
- Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease (Q29147547) (← links)
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (Q29417138) (← links)
- Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (Q29547208) (← links)
- Rare and low-frequency coding variants alter human adult height (Q29583867) (← links)
- Genome-wide association study identifies eight loci associated with blood pressure (Q29614414) (← links)
- Genotype imputation (Q29614590) (← links)
- LocusZoom: regional visualization of genome-wide association scan results (Q29614868) (← links)
- Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study (Q29615729) (← links)
- Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals (Q30276496) (← links)
- Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans. (Q30362046) (← links)
- Loss-of-function mutations in APOC3, triglycerides, and coronary disease (Q30408720) (← links)
- Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol (Q30411390) (← links)
- Common variants in the GDF5-UQCC region are associated with variation in human height (Q30435234) (← links)
- Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels (Q30441439) (← links)
- Association of exome sequences with plasma C-reactive protein levels in >9000 participants (Q30459027) (← links)
- A reference panel of 64,976 haplotypes for genotype imputation (Q33553419) (← links)
- Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve (Q33762797) (← links)
- Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations (Q33858783) (← links)
- No large-effect low-frequency coding variation found for myocardial infarction (Q33991765) (← links)
- Common variants show predicted polygenic effects on height in the tails of the distribution, except in extremely short individuals (Q34126353) (← links)
- Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (Q34142739) (← links)
- Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk (Q34213805) (← links)
- Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals (Q34221038) (← links)
- Defining the role of common variation in the genomic and biological architecture of adult human height (Q34441746) (← links)
- Twin concordance and sibling recurrence rates in multiple sclerosis. (Q34542659) (← links)
- Microchimerism in autoimmunity and transplantation: potential relevance to multiple sclerosis (Q34646812) (← links)
- Genomic inflation factors under polygenic inheritance (Q35108650) (← links)
- New genetic loci link adipose and insulin biology to body fat distribution (Q35114362) (← links)
- Genetically determined height and coronary artery disease (Q36288162) (← links)
- Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese (Q36438048) (← links)
- New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk (Q36541220) (← links)
- Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease (Q36851336) (← links)
- Finding genes and variants for lipid levels after genome-wide association analysis (Q36882615) (← links)
- Large-scale association analysis identifies new risk loci for coronary artery disease (Q36921066) (← links)