Pages that link to "Q56864510"
Jump to navigation
Jump to search
The following pages link to Benjamin F. Voight (Q56864510):
Displayed 50 items.
- Jonathan K. Pritchard (Q6273523) (← links)
- Confounding from cryptic relatedness in case-control association studies (Q21092505) (← links)
- A map of recent positive selection in the human genome (Q21563624) (← links)
- From mouse to human: evolutionary genomics analysis of human orthologs of essential genes (Q22065247) (← links)
- Common variants at 30 loci contribute to polygenic dyslipidemia (Q24598765) (← links)
- A common variant of HMGA2 is associated with adult and childhood height in the general population (Q24603211) (← links)
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (Q24609915) (← links)
- A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease (Q24615584) (← links)
- Biological, clinical and population relevance of 95 loci for blood lipids (Q24622541) (← links)
- Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk (Q24630394) (← links)
- Hundreds of variants clustered in genomic loci and biological pathways affect human height (Q24630979) (← links)
- Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes (Q24635872) (← links)
- Common variants near MC4R are associated with fat mass, weight and risk of obesity (Q24641880) (← links)
- Variants in MTNR1B influence fasting glucose levels (Q24642630) (← links)
- Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans (Q24643492) (← links)
- Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants (Q24645076) (← links)
- Common missense variant in the glucokinase regulatory protein gene is associated with increased plasma triglyceride and C-reactive protein but lower fasting glucose concentrations (Q24650362) (← links)
- Convergent adaptation of human lactase persistence in Africa and Europe (Q24655819) (← links)
- Patterns and rates of exonic de novo mutations in autism spectrum disorders (Q28264242) (← links)
- New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Q28270700) (← links)
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (Q28272915) (← links)
- Identification of ten loci associated with height highlights new biological pathways in human growth (Q28275237) (← 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)
- A genome-wide association search for type 2 diabetes genes in African Americans (Q28740367) (← links)
- Practical aspects of imputation-driven meta-analysis of genome-wide association studies (Q28749837) (← links)
- Linkage disequilibrium mapping of the replicated type 2 diabetes linkage signal on chromosome 1q (Q28752440) (← links)
- Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia (Q28943439) (← links)
- Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge (Q29147442) (← links)
- An expanded sequence context model broadly explains variability in polymorphism levels across the human genome (Q29307337) (← links)
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (Q29417007) (← links)
- Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease (Q29417023) (← links)
- Common body mass index-associated variants confer risk of extreme obesity (Q29417063) (← links)
- Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases (Q29417103) (← links)
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (Q29417138) (← links)
- The genetic architecture of type 2 diabetes (Q29583824) (← links)
- Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study (Q29615729) (← links)
- Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci (Q30425020) (← links)
- Pervasive sharing of genetic effects in autoimmune disease (Q30431030) (← links)
- Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies (Q30499949) (← links)
- Interrogating multiple aspects of variation in a full resequencing data set to infer human population size changes (Q31026014) (← links)
- Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study (Q31060192) (← links)
- A central role for GRB10 in regulation of islet function in man. (Q31156020) (← links)
- Coverage and characteristics of the Affymetrix GeneChip Human Mapping 100K SNP set. (Q33242615) (← links)
- Relative contribution of type 1 and type 2 diabetes loci to the genetic etiology of adult-onset, non-insulin-requiring autoimmune diabetes (Q33601181) (← links)
- Serum calcium and risk of migraine: a Mendelian randomization study (Q33614592) (← links)
- Multiethnic genetic association studies improve power for locus discovery (Q33691513) (← links)
- Gene Set Enrichment Analyses: lessons learned from the heart failure phenotype (Q33733871) (← links)
- Loss-of-function mutations in SLC30A8 protect against type 2 diabetes (Q33734046) (← links)
- Testing for an unusual distribution of rare variants (Q33847792) (← links)