Pages that link to "Q36508365"
The following pages link to Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes. (Q36508365):
Displaying 50 items.
- Genetics of Insulin Resistance and the Metabolic Syndrome (Q26745624) (← links)
- Challenges in elucidating the genetics of diabetic retinopathy (Q26998699) (← links)
- Pharmacogenomics of adverse drug reactions (Q27015820) (← links)
- Insights from exome sequencing for endocrine disorders (Q28088772) (← links)
- Gene-Lifestyle Interactions in Complex Diseases: Design and Description of the GLACIER and VIKING Studies (Q28397345) (← links)
- Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels (Q28596453) (← links)
- The genetic architecture of type 2 diabetes (Q29583824) (← links)
- Molecular Analysis of Alternative Transcripts of the Equine Cordon-Bleu WH2 Repeat Protein-Like 1 (COBLL1) Gene. (Q30374254) (← links)
- Type 2 diabetes: genetic data sharing to advance complex disease research (Q30390388) (← links)
- Association of exome sequences with plasma C-reactive protein levels in >9000 participants (Q30459027) (← links)
- β-cell failure in type 2 diabetes: postulated mechanisms and prospects for prevention and treatment (Q33570085) (← links)
- High frequency of rare variants with a moderate-to-high predicted biological effect in protocadherin genes of extremely obese (Q33632927) (← links)
- Pleiotropic genes for metabolic syndrome and inflammation (Q34005816) (← links)
- A polygenic burden of rare disruptive mutations in schizophrenia (Q34060200) (← links)
- Blood pressure levels in male carriers of Arg82Cys in CD300LG (Q34338304) (← links)
- The promise of whole-exome sequencing in medical genetics (Q34382912) (← links)
- Studies of association of AGPAT6 variants with type 2 diabetes and related metabolic phenotypes in 12,068 Danes (Q34508391) (← links)
- Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets (Q34765381) (← links)
- Dynamic changes in endothelial cell adhesion molecule nepmucin/CD300LG expression under physiological and pathological conditions. (Q35078143) (← links)
- A glycogene mutation map for discovery of diseases of glycosylation (Q35152903) (← links)
- A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes (Q35209761) (← links)
- Genetics of type 2 diabetes-pitfalls and possibilities (Q35227765) (← links)
- Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population (Q35588251) (← links)
- Exome sequencing followed by genotyping suggests SYPL2 as a susceptibility gene for morbid obesity (Q35959652) (← links)
- Reduced CD300LG mRNA tissue expression, increased intramyocellular lipid content and impaired glucose metabolism in healthy male carriers of Arg82Cys in CD300LG: a novel genometabolic cross-link between CD300LG and common metabolic phenotypes (Q36008752) (← links)
- Recent advances in understanding the genetic architecture of type 2 diabetes (Q36065329) (← links)
- Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes (Q36536523) (← links)
- The impact of low-frequency and rare variants on lipid levels (Q36591109) (← links)
- A Human Variant of Glucose-Regulated Protein 94 That Inefficiently Supports IGF Production (Q36911625) (← links)
- Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes (Q37367893) (← links)
- Vejle Diabetes Biobank - a resource for studies of the etiologies of diabetes and its comorbidities (Q37376704) (← links)
- Meta-analysis of gene-level tests for rare variant association (Q37610893) (← links)
- Genetic discoveries in hypertension: steps on the road to therapeutic translation (Q38087825) (← links)
- The potential of novel biomarkers to improve risk prediction of type 2 diabetes (Q38146916) (← links)
- Genetic susceptibility to type 2 diabetes and obesity: from genome-wide association studies to rare variants and beyond (Q38214522) (← links)
- Insights into the genetic susceptibility to type 2 diabetes from genome-wide association studies of glycaemic traits. (Q38262599) (← links)
- Recent Progress in the Understanding of Obesity: Contributions of Genome-Wide Association Studies (Q38587726) (← links)
- The Hoorn Diabetes Care System (DCS) cohort. A prospective cohort of persons with type 2 diabetes treated in primary care in the Netherlands (Q38674042) (← links)
- Pancreatic Islet Protein Complexes and Their Dysregulation in Type 2 Diabetes (Q38803129) (← links)
- Next generation sequencing: implications in personalized medicine and pharmacogenomics (Q38804924) (← links)
- Complex Genetics of Type 2 Diabetes and Effect Size: What have We Learned from Isolated Populations? (Q38816592) (← links)
- Diabetes in Population Isolates: Lessons from Greenland (Q38816596) (← links)
- Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family-Based Linkage and Association in the IRAS Family Study (Q39032260) (← links)
- MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing (Q40621425) (← links)
- Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project (Q40983057) (← links)
- Variation and association to diabetes in 2000 full mtDNA sequences mined from an exome study in a Danish population (Q43177334) (← links)
- Exome-wide association study of plasma lipids in >300,000 individuals (Q45071322) (← links)
- Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes (Q47677207) (← links)
- Exome-chip association analysis reveals an Asian-specific missense variant in PAX4 associated with type 2 diabetes in Chinese individuals. (Q48477844) (← links)
- A Decade of Genetic and Metabolomic Contributions to Type 2 Diabetes Risk Prediction (Q48561722) (← links)