Pages that link to "Q34372347"
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The following pages link to The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits (Q34372347):
Displaying 50 items.
- Genetic studies of body mass index yield new insights for obesity biology (Q22305005) (← links)
- In search of low-frequency and rare variants affecting complex traits (Q24618492) (← links)
- A global reference for human genetic variation (Q25909434) (← links)
- Genetics of Insulin Resistance and the Metabolic Syndrome (Q26745624) (← links)
- Recent progress in genetic and epigenetic research on type 2 diabetes (Q26766482) (← links)
- Making sense of GWAS: using epigenomics and genome engineering to understand the functional relevance of SNPs in non-coding regions of the human genome (Q26771497) (← links)
- Insights into blood lipids from rare variant discovery (Q26799138) (← links)
- Analysis of protein-coding genetic variation in 60,706 humans (Q26831375) (← links)
- Analysis of protein-coding genetic variation in 60,706 humans (Q26831376) (← links)
- Rare-variant association analysis: study designs and statistical tests (Q26852733) (← links)
- Genetics of coronary artery disease (Q26866396) (← links)
- A review of post-GWAS prioritization approaches (Q26995408) (← links)
- Exome sequencing and complex disease: practical aspects of rare variant association studies (Q27027055) (← links)
- Genetic loci on chromosome 5 are associated with circulating levels of interleukin-5 and eosinophil count in a European population with high risk for cardiovascular disease (Q27315831) (← links)
- Genetic Research and Women's Heart Disease: a Primer (Q28069638) (← links)
- A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease (Q28267020) (← links)
- Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers (Q28267312) (← links)
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (Q28272915) (← links)
- Pleiotropy in complex traits: challenges and strategies (Q28390545) (← links)
- Analysis of metabolic syndrome components in >15 000 african americans identifies pleiotropic variants: results from the population architecture using genomics and epidemiology study (Q28392948) (← links)
- Gene-Lifestyle Interactions in Complex Diseases: Design and Description of the GLACIER and VIKING Studies (Q28397345) (← links)
- Association of Cardiometabolic Genes with Arsenic Metabolism Biomarkers in American Indian Communities: The Strong Heart Family Study (SHFS) (Q28397971) (← links)
- Metabolic signatures of adiposity in young adults: Mendelian randomization analysis and effects of weight change (Q28542592) (← links)
- Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization (Q28654771) (← links)
- Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data (Q28655857) (← links)
- Quality control and conduct of genome-wide association meta-analyses (Q28656219) (← links)
- Discovery and refinement of loci associated with lipid levels (Q28661470) (← links)
- Population genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) Consortium (Q28681745) (← links)
- The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation (Q28685216) (← links)
- Circadian clock-related genetic risk scores and risk of placental abruption (Q28917067) (← links)
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (Q29417007) (← links)
- A Hidden Markov Model Approach for Simultaneously Estimating Local Ancestry and Admixture Time Using Next Generation Sequence Data in Samples of Arbitrary Ploidy (Q30000284) (← links)
- Causal Associations of Adiposity and Body Fat Distribution with Coronary Heart Disease, Stroke Subtypes and Type 2 Diabetes: A Mendelian Randomization Analysis (Q30252417) (← links)
- Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci (Q30252583) (← links)
- Fine mapping of QT interval regions in global populations refines previously identified QT interval loci and identifies signals unique to African and Hispanic descent populations (Q30275202) (← links)
- Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans (Q30275744) (← links)
- Multi-ethnic analysis reveals soluble L-selectin may be post-transcriptionally regulated by 3'UTR polymorphism: the Multi-Ethnic Study of Atherosclerosis (MESA). (Q30359866) (← links)
- The architecture of risk for type 2 diabetes: understanding Asia in the context of global findings. (Q30361503) (← links)
- Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations (Q30370866) (← links)
- Type 2 diabetes: genetic data sharing to advance complex disease research (Q30390388) (← links)
- Mendelian randomization of blood lipids for coronary heart disease (Q30407506) (← links)
- Evidence of a causal relationship between adiponectin levels and insulin sensitivity: a Mendelian randomization study (Q30538088) (← links)
- Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data (Q30574894) (← links)
- Imputation of coding variants in African Americans: better performance using data from the exome sequencing project (Q30662194) (← links)
- Genetic Predictors of Depressive Symptoms in the Look AHEAD Trial (Q30676637) (← links)
- Joint analysis of functional genomic data and genome-wide association studies of 18 human traits (Q30794057) (← links)
- Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data (Q30799619) (← links)
- Across-cohort QC analyses of GWAS summary statistics from complex traits (Q30832101) (← links)
- Harmonization of study and reference data by PhaseLift: saving time when imputing study data (Q30833273) (← links)
- Extension of GWAS results for lipid-related phenotypes to extreme obesity using electronic health record (EHR) data and the Metabochip (Q30844245) (← links)