Pages that link to "Q91168271"
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The following pages link to Alisa Manning (Q91168271):
Displaying 50 items.
- 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)
- Variants in MTNR1B influence fasting glucose levels (Q24642630) (← links)
- New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Q28270700) (← links)
- Age-related clonal hematopoiesis associated with adverse outcomes (Q28386602) (← links)
- Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function (Q28392223) (← links)
- The study to understand the genetics of the acute response to metformin and glipizide in humans (SUGAR-MGH): design of a pharmacogenetic resource for type 2 diabetes (Q28545045) (← links)
- Testing the role of predicted gene knockouts in human anthropometric trait variation (Q28597672) (← links)
- A genome-wide association search for type 2 diabetes genes in African Americans (Q28740367) (← links)
- Association of variants in RETN with plasma resistin levels and diabetes-related traits in the Framingham Offspring Study (Q28755370) (← links)
- Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge (Q29147442) (← 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)
- The genetic architecture of type 2 diabetes (Q29583824) (← links)
- Rare and low-frequency coding variants alter human adult height (Q29583867) (← links)
- Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol (Q30411390) (← links)
- Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19. (Q31149227) (← links)
- The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports (Q33300809) (← links)
- Genome-wide association with diabetes-related traits in the Framingham Heart Study (Q33300811) (← links)
- Incorporating biological knowledge in the search for gene x gene interaction in genome-wide association studies. (Q33519385) (← links)
- Distribution and medical impact of loss-of-function variants in the Finnish founder population (Q33981677) (← links)
- Mining the LIPG allelic spectrum reveals the contribution of rare and common regulatory variants to HDL cholesterol (Q34102781) (← links)
- Genetic risk reclassification for type 2 diabetes by age below or above 50 years using 40 type 2 diabetes risk single nucleotide polymorphisms. (Q34141398) (← links)
- Pathway analysis following association study (Q34175618) (← 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)
- Variants in the CNR1 and the FAAH genes and adiposity traits in the community (Q34575400) (← links)
- Genotype score in addition to common risk factors for prediction of type 2 diabetes (Q34884376) (← links)
- Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus (Q35018875) (← links)
- Meta-analysis of gene-environment interaction: joint estimation of SNP and SNP × environment regression coefficients (Q35852977) (← links)
- No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels (Q35902855) (← links)
- A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study (Q36016822) (← links)
- TCF7L2 variants are associated with increased proinsulin/insulin ratios but not obesity traits in the Framingham Heart Study (Q36199575) (← links)
- A common polymorphism decreases low-density lipoprotein receptor exon 12 splicing efficiency and associates with increased cholesterol. (Q36613682) (← links)
- A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance (Q36731268) (← links)
- Haplotype structure of the ENPP1 Gene and Nominal Association of the K121Q missense single nucleotide polymorphism with glycemic traits in the Framingham Heart Study (Q36756473) (← links)
- Variants at the endocannabinoid receptor CB1 gene (CNR1) and insulin sensitivity, type 2 diabetes, and coronary heart disease (Q36940105) (← links)
- The challenge of detecting epistasis (G x G interactions): Genetic Analysis Workshop 16 (Q36954418) (← links)
- Common variants in the adiponectin gene (ADIPOQ) associated with plasma adiponectin levels, type 2 diabetes, and diabetes-related quantitative traits: the Framingham Offspring Study (Q36975510) (← links)
- An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group (Q37014024) (← links)
- Multiple testing in the genomics era: findings from Genetic Analysis Workshop 15, Group 15. (Q37018787) (← links)
- Ordered stratification to reduce heterogeneity in linkage to diabetes-related quantitative traits (Q37105829) (← links)
- Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension (Q37324554) (← links)
- Mapping quantitative traits in unselected families: algorithms and examples (Q37396852) (← links)
- Independent test assessment using the extreme value distribution theory (Q37464371) (← links)
- Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits (Q38759579) (← links)
- Prosaposin is a regulator of progranulin levels and oligomerization (Q38847140) (← links)
- A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk (Q38877389) (← links)
- Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci (Q39601786) (← links)
- A method of moments estimator for random effect multivariate meta-analysis (Q39855140) (← links)
- The (in)famous GWAS P-value threshold revisited and updated for low-frequency variants (Q40143010) (← links)
- Variation in Maturity-Onset Diabetes of the Young Genes Influence Response to Interventions for Diabetes Prevention (Q40223049) (← links)
- A 100K genome-wide association scan for diabetes and related traits in the Framingham Heart Study: replication and integration with other genome-wide datasets (Q44797798) (← links)