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1. Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height

2. Bioinformatics pipeline for the systematic mining genomic and proteomic variation linked to rare diseases: The example of monogenic diabetes.

3. Building a collaborative cloud platform to accelerate heart, lung, blood, and sleep research.

4. Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthmaResearch in context

6. Deriving stratified effects from joint models investigating gene-environment interactions

8. Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration

9. Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

10. New insights into the genetic etiology of Alzheimer's disease and related dementias

11. Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease

12. A systematic mapping of the genomic and proteomic variation associated with monogenic diabetes

13. Abstract 66: Clonal Hematopoiesis of Indeterminate Potential and Incident Type 2 Diabetes Risk

14. The power of TOPMed imputation for the discovery of Latino enriched rare variants associated with type 2 diabetes

15. 137-OR: A Genetic Approach to Detangling the Heterogeneity of Fasting Insulin Levels

16. Opportunities and challenges for the use of common controls in sequencing studies

17. Nontargeted and Targeted Metabolomic Profiling Reveals Novel Metabolite Biomarkers of Incident Diabetes in African Americans

18. Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus.

19. Distribution and medical impact of loss-of-function variants in the Finnish founder population.

20. 73-OR: Clonal Hematopoiesis of Indeterminate Potential (CHIP), Glycemic Traits, and Type 2 Diabetes (T2D) Risk

22. The First Genome-Wide Association Study (GWAS) for Type 2 Diabetes in Youth from the Progress in Diabetes Genetics in Youth (ProDiGY) Collaboration

23. Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms

24. Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

25. Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland

26. Multiple testing in the genomics era: findings from Genetic Analysis Workshop 15, Group 15

27. The Type 2 Deiodinase (DIO2) A/G Polymorphism Is Not Associated with Glycemic Traits: The Framingham Heart Study.

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