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1. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

2. A Genome-Wide Association Study Identifies Blood Disorder–Related Variants Influencing Hemoglobin A1c With Implications for Glycemic Status in U.S. Hispanics/Latinos

3. Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

4. Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino Americans

5. GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations

6. Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep

7. The Epithelial Sodium Channel Is a Modifier of the Long-Term Nonprogressive Phenotype Associated with F508del CFTR Mutations

8. Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation?

10. Genome-Wide Association Study of Heavy Smoking and Daily/Nondaily Smoking in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)

11. SMIM1 absence is associated with reduced energy expenditure and excess weight

12. A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

13. The Genome of the Kinetoplastid Parasite, Leishmania major

14. The Genome Sequence of Trypanosoma cruzi, Etiologic Agent of Chagas Disease

15. Discovery of common and rare genetic risk variants for colorectal cancer

16. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications

17. Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

18. Multi-ancestry genome-wide analysis identifies common genetic variants for self-reported sleep duration and shared genetic effects

20. The trans-ancestral genomic architecture of glycemic traits

21. The genome sequence of Trypanosoma cruzi, etiologic agent of Chagas disease

22. Multi-ethnic GWAS and meta-analysis of sleep quality identify MPP6 as a novel gene that functions in sleep center neurons

23. The Trans-Ancestral Genomic Architecture of Glycaemic Traits

24. Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

25. SMIM1absence is associated with reduced energy expenditure and excess weight

26. A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

27. Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

28. Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

29. Discovery of common and rare genetic risk variants for colorectal cancer

30. Multi-ethnic GWAS and meta-analysis of sleep quality identify MPP6 as a novel gene that functions in sleep center neurons.

31. Discovery of common and rare genetic risk variants for colorectal cancer

32. Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino Americans

33. GWAS of QRS Duration Identifies New Loci Specific to Hispanic/Latino Populations Swenson Hispanic/Latino QRS GWAS

35. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries

36. Genetic variation near IRS1 is associated with adiposity and a favorable metabolic profile in US Hispanics/Latinos

37. Genetic variation near IRS 1 is associated with adiposity and a favorable metabolic profile in U.S.Hispanics/Latinos: IRS1Variation, Adiposity, and Metabolic Profile

38. Genome-Wide Association Study of Heavy Smoking and Daily/Nondaily Smoking in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)

39. A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A1c With Implications for Glycemic Status in U.S. Hispanics/Latinos.

40. Correction: Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis

41. Genetic variation nearIRS1is associated with adiposity and a favorable metabolic profile in U.S.Hispanics/Latinos

42. Exome Sequencing Identifies a GNPAT Variant Associated with Severe Iron Overload in HFE C282Y Homozygous Men with Extreme Phenotypes; Possible Role in Regulation of Hepcidin Expression

43. Exome Sequencing Identifies Genes and Variant Alleles Associated With Severity Of Iron Overload In Hemochromatosis HFE C282Y Homozygotes

44. Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

45. Exome Sequencing Identifies Genes and Variant Alleles Associated With Severity Of Iron Overload In Hemochromatosis HFE C282Y Homozygotes

47. Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis.

48. The Genome of the Kinetoplastid Parasite,Leishmania major

49. Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis.

50. Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

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