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115 results on '"Mohlke, K.L."'

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1. Genetic insights into resting heart rate and its role in cardiovascular disease.

3. Identification of novel candidate genes and variants for hearing loss and temporal bone anomalies

4. Genetic effects on liver chromatin accessibility identify disease regulatory variants

5. Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts

6. Assessing exposure effects on gene expression

7. Inferring Regulatory Networks From Mixed Observational Data Using Directed Acyclic Graphs

8. A New Liver Expression Quantitative Trait Locus Map From 1,183 Individuals Provides Evidence for Novel Expression Quantitative Trait Loci of Drug Response, Metabolic, and Sex-Biased Phenotypes

9. The Polygenic and Monogenic Basis of Blood Traits and Diseases

10. Enhancer deletion and allelic effects define a regulatory molecular mechanism at the VLDLR cholesterol GWAS locus

11. A2ML1 and otitis media: novel variants, differential expression, and relevant pathways

12. Associations of autozygosity with a broad range of human phenotypes

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

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

15. Deciphering the Emerging Complexities of Molecular Mechanisms at GWAS Loci

16. FUT2 Variants Confer Susceptibility to Familial Otitis Media

17. Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

18. Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article

19. Phenotype-Specific Enrichment of Mendelian Disorder Genes near GWAS Regions across 62 Complex Traits

20. A Common Type 2 Diabetes Risk Variant Potentiates Activity of an Evolutionarily Conserved Islet Stretch Enhancer and Increases C2CD4A and C2CD4B Expression

21. A partial loss-of-function variant in AKT2 is associated with reduced insulin-mediated glucose uptake in multiple insulin-sensitive tissues: A genotype-based callback positron emission tomography study

22. Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study

23. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K i

24. New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475,000 Individuals

25. Genetic risk scores in the prediction of plasma glucose, impaired insulin secretion, insulin resistance and incident type 2 diabetes in the METSIM study

26. Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

27. Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits

28. Rare and low-frequency coding variants alter human adult height

29. Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults

30. Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.

31. Evidence for Association between SH2B1 Gene Variants and Glycated Hemoglobin in Nondiabetic European American Young Adults: The Add Health Study

32. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

33. Parental origin of sequence variants associated with complex diseases

34. Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus

35. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

36. Genome-wide associations for birth weight and correlations with adult disease

37. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

38. A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease

39. Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

40. A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

41. Quantifying prion disease penetrance using large population control cohorts

42. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

43. Correction: The influence of age and sex on genetic associations with adult body size and shape : a large-scale genome-wide interaction study.

45. Evaluating resistin as a susceptibility gene for type 2 diabetes in the Finnish population

47. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

48. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

49. New genetic loci link adipose and insulin biology to body fat distribution.

50. Directional dominance on stature and cognition in diverse human populations.

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