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1. Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

2. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

3. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

4. Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake

5. Circulatory levels of lysophosphatidylcholine species in obese adolescents: Findings from cross-sectional and prospective lipidomics analyses

6. GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification

7. Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets

8. Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits

10. Author Correction: Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets

11. A saturated map of common genetic variants associated with human height

12. Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density

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

15. Epigenome-wide association study of incident type 2 diabetes: a meta-analysis of five prospective European cohorts

16. Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology

17. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

18. Disentangling the genetics of lean mass.

19. An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis

21. Colocalization analysis of pancreas eQTLs with risk loci from alcoholic and novel non-alcoholic chronic pancreatitis GWAS suggests potential disease causing mechanisms

23. Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy

24. Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function

26. Association of transketolase polymorphisms with diabetic polyneuropathy in the general population: The KORA F4 study.

27. Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy

28. Identification of genetic elements in metabolism by high-throughput mouse phenotyping

29. Genome-wide methylation data mirror ancestry information

30. Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.

31. An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

32. The Interpretable Multimodal Machine Learning (IMML) framework reveals pathological signatures of distal sensorimotor polyneuropathy

33. Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.

34. Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk.

35. Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome

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

38. Mendelian Randomization Study Highlights the Role of Haematological Traits on Type-2 Diabetes Mellitus in African Ancestry Individuals

39. Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

40. Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

44. Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation.

45. A meta-analysis of gene expression signatures of blood pressure and hypertension.

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

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

48. Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration

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