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1. Genome-wide association meta-analysis identifies five loci associated with postpartum hemorrhage

4. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

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

6. The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

7. A New Graph Node Classification Benchmark: Learning Structure from Histology Cell Graphs

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

10. A non-coding variant linked to metabolic obesity with normal weight affects actin remodelling in subcutaneous adipocytes

11. The genetic architecture of sporadic and multiple consecutive miscarriage.

12. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.

13. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.

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

15. Adjusting for Confounding in Unsupervised Latent Representations of Images

16. Towards Deep Cellular Phenotyping in Placental Histology

17. Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.

18. Disentangling the genetics of lean mass.

19. Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies.

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

22. Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

24. Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

25. Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

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

29. Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk.

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

31. Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness.

32. Genetic loci associated with heart rate variability and their effects on cardiac disease risk.

33. Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function

34. Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation

35. Genome-wide association study identifies 48 common genetic variants associated with handedness

36. Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci

37. Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity

38. Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene.

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

40. Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

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

42. Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene

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

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

45. Mouse-Human Experimental Epigenetic Analysis Unmasks Dietary Targets and Genetic Liability for Diabetic Phenotypes

46. Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes

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

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

49. Large-Scale Genome-Wide Association Studies and Meta-Analyses of Longitudinal Change in Adult Lung Function

50. The miRNA profile of human pancreatic islets and beta-cells and relationship to type 2 diabetes pathogenesis.

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