Search

Your search keyword '"Lindgren, Cecilia"' showing total 1,962 results

Search Constraints

Start Over You searched for: Author "Lindgren, Cecilia" Remove constraint Author: "Lindgren, Cecilia"
1,962 results on '"Lindgren, Cecilia"'

Search Results

1. Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy

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

5. Enhancing Cross-Institute Generalisation of GNNs in Histopathology Through Multiple Embedding Graph Augmentation (MEGA)

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

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

8. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

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

11. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

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

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

15. Association between maternal haemoglobin concentrations and maternal and neonatal outcomes: the prospective, observational, multinational, INTERBIO-21st fetal study

16. Discovering cellular programs of intrinsic and extrinsic drivers of metabolic traits using LipocyteProfiler

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

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

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

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

21. Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

22. Adjusting for Confounding in Unsupervised Latent Representations of Images

23. Towards Deep Cellular Phenotyping in Placental Histology

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

25. Disentangling the genetics of lean mass.

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

27. Meta-analysis fine-mapping is often miscalibrated at single-variant resolution

28. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease

29. Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

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

31. Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

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

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

37. Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

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

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

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

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

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

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

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

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

48. A regulatory variant at 3q21.1 confers an increased pleiotropic risk for hyperglycemia and altered bone mineral density

49. Är intresset för att bli familjehem tillräckligt stort?

50. ”Nämen vadå, det är ju så här vi lever alltid”: föräldrar till barn med neuropsykiatriska funktionsnedsättningar berättar om fritiden under covid-19-pandemin

Catalog

Books, media, physical & digital resources