Search

Your search keyword '"Steinthorsdottir, Valgerdur"' showing total 145 results

Search Constraints

Start Over You searched for: Author "Steinthorsdottir, Valgerdur" Remove constraint Author: "Steinthorsdottir, Valgerdur" Journal nature genetics Remove constraint Journal: nature genetics
145 results on '"Steinthorsdottir, Valgerdur"'

Search Results

1. Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency

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

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

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

5. Genetic effects on the timing of parturition and links to fetal birth weight

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

7. Multiomics study of nonalcoholic fatty liver disease

8. Author Correction: Genetic effects on the timing of parturition and links to fetal birth weight

9. Large-scale integration of the plasma proteome with genetics and disease

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

11. Homozygosity for a stop-gain variant in CCDC201causes primary ovarian insufficiency

12. Distinction between the effects of parental and fetal genomes on fetal growth

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

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

15. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

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

17. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

18. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

19. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

20. Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritability

21. Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease

22. Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes

23. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

24. Variants in the fetal genome near FLT1 are associated with risk of preeclampsia

25. Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

26. Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

27. Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

28. New common variants affecting susceptibility to basal cell carcinoma

29. Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche

30. Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

31. Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity

32. Variants in MTNR1B influence fasting glucose levels

33. Many sequence variants affecting diversity of adult human height

34. The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

35. Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes

36. A variant in CDKAL1 influences insulin response and risk of type 2 diabetes

37. A common inversion under selection in Europeans

38. Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.

39. Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.

40. Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.

41. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.

42. Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.

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

44. Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.

45. Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.

46. The impact of low-frequency and rare variants on lipid levels.

47. Defining the role of common variation in the genomic and biological architecture of adult human height.

48. Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.

49. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.

50. A germline variant in the TP53 polyadenylation signal confers cancer susceptibility.

Catalog

Books, media, physical & digital resources