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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. Sequence variants associated with BMI affect disease risk through BMI itself

4. Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination

5. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

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

7. Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study

8. Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

9. Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

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

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

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

13. Cell-free fetal DNA for genetic evaluation in Copenhagen Pregnancy Loss Study (COPL): a prospective cohort study

14. Multiomics study of nonalcoholic fatty liver disease

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

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

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

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

19. Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes

20. Genetic propensities for verbal and spatial ability have opposite effects on body mass index and risk of schizophrenia

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

22. Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry.

23. Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism.

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

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

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

27. Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes

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

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

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

31. Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets.

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

33. A genome-wide association search for type 2 diabetes genes in African Americans.

34. Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank

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

36. Hundreds of variants clustered in genomic loci and biological pathways affect human height

37. Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events

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

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

40. Data from Loss-of-Function Variants in the Tumor-Suppressor Gene PTPN14 Confer Increased Cancer Risk

41. Cell-free fetal DNA for genetic evaluation in Copenhagen Pregnancy Loss Study (COPL): a prospective cohort study

42. Genetic effects on the timing of parturition and links to fetal birth weight:[Inkl. Correction]

43. Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes:A genetic association study in Europeans

44. Cell-free fetal DNA for genetic evaluation in Copenhagen Pregnancy Loss Study (COPL):a prospective cohort study

45. Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans.

46. Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events

47. Pregnancy-Associated Bleeding and Genetics:Five Sequence Variants in the Myometrium and Progesterone Signaling Pathway are associated with postpartum hemorrhage

48. Genetic variants associated with syncope implicate neural and autonomic processes

49. A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy

50. Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans

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