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110 results on '"Steinthorsdottir, Valgerdur"'

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

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

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

4. Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling.

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

6. Genome-wide analyses identify 21 infertility loci and over 400 reproductive hormone loci across the allele frequency spectrum.

7. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.

8. Actionable Genotypes and Their Association with Life Span in Iceland.

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

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

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

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

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

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

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

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

17. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.

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

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

20. 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.

21. Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles: a Mendelian randomization analysis.

22. Multiomics study of nonalcoholic fatty liver disease.

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

24. Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes.

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

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

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

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

29. Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women.

30. Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease.

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

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

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

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

35. Sequence variants associating with urinary biomarkers.

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

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

38. Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.

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

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

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

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

43. Genome-wide analysis yields new loci associating with aortic valve stenosis.

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

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

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

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

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

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

50. Rare and low-frequency coding variants alter human adult height.

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