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95 results on '"Martina Müller-Nurasyid"'

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1. Network reconstruction for trans acting genetic loci using multi-omics data and prior information

2. Proteomics biomarker discovery for individualized prevention of familial pancreatic cancer using statistical learning.

3. Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.

4. Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes

5. Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke.

6. Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.

7. Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.

8. Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes.

9. META-GSA: Combining Findings from Gene-Set Analyses across Several Genome-Wide Association Studies.

10. No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects.

11. RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-Express and CARDIoGRAM studies.

12. Genome-wide association study of circulating interleukin 6 levels identifies novel loci

13. Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes

14. Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation

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

16. Heterogeneous contributions of change in population distribution of body mass index to change in obesity and underweight

17. Genetic Contributions to Early and Late Onset Ischemic Stroke

18. Genetic analyses of the QT interval and its components in over 250K individuals identifies new loci and pathways affecting ventricular depolarization and repolarization

19. Genetic Variation and Cardiovascular Risk Factors: A Cohort Study on Migrants from the Former Soviet Union and a Native German Population

20. Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

21. Deoxyribonuclease 1 Q222R single nucleotide polymorphism and long-term mortality after acute myocardial infarction

22. Random glucose GWAS in 493,036 individuals provides insights into diabetes pathophysiology, complications and treatment stratification

23. Chronically elevated branched chain amino acid levels are pro-arrhythmic

24. Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

25. Author response: Heterogeneous contributions of change in population distribution of body mass index to change in obesity and underweight

26. Comparison of genetic risk prediction models to improve prediction of coronary heart disease in two large cohorts of the MONICA/KORA study

27. DNA methylation and lipid metabolism: an EWAS of 226 metabolic measures

28. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

29. Genetic Susceptibility for Atrial Fibrillation in Patients Undergoing Atrial Fibrillation Ablation

30. Genome wide association analysis in dilated cardiomyopathy reveals two new key players in systolic heart failure on chromosome 3p25.1 and 22q11.23

31. Private variants in PRKN are associated with late-onset Parkinson's disease

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

33. Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced disease

34. Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease

35. Incidence of complications related to catheter ablation of atrial fibrillation and atrial flutter: a nationwide in-hospital analysis of administrative data for Germany in 2014

36. A comprehensive evaluation of the genetic architecture of sudden cardiac arrest

37. Epigenetic Link Between Statin Therapy and Type 2 Diabetes

38. A genome-wide genetic pleiotropy approach identified shared loci between multiple system atrophy and inflammatory bowel disease

39. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

40. Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals

41. Integrative clinical transcriptome analysis reveals TMPRSS2-ERG dependency of prognostic biomarkers in prostate adenocarcinoma

42. Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

43. Effects of Calcium, Magnesium, and Potassium concentrations on ventricular repolarization in unselected individuals

44. Serum magnesium and calcium levels in relation to ischemic stroke Mendelian randomization study

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

46. 52 Genetic Loci Influencing Myocardial Mass

47. PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity

48. Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

49. Abstract 053: Genome-wide Tcea3 -SNP Interaction Study Identifies Novel QT Interval Loci

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

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