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1. Atom probe tomography: a local probe for chemical bonds in solids

4. Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

5. X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements

6. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

8. SLC17A1/3 transporters mediate renal excretion of Lac-Phe in mice and humans

9. New insights into the hypothalamic–pituitary– thyroid axis: a transcriptome- and proteome-wide association study

10. Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.

11. Serum and Urine Metabolites and Kidney Function

13. Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine

14. Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

15. X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements

17. Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy

18. Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

25. Imputation-powered whole-exome analysis identifies genes associated with kidney function and disease in the UK Biobank

26. Wildtype heterogeneity contributes to clonal variability in genome edited cells

27. Copeptin, Natriuretic Peptides, and Cardiovascular Outcomes in Patients With CKD: The German Chronic Kidney Disease (GCKD) Study

28. Regional Variation in Hemoglobin Distribution Among Individuals With CKD: the ISN International Network of CKD Cohorts

29. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

30. Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

31. Copeptin, Natriuretic Peptides, and Cardiovascular Outcomes in Patients With CKD: The German Chronic Kidney Disease (GCKD) Study

32. Differential Prognostic Utility of Adiposity Measures in Chronic Kidney Disease

33. Development of Risk Prediction Equations for Incident Chronic Kidney Disease

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

37. Framework and baseline examination of the German National Cohort (NAKO)

39. Prospective Cohort Study of Soluble Urokinase Plasminogen Activation Receptor and Cardiovascular Events in Patients With CKD

40. A slit-diaphragm-associated protein network for dynamic control of renal filtration

42. Fully integrative data analysis of NMR metabolic fingerprints with comprehensive patient data: a case report based on the German Chronic Kidney Disease (GCKD) study

44. Relationship of Estimated GFR and Albuminuria to Concurrent Laboratory Abnormalities: An Individual Participant Data Meta-analysis in a Global Consortium

45. Adiposity and risk of decline in glomerular filtration rate: meta-analysis of individual participant data in a global consortium

46. Epigenome-wide DNA methylation in obsessive-compulsive disorder

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

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

49. Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

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

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