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1. The chromatin landscape of healthy and injured cell types in the human kidney.

3. Cell subtype-specific effects of genetic variation in the Alzheimer’s disease brain

5. Increased risk of kidney failure in patients with genetic kidney disorders

6. An atlas of healthy and injured cell states and niches in the human kidney.

7. Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

12. Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

15. Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome

16. Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network

17. Author Correction: Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits

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

23. Precision Medicine in Nephrology: An Integrative Framework of Multidimensional Data in the Kidney Precision Medicine Project

25. Advancing Genetic Testing in Kidney Diseases: Report From a National Kidney Foundation Working Group

26. Association of COVID-19 Versus COVID-19 Vaccination With Kidney Function and Disease Activity in Primary Glomerular Disease: A Report of the Cure Glomerulonephropathy Study

27. Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies

29. Rationale and design of the Kidney Precision Medicine Project

30. Molecular Signatures of Glomerular Neovascularization in a Patient with Diabetic Kidney Disease

31. Participant Experience with Protocol Research Kidney Biopsies in the Kidney Precision Medicine Project

32. The Significance of Hematuria in Podocytopathies

33. Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing

34. Racial and Ethnic Disparities in Acute Care Utilization Among Patients With Glomerular Disease

35. Anti-PLA2R Antibody Levels and Clinical Risk Factors for Treatment Nonresponse in Membranous Nephropathy

36. Returning integrated genomic risk and clinical recommendations: The eMERGE study

37. Genome-wide polygenic score to predict chronic kidney disease across ancestries

38. Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies.

39. The copy number variation landscape of congenital anomalies of the kidney and urinary tract.

42. IgA vasculitis with nephritis: update of pathogenesis with clinical implications

43. Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis

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

45. Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations

46. Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits

47. Improving Clinical Trials for Anticomplement Therapies in Complement-Mediated Glomerulopathies: Report of a Scientific Workshop Sponsored by the National Kidney Foundation

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