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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. Natural History and Clinicopathological Associations of TRPC6-Associated Podocytopathy

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

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

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

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

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

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

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

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

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

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

27. 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

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

30. Rationale and design of the Kidney Precision Medicine Project

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

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

33. The Significance of Hematuria in Podocytopathies

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

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

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

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

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

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

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

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

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

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

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

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

48. 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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