| # | Title | Journal | Year | Citations |
|---|
|
| 1 | Joint European League Against Rheumatism and European Renal Association–European Dialysis and Transplant Association (EULAR/ERA-EDTA) recommendations for the management of adult and paediatric lupus nephritis | Annals of the Rheumatic Diseases | 2012 | 890 |
| 2 | Dialysis Accelerates Medial Vascular Calcification in Part by Triggering Smooth Muscle Cell Apoptosis | Circulation | 2008 | 445 |
| 3 | Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10 | Proceedings of the National Academy of Sciences of the United States of America | 2009 | 437 |
| 4 | Nomenclature for kidney function and disease: report of a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference | Kidney International | 2020 | 437 |
| 5 | Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test | Genetics in Medicine | 2018 | 423 |
| 6 | Idiopathic nephrotic syndrome in children | Lancet, The | 2018 | 366 |
| 7 | Efficacy and safety of eculizumab in atypical hemolytic uremic syndrome from 2-year extensions of phase 2 studies | Kidney International | 2015 | 352 |
| 8 | Long‐term Outcome of Boys with Posterior Urethral Valves | British Journal of Urology | 1988 | 349 |
| 9 | Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia | Nature Reviews Nephrology | 2019 | 349 |
| 10 | Renal expression of genes that promote interstitial inflammation and fibrosis in rats with protein-overload proteinuria | Kidney International | 1995 | 340 |
| 11 | Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency | Blood | 2008 | 339 |
| 12 | Prelamin A Acts to Accelerate Smooth Muscle Cell Senescence and Is a Novel Biomarker of Human Vascular Aging | Circulation | 2010 | 317 |
| 13 | Lumasiran, an RNAi Therapeutic for Primary Hyperoxaluria Type 1 | New England Journal of Medicine | 2021 | 311 |
| 14 | Deletion of Complement Factor H–Related Genes CFHR1 and CFHR3 Is Associated with Atypical Hemolytic Uremic Syndrome | PLoS Genetics | 2007 | 292 |
| 15 | Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease | Kidney International | 2009 | 254 |
| 16 | Global Prevalence of Protein-Energy Wasting in Kidney Disease: A Meta-analysis of Contemporary Observational Studies From the International Society of Renal Nutrition and Metabolism | | 2018 | 251 |
| 17 | Abnormalities in the alternative pathway of complement in children with hematopoietic stem cell transplant-associated thrombotic microangiopathy | Blood | 2013 | 244 |
| 18 | Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference | Kidney International | 2017 | 242 |
| 19 | Subjective Global Nutritional Assessment for children | American Journal of Clinical Nutrition | 2007 | 239 |
| 20 | Renovascular hypertension in children | Lancet, The | 2008 | 238 |
| 21 | Eculizumab Therapy in Children with Severe Hematopoietic Stem Cell Transplantation–Associated Thrombotic Microangiopathy | Biology of Blood and Marrow Transplantation | 2014 | 224 |
| 22 | Prelamin A Accelerates Vascular Calcification Via Activation of the DNA Damage Response and Senescence-Associated Secretory Phenotype in Vascular Smooth Muscle Cells | Circulation Research | 2013 | 199 |
| 23 | VASCULAR CALCIFICATION IN PATIENTS WITH KIDNEY DISEASE: The Vascular Biology of Calcification | Seminars in Dialysis | 2007 | 192 |
| 24 | Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectruma | Human Mutation | 2010 | 187 |
| 25 | ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3 | Nature Genetics | 2013 | 186 |
| 26 | Retrospective study of children with renal scarring associated with reflux and urinary infection | BMJ: British Medical Journal | 1994 | 183 |
| 27 | Glypican-3 Modulates BMP- and FGF-Mediated Effects during Renal Branching Morphogenesis | Developmental Biology | 2001 | 175 |
| 28 | Outcome of isolated antenatal hydronephrosis: a systematic review and meta-analysis | Pediatric Nephrology | 2006 | 173 |
| 29 | Extracellular Signal-regulated Kinase and the Small GTP-binding Protein, Rac, Contribute to the Effects of Transforming Growth Factor-β1 on Gene Expression | Journal of Biological Chemistry | 1996 | 170 |
| 30 | GLI3-dependent transcriptional repression ofGli1, Gli2and kidney patterning genes disrupts renal morphogenesis | Development (Cambridge) | 2006 | 164 |
| 31 | Cell and Molecular Biology of Kidney Development | Seminars in Nephrology | 2009 | 160 |
| 32 | The polymorphonuclear leucocyte count in childhood haemolytic uraemic syndrome | Pediatric Nephrology | 1989 | 159 |
| 33 | Subjective Global Assessment in chronic kidney disease: A review | | 2004 | 158 |
| 34 | Frailty and Cognitive Function in Incident Hemodialysis Patients | Clinical Journal of the American Society of Nephrology: CJASN | 2015 | 155 |
| 35 | Rituximab in refractory nephrotic syndrome | Pediatric Nephrology | 2010 | 145 |
| 36 | Consensus Expert Recommendations for the Diagnosis and Management of Autosomal Recessive Polycystic Kidney Disease: Report of an International Conference | Journal of Pediatrics | 2014 | 144 |
| 37 | Long-term outcome of peritoneal dialysis in infants | Journal of Pediatrics | 2000 | 143 |
| 38 | B lymphocyte depletion therapy in children with refractory systemic lupus erythematosus | Arthritis and Rheumatism | 2005 | 143 |
| 39 | Acquired Renal Scars in Children | Journal of Urology | 1983 | 137 |
| 40 | Factors Influencing Patient and Graft Survival in 300 Cadaveric Pediatric Renal Transplants | Journal of Urology | 1988 | 135 |
| 41 | Genetic causes of hypomagnesemia, a clinical overview | Pediatric Nephrology | 2017 | 131 |
| 42 | NETosing Neutrophils Activate Complement Both on Their Own NETs and Bacteria via Alternative and Non-alternative Pathways | Frontiers in Immunology | 2016 | 129 |
| 43 | Quality of life in children with chronic kidney disease—patient and caregiver assessments | Nephrology Dialysis Transplantation | 2006 | 128 |
| 44 | Clinical and genetic predictors of atypical hemolytic uremic syndrome phenotype and outcome | Kidney International | 2018 | 128 |
| 45 | aHUS caused by complement dysregulation: new therapies on the horizon | Pediatric Nephrology | 2011 | 124 |
| 46 | Patient-, Provider-, and Clinic-Level Predictors of Unrecognized Elevated Blood Pressure in Children | Pediatrics | 2010 | 122 |
| 47 | Clinical practice recommendations for the treatment of Alport syndrome: a statement of the Alport Syndrome Research Collaborative | Pediatric Nephrology | 2013 | 122 |
| 48 | Spectrum of Complement-Mediated Thrombotic Microangiopathies: Pathogenetic Insights Identifying Novel Treatment Approaches | Seminars in Thrombosis and Hemostasis | 2014 | 122 |
| 49 | Renal Phenotype in Lowe Syndrome | Clinical Journal of the American Society of Nephrology: CJASN | 2008 | 120 |
| 50 | Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations | Kidney International | 2012 | 120 |
