Rufeng Dai

The share of this author’s assessed papers carrying a ⚑ flag. A concentration is a prompt for expert review — never, on its own, a determination about the person.

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How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.

Assessed papers (1)

• Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs.
  2023 L1 85/100

1 assessed by us (1 reproduced) · 38 not yet assessed — every PubMed paper on record, linked below.

• Urinary ANGPTL3: A Novel Noninvasive Biomarker for Podocyte Injury in Pediatric Glomerular Diseases ↗

  Research Square · 2026
  not yet assessed
• Vitamin D Deficiency Activates Gdnf-Ret-pErk1/2 Signal and Induces Kidney Malformations in Mice ↗

  International Journal of Molecular Sciences · 2026 · PMID 41977230
  not yet assessed
• Urinary ANGPTL3: a novel noninvasive biomarker for podocyte injury in pediatric glomerular diseases ↗

  Journal of Translational Medicine · 2026 · PMID 42337674
  not yet assessed
• Genome sequencing based sequential diagnostic strategy improve diagnosed yield of pediatric genetic kidney disease: a national multicenter study ↗

  npj Genomic Medicine · 2026
  not yet assessed
• Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families ↗

  Genetics in Medicine · 2025 · PMID 40223730
  not yet assessed
• Correlation between polymorphisms of the aquaporin-1 gene and peritoneal function in children on chronic peritoneal dialysis ↗

  Pediatric Nephrology · 2025 · PMID 40999036
  not yet assessed
• Genitourinary defects, anxiety and aggressive-like behavior and glucose metabolism disorders in Zmym2 mutant mice with inserted piggyBac transposon ↗

  Frontiers in Cell and Developmental Biology · 2025 · PMID 40313719
  not yet assessed
• From mutation to symptoms: a multi-center study on HNF1B-related nephropathy in Chinese children ↗

  BMC Nephrology · 2025 · PMID 41437330
  not yet assessed
• From Mutation to Symptoms: A Multi-Center Study on HNF1B-Related Nephropathy in Chinese Children ↗

  Research Square · 2025
  not yet assessed
• Clinical Spectrum and Genotype-Phenotype Associations in Coenzyme Q10 Deficiency Nephropathy in a Chinese Cohort ↗

  Journal of the American Society of Nephrology · 2025
  not yet assessed
• GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tract ↗

  Human Genomics · 2024 · PMID 38654324
  not yet assessed
• The emerging role of clinical genetics in pediatric patients with chronic kidney disease ↗

  Pediatric Nephrology · 2024 · PMID 38502225
  not yet assessed
• Noninvasive genetic testing for type IV collagen nephropathy using oral mucosa DNA sampling in children with haematuria ↗

  Renal Failure · 2024 · PMID 39540369
  not yet assessed
• Protein-losing enteropathy as a new phenotype in atypical hemolytic uremic syndrome caused by CD46 gene mutation and recovery from chronic kidney failure by eculizumab treatment ↗

  Research Square · 2024
  not yet assessed
• Angiopoietin-like protein 3: a novel potential biomarker for nephrotic syndrome in children ↗

  Frontiers in Pediatrics · 2023 · PMID 37266537
  not yet assessed
• Prioritization of Monogenic Congenital Anomalies of the Kidney and Urinary Tract Candidate Genes with Existing Single-Cell Transcriptomics Data of the Human Fetal Kidney ↗

  ˜The œNephron journals/Nephron journals · 2023 · PMID 37499630
  not yet assessed
• Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract ↗

  European Urology Open Science · 2022 · PMID 36185583
  not yet assessed
• Anti-ANGPTL3-FLD monoclonal antibody treatment ameliorates podocyte lesions through attenuating mitochondrial damage ↗

  Cell Death and Disease · 2022 · PMID 36229446
  not yet assessed
• Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs

  Journal of the American Society of Nephrology · 2022 · PMID 36414417
  L1 85/100
• Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models ↗

  American Journal of Medical Genetics Part A · 2022 · PMID 35040250
  not yet assessed
• Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT ↗

  Genetics in Medicine · 2021 · PMID 34906515
  not yet assessed
• Recessive <i>NOS1AP</i> variants impair actin remodeling and cause glomerulopathy in humans and mice ↗

  Science Advances · 2021 · PMID 33523862
  not yet assessed
• Exome survey of individuals affected by <scp>VATER</scp>/<scp>VACTERL</scp> with renal phenotypes identifies phenocopies and novel candidate genes ↗

  American Journal of Medical Genetics Part A · 2021 · PMID 34338422
  not yet assessed
• Whole-exome sequencing identifies<i>FOXL2</i>,<i>FOXA2</i>and<i>FOXA3</i>as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract ↗

  Nephrology Dialysis Transplantation · 2021 · PMID 34473308
  not yet assessed
• A truncating <scp><i>NRIP1</i></scp> variant in an Arabic family with congenital anomalies of the kidneys and urinary tract ↗

  American Journal of Medical Genetics Part A · 2021 · PMID 34525250
  not yet assessed
• PPARα agonist exerts protective effects in podocyte injury via inhibition of the ANGPTL3 pathway ↗

  Experimental Cell Research · 2021 · PMID 34499887
  not yet assessed
• Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations ↗

  The American Journal of Human Genetics · 2020 · PMID 32891193
  not yet assessed
• Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT) ↗

  Genetics in Medicine · 2020 · PMID 32475988
  not yet assessed
• In the Presence of Genetic Heterogeneity of CAKUT, Whole-Exome Sequencing Establishes a Molecular Genetic Diagnosis in 14% of Cases ↗

  Journal of the American Society of Nephrology · 2020
  not yet assessed
• Monogenic causes of chronic kidney disease in adults ↗

  Kidney International · 2019 · PMID 30773290
  not yet assessed
• CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor Mutations ↗

  The American Journal of Human Genetics · 2019 · PMID 31708116
  not yet assessed
• Angiopoietin-like-3 knockout protects against glomerulosclerosis in murine adriamycin-induced nephropathy by attenuating podocyte loss ↗

  BMC Nephrology · 2019 · PMID 31126248
  not yet assessed
• COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans ↗

  Human Genetics · 2019 · PMID 31230195
  not yet assessed
• Anti-proteinuria effect of antibody against ANGPTL3 coil-coiled domain on adriamycin-induced nephropathy in mice ↗

  Biochemical and Biophysical Research Communications · 2019 · PMID 31256934
  not yet assessed
• Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract ↗

  Journal of the American Society of Nephrology · 2018 · PMID 30143558
  not yet assessed
• A vital role for Angptl3 in the PAN-induced podocyte loss by affecting detachment and apoptosis in vitro ↗

  BMC Nephrology · 2015 · PMID 25884163
  not yet assessed
• Potential function of angiopoietin-like protein 3 in hyperlipidemia of nephrotic syndrome ↗

  2015
  not yet assessed
• Clinical significance of serum and urine angiopoietin - like 3 and 4 in children with primary nephrotic syndrome ↗

  2015
  not yet assessed
• The Study on Oil Field Enterprises' Intention of Energy Conservation and Emissions Reduction Based on Evolutionary Game

  2013
  not yet assessed