Ethan Lai

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.

Collaborators, sized by shared output and coloured by their own reproducibility (green = high, red = low). Click a node to open their card. A pattern is a prompt for review, never a determination.

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) · 5 not yet assessed — every PubMed paper on record, linked below.

• Important food sources of fructose-containing sugars and adiposity: A systematic review and meta-analysis of controlled feeding trials ↗

  American Journal of Clinical Nutrition · 2023 · PMID 36842451
  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
• 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
• 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
• Neutralizing Activity of Anti-interferon-γ Autoantibodies in Adult-Onset Immunodeficiency Is Associated With Their Binding Domains ↗

  Frontiers in Immunology · 2019 · PMID 31474987
  not yet assessed