Juliane Köhler

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)

• Evaluating genome sequencing strategies: trio, singleton, and standard testing in rare disease diagnosis
  2025 L1 88/100

1 assessed by us (1 reproduced) · 3 not yet assessed — every PubMed paper on record, linked below.

• Evaluating genome sequencing strategies: trio, singleton, and standard testing in rare disease diagnosis

  Genome Medicine · 2025 · PMID 40963120
  L1 88/100
• Evaluating Genome Sequencing Strategies: Trio, Singleton, and Standard Testing in Rare Disease Diagnosis ↗

  medRxiv · 2024
  not yet assessed
• Classification of putative <i>BRCA1</i> splicing mutations. ↗

  INDIGO (University of Illinois at Chicago) · 2015
  not yet assessed
• Analysis of 30 Putative BRCA1 Splicing Mutations in Hereditary Breast and Ovarian Cancer Families Identifies Exonic Splice Site Mutations That Escape In Silico Prediction ↗

  PLoS ONE · 2012 · PMID 23239986
  not yet assessed