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 (7)

• Pleiotropic effects of <i>MORC2</i> derive from its epigenetic signature
  2025 L1 No data access
• Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings
  2025 L1 76/100
• Fatty acid synthesis suppresses dietary polyunsaturated fatty acid use
  2024 L1 94/100
• Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findi
  2024 L1 87/100
• Expanding the clinical spectrum of COL2A1 related disorders by a mass like phenotype.
  2022 L1 84/100
• Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
  2019 L1 93/100
• 16p13.11 microdeletion uncovers loss-of-function of a MYH11 missense variant in a patient with megacystis-microcolon-intestinal-hypoperistalsis syndrome.
  2019 L1 78/100