Corpus 1,280 assessed · 1,181 scored · 646 reproduced ≥75 · 170 flagged ·∅ 74/100

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4 matching publication(s)

Publication	Journal	Year	Score	Verdict
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings PMID 40555819	Nature Genetics (Author Correction 2025; orig 2024;56:1644)	2025	76	L1 76/100
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findi PMID 39039281	Nat Genet	2024	87	L1 87/100
Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. PMID 35922433	Nat Commun	2022	—	L1 No data access
Severe COVID-19 Shares a Common Neutrophil Activation Signature with Other Acute Inflammatory States. PMID 35269470	Cells	2022	88	L2 88/100

Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

PMID 40555819 · Nature Genetics (Author Correction 2025; orig 2024;56:1644) · 2025

L1 76/100

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findi

PMID 39039281 · Nat Genet · 2024

L1 87/100

Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities.

PMID 35922433 · Nat Commun · 2022

L1 No data access

Severe COVID-19 Shares a Common Neutrophil Activation Signature with Other Acute Inflammatory States.

PMID 35269470 · Cells · 2022

L2 88/100