Corpus 1,272 assessed · 1,173 scored · 643 reproduced ≥75 · 168 flagged ·∅ 74.1/100

Publications 6 Datasets 392.5k Experiments 4.7k

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6 matching publication(s)

Publication	Journal	Year	Score	Verdict
Multi-omic identification of perineurial hyperplasia and lipid-associated nerve macrophages in human polyneuropathies. PMID 40849297	Nat Commun	2025	90	L1 90/100
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	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
Clinical and pathological characteristics of familial melanoma with germline <scp>TERT</scp> promoter variants PMID 35912549	—	2022	—	L1 No computation
Course of HEV viremia and anti-HEV IgM/IgG response in asymptomatic blood donors PMID 29860111	—	2018	—	L1 No computation
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. PMID 20890276	—	2010	96	96/100

Multi-omic identification of perineurial hyperplasia and lipid-associated nerve macrophages in human polyneuropathies.

PMID 40849297 · Nat Commun · 2025

L1 90/100

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

Clinical and pathological characteristics of familial melanoma with germline <scp>TERT</scp> promoter variants

PMID 35912549 · · 2022

L1 No computation

Course of HEV viremia and anti-HEV IgM/IgG response in asymptomatic blood donors

PMID 29860111 · · 2018

L1 No computation

Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.

PMID 20890276 · · 2010

96/100