Corpus 1,277 assessed · 1,178 scored · 644 reproduced ≥75 · 170 flagged ·∅ 74/100

Publications 5 Datasets 392.5k Experiments 4.8k

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5 matching publication(s)

Publication	Journal	Year	Score	Verdict
Compression of structured high-throughput sequencing data. ⚑ PMID 24260313	PLoS One	2013	43	L1 43/100 ⚑
CDKL1 variants affecting ciliary formation predispose to thoracic aortic aneurysm and dissection. PMID 41056017	—	2025	67	L1 67/100
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
Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs. PMID 36414417	—	2023	85	L1 85/100
Integrative analyses reveal signaling pathways underlying familial breast cancer susceptibility. PMID 26969729	Mol Syst Biol	2016	67	L1 67/100

Compression of structured high-throughput sequencing data.⚑

PMID 24260313 · PLoS One · 2013

L1 43/100 ⚑

CDKL1 variants affecting ciliary formation predispose to thoracic aortic aneurysm and dissection.

PMID 41056017 · · 2025

L1 67/100

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

Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs.

PMID 36414417 · · 2023

L1 85/100

Integrative analyses reveal signaling pathways underlying familial breast cancer susceptibility.

PMID 26969729 · Mol Syst Biol · 2016

L1 67/100