Corpus 1,284 assessed · 1,185 scored · 647 reproduced ≥75 · 173 flagged ·∅ 73.9/100

Publications 3 Datasets 392.5k Experiments 5.7k

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3 matching publication(s)

Publication	Journal	Year	Score	Verdict
Single duplex DNA sequencing with CODEC detects mutations with high sensitivity. PMID 37106072	Nat Genet	2023	78	L1 78/100
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
Vaccine-induced ICOS+CD38+ circulating Tfh are sensitive biosensors of age-related changes in inflammatory pathway PMID 34095875	Cell Rep Med	2021	88	L1 88/100

Single duplex DNA sequencing with CODEC detects mutations with high sensitivity.

PMID 37106072 · Nat Genet · 2023

L1 78/100

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

PMID 36414417 · · 2023

L1 85/100

Vaccine-induced ICOS+CD38+ circulating Tfh are sensitive biosensors of age-related changes in inflammatory pathway

PMID 34095875 · Cell Rep Med · 2021

L1 88/100