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

Publications 3 Datasets 392.5k Experiments 4.7k

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3 matching publication(s)

Publication	Journal	Year	Score	Verdict
KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness. PMID 10025409	Cell	1999	88	L1 88/100
Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors PMID 39256359	—	2024	87	L1 87/100
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. PMID 20890276	—	2010	96	96/100

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness.

PMID 10025409 · Cell · 1999

L1 88/100

Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors

PMID 39256359 · · 2024

L1 87/100

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

PMID 20890276 · · 2010

96/100