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Connection

HONGZHENG DAI to Epilepsy

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This is a "connection" page, showing publications HONGZHENG DAI has written about Epilepsy.
HONGZHENG DAI
Connection Strength
0.480
Epilepsy
  1. Diagnostic utility of DNA methylation analysis in genetically unsolved pediatric epilepsies and CHD2 episignature refinement. Nat Commun. 2024 Aug 06; 15(1):6524.
    View in: PubMed
    Score: 0.134
  2. KCNA1 gain-of-function epileptic encephalopathy treated with 4-aminopyridine. Ann Clin Transl Neurol. 2023 04; 10(4):656-663.
    View in: PubMed
    Score: 0.121
  3. Biallelic CACNA2D1 loss-of-function variants cause early-onset developmental epileptic encephalopathy. Brain. 2022 08 27; 145(8):2721-2729.
    View in: PubMed
    Score: 0.117
  4. PPP3CA truncating variants clustered in the regulatory domain cause early-onset refractory epilepsy. Clin Genet. 2021 08; 100(2):227-233.
    View in: PubMed
    Score: 0.108
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.