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Connection

T. Conrad Gilliam to Epilepsy

This is a "connection" page, showing publications T. Conrad Gilliam has written about Epilepsy.
Connection Strength

0.442
  1. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nat Genet. 2002 Mar; 30(3):335-41.
    View in: PubMed
    Score: 0.155
  2. High-resolution mapping and transcript identification at the progressive epilepsy with mental retardation locus on chromosome 8p. Genome Res. 1997 Sep; 7(9):887-96.
    View in: PubMed
    Score: 0.115
  3. Genetic and physical mapping of the progressive epilepsy with mental retardation (EPMR) locus on chromosome 8p. Genome Res. 1996 May; 6(5):351-60.
    View in: PubMed
    Score: 0.104
  4. Positional cloning and characterisation of the human DLGAP2 gene and its exclusion in progressive epilepsy with mental retardation. Eur J Hum Genet. 2000 May; 8(5):381-4.
    View in: PubMed
    Score: 0.034
  5. The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8. Nat Genet. 1999 Oct; 23(2):233-6.
    View in: PubMed
    Score: 0.033
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.