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Connection

T. Conrad Gilliam to Chromosomes, Human, Pair 10

This is a "connection" page, showing publications T. Conrad Gilliam has written about Chromosomes, Human, Pair 10.
  1. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nat Genet. 2002 Mar; 30(3):335-41.
    View in: PubMed
    Score: 0.050
  2. Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24. Epilepsia. 2002 Jan; 43(1):60-7.
    View in: PubMed
    Score: 0.050
  3. Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12. Mol Psychiatry. 2003 Mar; 8(3):333-42.
    View in: PubMed
    Score: 0.014
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.