The University of Chicago Header Logo

Connection

T. Conrad Gilliam to Genes, Dominant

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

0.360
  1. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nat Genet. 2002 Mar; 30(3):335-41.
    View in: PubMed
    Score: 0.208
  2. LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Neurology. 2004 Apr 13; 62(7):1120-6.
    View in: PubMed
    Score: 0.061
  3. Results of a genome-wide genetic screen for panic disorder. Am J Med Genet. 1998 Mar 28; 81(2):139-47.
    View in: PubMed
    Score: 0.040
  4. Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy. Ann Neurol. 1996 Apr; 39(4):507-20.
    View in: PubMed
    Score: 0.035
  5. 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: 0.013
  6. Genetic linkage analysis of neurofibromatosis with DNA markers. Ann N Y Acad Sci. 1986; 486:304-10.
    View in: PubMed
    Score: 0.004
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.