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Connection

T. Conrad Gilliam to DNA

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

0.286
DNA
  1. Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues. Ann Neurol. 1997 Jul; 42(1):41-9.
    View in: PubMed
    Score: 0.096
  2. Catechol-O-methyltransferase (COMT) genotypes and working memory: associations with differing cognitive operations. Biol Psychiatry. 2005 Dec 01; 58(11):901-7.
    View in: PubMed
    Score: 0.042
  3. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nat Genet. 2002 Mar; 30(3):335-41.
    View in: PubMed
    Score: 0.033
  4. Isolation of multiple genomic sequences coding for chicken myosin heavy chain protein. J Biol Chem. 1982 Jan 10; 257(1):549-56.
    View in: PubMed
    Score: 0.033
  5. Dinucleotide repeat polymorphism at the D4S251 locus. Hum Mol Genet. 1992 Aug; 1(5):349.
    View in: PubMed
    Score: 0.017
  6. Spinal muscular atrophy is not the result of mutations at the beta-hexosaminidase or GM2-activator locus. Neurology. 1991 Sep; 41(9):1418-22.
    View in: PubMed
    Score: 0.016
  7. Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomere. Cell. 1987 Aug 14; 50(4):565-71.
    View in: PubMed
    Score: 0.012
  8. DNA markers for nervous system diseases. Science. 1984 Sep 21; 225(4668):1320-6.
    View in: PubMed
    Score: 0.010
  9. Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration. Invest Ophthalmol Vis Sci. 1999 Aug; 40(9):2106-14.
    View in: PubMed
    Score: 0.007
  10. Cloning and genomic organization of beclin 1, a candidate tumor suppressor gene on chromosome 17q21. Genomics. 1999 Jul 01; 59(1):59-65.
    View in: PubMed
    Score: 0.007
  11. Report of the first international workshop on human chromosome 18 mapping. Cytogenet Cell Genet. 1993; 63(2):78-96.
    View in: PubMed
    Score: 0.004
  12. A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene. Genomics. 1989 Nov; 5(4):802-9.
    View in: PubMed
    Score: 0.004
  13. A somatic cell hybrid panel for localizing DNA segments near the Huntington's disease gene. Genomics. 1987 Sep; 1(1):29-34.
    View in: PubMed
    Score: 0.003
  14. Molecular genetics of Huntington's disease. Cold Spring Harb Symp Quant Biol. 1986; 51 Pt 1:359-64.
    View in: PubMed
    Score: 0.003
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.