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Connection

T. Conrad Gilliam to Polymorphism, Genetic

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

0.947
  1. DRD2 C957T polymorphism interacts with the COMT Val158Met polymorphism in human working memory ability. Schizophr Res. 2007 Feb; 90(1-3):104-7.
    View in: PubMed
    Score: 0.213
  2. Hardy-Weinberg disequilibrium identified genotyping error of the serotonin transporter (SLC6A4) promoter polymorphism. Psychiatr Genet. 2006 Feb; 16(1):31-4.
    View in: PubMed
    Score: 0.201
  3. Dinucleotide repeat polymorphism at the D1S182 locus. Hum Mol Genet. 1992 Sep; 1(6):454.
    View in: PubMed
    Score: 0.079
  4. Dinucleotide repeat polymorphism at the D19S206 locus. Hum Mol Genet. 1992 Sep; 1(6):454.
    View in: PubMed
    Score: 0.079
  5. Dinucleotide repeat polymorphism at the D4S251 locus. Hum Mol Genet. 1992 Aug; 1(5):349.
    View in: PubMed
    Score: 0.079
  6. Molecular genetic strategies to investigate Huntington's disease. Adv Neurol. 1988; 48:17-29.
    View in: PubMed
    Score: 0.057
  7. Isolation of polymorphic DNA fragments from human chromosome 4. Nucleic Acids Res. 1987 Feb 25; 15(4):1445-58.
    View in: PubMed
    Score: 0.054
  8. Large-scale copy number polymorphism in the human genome. Science. 2004 Jul 23; 305(5683):525-8.
    View in: PubMed
    Score: 0.045
  9. Population-based study of SR-BI genetic variation and lipid profile. Atherosclerosis. 2004 Jul; 175(1):159-68.
    View in: PubMed
    Score: 0.045
  10. The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers. Hum Genet. 1984; 68(2):154-8.
    View in: PubMed
    Score: 0.044
  11. A human anonymous low copy number clone, 4c11 (D6S4), localized to 6p12-6p21, detects 2 RFLPs, one of which is moderately polymorphic. Nucleic Acids Res. 1987 Jul 24; 15(14):5902.
    View in: PubMed
    Score: 0.014
  12. Linkage studies between polymorphic markers on chromosome 4 and cystic fibrosis. Hum Genet. 1985; 69(3):250-4.
    View in: PubMed
    Score: 0.012
  13. An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy. Genomics. 1994 May 01; 21(1):27-33.
    View in: PubMed
    Score: 0.006
  14. Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q. Nat Genet. 1992 Dec; 2(4):315-7.
    View in: PubMed
    Score: 0.005
  15. Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28. Genomics. 1992 Apr; 12(4):710-4.
    View in: PubMed
    Score: 0.005
  16. Molecular genetics of human chromosome 4. J Med Genet. 1986 Jun; 23(3):193-9.
    View in: PubMed
    Score: 0.003
  17. DNA markers for nervous system diseases. Science. 1984 Sep 21; 225(4668):1320-6.
    View in: PubMed
    Score: 0.003
  18. Cystic fibrosis is not caused by a defect in the gene coding for human complement C3. Mol Biol Med. 1983 Sep; 1(2):185-90.
    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.