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Connection

T. Conrad Gilliam to Middle Aged

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

0.126
  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: 0.018
  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: 0.017
  3. Population-based study of SR-BI genetic variation and lipid profile. Atherosclerosis. 2004 Jul; 175(1):159-68.
    View in: PubMed
    Score: 0.015
  4. Association of extreme blood lipid profile phenotypic variation with 11 reverse cholesterol transport genes and 10 non-genetic cardiovascular disease risk factors. Hum Mol Genet. 2003 Nov 01; 12(21):2733-43.
    View in: PubMed
    Score: 0.015
  5. 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: 0.010
  6. 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: 0.010
  7. Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy. Hum Mol Genet. 1996 Mar; 5(3):359-65.
    View in: PubMed
    Score: 0.009
  8. Autosomal dominant distal spinal muscular atrophy in four generations. Neurology. 1995 Apr; 45(4):699-704.
    View in: PubMed
    Score: 0.008
  9. Linkage disequilibrium and haplotype analysis among Polish families with spinal muscular atrophy. Am J Hum Genet. 1995 Jan; 56(1):210-5.
    View in: PubMed
    Score: 0.008
  10. Genetic mapping of "Lubag" (X-linked dystonia-parkinsonism) in a Filipino kindred to the pericentromeric region of the X chromosome. Ann Neurol. 1991 Feb; 29(2):124-31.
    View in: PubMed
    Score: 0.006
  11. Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR). Mol Psychiatry. 2010 Feb; 15(2):166-76.
    View in: PubMed
    Score: 0.005
  12. Screen for expanded FMR1 alleles in patients with essential tremor. Mov Disord. 2004 Aug; 19(8):930-3.
    View in: PubMed
    Score: 0.004
  13. Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy. Ann Neurol. 1996 Apr; 39(4):507-20.
    View in: PubMed
    Score: 0.002
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.