T. Conrad Gilliam to Polymorphism, Genetic
This is a "connection" page, showing publications T. Conrad Gilliam has written about Polymorphism, Genetic.
Connection Strength
0.979
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DRD2 C957T polymorphism interacts with the COMT Val158Met polymorphism in human working memory ability. Schizophr Res. 2007 Feb; 90(1-3):104-7.
Score: 0.220
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Hardy-Weinberg disequilibrium identified genotyping error of the serotonin transporter (SLC6A4) promoter polymorphism. Psychiatr Genet. 2006 Feb; 16(1):31-4.
Score: 0.208
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Dinucleotide repeat polymorphism at the D1S182 locus. Hum Mol Genet. 1992 Sep; 1(6):454.
Score: 0.082
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Dinucleotide repeat polymorphism at the D19S206 locus. Hum Mol Genet. 1992 Sep; 1(6):454.
Score: 0.082
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Dinucleotide repeat polymorphism at the D4S251 locus. Hum Mol Genet. 1992 Aug; 1(5):349.
Score: 0.082
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Molecular genetic strategies to investigate Huntington's disease. Adv Neurol. 1988; 48:17-29.
Score: 0.059
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Isolation of polymorphic DNA fragments from human chromosome 4. Nucleic Acids Res. 1987 Feb 25; 15(4):1445-58.
Score: 0.056
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Large-scale copy number polymorphism in the human genome. Science. 2004 Jul 23; 305(5683):525-8.
Score: 0.047
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Population-based study of SR-BI genetic variation and lipid profile. Atherosclerosis. 2004 Jul; 175(1):159-68.
Score: 0.047
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The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers. Hum Genet. 1984; 68(2):154-8.
Score: 0.045
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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.
Score: 0.014
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Linkage studies between polymorphic markers on chromosome 4 and cystic fibrosis. Hum Genet. 1985; 69(3):250-4.
Score: 0.012
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An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy. Genomics. 1994 May 01; 21(1):27-33.
Score: 0.006
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Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q. Nat Genet. 1992 Dec; 2(4):315-7.
Score: 0.005
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Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28. Genomics. 1992 Apr; 12(4):710-4.
Score: 0.005
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Molecular genetics of human chromosome 4. J Med Genet. 1986 Jun; 23(3):193-9.
Score: 0.003
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DNA markers for nervous system diseases. Science. 1984 Sep 21; 225(4668):1320-6.
Score: 0.003
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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.
Score: 0.003