T. Conrad Gilliam to Genetic Variation
This is a "connection" page, showing publications T. Conrad Gilliam has written about Genetic Variation.
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Population-based study of SR-BI genetic variation and lipid profile. Atherosclerosis. 2004 Jul; 175(1):159-68.
Score: 0.143
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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.
Score: 0.136
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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder. Biol Psychiatry. 2008 Jun 15; 63(12):1111-7.
Score: 0.046
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Large-scale copy number polymorphism in the human genome. Science. 2004 Jul 23; 305(5683):525-8.
Score: 0.036
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Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues. Ann Neurol. 1997 Jul; 42(1):41-9.
Score: 0.022
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Genetic analysis of childhood-onset spinal muscular atrophy. Adv Neurol. 1991; 56:181-7.
Score: 0.014
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Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet. 2007 Mar; 39(3):319-28.
Score: 0.011
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Molecular triangulation: bridging linkage and molecular-network information for identifying candidate genes in Alzheimer's disease. Proc Natl Acad Sci U S A. 2004 Oct 19; 101(42):15148-53.
Score: 0.009
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The implications of genetic variation in human pathology. Biochem Soc Symp. 1984; 49:183-8.
Score: 0.009
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Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy. Hum Hered. 1993 Nov-Dec; 43(6):380-7.
Score: 0.004