T. Conrad Gilliam to Alleles
This is a "connection" page, showing publications T. Conrad Gilliam has written about Alleles.
Connection Strength
0.440
-
Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues. Ann Neurol. 1997 Jul; 42(1):41-9.
Score: 0.118
-
DRD2 C957T polymorphism interacts with the COMT Val158Met polymorphism in human working memory ability. Schizophr Res. 2007 Feb; 90(1-3):104-7.
Score: 0.056
-
Evidence for sex-specific risk alleles in autism spectrum disorder. Am J Hum Genet. 2004 Dec; 75(6):1117-23.
Score: 0.049
-
Screen for expanded FMR1 alleles in patients with essential tremor. Mov Disord. 2004 Aug; 19(8):930-3.
Score: 0.048
-
Perils of gene mapping with microsatellite markers. Am J Hum Genet. 1992 Oct; 51(4):905-9.
Score: 0.021
-
Dinucleotide repeat polymorphism at the D4S251 locus. Hum Mol Genet. 1992 Aug; 1(5):349.
Score: 0.021
-
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder. Biol Psychiatry. 2008 Jun 15; 63(12):1111-7.
Score: 0.016
-
Rapid selection response for contextual fear conditioning in a cross between C57BL/6J and A/J: behavioral, QTL and gene expression analysis. Behav Genet. 2008 May; 38(3):277-91.
Score: 0.016
-
A DNA segment encoding two genes very tightly linked to Huntington's disease. Science. 1987 Nov 13; 238(4829):950-2.
Score: 0.015
-
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.
Score: 0.015
-
Large-scale copy number polymorphism in the human genome. Science. 2004 Jul 23; 305(5683):525-8.
Score: 0.012
-
Genomewide linkage analysis of celiac disease in Finnish families. Am J Hum Genet. 2002 Jan; 70(1):51-9.
Score: 0.010
-
Cloning and genomic organization of beclin 1, a candidate tumor suppressor gene on chromosome 17q21. Genomics. 1999 Jul 01; 59(1):59-65.
Score: 0.008
-
Genetic alterations of microsatellites on chromosome 18 in human breast carcinoma. Diagn Mol Pathol. 1995 Mar; 4(1):66-72.
Score: 0.006
-
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
-
Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy. Hum Hered. 1993 Nov-Dec; 43(6):380-7.
Score: 0.006
-
A microsatellite genetic linkage map of human chromosome 13. Genomics. 1993 Jan; 15(1):76-85.
Score: 0.005
-
Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28. Genomics. 1992 Apr; 12(4):710-4.
Score: 0.005
-
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: 0.004
-
DNA markers for nervous system diseases. Science. 1984 Sep 21; 225(4668):1320-6.
Score: 0.003