T. Conrad Gilliam to Female
This is a "connection" page, showing publications T. Conrad Gilliam has written about Female.
Connection Strength
0.279
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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: 0.014
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Catechol-O-methyltransferase (COMT) genotypes and working memory: associations with differing cognitive operations. Biol Psychiatry. 2005 Dec 01; 58(11):901-7.
Score: 0.013
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Population-based study of SR-BI genetic variation and lipid profile. Atherosclerosis. 2004 Jul; 175(1):159-68.
Score: 0.012
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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: 0.011
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Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nat Genet. 2002 Mar; 30(3):335-41.
Score: 0.010
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Mapping complex traits in diseases of the hair and skin. Exp Dermatol. 1999 Dec; 8(6):439-52.
Score: 0.009
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Results of a genome-wide genetic screen for panic disorder. Am J Med Genet. 1998 Mar 28; 81(2):139-47.
Score: 0.008
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TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa. Nat Genet. 1998 Feb; 18(2):177-9.
Score: 0.008
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High-resolution mapping and transcript identification at the progressive epilepsy with mental retardation locus on chromosome 8p. Genome Res. 1997 Sep; 7(9):887-96.
Score: 0.008
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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: 0.007
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Genetic and physical mapping of the progressive epilepsy with mental retardation (EPMR) locus on chromosome 8p. Genome Res. 1996 May; 6(5):351-60.
Score: 0.007
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Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy. Hum Mol Genet. 1996 Mar; 5(3):359-65.
Score: 0.007
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Autosomal dominant distal spinal muscular atrophy in four generations. Neurology. 1995 Apr; 45(4):699-704.
Score: 0.006
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Linkage disequilibrium and haplotype analysis among Polish families with spinal muscular atrophy. Am J Hum Genet. 1995 Jan; 56(1):210-5.
Score: 0.006
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An integrative computational approach for prioritization of genomic variants. PLoS One. 2014; 9(12):e114903.
Score: 0.006
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Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions. Hum Mol Genet. 1994 Sep; 3(9):1647-56.
Score: 0.006
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Refinement of the spinal muscular atrophy locus to the interval between D5S435 and MAP1B. Genomics. 1993 Feb; 15(2):365-71.
Score: 0.005
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A microsatellite genetic linkage map of human chromosome 18. Genomics. 1993 Jan; 15(1):48-56.
Score: 0.005
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Perils of gene mapping with microsatellite markers. Am J Hum Genet. 1992 Oct; 51(4):905-9.
Score: 0.005
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Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia. Genomics. 1989 Nov; 5(4):940-4.
Score: 0.004
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Physical mapping, linkage analysis of a putative schizophrenia locus on chromosome 5q. Schizophr Bull. 1989; 15(3):441-52.
Score: 0.004
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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.
Score: 0.004
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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder. Biol Psychiatry. 2008 Jun 15; 63(12):1111-7.
Score: 0.004
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Recurrent 16p11.2 microdeletions in autism. Hum Mol Genet. 2008 Feb 15; 17(4):628-38.
Score: 0.004
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Genetic architecture of fear conditioning in chromosome substitution strains: relationship to measures of innate (unlearned) anxiety-like behavior. Mamm Genome. 2007 Apr; 18(4):221-8.
Score: 0.004
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Strong association of de novo copy number mutations with autism. Science. 2007 Apr 20; 316(5823):445-9.
Score: 0.004
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Isolation of polymorphic DNA fragments from human chromosome 4. Nucleic Acids Res. 1987 Feb 25; 15(4):1445-58.
Score: 0.004
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Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet. 2007 Mar; 39(3):319-28.
Score: 0.004
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Selection for contextual fear conditioning affects anxiety-like behaviors and gene expression. Genes Brain Behav. 2007 Nov; 6(8):736-49.
Score: 0.004
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Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata. Am J Hum Genet. 2007 Feb; 80(2):316-28.
Score: 0.004
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Consequences of copper accumulation in the livers of the Atp7b-/- (Wilson disease gene) knockout mice. Am J Pathol. 2006 Feb; 168(2):423-34.
Score: 0.003
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Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs. Mol Psychiatry. 2005 Aug; 10(8):747-57.
Score: 0.003
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Gene expression differences in mice divergently selected for methamphetamine sensitivity. Mamm Genome. 2005 May; 16(5):291-305.
Score: 0.003
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Evidence for sex-specific risk alleles in autism spectrum disorder. Am J Hum Genet. 2004 Dec; 75(6):1117-23.
Score: 0.003
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Screen for expanded FMR1 alleles in patients with essential tremor. Mov Disord. 2004 Aug; 19(8):930-3.
Score: 0.003
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Large-scale copy number polymorphism in the human genome. Science. 2004 Jul 23; 305(5683):525-8.
Score: 0.003
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LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Neurology. 2004 Apr 13; 62(7):1120-6.
Score: 0.003
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Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome. Cytogenet Genome Res. 2004; 107(1-2):68-76.
Score: 0.003
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Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24. J Med Genet. 2003 Dec; 40(12):872-8.
Score: 0.003
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Association between lipoprotein lipase (LPL) gene and blood lipids: a common variant for a common trait? Genet Epidemiol. 2003 May; 24(4):309-21.
Score: 0.003
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Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris. Cell. 2003 Apr 18; 113(2):249-60.
Score: 0.003
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Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24. Epilepsia. 2002 Jan; 43(1):60-7.
Score: 0.003
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Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families. Am J Hum Genet. 2002 Jan; 70(1):60-71.
Score: 0.003
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A genomewide screen for autism susceptibility loci. Am J Hum Genet. 2001 Aug; 69(2):327-40.
Score: 0.002
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A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22. Am J Med Genet. 2001 Mar 08; 105(2):189-94.
Score: 0.002
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A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions. Exp Dermatol. 2000 Apr; 9(2):157-62.
Score: 0.002
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The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8. Nat Genet. 1999 Oct; 23(2):233-6.
Score: 0.002
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Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration. Invest Ophthalmol Vis Sci. 1999 Aug; 40(9):2106-14.
Score: 0.002
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No evidence for significant linkage between bipolar affective disorder and chromosome 18 pericentromeric markers in a large series of multiplex extended pedigrees. Am J Hum Genet. 1998 Apr; 62(4):916-24.
Score: 0.002
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Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3. Genomics. 1998 Mar 01; 48(2):171-7.
Score: 0.002
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A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions. Hum Mol Genet. 1997 Feb; 6(2):229-36.
Score: 0.002
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Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy. Ann Neurol. 1996 Apr; 39(4):507-20.
Score: 0.002
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Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21. Am J Hum Genet. 1995 Aug; 57(2):499-502.
Score: 0.002
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Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene. Proc Natl Acad Sci U S A. 1995 Apr 25; 92(9):3702-6.
Score: 0.002
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Genetic alterations of microsatellites on chromosome 18 in human breast carcinoma. Diagn Mol Pathol. 1995 Mar; 4(1):66-72.
Score: 0.002
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Bipolar disorder and linkage to Xq28. Nat Genet. 1994 Aug; 7(4):461-2.
Score: 0.002
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Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6p. Hum Mol Genet. 1994 Aug; 3(8):1401-3.
Score: 0.002
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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: 0.001
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Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q. Nat Genet. 1993 Dec; 5(4):386-91.
Score: 0.001
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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: 0.001
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High resolution physical map of the region surrounding the spinal muscular atrophy gene. Hum Mol Genet. 1993 Aug; 2(8):1169-76.
Score: 0.001
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A genetic linkage map of the chromosome 4 short arm. Somat Cell Mol Genet. 1993 Jan; 19(1):95-101.
Score: 0.001
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A microsatellite genetic linkage map of human chromosome 13. Genomics. 1993 Jan; 15(1):76-85.
Score: 0.001
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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: 0.001
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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: 0.001
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Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13. Proc Natl Acad Sci U S A. 1991 Sep 01; 88(17):7873-6.
Score: 0.001
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A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene. Genomics. 1989 Nov; 5(4):802-9.
Score: 0.001
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Linkage studies between polymorphic markers on chromosome 4 and cystic fibrosis. Hum Genet. 1985; 69(3):250-4.
Score: 0.001
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DNA markers for nervous system diseases. Science. 1984 Sep 21; 225(4668):1320-6.
Score: 0.001
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The implications of genetic variation in human pathology. Biochem Soc Symp. 1984; 49:183-8.
Score: 0.001
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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: 0.001