T. Conrad Gilliam to Genetic Linkage
This is a "connection" page, showing publications T. Conrad Gilliam has written about Genetic Linkage.
Connection Strength
1.686
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A microsatellite genetic linkage map of human chromosome 18. Genomics. 1993 Jan; 15(1):48-56.
Score: 0.093
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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.
Score: 0.081
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Physical mapping, linkage analysis of a putative schizophrenia locus on chromosome 5q. Schizophr Bull. 1989; 15(3):441-52.
Score: 0.070
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Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network. Genome Res. 2008 Jul; 18(7):1150-62.
Score: 0.067
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A DNA segment encoding two genes very tightly linked to Huntington's disease. Science. 1987 Nov 13; 238(4829):950-2.
Score: 0.065
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Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet. 2007 Mar; 39(3):319-28.
Score: 0.062
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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: 0.061
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Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis, suicide, and panic disorder. Mol Psychiatry. 2006 Mar; 11(3):252-60.
Score: 0.058
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Psychosis and the genetic spectrum of bipolar disorder: evidence from linkage analysis. Mol Psychiatry. 2006 Jan; 11(1):3-5.
Score: 0.057
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Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q. Am J Hum Genet. 2005 Oct; 77(4):582-95.
Score: 0.056
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Absence of psychosis may influence linkage results for bipolar disorder. Mol Psychiatry. 2005 Mar; 10(3):235-7.
Score: 0.054
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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: 0.052
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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: 0.052
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LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Neurology. 2004 Apr 13; 62(7):1120-6.
Score: 0.051
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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: 0.043
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Genomewide linkage analysis of celiac disease in Finnish families. Am J Hum Genet. 2002 Jan; 70(1):51-9.
Score: 0.043
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A genomewide screen for autism susceptibility loci. Am J Hum Genet. 2001 Aug; 69(2):327-40.
Score: 0.042
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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: 0.041
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Mapping complex traits in diseases of the hair and skin. Exp Dermatol. 1999 Dec; 8(6):439-52.
Score: 0.037
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A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus. Am J Hum Genet. 1999 Jan; 64(1):210-7.
Score: 0.035
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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: 0.033
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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: 0.033
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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: 0.029
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Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy. Ann Neurol. 1996 Apr; 39(4):507-20.
Score: 0.029
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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: 0.028
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Autosomal dominant distal spinal muscular atrophy in four generations. Neurology. 1995 Apr; 45(4):699-704.
Score: 0.027
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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: 0.026
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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: 0.023
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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: 0.023
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A microsatellite genetic linkage map of human chromosome 13. Genomics. 1993 Jan; 15(1):76-85.
Score: 0.023
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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: 0.023
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Mapping psychiatric disease genes: impact of new molecular strategies. J Psychiatr Res. 1992 Oct; 26(4):309-26.
Score: 0.023
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Genetic analysis of childhood-onset spinal muscular atrophy. Adv Neurol. 1991; 56:181-7.
Score: 0.020
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Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7q. Am J Med Genet B Neuropsychiatr Genet. 2011 Mar; 156(2):168-76.
Score: 0.020
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Genetic homogeneity between acute and chronic forms of spinal muscular atrophy. Nature. 1990 Jun 28; 345(6278):823-5.
Score: 0.019
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Report of a workshop on genetic linkage studies in schizophrenia. Schizophr Bull. 1990; 16(4):673-86.
Score: 0.019
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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: 0.019
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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: 0.019
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Pairwise linkage analysis of 11 loci on human chromosome 4. Am J Hum Genet. 1988 Mar; 42(3):490-7.
Score: 0.017
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Molecular genetic strategies to investigate Huntington's disease. Adv Neurol. 1988; 48:17-29.
Score: 0.016
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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: 0.016
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Genetic linkage analysis of neurofibromatosis with DNA markers. Ann N Y Acad Sci. 1986; 486:304-10.
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: 0.013
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DNA markers for nervous system diseases. Science. 1984 Sep 21; 225(4668):1320-6.
Score: 0.013
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Bipolar disorder and linkage to Xq28. Nat Genet. 1994 Aug; 7(4):461-2.
Score: 0.006
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Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q. Nat Genet. 1993 Dec; 5(4):386-91.
Score: 0.006
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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: 0.006
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Molecular and statistical approaches to the detection and correction of errors in genotype databases. Am J Hum Genet. 1993 Nov; 53(5):1137-45.
Score: 0.006
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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: 0.005
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Molecular genetics of human chromosome 4. J Med Genet. 1986 Jun; 23(3):193-9.
Score: 0.004
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Molecular genetics of Huntington's disease. Cold Spring Harb Symp Quant Biol. 1986; 51 Pt 1:359-64.
Score: 0.004
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The implications of genetic variation in human pathology. Biochem Soc Symp. 1984; 49:183-8.
Score: 0.003