T. Conrad Gilliam to Child
This is a "connection" page, showing publications T. Conrad Gilliam has written about Child.
Connection Strength
0.173
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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: 0.018
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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: 0.017
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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: 0.016
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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: 0.014
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An integrative computational approach for prioritization of genomic variants. PLoS One. 2014; 9(12):e114903.
Score: 0.014
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Genetic disorders of copper metabolism. Curr Opin Pediatr. 1994 Dec; 6(6):698-701.
Score: 0.014
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Progress toward cloning of the gene responsible for childhood spinal muscular atrophy. Semin Neurol. 1993 Sep; 13(3):276-82.
Score: 0.013
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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder. Biol Psychiatry. 2008 Jun 15; 63(12):1111-7.
Score: 0.009
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Recurrent 16p11.2 microdeletions in autism. Hum Mol Genet. 2008 Feb 15; 17(4):628-38.
Score: 0.009
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Strong association of de novo copy number mutations with autism. Science. 2007 Apr 20; 316(5823):445-9.
Score: 0.008
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LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Neurology. 2004 Apr 13; 62(7):1120-6.
Score: 0.007
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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: 0.006
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A genomewide screen for autism susceptibility loci. Am J Hum Genet. 2001 Aug; 69(2):327-40.
Score: 0.006
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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: 0.005
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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: 0.005
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Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses. Am J Hum Genet. 1997 Aug; 61(2):317-28.
Score: 0.004
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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: 0.003
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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: 0.003