RICHARD GIBBS to DNA
This is a "connection" page, showing publications RICHARD GIBBS has written about DNA.
Connection Strength
0.838
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Whole exome sequencing in a large pedigree with DCM identifies a novel mutation in RBM20. Acta Cardiol. 2020 Dec; 75(8):748-753.
Score: 0.105
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Elimination of residual natural nucleotides from 3'-O-modified-dNTP syntheses by enzymatic mop-up. Biotechniques. 1998 Nov; 25(5):814-7.
Score: 0.098
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Termination of DNA synthesis by novel 3'-modified-deoxyribonucleoside 5'-triphosphates. Nucleic Acids Res. 1994 Oct 11; 22(20):4259-67.
Score: 0.074
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Taking DNA from the dead. Nat Rev Genet. 2010 May; 11(5):318.
Score: 0.054
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Personalized copy number and segmental duplication maps using next-generation sequencing. Nat Genet. 2009 Oct; 41(10):1061-7.
Score: 0.052
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Detection of single DNA base differences by competitive oligonucleotide priming. Nucleic Acids Res. 1989 Apr 11; 17(7):2437-48.
Score: 0.051
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Identification of mutations leading to the Lesch-Nyhan syndrome by automated direct DNA sequencing of in vitro amplified cDNA. Proc Natl Acad Sci U S A. 1989 Mar; 86(6):1919-23.
Score: 0.050
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Pooled genomic indexing of rhesus macaque. Genome Res. 2005 Feb; 15(2):292-301.
Score: 0.038
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Association of Rare Protein-Truncating DNA Variants in APOB or PCSK9 With Low-density Lipoprotein Cholesterol Level and Risk of Coronary Heart Disease. JAMA Cardiol. 2023 03 01; 8(3):258-267.
Score: 0.033
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The multiple de novo copy number variant (MdnCNV) phenomenon presents with peri-zygotic DNA mutational signatures and multilocus pathogenic variation. Genome Med. 2022 10 27; 14(1):122.
Score: 0.032
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Reassessment of biochemically determined Hunter syndrome carrier status by DNA testing. J Med Genet. 1998 Aug; 35(8):646-9.
Score: 0.024
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Pressing ahead with human genome sequencing. Nat Genet. 1995 Oct; 11(2):121-5.
Score: 0.020
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Working on the assembly line. Trends Biochem Sci. 1995 Apr; 20(4):162-3.
Score: 0.019
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Detection and genetic analysis of beta-thalassemia mutations by competitive oligopriming. Hum Mutat. 1995; 6(1):30-5.
Score: 0.019
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Complete sequence of a 38.4-kb human cosmid insert containing the polymorphic marker DXS455 from Xq28. DNA Seq. 1995; 5(4):219-23.
Score: 0.019
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Large-scale sequencing library production: an adaptor-based strategy. Anal Biochem. 1993 Apr; 210(1):16-26.
Score: 0.017
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A human dimorphism resulting from loss of an Alu. Genomics. 1992 Nov; 14(3):590-7.
Score: 0.016
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The KAT6B-related disorders genitopatellar syndrome and Ohdo/SBBYS syndrome have distinct clinical features reflecting distinct molecular mechanisms. Hum Mutat. 2012 Nov; 33(11):1520-5.
Score: 0.016
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Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan families. Genomics. 1990 Jun; 7(2):235-44.
Score: 0.014
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Deletion screening at the hypoxanthine-guanine phosphoribosyltransferase locus in Chinese hamster cells using the polymerase chain reaction. Teratog Carcinog Mutagen. 1989; 9(3):177-87.
Score: 0.012
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Automated DNA sequencing methods for detection and analysis of mutations: applications to the Lesch-Nyhan syndrome. Trans Assoc Am Physicians. 1989; 102:185-94.
Score: 0.012
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Generation of cDNA probes directed by amino acid sequence: cloning of urate oxidase. Science. 1988 Mar 11; 239(4845):1288-91.
Score: 0.012
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Shedding genomic light on Aristotle's lantern. Dev Biol. 2006 Dec 01; 300(1):2-8.
Score: 0.011
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Genomic analysis of the nuclear receptor family: new insights into structure, regulation, and evolution from the rat genome. Genome Res. 2004 Apr; 14(4):580-90.
Score: 0.009
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An allylic/acyclic adenosine nucleoside triphosphate for termination of DNA synthesis by DNA template-dependent polymerases. Nucleic Acids Res. 1999 Mar 01; 27(5):1271-4.
Score: 0.006
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A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element. Nat Genet. 1996 Mar; 12(3):288-97.
Score: 0.005
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Identification of a 2 base pair nonsense mutation causing a cryptic splice site in a DMD patient. Hum Mol Genet. 1992 Nov; 1(8):645-6.
Score: 0.004
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A transposon-like element in the deletion-prone region of the dystrophin gene. Genomics. 1992 Jul; 13(3):594-600.
Score: 0.004
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Polymerase chain reaction-based comprehensive procedure for the analysis of the mutation spectrum at the hypoxanthine-guanine phosphoribosyltransferase locus in Chinese hamster cells. Environ Mol Mutagen. 1992; 19(4):267-73.
Score: 0.004
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Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification. Nucleic Acids Res. 1988 Dec 09; 16(23):11141-56.
Score: 0.003
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Expression of the murine Duchenne muscular dystrophy gene in muscle and brain. Science. 1988 Mar 18; 239(4846):1416-8.
Score: 0.003
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The molecular basis of the sparse fur mouse mutation. Science. 1987 Jul 24; 237(4813):415-7.
Score: 0.003