Connection

DAVID NELSON to Chromosome Mapping

This is a "connection" page, showing publications DAVID NELSON has written about Chromosome Mapping.
Connection Strength

0.861
  1. The human secretin gene: fine structure in 11p15.5 and sequence variation in patients with autism. Genomics. 2002 Aug; 80(2):185-94.
    View in: PubMed
    Score: 0.157
  2. Molecular definition of pericentric inversion breakpoints occurring during the evolution of humans and chimpanzees. Genomics. 1998 Jun 15; 50(3):368-72.
    View in: PubMed
    Score: 0.118
  3. Positional cloning reaches maturity. Curr Opin Genet Dev. 1995 Jun; 5(3):298-303.
    View in: PubMed
    Score: 0.096
  4. Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources. Proc Natl Acad Sci U S A. 1989 Sep; 86(17):6686-90.
    View in: PubMed
    Score: 0.064
  5. Metaphase chromosome transfer of introduced selectable markers. J Mol Appl Genet. 1984; 2(6):563-77.
    View in: PubMed
    Score: 0.043
  6. Haplotype and linkage disequilibrium architecture for human cancer-associated genes. Genome Res. 2002 Dec; 12(12):1846-53.
    View in: PubMed
    Score: 0.040
  7. Impaired conditioned fear and enhanced long-term potentiation in Fmr2 knock-out mice. J Neurosci. 2002 Apr 01; 22(7):2753-63.
    View in: PubMed
    Score: 0.038
  8. Physical and genetic characterization reveals a pseudogene, an evolutionary junction, and unstable loci in distal Xq28. Genomics. 2002 Jan; 79(1):31-40.
    View in: PubMed
    Score: 0.038
  9. MSG1 (melanocyte-specific gene 1): mapping to chromosome Xq13.1, genomic organization, and promoter analysis. Genomics. 1998 Aug 01; 51(3):401-7.
    View in: PubMed
    Score: 0.030
  10. Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution. Hum Mol Genet. 1996 Jul; 5(7):899-912.
    View in: PubMed
    Score: 0.026
  11. A de novo deletion in FMR1 in a patient with developmental delay. Hum Mol Genet. 1994 Sep; 3(9):1705-6.
    View in: PubMed
    Score: 0.023
  12. Regional assignment of 19 X-linked ESTs. Hum Mol Genet. 1993 Nov; 2(11):1901-5.
    View in: PubMed
    Score: 0.021
  13. Genome analysis and the human X chromosome. Science. 1992 Oct 02; 258(5079):103-9.
    View in: PubMed
    Score: 0.020
  14. Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locus. Proc Natl Acad Sci U S A. 1991 Jul 15; 88(14):6157-61.
    View in: PubMed
    Score: 0.018
  15. Report of the X chromosome workshop. Genomics. 1990 Aug; 7(4):647-54.
    View in: PubMed
    Score: 0.017
  16. Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequence polymerase chain reaction. Genomics. 1990 Mar; 6(3):475-81.
    View in: PubMed
    Score: 0.017
  17. Eucaryotic chromosome transfer: production of a murine-specific cosmid library from a neor-linked fragment of murine chromosome 17. Mol Cell Biol. 1986 Feb; 6(2):441-51.
    View in: PubMed
    Score: 0.013
  18. Positive selection of a pre-expansion CAG repeat of the human SCA2 gene. PLoS Genet. 2005 Sep; 1(3):e41.
    View in: PubMed
    Score: 0.012
  19. Eukaryotic chromosome transfer: linkage of the murine major histocompatibility complex to an inserted dominant selectable marker. Proc Natl Acad Sci U S A. 1984 Aug; 81(15):4879-83.
    View in: PubMed
    Score: 0.011
  20. Initial sequencing and analysis of the human genome. Nature. 2001 Feb 15; 409(6822):860-921.
    View in: PubMed
    Score: 0.009
  21. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. Nat Genet. 2000 Oct; 26(2):191-4.
    View in: PubMed
    Score: 0.009
  22. Filamin (FLN1), plexin (SEX), major palmitoylated protein p55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2. Am J Med Genet. 2000 Sep 04; 94(1):79-84.
    View in: PubMed
    Score: 0.009
  23. Mutation analysis of the DKC1 gene in incontinentia pigmenti. J Med Genet. 1999 Nov; 36(11):860-2.
    View in: PubMed
    Score: 0.008
  24. Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity. Hum Mol Genet. 1997 Jul; 6(7):991-1002.
    View in: PubMed
    Score: 0.007
  25. Molecular and phenotypic variation in patients with severe Hunter syndrome. Hum Mol Genet. 1997 Mar; 6(3):479-86.
    View in: PubMed
    Score: 0.007
  26. Report and abstracts of the Fourth International Workshop on Human X Chromosome Mapping 1993. St. Louis, Missouri, May 9-12, 1993. Cytogenet Cell Genet. 1993; 64(3-4):147-94.
    View in: PubMed
    Score: 0.005
  27. Direct cloning of human transcripts with HnRNA from hybrid cell lines. Science. 1990 Aug 10; 249(4969):652-5.
    View in: PubMed
    Score: 0.004
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.