Connection

DAVID NELSON to Polymorphism, Single Nucleotide

This is a "connection" page, showing publications DAVID NELSON has written about Polymorphism, Single Nucleotide.
Connection Strength

0.397
  1. Complex SNP-based haplotypes in three human helicases: implications for cancer association studies. Genome Res. 2002 Apr; 12(4):627-39.
    View in: PubMed
    Score: 0.099
  2. SNPs, lonkage disequilibrium, human genetic variation and Native American culture. Trends Genet. 2001 Jan; 17(1):15-6.
    View in: PubMed
    Score: 0.091
  3. Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium. Am J Hum Genet. 2000 Dec; 67(6):1437-51.
    View in: PubMed
    Score: 0.090
  4. CC genotype donors for the interleukin-28B single nucleotide polymorphism are associated with better outcomes in hepatitis C after liver transplant. Liver Int. 2013 Jan; 33(1):72-8.
    View in: PubMed
    Score: 0.052
  5. Haplotype and linkage disequilibrium architecture for human cancer-associated genes. Genome Res. 2002 Dec; 12(12):1846-53.
    View in: PubMed
    Score: 0.026
  6. 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: 0.024
  7. Positive selection of a pre-expansion CAG repeat of the human SCA2 gene. PLoS Genet. 2005 Sep; 1(3):e41.
    View in: PubMed
    Score: 0.008
  8. The DNA sequence of the human X chromosome. Nature. 2005 Mar 17; 434(7031):325-37.
    View in: PubMed
    Score: 0.008
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.