Connection

DAVID NELSON to Genetic Variation

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

1.141
  1. X-cess of variants in XLMR. Nat Genet. 2009 May; 41(5):510-2.
    View in: PubMed
    Score: 0.200
  2. Prevalence and cardiometabolic correlates of ketohexokinase gene variants among UK Biobank participants. PLoS One. 2021; 16(2):e0247683.
    View in: PubMed
    Score: 0.113
  3. SNPs, lonkage disequilibrium, human genetic variation and Native American culture. Trends Genet. 2001 Jan; 17(1):15-6.
    View in: PubMed
    Score: 0.112
  4. 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: 0.111
  5. Distribution and Diversity of Cytochrome P450 Monooxygenases in the Fungal Class Tremellomycetes. Int J Mol Sci. 2019 Jun 13; 20(12).
    View in: PubMed
    Score: 0.101
  6. Genetic variation and evolutionary stability of the FMR1 CGG repeat in six closed human populations. Am J Med Genet. 1996 Jul 12; 64(1):220-5.
    View in: PubMed
    Score: 0.082
  7. How Obstacles Perturb Population Fronts and Alter Their Genetic Structure. PLoS Comput Biol. 2015 Dec; 11(12):e1004615.
    View in: PubMed
    Score: 0.079
  8. Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions. Hum Mol Genet. 1995 Dec; 4(12):2199-208.
    View in: PubMed
    Score: 0.079
  9. Whole-Genome Resequencing Reveals Extensive Natural Variation in the Model Green Alga Chlamydomonas reinhardtii. Plant Cell. 2015 Sep; 27(9):2353-69.
    View in: PubMed
    Score: 0.078
  10. Diversity and evolution of cytochrome P450 monooxygenases in Oomycetes. Sci Rep. 2015 Jul 01; 5:11572.
    View in: PubMed
    Score: 0.077
  11. 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: 0.031
  12. 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: 0.031
  13. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell. 1991 May 31; 65(5):905-14.
    View in: PubMed
    Score: 0.029
  14. Genetic drift opposes mutualism during spatial population expansion. Proc Natl Acad Sci U S A. 2014 Jan 21; 111(3):1037-42.
    View in: PubMed
    Score: 0.017
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.