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Connection

KATHRYN OSTERMAIER to Polymorphism, Single Nucleotide

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This is a "connection" page, showing publications KATHRYN OSTERMAIER has written about Polymorphism, Single Nucleotide.
KATHRYN OSTERMAIER
Connection Strength
0.074
Polymorphism, Single Nucleotide
  1. Association of retinoic acid receptor genes with meningomyelocele. Birth Defects Res A Clin Mol Teratol. 2011 Jan; 91(1):39-43.
    View in: PubMed
    Score: 0.048
  2. Association of copper-zinc superoxide dismutase (SOD1) and manganese superoxide dismutase (SOD2) genes with nonsyndromic myelomeningocele. Birth Defects Res A Clin Mol Teratol. 2012 Oct; 94(10):762-9.
    View in: PubMed
    Score: 0.014
  3. Association of folate receptor (FOLR1, FOLR2, FOLR3) and reduced folate carrier (SLC19A1) genes with meningomyelocele. Birth Defects Res A Clin Mol Teratol. 2010 Aug; 88(8):689-94.
    View in: PubMed
    Score: 0.012
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.