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Connection

Yusuke Nakamura to Pedigree

This is a "connection" page, showing publications Yusuke Nakamura has written about Pedigree.
Connection Strength

0.112
  1. Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues. Am J Hum Genet. 2003 Jan; 72(1):73-82.
    View in: PubMed
    Score: 0.042
  2. Submicroscopic deletions at 13q32.1 cause congenital microcoria. Am J Hum Genet. 2015 Apr 02; 96(4):631-9.
    View in: PubMed
    Score: 0.024
  3. Aberrant splicing caused by a MLH1 splice donor site mutation found in a young Japanese patient with Lynch syndrome. Fam Cancer. 2012 Dec; 11(4):559-64.
    View in: PubMed
    Score: 0.021
  4. Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion. Nat Genet. 2007 Jun; 39(6):776-80.
    View in: PubMed
    Score: 0.014
  5. Heterozygous TGFBR2 mutations in Marfan syndrome. Nat Genet. 2004 Aug; 36(8):855-60.
    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.