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Connection

Yusuke Nakamura to Genetic Markers

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

0.666
  1. A genome-wide association study identifies three new risk loci for Kawasaki disease. Nat Genet. 2012 Mar 25; 44(5):517-21.
    View in: PubMed
    Score: 0.097
  2. Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population. Nat Genet. 2012 Mar 25; 44(5):511-6.
    View in: PubMed
    Score: 0.097
  3. Lack of association between variations of PDE4D and ischemic stroke in the Japanese population. Stroke. 2009 Apr; 40(4):1245-51.
    View in: PubMed
    Score: 0.079
  4. Pharmacogenomics and drug toxicity. N Engl J Med. 2008 Aug 21; 359(8):856-8.
    View in: PubMed
    Score: 0.076
  5. Gene expression patterns as marker for 5-year postoperative prognosis of primary breast cancers. J Cancer Res Clin Oncol. 2004 Sep; 130(9):537-45.
    View in: PubMed
    Score: 0.057
  6. Identification of 46 novel SNPs in the 130-kb region containing a myocardial infarction susceptibility gene on chromosomal band 6p21. J Hum Genet. 2003; 48(9):476-479.
    View in: PubMed
    Score: 0.054
  7. Association study of 71 European Crohn's disease susceptibility loci in a Japanese population. Inflamm Bowel Dis. 2013 Mar; 19(3):526-33.
    View in: PubMed
    Score: 0.026
  8. Physical localization of 70 polymorphic markers to human chromosome 5 by fluorescence in situ hybridization. Cytogenet Cell Genet. 1993; 62(4):207-10.
    View in: PubMed
    Score: 0.026
  9. Novel deletion mutations of OPTN in amyotrophic lateral sclerosis in Japanese. Neurobiol Aging. 2012 Aug; 33(8):1843.e19-24.
    View in: PubMed
    Score: 0.024
  10. Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients. J Hum Genet. 2007; 52(7):575-583.
    View in: PubMed
    Score: 0.017
  11. Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction. J Hum Genet. 2006; 51(12):1087-1099.
    View in: PubMed
    Score: 0.017
  12. Similarity of the allele frequency and linkage disequilibrium pattern of single nucleotide polymorphisms in drug-related gene loci between Thai and northern East Asian populations: implications for tagging SNP selection in Thais. J Hum Genet. 2006; 51(10):896-904.
    View in: PubMed
    Score: 0.017
  13. A SNP in the ABCC11 gene is the determinant of human earwax type. Nat Genet. 2006 Mar; 38(3):324-30.
    View in: PubMed
    Score: 0.016
  14. Inference from the relationships between linkage disequilibrium and allele frequency distributions of 240 candidate SNPs in 109 drug-related genes in four Asian populations. J Hum Genet. 2004; 49(10):558-572.
    View in: PubMed
    Score: 0.014
  15. Analysis of single-nucleotide polymorphisms in Japanese rheumatoid arthritis patients shows additional susceptibility markers besides the classic shared epitope susceptibility sequences. Arthritis Rheum. 2004 Jan; 50(1):63-71.
    View in: PubMed
    Score: 0.014
  16. Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseases. J Hum Genet. 2002; 47(6):275-8.
    View in: PubMed
    Score: 0.012
  17. Correlation of allelic losses and clinicopathological factors in 504 primary breast cancers. Breast Cancer. 2002; 9(3):208-15.
    View in: PubMed
    Score: 0.012
  18. A physical and genetic linkage map of the distal long arm of human chromosome 5. Cytogenet Cell Genet. 1992; 59(1):27-30.
    View in: PubMed
    Score: 0.006
  19. Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13. Diabetes. 1989 Aug; 38(8):1072-5.
    View in: PubMed
    Score: 0.005
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.