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Connection

Yusuke Nakamura to Phenotype

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

0.561
  1. Trans-ethnic meta-analysis of white blood cell phenotypes. Hum Mol Genet. 2014 Dec 20; 23(25):6944-60.
    View in: PubMed
    Score: 0.079
  2. Multiple loci are associated with white blood cell phenotypes. PLoS Genet. 2011 Jun; 7(6):e1002113.
    View in: PubMed
    Score: 0.063
  3. An association study of asthma and related phenotypes with polymorphisms in negative regulator molecules of the TLR signaling pathway. J Hum Genet. 2006; 51(4):284-291.
    View in: PubMed
    Score: 0.043
  4. Catalog of 178 variations in the Japanese population among eight human genes encoding G protein-coupled receptors (GPCRs). J Hum Genet. 2003; 48(9):461-468.
    View in: PubMed
    Score: 0.037
  5. Catalog of 680 variations among eight cytochrome p450 ( CYP) genes, nine esterase genes, and two other genes in the Japanese population. J Hum Genet. 2003; 48(5):249-270.
    View in: PubMed
    Score: 0.036
  6. Identification of 779 genetic variations in eight genes encoding members of the ATP-binding cassette, subfamily C (ABCC/MRP/CFTR. J Hum Genet. 2002; 47(4):147-71.
    View in: PubMed
    Score: 0.033
  7. 906 variations among 27 genes encoding cytochrome P450 (CYP) enzymes and aldehyde dehydrogenases (ALDHs) in the Japanese population. J Hum Genet. 2002; 47(8):419-44.
    View in: PubMed
    Score: 0.033
  8. Catalog of 238 variations among six human genes encoding solute carriers ( hSLCs) in the Japanese population. J Hum Genet. 2002; 47(11):576-84.
    View in: PubMed
    Score: 0.033
  9. A cross-population atlas of genetic associations for 220 human phenotypes. Nat Genet. 2021 10; 53(10):1415-1424.
    View in: PubMed
    Score: 0.032
  10. Integration of mouse and human genome-wide association data identifies KCNIP4 as an asthma gene. PLoS One. 2013; 8(2):e56179.
    View in: PubMed
    Score: 0.018
  11. Genome-wide association analysis in asthma subjects identifies SPATS2L as a novel bronchodilator response gene. PLoS Genet. 2012 Jul; 8(7):e1002824.
    View in: PubMed
    Score: 0.017
  12. Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). PLoS Genet. 2011 Jun; 7(6):e1002108.
    View in: PubMed
    Score: 0.016
  13. The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population. Hum Mol Genet. 2011 Jul 01; 20(13):2680-5.
    View in: PubMed
    Score: 0.016
  14. A functional single nucleotide polymorphism in mucin 1, at chromosome 1q22, determines susceptibility to diffuse-type gastric cancer. Gastroenterology. 2011 Mar; 140(3):892-902.
    View in: PubMed
    Score: 0.015
  15. Making a haplotype catalog with estimated frequencies based on SNP homozygotes. J Hum Genet. 2010 Aug; 55(8):500-6.
    View in: PubMed
    Score: 0.015
  16. A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. Hum Genet. 2010 Mar; 127(3):303-14.
    View in: PubMed
    Score: 0.014
  17. An algorithm for inferring complex haplotypes in a region of copy-number variation. Am J Hum Genet. 2008 Aug; 83(2):157-69.
    View in: PubMed
    Score: 0.013
  18. MOCSphaser: a haplotype inference tool from a mixture of copy number variation and single nucleotide polymorphism data. Bioinformatics. 2008 Jul 15; 24(14):1645-6.
    View in: PubMed
    Score: 0.013
  19. Functional promoter polymorphism in the TBX21 gene associated with aspirin-induced asthma. Hum Genet. 2005 Jun; 117(1):16-26.
    View in: PubMed
    Score: 0.010
  20. Fukutin is required for maintenance of muscle integrity, cortical histiogenesis and normal eye development. Hum Mol Genet. 2003 Jun 15; 12(12):1449-59.
    View in: PubMed
    Score: 0.009
  21. Nucleotide pyrophosphatase gene polymorphism associated with ossification of the posterior longitudinal ligament of the spine. J Bone Miner Res. 2002 Jan; 17(1):138-44.
    View in: PubMed
    Score: 0.008
  22. 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: 0.008
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.