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Yusuke Nakamura to Genome, Human

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This is a "connection" page, showing publications Yusuke Nakamura has written about Genome, Human.
Yusuke Nakamura
Connection Strength
3.303
Genome, Human
  1. Predicting response to docetaxel neoadjuvant chemotherapy for advanced breast cancers through genome-wide gene expression profiling. Int J Oncol. 2009 Feb; 34(2):361-70.
    View in: PubMed
    Score: 0.239
  2. Genome-wide gene expression profile analysis of esophageal squamous cell carcinomas. Int J Oncol. 2006 Jun; 28(6):1375-84.
    View in: PubMed
    Score: 0.199
  3. [BioBank Japan project]. Nihon Rinsho. 2005 Dec; 63 Suppl 12:35-41.
    View in: PubMed
    Score: 0.192
  4. Predicting response to methotrexate, vinblastine, doxorubicin, and cisplatin neoadjuvant chemotherapy for bladder cancers through genome-wide gene expression profiling. Clin Cancer Res. 2005 Apr 01; 11(7):2625-36.
    View in: PubMed
    Score: 0.183
  5. Comparison of gene-expression profiles between diffuse- and intestinal-type gastric cancers using a genome-wide cDNA microarray. Oncogene. 2004 Sep 02; 23(40):6830-44.
    View in: PubMed
    Score: 0.176
  6. Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome. Hum Mol Genet. 2004 Aug 01; 13(15):1623-32.
    View in: PubMed
    Score: 0.173
  7. Genome-wide analysis of organ-preferential metastasis of human small cell lung cancer in mice. Mol Cancer Res. 2003 May; 1(7):485-99.
    View in: PubMed
    Score: 0.161
  8. Genome-wide profiling of gene expression in 29 normal human tissues with a cDNA microarray. DNA Res. 2002 Apr 30; 9(2):35-45.
    View in: PubMed
    Score: 0.150
  9. 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: 0.146
  10. 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: 0.146
  11. Trans-ethnic meta-analysis of white blood cell phenotypes. Hum Mol Genet. 2014 Dec 20; 23(25):6944-60.
    View in: PubMed
    Score: 0.088
  12. Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes. PLoS One. 2013; 8(11):e78511.
    View in: PubMed
    Score: 0.083
  13. Pathway analysis of genome-wide data improves warfarin dose prediction. BMC Genomics. 2013; 14 Suppl 3:S11.
    View in: PubMed
    Score: 0.081
  14. A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population. J Hum Genet. 2012 Apr; 57(4):235-7.
    View in: PubMed
    Score: 0.074
  15. Meta-analysis of published studies identified eight additional common susceptibility loci for Crohn's disease and ulcerative colitis. Inflamm Bowel Dis. 2011 Dec; 17(12):2407-15.
    View in: PubMed
    Score: 0.069
  16. Whole-genome sequencing and comprehensive variant analysis of a Japanese individual using massively parallel sequencing. Nat Genet. 2010 Nov; 42(11):931-6.
    View in: PubMed
    Score: 0.067
  17. A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B. Nat Genet. 2010 Oct; 42(10):864-8.
    View in: PubMed
    Score: 0.067
  18. International network of cancer genome projects. Nature. 2010 Apr 15; 464(7291):993-8.
    View in: PubMed
    Score: 0.065
  19. Population-genetic nature of copy number variations in the human genome. Hum Mol Genet. 2010 Mar 01; 19(5):761-73.
    View in: PubMed
    Score: 0.063
  20. Genetic variation in PSCA is associated with susceptibility to diffuse-type gastric cancer. Nat Genet. 2008 Jun; 40(6):730-40.
    View in: PubMed
    Score: 0.057
  21. Multiplex PCR-based real-time invader assay (mPCR-RETINA): a novel SNP-based method for detecting allelic asymmetries within copy number variation regions. Hum Mutat. 2008 Jan; 29(1):182-9.
    View in: PubMed
    Score: 0.055
  22. Recombination rates of genes expressed in human tissues. Hum Mol Genet. 2008 Feb 15; 17(4):577-86.
    View in: PubMed
    Score: 0.055
  23. Genome-wide detection and characterization of positive selection in human populations. Nature. 2007 Oct 18; 449(7164):913-8.
    View in: PubMed
    Score: 0.055
  24. Prediction of risk of disease recurrence by genome-wide cDNA microarray analysis in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia treated with imatinib-combined chemotherapy. Int J Oncol. 2007 Aug; 31(2):313-22.
    View in: PubMed
    Score: 0.054
  25. Linkage disequilibrium of evolutionarily conserved regions in the human genome. BMC Genomics. 2006 Dec 28; 7:326.
    View in: PubMed
    Score: 0.052
  26. A genomewide linkage analysis of Kawasaki disease: evidence for linkage to chromosome 12. J Hum Genet. 2007; 52(2):179-190.
    View in: PubMed
    Score: 0.052
  27. Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. Hum Mol Genet. 2005 Nov 15; 14(22):3499-506.
    View in: PubMed
    Score: 0.048
  28. Genome-wide analysis of gene expression in human intrahepatic cholangiocarcinoma. Hepatology. 2005 Jun; 41(6):1339-48.
    View in: PubMed
    Score: 0.046
  29. Association of solute carrier family 12 (sodium/chloride) member 3 with diabetic nephropathy, identified by genome-wide analyses of single nucleotide polymorphisms. Diabetes. 2003 Nov; 52(11):2848-53.
    View in: PubMed
    Score: 0.042
  30. Genome-wide analysis of gene-expression profiles in chronic myeloid leukemia cells using a cDNA microarray. Int J Oncol. 2003 Sep; 23(3):681-91.
    View in: PubMed
    Score: 0.041
  31. Genome-wide analysis of gene expression in intestinal-type gastric cancers using a complementary DNA microarray representing 23,040 genes. Cancer Res. 2002 Dec 01; 62(23):7012-7.
    View in: PubMed
    Score: 0.039
  32. Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism. J Hum Genet. 2002; 47(11):605-10.
    View in: PubMed
    Score: 0.037
  33. Molecular features of triple negative breast cancer cells by genome-wide gene expression profiling analysis. Int J Oncol. 2013 Feb; 42(2):478-506.
    View in: PubMed
    Score: 0.020
  34. New gene functions in megakaryopoiesis and platelet formation. Nature. 2011 Nov 30; 480(7376):201-8.
    View in: PubMed
    Score: 0.018
  35. Genome-wide association study identifies two susceptibility loci for exudative age-related macular degeneration in the Japanese population. Nat Genet. 2011 Sep 11; 43(10):1001-4.
    View in: PubMed
    Score: 0.018
  36. hzAnalyzer: detection, quantification, and visualization of contiguous homozygosity in high-density genotyping datasets. Genome Biol. 2011; 12(3):R21.
    View in: PubMed
    Score: 0.017
  37. Identification of evidence suggestive of an association with peripheral arterial disease at the OSBPL10 locus by genome-wide investigation in the Japanese population. J Atheroscler Thromb. 2010 Oct 27; 17(10):1054-62.
    View in: PubMed
    Score: 0.016
  38. Establishment of a standardized system to perform population structure analyses with limited sample size or with different sets of SNP genotypes. J Hum Genet. 2010 Aug; 55(8):525-33.
    View in: PubMed
    Score: 0.016
  39. Making a haplotype catalog with estimated frequencies based on SNP homozygotes. J Hum Genet. 2010 Aug; 55(8):500-6.
    View in: PubMed
    Score: 0.016
  40. Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nat Genet. 2009 Dec; 41(12):1303-7.
    View in: PubMed
    Score: 0.016
  41. Criterion values for multiplex SNP genotyping by the invader assay. Forensic Sci Int Genet. 2010 Feb; 4(2):130-6.
    View in: PubMed
    Score: 0.016
  42. A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians. Nat Genet. 2009 May; 41(5):591-5.
    View in: PubMed
    Score: 0.015
  43. Functional SNPs in CD244 increase the risk of rheumatoid arthritis in a Japanese population. Nat Genet. 2008 Oct; 40(10):1224-9.
    View in: PubMed
    Score: 0.015
  44. 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: 0.014
  45. Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. Nat Genet. 2008 May; 40(5):631-7.
    View in: PubMed
    Score: 0.014
  46. Molecular features of hormone-refractory prostate cancer cells by genome-wide gene expression profiles. Cancer Res. 2007 Jun 01; 67(11):5117-25.
    View in: PubMed
    Score: 0.013
  47. Novel tumor marker REG4 detected in serum of patients with resectable pancreatic cancer and feasibility for antibody therapy targeting REG4. Cancer Sci. 2006 Nov; 97(11):1191-7.
    View in: PubMed
    Score: 0.013
  48. Genome-wide analysis of gene expression in synovial sarcomas using a cDNA microarray. Cancer Res. 2002 Oct 15; 62(20):5859-66.
    View in: PubMed
    Score: 0.010
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.