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Connection

CHRIS AMOS to Genome, Human

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This is a "connection" page, showing publications CHRIS AMOS has written about Genome, Human.
CHRIS AMOS
Connection Strength
3.505
Genome, Human
  1. Untouchable genes in the human genome: Identifying ideal targets for cancer treatment. Cancer Genet. 2019 02; 231-232:67-79.
    View in: PubMed
    Score: 0.370
  2. Genome-wide association tests of inversions with application to psoriasis. Hum Genet. 2014 Aug; 133(8):967-74.
    View in: PubMed
    Score: 0.264
  3. Genomic sequencing in cancer. Cancer Lett. 2013 Nov 01; 340(2):161-70.
    View in: PubMed
    Score: 0.241
  4. Building a statistical model for predicting cancer genes. PLoS One. 2012; 7(11):e49175.
    View in: PubMed
    Score: 0.241
  5. Investigation of inversion polymorphisms in the human genome using principal components analysis. PLoS One. 2012; 7(7):e40224.
    View in: PubMed
    Score: 0.235
  6. Relative effects of mutability and selection on single nucleotide polymorphisms in transcribed regions of the human genome. BMC Genomics. 2008 Jun 17; 9:292.
    View in: PubMed
    Score: 0.177
  7. Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms. Am J Hum Genet. 2008 Jan; 82(1):100-12.
    View in: PubMed
    Score: 0.172
  8. Successful design and conduct of genome-wide association studies. Hum Mol Genet. 2007 Oct 15; 16 Spec No. 2:R220-5.
    View in: PubMed
    Score: 0.166
  9. Bias in estimates of quantitative-trait-locus effect in genome scans: demonstration of the phenomenon and a method-of-moments procedure for reducing bias. Am J Hum Genet. 2002 Mar; 70(3):575-85.
    View in: PubMed
    Score: 0.114
  10. Ancestry inference using principal component analysis and spatial analysis: a distance-based analysis to account for population substructure. BMC Genomics. 2017 Oct 16; 18(1):789.
    View in: PubMed
    Score: 0.085
  11. Allelic Spectra of Risk SNPs Are Different for Environment/Lifestyle Dependent versus Independent Diseases. PLoS Genet. 2015 Jul; 11(7):e1005371.
    View in: PubMed
    Score: 0.072
  12. Characterization of large structural genetic mosaicism in human autosomes. Am J Hum Genet. 2015 Mar 05; 96(3):487-97.
    View in: PubMed
    Score: 0.071
  13. Association and linkage with quantitative traits. Genet Epidemiol. 1995; 12(6):771-5.
    View in: PubMed
    Score: 0.070
  14. Genome-wide scan of 29,141 African Americans finds no evidence of directional selection since admixture. Am J Hum Genet. 2014 Oct 02; 95(4):437-44.
    View in: PubMed
    Score: 0.068
  15. How to get the most from microarray data: advice from reverse genomics. BMC Genomics. 2014 Mar 21; 15:223.
    View in: PubMed
    Score: 0.066
  16. Genes with a large intronic burden show greater evolutionary conservation on the protein level. BMC Evol Biol. 2014 Mar 16; 14(1):50.
    View in: PubMed
    Score: 0.066
  17. Genome-wide gene-environment interaction analysis for asbestos exposure in lung cancer susceptibility. Carcinogenesis. 2012 Aug; 33(8):1531-7.
    View in: PubMed
    Score: 0.058
  18. Genome-wide algorithm for detecting CNV associations with diseases. BMC Bioinformatics. 2011 Aug 09; 12:331.
    View in: PubMed
    Score: 0.055
  19. The landscape of recombination in African Americans. Nature. 2011 Jul 20; 476(7359):170-5.
    View in: PubMed
    Score: 0.055
  20. Association between acquired uniparental disomy and homozygous mutations and HER2/ER/PR status in breast cancer. PLoS One. 2010 Nov 30; 5(11):e15094.
    View in: PubMed
    Score: 0.053
  21. Evolutionary evidence of the effect of rare variants on disease etiology. Clin Genet. 2011 Mar; 79(3):199-206.
    View in: PubMed
    Score: 0.052
  22. Forward-time simulation of realistic samples for genome-wide association studies. BMC Bioinformatics. 2010 Sep 01; 11:442.
    View in: PubMed
    Score: 0.052
  23. Locus category based analysis of a large genome-wide association study of rheumatoid arthritis. Hum Mol Genet. 2010 Oct 01; 19(19):3863-72.
    View in: PubMed
    Score: 0.051
  24. Genome-wide gene and pathway analysis. Eur J Hum Genet. 2010 Sep; 18(9):1045-53.
    View in: PubMed
    Score: 0.051
  25. A modified forward multiple regression in high-density genome-wide association studies for complex traits. Genet Epidemiol. 2009 Sep; 33(6):518-25.
    View in: PubMed
    Score: 0.048
  26. Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. Nat Genet. 2008 May; 40(5):616-22.
    View in: PubMed
    Score: 0.044
  27. Detecting haplotype effects in genomewide association studies. Genet Epidemiol. 2007 Dec; 31(8):803-12.
    View in: PubMed
    Score: 0.043
  28. Introduction to Genetic Analysis Workshop 15 summaries. Genet Epidemiol. 2007; 31 Suppl 1:S1-6.
    View in: PubMed
    Score: 0.040
  29. A genome-wide screen for nicotine dependence susceptibility loci. Am J Med Genet B Neuropsychiatr Genet. 2006 Jun 05; 141B(4):354-60.
    View in: PubMed
    Score: 0.039
  30. Genome-wide meta-analysis for rheumatoid arthritis. Hum Genet. 2006 Jul; 119(6):634-41.
    View in: PubMed
    Score: 0.038
  31. Strength of the purifying selection against different categories of the point mutations in the coding regions of the human genome. Hum Mol Genet. 2006 Apr 01; 15(7):1143-50.
    View in: PubMed
    Score: 0.038
  32. Genome-wide linkage scan for spontaneous DZ twinning. Eur J Hum Genet. 2006 Jan; 14(1):117-22.
    View in: PubMed
    Score: 0.037
  33. An evolutionary perspective on single-nucleotide polymorphism screening in molecular cancer epidemiology. Cancer Res. 2004 Mar 15; 64(6):2251-7.
    View in: PubMed
    Score: 0.033
  34. Screening the genome for rheumatoid arthritis susceptibility genes: a replication study and combined analysis of 512 multicase families. Arthritis Rheum. 2003 Apr; 48(4):906-16.
    View in: PubMed
    Score: 0.031
  35. Testing for genetic linkage in families by a variance-components approach in the presence of genomic imprinting. Am J Hum Genet. 2002 Mar; 70(3):751-7.
    View in: PubMed
    Score: 0.029
  36. Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer. Cancer Res. 2021 06 15; 81(12):3162-3173.
    View in: PubMed
    Score: 0.027
  37. A genomewide screen in multiplex rheumatoid arthritis families suggests genetic overlap with other autoimmune diseases. Am J Hum Genet. 2001 Apr; 68(4):927-36.
    View in: PubMed
    Score: 0.027
  38. Human genes differ by their UV sensitivity estimated through analysis of UV-induced silent mutations in melanoma. Hum Mutat. 2020 10; 41(10):1751-1760.
    View in: PubMed
    Score: 0.026
  39. The quantitative LOD score: test statistic and sample size for exclusion and linkage of quantitative traits in human sibships. Am J Hum Genet. 1998 Apr; 62(4):962-8.
    View in: PubMed
    Score: 0.022
  40. A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing. Genet Epidemiol. 2017 Jan; 41(1):18-34.
    View in: PubMed
    Score: 0.020
  41. Empirical hierarchical bayes approach to gene-environment interactions: development and application to genome-wide association studies of lung cancer in TRICL. Genet Epidemiol. 2013 Sep; 37(6):551-559.
    View in: PubMed
    Score: 0.016
  42. Derived SNP alleles are used more frequently than ancestral alleles as risk-associated variants in common human diseases. J Bioinform Comput Biol. 2012 Apr; 10(2):1241008.
    View in: PubMed
    Score: 0.014
  43. Genetic Analysis Workshop 16: introduction to workshop summaries. Genet Epidemiol. 2009; 33 Suppl 1:S1-7.
    View in: PubMed
    Score: 0.012
  44. Common variants at CD40 and other loci confer risk of rheumatoid arthritis. Nat Genet. 2008 Oct; 40(10):1216-23.
    View in: PubMed
    Score: 0.011
  45. A major lung cancer susceptibility locus maps to chromosome 6q23-25. Am J Hum Genet. 2004 Sep; 75(3):460-74.
    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.