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CHRIS AMOS to Quantitative Trait Loci

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This is a "connection" page, showing publications CHRIS AMOS has written about Quantitative Trait Loci.
CHRIS AMOS
Connection Strength
3.708
Quantitative Trait Loci
  1. SNP eQTL status and eQTL density in the adjacent region of the SNP are associated with its statistical significance in GWA studies. BMC Genet. 2019 11 12; 20(1):85.
    View in: PubMed
    Score: 0.564
  2. A unified framework integrating parent-of-origin effects for association study. PLoS One. 2013; 8(8):e72208.
    View in: PubMed
    Score: 0.366
  3. Imprinting detection by extending a regression-based QTL analysis method. Hum Genet. 2007 Sep; 122(2):159-74.
    View in: PubMed
    Score: 0.238
  4. Genomic imprinting and linkage test for quantitative-trait Loci in extended pedigrees. Am J Hum Genet. 2003 Oct; 73(4):933-8.
    View in: PubMed
    Score: 0.184
  5. Effect of Box-Cox transformation on power of Haseman-Elston and maximum-likelihood variance components tests to detect quantitative trait Loci. Hum Hered. 2003; 55(2-3):108-16.
    View in: PubMed
    Score: 0.175
  6. Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer. Nat Genet. 2022 08; 54(8):1167-1177.
    View in: PubMed
    Score: 0.170
  7. Genetic variants associated mRNA stability in lung. BMC Genomics. 2022 Mar 11; 23(1):196.
    View in: PubMed
    Score: 0.166
  8. Incorporating multiple sets of eQTL weights into gene-by-environment interaction analysis identifies novel susceptibility loci for pancreatic cancer. Genet Epidemiol. 2020 11; 44(8):880-892.
    View in: PubMed
    Score: 0.148
  9. Functional annotation of melanoma risk loci identifies novel susceptibility genes. Carcinogenesis. 2020 06 17; 41(4):452-457.
    View in: PubMed
    Score: 0.147
  10. Joint modeling of eQTLs and parent-of-origin effects using an orthogonal framework with RNA-seq data. Hum Genet. 2020 Aug; 139(8):1107-1117.
    View in: PubMed
    Score: 0.145
  11. A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits. Genet Epidemiol. 2016 Dec; 40(8):702-721.
    View in: PubMed
    Score: 0.112
  12. Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population. Lung Cancer. 2016 08; 98:33-42.
    View in: PubMed
    Score: 0.111
  13. Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans. Hum Mol Genet. 2013 Jul 15; 22(14):2948-59.
    View in: PubMed
    Score: 0.089
  14. Ascertainment correction for Markov chain Monte Carlo segregation and linkage analysis of a quantitative trait. Genet Epidemiol. 2007 Sep; 31(6):594-604.
    View in: PubMed
    Score: 0.060
  15. An empirical Bayes method for updating inferences in analysis of quantitative trait loci using information from related genome scans. Genetics. 2006 Aug; 173(4):2283-96.
    View in: PubMed
    Score: 0.056
  16. Empirical bayes method for incorporating data from multiple genome scans. Hum Hered. 2005; 60(1):36-42.
    View in: PubMed
    Score: 0.053
  17. Genetic Architecture of Idiopathic Inflammatory Myopathies From Meta-Analyses. Arthritis Rheumatol. 2025 Jun; 77(6):750-764.
    View in: PubMed
    Score: 0.051
  18. New joint covariance- and marginal-based tests for association and linkage for quantitative traits for random and non-random sampling. Genet Epidemiol. 2005 Jan; 28(1):48-57.
    View in: PubMed
    Score: 0.050
  19. Context-aware single-cell multiomics approach identifies cell-type-specific lung cancer susceptibility genes. Nat Commun. 2024 09 12; 15(1):7995.
    View in: PubMed
    Score: 0.049
  20. Effect of winsorization on power and type 1 error of variance components and related methods of QTL detection. Behav Genet. 2004 Mar; 34(2):153-9.
    View in: PubMed
    Score: 0.047
  21. Germline determinants of humoral immune response to HPV-16 protect against oropharyngeal cancer. Nat Commun. 2021 10 12; 12(1):5945.
    View in: PubMed
    Score: 0.040
  22. A Genome-Wide Association Study Identifies Two Novel Susceptible Regions for Squamous Cell Carcinoma of the Head and Neck. Cancer Res. 2020 06 15; 80(12):2451-2460.
    View in: PubMed
    Score: 0.036
  23. Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q. Cancer Epidemiol Biomarkers Prev. 2020 02; 29(2):434-442.
    View in: PubMed
    Score: 0.035
  24. Transcriptome-wide association study reveals candidate causal genes for lung cancer. Int J Cancer. 2020 04 01; 146(7):1862-1878.
    View in: PubMed
    Score: 0.035
  25. Systematic analyses of regulatory variants in DNase I hypersensitive sites identified two novel lung cancer susceptibility loci. Carcinogenesis. 2019 05 14; 40(3):432-440.
    View in: PubMed
    Score: 0.034
  26. Genetic variants in the calcium signaling pathway genes are associated with cutaneous melanoma-specific survival. Carcinogenesis. 2019 04 29; 40(2):279-288.
    View in: PubMed
    Score: 0.034
  27. Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women. Gynecol Oncol. 2019 05; 153(2):343-355.
    View in: PubMed
    Score: 0.034
  28. Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk. Nat Commun. 2018 08 13; 9(1):3221.
    View in: PubMed
    Score: 0.032
  29. Genetic variants in RORA and DNMT1 associated with cutaneous melanoma survival. Int J Cancer. 2018 06 01; 142(11):2303-2312.
    View in: PubMed
    Score: 0.031
  30. Novel genetic variants in the P38MAPK pathway gene ZAK and susceptibility to lung cancer. Mol Carcinog. 2018 02; 57(2):216-224.
    View in: PubMed
    Score: 0.031
  31. Metabolome-wide association study identified the association between a circulating polyunsaturated fatty acids variant rs174548 and lung cancer. Carcinogenesis. 2017 10 26; 38(11):1147-1154.
    View in: PubMed
    Score: 0.031
  32. Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence. Mol Psychiatry. 2018 09; 23(9):1911-1919.
    View in: PubMed
    Score: 0.030
  33. Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. Nat Genet. 2017 Jul; 49(7):1126-1132.
    View in: PubMed
    Score: 0.030
  34. Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. Nat Genet. 2017 May; 49(5):789-794.
    View in: PubMed
    Score: 0.029
  35. Associations between genetic variants in mRNA splicing-related genes and risk of lung cancer: a pathway-based analysis from published GWASs. Sci Rep. 2017 03 17; 7:44634.
    View in: PubMed
    Score: 0.029
  36. Gene-set meta-analysis of lung cancer identifies pathway related to systemic lupus erythematosus. PLoS One. 2017; 12(3):e0173339.
    View in: PubMed
    Score: 0.029
  37. 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: 0.029
  38. Susceptibility loci of CNOT6 in the general mRNA degradation pathway and lung cancer risk-A re-analysis of eight GWASs. Mol Carcinog. 2017 04; 56(4):1227-1238.
    View in: PubMed
    Score: 0.029
  39. Genetic variants in the PIWI-piRNA pathway gene DCP1A predict melanoma disease-specific survival. Int J Cancer. 2016 Dec 15; 139(12):2730-2737.
    View in: PubMed
    Score: 0.028
  40. Prediction of the gene expression in normal lung tissue by the gene expression in blood. BMC Med Genomics. 2015 Nov 17; 8:77.
    View in: PubMed
    Score: 0.027
  41. Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups. Ann Rheum Dis. 2016 Aug; 75(8):1558-66.
    View in: PubMed
    Score: 0.026
  42. Functional characterization of RAD52 as a lung cancer susceptibility gene in the 12p13.33 locus. Mol Carcinog. 2016 May; 55(5):953-63.
    View in: PubMed
    Score: 0.026
  43. Forward-time simulations of human populations with complex diseases. PLoS Genet. 2007 Mar 23; 3(3):e47.
    View in: PubMed
    Score: 0.015
  44. 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: 0.014
  45. Possible genomic imprinting of three human obesity-related genetic loci. Am J Hum Genet. 2005 Mar; 76(3):427-37.
    View in: PubMed
    Score: 0.013
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.