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Connection

CHRIS AMOS to Genetic Association Studies

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This is a "connection" page, showing publications CHRIS AMOS has written about Genetic Association Studies.
CHRIS AMOS
Connection Strength
1.285
Genetic Association Studies
  1. Linear mixed models for association analysis of quantitative traits with next-generation sequencing data. Genet Epidemiol. 2019 Mar; 43(2):189-206.
    View in: PubMed
    Score: 0.113
  2. Identifying Associations between Somatic Mutations and Clinicopathologic Findings in Lung Cancer Pathology Reports. Methods Inf Med. 2018 02; 57(1):63-73.
    View in: PubMed
    Score: 0.108
  3. Functional variants in DCAF4 associated with lung cancer risk in European populations. Carcinogenesis. 2017 05 01; 38(5):541-551.
    View in: PubMed
    Score: 0.101
  4. 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: 0.098
  5. 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: 0.095
  6. Meta-analysis of Complex Diseases at Gene Level with Generalized Functional Linear Models. Genetics. 2016 Feb; 202(2):457-70.
    View in: PubMed
    Score: 0.092
  7. The role of haplotype in 15q25.1 locus in lung cancer risk: results of scanning chromosome 15. Carcinogenesis. 2015 Nov; 36(11):1275-83.
    View in: PubMed
    Score: 0.090
  8. TERT Polymorphism rs2736100-C Is Associated with EGFR Mutation-Positive Non-Small Cell Lung Cancer. Clin Cancer Res. 2015 Nov 15; 21(22):5173-5180.
    View in: PubMed
    Score: 0.089
  9. A unified framework integrating parent-of-origin effects for association study. PLoS One. 2013; 8(8):e72208.
    View in: PubMed
    Score: 0.078
  10. SNP characteristics and validation success in genome wide association studies. Hum Genet. 2022 Feb; 141(2):229-238.
    View in: PubMed
    Score: 0.035
  11. Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics. Int J Cancer. 2020 02 01; 146(3):739-748.
    View in: PubMed
    Score: 0.029
  12. Multi-Omics Analysis Reveals a HIF Network and Hub Gene EPAS1 Associated with Lung Adenocarcinoma. EBioMedicine. 2018 Jun; 32:93-101.
    View in: PubMed
    Score: 0.027
  13. Inherited variation in circadian rhythm genes and risks of prostate cancer and three other cancer sites in combined cancer consortia. Int J Cancer. 2017 11 01; 141(9):1794-1802.
    View in: PubMed
    Score: 0.026
  14. A PGC1? genetic variant associated with nevus count and melanoma mortality. Int J Cancer. 2017 09 01; 141(5):1066-1067.
    View in: PubMed
    Score: 0.025
  15. Genetic variants in the genes encoding rho GTPases and related regulators predict cutaneous melanoma-specific survival. Int J Cancer. 2017 08 15; 141(4):721-730.
    View in: PubMed
    Score: 0.025
  16. Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum. Arthritis Rheumatol. 2017 05; 69(5):1090-1099.
    View in: PubMed
    Score: 0.025
  17. Telomere structure and maintenance gene variants and risk of five cancer types. Int J Cancer. 2016 Dec 15; 139(12):2655-2670.
    View in: PubMed
    Score: 0.024
  18. Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes. Genes Immun. 2015 Oct; 16(7):470-80.
    View in: PubMed
    Score: 0.022
  19. Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study. Hum Mol Genet. 2015 Sep 15; 24(18):5356-66.
    View in: PubMed
    Score: 0.022
  20. Association of granulomatosis with polyangiitis (Wegener's) with HLA-DPB1*04 and SEMA6A gene variants: evidence from genome-wide analysis. Arthritis Rheum. 2013 Sep; 65(9):2457-68.
    View in: PubMed
    Score: 0.020
  21. Association between functional polymorphisms in genes involved in the MAPK signaling pathways and cutaneous melanoma risk. Carcinogenesis. 2013 Apr; 34(4):885-92.
    View in: PubMed
    Score: 0.019
  22. PGC-1 coactivators regulate MITF and the tanning response. Mol Cell. 2013 Jan 10; 49(1):145-57.
    View in: PubMed
    Score: 0.019
  23. Genetic variants in the vitamin D pathway and breast cancer disease-free survival. Carcinogenesis. 2013 Mar; 34(3):587-94.
    View in: PubMed
    Score: 0.019
  24. Method for evaluating multiple mediators: mediating effects of smoking and COPD on the association between the CHRNA5-A3 variant and lung cancer risk. PLoS One. 2012; 7(10):e47705.
    View in: PubMed
    Score: 0.018
  25. Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Arch Gen Psychiatry. 2012 Aug; 69(8):854-60.
    View in: PubMed
    Score: 0.018
  26. Association of smoking with tumor size at diagnosis in non-small cell lung cancer. Lung Cancer. 2011 Dec; 74(3):378-83.
    View in: PubMed
    Score: 0.017
  27. Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium. J Natl Cancer Inst. 2010 Jul 07; 102(13):959-71.
    View in: PubMed
    Score: 0.016
  28. Cumulative effect of multiple loci on genetic susceptibility to familial lung cancer. Cancer Epidemiol Biomarkers Prev. 2010 Feb; 19(2):517-24.
    View in: PubMed
    Score: 0.015
Connection Strength

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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.