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CHRIS AMOS to Linkage Disequilibrium

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This is a "connection" page, showing publications CHRIS AMOS has written about Linkage Disequilibrium.
CHRIS AMOS
Connection Strength
3.397
Linkage Disequilibrium
  1. Shared genomic architecture between COVID-19 severity and numerous clinical and physiologic parameters revealed by LD score regression analysis. Sci Rep. 2022 02 03; 12(1):1891.
    View in: PubMed
    Score: 0.696
  2. Examining the effect of linkage disequilibrium on multipoint linkage analysis. BMC Genet. 2005 Dec 30; 6 Suppl 1:S83.
    View in: PubMed
    Score: 0.228
  3. Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis. Am J Hum Genet. 2004 Dec; 75(6):1106-12.
    View in: PubMed
    Score: 0.210
  4. An Atlas Characterizing the Shared Genetic Architecture of Inflammatory Bowel Disease with Clinical and Behavioral Traits. Inflamm Bowel Dis. 2024 06 03; 30(6):884-893.
    View in: PubMed
    Score: 0.204
  5. The shared genetic architecture between epidemiological and behavioral traits with lung cancer. Sci Rep. 2021 09 02; 11(1):17559.
    View in: PubMed
    Score: 0.169
  6. Comparison of linkage-disequilibrium methods for localization of genes influencing quantitative traits in humans. Am J Hum Genet. 1999 Apr; 64(4):1194-205.
    View in: PubMed
    Score: 0.143
  7. Genome scans for genetic predisposition to alcoholism by use of transmission disequilibrium test analyses. Genet Epidemiol. 1999; 17 Suppl 1:S277-81.
    View in: PubMed
    Score: 0.140
  8. Estimating the strength of genetic effects: a comparison of maximum likelihood and transmission disequilibrium methods in the study of ankylosing spondylitis. Hum Immunol. 1997 Sep 15; 57(1):44-50.
    View in: PubMed
    Score: 0.128
  9. A unified framework integrating parent-of-origin effects for association study. PLoS One. 2013; 8(8):e72208.
    View in: PubMed
    Score: 0.097
  10. Obesity-related genetic variants, human pigmentation, and risk of melanoma. Hum Genet. 2013 Jul; 132(7):793-801.
    View in: PubMed
    Score: 0.094
  11. Pathway-based analysis of primary biliary cirrhosis genome-wide association studies. Genes Immun. 2013 Apr; 14(3):179-86.
    View in: PubMed
    Score: 0.093
  12. Fine-mapping of the 5p15.33, 6p22.1-p21.31, and 15q25.1 regions identifies functional and histology-specific lung cancer susceptibility loci in African-Americans. Cancer Epidemiol Biomarkers Prev. 2013 Feb; 22(2):251-60.
    View in: PubMed
    Score: 0.092
  13. Novel genetic variants in the chromosome 5p15.33 region associate with lung cancer risk. Carcinogenesis. 2011 Oct; 32(10):1493-9.
    View in: PubMed
    Score: 0.084
  14. Re: Discriminatory accuracy from single-nucleotide polymorphisms in models to predict breast cancer risk. J Natl Cancer Inst. 2009 Dec 16; 101(24):1731-2; author reply 1732.
    View in: PubMed
    Score: 0.075
  15. Detection of disease-associated deletions in case-control studies using SNP genotypes with application to rheumatoid arthritis. Hum Genet. 2009 Aug; 126(2):303-15.
    View in: PubMed
    Score: 0.072
  16. TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. N Engl J Med. 2007 Sep 20; 357(12):1199-209.
    View in: PubMed
    Score: 0.064
  17. Joint tests for quantitative trait loci in experimental crosses. Genet Sel Evol. 2004 Nov-Dec; 36(6):601-19.
    View in: PubMed
    Score: 0.053
  18. High-throughput characterization of functional variants highlights heterogeneity and polygenicity underlying lung cancer susceptibility. Am J Hum Genet. 2024 07 11; 111(7):1405-1419.
    View in: PubMed
    Score: 0.051
  19. Partitioned glioma heritability shows subtype-specific enrichment in immune cells. Neuro Oncol. 2021 08 02; 23(8):1304-1314.
    View in: PubMed
    Score: 0.042
  20. The Shared Genetic Architectures Between Lung Cancer and Multiple Polygenic Phenotypes in Genome-Wide Association Studies. Cancer Epidemiol Biomarkers Prev. 2021 06; 30(6):1156-1164.
    View in: PubMed
    Score: 0.041
  21. Genetic linkage methods for quantitative traits. Stat Methods Med Res. 2001 Feb; 10(1):3-25.
    View in: PubMed
    Score: 0.041
  22. Adaptations of linkage and association methods for the study of asthma, a complex trait. Genet Epidemiol. 2001; 21 Suppl 1:S89-96.
    View in: PubMed
    Score: 0.040
  23. Genetic modifiers of radon-induced lung cancer risk: a genome-wide interaction study in former uranium miners. Int Arch Occup Environ Health. 2018 Nov; 91(8):937-950.
    View in: PubMed
    Score: 0.034
  24. Functional variants in DCAF4 associated with lung cancer risk in European populations. Carcinogenesis. 2017 05 01; 38(5):541-551.
    View in: PubMed
    Score: 0.031
  25. 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: 0.031
  26. 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: 0.030
  27. 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: 0.030
  28. Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genet Epidemiol. 2013 Dec; 37(8):846-59.
    View in: PubMed
    Score: 0.025
  29. A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry. Nat Genet. 2013 Jun; 45(6):690-6.
    View in: PubMed
    Score: 0.024
  30. Genetic variants in the vitamin D pathway and breast cancer disease-free survival. Carcinogenesis. 2013 Mar; 34(3):587-94.
    View in: PubMed
    Score: 0.023
  31. 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: 0.022
  32. Susceptibility locus for lung cancer at 15q25.1 is not associated with risk of pancreatic cancer. Pancreas. 2011 Aug; 40(6):872-5.
    View in: PubMed
    Score: 0.021
  33. Genome-wide association study of survival in non-small cell lung cancer patients receiving platinum-based chemotherapy. J Natl Cancer Inst. 2011 May 18; 103(10):817-25.
    View in: PubMed
    Score: 0.021
  34. A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity. Hum Mol Genet. 2011 Feb 15; 20(4):820-6.
    View in: PubMed
    Score: 0.020
  35. 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: 0.020
  36. 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: 0.019
  37. A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. Am J Hum Genet. 2009 11; 85(5):679-91.
    View in: PubMed
    Score: 0.019
  38. Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. Cancer Res. 2009 Aug 15; 69(16):6633-41.
    View in: PubMed
    Score: 0.018
  39. Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer. Nat Genet. 2009 Sep; 41(9):991-5.
    View in: PubMed
    Score: 0.018
  40. CTLA4/ICOS gene variants and haplotypes are associated with rheumatoid arthritis and primary biliary cirrhosis in the Canadian population. Arthritis Rheum. 2009 Apr; 60(4):931-7.
    View in: PubMed
    Score: 0.018
  41. The chromosome 7q region association with rheumatoid arthritis in females in a British population is not replicated in a North American case-control series. Arthritis Rheum. 2009 Jan; 60(1):47-52.
    View in: PubMed
    Score: 0.018
  42. A large-scale rheumatoid arthritis genetic study identifies association at chromosome 9q33.2. PLoS Genet. 2008 Jun 27; 4(6):e1000107.
    View in: PubMed
    Score: 0.017
  43. Mutagen sensitivity and genetic variants in nucleotide excision repair pathway: genotype-phenotype correlation. Cancer Epidemiol Biomarkers Prev. 2007 Oct; 16(10):2065-71.
    View in: PubMed
    Score: 0.016
  44. Forward-time simulations of human populations with complex diseases. PLoS Genet. 2007 Mar 23; 3(3):e47.
    View in: PubMed
    Score: 0.015
  45. 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: 0.013
  46. Functional variants of OCTN cation transporter genes are associated with Crohn disease. Nat Genet. 2004 May; 36(5):471-5.
    View in: PubMed
    Score: 0.013
  47. Dissecting the genetic complexity of the association between human leukocyte antigens and rheumatoid arthritis. Am J Hum Genet. 2002 Sep; 71(3):585-94.
    View in: PubMed
    Score: 0.011
  48. No linkage or association of telomeric and centromeric T-cell receptor beta-chain markers with susceptibility to type 1 insulin-dependent diabetes in HLA-DR4 multiplex families. Eur J Immunogenet. 1996 Oct; 23(5):361-70.
    View in: PubMed
    Score: 0.008
  49. Genetic variability in the tumor necrosis factor-lymphotoxin region influences susceptibility to rheumatoid arthritis. Am J Hum Genet. 1996 Sep; 59(3):676-83.
    View in: PubMed
    Score: 0.007
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.