Connection

CHRIS AMOS to Humans

This is a "connection" page, showing publications CHRIS AMOS has written about Humans.
Connection Strength

3.934
  1. Pre-diagnostic body mass index trajectories and associations with lung cancer risk. Am J Epidemiol. 2026 Feb 05; 195(2):358-366.
    View in: PubMed
    Score: 0.027
  2. Exonic Variation in HLA-C, CFB, and TAP2 Associated With Increased Risk for Comorbid Crohn's Disease and Psoriasis. Int J Dermatol. 2026 Mar; 65(3):553-562.
    View in: PubMed
    Score: 0.026
  3. Linkage disequilibrium score regression identifies genetic correlations between hepatocellular carcinoma and clinically relevant traits. Int J Cancer. 2026 Mar 01; 158(5):1193-1203.
    View in: PubMed
    Score: 0.026
  4. Exposure-inducible genes may contribute to missingness in RNAseq-based gene expression analyses. Sci Rep. 2025 Aug 22; 15(1):30889.
    View in: PubMed
    Score: 0.026
  5. The role of long non-coding RNAs in lung cancer metastasis: Molecular mechanisms, pathogenesis and clinical implications. Clin Transl Med. 2025 Aug; 15(8):e70429.
    View in: PubMed
    Score: 0.026
  6. Gene expression in tumor and adjacent normal tissues in lung adenocarcinoma subtypes. BMC Cancer. 2025 Jul 14; 25(1):1169.
    View in: PubMed
    Score: 0.026
  7. A hybrid cloud data lake architecture supporting the integration of clinical and genomics data. Health Informatics J. 2025 Apr-Jun; 31(2):14604582251353440.
    View in: PubMed
    Score: 0.026
  8. Uncovering shared genetic features between inflammatory bowel disease and systemic lupus erythematosus. Sci Rep. 2025 May 01; 15(1):15309.
    View in: PubMed
    Score: 0.025
  9. Effects of smoking behavior on lung metastasis in the All of Us Research Program. Sci Rep. 2025 Apr 01; 15(1):11114.
    View in: PubMed
    Score: 0.025
  10. Alternative polyadenylation shapes the molecular and clinical features of lung adenocarcinoma. Hum Mol Genet. 2025 Jan 23; 34(1):1-10.
    View in: PubMed
    Score: 0.025
  11. 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: 0.024
  12. Strength of selection in lung tumors correlates with clinical features better than tumor mutation burden. Sci Rep. 2024 06 03; 14(1):12732.
    View in: PubMed
    Score: 0.024
  13. Lung Cancer in Ever- and Never-Smokers: Findings from Multi-Population GWAS Studies. Cancer Epidemiol Biomarkers Prev. 2024 03 01; 33(3):389-399.
    View in: PubMed
    Score: 0.023
  14. Genome-wide association study identifies high-impact susceptibility loci for HCC in North America. Hepatology. 2024 07 01; 80(1):87-101.
    View in: PubMed
    Score: 0.023
  15. Common and distinct patterns of acquired uniparental disomy and homozygous deletions between lung squamous cell carcinomas and lung adenocarcinoma. Neoplasia. 2023 11; 45:100932.
    View in: PubMed
    Score: 0.023
  16. Heritable Traits and Lung Cancer Risk: A Two-Sample Mendelian Randomization Study. Cancer Epidemiol Biomarkers Prev. 2023 10 02; 32(10):1421-1435.
    View in: PubMed
    Score: 0.023
  17. Candidate pathway analysis of surfactant proteins identifies CTSH and SFTA2 that influences lung cancer risk. Hum Mol Genet. 2023 09 05; 32(18):2842-2855.
    View in: PubMed
    Score: 0.023
  18. A comprehensive analysis of lung cancer highlighting epidemiological factors and psychiatric comorbidities from the All of Us Research Program. Sci Rep. 2023 07 05; 13(1):10852.
    View in: PubMed
    Score: 0.022
  19. Immune Infiltration in Tumor and Adjacent Non-Neoplastic Regions Codetermines Patient Clinical Outcomes in Early-Stage Lung Cancer. J Thorac Oncol. 2023 09; 18(9):1184-1198.
    View in: PubMed
    Score: 0.022
  20. Why does the X chromosome lag behind autosomes in GWAS findings? PLoS Genet. 2023 02; 19(2):e1010472.
    View in: PubMed
    Score: 0.022
  21. Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis. Nat Commun. 2023 02 24; 14(1):1069.
    View in: PubMed
    Score: 0.022
  22. Optimized workplace risk mitigation measures for SARS-CoV-2 in 2022. Sci Rep. 2023 02 16; 13(1):2779.
    View in: PubMed
    Score: 0.022
  23. A refined use of mutations to guide immunotherapy decisions. Nature. 2022 12; 612(7941):639-641.
    View in: PubMed
    Score: 0.021
  24. Synergistic Associations of PNPLA3 I148M Variant, Alcohol Intake, and Obesity With Risk of Cirrhosis, Hepatocellular Carcinoma, and Mortality. JAMA Netw Open. 2022 10 03; 5(10):e2234221.
    View in: PubMed
    Score: 0.021
  25. 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: 0.021
  26. Smoking Status and Factors associated with COVID-19 In-Hospital Mortality among US Veterans. Nicotine Tob Res. 2022 03 26; 24(5):785-793.
    View in: PubMed
    Score: 0.020
  27. 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: 0.020
  28. The shared genetic architecture between epidemiological and behavioral traits with lung cancer. Sci Rep. 2021 09 02; 11(1):17559.
    View in: PubMed
    Score: 0.020
  29. Reducing COVID-19 quarantine with SARS-CoV-2 testing: a simulation study. BMJ Open. 2021 07 16; 11(7):e050473.
    View in: PubMed
    Score: 0.020
  30. COVID-19 Community Incidence and Associated Neighborhood-Level Characteristics in Houston, Texas, USA. Int J Environ Res Public Health. 2021 02 04; 18(4).
    View in: PubMed
    Score: 0.019
  31. Psychosocial and health behavioural impacts of COVID-19 pandemic on adults in the USA: protocol for a longitudinal cohort study. BMJ Open. 2020 12 22; 10(12):e044642.
    View in: PubMed
    Score: 0.019
  32. Tumor somatic mutations also existing as germline polymorphisms may help to identify functional SNPs from genome-wide association studies. Carcinogenesis. 2020 10 15; 41(10):1353-1362.
    View in: PubMed
    Score: 0.019
  33. The tumor microenvironment of colorectal cancer metastases: opportunities in cancer immunotherapy. Immunotherapy. 2020 10; 12(14):1083-1100.
    View in: PubMed
    Score: 0.018
  34. An EGFR signature predicts cell line and patient sensitivity to multiple tyrosine kinase inhibitors. Int J Cancer. 2020 11 01; 147(9):2621-2633.
    View in: PubMed
    Score: 0.018
  35. Genetic variants in PDSS1 and SLC16A6 of the ketone body metabolic pathway predict cutaneous melanoma-specific survival. Mol Carcinog. 2020 06; 59(6):640-650.
    View in: PubMed
    Score: 0.018
  36. 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: 0.017
  37. Untouchable genes in the human genome: Identifying ideal targets for cancer treatment. Cancer Genet. 2019 02; 231-232:67-79.
    View in: PubMed
    Score: 0.016
  38. A multi-omics approach for identifying important pathways and genes in human cancer. BMC Bioinformatics. 2018 Dec 12; 19(1):479.
    View in: PubMed
    Score: 0.016
  39. Gene characteristics predicting missense, nonsense and frameshift mutations in tumor samples. BMC Bioinformatics. 2018 Nov 19; 19(1):430.
    View in: PubMed
    Score: 0.016
  40. Identification of gene expression levels in primary melanoma associated with clinically meaningful characteristics. Melanoma Res. 2018 10; 28(5):380-389.
    View in: PubMed
    Score: 0.016
  41. 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: 0.015
  42. Opportunities and Challenges for Environmental Exposure Assessment in Population-Based Studies. Cancer Epidemiol Biomarkers Prev. 2017 09; 26(9):1370-1380.
    View in: PubMed
    Score: 0.015
  43. Pathway-Based Kernel Boosting for the Analysis of Genome-Wide Association Studies. Comput Math Methods Med. 2017; 2017:6742763.
    View in: PubMed
    Score: 0.015
  44. Gene set selection via LASSO penalized regression (SLPR). Nucleic Acids Res. 2017 Jul 07; 45(12):e114.
    View in: PubMed
    Score: 0.015
  45. A Decade of GWAS Results in Lung Cancer. Cancer Epidemiol Biomarkers Prev. 2018 04; 27(4):363-379.
    View in: PubMed
    Score: 0.015
  46. Hyper-Methylated Loci Persisting from Sessile Serrated Polyps to Serrated Cancers. Int J Mol Sci. 2017 Mar 02; 18(3).
    View in: PubMed
    Score: 0.014
  47. seXY: a tool for sex inference from genotype arrays. Bioinformatics. 2017 02 15; 33(4):561-563.
    View in: PubMed
    Score: 0.014
  48. Next generation sequencing and its applications in HPV-associated cancers. Oncotarget. 2017 Jan 31; 8(5):8877-8889.
    View in: PubMed
    Score: 0.014
  49. Unsupervised gene set testing based on random matrix theory. BMC Bioinformatics. 2016 Nov 04; 17(1):442.
    View in: PubMed
    Score: 0.014
  50. The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers. Cancer Epidemiol Biomarkers Prev. 2017 01; 26(1):126-135.
    View in: PubMed
    Score: 0.014
  51. A Novel Pathway-Based Approach Improves Lung Cancer Risk Prediction Using Germline Genetic Variations. Cancer Epidemiol Biomarkers Prev. 2016 08; 25(8):1208-15.
    View in: PubMed
    Score: 0.014
  52. FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data. BMC Bioinformatics. 2016 Mar 09; 17:122.
    View in: PubMed
    Score: 0.013
  53. Gene by Environment Interaction Linking the Chromosome 15q25 Locus with Cigarette Consumption and Lung Cancer Susceptibility--Are African American Affected Differently?--Authors' Reply. EBioMedicine. 2016 Feb; 4:15.
    View in: PubMed
    Score: 0.013
  54. META-GSA: Combining Findings from Gene-Set Analyses across Several Genome-Wide Association Studies. PLoS One. 2015; 10(10):e0140179.
    View in: PubMed
    Score: 0.013
  55. 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: 0.013
  56. 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: 0.013
  57. RNA-seq analysis of lung adenocarcinomas reveals different gene expression profiles between smoking and nonsmoking patients. Tumour Biol. 2015 Nov; 36(11):8993-9003.
    View in: PubMed
    Score: 0.013
  58. Mutations of HNRNPA0 and WIF1 predispose members of a large family to multiple cancers. Fam Cancer. 2015 Jun; 14(2):297-306.
    View in: PubMed
    Score: 0.013
  59. BRCA2-branching out too? J Natl Cancer Inst. 2015 May; 107(5).
    View in: PubMed
    Score: 0.013
  60. SNP characteristics predict replication success in association studies. Hum Genet. 2014 Dec; 133(12):1477-86.
    View in: PubMed
    Score: 0.012
  61. Bayesian variable selection for hierarchical gene-environment and gene-gene interactions. Hum Genet. 2015 Jan; 134(1):23-36.
    View in: PubMed
    Score: 0.012
  62. Routine use of the Ion Torrent AmpliSeq? Cancer Hotspot Panel for identification of clinically actionable somatic mutations. Clin Chem Lab Med. 2014 May; 52(5):707-14.
    View in: PubMed
    Score: 0.012
  63. How to get the most from microarray data: advice from reverse genomics. BMC Genomics. 2014 Mar 21; 15:223.
    View in: PubMed
    Score: 0.012
  64. Genome-wide association tests of inversions with application to psoriasis. Hum Genet. 2014 Aug; 133(8):967-74.
    View in: PubMed
    Score: 0.012
  65. The national alopecia areata registry-update. J Investig Dermatol Symp Proc. 2013 Dec; 16(1):S53.
    View in: PubMed
    Score: 0.012
  66. Natural and orthogonal model for estimating gene-gene interactions applied to cutaneous melanoma. Hum Genet. 2014 May; 133(5):559-74.
    View in: PubMed
    Score: 0.011
  67. A unified framework integrating parent-of-origin effects for association study. PLoS One. 2013; 8(8):e72208.
    View in: PubMed
    Score: 0.011
  68. A novel kernel for correcting size bias in the logistic kernel machine test with an application to rheumatoid arthritis. Hum Hered. 2012; 74(2):97-108.
    View in: PubMed
    Score: 0.011
  69. Pathway-based analysis of primary biliary cirrhosis genome-wide association studies. Genes Immun. 2013 Apr; 14(3):179-86.
    View in: PubMed
    Score: 0.011
  70. Whole-genome detection of disease-associated deletions or excess homozygosity in a case-control study of rheumatoid arthritis. Hum Mol Genet. 2013 Mar 15; 22(6):1249-61.
    View in: PubMed
    Score: 0.011
  71. 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: 0.011
  72. Genomic sequencing in cancer. Cancer Lett. 2013 Nov 01; 340(2):161-70.
    View in: PubMed
    Score: 0.011
  73. Building a statistical model for predicting cancer genes. PLoS One. 2012; 7(11):e49175.
    View in: PubMed
    Score: 0.011
  74. Genetic association analysis of complex diseases incorporating intermediate phenotype information. PLoS One. 2012; 7(10):e46612.
    View in: PubMed
    Score: 0.011
  75. Model-free tests for genetic linkage. Curr Protoc Hum Genet. 2012 Oct; Chapter 1:Unit1.8.
    View in: PubMed
    Score: 0.011
  76. Natural and orthogonal interaction framework for modeling gene-environment interactions with application to lung cancer. Hum Hered. 2012; 73(4):185-94.
    View in: PubMed
    Score: 0.011
  77. Principal components analysis of population admixture. PLoS One. 2012; 7(7):e40115.
    View in: PubMed
    Score: 0.010
  78. Investigation of inversion polymorphisms in the human genome using principal components analysis. PLoS One. 2012; 7(7):e40224.
    View in: PubMed
    Score: 0.010
  79. Multistage analysis of variants in the inflammation pathway and lung cancer risk in smokers. Cancer Epidemiol Biomarkers Prev. 2012 Jul; 21(7):1213-21.
    View in: PubMed
    Score: 0.010
  80. A case-control study of a sex-specific association between a 15q25 variant and lung cancer risk. Cancer Epidemiol Biomarkers Prev. 2011 Dec; 20(12):2603-9.
    View in: PubMed
    Score: 0.010
  81. Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. Hum Mol Genet. 2011 Dec 15; 20(24):5012-23.
    View in: PubMed
    Score: 0.010
  82. Genome-wide algorithm for detecting CNV associations with diseases. BMC Bioinformatics. 2011 Aug 09; 12:331.
    View in: PubMed
    Score: 0.010
  83. 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: 0.010
  84. Family-based designs. IARC Sci Publ. 2011; (163):261-80.
    View in: PubMed
    Score: 0.009
  85. 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: 0.009
  86. Ordered subset analysis identifies loci influencing lung cancer risk on chromosomes 6q and 12q. Cancer Epidemiol Biomarkers Prev. 2010 Dec; 19(12):3157-66.
    View in: PubMed
    Score: 0.009
  87. Theoretical formulation of principal components analysis to detect and correct for population stratification. PLoS One. 2010 Sep 17; 5(9).
    View in: PubMed
    Score: 0.009
  88. Evolutionary evidence of the effect of rare variants on disease etiology. Clin Genet. 2011 Mar; 79(3):199-206.
    View in: PubMed
    Score: 0.009
  89. Forward-time simulation of realistic samples for genome-wide association studies. BMC Bioinformatics. 2010 Sep 01; 11:442.
    View in: PubMed
    Score: 0.009
  90. Nicotinic acetylcholine receptor region on chromosome 15q25 and lung cancer risk among African Americans: a case-control study. J Natl Cancer Inst. 2010 Aug 04; 102(15):1199-205.
    View in: PubMed
    Score: 0.009
  91. Power of competing strategies of linkage analysis for complex traits. Hum Hered. 2010; 70(1):55-62.
    View in: PubMed
    Score: 0.009
  92. Effects of MDM2, MDM4 and TP53 codon 72 polymorphisms on cancer risk in a cohort study of carriers of TP53 germline mutations. PLoS One. 2010 May 26; 5(5):e10813.
    View in: PubMed
    Score: 0.009
  93. Chipping away at the genetics of smoking behavior. Nat Genet. 2010 May; 42(5):366-8.
    View in: PubMed
    Score: 0.009
  94. Power analysis for case-control association studies of samples with known family histories. Hum Genet. 2010 Jun; 127(6):699-704.
    View in: PubMed
    Score: 0.009
  95. A susceptibility locus on chromosome 6q greatly increases lung cancer risk among light and never smokers. Cancer Res. 2010 Mar 15; 70(6):2359-67.
    View in: PubMed
    Score: 0.009
  96. Smoking and colorectal cancer in Lynch syndrome: results from the Colon Cancer Family Registry and the University of Texas M.D. Anderson Cancer Center. Clin Cancer Res. 2010 Feb 15; 16(4):1331-9.
    View in: PubMed
    Score: 0.009
  97. Racial differences in the association between SNPs on 15q25.1, smoking behavior, and risk of non-small cell lung cancer. J Thorac Oncol. 2009 Oct; 4(10):1195-201.
    View in: PubMed
    Score: 0.009
  98. Less common colorectal cancer predisposition syndromes. Surg Oncol Clin N Am. 2009 Oct; 18(4):647-61.
    View in: PubMed
    Score: 0.009
  99. 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: 0.009
  100. 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: 0.008
  101. Shared susceptibility variations in autoimmune diseases: a brief perspective on common issues. Genes Immun. 2009 Jan; 10(1):1-4.
    View in: PubMed
    Score: 0.008
  102. 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: 0.008
  103. Forward-time simulations of non-random mating populations using simuPOP. Bioinformatics. 2008 Jun 01; 24(11):1408-9.
    View in: PubMed
    Score: 0.008
  104. 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: 0.008
  105. An investigation of a personal norm of condom-use responsibility among African American crack cocaine smokers. AIDS Care. 2008 Feb; 20(2):218-227.
    View in: PubMed
    Score: 0.008
  106. 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: 0.008
  107. Seizure 6-like (SEZ6L) gene and risk for lung cancer. Cancer Res. 2007 Sep 01; 67(17):8406-11.
    View in: PubMed
    Score: 0.007
  108. 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: 0.007
  109. Imprinting detection by extending a regression-based QTL analysis method. Hum Genet. 2007 Sep; 122(2):159-74.
    View in: PubMed
    Score: 0.007
  110. Dissecting the heterogeneity of rheumatoid arthritis through linkage analysis of quantitative traits. Arthritis Rheum. 2007 Jan; 56(1):58-68.
    View in: PubMed
    Score: 0.007
  111. Peutz-Jeghers syndrome: clinicopathology and molecular alterations. Cell Mol Life Sci. 2006 Sep; 63(18):2135-44.
    View in: PubMed
    Score: 0.007
  112. Stochastic search gene suggestion: a Bayesian hierarchical model for gene mapping. Biometrics. 2006 Jun; 62(2):495-503.
    View in: PubMed
    Score: 0.007
  113. High-density SNP analysis of 642 Caucasian families with rheumatoid arthritis identifies two new linkage regions on 11p12 and 2q33. Genes Immun. 2006 Jun; 7(4):277-86.
    View in: PubMed
    Score: 0.007
  114. 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: 0.007
  115. Assessing BRCA carrier probabilities in extended families. J Clin Oncol. 2006 Jan 20; 24(3):354-60.
    View in: PubMed
    Score: 0.007
  116. Advances in the Basic Sciences in Thoracic Oncology in the Last 20 Years and Their Translational Impact. J Thorac Oncol. 2026 Jan; 21(1):41-76.
    View in: PubMed
    Score: 0.007
  117. Examining the effect of linkage disequilibrium on multipoint linkage analysis. BMC Genet. 2005 Dec 30; 6 Suppl 1:S83.
    View in: PubMed
    Score: 0.007
  118. Tumor miRNA Signatures Associate with Outcomes of Patients with Stage II/III Melanoma. Clin Cancer Res. 2025 Dec 15; 31(24):5225-5236.
    View in: PubMed
    Score: 0.007
  119. Validation of a Risk Score for Cancer-Associated Thrombosis Using Nationwide EHR Data. JAMA Netw Open. 2025 Nov 03; 8(11):e2544428.
    View in: PubMed
    Score: 0.007
  120. Predicting the oncogenicity of missense mutations reported in the International Agency for Cancer Research (IARC) mutation database on p53. Hum Mutat. 2005 Nov; 26(5):446-54.
    View in: PubMed
    Score: 0.007
  121. Associations of genetic risk and modifiable lifestyle factors with comorbid psoriasis and Crohns disease. Clin Exp Dermatol. 2025 Oct 27; 50(11):2232-2239.
    View in: PubMed
    Score: 0.007
  122. HLA loci heterozygosity modulates genetic risk in idiopathic inflammatory myopathies. Ann Rheum Dis. 2025 Oct; 84(10):1696-1705.
    View in: PubMed
    Score: 0.006
  123. N-acetylaspartate from fat cells regulates postprandial body temperature. Nat Metab. 2025 Aug; 7(8):1524-1535.
    View in: PubMed
    Score: 0.006
  124. Genome-wide association study for lung cancer in 6531 African Americans reveals new susceptibility loci. Hum Mol Genet. 2025 Jul 03; 34(14):1227-1237.
    View in: PubMed
    Score: 0.006
  125. A Survey Study of Roadblocks in Translational Science. Clin Transl Sci. 2025 Jul; 18(7):e70259.
    View in: PubMed
    Score: 0.006
  126. Genome-wide association study of early-stage non-small cell lung cancer prognosis: a pooled analysis in the International Lung Cancer Consortium. Carcinogenesis. 2025 Apr 03; 46(2).
    View in: PubMed
    Score: 0.006
  127. Sensitivity to Environmental Stress and Adversity and Lung Cancer. JAMA Netw Open. 2025 01 02; 8(1):e2457079.
    View in: PubMed
    Score: 0.006
  128. Linkage analysis of affected sib pairs allowing for parent-of-origin effects. Ann Hum Genet. 2005 Jan; 69(Pt 1):113-26.
    View in: PubMed
    Score: 0.006
  129. The relative efficiency of penetrance estimators for sib pairs. Hum Hered. 2005; 59(1):61-6.
    View in: PubMed
    Score: 0.006
  130. Self-Collection for Primary HPV Testing: Acceptability in a Large Urban Emergency Department. Ann Emerg Med. 2025 Mar; 85(3):249-257.
    View in: PubMed
    Score: 0.006
  131. DNA Methylation Classes of Stage II and III Primary Melanomas and Their Clinical and Prognostic Significance. JCO Precis Oncol. 2024 Nov; 8:e2400375.
    View in: PubMed
    Score: 0.006
  132. Multi-ancestry GWAS meta-analyses of lung cancer reveal susceptibility loci and elucidate smoking-independent genetic risk. Nat Commun. 2024 10 04; 15(1):8629.
    View in: PubMed
    Score: 0.006
  133. Clonal hematopoiesis of indeterminate potential and cardiovascular disease: Pathogenesis, clinical presentation, and future directions. Prog Cardiovasc Dis. 2024 Sep-Oct; 86:79-85.
    View in: PubMed
    Score: 0.006
  134. 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: 0.006
  135. The prognostic effect of infiltrating immune cells is shaped by proximal M2 macrophages in lung adenocarcinoma. Mol Cancer. 2024 Sep 04; 23(1):185.
    View in: PubMed
    Score: 0.006
  136. Prognostic stratification in DLBCL patients with aberrant MYC gene. Br J Haematol. 2024 Nov; 205(5):1782-1793.
    View in: PubMed
    Score: 0.006
  137. On the informative value of community-based indoor radon values in relation to lung cancer. Cancer Med. 2024 Aug; 13(16):e70126.
    View in: PubMed
    Score: 0.006
  138. Discovery of new myositis genetic associations through leveraging other immune-mediated diseases. HGG Adv. 2024 Oct 10; 5(4):100336.
    View in: PubMed
    Score: 0.006
  139. Asbestos-Related lung Cancer: An underappreciated oncological issue. Lung Cancer. 2024 Aug; 194:107861.
    View in: PubMed
    Score: 0.006
  140. 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: 0.006
  141. PNPLA3, Obesity, and Heavy Alcohol Use in Cirrhosis Patients May Exert a Synergistic Increase Hepatocellular Carcinoma Risk. Clin Gastroenterol Hepatol. 2024 Sep; 22(9):1858-1866.e4.
    View in: PubMed
    Score: 0.006
  142. Genotype-phenotype correlations in Peutz-Jeghers syndrome. J Med Genet. 2004 May; 41(5):327-33.
    View in: PubMed
    Score: 0.006
  143. What is the additive value of nutritional deficiency to VA-FI in the risk assessment for heart failure patients? J Nutr Health Aging. 2024 Jul; 28(7):100253.
    View in: PubMed
    Score: 0.006
  144. Identifying therapeutic targets for cancer among 2074 circulating proteins and risk of nine cancers. Nat Commun. 2024 Apr 29; 15(1):3621.
    View in: PubMed
    Score: 0.006
  145. Thrombosis risk prediction in lymphoma patients: A multi-institutional, retrospective model development and validation study. Am J Hematol. 2024 07; 99(7):1230-1239.
    View in: PubMed
    Score: 0.006
  146. Adaptive Time-Location Sampling for COMPASS: A SARS-CoV-2 Prevalence Study in Fifteen Diverse Communities in the United States. Epidemiology. 2024 May 01; 35(3):389-397.
    View in: PubMed
    Score: 0.006
  147. Somatic mutations of esophageal adenocarcinoma: a comparison between Black and White patients. Sci Rep. 2024 04 18; 14(1):8988.
    View in: PubMed
    Score: 0.006
  148. CYP2A6 Activity and Cigarette Consumption Interact in Smoking-Related Lung Cancer Susceptibility. Cancer Res. 2024 02 15; 84(4):616-625.
    View in: PubMed
    Score: 0.006
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  713. The hamartomatous polyposis syndromes: a clinical and molecular review. Am J Gastroenterol. 2005 Feb; 100(2):476-90.
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    Score: 0.002
  714. A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn's disease. Gastroenterology. 2005 Feb; 128(2):260-9.
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    Score: 0.002
  715. SLC22A4 polymorphisms implicated in rheumatoid arthritis and Crohn's disease are not associated with rheumatoid arthritis in a Canadian Caucasian population. Arthritis Rheum. 2005 Feb; 52(2):425-9.
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    Score: 0.002
  716. Genetic mapping of a third Li-Fraumeni syndrome predisposition locus to human chromosome 1q23. Cancer Res. 2005 Jan 15; 65(2):427-31.
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    Score: 0.002
  717. Possible genomic imprinting of three human obesity-related genetic loci. Am J Hum Genet. 2005 Mar; 76(3):427-37.
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    Score: 0.002
  718. 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.
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    Score: 0.002
  719. Relationship between plasma carotenoids and prostate cancer. Nutr Cancer. 2005; 53(2):127-34.
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    Score: 0.002
  720. An informatics tool to assess colon cancer risk. AMIA Annu Symp Proc. 2005; 998.
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    Score: 0.002
  721. Complex segregation analysis reveals a multigene model for lung cancer. Hum Genet. 2005 Jan; 116(1-2):121-7.
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    Score: 0.002
  722. Joint tests for quantitative trait loci in experimental crosses. Genet Sel Evol. 2004 Nov-Dec; 36(6):601-19.
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    Score: 0.002
  723. p73 G4C14-to-A4T14 polymorphism and risk of lung cancer. Cancer Res. 2004 Oct 01; 64(19):6863-6.
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    Score: 0.002
  724. p53 polymorphism and age of onset of hereditary nonpolyposis colorectal cancer in a Caucasian population. Clin Cancer Res. 2004 Sep 01; 10(17):5845-9.
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    Score: 0.002
  725. A major lung cancer susceptibility locus maps to chromosome 6q23-25. Am J Hum Genet. 2004 Sep; 75(3):460-74.
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    Score: 0.002
  726. A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis. Am J Hum Genet. 2004 Aug; 75(2):330-7.
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    Score: 0.001
  727. Association of a p73 exon 2 G4C14-to-A4T14 polymorphism with risk of squamous cell carcinoma of the head and neck. Carcinogenesis. 2004 Oct; 25(10):1911-6.
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    Score: 0.001
  728. Functional variants of OCTN cation transporter genes are associated with Crohn disease. Nat Genet. 2004 May; 36(5):471-5.
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    Score: 0.001
  729. GSTM1 polymorphism does not affect hereditary nonpolyposis colorectal cancer age of onset. Cancer Epidemiol Biomarkers Prev. 2004 Apr; 13(4):676-8.
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    Score: 0.001
  730. An evolutionary perspective on single-nucleotide polymorphism screening in molecular cancer epidemiology. Cancer Res. 2004 Mar 15; 64(6):2251-7.
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    Score: 0.001
  731. 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.
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    Score: 0.001
  732. Clustering of disease features within 512 multicase rheumatoid arthritis families. Arthritis Rheum. 2004 Mar; 50(3):736-41.
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    Score: 0.001
  733. CARD15 and HLA DRB1 alleles influence susceptibility and disease localization in Crohn's disease. Am J Gastroenterol. 2004 Feb; 99(2):306-15.
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    Score: 0.001
  734. Correlation of staining for LKB1 and COX-2 in hamartomatous polyps and carcinomas from patients with Peutz-Jeghers syndrome. J Histochem Cytochem. 2003 Dec; 51(12):1665-72.
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    Score: 0.001
  735. Risk for smoking-related cancer among relatives of lung cancer patients. Cancer Res. 2003 Dec 01; 63(23):8531-5.
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    Score: 0.001
  736. The worldwide distribution of the VHL 598C>T mutation indicates a single founding event. Blood. 2004 Mar 01; 103(5):1937-40.
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    Score: 0.001
  737. Smoking, DNA repair capacity and risk of nonsmall cell lung cancer. Int J Cancer. 2003 Oct 20; 107(1):84-8.
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    Score: 0.001
  738. XRCC3 genetic polymorphism, smoking, and lung carcinoma risk in minority populations. Cancer. 2003 Oct 15; 98(8):1701-6.
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    Score: 0.001
  739. Dietary folate intake and lung cancer risk in former smokers: a case-control analysis. Cancer Epidemiol Biomarkers Prev. 2003 Oct; 12(10):980-6.
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  740. Telomere dysfunction: a potential cancer predisposition factor. J Natl Cancer Inst. 2003 Aug 20; 95(16):1211-8.
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  741. Association of the CpG island methylator phenotype with family history of cancer in patients with colorectal cancer. Cancer Res. 2003 Aug 15; 63(16):4805-8.
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  742. Genetic susceptibility to lung cancer: the role of DNA damage and repair. Cancer Epidemiol Biomarkers Prev. 2003 Aug; 12(8):689-98.
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  743. Lung cancer risk in germline p53 mutation carriers: association between an inherited cancer predisposition, cigarette smoking, and cancer risk. Hum Genet. 2003 Aug; 113(3):238-43.
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  744. Genetic linkage and imprinting effects on body mass index in children and young adults. Eur J Hum Genet. 2003 Jun; 11(6):425-32.
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    Score: 0.001
  745. 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.
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    Score: 0.001
  746. Overexpression of cyclooxygenase 2 in hamartomatous polyps of Peutz-Jeghers syndrome. Am J Gastroenterol. 2003 Mar; 98(3):671-8.
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    Score: 0.001
  747. XPA polymorphism associated with reduced lung cancer risk and a modulating effect on nucleotide excision repair capacity. Carcinogenesis. 2003 Mar; 24(3):505-9.
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  748. Germline p53 mutations in a cohort with childhood sarcoma: sex differences in cancer risk. Am J Hum Genet. 2003 Apr; 72(4):975-83.
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  749. Repair of UV light-induced DNA damage and risk of cutaneous malignant melanoma. J Natl Cancer Inst. 2003 Feb 19; 95(4):308-15.
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  750. Genetic susceptibility for lung cancer: interactions with gender and smoking history and impact on early detection policies. Hum Hered. 2003; 56(1-3):139-45.
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  751. A case-control analysis of lymphocytic chromosome 9 aberrations in lung cancer. Int J Cancer. 2002 Dec 10; 102(5):536-40.
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  752. Power of a simplified multivariate test for genetic linkage. Ann Hum Genet. 2002 Nov; 66(Pt 5-6):407-17.
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    Score: 0.001
  753. Dissecting the genetic complexity of the association between human leukocyte antigens and rheumatoid arthritis. Am J Hum Genet. 2002 Sep; 71(3):585-94.
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    Score: 0.001
  754. Bleomycin hydrolase and a genetic locus within the MHC affect risk for pulmonary fibrosis in mice. Hum Mol Genet. 2002 Aug 01; 11(16):1855-63.
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  755. An analysis of DNA repair as a determinant of survival in patients with non-small-cell lung cancer. J Natl Cancer Inst. 2002 Jul 17; 94(14):1091-9.
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  756. p53 Genotypes and Haplotypes Associated With Lung Cancer Susceptibility and Ethnicity. J Natl Cancer Inst. 2002 May 01; 94(9):681-90.
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    Score: 0.001
  757. Common deletion of SMAD4 in juvenile polyposis is a mutational hotspot. Am J Hum Genet. 2002 May; 70(5):1357-62.
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    Score: 0.001
  758. Extension of variance components approach to incorporate temporal trends and longitudinal pedigree data analysis. Genet Epidemiol. 2002 Mar; 22(3):221-32.
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    Score: 0.001
  759. Individual-specific liability groups in genetic linkage, with applications to kindreds with Li-Fraumeni syndrome. Am J Hum Genet. 2002 Mar; 70(3):813-7.
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  760. Contrasting molecular pathology of colorectal carcinoma in Egyptian and Western patients. Br J Cancer. 2001 Sep 28; 85(7):1037-46.
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  761. International Genetic Epidemiology Society: commentary on Darkness in El Dorado by Patrick Tierney. Genet Epidemiol. 2001 Sep; 21(2):81-104.
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  762. Cyclin D1 polymorphism and increased risk of colorectal cancer at young age. J Natl Cancer Inst. 2001 Jul 18; 93(14):1106-8.
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  763. The association of microsomal epoxide hydrolase polymorphisms and lung cancer risk in African-Americans and Mexican-Americans. Carcinogenesis. 2001 Jun; 22(6):923-8.
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  764. Tumour necrosis factor 5' promoter single nucleotide polymorphisms influence susceptibility to rheumatoid arthritis (RA) in immunogenetically defined multiplex RA families. Genes Immun. 2001 Apr; 2(2):82-7.
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  765. 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.
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  766. Modulation of nucleotide excision repair capacity by XPD polymorphisms in lung cancer patients. Cancer Res. 2001 Feb 15; 61(4):1354-7.
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    Score: 0.001
  767. Segregation analysis of cancer in families of glioma patients. Genet Epidemiol. 2001 Feb; 20(2):258-70.
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    Score: 0.001
  768. Leptin and prostate cancer. Prostate. 2001 Jan 01; 46(1):62-7.
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    Score: 0.001
  769. Adaptations of linkage and association methods for the study of asthma, a complex trait. Genet Epidemiol. 2001; 21 Suppl 1:S89-96.
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  770. Frequent association of beta-catenin and WT1 mutations in Wilms tumors. Cancer Res. 2000 Nov 15; 60(22):6288-92.
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  771. Repair of tobacco carcinogen-induced DNA adducts and lung cancer risk: a molecular epidemiologic study. J Natl Cancer Inst. 2000 Nov 01; 92(21):1764-72.
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    Score: 0.001
  772. Current applications of genetic technology in predisposition testing and microsatellite instability assays. J Clin Oncol. 2000 Nov 01; 18(21 Suppl):70S-4S.
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    Score: 0.001
  773. Dietary intake of isothiocyanates: evidence of a joint effect with glutathione S-transferase polymorphisms in lung cancer risk. Cancer Epidemiol Biomarkers Prev. 2000 Oct; 9(10):1017-20.
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    Score: 0.001
  774. Epidemiologic determinants of clinically relevant prostate cancer. Int J Cancer. 2000 May 20; 89(3):259-64.
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    Score: 0.001
  775. Joint effect of insulin-like growth factors and mutagen sensitivity in lung cancer risk. J Natl Cancer Inst. 2000 May 03; 92(9):737-43.
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    Score: 0.001
  776. Joint effect of insulin-like growth factors and mutagen sensitivity in lung cancer risk. Growth Horm IGF Res. 2000 Apr; 10 Suppl A:S26-7.
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    Score: 0.001
  777. Effects of cyclin D1 polymorphism on age of onset of hereditary nonpolyposis colorectal cancer. Cancer Res. 2000 Jan 15; 60(2):249-52.
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    Score: 0.001
  778. Nonsyndromic cleft lip and palate is not associated with cancer or other birth defects. Am J Med Genet. 2000 Jan 03; 90(1):17-24.
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    Score: 0.001
  779. SMAD genes in juvenile polyposis. Genes Chromosomes Cancer. 1999 Sep; 26(1):54-61.
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    Score: 0.001
  780. Genetic analysis of multiplex rheumatoid arthritis families. Genes Immun. 1999 Sep; 1(1):28-36.
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    Score: 0.001
  781. Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure. Am J Hum Genet. 1999 Aug; 65(2):531-44.
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    Score: 0.001
  782. Testing for linkage under robust genetic models. Hum Hered. 1999 Jun; 49(3):146-53.
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    Score: 0.001
  783. The genetics revolution and the assault on rheumatoid arthritis. Arthritis Rheum. 1999 Jun; 42(6):1071-9.
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    Score: 0.001
  784. Loci for efficient detection of microsatellite instability in hereditary non-polyposis colorectal cancer. Oncol Rep. 1999 May-Jun; 6(3):497-505.
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  785. Associations among telomerase activity, p53 protein overexpression, and genetic instability in lung cancer. Br J Cancer. 1999 May; 80(3-4):453-7.
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  786. Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes. Cell. 1999 Apr 02; 97(1):133-44.
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    Score: 0.001
  787. Intention to learn results of genetic testing for hereditary colon cancer. Cancer Epidemiol Biomarkers Prev. 1999 Apr; 8(4 Pt 2):353-60.
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    Score: 0.001
  788. Familial antiphospholipid antibody syndrome: criteria for disease and evidence for autosomal dominant inheritance. Arthritis Rheum. 1999 Feb; 42(2):318-27.
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    Score: 0.001
  789. Methods to estimate genetic components of variance for quantitative traits in family studies. Genet Epidemiol. 1999; 17(1):64-76.
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    Score: 0.001
  790. Segregation analysis of squamous cell carcinoma of the head and neck: evidence for a major gene determining risk. Ann Hum Genet. 1998 Nov; 62(Pt 6):505-10.
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    Score: 0.001
  791. Chromosome 5 aberrations and genetic predisposition to lung cancer. Int J Cancer. 1998 Oct 23; 79(5):490-3.
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    Score: 0.001
  792. Familial clustering of rheumatoid arthritis with other autoimmune diseases. Hum Genet. 1998 Oct; 103(4):475-82.
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    Score: 0.001
  793. Benzo[a]pyrene diol epoxide and bleomycin sensitivity and susceptibility to cancer of upper aerodigestive tract. J Natl Cancer Inst. 1998 Sep 16; 90(18):1393-9.
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    Score: 0.001
  794. A parallel study of in vitro sensitivity to benzo[a]pyrene diol epoxide and bleomycin in lung carcinoma cases and controls. Cancer. 1998 Sep 15; 83(6):1118-27.
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    Score: 0.001
  795. Segregation analysis of idiopathic talipes equinovarus in a Texan population. Am J Med Genet. 1998 Sep 01; 79(2):97-102.
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  796. Linkage of familial Hibernian fever to chromosome 12p13. Am J Hum Genet. 1998 Jun; 62(6):1446-51.
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    Score: 0.001
  797. Exclusion of a p53 germline mutation in a classic Li-Fraumeni syndrome family. Hum Genet. 1998 Jun; 102(6):681-6.
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  798. Variation in the region of the angiotensin-converting enzyme gene influences interindividual differences in blood pressure levels in young white males. Circulation. 1998 May 12; 97(18):1773-9.
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  799. 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.
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  800. The role of germline polymorphisms in the T-cell receptor in susceptibility to ankylosing spondylitis. Br J Rheumatol. 1998 Apr; 37(4):454-8.
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  801. Case-control study of the D2 dopamine receptor gene and smoking status in lung cancer patients. J Natl Cancer Inst. 1998 Mar 04; 90(5):358-63.
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  802. Linkage analysis of chromosome 1q markers in 136 prostate cancer families. The Cancer Research Campaign/British Prostate Group U.K. Familial Prostate Cancer Study Collaborators. Am J Hum Genet. 1998 Mar; 62(3):653-8.
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  803. Chromosome breaks and sister chromatid exchange as predictors of second cancers in Hodgkin's disease. Leuk Lymphoma. 1998 Feb; 28(5-6):561-6.
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  804. Cytochrome P450 2E1 DraI polymorphisms in lung cancer in minority populations. Cancer Epidemiol Biomarkers Prev. 1998 Jan; 7(1):13-8.
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  805. Deletion in poly(ADP-ribose)polymerase pseudogene and lung cancer risk. Carcinogenesis. 1998 Jan; 19(1):93-8.
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  806. Design and methodology of a study of psychosocial aspects of genetic testing for hereditary colorectal cancer. Ann N Y Acad Sci. 1997 Dec 29; 833:190-4.
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  807. A clinical trial to evaluate the effect of vitamin C supplementation on in vitro mutagen sensitivity. The University of Texas M. D. Anderson Clinical Community Oncology Program Network. Cancer Epidemiol Biomarkers Prev. 1997 Jul; 6(7):537-42.
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  808. Evidence for genetic heterogeneity in familial Wilms' tumor. Cancer Res. 1997 May 15; 57(10):1859-62.
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  809. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. Nat Genet. 1997 Jan; 15(1):62-9.
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  810. Correlates of psychologic distress in colorectal cancer patients undergoing genetic testing for hereditary colon cancer. Health Psychol. 1997 Jan; 16(1):73-86.
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  811. 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.
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  812. Genetic variability in the tumor necrosis factor-lymphotoxin region influences susceptibility to rheumatoid arthritis. Am J Hum Genet. 1996 Sep; 59(3):676-83.
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  813. Higher lung cancer risk for younger African-Americans with the Pro/Pro p53 genotype. Carcinogenesis. 1995 Sep; 16(9):2205-8.
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  814. Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families. Am J Hum Genet. 1995 Aug; 57(2):257-72.
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  815. Mutagen sensitivity as a biological marker of lung cancer risk in African Americans. Cancer Epidemiol Biomarkers Prev. 1995 Mar; 4(2):99-103.
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  816. A case-control study of nonrandom distribution of bleomycin-induced chromatid breaks in lymphocytes of lung cancer cases. Cancer Res. 1995 Feb 01; 55(3):557-61.
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  817. Late onset and reactivation of chorioretinitis in children with congenital cytomegalovirus infection. Pediatr Infect Dis J. 1994 Dec; 13(12):1139-42.
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  818. Mutagen sensitivity as a risk factor for second malignant tumors following malignancies of the upper aerodigestive tract. J Natl Cancer Inst. 1994 Nov 16; 86(22):1681-4.
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  819. Investigating the genetic basis for ankylosing spondylitis. Linkage studies with the major histocompatibility complex region. Arthritis Rheum. 1994 Aug; 37(8):1212-20.
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  820. Linkage between the APOB gene and serum ApoB levels in a large pedigree from the Bogalusa Heart Study. Genet Epidemiol. 1994; 11(1):29-40.
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  821. Genetic contributions to quantitative lipoprotein traits associated with coronary artery disease: analysis of a large pedigree from the Bogalusa Heart Study. Am J Med Genet. 1993 Nov 01; 47(6):875-83.
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  822. Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q. Nat Genet. 1992 Jul; 1(4):301-5.
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  823. High risk of HIV-1 infection for first-born twins. The International Registry of HIV-exposed Twins. Lancet. 1991 Dec 14; 338(8781):1471-5.
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  824. Relationship between head circumference and height in normal adults and in the nevoid basal cell carcinoma syndrome and neurofibromatosis type I. Am J Med Genet. 1991 Aug 01; 40(2):206-10.
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  825. Stepwise oligogenic segregation and linkage analysis illustrated with dopamine-beta-hydroxylase activity. Am J Med Genet. 1990 Mar; 35(3):425-32.
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  826. Cigarette smoking, alcohol, and oral contraceptive use by type A adolescent--the Bogalusa Heart Study. J Behav Med. 1989 Feb; 12(1):13-24.
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  827. Hereditary medullary thyroid carcinoma: genetic annalysis of three related syndromes. Groupe d'Etude des Tumeurs a Calcitonine. Henry Ford Hosp Med J. 1989; 37(3-4):109-11.
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  828. Association between polymorphic blood markers and risk factors for cardiovascular disease in a large pedigree. Genet Epidemiol. 1987; 4(4):267-75.
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  829. Description of a large pedigree with an adverse lipoprotein cholesterol phenotype: the Bogalusa Heart Study. Genet Epidemiol. 1986; 3(4):241-53.
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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.