Connection

CHRIS AMOS to Adolescent

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

0.583
  1. 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: 0.043
  2. 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: 0.031
  3. 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: 0.022
  4. 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: 0.021
  5. 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: 0.019
  6. Genotype-phenotype correlations in Peutz-Jeghers syndrome. J Med Genet. 2004 May; 41(5):327-33.
    View in: PubMed
    Score: 0.014
  7. Prospective Clinical and Biomarker Validation of the American Society for Transplantation and Cellular Therapy Consensus Definition for Transplantation-Associated Thrombotic Microangiopathy. Transplant Cell Ther. 2023 11; 29(11):685.e1-685.e7.
    View in: PubMed
    Score: 0.014
  8. Genetic variants of SDCCAG8 and MAGI2 in mitosis-related pathway genes are independent predictors of cutaneous melanoma-specific survival. Cancer Sci. 2021 Oct; 112(10):4355-4364.
    View in: PubMed
    Score: 0.012
  9. Modeling age x major gene interaction by a variance component approach. Genet Epidemiol. 2001; 21 Suppl 1:S849-53.
    View in: PubMed
    Score: 0.011
  10. A new efficient method to detect genetic interactions for lung cancer GWAS. BMC Med Genomics. 2020 10 30; 13(1):162.
    View in: PubMed
    Score: 0.011
  11. 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: 0.011
  12. Penetrance Estimates Over Time to First and Second Primary Cancer Diagnosis in Families with Li-Fraumeni Syndrome: A Single Institution Perspective. Cancer Res. 2020 01 15; 80(2):347-353.
    View in: PubMed
    Score: 0.011
  13. Genetic variants in glutamine metabolic pathway genes predict cutaneous melanoma-specific survival. Mol Carcinog. 2019 11; 58(11):2091-2103.
    View in: PubMed
    Score: 0.010
  14. 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: 0.010
  15. Genetic variants in ELOVL2 and HSD17B12 predict melanoma-specific survival. Int J Cancer. 2019 11 15; 145(10):2619-2628.
    View in: PubMed
    Score: 0.010
  16. Age-specific genome-wide association study in glioblastoma identifies increased proportion of 'lower grade glioma'-like features associated with younger age. Int J Cancer. 2018 11 15; 143(10):2359-2366.
    View in: PubMed
    Score: 0.010
  17. 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: 0.010
  18. Cigarette smoking in a multiethnic population of youth: methods and baseline findings. Prev Med. 1998 May-Jun; 27(3):365-84.
    View in: PubMed
    Score: 0.010
  19. Glioma-related seizures in relation to histopathological subtypes: a report from the glioma international case-control study. J Neurol. 2018 Jun; 265(6):1432-1442.
    View in: PubMed
    Score: 0.009
  20. 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: 0.009
  21. Genetic Variants in WNT2B and BTRC Predict Melanoma Survival. J Invest Dermatol. 2017 08; 137(8):1749-1756.
    View in: PubMed
    Score: 0.009
  22. Genetic regulation of the capacity to make immunoglobulin G to pneumococcal capsular polysaccharides. J Investig Med. 1997 Feb; 45(2):57-68.
    View in: PubMed
    Score: 0.009
  23. Genetic variants in the integrin signaling pathway genes predict cutaneous melanoma survival. Int J Cancer. 2017 03 15; 140(6):1270-1279.
    View in: PubMed
    Score: 0.009
  24. History of chickenpox in glioma risk: a report from the glioma international case-control study (GICC). Cancer Med. 2016 06; 5(6):1352-8.
    View in: PubMed
    Score: 0.008
  25. Approaching a Scientific Consensus on the Association between Allergies and Glioma Risk: A Report from the Glioma International Case-Control Study. Cancer Epidemiol Biomarkers Prev. 2016 Feb; 25(2):282-90.
    View in: PubMed
    Score: 0.008
  26. The Glioma International Case-Control Study: A Report From the Genetic Epidemiology of Glioma International Consortium. Am J Epidemiol. 2016 Jan 15; 183(2):85-91.
    View in: PubMed
    Score: 0.008
  27. 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: 0.008
  28. Functional Variants in Notch Pathway Genes NCOR2, NCSTN, and MAML2 Predict Survival of Patients with Cutaneous Melanoma. Cancer Epidemiol Biomarkers Prev. 2015 Jul; 24(7):1101-10.
    View in: PubMed
    Score: 0.008
  29. Genetic variants in Hippo pathway genes YAP1, TEAD1 and TEAD4 are associated with melanoma-specific survival. Int J Cancer. 2015 Aug 01; 137(3):638-45.
    View in: PubMed
    Score: 0.008
  30. Community-wide cardiovascular disease prevention programs and health outcomes in a rural county, 1970-2010. JAMA. 2015 Jan 13; 313(2):147-55.
    View in: PubMed
    Score: 0.008
  31. Genetic variants in fanconi anemia pathway genes BRCA2 and FANCA predict melanoma survival. J Invest Dermatol. 2015 Feb; 135(2):542-550.
    View in: PubMed
    Score: 0.007
  32. Genome-wide association study of dermatomyositis reveals genetic overlap with other autoimmune disorders. Arthritis Rheum. 2013 Dec; 65(12):3239-47.
    View in: PubMed
    Score: 0.007
  33. 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: 0.007
  34. Gene variants in angiogenesis and lymphangiogenesis and cutaneous melanoma progression. Cancer Epidemiol Biomarkers Prev. 2013 May; 22(5):827-34.
    View in: PubMed
    Score: 0.007
  35. Polymorphisms of nucleotide excision repair genes predict melanoma survival. J Invest Dermatol. 2013 Jul; 133(7):1813-21.
    View in: PubMed
    Score: 0.007
  36. Description of selected characteristics of familial glioma patients - results from the Gliogene Consortium. Eur J Cancer. 2013 Apr; 49(6):1335-45.
    View in: PubMed
    Score: 0.007
  37. On the interplay of telomeres, nevi and the risk of melanoma. PLoS One. 2012; 7(12):e52466.
    View in: PubMed
    Score: 0.007
  38. Cell cycle-related genes as modifiers of age of onset of colorectal cancer in Lynch syndrome: a large-scale study in non-Hispanic white patients. Carcinogenesis. 2013 Feb; 34(2):299-306.
    View in: PubMed
    Score: 0.007
  39. Twins, tissue, and time: an assessment of SNPs and CNVs. Twin Res Hum Genet. 2012 Dec; 15(6):737-45.
    View in: PubMed
    Score: 0.006
  40. Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Arch Gen Psychiatry. 2012 Aug; 69(8):854-60.
    View in: PubMed
    Score: 0.006
  41. Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma. Hum Genet. 2012 Sep; 131(9):1507-17.
    View in: PubMed
    Score: 0.006
  42. Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nat Genet. 2012 May 06; 44(6):642-50.
    View in: PubMed
    Score: 0.006
  43. Smoking and genetic risk variation across populations of European, Asian, and African American ancestry--a meta-analysis of chromosome 15q25. Genet Epidemiol. 2012 May; 36(4):340-51.
    View in: PubMed
    Score: 0.006
  44. Joint effects of germ-line TP53 mutation, MDM2 SNP309, and gender on cancer risk in family studies of Li-Fraumeni syndrome. Hum Genet. 2011 Jun; 129(6):663-73.
    View in: PubMed
    Score: 0.006
  45. Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD. PLoS Genet. 2010 Aug 05; 6(8).
    View in: PubMed
    Score: 0.006
  46. Reduced DNA repair capacity for removing tobacco carcinogen-induced DNA adducts contributes to risk of head and neck cancer but not tumor characteristics. Clin Cancer Res. 2010 Jan 15; 16(2):764-74.
    View in: PubMed
    Score: 0.005
  47. Genetic variants in the cell cycle control pathways contribute to early onset colorectal cancer in Lynch syndrome. Cancer Causes Control. 2009 Nov; 20(9):1769-77.
    View in: PubMed
    Score: 0.005
  48. Evidence for a founder effect of the MPL-S505N mutation in eight Italian pedigrees with hereditary thrombocythemia. Haematologica. 2009 Oct; 94(10):1368-74.
    View in: PubMed
    Score: 0.005
  49. Genetic variation in genes for the xenobiotic-metabolizing enzymes CYP1A1, EPHX1, GSTM1, GSTT1, and GSTP1 and susceptibility to colorectal cancer in Lynch syndrome. Cancer Epidemiol Biomarkers Prev. 2008 Sep; 17(9):2393-401.
    View in: PubMed
    Score: 0.005
  50. Several regions in the major histocompatibility complex confer risk for anti-CCP-antibody positive rheumatoid arthritis, independent of the DRB1 locus. Mol Med. 2008 May-Jun; 14(5-6):293-300.
    View in: PubMed
    Score: 0.005
  51. Statistical methods for anomalous discrete time series based on minimum cell count. Biom J. 2008 Feb; 50(1):86-96.
    View in: PubMed
    Score: 0.005
  52. Detecting haplotype effects in genomewide association studies. Genet Epidemiol. 2007 Dec; 31(8):803-12.
    View in: PubMed
    Score: 0.005
  53. Influence of methylenetetrahydrofolate reductase gene polymorphisms C677T and A1298C on age-associated risk for colorectal cancer in a caucasian lynch syndrome population. Cancer Epidemiol Biomarkers Prev. 2007 Sep; 16(9):1753-9.
    View in: PubMed
    Score: 0.005
  54. Association between Aurora-A kinase polymorphisms and age of onset of hereditary nonpolyposis colorectal cancer in a Caucasian population. Mol Carcinog. 2007 Apr; 46(4):249-56.
    View in: PubMed
    Score: 0.004
  55. Polymorphisms of FAS and FAS ligand genes involved in the death pathway and risk and progression of squamous cell carcinoma of the head and neck. Clin Cancer Res. 2006 Sep 15; 12(18):5596-602.
    View in: PubMed
    Score: 0.004
  56. Joint effects of germ-line p53 mutation and sex on cancer risk in Li-Fraumeni syndrome. Cancer Res. 2006 Aug 15; 66(16):8287-92.
    View in: PubMed
    Score: 0.004
  57. Differing DNA methylation patterns and gene mutation frequencies in colorectal carcinomas from Middle Eastern countries. Clin Cancer Res. 2005 Dec 01; 11(23):8281-7.
    View in: PubMed
    Score: 0.004
  58. 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.
    View in: PubMed
    Score: 0.004
  59. 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.
    View in: PubMed
    Score: 0.004
  60. CARD15 and HLA DRB1 alleles influence susceptibility and disease localization in Crohn's disease. Am J Gastroenterol. 2004 Feb; 99(2):306-15.
    View in: PubMed
    Score: 0.004
  61. Genetic linkage and imprinting effects on body mass index in children and young adults. Eur J Hum Genet. 2003 Jun; 11(6):425-32.
    View in: PubMed
    Score: 0.003
  62. Germline p53 mutations in a cohort with childhood sarcoma: sex differences in cancer risk. Am J Hum Genet. 2003 Apr; 72(4):975-83.
    View in: PubMed
    Score: 0.003
  63. Contrasting molecular pathology of colorectal carcinoma in Egyptian and Western patients. Br J Cancer. 2001 Sep 28; 85(7):1037-46.
    View in: PubMed
    Score: 0.003
  64. Segregation analysis of cancer in families of glioma patients. Genet Epidemiol. 2001 Feb; 20(2):258-70.
    View in: PubMed
    Score: 0.003
  65. 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: 0.003
  66. Frequent association of beta-catenin and WT1 mutations in Wilms tumors. Cancer Res. 2000 Nov 15; 60(22):6288-92.
    View in: PubMed
    Score: 0.003
  67. 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.
    View in: PubMed
    Score: 0.003
  68. SMAD genes in juvenile polyposis. Genes Chromosomes Cancer. 1999 Sep; 26(1):54-61.
    View in: PubMed
    Score: 0.003
  69. Familial antiphospholipid antibody syndrome: criteria for disease and evidence for autosomal dominant inheritance. Arthritis Rheum. 1999 Feb; 42(2):318-27.
    View in: PubMed
    Score: 0.003
  70. 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.
    View in: PubMed
    Score: 0.002
  71. Chromosome breaks and sister chromatid exchange as predictors of second cancers in Hodgkin's disease. Leuk Lymphoma. 1998 Feb; 28(5-6):561-6.
    View in: PubMed
    Score: 0.002
  72. 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: 0.002
  73. Investigating the genetic basis for ankylosing spondylitis. Linkage studies with the major histocompatibility complex region. Arthritis Rheum. 1994 Aug; 37(8):1212-20.
    View in: PubMed
    Score: 0.002
  74. 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.
    View in: PubMed
    Score: 0.002
  75. Cigarette smoking, alcohol, and oral contraceptive use by type A adolescent--the Bogalusa Heart Study. J Behav Med. 1989 Feb; 12(1):13-24.
    View in: PubMed
    Score: 0.001
  76. Description of a large pedigree with an adverse lipoprotein cholesterol phenotype: the Bogalusa Heart Study. Genet Epidemiol. 1986; 3(4):241-53.
    View in: PubMed
    Score: 0.001
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.