Connection

CHRIS AMOS to Genetic Linkage

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

6.331
  1. Model-free tests for genetic linkage. Curr Protoc Hum Genet. 2012 Oct; Chapter 1:Unit1.8.
    View in: PubMed
    Score: 0.352
  2. Family-based designs. IARC Sci Publ. 2011; (163):261-80.
    View in: PubMed
    Score: 0.311
  3. Power of competing strategies of linkage analysis for complex traits. Hum Hered. 2010; 70(1):55-62.
    View in: PubMed
    Score: 0.299
  4. Dissecting the heterogeneity of rheumatoid arthritis through linkage analysis of quantitative traits. Arthritis Rheum. 2007 Jan; 56(1):58-68.
    View in: PubMed
    Score: 0.236
  5. 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: 0.205
  6. The relative efficiency of penetrance estimators for sib pairs. Hum Hered. 2005; 59(1):61-6.
    View in: PubMed
    Score: 0.205
  7. 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: 0.203
  8. 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: 0.188
  9. Statistical properties of affected sib-pair linkage tests. Hum Hered. 2003; 55(4):153-62.
    View in: PubMed
    Score: 0.179
  10. Model-free tests for genetic linkage. Curr Protoc Hum Genet. 2001 May; Chapter 1:Unit 1.8.
    View in: PubMed
    Score: 0.159
  11. Genetic linkage methods for quantitative traits. Stat Methods Med Res. 2001 Feb; 10(1):3-25.
    View in: PubMed
    Score: 0.157
  12. Comparison of multivariate tests for genetic linkage. Hum Hered. 2001; 51(3):133-44.
    View in: PubMed
    Score: 0.156
  13. Least squares estimation of variance components for linkage. Genet Epidemiol. 2000; 19 Suppl 1:S1-7.
    View in: PubMed
    Score: 0.145
  14. Assessing linkage of monoamine oxidase B in a genome-wide scan using a univariate variance components approach. Genet Epidemiol. 1999; 17 Suppl 1:S49-54.
    View in: PubMed
    Score: 0.136
  15. Genetic linkage analysis using lognormal variance components. Ann Hum Genet. 1998 Nov; 62(Pt 6):521-30.
    View in: PubMed
    Score: 0.134
  16. Comparison of model-free linkage mapping strategies for the study of a complex trait. Genet Epidemiol. 1997; 14(6):743-8.
    View in: PubMed
    Score: 0.118
  17. Assessing linkage on chromosome 5 using components of variance approach: univariate versus multivariate. Genet Epidemiol. 1997; 14(6):773-8.
    View in: PubMed
    Score: 0.118
  18. Assessing genetic linkage and association with robust components of variance approaches. Ann Hum Genet. 1996 03; 60(2):143-60.
    View in: PubMed
    Score: 0.111
  19. 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: 0.106
  20. Targeted sequencing in chromosome 17q linkage region identifies familial glioma candidates in the Gliogene Consortium. Sci Rep. 2015 Feb 05; 5:8278.
    View in: PubMed
    Score: 0.103
  21. Guess LOD approach: sufficient conditions for robustness. Genet Epidemiol. 1995; 12(2):163-76.
    View in: PubMed
    Score: 0.103
  22. Robust variance-components approach for assessing genetic linkage in pedigrees. Am J Hum Genet. 1994 Mar; 54(3):535-43.
    View in: PubMed
    Score: 0.097
  23. A comparison of univariate and multivariate tests for genetic linkage. Genet Epidemiol. 1993; 10(6):671-6.
    View in: PubMed
    Score: 0.089
  24. A variable age of onset segregation model for linkage analysis, with correction for ascertainment, applied to glioma. Cancer Epidemiol Biomarkers Prev. 2012 Dec; 21(12):2242-51.
    View in: PubMed
    Score: 0.087
  25. Preliminary evaluation of linkage between chromosome 1p markers and nevus densities in the Utah data. Cytogenet Cell Genet. 1992; 59(2-3):173-5.
    View in: PubMed
    Score: 0.083
  26. A multivariate method for detecting genetic linkage, with application to a pedigree with an adverse lipoprotein phenotype. Am J Hum Genet. 1990 Aug; 47(2):247-54.
    View in: PubMed
    Score: 0.076
  27. 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: 0.074
  28. Estimating the power of linkage analysis in hereditary breast cancer. Am J Hum Genet. 1990 Feb; 46(2):266-72.
    View in: PubMed
    Score: 0.073
  29. On the asymptotic behavior of the estimate of the recombination fraction under the null hypothesis of no linkage when the model is misspecified. Genet Epidemiol. 1990; 7(5):309-18.
    View in: PubMed
    Score: 0.073
  30. A comparison of some sib-pair linkage methods and multiple locus extensions. Prog Clin Biol Res. 1989; 329:129-34.
    View in: PubMed
    Score: 0.068
  31. Power of the sib-pair and lod-score methods for linkage analysis of quantitative traits. Prog Clin Biol Res. 1989; 329:201-6.
    View in: PubMed
    Score: 0.068
  32. Information for detecting linkage when sampling affected individuals. Prog Clin Biol Res. 1989; 329:207-12.
    View in: PubMed
    Score: 0.068
  33. Robust methods for the detection of genetic linkage for quantitative data from pedigrees. Genet Epidemiol. 1989; 6(2):349-60.
    View in: PubMed
    Score: 0.068
  34. A more powerful robust sib-pair test of linkage for quantitative traits. Genet Epidemiol. 1989; 6(3):435-49.
    View in: PubMed
    Score: 0.068
  35. Design considerations in a sib-pair study of linkage for susceptibility loci in cancer. BMC Med Genet. 2008 Jul 10; 9:64.
    View in: PubMed
    Score: 0.066
  36. 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: 0.064
  37. 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: 0.062
  38. Imprinting detection by extending a regression-based QTL analysis method. Hum Genet. 2007 Sep; 122(2):159-74.
    View in: PubMed
    Score: 0.061
  39. Linkage and segregation analyses of apolipoproteins A1 and B, and lipoprotein cholesterol levels in a large pedigree with excess coronary heart disease: the Bogalusa Heart Study. Genet Epidemiol. 1987; 4(2):115-28.
    View in: PubMed
    Score: 0.059
  40. Linkage analyses of rheumatoid arthritis and related quantitative phenotypes: the GAW15 experience. Genet Epidemiol. 2007; 31 Suppl 1:S86-95.
    View in: PubMed
    Score: 0.059
  41. 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: 0.057
  42. 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: 0.056
  43. Linkage analysis of rheumatoid arthritis in US and UK families reveals interactions between HLA-DRB1 and loci on chromosomes 6q and 16p. Arthritis Rheum. 2006 May; 54(5):1482-90.
    View in: PubMed
    Score: 0.056
  44. Genome-wide meta-analysis for rheumatoid arthritis. Hum Genet. 2006 Jul; 119(6):634-41.
    View in: PubMed
    Score: 0.056
  45. Genome-wide linkage scan for spontaneous DZ twinning. Eur J Hum Genet. 2006 Jan; 14(1):117-22.
    View in: PubMed
    Score: 0.055
  46. Empirical bayes method for incorporating data from multiple genome scans. Hum Hered. 2005; 60(1):36-42.
    View in: PubMed
    Score: 0.054
  47. 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: 0.051
  48. 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: 0.046
  49. 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: 0.045
  50. Power of a simplified multivariate test for genetic linkage. Ann Hum Genet. 2002 Nov; 66(Pt 5-6):407-17.
    View in: PubMed
    Score: 0.044
  51. Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer. Cancer Res. 2021 06 15; 81(12):3162-3173.
    View in: PubMed
    Score: 0.040
  52. 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.
    View in: PubMed
    Score: 0.035
  53. Testing for linkage under robust genetic models. Hum Hered. 1999 Jun; 49(3):146-53.
    View in: PubMed
    Score: 0.035
  54. A genome-wide search for susceptibility genes linked to alcohol dependence. Genet Epidemiol. 1999; 17 Suppl 1:S295-300.
    View in: PubMed
    Score: 0.034
  55. 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.
    View in: PubMed
    Score: 0.032
  56. 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.
    View in: PubMed
    Score: 0.032
  57. Identification of quantitative trait loci controlling levels of radiation-induced thymocyte apoptosis in mice. Genomics. 1997 Nov 01; 45(3):626-8.
    View in: PubMed
    Score: 0.031
  58. Evidence for genetic heterogeneity in familial Wilms' tumor. Cancer Res. 1997 May 15; 57(10):1859-62.
    View in: PubMed
    Score: 0.030
  59. Genetic analysis of simulated oligogenic traits in nuclear and extended pedigrees: summary of GAW10 contributions. Genet Epidemiol. 1997; 14(6):719-35.
    View in: PubMed
    Score: 0.029
  60. 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: 0.029
  61. Nonsyndromic cleft lip with or without cleft palate: new BCL3 information. Am J Hum Genet. 1996 Sep; 59(3):743-4.
    View in: PubMed
    Score: 0.029
  62. 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.
    View in: PubMed
    Score: 0.027
  63. Major gene analysis for diseases and disorders of complex etiology. Exp Clin Immunogenet. 1995; 12(3):141-55.
    View in: PubMed
    Score: 0.026
  64. Genetic epidemiologic studies in the etiology of skin diseases. J Invest Dermatol. 1994 Jun; 102(6):46S-48S.
    View in: PubMed
    Score: 0.025
  65. Can a susceptibility locus for schizophrenia be excluded from chromosome 5q11-13? Am J Hum Genet. 1991 Jun; 48(6):1206-9.
    View in: PubMed
    Score: 0.020
  66. The probabilistic determination of identity-by-descent sharing for pairs of relatives from pedigrees. Am J Hum Genet. 1990 Nov; 47(5):842-53.
    View in: PubMed
    Score: 0.019
  67. Stepwise oligogenic segregation and linkage analysis illustrated with dopamine-beta-hydroxylase activity. Am J Med Genet. 1990 Mar; 35(3):425-32.
    View in: PubMed
    Score: 0.018
  68. Common variants at CD40 and other loci confer risk of rheumatoid arthritis. Nat Genet. 2008 Oct; 40(10):1216-23.
    View in: PubMed
    Score: 0.017
  69. STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus. N Engl J Med. 2007 Sep 06; 357(10):977-86.
    View in: PubMed
    Score: 0.015
  70. Introduction to Genetic Analysis Workshop 15 summaries. Genet Epidemiol. 2007; 31 Suppl 1:S1-6.
    View in: PubMed
    Score: 0.015
  71. 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
  72. Support for previously identified alcoholism susceptibility Loci in a cohort selected for smoking behavior. Alcohol Clin Exp Res. 2005 Dec; 29(12):2108-15.
    View in: PubMed
    Score: 0.014
  73. Genetic mapping of a third Li-Fraumeni syndrome predisposition locus to human chromosome 1q23. Cancer Res. 2005 Jan 15; 65(2):427-31.
    View in: PubMed
    Score: 0.013
  74. 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
  75. A major lung cancer susceptibility locus maps to chromosome 6q23-25. Am J Hum Genet. 2004 Sep; 75(3):460-74.
    View in: PubMed
    Score: 0.012
  76. 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.
    View in: PubMed
    Score: 0.011
  77. Universal and radiation-specific loci influence murine susceptibility to radiation-induced pulmonary fibrosis. Cancer Res. 2002 Jul 01; 62(13):3782-8.
    View in: PubMed
    Score: 0.011
  78. Extension of variance components approach to incorporate temporal trends and longitudinal pedigree data analysis. Genet Epidemiol. 2002 Mar; 22(3):221-32.
    View in: PubMed
    Score: 0.011
  79. Genetic analysis of multiplex rheumatoid arthritis families. Genes Immun. 1999 Sep; 1(1):28-36.
    View in: PubMed
    Score: 0.009
  80. The genetics revolution and the assault on rheumatoid arthritis. Arthritis Rheum. 1999 Jun; 42(6):1071-9.
    View in: PubMed
    Score: 0.009
  81. 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: 0.009
  82. Methods to estimate genetic components of variance for quantitative traits in family studies. Genet Epidemiol. 1999; 17(1):64-76.
    View in: PubMed
    Score: 0.008
  83. Linkage of familial Hibernian fever to chromosome 12p13. Am J Hum Genet. 1998 Jun; 62(6):1446-51.
    View in: PubMed
    Score: 0.008
  84. Exclusion of a p53 germline mutation in a classic Li-Fraumeni syndrome family. Hum Genet. 1998 Jun; 102(6):681-6.
    View in: PubMed
    Score: 0.008
  85. 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: 0.008
  86. The role of germline polymorphisms in the T-cell receptor in susceptibility to ankylosing spondylitis. Br J Rheumatol. 1998 Apr; 37(4):454-8.
    View in: PubMed
    Score: 0.008
  87. 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: 0.006
  88. 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.
    View in: PubMed
    Score: 0.006
  89. Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q. Nat Genet. 1992 Jul; 1(4):301-5.
    View in: PubMed
    Score: 0.005
  90. 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.
    View in: PubMed
    Score: 0.004
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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.