PubRank

C I Amos

Author PubWeight™ 121.31‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes. Cell 1999 5.01
2 Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure. Am J Hum Genet 1999 4.54
3 A genomewide screen in multiplex rheumatoid arthritis families suggests genetic overlap with other autoimmune diseases. Am J Hum Genet 2001 4.17
4 Genetic analysis of simulated oligogenic traits in nuclear and extended pedigrees: summary of GAW10 contributions. Genet Epidemiol 1997 3.45
5 A major lung cancer susceptibility locus maps to chromosome 6q23-25. Am J Hum Genet 2004 3.05
6 The genetics revolution and the assault on rheumatoid arthritis. Arthritis Rheum 1999 2.92
7 High risk of HIV-1 infection for first-born twins. The International Registry of HIV-exposed Twins. Lancet 1991 2.51
8 Modulation of nucleotide excision repair capacity by XPD polymorphisms in lung cancer patients. Cancer Res 2001 2.37
9 Repair of tobacco carcinogen-induced DNA adducts and lung cancer risk: a molecular epidemiologic study. J Natl Cancer Inst 2000 2.33
10 Case-control study of the D2 dopamine receptor gene and smoking status in lung cancer patients. J Natl Cancer Inst 1998 2.16
11 Mutagen sensitivity as a risk factor for second malignant tumors following malignancies of the upper aerodigestive tract. J Natl Cancer Inst 1994 2.15
12 Familial clustering of rheumatoid arthritis with other autoimmune diseases. Hum Genet 1998 1.99
13 Frequent association of beta-catenin and WT1 mutations in Wilms tumors. Cancer Res 2000 1.82
14 Benzo[a]pyrene diol epoxide and bleomycin sensitivity and susceptibility to cancer of upper aerodigestive tract. J Natl Cancer Inst 1998 1.81
15 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 1.77
16 Variation in the region of the angiotensin-converting enzyme gene influences interindividual differences in blood pressure levels in young white males. Circulation 1998 1.65
17 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 1.61
18 Evolutionary evidence of the effect of rare variants on disease etiology. Clin Genet 2010 1.54
19 Segregation analysis of breast cancer from the cancer and steroid hormone study: histologic subtypes. J Natl Cancer Inst 1990 1.49
20 Guess LOD approach: sufficient conditions for robustness. Genet Epidemiol 1995 1.37
21 Detecting haplotype effects in genomewide association studies. Genet Epidemiol 2007 1.33
22 Segregation analysis of idiopathic talipes equinovarus in a Texan population. Am J Med Genet 1998 1.32
23 Power of the sib-pair and lod-score methods for linkage analysis of quantitative traits. Prog Clin Biol Res 1989 1.32
24 Genetic regulation of the capacity to make immunoglobulin G to pneumococcal capsular polysaccharides. J Investig Med 1997 1.29
25 Dietary intake of isothiocyanates: evidence of a joint effect with glutathione S-transferase polymorphisms in lung cancer risk. Cancer Epidemiol Biomarkers Prev 2000 1.25
26 Correlates of psychologic distress in colorectal cancer patients undergoing genetic testing for hereditary colon cancer. Health Psychol 1997 1.23
27 Genetic variability in the tumor necrosis factor-lymphotoxin region influences susceptibility to rheumatoid arthritis. Am J Hum Genet 1996 1.23
28 Effect of Box-Cox transformation on power of Haseman-Elston and maximum-likelihood variance components tests to detect quantitative trait Loci. Hum Hered 2003 1.22
29 Ascertainment issues in variance components models. Genet Epidemiol 2000 1.21
30 Effects of cyclin D1 polymorphism on age of onset of hereditary nonpolyposis colorectal cancer. Cancer Res 2000 1.20
31 Investigating the genetic basis for ankylosing spondylitis. Linkage studies with the major histocompatibility complex region. Arthritis Rheum 1994 1.20
32 Genetic analysis of multiplex rheumatoid arthritis families. Genes Immun 1999 1.18
33 Entropy-based information gain approaches to detect and to characterize gene-gene and gene-environment interactions/correlations of complex diseases. Genet Epidemiol 2011 1.16
34 Linkage of familial Hibernian fever to chromosome 12p13. Am J Hum Genet 1998 1.14
35 Higher lung cancer risk for younger African-Americans with the Pro/Pro p53 genotype. Carcinogenesis 1995 1.13
36 International Genetic Epidemiology Society: commentary on Darkness in El Dorado by Patrick Tierney. Genet Epidemiol 2001 1.13
37 SMAD genes in juvenile polyposis. Genes Chromosomes Cancer 1999 1.10
38 Methods to estimate genetic components of variance for quantitative traits in family studies. Genet Epidemiol 1999 1.09
39 Re: Discriminatory accuracy from single-nucleotide polymorphisms in models to predict breast cancer risk. J Natl Cancer Inst 2009 1.08
40 Association of primary biliary cirrhosis with variants in the CLEC16A, SOCS1, SPIB and SIAE immunomodulatory genes. Genes Immun 2012 1.08
41 Comparison of linkage-disequilibrium methods for localization of genes influencing quantitative traits in humans. Am J Hum Genet 1999 1.07
42 The association of microsomal epoxide hydrolase polymorphisms and lung cancer risk in African-Americans and Mexican-Americans. Carcinogenesis 2001 1.07
43 Cigarette smoking in a multiethnic population of youth: methods and baseline findings. Prev Med 1998 1.06
44 Leptin and prostate cancer. Prostate 2001 1.06
45 Intention to learn results of genetic testing for hereditary colon cancer. Cancer Epidemiol Biomarkers Prev 1999 1.05
46 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 1.04
47 Age-associated risk of cancer among individuals with N-acetyltransferase 2 (NAT2) mutations and mutations in DNA mismatch repair genes. Cancer Res 2001 1.03
48 Contrasting molecular pathology of colorectal carcinoma in Egyptian and Western patients. Br J Cancer 2001 1.03
49 Assessing linkage on chromosome 5 using components of variance approach: univariate versus multivariate. Genet Epidemiol 1997 1.02
50 Cyclin D1 polymorphism and increased risk of colorectal cancer at young age. J Natl Cancer Inst 2001 1.01
51 Inheritance of susceptibility to bleomycin-induced pulmonary fibrosis in the mouse. Cancer Res 1996 1.00
52 Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q. Nat Genet 1992 0.98
53 Segregation analysis of cancer in families of glioma patients. Genet Epidemiol 2001 0.98
54 Joint effect of insulin-like growth factors and mutagen sensitivity in lung cancer risk. J Natl Cancer Inst 2000 0.96
55 A parallel study of in vitro sensitivity to benzo[a]pyrene diol epoxide and bleomycin in lung carcinoma cases and controls. Cancer 1998 0.95
56 Exclusion of a p53 germline mutation in a classic Li-Fraumeni syndrome family. Hum Genet 1998 0.91
57 Classical HLA-DRB1 and DPB1 alleles account for HLA associations with primary biliary cirrhosis. Genes Immun 2012 0.91
58 Testing for linkage under robust genetic models. Hum Hered 1999 0.91
59 Cigarette smoking, alcohol, and oral contraceptive use by type A adolescent--the Bogalusa Heart Study. J Behav Med 1989 0.90
60 Birth order, delivery route, and concordance in the transmission of human immunodeficiency virus type 1 from mothers to twins. International Registry of HIV-Exposed Twins. J Pediatr 1995 0.90
61 Pathway-based analysis of primary biliary cirrhosis genome-wide association studies. Genes Immun 2013 0.90
62 Stepwise oligogenic segregation and linkage analysis illustrated with dopamine-beta-hydroxylase activity. Am J Med Genet 1990 0.90
63 Segregation analysis of squamous cell carcinoma of the head and neck: evidence for a major gene determining risk. Ann Hum Genet 1998 0.89
64 Cytochrome P450 2E1 DraI polymorphisms in lung cancer in minority populations. Cancer Epidemiol Biomarkers Prev 1998 0.89
65 Changes in screening behaviors and attitudes toward screening from pre-test genetic counseling to post-disclosure in Lynch syndrome families. Clin Genet 2013 0.88
66 Chromosome 5 aberrations and genetic predisposition to lung cancer. Int J Cancer 1998 0.88
67 Mutagen sensitivity as a biological marker of lung cancer risk in African Americans. Cancer Epidemiol Biomarkers Prev 1995 0.88
68 A case-control study of nonrandom distribution of bleomycin-induced chromatid breaks in lymphocytes of lung cancer cases. Cancer Res 1995 0.87
69 Associations among telomerase activity, p53 protein overexpression, and genetic instability in lung cancer. Br J Cancer 1999 0.86
70 Evidence for genetic heterogeneity in familial Wilms' tumor. Cancer Res 1997 0.86
71 Association between polymorphic blood markers and risk factors for cardiovascular disease in a large pedigree. Genet Epidemiol 1987 0.85
72 Strain difference in jejunal crypt cell susceptibility to radiation-induced apoptosis. Int J Radiat Biol 1996 0.85
73 Shared susceptibility variations in autoimmune diseases: a brief perspective on common issues. Genes Immun 2009 0.85
74 Assessing linkage of monoamine oxidase B in a genome-wide scan using a univariate variance components approach. Genet Epidemiol 1999 0.84
75 Epidemiologic determinants of clinically relevant prostate cancer. Int J Cancer 2000 0.84
76 The quantitative LOD score: test statistic and sample size for exclusion and linkage of quantitative traits in human sibships. Am J Hum Genet 1998 0.83
77 An approach to the multivariate analysis of high-density-lipoprotein cholesterol in a large kindred: the Bogalusa Heart Study. Genet Epidemiol 1986 0.82
78 Robustness of the maximum-likelihood (LOD) method for detecting linkage. Am J Hum Genet 1993 0.82
79 Description of a large pedigree with an adverse lipoprotein cholesterol phenotype: the Bogalusa Heart Study. Genet Epidemiol 1986 0.81
80 Genome scans for genetic predisposition to alcoholism by use of transmission disequilibrium test analyses. Genet Epidemiol 1999 0.81
81 A comparison of some sib-pair linkage methods and multiple locus extensions. Prog Clin Biol Res 1989 0.80
82 Update on genetic risk factors for systemic lupus erythematosus and rheumatoid arthritis. Curr Opin Rheumatol 2000 0.80
83 Genetic linkage analysis using lognormal variance components. Ann Hum Genet 1998 0.79
84 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 0.79
85 Genetic basis of strain variation in levels of radiation-induced apoptosis of thymocytes. Radiat Res 1996 0.79
86 Loci for efficient detection of microsatellite instability in hereditary non-polyposis colorectal cancer. Oncol Rep 1999 0.79
87 A chromosome 15 quantitative trait locus controls levels of radiation-induced jejunal crypt cell apoptosis in mice. Genomics 2001 0.78
88 Current applications of genetic technology in predisposition testing and microsatellite instability assays. J Clin Oncol 2000 0.78
89 Design and methodology of a study of psychosocial aspects of genetic testing for hereditary colorectal cancer. Ann N Y Acad Sci 1997 0.77
90 A genome-wide search for susceptibility genes linked to alcohol dependence. Genet Epidemiol 1999 0.77
91 Chromosome breaks and sister chromatid exchange as predictors of second cancers in Hodgkin's disease. Leuk Lymphoma 1998 0.77
92 The role of germline polymorphisms in the T-cell receptor in susceptibility to ankylosing spondylitis. Br J Rheumatol 1998 0.77
93 Joint effect of insulin-like growth factors and mutagen sensitivity in lung cancer risk. Growth Horm IGF Res 2000 0.76
94 Modeling age x major gene interaction by a variance component approach. Genet Epidemiol 2001 0.76
95 Deletion in poly(ADP-ribose)polymerase pseudogene and lung cancer risk. Carcinogenesis 1998 0.75
96 Can a susceptibility locus for schizophrenia be excluded from chromosome 5q11-13? Am J Hum Genet 1991 0.75
97 Linkage between the APOB gene and serum ApoB levels in a large pedigree from the Bogalusa Heart Study. Genet Epidemiol 1994 0.75
98 Identification of quantitative trait loci controlling levels of radiation-induced thymocyte apoptosis in mice. Genomics 1997 0.75
99 Association and linkage with quantitative traits. Genet Epidemiol 1995 0.75
100 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 0.75
101 Informed consent for tissue research. JAMA 1999 0.75
102 Power of a simplified multivariate test for genetic linkage. Ann Hum Genet 2002 0.75
103 Adaptations of linkage and association methods for the study of asthma, a complex trait. Genet Epidemiol 2001 0.75
104 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 0.75