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Results 1 to 25 of 173

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Successful design and conduct of genome-wide association studiesAMOS, Christopher I.Human molecular genetics (Print). 2007, Vol 16, issn 0964-6906, R220-R225, NS2Article

Testing for genetic linkage in families by a variance-components approach in the presence of genomic imprintingSHETE, Sanjay; AMOS, Christopher I.American journal of human genetics. 2002, Vol 70, Num 3, pp 751-757, issn 0002-9297Article

Forward-time simulations of non-random mating populations using simuPOPBO PENG; AMOS, Christopher I.Bioinformatics (Oxford. Print). 2008, Vol 24, Num 11, pp 1408-1409, issn 1367-4803, 2 p.Article

Ascertainment issues in variance components modelsDE ANDRADE, Mariza; AMOS, Christopher I.Genetic epidemiology. 2000, Vol 19, Num 4, pp 333-344, issn 0741-0395Article

Genomic imprinting and linkage test for quantitative-trait loci in extended pedigreesSHETE, Sanjay; XIAOJUN ZHOU; AMOS, Christopher I et al.American journal of human genetics. 2003, Vol 73, Num 4, pp 933-938, issn 0002-9297, 6 p.Article

Strength of the purifying selection against different categories of the point mutations in the coding regions of the human genomeGORLOV, Ivan P; KIMMEL, Marek; AMOS, Christopher I et al.Human molecular genetics (Print). 2006, Vol 15, Num 7, pp 1143-1150, issn 0964-6906, 8 p.Article

Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysisQIQING HUANG; SHETE, Sanjay; AMOS, Christopher I et al.American journal of human genetics. 2004, Vol 75, Num 6, pp 1106-1112, issn 0002-9297, 7 p.Article

Complex segregation analysis reveals a multigene model for lung cancerHONGYAN XU; SPITZ, Margaret R; AMOS, Christopher I et al.Human genetics. 2005, Vol 116, Num 1-2, pp 121-127, issn 0340-6717, 7 p.Article

Expression of a 65 kDa oncofetal protein in human prostatic carcinomaHANAUSEK, Margaret; WALASZEK, Zbigniew; KING, Terri M et al.Oncology reports. 2003, Vol 10, Num 5, pp 1387-1392, issn 1021-335X, 6 p.Article

Risk for smoking-related Cancer among relatives of lung Cancer patientsETZEL, Carol J; AMOS, Christopher I; SPITZ, Margaret R et al.Cancer research (Baltimore). 2003, Vol 63, Num 23, pp 8531-8535, issn 0008-5472, 5 p.Article

Power analysis for case-control association studies of samples with known family historiesBO PENG; BIAO LI; YOUNGHUN HAN et al.Human genetics. 2010, Vol 127, Num 6, pp 699-704, issn 0340-6717, 6 p.Article

Frequent association of β-catenin and WT1 mutations in Wilms tumorsMAITI, Sourindra; ALAM, Rita; AMOS, Christopher I et al.Cancer research (Baltimore). 2000, Vol 60, Num 22, pp 6288-6292, issn 0008-5472Article

Genetic susceptibility to lung cancer: The role of DNA damage and repairSPITZ, Margaret R; QINGYI WEI; QIONG DONG et al.Cancer epidemiology, biomarkers & prevention. 2003, Vol 12, Num 8, pp 689-698, issn 1055-9965, 10 p.Article

Germline p53 mutations in a cohort with childhood sarcoma : Sex differences in Cancer riskHWANG, Shih-Jen; LOZANO, Guillermina; AMOS, Christopher I et al.American journal of human genetics. 2003, Vol 72, Num 4, pp 975-983, issn 0002-9297, 9 p.Article

Clustering of disease features within 512 multicase Rheumatoid Arthritis familiesJAWAHEER, Damini; LUM, Raymond F; AMOS, Christopher I et al.Arthritis and rheumatism. 2004, Vol 50, Num 3, pp 736-741, issn 0004-3591, 6 p.Article

Accuracy of family history of cancer as reported by men with prostate cancerKING, Terri M; TONG, L; PACK, Rebecca J et al.Urology (Ridgewood, NJ). 2002, Vol 59, Num 4, pp 546-550, issn 0090-4295Article

The CHRNA5-A3 Region on Chromosome 15q24-25.1 Is a Risk Factor Both for Nicotine Dependence and for Lung CancerSPITZ, Margaret R; AMOS, Christopher I; QIONG DONG et al.Journal of the National Cancer Institute. 2008, Vol 100, Num 21, pp 1552-1556, issn 0027-8874, 5 p.Article

Joint effects of germ-line p53 mutation and sex on cancer risk in Li-fraumeni syndromeWU, Chih-Chieh; SHETE, Sanjay; AMOS, Christopher I et al.Cancer research (Baltimore). 2006, Vol 66, Num 16, pp 8287-8292, issn 0008-5472, 6 p.Article

Genetic Variants in IL-23R and ATG16L1 Independently Predispose to Increased Susceptibility to Crohn's Disease in a Canadian PopulationNEWMAN, William G; QING ZHANG; XIANGDONG LIU et al.Journal of clinical gastroenterology. 2009, Vol 43, Num 5, pp 444-447, issn 0192-0790, 4 p.Article

Missense mutations in hMLH1 and hMSH2 are associated with exonic splicing enhancersGORLOV, Ivan P; GORLOVA, Olga Y; FRAZIER, Marsha L et al.American journal of human genetics. 2003, Vol 73, Num 5, pp 1157-1161, issn 0002-9297, 5 p.Article

Individual-specific liability groups in genetic linkage, with applications to kindreds with Li-Fraumeni syndromeSHETE, Sanjay; AMOS, Christopher I; HWANG, Shih-Jen et al.American journal of human genetics. 2002, Vol 70, Num 3, pp 813-817, issn 0002-9297Article

Current applications of genetic technology in predisposition testing and microsatellite instability assaysFRAZIER, Marsha L; SU, Li-Kuo; AMOS, Christopher I et al.Journal of clinical oncology. 2000, Vol 18, Num 21, pp 70s-74s, issn 0732-183X, SUPArticle

Statistical Methods for Anomalous Discrete Time Series Based on Minimum Cell CountWU, Chih-Chieh; GRIMSON, Roger C; AMOS, Christopher I et al.Biometrical journal. 2008, Vol 50, Num 1, pp 86-96, issn 0323-3847, 11 p.Article

Aggregation of cancer among relatives of never-smoking lung cancer patientsGORLOVA, Olga Y; WENG, Shih-Feng; YIQUN ZHANG et al.International journal of cancer. 2007, Vol 121, Num 1, pp 111-118, issn 0020-7136, 8 p.Article

Extension of variance components approach to incorporate temporal trends and longitudinal pedigree data analysisDE ANDRADE, Mariza; GUEGUEN, René; VISVIKIS, Sophie et al.Genetic epidemiology. 2002, Vol 22, Num 3, pp 221-232, issn 0741-0395Article

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