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Candidate genes and single nucleotide polymorphisms (SNPs) in the study of human disease : Cancer genomicsCHANOCK, Stephen.Disease markers. 2001, Vol 17, Num 2, pp 89-98, issn 0278-0240Article

Reflections on events surrounding the time of diagnosis in pediatric oncologyCHANOCK, Stephen.Journal of pediatric hematology/oncology. 2001, Vol 23, Num 4, pp 211-212, issn 1077-4114Article

Genetic variation and hematology: Single-nucleotide polymorphisms, haplotypes, and complex diseaseCHANOCK, Stephen.Seminars in hematology. 2003, Vol 40, Num 4, pp 321-328, issn 0037-1963, 8 p.Article

Current status of genome-wide association studies in cancerCHUNG, Charles C; CHANOCK, Stephen J.Human genetics. 2011, Vol 130, Num 1, pp 59-78, issn 0340-6717, 20 p.Article

Detectable Clonal Mosaicism in the Human Genome : Next-Generation Sequencing in Hematologic CancersMACHIELA, Mitchell J; CHANOCK, Stephen J.Seminars in hematology. 2013, Vol 50, Num 4, pp 348-359, issn 0037-1963, 12 p.Article

Personalized medicine: new genomics, old lessonsOFFIT, Kenneth.Human genetics. 2011, Vol 130, Num 1, pp 3-14, issn 0340-6717, 12 p.Article

Special Issue on Personalized MedicineCHANOCK, Stephen J; BIANKIN, Andrew V.Human genetics. 2011, Vol 130, Num 1, issn 0340-6717, 167 p.Serial Issue

Direct-to-consumer testing: if consumers are not anxious, why are policymakers?CAULFIELD, Timothy.Human genetics. 2011, Vol 130, Num 1, pp 23-25, issn 0340-6717, 3 p.Article

Human pharmacogenomic variations and their implications for antifungal efficacyMELETIADIS, Joseph; CHANOCK, Stephen; WALSH, Thomas J et al.Clinical microbiology reviews (Print). 2006, Vol 19, Num 4, issn 0893-8512, 594, 763-787 [26 p.]Article

Using germ-line genetic variation to investigate and treat cancerSAVAGE, Sharon A; CHANOCK, Stephen J.Drug discovery today. 2004, Vol 9, Num 14, pp 610-618, issn 1359-6446, 9 p.Article

Genetic counselling for personalised medicineCLARKE, Angus; THIRLAWAY, Katie.Human genetics. 2011, Vol 130, Num 1, pp 27-31, issn 0340-6717, 5 p.Article

Characterization of the genomic structure of the human Vitamin C transporter SVCT1 (SLC23A2)ERICHSEN, Hans Christian; ECK, Peter; LEVINE, Mark et al.The Journal of nutrition. 2001, Vol 131, Num 10, pp 2623-2627, issn 0022-3166Article

The expression of NA antigens in people with unusual Fcγ receptor III genotypesMATSUO, Kazuhiko; PROCTER, Jo L; CHANOCK, Stephen et al.Transfusion (Philadelphia, PA). 2001, Vol 41, Num 6, pp 775-782, issn 0041-1132Article

Translating genomics into improved population screening: hype or hope?PASHAYAN, Nora; PHAROAH, Paul.Human genetics. 2011, Vol 130, Num 1, pp 19-21, issn 0340-6717, 3 p.Article

Telomere Length in White Blood Cell DNA and Lung Cancer: A Pooled Analysis of Three Prospective CohortsWEI JIE SEOW; CAWTHON, Richard M; BASSIG, Bryan A et al.Cancer research (Chicago, Ill.). 2014, Vol 74, Num 15, pp 4090-4098, issn 0008-5472, 9 p.Article

Common Genetic Variants in the 8q24 Region and Risk of Papillary Thyroid CancerNETA, Gila; YU, Chu-Ling; CHANOCK, Stephen et al.The Laryngoscope. 2012, Vol 122, Num 5, pp 1040-1042, issn 0023-852X, 3 p.Article

A single nucleotide polymorphism tags variation in the arylamine N-acetyltransferase 2 phenotype in populations of European backgroundGARCIA-CLOSAS, Montserrat; HEIN, David W; KOGEVINAS, Manolis et al.Pharmacogenetics and genomics (Print). 2011, Vol 21, Num 4, pp 231-236, issn 1744-6872, 6 p.Article

Genome-wide association study identifies a common variant associated with risk of endometrial cancerSPURDLE, Amanda B; THOMPSON, Deborah J; MONTGOMERY, Grant W et al.Nature genetics. 2011, Vol 43, Num 5, pp 451-454, issn 1061-4036, 4 p.Article

Polymorphism in the GALNT1 Gene and Epithelial Ovarian Cancer in Non-Hispanic White Women: The Ovarian Cancer Association ConsortiumPHELAN, Catherine M; TSAI, Ya-Yu; MOYSICH, Kirsten et al.Cancer epidemiology, biomarkers & prevention. 2010, Vol 19, Num 2, pp 600-604, issn 1055-9965, 5 p.Article

CYP19A1 Genetic Variation in Relation to Prostate Cancer Risk and Circulating Sex Hormone Concentrations in Men from the Breast and Prostate Cancer Cohort ConsortiumTRAVIS, Ruth C; SCHUMACHER, Fredrick; CALLE, Eugenia E et al.Cancer epidemiology, biomarkers & prevention. 2009, Vol 18, Num 10, pp 2734-2744, issn 1055-9965, 11 p.Article

Identification of modifier genes for cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutationsYANG, Xiaohong Rose; PFEIFFER, Ruth M; WHEELER, William et al.International journal of cancer (Print). 2009, Vol 125, Num 12, pp 2912-2917, issn 0020-7136, 6 p.Article

Large-Scale Evaluation of Genetic Variants in Candidate Genes for Colorectal Cancer Risk in the Nurses' Health Study and the Health Professionals' Follow-up StudyHAZRA, Aditi; CHANOCK, Stephen; GIOVANNUCCI, Edward et al.Cancer epidemiology, biomarkers & prevention. 2008, Vol 17, Num 2, pp 311-319, issn 1055-9965, 9 p.Article

Polymorphisms of Genes in the Lipid Metabolism Pathway and Risk of Biliary Tract Cancers and Stones : A Population-Based Case-Control Study in Shanghai, ChinaANDREOTTI, Gabriella; JINBO CHEN; HAN, Tian-Quan et al.Cancer epidemiology, biomarkers & prevention. 2008, Vol 17, Num 3, pp 525-534, issn 1055-9965, 10 p.Article

Genetic variants in caspase genes and susceptibility to non-Hodgkin lymphomaQING LAN; TONGZHANG ZHENG; YEAGER, Meredith et al.Carcinogenesis (New York. Print). 2007, Vol 28, Num 4, pp 823-827, issn 0143-3334, 5 p.Article

Polymorphisms in immunoregulatory genes, smoky coal exposure and lung cancer risk in Xuan Wei, ChinaLEE, Kyoung-Mu; MIN SHEN; CHANOCK, Stephen et al.Carcinogenesis (New York. Print). 2007, Vol 28, Num 7, pp 1437-1441, issn 0143-3334, 5 p.Article

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