المؤلفون: Morton LM; Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD 20852, USA. mortonli@mail.nih.gov, Wang SS, Bergen AW, Chatterjee N, Kvale P, Welch R, Yeager M, Hayes RB, Chanock SJ, Caporaso NE

المصدر: Pharmacogenetics and genomics [Pharmacogenet Genomics] 2006 Dec; Vol. 16 (12), pp. 901-10.

نوع المنشور: Clinical Trial; Journal Article; Research Support, N.I.H., Intramural

بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101231005 Publication Model: Print Cited Medium: Print ISSN: 1744-6872 (Print) Linking ISSN: 17446872 NLM ISO Abbreviation: Pharmacogenet Genomics Subsets: MEDLINE

مواضيع طبية MeSH: Obesity/*genetics , Receptors, Dopamine D2/*genetics , Smoking/*genetics, Aged ; Alcohol Drinking/genetics ; Alcohol Drinking/psychology ; Body Mass Index ; Female ; Genetic Variation ; Haplotypes ; Humans ; Male ; Middle Aged ; Obesity/psychology ; Polymorphism, Single Nucleotide ; Reward ; Smoking/psychology ; Smoking Cessation ; Tobacco Use Disorder/genetics ; Tobacco Use Disorder/psychology

المؤلفون: Morton LM; Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Rockville, Maryland 20852, USA. mortonli@mail.nih.gov, Schenk M, Hein DW, Davis S, Zahm SH, Cozen W, Cerhan JR, Hartge P, Welch R, Chanock SJ, Rothman N, Wang SS

المصدر: Pharmacogenetics and genomics [Pharmacogenet Genomics] 2006 Aug; Vol. 16 (8), pp. 537-45.

نوع المنشور: Journal Article; Research Support, N.I.H., Intramural; Research Support, U.S. Gov't, P.H.S.

بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101231005 Publication Model: Print Cited Medium: Print ISSN: 1744-6872 (Print) Linking ISSN: 17446872 NLM ISO Abbreviation: Pharmacogenet Genomics Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Variation*, Arylamine N-Acetyltransferase/*genetics , Isoenzymes/*genetics , Lymphoma, Non-Hodgkin/*genetics, Adult ; Aged ; Case-Control Studies ; Female ; Genotype ; Humans ; Male ; Middle Aged ; Phenotype ; Polymorphism, Single Nucleotide ; Risk Factors