Zobrazeno 1 - 10
of 70
pro vyhledávání: '"C. I. Amos"'
Autor:
F W, Miller, W, Chen, T P, O'Hanlon, R G, Cooper, J, Vencovsky, L G, Rider, K, Danko, L R, Wedderburn, I E, Lundberg, L M, Pachman, A M, Reed, S R, Ytterberg, L, Padyukov, A, Selva-O'Callaghan, T R, Radstake, D A, Isenberg, H, Chinoy, W E R, Ollier, P, Scheet, B, Peng, A, Lee, J, Byun, J A, Lamb, P K, Gregersen, C I, Amos, Hemlata, Varsani
Publikováno v:
Genes & Immunity. 16:470-480
Autoimmune muscle diseases (myositis) comprise a group of complex phenotypes influenced by genetic and environmental factors. To identify genetic risk factors in patients of European ancestry, we conducted a genome-wide association study (GWAS) of th
Autor:
D B, Hancock, Y, Guo, G W, Reginsson, N C, Gaddis, S M, Lutz, R, Sherva, A, Loukola, C C, Minica, C A, Markunas, Y, Han, K A, Young, D F, Gudbjartsson, F, Gu, D W, McNeil, B, Qaiser, C, Glasheen, S, Olson, M T, Landi, P A F, Madden, L A, Farrer, J, Vink, N L, Saccone, M C, Neale, H R, Kranzler, J, McKay, R J, Hung, C I, Amos, M L, Marazita, D I, Boomsma, T B, Baker, J, Gelernter, J, Kaprio, N E, Caporaso, T E, Thorgeirsson, J E, Hokanson, L J, Bierut, K, Stefansson, E O, Johnson
Publikováno v:
Molecular psychiatry
Cigarette smoking is a leading cause of preventable mortality worldwide. Nicotine dependence, which reduces the likelihood of quitting smoking, is a heritable trait with firmly established associations with sequence variants in nicotine acetylcholine
Publikováno v:
Annals of Human Genetics. 66:407-417
Publikováno v:
Annals of Human Genetics. 62:505-510
Autor:
A M, Burton-Chase, S R, Hovick, S K, Peterson, S K, Marani, S W, Vernon, C I, Amos, M L, Frazier, P M, Lynch, E R, Gritz
Publikováno v:
Clinical genetics. 83(3)
The purpose of this study was to examine colonoscopy adherence and attitudes toward colorectal cancer (CRC) screening in individuals who underwent Lynch syndrome genetic counseling and testing. We evaluated changes in colonoscopy adherence and CRC sc
Autor:
C. I. Amos
Publikováno v:
JAMA: The Journal of the American Medical Association. 268:1896-1899
Publikováno v:
Cancer research. 61(4)
Mutations in N-acetyltransferase 2 (NAT2), a highly polymorphic enzyme involved in the metabolism of xenobiotics and carcinogens, may affect risk for colorectal cancer (CRC), especially among individuals with germ-line mutations in DNA mismatch repai
Publikováno v:
Genetic epidemiology. 20(2)
A small proportion of brain tumors are attributed to a genetic predisposition; however, the hereditary proportion is undetermined. This study evaluates the degree of familial aggregation of cancer in a large series of brain tumor patients. Our study
Autor:
S, Chang, S D, Hursting, J H, Contois, S S, Strom, Y, Yamamura, R J, Babaian, P, Troncoso, P S, Scardino, T M, Wheeler, C I, Amos, M R, Spitz
Publikováno v:
The Prostate. 46(1)
Higher prostate cancer mortality rates among US immigrants from countries with lower rates suggest environmental influences on prostate carcinogenesis (e.g., diet, body composition).In a study identifying determinants of clinically relevant prostate
Publikováno v:
Cancer research. 60(22)
The etiology of Wilms tumor, an embryonic kidney tumor, is genetically heterogeneous. One Wilms tumor gene, WT1, which encodes a zinc finger transcription factor, is mutated in 10-20% of Wilms tumors, but it is still not clear what critical cellular