Amos CI - Search Results

1

Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis.

Hirschfield GM, Liu X, Han Y, Gorlov IP, Lu Y, Xu C, Lu Y, Chen W, Juran BD, Coltescu C, Mason AL, Milkiewicz P, Myers RP, Odin JA, Luketic VA, Speiciene D, Vincent C, Levy C, Gregersen PK, Zhang J, Heathcote EJ, Lazaridis KN, Amos CI, Siminovitch KA. Hirschfield GM, et al. Among authors: amos ci. Nat Genet. 2010 Aug;42(8):655-7. doi: 10.1038/ng.631. Epub 2010 Jul 18. Nat Genet. 2010. PMID: 20639879 Free PMC article.

2

Missense mutations in hMLH1 and hMSH2 are associated with exonic splicing enhancers.

Gorlov IP, Gorlova OY, Frazier ML, Amos CI. Gorlov IP, et al. Among authors: amos ci. Am J Hum Genet. 2003 Nov;73(5):1157-61. doi: 10.1086/378819. Epub 2003 Oct 1. Am J Hum Genet. 2003. PMID: 14526391 Free PMC article.

3

Clustering of disease features within 512 multicase rheumatoid arthritis families.

Jawaheer D, Lum RF, Amos CI, Gregersen PK, Criswell LA. Jawaheer D, et al. Among authors: amos ci. Arthritis Rheum. 2004 Mar;50(3):736-41. doi: 10.1002/art.20066. Arthritis Rheum. 2004. PMID: 15022313 Free article.

4

CARD15 and HLA DRB1 alleles influence susceptibility and disease localization in Crohn's disease.

Newman B, Silverberg MS, Gu X, Zhang Q, Lazaro A, Steinhart AH, Greenberg GR, Griffiths AM, McLeod RS, Cohen Z, Fernández-Viña M, Amos CI, Siminovitch K. Newman B, et al. Among authors: amos ci. Am J Gastroenterol. 2004 Feb;99(2):306-15. doi: 10.1111/j.1572-0241.2004.04038.x. Am J Gastroenterol. 2004. PMID: 15046222

5

Functional variants of OCTN cation transporter genes are associated with Crohn disease.

Peltekova VD, Wintle RF, Rubin LA, Amos CI, Huang Q, Gu X, Newman B, Van Oene M, Cescon D, Greenberg G, Griffiths AM, St George-Hyslop PH, Siminovitch KA. Peltekova VD, et al. Among authors: amos ci. Nat Genet. 2004 May;36(5):471-5. doi: 10.1038/ng1339. Epub 2004 Apr 11. Nat Genet. 2004. PMID: 15107849

6

Missense mutations in cancer suppressor gene TP53 are colocalized with exonic splicing enhancers (ESEs).

Gorlov IP, Gorlova OY, Frazier ML, Amos CI. Gorlov IP, et al. Among authors: amos ci. Mutat Res. 2004 Oct 4;554(1-2):175-83. doi: 10.1016/j.mrfmmm.2004.04.014. Mutat Res. 2004. PMID: 15450416

7

A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn's disease.

Newman B, Gu X, Wintle R, Cescon D, Yazdanpanah M, Liu X, Peltekova V, Van Oene M, Amos CI, Siminovitch KA. Newman B, et al. Among authors: amos ci. Gastroenterology. 2005 Feb;128(2):260-9. doi: 10.1053/j.gastro.2004.11.056. Gastroenterology. 2005. PMID: 15685536

8

SLC22A4 polymorphisms implicated in rheumatoid arthritis and Crohn's disease are not associated with rheumatoid arthritis in a Canadian Caucasian population.

Newman B, Wintle RF, van Oene M, Yazdanpanah M, Owen J, Johnson B, Gu X, Amos CI, Keystone E, Rubin LA, Siminovitch KA. Newman B, et al. Among authors: amos ci. Arthritis Rheum. 2005 Feb;52(2):425-9. doi: 10.1002/art.20854. Arthritis Rheum. 2005. PMID: 15693005 Free article.

9

Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations.

van Oene M, Wintle RF, Liu X, Yazdanpanah M, Gu X, Newman B, Kwan A, Johnson B, Owen J, Greer W, Mosher D, Maksymowych W, Keystone E, Rubin LA, Amos CI, Siminovitch KA. van Oene M, et al. Among authors: amos ci. Arthritis Rheum. 2005 Jul;52(7):1993-8. doi: 10.1002/art.21123. Arthritis Rheum. 2005. PMID: 15986374 Free article.

10

Predicting the oncogenicity of missense mutations reported in the International Agency for Cancer Research (IARC) mutation database on p53.

Gorlov IP, Gorlova OY, Amos CI. Gorlov IP, et al. Among authors: amos ci. Hum Mutat. 2005 Nov;26(5):446-54. doi: 10.1002/humu.20242. Hum Mutat. 2005. PMID: 16173033

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