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Page 1
Classical HLA-DRB1 and DPB1 alleles account for HLA associations with primary biliary cirrhosis.
Invernizzi P, Ransom M, Raychaudhuri S, Kosoy R, Lleo A, Shigeta R, Franke A, Bossa F, Amos CI, Gregersen PK, Siminovitch KA, Cusi D, de Bakker PI, Podda M, Gershwin ME, Seldin MF; Italian PBC Genetics Study Group. Invernizzi P, et al. Among authors: amos ci. Genes Immun. 2012 Sep;13(6):461-8. doi: 10.1038/gene.2012.17. Epub 2012 May 10. Genes Immun. 2012. PMID: 22573116 Free PMC article.
Pathway-based analysis of primary biliary cirrhosis genome-wide association studies.
Kar SP, Seldin MF, Chen W, Lu E, Hirschfield GM, Invernizzi P, Heathcote J, Cusi D; Italian PBC Genetics Study Group; Gershwin ME, Siminovitch KA, Amos CI. Kar SP, et al. Among authors: amos ci. Genes Immun. 2013 Apr;14(3):179-86. doi: 10.1038/gene.2013.1. Epub 2013 Feb 7. Genes Immun. 2013. PMID: 23392275 Free PMC article.
Genetic analysis of multiplex rheumatoid arthritis families.
Bali D, Gourley S, Kostyu DD, Goel N, Bruce I, Bell A, Walker DJ, Tran K, Zhu DK, Costello TJ, Amos CI, Seldin MF. Bali D, et al. Among authors: amos ci. Genes Immun. 1999 Sep;1(1):28-36. doi: 10.1038/sj.gene.6363635. Genes Immun. 1999. PMID: 11197302
A genomewide screen in multiplex rheumatoid arthritis families suggests genetic overlap with other autoimmune diseases.
Jawaheer D, Seldin MF, Amos CI, Chen WV, Shigeta R, Monteiro J, Kern M, Criswell LA, Albani S, Nelson JL, Clegg DO, Pope R, Schroeder HW Jr, Bridges SL Jr, Pisetsky DS, Ward R, Kastner DL, Wilder RL, Pincus T, Callahan LF, Flemming D, Wener MH, Gregersen PK. Jawaheer D, et al. Among authors: amos ci. Am J Hum Genet. 2001 Apr;68(4):927-36. doi: 10.1086/319518. Epub 2001 Mar 9. Am J Hum Genet. 2001. PMID: 11254450 Free PMC article.
The genetics revolution and the assault on rheumatoid arthritis.
Seldin MF, Amos CI, Ward R, Gregersen PK. Seldin MF, et al. Among authors: amos ci. Arthritis Rheum. 1999 Jun;42(6):1071-9. doi: 10.1002/1529-0131(199906)42:6<1071::AID-ANR1>3.0.CO;2-8. Arthritis Rheum. 1999. PMID: 10366098 Free article. Review. No abstract available.
Genotype-phenotype correlations in Peutz-Jeghers syndrome.
Amos CI, Keitheri-Cheteri MB, Sabripour M, Wei C, McGarrity TJ, Seldin MF, Nations L, Lynch PM, Fidder HH, Friedman E, Frazier ML. Amos CI, et al. J Med Genet. 2004 May;41(5):327-33. doi: 10.1136/jmg.2003.010900. J Med Genet. 2004. PMID: 15121768 Free PMC article.
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes.
Miller FW, Chen W, O'Hanlon TP, Cooper RG, Vencovsky J, Rider LG, Danko K, Wedderburn LR, Lundberg IE, Pachman LM, Reed AM, Ytterberg SR, Padyukov L, Selva-O'Callaghan A, Radstake TR, Isenberg DA, Chinoy H, Ollier WE, Scheet P, Peng B, Lee A, Byun J, Lamb JA, Gregersen PK, Amos CI; Myositis Genetics Consortium. Miller FW, et al. Among authors: amos ci. Genes Immun. 2015 Oct;16(7):470-80. doi: 10.1038/gene.2015.28. Epub 2015 Aug 20. Genes Immun. 2015. PMID: 26291516 Free PMC article.
864 results