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Results: 1 to 20 of 90

1.

Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.

Mells GF, Floyd JA, Morley KI, Cordell HJ, Franklin CS, Shin SY, Heneghan MA, Neuberger JM, Donaldson PT, Day DB, Ducker SJ, Muriithi AW, Wheater EF, Hammond CJ, Dawwas MF; UK PBC Consortium; Wellcome Trust Case Control Consortium 3, Jones DE, Peltonen L, Alexander GJ, Sandford RN, Anderson CA.

Nat Genet. 2011 Mar 13;43(4):329-32. doi: 10.1038/ng.789. Erratum in: Nat Genet. 2011 Nov;43(11):1164. Richardson,Paul [added]; Nasr, Ikram [added]; Aspinall,Richard [added].

PMID:
21399635
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population.

Nakamura M, Nishida N, Kawashima M, Aiba Y, Tanaka A, Yasunami M, Nakamura H, Komori A, Nakamuta M, Zeniya M, Hashimoto E, Ohira H, Yamamoto K, Onji M, Kaneko S, Honda M, Yamagiwa S, Nakao K, Ichida T, Takikawa H, Seike M, Umemura T, Ueno Y, Sakisaka S, Kikuchi K, Ebinuma H, Yamashiki N, Tamura S, Sugawara Y, Mori A, Yagi S, Shirabe K, Taketomi A, Arai K, Monoe K, Ichikawa T, Taniai M, Miyake Y, Kumagi T, Abe M, Yoshizawa K, Joshita S, Shimoda S, Honda K, Takahashi H, Hirano K, Takeyama Y, Harada K, Migita K, Ito M, Yatsuhashi H, Fukushima N, Ota H, Komatsu T, Saoshiro T, Ishida J, Kouno H, Kouno H, Yagura M, Kobayashi M, Muro T, Masaki N, Hirata K, Watanabe Y, Nakamura Y, Shimada M, Hirashima N, Komeda T, Sugi K, Koga M, Ario K, Takesaki E, Maehara Y, Uemoto S, Kokudo N, Tsubouchi H, Mizokami M, Nakanuma Y, Tokunaga K, Ishibashi H.

Am J Hum Genet. 2012 Oct 5;91(4):721-8. doi: 10.1016/j.ajhg.2012.08.010. Epub 2012 Sep 20.

PMID:
23000144
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

[Analysis of disease-pathway by identifying susceptible genes to primary biliary cirrhosis].

Nakamura M.

Nihon Rinsho Meneki Gakkai Kaishi. 2012;35(6):503-10. Review. Japanese. Erratum in: Nihon Rinsho Meneki Gakkai Kaishi. 2013;36(1):1. Makamura, Minoru [corrected to Nakamura, Minoru].

PMID:
23291485
[PubMed - indexed for MEDLINE]
Free Article
4.

Association of primary biliary cirrhosis with variants in the CLEC16A, SOCS1, SPIB and SIAE immunomodulatory genes.

Hirschfield GM, Xie G, Lu E, Sun Y, Juran BD, Chellappa V, Coltescu C, Mason AL, Milkiewicz P, Myers RP, Odin JA, Luketic VA, Bacon B, Bodenheimer H, Liakina V, Vincent C, Levy C, Pillai S, Lazaridis KN, Amos CI, Siminovitch KA.

Genes Immun. 2012 Jun;13(4):328-35. doi: 10.1038/gene.2011.89. Epub 2012 Jan 19.

PMID:
22257840
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

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.

Genes Immun. 2013 Apr;14(3):179-86. doi: 10.1038/gene.2013.1. Epub 2013 Feb 7.

PMID:
23392275
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.

Liu JZ, Almarri MA, Gaffney DJ, Mells GF, Jostins L, Cordell HJ, Ducker SJ, Day DB, Heneghan MA, Neuberger JM, Donaldson PT, Bathgate AJ, Burroughs A, Davies MH, Jones DE, Alexander GJ, Barrett JC, Sandford RN, Anderson CA; UK Primary Biliary Cirrhosis (PBC) Consortium; Wellcome Trust Case Control Consortium 3.

Nat Genet. 2012 Oct;44(10):1137-41. doi: 10.1038/ng.2395. Epub 2012 Sep 9.

PMID:
22961000
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis.

Hoppenbrouwers IA, Aulchenko YS, Janssens AC, Ramagopalan SV, Broer L, Kayser M, Ebers GC, Oostra BA, van Duijn CM, Hintzen RQ.

J Hum Genet. 2009 Nov;54(11):676-80. doi: 10.1038/jhg.2009.96. Epub 2009 Oct 16.

PMID:
19834503
[PubMed - indexed for MEDLINE]
8.

Progress in the genetics of primary biliary cirrhosis.

Hirschfield GM, Invernizzi P.

Semin Liver Dis. 2011 May;31(2):147-56. doi: 10.1055/s-0031-1276644. Epub 2011 May 2. Review.

PMID:
21538281
[PubMed - indexed for MEDLINE]
9.

Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance.

Jagielska D, Redler S, Brockschmidt FF, Herold C, Pasternack SM, Garcia Bartels N, Hanneken S, Eigelshoven S, Refke M, Barth S, Giehl KA, Kruse R, Lutz G, Wolff H, Blaumeiser B, Böhm M, Blume-Peytavi U, Becker T, Nöthen MM, Betz RC.

J Invest Dermatol. 2012 Sep;132(9):2192-7. doi: 10.1038/jid.2012.129. Epub 2012 Apr 26.

PMID:
22534877
[PubMed - indexed for MEDLINE]
Free Article
10.

Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.

Hirschfield GM, Liu X, Xu C, Lu Y, Xie G, Lu Y, Gu X, Walker EJ, Jing K, Juran BD, Mason AL, Myers RP, Peltekian KM, Ghent CN, Coltescu C, Atkinson EJ, Heathcote EJ, Lazaridis KN, Amos CI, Siminovitch KA.

N Engl J Med. 2009 Jun 11;360(24):2544-55. doi: 10.1056/NEJMoa0810440. Epub 2009 May 20. Erratum in: N Engl J Med. 2009 Jun 25;360(26):2797-8.

PMID:
19458352
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Risk alleles for multiple sclerosis in multiplex families.

D'Netto MJ, Ward H, Morrison KM, Ramagopalan SV, Dyment DA, DeLuca GC, Handunnetthi L, Sadovnick AD, Ebers GC.

Neurology. 2009 Jun 9;72(23):1984-8. doi: 10.1212/WNL.0b013e3181a92c25.

PMID:
19506219
[PubMed - indexed for MEDLINE]
12.

Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians.

Rubio JP, Stankovich J, Field J, Tubridy N, Marriott M, Chapman C, Bahlo M, Perera D, Johnson LJ, Tait BD, Varney MD, Speed TP, Taylor BV, Foote SJ, Butzkueven H, Kilpatrick TJ.

Genes Immun. 2008 Oct;9(7):624-30. doi: 10.1038/gene.2008.59. Epub 2008 Jul 24.

PMID:
18650830
[PubMed - indexed for MEDLINE]
13.

Variants of DENND1B associated with asthma in children.

Sleiman PM, Flory J, Imielinski M, Bradfield JP, Annaiah K, Willis-Owen SA, Wang K, Rafaels NM, Michel S, Bonnelykke K, Zhang H, Kim CE, Frackelton EC, Glessner JT, Hou C, Otieno FG, Santa E, Thomas K, Smith RM, Glaberson WR, Garris M, Chiavacci RM, Beaty TH, Ruczinski I, Orange JS, Allen J, Spergel JM, Grundmeier R, Mathias RA, Christie JD, von Mutius E, Cookson WO, Kabesch M, Moffatt MF, Grunstein MM, Barnes KC, Devoto M, Magnusson M, Li H, Grant SF, Bisgaard H, Hakonarson H.

N Engl J Med. 2010 Jan 7;362(1):36-44. doi: 10.1056/NEJMoa0901867. Epub 2009 Dec 23. Erratum in: N Engl J Med. 2012 Feb 16;366(7):672. Orange, Jordan M [corrected to Orange, Jordan S]. N Engl J Med. 2010 Sep 2;363(10):994.

PMID:
20032318
[PubMed - indexed for MEDLINE]
Free Article
14.

Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants.

Juran BD, Hirschfield GM, Invernizzi P, Atkinson EJ, Li Y, Xie G, Kosoy R, Ransom M, Sun Y, Bianchi I, Schlicht EM, Lleo A, Coltescu C, Bernuzzi F, Podda M, Lammert C, Shigeta R, Chan LL, Balschun T, Marconi M, Cusi D, Heathcote EJ, Mason AL, Myers RP, Milkiewicz P, Odin JA, Luketic VA, Bacon BR, Bodenheimer HC Jr, Liakina V, Vincent C, Levy C, Franke A, Gregersen PK, Bossa F, Gershwin ME, deAndrade M, Amos CI; Italian PBC Genetics Study Group, Lazaridis KN, Seldin MF, Siminovitch KA.

Hum Mol Genet. 2012 Dec 1;21(23):5209-21. doi: 10.1093/hmg/dds359. Epub 2012 Aug 29.

PMID:
22936693
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Implications of genome-wide association studies in novel therapeutics in primary biliary cirrhosis.

Carbone M, Lleo A, Sandford RN, Invernizzi P.

Eur J Immunol. 2014 Apr;44(4):945-54. doi: 10.1002/eji.201344270. Epub 2014 Feb 27. Review.

PMID:
24481870
[PubMed - indexed for MEDLINE]
16.

An association study of TOLL and CARD with leprosy susceptibility in Chinese population.

Liu H, Bao F, Irwanto A, Fu X, Lu N, Yu G, Yu Y, Sun Y, Low H, Li Y, Liany H, Yuan C, Li J, Liu J, Chen M, Liu H, Wang N, You J, Ma S, Niu G, Zhou Y, Chu T, Tian H, Chen S, Zhang X, Liu J, Zhang F.

Hum Mol Genet. 2013 Nov 1;22(21):4430-7. doi: 10.1093/hmg/ddt286. Epub 2013 Jun 19.

PMID:
23784377
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Novel insights into autoimmune liver diseases provided by genome-wide association studies.

Mells GF, Kaser A, Karlsen TH.

J Autoimmun. 2013 Oct;46:41-54. doi: 10.1016/j.jaut.2013.07.004. Epub 2013 Aug 7. Review.

PMID:
23931959
[PubMed - indexed for MEDLINE]
18.

Role of STAT4 polymorphisms in systemic lupus erythematosus in a Japanese population: a case-control association study of the STAT1-STAT4 region.

Kawasaki A, Ito I, Hikami K, Ohashi J, Hayashi T, Goto D, Matsumoto I, Ito S, Tsutsumi A, Koga M, Arinami T, Graham RR, Hom G, Takasaki Y, Hashimoto H, Behrens TW, Sumida T, Tsuchiya N.

Arthritis Res Ther. 2008;10(5):R113. doi: 10.1186/ar2516. Epub 2008 Sep 19.

PMID:
18803832
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study.

Hou S, Yang Z, Du L, Jiang Z, Shu Q, Chen Y, Li F, Zhou Q, Ohno S, Chen R, Kijlstra A, Rosenbaum JT, Yang P.

Arthritis Rheum. 2012 Dec;64(12):4104-13. doi: 10.1002/art.37708.

PMID:
23001997
[PubMed - indexed for MEDLINE]
Free Article
20.

The genetics of multiple sclerosis: an update 2010.

Hoffjan S, Akkad DA.

Mol Cell Probes. 2010 Oct;24(5):237-43. doi: 10.1016/j.mcp.2010.04.006. Epub 2010 May 5. Review.

PMID:
20450971
[PubMed - indexed for MEDLINE]

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