226 related articles for article (PubMed ID: 33393726)
1. Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet's Disease.
Ortiz Fernández L; Coit P; Yilmaz V; Yentür SP; Alibaz-Oner F; Aksu K; Erken E; Düzgün N; Keser G; Cefle A; Yazici A; Ergen A; Alpsoy E; Salvarani C; Casali B; Kısacık B; Kötter I; Henes J; Çınar M; Schaefer A; Nohutcu RM; Zhernakova A; Wijmenga C; Takeuchi F; Harihara S; Kaburaki T; Messedi M; Song YW; Kaşifoğlu T; Carmona FD; Guthridge JM; James JA; Martin J; González Escribano MF; Saruhan-Direskeneli G; Direskeneli H; Sawalha AH
Arthritis Rheumatol; 2021 Jul; 73(7):1244-1252. PubMed ID: 33393726
[TBL] [Abstract][Full Text] [Related]
2. Two-stage association study in Chinese Han identifies two independent associations in CCR1/CCR3 locus as candidate for Behçet's disease susceptibility.
Hou S; Xiao X; Li F; Jiang Z; Kijlstra A; Yang P
Hum Genet; 2012 Dec; 131(12):1841-50. PubMed ID: 22829007
[TBL] [Abstract][Full Text] [Related]
3. Behçet's disease risk association fine-mapped on the IL23R-IL12RB2 intergenic region in Koreans.
Kang EH; Kim S; Park MY; Choi JY; Choi IA; Kim MJ; Ha YJ; Lee EY; Lee YJ; Lee EB; Kang C; Song YW
Arthritis Res Ther; 2017 Oct; 19(1):227. PubMed ID: 29017598
[TBL] [Abstract][Full Text] [Related]
4. Sex-specific analysis in Behçet's disease reveals higher genetic risk in male patients.
Jo YG; Ortiz-Fernández L; Coit P; Yilmaz V; Yentür SP; Alibaz-Oner F; Aksu K; Erken E; Düzgün N; Keser G; Cefle A; Yazici A; Ergen A; Alpsoy E; Salvarani C; Kısacık B; Kötter I; Henes J; Çınar M; Schaefer A; Nohutcu RM; Takeuchi F; Harihara S; Kaburaki T; Messedi M; Song YW; Kaşifoğlu T; Martin J; González Escribano MF; Saruhan-Direskeneli G; Direskeneli H; Sawalha AH
J Autoimmun; 2022 Oct; 132():102882. PubMed ID: 35987173
[TBL] [Abstract][Full Text] [Related]
5. A putative functional variant within the UBAC2 gene is associated with increased risk of Behçet's disease.
Sawalha AH; Hughes T; Nadig A; Yılmaz V; Aksu K; Keser G; Cefle A; Yazıcı A; Ergen A; Alarcón-Riquelme ME; Salvarani C; Casali B; Direskeneli H; Saruhan-Direskeneli G
Arthritis Rheum; 2011 Nov; 63(11):3607-12. PubMed ID: 21918955
[TBL] [Abstract][Full Text] [Related]
6. Clinical trait-specific genetic analysis in Behçet's disease identifies novel loci associated with ocular and neurological involvement.
Casares-Marfil D; Esencan D; Alibaz-Oner F; Çefle A; Yazıcı A; Duzgun N; Aşık MA; Özbek S; Cinar M; Alpsoy E; Bilge SY; Kasifoglu T; Saruhan-Direskeneli G; Direskeneli H; Sawalha AH
Clin Immunol; 2023 Aug; 253():109657. PubMed ID: 37271218
[TBL] [Abstract][Full Text] [Related]
7. The immunogenetics of Behçet's disease: A comprehensive review.
Takeuchi M; Kastner DL; Remmers EF
J Autoimmun; 2015 Nov; 64():137-48. PubMed ID: 26347074
[TBL] [Abstract][Full Text] [Related]
8. Identification of novel genetic susceptibility loci for Behçet's disease using a genome-wide association study.
Fei Y; Webb R; Cobb BL; Direskeneli H; Saruhan-Direskeneli G; Sawalha AH
Arthritis Res Ther; 2009; 11(3):R66. PubMed ID: 19442274
[TBL] [Abstract][Full Text] [Related]
9. Brief report: association of CCR1, KLRC4, IL12A-AS1, STAT4, and ERAP1 With Behçet's disease in Iranians.
Sousa I; Shahram F; Francisco D; Davatchi F; Abdollahi BS; Ghaderibarmi F; Nadji A; Mojarad Shafiee N; Xavier JM; Oliveira SA
Arthritis Rheumatol; 2015 Oct; 67(10):2742-8. PubMed ID: 26097239
[TBL] [Abstract][Full Text] [Related]
10. Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.
Kirino Y; Bertsias G; Ishigatsubo Y; Mizuki N; Tugal-Tutkun I; Seyahi E; Ozyazgan Y; Sacli FS; Erer B; Inoko H; Emrence Z; Cakar A; Abaci N; Ustek D; Satorius C; Ueda A; Takeno M; Kim Y; Wood GM; Ombrello MJ; Meguro A; Gül A; Remmers EF; Kastner DL
Nat Genet; 2013 Feb; 45(2):202-7. PubMed ID: 23291587
[TBL] [Abstract][Full Text] [Related]
11. The genetics of Behçet's disease in a Chinese population.
Hou S; Kijlstra A; Yang P
Front Med; 2012 Dec; 6(4):354-9. PubMed ID: 23161479
[TBL] [Abstract][Full Text] [Related]
12. Identification of multiple independent susceptibility loci in the HLA region in Behçet's disease.
Hughes T; Coit P; Adler A; Yilmaz V; Aksu K; Düzgün N; Keser G; Cefle A; Yazici A; Ergen A; Alpsoy E; Salvarani C; Casali B; Kötter I; Gutierrez-Achury J; Wijmenga C; Direskeneli H; Saruhan-Direskeneli G; Sawalha AH
Nat Genet; 2013 Mar; 45(3):319-24. PubMed ID: 23396137
[TBL] [Abstract][Full Text] [Related]
13. Genetic variants in the JAK1 gene confer higher risk of Behcet's disease with ocular involvement in Han Chinese.
Hou S; Qi J; Zhang Q; Liao D; Li Q; Hu K; Zhou Y; Kijlstra A; Yang P
Hum Genet; 2013 Sep; 132(9):1049-58. PubMed ID: 23674219
[TBL] [Abstract][Full Text] [Related]
14. Identification of susceptibility SNPs in IL10 and IL23R-IL12RB2 for Behçet's disease in Han Chinese.
Yu H; Zheng M; Zhang L; Li H; Zhu Y; Cheng L; Li L; Deng B; Kijlstra A; Yang P
J Allergy Clin Immunol; 2017 Feb; 139(2):621-627. PubMed ID: 27464962
[TBL] [Abstract][Full Text] [Related]
15. Genetics of Behçet's disease: lessons learned from genomewide association studies.
Gül A
Curr Opin Rheumatol; 2014 Jan; 26(1):56-63. PubMed ID: 24257369
[TBL] [Abstract][Full Text] [Related]
16. Targeted resequencing of candidate genes reveals novel variants associated with severe Behçet's uveitis.
Kim SJ; Lee S; Park C; Seo JS; Kim JI; Yu HG
Exp Mol Med; 2013 Oct; 45(10):e49. PubMed ID: 24136464
[TBL] [Abstract][Full Text] [Related]
17. Dense genotyping of immune-related loci implicates host responses to microbial exposure in Behçet's disease susceptibility.
Takeuchi M; Mizuki N; Meguro A; Ombrello MJ; Kirino Y; Satorius C; Le J; Blake M; Erer B; Kawagoe T; Ustek D; Tugal-Tutkun I; Seyahi E; Ozyazgan Y; Sousa I; Davatchi F; Francisco V; Shahram F; Abdollahi BS; Nadji A; Shafiee NM; Ghaderibarmi F; Ohno S; Ueda A; Ishigatsubo Y; Gadina M; Oliveira SA; Gül A; Kastner DL; Remmers EF
Nat Genet; 2017 Mar; 49(3):438-443. PubMed ID: 28166214
[TBL] [Abstract][Full Text] [Related]
18. Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci.
Mizuki N; Meguro A; Ota M; Ohno S; Shiota T; Kawagoe T; Ito N; Kera J; Okada E; Yatsu K; Song YW; Lee EB; Kitaichi N; Namba K; Horie Y; Takeno M; Sugita S; Mochizuki M; Bahram S; Ishigatsubo Y; Inoko H
Nat Genet; 2010 Aug; 42(8):703-6. PubMed ID: 20622879
[TBL] [Abstract][Full Text] [Related]
19. IL10 low-frequency variants in Behçet's disease patients.
Matos M; Xavier JM; Abrantes P; Sousa I; Rei N; Davatchi F; Shahram F; Jesus G; Barcelos F; Vedes J; Salgado M; Abdollahi BS; Nadji A; Moraes-Fontes MF; Shafiee NM; Ghaderibarmi F; Vaz Patto J; Crespo J; Oliveira SA
Int J Rheum Dis; 2017 May; 20(5):622-627. PubMed ID: 24708170
[TBL] [Abstract][Full Text] [Related]
20. Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease.
Remmers EF; Cosan F; Kirino Y; Ombrello MJ; Abaci N; Satorius C; Le JM; Yang B; Korman BD; Cakiris A; Aglar O; Emrence Z; Azakli H; Ustek D; Tugal-Tutkun I; Akman-Demir G; Chen W; Amos CI; Dizon MB; Kose AA; Azizlerli G; Erer B; Brand OJ; Kaklamani VG; Kaklamanis P; Ben-Chetrit E; Stanford M; Fortune F; Ghabra M; Ollier WE; Cho YH; Bang D; O'Shea J; Wallace GR; Gadina M; Kastner DL; Gül A
Nat Genet; 2010 Aug; 42(8):698-702. PubMed ID: 20622878
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
