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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. Jo YG, et al. Among authors: harihara s. J Autoimmun. 2022 Oct;132:102882. doi: 10.1016/j.jaut.2022.102882. Epub 2022 Aug 18. J Autoimmun. 2022. PMID: 35987173 Free PMC article.
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. Ortiz Fernández L, et al. Among authors: harihara s. Arthritis Rheumatol. 2021 Jul;73(7):1244-1252. doi: 10.1002/art.41637. Epub 2021 May 18. Arthritis Rheumatol. 2021. PMID: 33393726 Free PMC article.
The mitochondrial DNA A3243G mutation in Werner's syndrome.
Takeuchi F, Harihara S, Nakamura K, Takubo K, Kanamori M, Goto M. Takeuchi F, et al. Among authors: harihara s. Exp Gerontol. 2003 Mar;38(3):339-42. doi: 10.1016/s0531-5565(02)002090-7. Exp Gerontol. 2003. PMID: 12581800
Mitochondrial DNA polymorphism among five Asian populations.
Harihara S, Saitou N, Hirai M, Gojobori T, Park KS, Misawa S, Ellepola SB, Ishida T, Omoto K. Harihara S, et al. Am J Hum Genet. 1988 Aug;43(2):134-43. Am J Hum Genet. 1988. PMID: 2840820 Free PMC article.
105 results