Human Genome Epidemiology Literature Finder
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Records 1 - 20 (of 20 Records) |
| Query Trace: Disease and ANXA11[original query] |
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| Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis. Nature genetics 2008 Sep 40 (9): 1103-6. Hofmann Sylvia, Franke Andre, Fischer Annegret, Jacobs Gunnar, Nothnagel Michael, Gaede Karoline I, Schürmann Manfred, Müller-Quernheim Joachim, Krawczak Michael, Rosenstiel Philip, Schreiber Stef |
| Functional variant ANXA11 R230C: true marker of protection and candidate disease modifier in sarcoidosis. Genes and immunity 2011 Sep 12 (6): 490-4. Mrazek F, Stahelova A, Kriegova E, Fillerova R, Zurkova M, Kolek V, Petrek |
| Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. PloS one 2012 7 (8): e43907. Adrianto Indra, Lin Chee Paul, Hale Jessica J, Levin Albert M, Datta Indrani, Parker Ryan, Adler Adam, Kelly Jennifer A, Kaufman Kenneth M, Lessard Christopher J, Moser Kathy L, Kimberly Robert P, Harley John B, Iannuzzi Michael C, Rybicki Benjamin A, Montgomery Courtney |
| Fine-mapping in African-American women confirms the importance of the 10p12 locus to sarcoidosis. Genes and immunity 2012 Oct 13 (7): 573-8. Cozier Y C, Ruiz-Narvaez E A, McKinnon C J, Berman J S, Rosenberg L, Palmer J |
| IL12RB2 gene is associated with the age of type 1 diabetes onset in Croatian family Trios. PloS one 2012 7 (11): 11. Pehli? M, Vrki? D, Skrabi? V, Jeron?i? A, Stipan?i? G, Uroji? AŠ, Marjanac I, Jakši? J, Ka?i? Z, Boraska V, Zemunik T |
| Associations between sarcoidosis clinical course and ANXA11 rs1049550 C/T, BTNL2 rs2076530 G/A, and HLA class I and II alleles. The clinical respiratory journal 2016 Sep . Morais Antonio, Lima Bruno, Alves Helena, Melo Natalia, Mota Patricia C, Marques Agostinho, Delgado Lu |
| The Association between ANXA11 Gene Polymorphisms and Sarcoidosis: a Meta-Analysis and systematic review. Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG 2016 Aug 33 (2): 102-11. Zhou Hongfei, Diao Mengyuan, Zhang Mingy |
| Feasibility of novel PPP1R15A and proposed ANXA11 single nucleotide polymorphisms as predictive markers for bevacizumab regimen in metastatic colorectal cancer. Journal of cancer research and clinical oncology 2016 May . Roh Seon Ae, Park In Ja, Yoon Yong Sik, Kwon Yi Hong, Chung Jin Hwa, Kim Tae Won, Cho Dong Hyung, Lim Byung Ho, Kim Seon Kyu, Kim Seon Young, Kim Yong Sung, Kim Jin Che |
| TNFA, ANXA11 and BTNL2 Polymorphisms in CVID Patients with Granulomatous Disease. Journal of clinical immunology 2016 Jan . Boutboul David, Vince Nicolas, Mahevas Matthieu, Bories Jean-Christophe, Fieschi Claire, |
| ALS Genes in the Genomic Era and their Implications for FTD. Trends in genetics : TIG 2018 4 34 (6): 404-423. Nguyen Hung Phuoc, Van Broeckhoven Christine, van der Zee Jul |
| Unique characteristics of the genetics epidemiology of amyotrophic lateral sclerosis in China. Science China. Life sciences 2019 3 62 (4): 517-525. Wei Qianqian, Chen Xueping, Chen Yongping, Ou Ruwei, Cao Bei, Hou Yanbing, Zhang Lingyu, Shang Hui-Fa |
| Re-analysis of the Hungarian amyotrophic lateral sclerosis population and evaluation of novel ALS genetic risk variants. Neurobiology of aging 2022 Aug 116 1-11. Nagy Zsófia Flóra, Pál Margit, Salamon András, Kafui Esi Zodanu Gloria, Füstös Dalma, Klivényi Péter, Széll Már |
| ANXA11 rs1049550 Associates with Löfgren's Syndrome and Chronic Sarcoidosis Patients. Cells 2022 5 11 (9): . Karakaya Bekir, van der Vis Joanne J, Veltkamp Marcel, Biesma Douwe H, Grutters Jan C, van Moorsel Coline H |
| Mutation spectrum of chinese amyotrophic lateral sclerosis patients with frontotemporal dementia. Orphanet journal of rare diseases 2022 11 17 (1): 404. Yang Xunzhe, Sun Xiaohai, Liu Qing, Liu Liyang, Li Jinyue, Cai Zhengyi, Zhang Kang, Liu Shuangwu, He Di, Shen Dongchao, Liu Mingsheng, Cui Liying, Zhang X |
| Genetic analysis of and clinical characteristics associated with ANXA11 variants in a Chinese cohort with amyotrophic lateral sclerosis. Neurobiology of disease 2022 10 175 105907. Jiang Qirui, Lin Junyu, Wei Qianqian, Li Chunyu, Hou Yanbing, Cao Bei, Zhang Lingyu, Ou Ruwei, Liu Kuncheng, Yang Tianmi, Xiao Yi, Shang Huifa |
| Revealing the Mutational Spectrum in Southern Africans With Amyotrophic Lateral Sclerosis. Neurology. Genetics 2022 Feb 8 (1): e654. Nel Melissa, Mahungu Amokelani C, Monnakgotla Nomakhosazana, Botha Gerrit R, Mulder Nicola J, Wu Gang, Rampersaud Evadnie, van Blitterswijk Marka, Wuu Joanne, Cooley Anne, Myers Jason, Rademakers Rosa, Taylor J Paul, Benatar Michael, Heckmann Jeannine |
| Evaluation of genetic risk, its clinical manifestation and disease management based on 18 susceptibility gene markers among West-Slavonic patients with sarcoidosis. Gene 2023 6 878 147577. Amit Kishore, Katerina Sikorova, Lenka Kocourkova, Jana Petrkova, Martina Doubkova, Petr Jakubec, Krzysztof R?ba?a, Anna Dubaniewicz, Martin Petr |
| Sex differences in the genetics of sarcoidosis across European and African ancestry populations. Frontiers in medicine 2023 5 10 1132799. Ying Xiong, Susanna Kullberg, Lori Garman, Nathan Pezant, David Ellinghaus, Vasiliki Vasila, Anders Eklund, Benjamin A Rybicki, Michael C Iannuzzi, Stefan Schreiber, Joachim Müller-Quernheim, Courtney G Montgomery, Johan Grunewald, Leonid Padyukov, Natalia V Rive |
| Clinical and genetic characteristics of 1672 cases of amyotrophic lateral sclerosis in China: a single-center retrospective study. Journal of neurology 2024 6 . Dongchao Shen, Xunzhe Yang, Di He, Kang Zhang, Shuangwu Liu, Xiaohan Sun, Jinyue Li, Zhengyi Cai, Mingsheng Liu, Xue Zhang, Qing Liu, Liying C |
| Genetic Screening of Patients with Sporadic Alzheimer's Disease and Frontotemporal Lobar Degeneration in the Chinese Population. Journal of Alzheimer's disease : JAD 2024 5 . Yaoru Li, Ziying Yang, Yanxin Zhang, Fang Liu, Jing Xu, Yaping Meng, Gebeili Xing, Xuqin Ruan, Jun Sun, Nan Zha |
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