Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 32 Records) |
Query Trace: ANXA11[original query] |
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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 |
Novel chemosensitive single-nucleotide polymorphism markers to targeted regimens in metastatic colorectal cancer. Clinical cancer research : an official journal of the American Association for Cancer Research 2011 Mar 17 (5): 1200-9. Kim Jin C, Kim Seon Y, Cho Dong H, Ha Ye J, Choi Eun Y, Kim Chan W, Roh Seon A, Kim Tae W, Ju Hyoungseok, Kim Yong |
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 |
Association of ANXA11 genetic variation with sarcoidosis in African Americans and European Americans. Genes and immunity 2012 Nov . Levin AM, Iannuzzi MC, Montgomery CG, Trudeau S, Datta I, McKeigue P, Fischer A, Nebel A, Rybicki BA |
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 |
Feasibility of proposed single-nucleotide polymorphisms as predictive markers for targeted regimens in metastatic colorectal cancer. British journal of cancer 2013 May 108 (9): 1862-9. Kim J C, Ha Y J, Roh S A, Choi E Y, Yoon Y S, Kim K P, Hong Y S, Kim T W, Cho D H, Kim S Y, Kim Y |
Annexin A11 (ANXA11) gene polymorphisms are associated with sarcoidosis in a Han Chinese population: a case-control study. BMJ open 2014 4 (7): e004466. Feng Xianjun, Zang Shuzhi, Yang Yanrong, Zhao Shasha, Li Yunxia, Gao Xinyuan, Zhang Ligo |
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, |
Genetic analysis of ANXA11 variants in a Han Chinese cohort with amyotrophic lateral sclerosis in Taiwan. Neurobiology of aging 2018 Jul . Tsai Pei-Chien, Liao Yi-Chu, Jih Kang-Yang, Soong Bing-Wen, Lin Kon-Ping, Lee Yi-Chu |
ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia. Neurology. Genetics 2018 5 4 (3): e237. Zhang Kang, Liu Qing, Liu Keqiang, Shen Dongchao, Tai Hongfei, Shu Shi, Ding Qingyun, Fu Hanhui, Liu Shuangwu, Wang Zhili, Li Xiaoguang, Liu Mingsheng, Zhang Xue, Cui Liyi |
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 |
Association of genetic variants in RAB23 and ANXA11 with uveitis in sarcoidosis. Molecular vision 2018 24 59-74. Davoudi Samaneh, Chang Victoria S, Navarro-Gomez Daniel, Stanwyck Lynn K, Sevgi Damla Duriye, Papavasileiou Evangelia, Ren Aiai, Uchiyama Eduardo, Sullivan Lynn, Lobo Ann-Marie, Papaliodis George N, Sobrin Luc |
Two rare variants of the ANXA11 gene identified in Chinese patients with amyotrophic lateral sclerosis. Neurobiology of aging 2019 02 74 235.e9-235.e12. Liu Xiangyi, Wu Chujun, He Ji, Zhang Nan, Fan Dongshe |
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 |
Genetic epidemiology of familial ALS in Brazil. Neurobiology of aging 2021 2 102 227.e1-227.e4. Nunes Gonçalves João Pedro, Leoni Tauana Bernardes, Martins Melina Pazian, Peluzzo Thiago Mazzo, Dourado Mario Emílio T, Saute Jonas Alex M, Paranhos Miranda Covaleski Anna Paula, Bulle de Oliveira Acary Souza, Claudino Rinaldo, Marques Wilson, Nucci Anamarli, França Marcondes |
Generation of six induced pluripotent stem cell lines from patients with amyotrophic lateral sclerosis with associated genetic mutations in either FUS or ANXA11. Stem cell research 2021 2 52 102246. Hedges Erin C, Topp Simon, Shaw Christopher E, Nishimura Agnes |
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 |
A genome-wide association study on frequent exacerbation of asthma depending on smoking status. Respiratory medicine 2022 5 199 106877. Son Ji-Hye, Park Jong-Sook, Lee Jong-Uk, Kim Min Kyung, Min Sun-Ah, Park Choon-Sik, Chang Hun S |
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 |
Semantic variant primary progressive aphasia with a pathogenic variant p.Asp40Gly in the ANXA11 gene. European journal of neurology 2022 Oct 29 (10): 3124-3126. Kim Eun-Joo, Moon So Young, Kim Hee-Jin, Jung Na-Yeon, Lee Sun Min, Kim Young E |
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 |
Whole genome sequencing versus chromosomal microarray analysis in prenatal diagnosis. American journal of obstetrics and gynecology 2023 3 . Hu Ping, Zhang Qinxin, Cheng Qing, Luo Chunyu, Zhang Cuiping, Zhou Ran, Meng Lulu, Huang Mingtao, Wang Yuguo, Wang Yan, Qiao Fengchang, Xu Zhengfe |
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- Page last updated:Apr 22, 2024
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