Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 128 Records) |
Query Trace: CFB[original query] |
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Identification of susceptibility locus shared by IgA nephropathy and inflammatory bowel disease in a Chinese Han population. Journal of human genetics 2019 Dec . Shi Dianchun, Zhong Zhong, Wang Meng, Cai Lu, Fu Dongying, Peng Yuan, Guo Lin, Mao Haiping, Yu Xueqing, Li Mi |
Role of complement factor B rs4151667 (L9H) polymorphisms and its interactional role with CFH Y402H and C3 rs2230199 (R102G) risk variants in age-related macular degeneration: a case control study. BMC ophthalmology 2020 Aug 20 (1): 323. Roshanipour Nasrin, Laleh Maryam Ghaffari, Bonyadi Mortaza, Bonyadi Mohammad Hossein Jabbarpoor, Soheilian Masoud, Javadzadeh Alireza, Yaseri Meh |
Development of a Genotype Assay for Age-Related Macular Degeneration: The EYE-RISK Consortium. Ophthalmology 2020 Jul . de Breuk Anita, Acar Ilhan E, Kersten Eveline, Schijvenaars Mascha M V A P, Colijn Johanna M, Haer-Wigman Lonneke, Bakker Bjorn, de Jong Sarah, Meester-Smoor Magda A, Verzijden Timo, Missotten Tom O A R, Monés Jordi, Biarnés Marc, Pauleikhoff Daniel, Hense Hans W, Silva Rufino, Nunes Sandrina, Melo Joana B, Fauser Sascha, Hoyng Carel B, Ueffing Marius, Coenen Marieke J H, Klaver Caroline C W, den Hollander Anneke I, |
Genetic factors associated with response to as-needed aflibercept therapy for typical neovascular age-related macular degeneration and polypoidal choroidal vasculopathy. Scientific reports 2020 Apr 10 (1): 7188. Yoneyama Seigo, Sakurada Yoichi, Kikushima Wataru, Sugiyama Atsushi, Matsubara Mio, Fukuda Yoshiko, Tanabe Naohiko, Parikh Ravi, Mabuchi Fumihiko, Kashiwagi Kenji, Iijima Hiroyu |
Genetic Association of Age-Related Macular Degeneration and Polypoidal Choroidal Vasculopathy. Asia-Pacific journal of ophthalmology (Philadelphia, Pa.) 2020 3 9 (2): 104-109. Chen Li J |
Complement Activation Levels Are Related to Disease Stage in AMD. Investigative ophthalmology & visual science 2020 3 61 (3): 18. Heesterbeek Thomas J, Lechanteur Yara T E, Lorés-Motta Laura, Schick Tina, Daha Mohamed R, Altay Lebriz, Liakopoulos Sandra, Smailhodzic Dzenita, den Hollander Anneke I, Hoyng Carel B, de Jong Eiko K, Klevering B Jero |
A non-synonymous variant rs12614 of complement factor B associated with risk of chronic hepatitis B in a Korean population. BMC medical genetics 2020 Dec 21 (1): 241. Seo Jung Yeon, Shin Joong-Gon, Youn Byeong Ju, Namgoong Suhg, Cheong Hyun Sub, Kim Lyoung Hyo, Kim Ji On, Shin Hyoung Doo, Kim Yoon J |
The Effect of Genetic Variants Associated With Age-Related Macular Degeneration Varies With Age. Investigative ophthalmology & visual science 2020 12 61 (14): 17. Schick Tina, Lorés-Motta Laura, Altay Lebriz, Fritsche Lars G, den Hollander Anneke I, Fauser Sasc |
Distinct genetic profile with recurrent population-specific missense variants in Korean adult atypical hemolytic uremic syndrome. Thrombosis research 2020 11 194 45-53. Yun Jae Won, Oh Jisu, Lee Ki-O, Lee Seon Ju, Kim Jung Oh, Kim Nam Keun, Kim Jin Seok, Koh Youngil, Yoon Sung-Soo, Yhim Ho-Young, Jo Sang-Kyung, Park Yong, Lee Jung Eun, Park Jinny, Lee Jong Wook, Kim Sun-Hee, Kim Hee-Jin, Oh Doyeun, , |
A missense variant in complement factor B (CFB) is a potential predictor of 24-week off-treatment response to PegIFNa therapy in Chinese HBeAg-positive chronic hepatitis B patients. Alimentary pharmacology & therapeutics 2020 Jan . Chen Haitao, Sun Jian, Zhou Bin, Peng Jinxin, Xie Qing, Liang Xieer, Fan Rong, Conran Carly, Xu Jianfeng, Ji Yuan, Zhang Xinxin, Sun Li, Jia Jidong, Wang Guiqiang, Hou Jinlin, Jiang De- |
Investigation of genetic base in the treatment of age-related macular degeneration. International ophthalmology 2020 Jan . Gourgouli Kalliopi, Gourgouli Ioanna, Tsaousis Georgios, Spai Sofia, Niskopoulou Maria, Efthimiopoulos Spiros, Lamnissou Kl |
Gene polymorphisms associated with an increased risk of exudative age-related macular degeneration in a Spanish population. European journal of ophthalmology 2021 Mar 11206721211002698. Gili Pablo, Lloreda Martín Leyre, Martín-Rodrigo José-Carlos, Kim-Yeon Naon, Modamio-Gardeta Laura, Fernández-García Javier L, Rebolledo-Poves Ana Belén, Gómez-Blazquez Elena, Pazos-Rodriguez Ruth, Pérez-Fernández Elia, Velasco Mar |
CFH I62V as a Putative Genetic Marker for Posner-Schlossman Syndrome. Frontiers in immunology 2021 3 12 608723. Yang Ming Ming, Sun Hong Yan, Meng Ting, Qiu Shan Hu, Zeng Qi Qiao, Ng Tsz Kin, Jiang Li, Deng Ting Ming, Zeng Ai Neng, Wang Jun, Luo Xiao Li |
A Missense Variant in Granulysin is Associated with the Efficacy of Pegylated-Interferon-Alpha Therapy in Chinese Patients with HBeAg-Positive Chronic Hepatitis B. Pharmacogenomics and personalized medicine 2021 12 14 1505-1515. Li Jing, Chen Haitao, Chen Jiaxuan, Zhou Bin, Hou Jinlin, Jiang De- |
The effect of systemic levels of TNF-alpha and complement pathway activity on outcomes of VEGF inhibition in neovascular AMD. Eye (London, England) 2021 Nov . Khan Adnan H, Pierce Charles O, De Salvo Gabriella, Griffiths Helen, Nelson Marie, Cree Angela J, Menon Geeta, Lotery Andrew |
Evaluating the Occurrence of Rare Variants in the Complement Factor H Gene in Patients With Early-Onset Drusen Maculopathy. JAMA ophthalmology 2021 Oct . de Breuk Anita, Heesterbeek Thomas J, Bakker Bjorn, Verzijden Timo, Lechanteur Yara T E, Klaver Caroline C W, den Hollander Anneke I, Hoyng Carel |
Exome Chip Analyses and Genetic Risk for IgA Nephropathy among Han Chinese. Clinical journal of the American Society of Nephrology : CJASN 2021 Jan . Zhou Xu-Jie, Tsoi Lam C, Hu Yong, Patrick Matthew T, He Kevin, Berthier Celine C, Li Yanming, Wang Yan-Na, Qi Yuan-Yuan, Zhang Yue-Miao, Gan Ting, Li Yang, Hou Ping, Liu Li-Jun, Shi Su-Fang, Lv Ji-Cheng, Xu Hu-Ji, Zhang Ho |
Targeted Genotyping of MIS-C Patients Reveals a Potential Alternative Pathway Mediated Complement Dysregulation during COVID-19 Infection. Current issues in molecular biology 2022 7 44 (7): 2811-2824. Gavriilaki Eleni, Tsiftsoglou Stefanos A, Touloumenidou Tasoula, Farmaki Evangelia, Panagopoulou Paraskevi, Michailidou Elissavet, Koravou Evaggelia-Evdoxia, Mavrikou Ioulia, Iosifidis Elias, Tsiatsiou Olga, Papadimitriou Eleni, Papadopoulou-Alataki Efimia, Papayanni Penelope Georgia, Varelas Christos, Kokkoris Styliani, Papalexandri Apostolia, Fotoulaki Maria, Galli-Tsinopoulou Assimina, Zafeiriou Dimitrios, Roilides Emmanuel, Sakellari Ioanna, Anagnostopoulos Achilles, Tragiannidis Athanasi |
TRIM26 inhibits hepatitis B virus replication by promoting HBx degradation and TRIM26 genetic polymorphism predicts PegIFN? treatment response of HBeAg-positive chronic hepatitis B Patients. Alimentary pharmacology & therapeutics 2022 Jul . Luo Mengqi, Hou Jia, Mai Haoming, Chen Jiaxuan, Chen Haitao, Zhou Bin, Hou Jinlin, Jiang De- |
Hypomethylation of miR-17-92 cluster in lupus T cells and no significant role for genetic factors in the lupus-associated DNA methylation signature. Annals of the rheumatic diseases 2022 6 81 (10): 1428-1437. Coit Patrick, Roopnarinesingh Xiavan, Ortiz-Fernández Lourdes, McKinnon-Maksimowicz Kathleen, Lewis Emily E, Merrill Joan T, McCune W Joseph, Wren Jonathan D, Sawalha Amr |
Relationships between Lipid-Related Metabolites and Age-Related Macular Degeneration Vary with Complement Genotype. Ophthalmology science 2022 12 2 (4): 100211. Sim Ralene Zi Hui, Tham Yih-Chung, Betzler Bjorn Kaijun, Zhou Lei, Wang Xiaomeng, Sabanayagam Charumathi, Cheung Gemmy Chiu Ming, Wong Tien Yin, Cheng Ching-Yu, Nusinovici Sim |
HSP70 and TNF Loci Polymorphism Associated with the Posner-Schlossman Syndrome in a Southern Chinese Population. Journal of immunology research 2022 12 2022 5242948. Bai Wei, Huang Xiaosheng, Shen Xiaoli, Ye Ye, Peng Shiming, Zhu Tianhui, Mei Shaoyi, Kuang Jiajie, Yu Sejie, Ma Xiaochen, Zhao J |
Functional variant rs12614 in CFB confers a low risk of IgA nephropathy by attenuating complement alternative pathway activation in Han Chinese. Frontiers in immunology 2022 10 13 973169. Shi Dian-Chun, Feng Shao-Zhen, Zhong Zhong, Cai Lu, Wang Meng, Fu Dong-Ying, Yu Xue-Qing, Li Mi |
MCPggaac haplotype is associated with poor graft survival in kidney transplant recipients with de novo thrombotic microangiopathy. Frontiers in immunology 2022 10 13 985766. Petr Vojtech, Csuka Dorottya, Hruba Petra, Szilágyi Ágnes, Kollar Marek, Slavcev Antonij, Prohászka Zoltán, Viklicky Ondr |
An extremes of phenotype approach confirms significant genetic heterogeneity in patients with ulcerative colitis. Journal of Crohn's & colitis 2022 Sep . Mortlock Sally, Lord Anton, Montgomery Grant, Zakrzewski Martha, Simms Lisa A, Krishnaprasad Krupa, Hanigan Katherine, Doecke James D, Walsh Alissa, Lawrance Ian C, Bampton Peter A, Andrews Jane M, Mahy Gillian, Connor Susan J, Sparrow Miles P, Bell Sally, Florin Timothy H, Begun Jakob, Gearry Richard B, Radford-Smith Graham |
CSMD1 rs10503253 increases schizophrenia risk in a Tunisian population-group. L'Encephale 2023 9 . Ons Mihoub, Arij Ben Chaaben, Wahid Boukouaci, Mohamed Lajnef, Fayza Ayari, Hamdi El Kefi, Hanen Ben Ammar, Hajer Abazza, Zouhair El Hechmi, Fathi Guemira, Marion Leboyer, Ryad Tamouza, Maher Kharr |
Spatial Distribution of Missense Variants within Complement Proteins Associates with Age Related Macular Degeneration. medRxiv : the preprint server for health sciences 2023 9 . Michelle Grunin, Sarah de Jong, Ellen L Palmer, Bowen Jin, David Rinker, Christopher Moth, Anthony Capra, Jonathan L Haines, William S Bush, Anneke I den Hollander, |
Genome-wide identification of RNA modification-related single nucleotide polymorphisms associated with rheumatoid arthritis. BMC genomics 2023 3 24 (1): 153. Wang Mimi, Wu Jingyun, Lei Shufeng, Mo Xing |
Targeted genotyping of COVID-19 patients reveals a signature of complement C3 and factor B coding SNPs associated with severe infection. Immunobiology 2023 2 228 (2): 152351. Tsiftsoglou Stefanos A, Gavriilaki Eleni, Touloumenidou Tasoula, Koravou Evaggelia-Evdoxia, Koutra Maria, Papayanni Penelope Georgia, Karali Vassiliki, Papalexandri Apostolia, Varelas Christos, Chatzopoulou Fani, Chatzidimitriou Maria, Chatzidimitriou Dimitrios, Veleni Anastasia, Rapti Evdoxia, Kioumis Ioannis, Kaimakamis Evaggelos, Bitzani Milly, Boumpas Dimitrios T, Tsantes Argyris, Sotiropoulos Damianos, Papadopoulou Anastasia, Sakellari Ioanna, Kokoris Styliani, Anagnostopoulos Achill |
Complement alternative pathway determines disease susceptibility and severity in antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis. Kidney international 2023 11 . Laura Lucientes-Continente, Gema Fernández-Juárez, Bárbara Márquez-Tirado, Laura Jiménez-Villegas, Mercedes Acevedo, Teresa Cavero, Luís Sánchez Cámara, Juliana Draibe, Paula Anton-Pampols, Fernando Caravaca-Fontán, Manuel Praga, Javier Villacorta, Elena Goicoechea de Jor |
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- Page last updated:Apr 22, 2024
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