Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: Infection and CFH[original query] |
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A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration. Proceedings of the National Academy of Sciences of the United States of America 2005 May 102 (20): 7227-32. Hageman Gregory S, Anderson Don H, Johnson Lincoln V, Hancox Lisa S, Taiber Andrew J, Hardisty Lisa I, Hageman Jill L, Stockman Heather A, Borchardt James D, Gehrs Karen M, Smith Richard J H, Silvestri Giuliana, Russell Stephen R, Klaver Caroline C W, Barbazetto Irene, Chang Stanley, Yannuzzi Lawrence A, Barile Gaetano R, Merriam John C, Smith R Theodore, Olsh Adam K, Bergeron Julie, Zernant Jana, Merriam Joanna E, Gold Bert, Dean Michael, Allikmets Ran |
Host polymorphisms in interleukin 4, complement factor H, and C-reactive protein associated with nasal carriage of Staphylococcus aureus and occurrence of boils. The Journal of infectious diseases 2008 May 197 (9): 1244-53. Emonts Marieke, Uitterlinden André G, Nouwen Jan L, Kardys Isabella, Maat Moniek P M de, Melles Damian C, Witteman Jacqueline, Jong Paulus T V M de, Verbrugh Henri A, Hofman Albert, Hermans Peter W M, Belkum Alex v |
Chlamydia pneumoniae infection, complement factor H variants and age-related macular degeneration. The British journal of ophthalmology 2009 Mar 93 (3): 405-8. Shen D, Tuo J, Patel M, Herzlich A A, Ding X, Chew E Y, Chan C |
Gene-environment interaction in progression of AMD: the CFH gene, smoking and exposure to chronic infection. Human molecular genetics 2008 May 17 (9): 1299-305. Baird Paul N, Robman Luba D, Richardson Andrea J, Dimitrov Peter N, Tikellis Gabriella, McCarty Catherine A, Guymer Robyn |
Thrombomodulin mutations in atypical hemolytic-uremic syndrome. The New England journal of medicine 2009 Jul 361 (4): 345-57. Delvaeye Mieke, Noris Marina, De Vriese Astrid, Esmon Charles T, Esmon Naomi L, Ferrell Gary, Del-Favero Jurgen, Plaisance Stephane, Claes Bart, Lambrechts Diether, Zoja Carla, Remuzzi Giuseppe, Conway Edward |
Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease.
Nature genetics 2010 Sep 42 (9): 772-6. Davila Sonia, Wright Victoria J, Khor Chiea Chuen, Sim Kar Seng, Binder Alexander, Breunis Willemijn B, Inwald David, Nadel Simon, Betts Helen, Carrol Enitan D, de Groot Ronald, Hermans Peter W M, Hazelzet Jan, Emonts Marieke, Lim Chui Chin, Kuijpers Taco W, Martinon-Torres Federico, Salas Antonio, Zenz Werner, Levin Michael, Hibberd Martin L, |
Chlamydia infection status, genotype, and age-related macular degeneration. Molecular vision 2012 18 29-37. Khandhadia Sam, Foster Sebastian, Cree Angela, Griffiths Helen, Osmond Clive, Goverdhan Srinivas, Lotery Andr |
Complement alternative pathway genetic variation and Dengue infection in the Thai population. Clinical and experimental immunology 2013 Nov 174 (2): 326-34. Kraivong R, Vasanawathana S, Limpitikul W, Malasit P, Tangthawornchaikul N, Botto M, Screaton G R, Mongkolsapaya J, Pickering M |
Genetic variants of complement genes ficolin-2, mannose-binding lectin and complement factor H are associated with leprosy in Han Chinese from Southwest China. Human genetics 2013 Jun 132 (6): 629-40. Zhang Deng-Feng, Huang Xian-Qiong, Wang Dong, Li Yu-Ye, Yao Yong-Ga |
A novel quantitative hemolytic assay coupled with restriction fragment length polymorphisms analysis enabled early diagnosis of atypical hemolytic uremic syndrome and identified unique predisposing mutations in Japan. PloS one 2015 10 (5): e0124655. Yoshida Yoko, Miyata Toshiyuki, Matsumoto Masanori, Shirotani-Ikejima Hiroko, Uchida Yumiko, Ohyama Yoshifumi, Kokubo Tetsuro, Fujimura Yoshihi |
Susceptibility to invasive meningococcal disease: polymorphism of complement system genes and Neisseria meningitidis factor H binding protein. PloS one 2015 10 (3): e0120757. Bradley Declan T, Bourke Thomas W, Fairley Derek J, Borrow Raymond, Shields Michael D, Zipfel Peter F, Hughes Anne |
Natural resistance to Meningococcal Disease related to CFH loci: Meta-analysis of genome-wide association studies. Scientific reports 2016 Nov 6 35842. Martinón-Torres Federico, Png Eileen, Khor Chiea Chuen, Davila Sonia, Wright Victoria J, Sim Kar Seng, Vega Ana, Fachal Laura, Inwald David, Nadel Simon, Carrol Enitan D, Martinón-Torres Nazareth, Alonso Sonia Marcos, Carracedo Angel, Morteruel Elvira, López-Bayón Julio, Torre Andrés Concha, Monge Cristina Calvo, de Aguilar Pilar Azcón González, Torné Elisabeth Esteban, Martínez-Padilla María Del Carmen, Martinón-Sánchez José María, Levin Michael, Hibberd Martin L, Salas Antonio, , , |
A polymorphism in the haptoglobin, haptoglobin related protein locus is associated with risk of human sleeping sickness within Cameroonian populations. PLoS neglected tropical diseases 2017 Oct 11 (10): e0005979. Ofon Elvis, Noyes Harry, Mulindwa Julius, Ilboudo Hamidou, Simuunza Martin, Ebo'o Vincent, Njiokou Flobert, Koffi Mathurin, Bucheton Bruno, Fogue Pythagore, Hertz-Fowler Christiane, MacLeod Annette, Simo Gustave, |
Candidate genes-based investigation of susceptibility to Human African Trypanosomiasis in Côte d'Ivoire. PLoS neglected tropical diseases 2017 10 11 (10): e0005992. Ahouty Bernardin, Koffi Mathurin, Ilboudo Hamidou, Simo Gustave, Matovu Enock, Mulindwa Julius, Hertz-Fowler Christiane, Bucheton Bruno, Sidibé Issa, Jamonneau Vincent, MacLeod Annette, Noyes Harry, N'Guetta Simon-Pierre, |
No evidence for association between APOL1 kidney disease risk alleles and Human African Trypanosomiasis in two Ugandan populations. PLoS neglected tropical diseases 2018 02 12 (2): e0006300. Kimuda Magambo Phillip, Noyes Harry, Mulindwa Julius, Enyaru John, Alibu Vincent Pius, Sidibe Issa, Mumba Ngoyi Dieuodonne, Hertz-Fowler Christiane, MacLeod Annette, Tastan Bishop Özlem, Matovu Enock, |
Association of CFH polymorphism with susceptibility to sepsis caused by Pseudomonas aeruginosa in Chinese Han populations: A multi-center study. Gene 2019 Sep 144127. Li Jia, Long Ding, Wu Sisi, Wu Xiaoling, Wei Bohua, Chen Dan, Shao Yiming, Wang Hongliang, Cui Lili, Chen Xiangyan, Yu |
Association of APOL1 renal disease risk alleles with Trypanosoma brucei rhodesiense infection outcomes in the northern part of Malawi. PLoS neglected tropical diseases 2019 Aug 13 (8): e0007603. Kamoto Kelita, Noyes Harry, Nambala Peter, Senga Edward, Musaya Janelisa, Kumwenda Benjamin, Bucheton Bruno, Macleod Annette, Cooper Anneli, Clucas Caroline, Herz-Fowler Christiane, Matove Enock, Chiwaya Arthur M, Chisi John E, |
SNPs in IL4 and IFNG show no protective associations with human African trypanosomiasis in the Democratic Republic of the Congo: a case-control study. AAS open research 2020 9 3 35. Fataki Asina Olivier, Noyes Harry, Bucheton Bruno, Ilboudo Hamidou, MacLeod Annette, Mumba Ngoyi Dieudonné, |
Exome array identifies functional exonic biomarkers for pediatric dental caries.
Computers in biology and medicine 2021 Nov 105019. Borgio J Francis, Alsuwat Hind Saleh, Alamoudi Widyan, Hegazi Fatma Mohammed, Al Otaibi Waad Mohammed, M Ibrahim Abdallah, Almandil Noor B, Al-Amodi Amani M, Alyousef Yousef M, AlShwaimi Emad, Almasoud Naif, Kamaraj Balu, Sayed AbdulAze |
Genetic analysis of CFH and MCP in Egyptian patients with immune-complex proliferative glomerulonephritis. Frontiers in immunology 2022 10 13 960068. Gouda Heba R, Talaat Iman M, Bouzid Amal, El-Assi Hoda, Nabil Amira, Venkatachalam Thenmozhi, Manasa Bhamidimarri Poorna, Wohlers Inken, Mahdami Amena, El-Gendi Saba, ElKoraie Ahmed, Busch Hauke, Saber-Ayad Maha, Hamoudi Rifat, Baddour Nah |
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