Human Genome Epidemiology Literature Finder
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Records 1 - 22 (of 22 Records) |
| Query Trace: Disease and CFHR3[original query] |
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| A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration. Nature genetics 2006 Oct 38 (10): 1173-7. Hughes Anne E, Orr Nick, Esfandiary Hossein, Diaz-Torres Martha, Goodship Timothy, Chakravarthy Us |
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, |
| Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility. PLoS genetics 2011 May 7 (5): e1002079. Zhao Jian, Wu Hui, Khosravi Melanie, Cui Huijuan, Qian Xiaoxia, Kelly Jennifer A, Kaufman Kenneth M, Langefeld Carl D, Williams Adrienne H, Comeau Mary E, Ziegler Julie T, Marion Miranda C, Adler Adam, Glenn Stuart B, Alarcón-Riquelme Marta E, , , Pons-Estel Bernardo A, Harley John B, Bae Sang-Cheol, Bang So-Young, Cho Soo-Kyung, Jacob Chaim O, Vyse Timothy J, Niewold Timothy B, Gaffney Patrick M, Moser Kathy L, Kimberly Robert P, Edberg Jeffrey C, Brown Elizabeth E, Alarcon Graciela S, Petri Michelle A, Ramsey-Goldman Rosalind, Vilá Luis M, Reveille John D, James Judith A, Gilkeson Gary S, Kamen Diane L, Freedman Barry I, Anaya Juan-Manuel, Merrill Joan T, Criswell Lindsey A, Scofield R Hal, Stevens Anne M, Guthridge Joel M, Chang Deh-Ming, Song Yeong Wook, Park Ji Ah, Lee Eun Young, Boackle Susan A, Grossman Jennifer M, Hahn Bevra H, Goodship Timothy H J, Cantor Rita M, Yu Chack-Yung, Shen Nan, Tsao Betty |
| Investigation of modifier genes within copy number variations in Rett syndrome. Journal of human genetics 2011 Jul 56 (7): 508-15. Artuso Rosangela, Papa Filomena T, Grillo Elisa, Mucciolo Mafalda, Yasui Dag H, Dunaway Keith W, Disciglio Vittoria, Mencarelli Maria A, Pollazzon Marzia, Zappella Michele, Hayek Giuseppe, Mari Francesca, Renieri Alessandra, Lasalle Janine M, Ariani Frances |
| Genome-wide association study identifies susceptibility loci for IgA nephropathy.
Nature genetics 2011 Apr 43 (4): 321-7. Gharavi Ali G, Kiryluk Krzysztof, Choi Murim, Li Yifu, Hou Ping, Xie Jingyuan, Sanna-Cherchi Simone, Men Clara J, Julian Bruce A, Wyatt Robert J, Novak Jan, He John C, Wang Haiyan, Lv Jicheng, Zhu Li, Wang Weiming, Wang Zhaohui, Yasuno Kasuhito, Gunel Murat, Mane Shrikant, Umlauf Sheila, Tikhonova Irina, Beerman Isabel, Savoldi Silvana, Magistroni Riccardo, Ghiggeri Gian Marco, Bodria Monica, Lugani Francesca, Ravani Pietro, Ponticelli Claudio, Allegri Landino, Boscutti Giuliano, Frasca Giovanni, Amore Alessandro, Peruzzi Licia, Coppo Rosanna, Izzi Claudia, Viola Battista Fabio, Prati Elisabetta, Salvadori Maurizio, Mignani Renzo, Gesualdo Loreto, Bertinetto Francesca, Mesiano Paola, Amoroso Antonio, Scolari Francesco, Chen Nan, Zhang Hong, Lifton Richard |
| Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis. PLoS genetics 2012 8 (6): e1002765. Kiryluk Krzysztof, Li Yifu, Sanna-Cherchi Simone, Rohanizadegan Mersedeh, Suzuki Hitoshi, Eitner Frank, Snyder Holly J, Choi Murim, Hou Ping, Scolari Francesco, Izzi Claudia, Gigante Maddalena, Gesualdo Loreto, Savoldi Silvana, Amoroso Antonio, Cusi Daniele, Zamboli Pasquale, Julian Bruce A, Novak Jan, Wyatt Robert J, Mucha Krzysztof, Perola Markus, Kristiansson Kati, Viktorin Alexander, Magnusson Patrik K, Thorleifsson Gudmar, Thorsteinsdottir Unnur, Stefansson Kari, Boland Anne, Metzger Marie, Thibaudin Lise, Wanner Christoph, Jager Kitty J, Goto Shin, Maixnerova Dita, Karnib Hussein H, Nagy Judit, Panzer Ulf, Xie Jingyuan, Chen Nan, Tesar Vladimir, Narita Ichiei, Berthoux Francois, Floege Jürgen, Stengel Benedicte, Zhang Hong, Lifton Richard P, Gharavi Ali |
| Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration. PloS one 2012 7 (4): e35255. Cantsilieris Stuart, White Stefan J, Richardson Andrea J, Guymer Robyn H, Baird Paul |
| Age-related macular degeneration and coronary heart disease: evaluation of genetic and environmental associations. European journal of medical genetics 2013 Feb 56 (2): 72-9. Keilhauer Claudia N, Fritsche Lars G, Guthoff Rainer, Haubitz Imme, Weber Bernhard |
| Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32. PloS one 2013 8 (4): e60352. Holmes Lucy V, Strain Lisa, Staniforth Scott J, Moore Iain, Marchbank Kevin, Kavanagh David, Goodship Judith A, Cordell Heather J, Goodship Timothy H |
| Variants in Complement Factor H and Complement Factor H-Related Protein Genes, CFHR3 and CFHR1, Affect Complement Activation in IgA Nephropathy. Journal of the American Society of Nephrology : JASN 2015 May 26 (5): 1195-204. Zhu Li, Zhai Ya-Ling, Wang Feng-Mei, Hou Ping, Lv Ji-Cheng, Xu Da-Min, Shi Su-Fang, Liu Li-Jun, Yu Feng, Zhao Ming-Hui, Novak Jan, Gharavi Ali G, Zhang Ho |
| Comprehensive Analysis of Complement Genes in Patients with Atypical Hemolytic Uremic Syndrome. American journal of nephrology 2016 Apr 43 (3): 160-169. Zhang Tao, Lu Jianping, Liang Shaoshan, Chen Dachen, Zhang Haitao, Zeng Caihong, Liu Zhihong, Chen Huim |
| The clinical and laboratory features of Chinese Han anti-factor H autoantibody-associated hemolytic uremic syndrome. Pediatric nephrology (Berlin, Germany) 2016 12 32 (5): 811-822. Song Di, Liu Xiao-Rong, Chen Zhi, Xiao Hui-Jie, Ding Jie, Sun Shu-Zhen, Liu Hong-Yan, Guo Wei-Yi, Wang Su-Xia, Yu Feng, Zhao Ming-Hui, |
| Routine use of clinical exome-based next-generation sequencing for evaluation of patients with thrombotic microangiopathies. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2017 7 30 (12): 1739-1747. Gaut Joseph P, Jain Sanjay, Pfeifer John D, Vigh-Conrad Katinka A, Corliss Meagan, Sharma Mukesh K, Heusel Jonathan W, Cottrell Catherine |
| Association of copy number variations in complement factor H-Related genes among age-related macular degenerative subjects. The Kaohsiung journal of medical sciences 2017 Dec 33 (12): 602-608. Bakri Norshakimah Md, Ramachandran Vasudevan, Kee Hoo Fan, Subrayan Visvaraja, Isa Hazlita, Ngah Nor Fariza, Mohamad Nur Afiqah, Mooi Ching Siew, Mun Chan Yoke, Ismail Patimah, Ismail Fazliana, Sukiman Erma Suryana, Wan Sulaiman Wan Al |
| High Complement Factor H-Related (FHR)-3 Levels Are Associated With the Atypical Hemolytic-Uremic Syndrome-Risk Allele CFHR3*B. Frontiers in immunology 2018 9 848. Pouw Richard B, Gómez Delgado Irene, López Lera Alberto, Rodríguez de Córdoba Santiago, Wouters Diana, Kuijpers Taco W, Sánchez-Corral Pil |
| Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 loci. Human genomics 2021 9 15 (1): 60. Pappas Chris M, Zouache Moussa A, Matthews Stacie, Faust Caitlin D, Hageman Jill L, Williams Brandi L, Richards Burt T, Hageman Gregory |
| Clinical and Genetic Characteristics of Atypical Hemolytic Uremic Syndrome in Children: A Chinese Cohort Study. Nephron 2021 4 145 (4): 415-427. Wu Dan, Chen Jiahui, Ling Chen, Chen Zhi, Fan Jianfeng, Sun Qiang, Meng Qun, Liu Xiaoro |
| Complement Genetic Variants and FH Desialylation in S. pneumoniae-Haemolytic Uraemic Syndrome. Frontiers in immunology 2021 3 12 641656. Gómez Delgado Irene, Corvillo Fernando, Nozal Pilar, Arjona Emilia, Madrid Álvaro, Melgosa Marta, Bravo Juan, Szilágyi Ágnes, Csuka Dorottya, Veszeli Nóra, Prohászka Zoltán, Sánchez-Corral Pil |
| Variation in CFHR3 determines susceptibility to meningococcal disease by controlling factor H concentrations. American journal of human genetics 2022 8 109 (9): 1680-1691. Kumar Vikrant, Pouw Richard B, Autio Matias I, Sagmeister Manfred G, Phua Zai Yang, Borghini Lisa, Wright Victoria J, Hoggart Clive, Pan Bangfen, Tan Antson Kiat Yee, Binder Alexander, Brouwer Mieke C, Pinnock Ellie, De Groot Ronald, Hazelzet Jan, Emonts Marieke, Van Der Flier Michiel, Reiter Karl, Nöthen Markus M, Hoffmann Per, , Schlapbach Luregn J, Bellos Evangelos, Anderson Suzanne, Secka Fatou, Martinón-Torres Federico, Salas Antonio, Fink Colin, Carrol Enitan D, Pollard Andrew J, Coin Lachlan J, Zenz Werner, Wouters Diana, Ang Lay Teng, Hibberd Martin L, Levin Michael, Kuijpers Taco W, Davila Son |
| Beyond Panel-Based Testing: Exome Analysis Increases Sensitivity for Diagnosis of Genetic Kidney Disease. Kidney360 2022 4 1 (8): 772-780. Wilson Parker C, Love-Gregory Latisha, Corliss Meagan, McNulty Samantha, Heusel Jonathan W, Gaut Joseph |
| Disease profiles in the Indigenous Australian population are suggestive of a common complement control haplotype. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2023 5 112 105453. Joshua G Dubowsky, Jose J Estevez, Jamie E Craig, Binoy Appukuttan, Jillian M Ca |
| 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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