Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 35 Records) |
| Query Trace: Disease and CFHR1[original query] |
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| 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 |
| Factor H autoantibodies and deletion of Complement Factor H-Related protein-1 in rheumatic diseases in comparison to atypical hemolytic uremic syndrome. Arthritis research & therapy 2012 14 (4): R185. Foltyn Zadura Anna, Zipfel Peter F, Bokarewa Maria I, Sturfelt Gunnar, Jönsen Andreas, Nilsson Sara C, Hillarp Andreas, Saxne Tore, Trouw Leendert A, Blom Anna |
| 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 |
| Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as susceptibility loci for systemic lupus erythematosus in a large-scale multiracial replication study. American journal of human genetics 2012 Apr 90 (4): 648-60. Lessard Christopher J, Adrianto Indra, Ice John A, Wiley Graham B, Kelly Jennifer A, Glenn Stuart B, Adler Adam J, Li He, Rasmussen Astrid, Williams Adrienne H, Ziegler Julie, Comeau Mary E, Marion Miranda, Wakeland Benjamin E, Liang Chaoying, Ramos Paula S, Grundahl Kiely M, Gallant Caroline J, Alarcón-Riquelme Marta E, Alarcón Graciela S, Anaya Juan-Manuel, Bae Sang-Cheol, Boackle Susan A, Brown Elizabeth E, Chang Deh-Ming, Cho Soo-Kyung, Criswell Lindsey A, Edberg Jeffrey C, Freedman Barry I, Gilkeson Gary S, Jacob Chaim O, James Judith A, Kamen Diane L, Kimberly Robert P, Kim Jae-Hoon, Martin Javier, Merrill Joan T, Niewold Timothy B, Park So-Yeon, Petri Michelle A, Pons-Estel Bernardo A, Ramsey-Goldman Rosalind, Reveille John D, Scofield R Hal, Song Yeong Wook, Stevens Anne M, Tsao Betty P, Vila Luis M, Vyse Timothy J, Yu Chack-Yung, Guthridge Joel M, Kaufman Kenneth M, Harley John B, Wakeland Edward K, Langefeld Carl D, Gaffney Patrick M, Montgomery Courtney G, Moser Kathy L, , |
| Complement factor H-related protein 1 deficiency and factor H antibodies in pediatric patients with atypical hemolytic uremic syndrome. Clinical journal of the American Society of Nephrology : CJASN 2013 Mar 8 (3): 407-15. Hofer Johannes, Janecke Andreas R, Zimmerhackl L B, Riedl Magdalena, Rosales Alejandra, Giner Thomas, Cortina Gerard, Haindl Carola J, Petzelberger Barbara, Pawlik Miriam, Jeller Verena, Vester Udo, Gadner Bettina, van Husen Michael, Moritz Michael L, Würzner Reinhard, Jungraithmayr Therese, |
| 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 |
| Influence of genetic variation on plasma protein levels in older adults using a multi-analyte panel. PloS one 2013 8 (7): e70269. Kim Sungeun, Swaminathan Shanker, Inlow Mark, Risacher Shannon L, Nho Kwangsik, Shen Li, Foroud Tatiana M, Petersen Ronald C, Aisen Paul S, Soares Holly, Toledo Jon B, Shaw Leslie M, Trojanowski John Q, Weiner Michael W, McDonald Brenna C, Farlow Martin R, Ghetti Bernardino, Saykin Andrew J, |
| 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 |
| Factors determining penetrance in familial atypical haemolytic uraemic syndrome. Journal of medical genetics 2014 Nov 51 (11): 756-64. Sansbury Francis H, Cordell Heather J, Bingham Coralie, Bromilow Gilly, Nicholls Anthony, Powell Roy, Shields Bev, Smyth Lucy, Warwicker Paul, Strain Lisa, Wilson Valerie, Goodship Judith A, Goodship Timothy H J, Turnpenny Peter |
| 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 |
| Atypical hemolytic uremic syndrome: Korean pediatric series. Pediatrics international : official journal of the Japan Pediatric Society 2015 Jun 57 (3): 431-8. Lee Jiwon M, Park Young Seo, Lee Joo Hoon, Park Se Jin, Shin Jae Il, Park Yong-Hoon, Yoo Kee Hwan, Cho Min Hyun, Kim Su-Young, Kim Seong Heon, Namgoong Mee Kyung, Lee Seung Joo, Lee Jun Ho, Cho Hee Yeon, Han Kyoung Hee, Kang Hee Gyung, Ha Il Soo, Bae Jun-Seok, Kim Nayoung K D, Park Woong-Yang, Cheong Hae |
| 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 |
| Factor H Competitor Generated by Gene Conversion Events Associates with Atypical Hemolytic Uremic Syndrome. Journal of the American Society of Nephrology : JASN 2017 10 29 (1): 240-249. Goicoechea de Jorge Elena, Tortajada Agustín, García Sheila Pinto, Gastoldi Sara, Merinero Héctor Martín, García-Fernández Jesús, Arjona Emilia, Cao Mercedes, Remuzzi Giuseppe, Noris Marina, Rodríguez de Córdoba Santia |
| Copy number variations exploration of multiple genes in Graves' disease. Medicine 2017 Jan 96 (4): e5866. Song Rong-Hua, Shao Xiao-Qing, Li Ling, Wang Wen, Zhang Jin- |
Role of the Complement System in Chronic Central Serous Chorioretinopathy: A Genome-Wide Association Study.
JAMA ophthalmology 2018 Aug . Schellevis Rosa L, van Dijk Elon H C, Breukink Myrte B, Altay Lebriz, Bakker Bjorn, Koeleman Bobby P C, Kiemeney Lambertus A, Swinkels Dorine W, Keunen Jan E E, Fauser Sascha, Hoyng Carel B, den Hollander Anneke I, Boon Camiel J F, de Jong Eiko |
| Combined study of ADAMTS13 and complement genes in the diagnosis of thrombotic microangiopathies using next-generation sequencing. Research and practice in thrombosis and haemostasis 2018 7 1 (1): 69-80. Fidalgo Teresa, Martinho Patrícia, Pinto Catarina S, Oliveira Ana C, Salvado Ramon, Borràs Nina, Coucelo Margarida, Manco Licínio, Maia Tabita, Mendes M João, Del Orbe Barreto Rafael, Corrales Irene, Vidal Francisco, Ribeiro M Letíc |
| 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 |
| Macular retinal thickness differs markedly in age-related macular degeneration driven by risk polymorphisms on chromosomes 1 and 10. Scientific reports 2020 12 10 (1): 21093. Zouache Moussa A, Bennion Alex, Hageman Jill L, Pappas Christian, Richards Burt T, Hageman Gregory |
| DelCFHR3-1 influences graft survival in transplant patients with IgA nephropathy via complement-mediated cellular senescence. American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2020 10 21 (2): 838-845. Pesce Francesco, Stea Emma D, Divella Chiara, Accetturo Matteo, Laghetti Paola, Gallo Pasquale, Rossini Michele, Cianciotta Francesca, Crispino Lucia, Granata Antonio, Battaglia Michele, Lucarelli Giuseppe, de Cordoba Santiago R, Stallone Giovanni, Gesualdo Loreto, Castellano Giusep |
| Prognostic Genetic Biomarkers Based on Oncogenic Signaling Pathways for Outcome Prediction in Patients with Oral Cavity Squamous Cell Carcinoma. Cancers 2021 May 13 (11): . Fan Wen-Lang, Yang Lan-Yan, Hsieh Jason Chia-Hsun, Lin Tsung-Chieh, Lu Mei-Yeh Jade, Liao Chun- |
| 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 |
| Factor H-Related Protein 1 Drives Disease Susceptibility and Prognosis in C3 Glomerulopathy. Journal of the American Society of Nephrology : JASN 2022 5 33 (6): 1137-1153. Márquez-Tirado Bárbara, Gutiérrez-Tenorio Josué, Tortajada Agustín, Lucientes Continente Laura, Caravaca-Fontán Fernando, Malik Talat H, Roldán Montero Raquel, Elías Sandra, Saiz Gonzalez Ana, Fernández-Juarez Gema, Sánchez-Corral Pilar, Pickering Matthew C, Praga Manuel, Rodríguez de Córdoba Santiago, Goicoechea de Jorge Ele |
| 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 |
| 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 |
| Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood. medRxiv : the preprint server for health sciences 2024 5 . Yasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, Fulong Yu, Jason Bacon, Justin W Wong, Francois Aguet, Kristin Ardlie, Donna Arnett, Kathleen Barnes, Joshua C Bis, Tom Blackwell, Lewis C Becker, Eric Boerwinkle, Russell P Bowler, Matthew J Budoff, April P Carson, Jiawen Chen, Michael H Cho, Josef Coresh, Nancy Cox, Paul S de Vries, Dawn L DeMeo, David W Fardo, Myriam Fornage, Xiuqing Guo, Michael E Hall, Nancy Heard-Costa, Bertha Hidalgo, Marguerite Ryan Irvin, Andrew D Johnson, Eimear E Kenny, Dan Levy, Yun Li, Joao Ac Lima, Yongmei Liu, Ruth J F Loos, Mitchell J Machiela, Rasika A Mathias, Braxton D Mitchell, Joanne Murabito, Josyf C Mychaleckyj, Kari North, Peter Orchard, Stephen Cj Parker, Yash Pershad, Patricia A Peyser, Katherine A Pratte, Bruce M Psaty, Laura M Raffield, Susan Redline, Stephen S Rich, Jerome I Rotter, Sanjiv J Shah, Jennifer A Smith, Aaron P Smith, Albert Smith, Margaret Taub, Hemant K Tiwari, Russell Tracy, Bjoernar Tuftin, Alexander G Bick, Vijay G Sankaran, Alexander P Reiner, Paul Scheet, Paul L Au |
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