Human Genome Epidemiology Literature Finder
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Records 1 - 19 (of 19 Records) |
| Query Trace: Disease and CD46[original query] |
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| Genetic analysis of the complement factor H related 5 gene in haemolytic uraemic syndrome. Molecular immunology 2007 Mar 44 (7): 1704-8. Monteferrante G, Brioschi S, Caprioli J, Pianetti G, Bettinaglio P, Bresin E, Remuzzi G, Noris |
| Integrating host genomics with surveillance for invasive bacterial diseases. Emerging infectious diseases 2008 Jul 14 (7): 1138-40. Crawford Dana C, Zimmer Shanta M, Morin Craig A, Messonnier Nancy E, Lynfield Ruth, Yi Qian, Shephard Cynthia, Wong Michelle, Rieder Mark J, Livingston Robert J, Nickerson Deborah A, Whitney Cynthia G, Lingappa Jair |
| Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome. Human mutation 2010 Jun 31 (6): E1445-60. Maga Tara K, Nishimura Carla J, Weaver Amy E, Frees Kathy L, Smith Richard J |
| Identifying host genetic risk factors in the context of public health surveillance for invasive pneumococcal disease. PloS one 2011 6 (8): e23413. Lingappa Jairam R, Dumitrescu Logan, Zimmer Shanta M, Lynfield Ruth, McNicholl Janet M, Messonnier Nancy E, Whitney Cynthia G, Crawford Dana |
| The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia. Biological psychiatry 2011 Jul 70 (1): 35-42. Håvik Bjarte, Le Hellard Stephanie, Rietschel Marcella, Lybæk Helle, Djurovic Srdjan, Mattheisen Manuel, Mühleisen Thomas W, Degenhardt Franziska, Priebe Lutz, Maier Wolfgang, Breuer Rene, Schulze Thomas G, Agartz Ingrid, Melle Ingrid, Hansen Thomas, Bramham Clive R, Nöthen Markus M, Stevens Beth, Werge Thomas, Andreassen Ole A, Cichon Sven, Steen Vidar |
| Coding polymorphisms in the genes of the alternative complement pathway and abdominal aortic aneurysm. International journal of immunogenetics 2011 Jun 38 (3): 243-8. Bradley D T, Badger S A, Bown M J, Sayers R D, Hughes A |
| Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS. Molecular immunology 2012 Jan 49 (4): 640-8. Ermini Luca, Goodship Timothy H J, Strain Lisa, Weale Michael E, Sacks Steven H, Cordell Heather J, Fremeaux-Bacchi Veronique, Sheerin Neil |
| Genetic variation in complement regulators and susceptibility to age-related macular degeneration. Immunobiology 2012 Feb 217 (2): 158-61. Cipriani Valentina, Matharu Baljinder K, Khan Jane C, Shahid Humma, Stanton Chloe M, Hayward Caroline, Wright Alan F, Bunce Catey, Clayton David G, Moore Anthony T, Yates John R |
| 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 |
| The local complement activation on vascular bed of patients with systemic sclerosis: a hypothesis-generating study. PloS one 2015 10 (2): e0114856. Scambi Cinzia, Ugolini Sara, Jokiranta T Sakari, De Franceschi Lucia, Bortolami Oscar, La Verde Valentina, Guarini Patrizia, Caramaschi Paola, Ravagnani Viviana, Martignoni Guido, Colato Chiara, Pedron Serena, Benedetti Fabio, Sorio Marco, Poli Fabio, Biasi Domeni |
| Role of CD46 Polymorphisms in the Occurrence of Disease in Young Chinese Men With Human Adenovirus Type 55 Infection. Disaster medicine and public health preparedness 2016 Sep 1-4. Lv Qi, Ding Hui, Liu Zi-Quan, Gao Hong-Wei, Yu Bao-Guo, Wu Zhou-Wei, Fan Hao-Jun, Hou Shi- |
| Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome. Molecular immunology 2016 Feb 71 131-142. Iatropoulos Paraskevas, Noris Marina, Mele Caterina, Piras Rossella, Valoti Elisabetta, Bresin Elena, Curreri Manuela, Mondo Elena, Zito Anna, Gamba Sara, Bettoni Serena, Murer Luisa, Fremeaux-Bacchi Veronique, Vivarelli Marina, Emma Francesco, Daina Erica, Remuzzi Giusep |
| 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 |
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 |
| Genetic Analysis of 400 Patients Refines Understanding and Implicates a New Gene in Atypical Hemolytic Uremic Syndrome. Journal of the American Society of Nephrology : JASN 2018 11 29 (12): 2809-2819. Bu Fengxiao, Zhang Yuzhou, Wang Kai, Borsa Nicolo Ghiringhelli, Jones Michael B, Taylor Amanda O, Takanami Erika, Meyer Nicole C, Frees Kathy, Thomas Christie P, Nester Carla, Smith Richard J |
| Common variants of fetal and maternal complement genes in preeclampsia: pregnancy specific complotype. Scientific reports 2020 3 10 (1): 4811. Banadakoppa Manu, Balakrishnan Meena, Yallampalli Chand |
| 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 |
| Focused panel sequencing points to genetic predisposition in non-cirrhotic intrahepatic portal hypertension patients in India. Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology 2023 10 . Rekha Aaron, Kalpana Premkumar, Aaron Chapla, B Vijayalekshmi, Uday Zachariah, Elwyn Elias, Thomas Alex Kodiatte, Dolly Daniel, John Jude, K A Balasubramanian, Sukesh C Nair, Nihal Thomas, Banumathi Ramakrishna, C E Eapen, Ashish Go |
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