Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Autoimmune Diseases and C4A[original query] |
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| Genetic control of immune response in carriers of the 8.1 ancestral haplotype: correlation with levels of IgG subclasses: its relevance in the pathogenesis of autoimmune diseases. Annals of the New York Academy of Sciences 2007 Sep 1110 151-8. Candore Giuseppina, Campagna Anna Maria, Cuppari Irene, Di Carlo Daniele, Mineo Claudia, Caruso Caloge |
| Autoimmune-associated HLA-B8-DR3 haplotypes in Asian Indians are unique in C4 complement gene copy numbers and HSP-2 1267A/G. Human immunology 2008 Sep 69 (9): 580-7. Kaur Gurvinder, Kumar Neeraj, Szilagyi Agnes, Blasko Bernadett, Fust George, Rajczy Katalin, Pozsonyi Eva, Hosso Adrienn, Petranyi Gyozo, Tandon Nikhil, Mehra Narind |
| High C4 gene copy numbers protects against Vogt-Koyanagi-Harada syndrome in Chinese Han. The British journal of ophthalmology 2014 Dec 98 (12): 1733-7. Hou Shengping, Qi Jian, Liao Dan, Fang Jing, Chen Lu, Kijlstra Aize, Yang Peize |
| Corrigendum: Association between C4, C4A, and C4B copy number variations and susceptibility to autoimmune diseases: a meta-analysis. Scientific reports 2017 May 7 46785. Li Na, Zhang Jun, Liao Dan, Yang Lu, Wang Yingxiong, Hou Shengpi |
| Association between C4, C4A, and C4B copy number variations and susceptibility to autoimmune diseases: a meta-analysis. Scientific reports 2017 Feb 7 42628. Li Na, Zhang Jun, Liao Dan, Yang Lu, Wang Yingxiong, Hou Shengpi |
| Complement genes contribute sex-biased vulnerability in diverse disorders. Nature 2020 6 582 (7813): 577-581. Kamitaki Nolan, Sekar Aswin, Handsaker Robert E, de Rivera Heather, Tooley Katherine, Morris David L, Taylor Kimberly E, Whelan Christopher W, Tombleson Philip, Loohuis Loes M Olde, , Boehnke Michael, Kimberly Robert P, Kaufman Kenneth M, Harley John B, Langefeld Carl D, Seidman Christine E, Pato Michele T, Pato Carlos N, Ophoff Roel A, Graham Robert R, Criswell Lindsey A, Vyse Timothy J, McCarroll Steven |
| Strong Association of Combined Genetic Deficiencies in the Classical Complement Pathway With Risk of Systemic Lupus Erythematosus and Primary Sjögren's Syndrome. Arthritis & rheumatology (Hoboken, N.J.) 2022 6 74 (11): 1842-1850. Lundtoft Christian, Sjöwall Christopher, Rantapää-Dahlqvist Solbritt, Bengtsson Anders A, Jönsen Andreas, Pucholt Pascal, Wu Yee Ling, Lundström Emeli, Eloranta Maija-Leena, Gunnarsson Iva, Baecklund Eva, Jonsson Roland, Hammenfors Daniel, Forsblad-d'Elia Helena, Eriksson Per, Mandl Thomas, Bucher Sara, Norheim Katrine B, Auglaend Johnsen Svein Joar, Omdal Roald, Kvarnström Marika, Wahren-Herlenius Marie, Truedsson Lennart, Nilsson Bo, Kozyrev Sergey V, Bianchi Matteo, Lindblad-Toh Kerstin, , Yu Chack-Yung, Nordmark Gunnel, Sandling Johanna K, Svenungsson Elisabet, Leonard Dag, Rönnblom La |
| Complement C4 Copy Number Variation is Linked to SSA/Ro and SSB/La Autoantibodies in Systemic Inflammatory Autoimmune Diseases. Arthritis & rheumatology (Hoboken, N.J.) 2022 3 74 (8): 1440-1450. Lundtoft Christian, Pucholt Pascal, Martin Myriam, Bianchi Matteo, Lundström Emeli, Eloranta Maija-Leena, Sandling Johanna K, Sjöwall Christopher, Jönsen Andreas, Gunnarsson Iva, Rantapää-Dahlqvist Solbritt, Bengtsson Anders A, Leonard Dag, Baecklund Eva, Jonsson Roland, Hammenfors Daniel, Forsblad-d'Elia Helena, Eriksson Per, Mandl Thomas, Magnusson Bucher Sara, Norheim Katrine B, Auglaend Johnsen Svein Joar, Omdal Roald, Kvarnström Marika, Wahren-Herlenius Marie, Notarnicola Antonella, Andersson Helena, Molberg Øyvind, Diederichsen Louise Pyndt, Almlöf Jonas, Syvänen Ann-Christine, Kozyrev Sergey V, Lindblad-Toh Kerstin, , , Nilsson Bo, Blom Anna M, Lundberg Ingrid E, Nordmark Gunnel, Diaz-Gallo Lina Marcela, Svenungsson Elisabet, Rönnblom La |
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