Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 46 Records) |
| Query Trace: Disease and C4A[original query] |
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| Assessment of complement C4 gene copy number using the paralog ratio test. Human mutation 2010 Jul 31 (7): 866-74. Fernando Michelle M A, Boteva Lora, Morris David L, Zhou Bi, Wu Yee Ling, Lokki Marja-Liisa, Yu Chack Yung, Rioux John D, Hollox Edward J, Vyse Timothy |
| Genotypic diversity of complement component C4 does not predict kidney transplant outcome. Journal of the American Society of Nephrology : JASN 2010 Dec . Wahrmann M, Döhler B, Ruhenstroth A, Haslacher H, Perkmann T, Exner M, Rees AJ, Böhmig GA |
| Association between copy number variation of complement component C4 and Graves' disease. Journal of biomedical science 2011 18 (1): 71. Liu Yu-Huei, Wan Lei, Chang Chwen-Tzuei, Liao Wen-Ling, Chen Wen-Chi, Tsai Yuhsin, Tsai Chang-Hai, Tsai Fuu-J |
| Confirmation of C4 gene copy number variation and the association with systemic lupus erythematosus in Chinese Han population. Rheumatology international 2012 Oct 32 (10): 3047-53. Lv Yongmei, He Sumin, Zhang Zheng, Li Yang, Hu Dayan, Zhu Kunju, Cheng Hui, Zhou Fusheng, Chen Gang, Zheng Xiaodong, Li Pan, Ren Yunqing, Yin Xianyong, Cui Yong, Sun Liangdan, Yang Sen, Zhang Xuej |
| Gene CNVs and protein levels of complement C4A and C4B as novel biomarkers for partial disease remissions in new-onset type 1 diabetes patients. Pediatric diabetes 2012 Aug 13 (5): 408-18. Kingery Suzanne E, Wu Yee Ling, Zhou Bi, Hoffman Robert P, Yu C Yu |
| HLA-DRB1 allele frequencies and C4 copy number variation in Finnish sarcoidosis patients and associations with disease prognosis. Human immunology 2012 Jan 73 (1): 93-100. Wennerström Annika, Pietinalho Anne, Vauhkonen Hanna, Lahtela Laura, Palikhe Anil, Hedman Jouni, Purokivi Minna, Varkki Essi, Seppänen Mikko, Lokki Marja-Liisa, Selroos Olof, |
| Genetically determined partial complement C4 deficiency states are not independent risk factors for SLE in UK and Spanish populations. American journal of human genetics 2012 Mar 90 (3): 445-56. Boteva Lora, Morris David L, Cortés-Hernández Josefina, Martin Javier, Vyse Timothy J, Fernando Michelle M |
| Proinflammatory HLA-DRB1*01-haplotype predisposes to ST-elevation myocardial infarction. Atherosclerosis 2012 Apr 221 (2): 461-6. Paakkanen Riitta, Lokki Marja-Liisa, Seppänen Mikko, Tierala Ilkka, Nieminen Markku S, Sinisalo Ju |
| Copy number variations of complement component C4 are associated with Behçet's disease but not with ankylosing spondylitis associated with acute anterior uveitis. Arthritis and rheumatism 2013 Nov 65 (11): 2963-70. Hou Shengping, Qi Jian, Liao Dan, Zhang Qi, Fang Jing, Zhou Yan, Liu Yunjia, Bai Lin, Zhang Meifen, Kijlstra Aize, Yang Peize |
| Investigation of complement component C4 copy number variation in human longevity. PloS one 2014 9 (1): e86188. Flachsbart Friederike, Caliebe Amke, Heinsen Femke-Anouska, Hemming-Karlsen Tom, Schreiber Stefan, Franke Andre, Nebel Alm |
| Immunogenetics of complement in mixed cryoglobulinaemia. Clinical and experimental rheumatology 0 34 (3 Suppl 97): S12-5. Menegatti Elisa, Messina Margherita, Oddone Valentina, Rubini Elena, Sciascia Savino, Naretto Carla, Baldovino Simone, Roccatello Dar |
| Effects of Complement C4 Gene Copy Number Variations, Size Dichotomy, and C4A Deficiency on Genetic Risk and Clinical Presentation of Systemic Lupus Erythematosus in East Asian Populations. Arthritis & rheumatology (Hoboken, N.J.) 2016 Jan . Chen Ji Yih, Wu Yee Ling, Mok Mo Yin, Wu Yeong-Jian Jan, Lintner Katherine E, Wang Chin-Man, Chung Erwin K, Yang Yan, Zhou Bi, Wang Huanyu, Yu Denise J H C, Alhomosh Alaaedin, Jones Karla, Spencer Charles H, Nagaraja Haikady N, Lung Lau Yu, Lau Chak-Sing, Yu C Yu |
| Comprehensive approach to study complement C4 in systemic lupus erythematosus: Gene polymorphisms, protein levels and functional activity. Molecular immunology 2017 Oct 92 125-131. Tsang-A-Sjoe M W P, Bultink I E M, Korswagen L A, van der Horst A, Rensink I, de Boer M, Hamann D, Voskuyl A E, Wouters |
| Low copy numbers of complement C4 and homozygous deficiency of C4A may predispose to severe disease and earlier disease onset in patients with systemic lupus erythematosus. Lupus 2017 Jan 961203317735187. Jüptner M, Flachsbart F, Caliebe A, Lieb W, Schreiber S, Zeuner R, Franke A, Schröder J |
| Complement component 4 variations may influence psychopathology risk in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Human genetics 2018 11 137 (11-12): 955-960. Lao Qizong, Jardin Marcia Des, Jayakrishnan Rahul, Ernst Monique, Merke Deborah |
| Pneumonia: host susceptibility and shared genetics with pulmonary function and other traits. Clinical and experimental immunology 2019 Sep . Khadzhieva M B, Kuzovlev A N, Salnikova L |
| Impact of C4, C4A and C4B gene copy number variation in the susceptibility, phenotype and progression of systemic lupus erythematosus. Advances in rheumatology (London, England) 2019 8 59 (1): 36. Pereira Kaline Medeiros Costa, Perazzio Sandro, Faria Atila Granado A, Moreira Eloisa Sa, Santos Viviane C, Grecco Marcelle, da Silva Neusa Pereira, Andrade Luis Eduardo Coel |
| Elevated serum complement levels and higher gene copy number of complement C4B are associated with hypertension and effective response to statin therapy in childhood-onset systemic lupus erythematosus (SLE). Lupus science & medicine 2019 8 6 (1): e000333. Mulvihill Evan, Ardoin Stacy, Thompson Susan D, Zhou Bi, Yu Gakit Richard, King Emily, Singer Nora, Levy D M, Brunner Hermine, Wu Yee Ling, Nagaraja Haikady N, Schanberg Laura Eve, Yu Chack-Yu |
| Investigation of MHC gamma block C4A and C4B polymorphisms in unrelated hematopoietic stem cell transplantation. Hematology, transfusion and cell therapy 2019 Sep . Getz Joselito, Goldenstein Monica, Bonfim Carmem, Funke Vaneuza Moreira, Colturato Vergílio, Hamerschlak Nelson, Torres Margareth, Sayer David, Boldt Angelica, Pasquini Ricardo, Pereira Noemi Far |
| Association between complement 4 copy number variation and systemic lupus erythematosus: a meta-analysis. Clinical and experimental medicine 2020 Jul . Wu Ziyan, Zhang Shulan, Li Ping, Zhang Fengchun, Li Yongz |
| 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 |
| Integrative brain transcriptome analysis links complement component 4 and HSPA2 to the APOE ?2 protective effect in Alzheimer disease. Molecular psychiatry 2021 9 26 (10): 6054-6064. Panitch Rebecca, Hu Junming, Chung Jaeyoon, Zhu Congcong, Meng Gaoyuan, Xia Weiming, Bennett David A, Lunetta Kathryn L, Ikezu Tsuneya, Au Rhoda, Stein Thor D, Farrer Lindsay A, Jun Gyungah |
Medical Records-Based Genetic Studies of the Complement System.
Journal of the American Society of Nephrology : JASN 2021 5 32 (8): 2031-2047. Khan Atlas, Shang Ning, Petukhova Lynn, Zhang Jun, Shen Yufeng, Hebbring Scott J, Moncrieffe Halima, Kottyan Leah C, Namjou-Khales Bahram, Knevel Rachel, Raychaudhuri Soumya, Karlson Elizabeth W, Harley John B, Stanaway Ian B, Crosslin David, Denny Joshua C, Elkind Mitchell S V, Gharavi Ali G, Hripcsak George, Weng Chunhua, Kiryluk Krzyszt |
| Functional regulatory variants implicate distinct transcriptional networks in dementia. Science (New York, N.Y.) 2022 08 377 (6608): eabi8654. Cooper Yonatan A, Teyssier Noam, Dräger Nina M, Guo Qiuyu, Davis Jessica E, Sattler Sydney M, Yang Zhongan, Patel Abdulsamie, Wu Sarah, Kosuri Sriram, Coppola Giovanni, Kampmann Martin, Geschwind Daniel |
| Schizophrenia risk loci from xMHC region were associated with antipsychotic response in chronic schizophrenic patients with persistent positive symptom. Translational psychiatry 2022 3 12 (1): 92. Li Jiang, Yoshikawa Akane, Alliey-Rodriguez Ney, Meltzer Herbert |
| A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodies.
Brain : a journal of neurology 2022 3 . Strippel Christine, Herrera-Rivero Marisol, Wendorff Mareike, Tietz Anja K, Degenhardt Frauke, Witten Anika, Schroeter Christina, Nelke Christopher, Golombeck Kristin S, Madlener Marie, Rüber Theodor, Ernst Leon, Racz Attila, Baumgartner Tobias, Widman Guido, Doppler Kathrin, Thaler Franziska, Siebenbrodt Kai, Dik Andre, Kerin Constanze, Räuber Saskia, Gallus Marco, Kovac Stjepana, Grauer Oliver M, Grimm Alexander, Prüss Harald, Wickel Jonathan, Geis Christian, Lewerenz Jan, Goebels Norbert, Ringelstein Marius, Menge Til, Tackenberg Björn, Kellinghaus Christoph, Bien Christian G, Kraft Andrea, Zettl Uwe, Ismail Fatme Seval, Ayzenberg Ilya, Urbanek Christian, Sühs Kurt-Wolfram, Tauber Simone C, Mues Sigrid, Körtvélyessy Peter, Markewitz Robert, Paliantonis Asterios, Elger Christian E, Surges Rainer, Sommer Claudia, Kümpfel Tania, Gross Catharina C, Lerche Holger, Wellmer Jörg, Quesada Carlos M, Then Bergh Florian, Wandinger Klaus-Peter, Becker Albert J, Kunz Wolfram S, Meyer Zu Hörste Gerd, Malter Michael P, Rosenow Felix, Wiendl Heinz, Kuhlenbäumer Gregor, Leypoldt Frank, Lieb Wolfgang, Franke Andre, Meuth Sven G, Stoll Monika, Melzer Nico, |
| 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 |
| Evaluation of C4 gene copy number in Pediatric Acute Neuropsychiatric Syndrome. Developmental neuroscience 2023 6 . Agnieszka Kalinowski, Lu Tian, Reenal Pattni, Hanna Ollila, Maroof Khan, Cindy Manko, Melissa Silverman, Meiqian Ma, Laurie Columbo, Bahare Farhadian, Susan Swedo, Tanya Murphy, Mats Johnson, Elisabeth Fernell, Christopher Gillberg, Margo Thienemann, Elizabeth D Mellins, Douglas F Levinson, Alexander E Urban, Jennifer Frankovi |
| Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes. Nature communications 2024 9 15 (1): 7880. Kurt Farrell, Jack Humphrey, Timothy Chang, Yi Zhao, Yuk Yee Leung, Pavel P Kuksa, Vishakha Patil, Wan-Ping Lee, Amanda B Kuzma, Otto Valladares, Laura B Cantwell, Hui Wang, Ashvin Ravi, Claudia De Sanctis, Natalia Han, Thomas D Christie, Robina Afzal, Shrishtee Kandoi, Kristen Whitney, Margaret M Krassner, Hadley Ressler, SoongHo Kim, Diana Dangoor, Megan A Iida, Alicia Casella, Ruth H Walker, Melissa J Nirenberg, Alan E Renton, Bergan Babrowicz, Giovanni Coppola, Towfique Raj, Günter U Höglinger, Ulrich Müller, Lawrence I Golbe, Huw R Morris, John Hardy, Tamas Revesz, Tom T Warner, Zane Jaunmuktane, Kin Y Mok, Rosa Rademakers, Dennis W Dickson, Owen A Ross, Li-San Wang, Alison Goate, Gerard Schellenberg, Daniel H Geschwind, , John F Crary, Adam N |
| Low C4A copy numbers and higher HERV gene insertion contributes to increased risk of SLE, with absence of association with disease phenotype and disease activity. Immunologic research 2024 4 . Christina Mary Mariaselvam, Gaurav Seth, Chengappa Kavadichanda, Wahid Boukouaci, Ching-Lien Wu, Bruno Costes, Molly Mary Thabah, Rajagopal Krishnamoorthy, Marion Leboyer, Vir Singh Negi, Ryad Tamou |
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