Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Syndrome and C4A[original query] |
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| Low complement C4B gene copy number predicts short-term mortality after acute myocardial infarction. International immunology 2008 Jan 20 (1): 31-7. Blaskó Bernadett, Kolka Ragnhildur, Thorbjornsdottir Perla, Sigurdarson Sigurdur Thór, Sigurdsson Gardar, Rónai Zsolt, Sasvári-Székely Mária, Bödvarsson Sigurdur, Thorgeirsson Gudmundur, Prohászka Zoltán, Kovács Margit, Füst George, Arason Gudmundur Jóha |
| Human MHC region harbors both susceptibility and protective haplotypes for coronary artery disease. Tissue antigens 2007 Jan 69 (1): 47-55. Palikhe A, Sinisalo J, Seppänen M, Valtonen V, Nieminen M S, Lokki M |
| 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 |
| 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 |
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 |
| Association of C4 Null Alleles and Persistently Low C4 in Asian Indian Patients With Systemic Lupus Erythematosus. International journal of immunogenetics 2025 1 . Sachin R Jeevanagi, Pankti Mehta, Rekha Aaron, Debashish Danda, Sumita Danda, Jayakanthan Kabeerdo |
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