Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 95 Records) |
Query Trace: C4B[original query] |
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Plasma Levels of Complement Factor I and C4b Peptides Are Associated with HIV Suppression. ACS infectious diseases 2017 9 3 (12): 880-885. Wu Boyue, Ouyang Zhengyu, Lyon Christopher J, Zhang Wei, Clift Tori, Bone Christopher R, Li Boan, Zhao Zhen, Kimata Jason T, Yu Xu G, Hu |
Relationship between plasma protein S levels and apolipoprotein C-II in Japanese middle-aged obese women and young nonobese women. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2017 12 29 (1): 39-47. Otsuka Yukiko, Ueda Maiko, Nakazono Eri, Tsuda Tomohide, Jin Xiuri, Noguchi Kenta, Sata Shihoko, Miyazaki Hitomi, Abe Shimako, Imai Katsumi, Iwamoto Masako, Masuda Takashi, Moriguchi Ririko, Nakano Shuji, Tsuda Hiro |
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 |
Complement receptor 1 (CR1, CD35) association with susceptibility to leprosy. PLoS neglected tropical diseases 2018 8 12 (8): e0006705. Kretzschmar Gabriela Canalli, Oliveira Luana Caroline, Nisihara Renato Mitsunori, Velavan Thirumalaisamy P, Stinghen Sérvio Túlio, Stahlke Ewalda R S, Petzl-Erler Maria Luiza, Messias-Reason Iara José T de, Boldt Angelica Beate Wint |
Insights on the relationship between complement component C4 serum concentrations and C4 gene copy numbers in a Western Australian systemic lupus erythematosus cohort. Lupus 2018 7 27 (10): 1687-1696. Margery-Muir A A, Bundell C, Wetherall J D, Whidborne R, Martinez P, Groth D |
Complement receptor 1 gene (CR1) intragenic duplication and risk of Alzheimer's disease. Human genetics 2018 Apr . Kucukkilic Ezgi, Brookes Keeley, Barber Imelda, Guetta-Baranes Tamar, , Morgan Kevin, Hollox Edward |
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 |
GENETIC RISK FACTORS IN ACUTE CENTRAL SEROUS CHORIORETINOPATHY. Retina (Philadelphia, Pa.) 2018 Oct . Mohabati Danial, Schellevis Rosa L, van Dijk Elon H C, Altay Lebriz, Fauser Sascha, Hoyng Carel B, De Jong Eiko K, Boon Camiel J F, Yzer Suzan |
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 |
Relationships of complement components C3 and C4 and their genetics to cardiometabolic risk in healthy, non-Hispanic white adolescents. Pediatric research 2019 Aug . Copenhaver Melanie M, Yu Chack-Yung, Zhou Danlei, Hoffman Robert |
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 Study of the Complement Component C4 Gene in Tardive Dyskinesia. Frontiers in pharmacology 2019 12 10 1339. Zai Clement C, Tiwari Arun K, Zai Gwyneth C, Freeman Natalie, Pouget Jennie G, Greco James, Tampakeras Maria, Shaikh Sajid A, Herbert Deanna, Emmerson Heather, Cheema Sheraz Y, Braganza Nicole, Müller Daniel J, Voineskos Aristotle N, Remington Gary, Kennedy James |
GENETIC RISK FACTORS IN SEVERE, NONSEVERE AND ACUTE PHENOTYPES OF CENTRAL SEROUS CHORIORETINOPATHY. Retina (Philadelphia, Pa.) 2019 Dec . Mohabati Danial, Schellevis Rosa L, van Dijk Elon H C, Fauser Sascha, den Hollander Anneke I, Hoyng Carel B, De Jong Eiko K, Yzer Suzanne, Boon Camiel J |
Complement protein levels and MBL2 polymorphisms are associated with dengue and disease severity. Scientific reports 2020 Sep 10 (1): 14923. Giang Ngo Truong, van Tong Hoang, Quyet Do, Hoan Nghiem Xuan, Nghia Trinh Huu, Nam Nguyen Minh, Hung Hoang Vu, Anh Do Tuan, Van Mao Can, Son Ho Anh, Meyer Christian G, Velavan Thirumalaisamy P, Toan Nguyen Li |
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 |
CCL3L3-null status is associated with susceptibility to systemic lupus erythematosus. Scientific reports 2021 Sep 11 (1): 19172. Kim Young-Ho, Lee Eunyoung Emily, Sim Hye-Won, Kang Eun-Kyung, Won Yoon-Ho, Lee Dong-Eun, Hong Kyeong-Man, Song Yeong-Wo |
Variants at the MHC Region Associate With Susceptibility to Clostridioides difficile Infection: A Genome-Wide Association Study Using Comprehensive Electronic Health Records.
Frontiers in immunology 2021 12 638913. Li Jiang, Zhang Yanfei, Jilg Alexandria L, Wolk Donna M, Khara Harshit S, Kolinovsky Amy, Rolston David D K, Hontecillas Raquel, Bassaganya-Riera Josep, Williams Marc S, Abedi Vida, Lee Ming Ta Micha |
Association between complement component 4A expression, cognitive performance and brain imaging measures in UK Biobank. Psychological medicine 2021 3 52 (15): 1-11. O'Connell Kevin S, Sønderby Ida E, Frei Oleksandr, van der Meer Dennis, Athanasiu Lavinia, Smeland Olav B, Alnæs Dag, Kaufmann Tobias, Westlye Lars T, Steen Vidar M, Andreassen Ole A, Hughes Timothy, Djurovic Srdj |
Complement C4 associations with altered microbial biomarkers exemplify gene-by-environment interactions in schizophrenia. Schizophrenia research 2021 2 234 87-93. Severance Emily G, Leister Flora, Lea Ashley, Yang Shuojia, Dickerson Faith, Yolken Robert |
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 |
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 |
Synthesis of genetic association studies on autism spectrum disorders using a genetic model-free approach. Psychiatric genetics 2022 3 32 (3): 91-104. Mpoulimari Ioanna, Zintzaras Eli |
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 |
Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosis. NPJ genomic medicine 2022 Oct 7 (1): 57. Kerick Martin, Acosta-Herrera Marialbert, Simeón-Aznar Carmen Pilar, Callejas José Luis, Assassi Shervin, , Proudman Susanna M, Nikpour Mandana, , , Hunzelmann Nicolas, Moroncini Gianluca, de Vries-Bouwstra Jeska K, Orozco Gisela, Barton Anne, Herrick Ariane L, Terao Chikashi, Allanore Yannick, Fonseca Carmen, Alarcón-Riquelme Marta Eugenia, Radstake Timothy R D J, Beretta Lorenzo, Denton Christopher P, Mayes Maureen D, Martin Javi |
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 |
Exploring genes for immunoglobulin A nephropathy: a summary data-based mendelian randomization and FUMA analysis. BMC medical genomics 2023 1 16 (1): 16. Zhang Qian, Zhang Kang, Zhu Yining, Yuan Guangwei, Yang Jingyun, Zhang Minm |
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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- Page last updated:Apr 16, 2024
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