Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: PLCL2[original query] |
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Comprehensive assessment of rheumatoid arthritis susceptibility loci in a large psoriatic arthritis cohort. Annals of the rheumatic diseases 2012 Aug 71 (8): 1350-4. Bowes John, Ho Pauline, Flynn Edward, Ali Faisal, Marzo-Ortega Helena, Coates Laura C, Warren Richard B, McManus Ross, Ryan Anthony W, Kane David, Korendowych Eleanor, McHugh Neil, FitzGerald Oliver, Packham Jonathon, Morgan Ann W, Bruce Ian N, Barton An |
A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese.
European journal of human genetics : EJHG 2015 Mar 23 (3): 374-80. Hirokawa Megumi, Morita Hiroyuki, Tajima Tomoyuki, Takahashi Atsushi, Ashikawa Kyota, Miya Fuyuki, Shigemizu Daichi, Ozaki Kouichi, Sakata Yasuhiko, Nakatani Daisaku, Suna Shinichiro, Imai Yasushi, Tanaka Toshihiro, Tsunoda Tatsuhiko, Matsuda Koichi, Kadowaki Takashi, Nakamura Yusuke, Nagai Ryozo, Komuro Issei, Kubo Michia |
Enhanced meta-analysis and replication studies identify five new psoriasis susceptibility loci.
Nature communications 2015 6 7001. Tsoi Lam C, Spain Sarah L, Ellinghaus Eva, Stuart Philip E, Capon Francesca, Knight Jo, Tejasvi Trilokraj, Kang Hyun M, Allen Michael H, Lambert Sylviane, Stoll Stefan W, Weidinger Stephan, Gudjonsson Johann E, Koks Sulev, Kingo Külli, Esko Tonu, Das Sayantan, Metspalu Andres, Weichenthal Michael, Enerback Charlotta, Krueger Gerald G, Voorhees John J, Chandran Vinod, Rosen Cheryl F, Rahman Proton, Gladman Dafna D, Reis Andre, Nair Rajan P, Franke Andre, Barker Jonathan N W N, Abecasis Goncalo R, Trembath Richard C, Elder James |
Identification of NF-?B and PLCL2 as new susceptibility genes and highlights on a potential role of IRF8 through interferon signature modulation in systemic sclerosis. Arthritis research & therapy 2015 17 (1): 71. Arismendi Maria, Giraud Matthieu, Ruzehaji Nadira, Dieudé Philippe, Koumakis Eugenie, Ruiz Barbara, Airo Paolo, Cusi Daniele, Matucci-Cerinic Marco, Salvi Erika, Cuomo Giovanna, Hachulla Eric, Diot Elisabeth, Caramaschi Paola, Riccieri Valeria, Avouac Jérôme, Kayser Cristiane, Allanore Yanni |
Investigation of the genetic overlap between rheumatoid arthritis and psoriatic arthritis in a Greek population. Scandinavian journal of rheumatology 2017 May 46 (3): 180-186. Myrthianou E, Zervou M I, Budu-Aggrey A, Eliopoulos E, Kardassis D, Boumpas D T, Kougkas N, Barton A, Sidiropoulos P, Goulielmos G |
Two Novel SNPs in the PLCL2 Gene Associated with Large Artery Atherosclerotic Stroke Identified by Fine-Mapping. Journal of molecular neuroscience : MN 2020 Jan . Huang Xiaoya, Zhu Zhenguo, Chen Yanyan, Li Jia, Xia Niange, Chen Siyan, Geng Wujun, Ye Zus |
Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits.
HGG advances 2021 Jan 2 (1): . Sun Daokun, Richard Melissa, Musani Solomon K, Sung Yun Ju, Winkler Thomas W, Schwander Karen, Chai Jin Fang, Guo Xiuqing, Kilpeläinen Tuomas O, Vojinovic Dina, Aschard Hugues, Bartz Traci M, Bielak Lawrence F, Brown Michael R, Chitrala Kumaraswamy, Hartwig Fernando P, Horimoto Andrea R V R, Liu Yongmei, Manning Alisa K, Noordam Raymond, Smith Albert V, Harris Sarah E, Kühnel Brigitte, Lyytikäinen Leo-Pekka, Nolte Ilja M, Rauramaa Rainer, van der Most Peter J, Wang Rujia, Ware Erin B, Weiss Stefan, Wen Wanqing, Yanek Lisa R, Arking Dan E, Arnett Donna K, Barac Ana, Boerwinkle Eric, Broeckel Ulrich, Chakravarti Aravinda, Chen Yii-Der Ida, Cupples L Adrienne, Davigulus Martha L, de Las Fuentes Lisa, de Mutsert Renée, de Vries Paul S, Delaney Joseph A C, Roux Ana V Diez, Dörr Marcus, Faul Jessica D, Fretts Amanda M, Gallo Linda C, Grabe Hans Jörgen, Gu C Charles, Harris Tamara B, Hartman Catharina C A, Heikkinen Sami, Ikram M Arfan, Isasi Carmen, Johnson W Craig, Jonas Jost Bruno, Kaplan Robert C, Komulainen Pirjo, Krieger Jose E, Levy Daniel, , Liu Jianjun, Lohman Kurt, Luik Annemarie I, Martin Lisa W, Meitinger Thomas, Milaneschi Yuri, O'Connell Jeff R, Palmas Walter R, Peters Annette, Peyser Patricia A, Pulkki-Råback Laura, Raffel Leslie J, Reiner Alex P, Rice Kenneth, Robinson Jennifer G, Rosendaal Frits R, Schmidt Carsten Oliver, Schreiner Pamela J, Schwettmann Lars, Shikany James M, Shu Xiao-Ou, Sidney Stephen, Sims Mario, Smith Jennifer A, Sotoodehnia Nona, Strauch Konstantin, Tai E Shyong, Taylor Kent, Uitterlinden André G, van Duijn Cornelia M, Waldenberger Melanie, Wee Hwee-Lin, Wei Wen-Bin, Wilson Gregory, Xuan Deng, Yao Jie, Zeng Donglin, Zhao Wei, Zhu Xiaofeng, Zonderman Alan B, Becker Diane M, Deary Ian J, Gieger Christian, Lakka Timo A, Lehtimäki Terho, North Kari E, Oldehinkel Albertine J, Penninx Brenda W J H, Snieder Harold, Wang Ya-Xing, Weir David R, Zheng Wei, Evans Michele K, Gauderman W James, Gudnason Vilmundur, Horta Bernardo L, Liu Ching-Ti, Mook-Kanamori Dennis O, Morrison Alanna C, Pereira Alexandre C, Psaty Bruce M, Amin Najaf, Fox Ervin R, Kooperberg Charles, Sim Xueling, Bierut Laura, Rotter Jerome I, Kardia Sharon L R, Franceschini Nora, Rao Dabeeru C, Fornage Myri |
Association of rs4618210A>G variant in PLCL2 gene with myocardial infarction: A case-control study in Iran. Journal of cardiovascular and thoracic research 2021 1 12 (4): 303-306. Ramezanpour Najmeh, Nasiri Mahboobeh, Akbarpour Omid Re |
Genome-wide association study of SARS-CoV-2 infection in Chinese population.
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology 2022 Sep 41 (9): 1155-1163. Fan Jie, Long Quan-Xin, Ren Ji-Hua, Chen Hao, Li Meng-Meng, Cheng Zheng, Chen Juan, Zhou Li, Huang Ai-Lo |
Fine-Mapping of the PLCL2 Gene Identifies Candidate Variants Associated With Ischaemic Stroke Risk in Metabolic Syndrome Patients. Frontiers in neurology 2022 2 12 743169. Huang Xiaoya, Ye Qiang, Zhang Yanlei, Chen Yanyan, Li Jia, Sun Jun, Ye Zus |
Genome-wide identification of RNA modification-related single nucleotide polymorphisms associated with rheumatoid arthritis. BMC genomics 2023 3 24 (1): 153. Wang Mimi, Wu Jingyun, Lei Shufeng, Mo Xing |
Exome-wide analysis identify multiple variations in olfactory receptor genes (OR12D2 and OR5V1) associated with autism spectrum disorder in Saudi females. Frontiers in medicine 2023 2 10 1051039. Almandil Noor B, Alismail Maram Adnan, Alsuwat Hind Saleh, AlSulaiman Abdulla, AbdulAzeez Sayed, Borgio J Franc |
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