Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 41 Records) |
Query Trace: APOC2[original query] |
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Variants identified in a GWAS meta-analysis for blood lipids are associated with the lipid response to fenofibrate. PloS one 2012 7 (10): e48663. Aslibekyan Stella, Goodarzi Mark O, Frazier-Wood Alexis C, Yan Xiaofei, Irvin Marguerite R, Kim Eric, Tiwari Hemant K, Guo Xiuqing, Straka Robert J, Taylor Kent D, Tsai Michael Y, Hopkins Paul N, Korenman Stanley G, Borecki Ingrid B, Chen Yii-Der I, Ordovas Jose M, Rotter Jerome I, Arnett Donna |
Rare LPL gene variants attenuate triglyceride reduction and HDL cholesterol increase in response to fenofibric acid therapy in individuals with mixed dyslipidemia. Atherosclerosis 2014 Jun 234 (2): 249-53. Gao Feng, Ballantyne Christie, Ma Li, Virani Salim S, Keinan Alon, Brautbar Ari |
Genetic Variants Associated with Gestational Hypertriglyceridemia and Pancreatitis. PloS one 2015 10 (6): e0129488. Xie Sai-Li, Chen Tan-Zhou, Huang Xie-Lin, Chen Chao, Jin Rong, Huang Zhi-Ming, Zhou Meng-T |
Rare and common variants in LPL and APOA5 in Thai subjects with severe hypertriglyceridemia: A resequencing approach. Journal of clinical lipidology 0 10 (3): 505-511.e1. Khovidhunkit Weerapan, Charoen Supannika, Kiateprungvej Arunrat, Chartyingcharoen Palm, Muanpetch Suwanna, Plengpanich Wan |
Frequency of rare mutations and common genetic variations in severe hypertriglyceridemia in the general population of Spain. Lipids in health and disease 2016 15 (1): 82. Lamiquiz-Moneo Itziar, Blanco-Torrecilla Cristian, Bea Ana M, Mateo-Gallego Rocío, Pérez-Calahorra Sofía, Baila-Rueda Lucía, Cenarro Ana, Civeira Fernando, de Castro-Orós Isab |
Hypertriglyceridemic acute pancreatitis in emergency department: Typical clinical features and genetic variants. Journal of digestive diseases 2017 Jun 18 (6): 359-368. Chen Wan Jun, Sun Xiao Fan, Zhang Rui Xue, Xu Min Jie, Dou Tong Hai, Zhang Xiao Bin, Zhong Min, Yang Wei Qiang, Liu Li, Lu Xiao Ye, Zhu Chang Qi |
Genomic profile in gestational and non-gestational choriocarcinomas. Placenta 2017 02 50 8-15. Mello Julia Bette Homem de, Ramos Cirilo Priscila Daniele, Michelin Odair Carlito, Custódio Domingues Maria Aparecida, Cunha Rudge Marilza Vieira, Rogatto Silvia Regina, Maestá Izildin |
Variants of Lipolysis-Related Genes in Korean Patients with Very High Triglycerides. Yonsei medical journal 2017 12 59 (1): 148-153. Lee Chan Joo, Oum Chi Yoon, Lee Yunbeom, Park Sungha, Kang Seok Min, Choi Donghoon, Jang Yangsoo, Lee Ji Hyun, Lee Sang H |
Compound but non-linked heterozygous p.W14X and p.L279 V LPL gene mutations in a Chinese patient with long-term severe hypertriglyceridemia and recurrent acute pancreatitis. Lipids in health and disease 2018 6 17 (1): 144. Li Xiaoyao, Yang Qi, Shi Xiaolei, Chen Weiwei, Pu Na, Li Weiqin, Li Jiesh |
A Compound Heterozygous Mutation of Lipase Maturation Factor 1 is Responsible for Hypertriglyceridemia of a Patient. Journal of atherosclerosis and thrombosis 2018 6 26 (2): 136-144. Liu Yihui, Xu Jiang, Tao Wanyun, Yu Rong, Zhang Xinjia |
Clinical and biochemical features of different molecular etiologies of familial chylomicronemia. Journal of clinical lipidology 2018 Apr . Hegele Robert A, Berberich Amanda J, Ban Matthew R, Wang Jian, Digenio Andres, Alexander Veronica J, D'Erasmo Laura, Arca Marcello, Jones Alan, Bruckert Eric, Stroes Erik S, Bergeron Jean, Civeira Fernando, Witztum Joseph L, Gaudet Dani |
Severe hypertriglyceridemia is primarily polygenic. Journal of clinical lipidology 0 13 (1): 80-88. Dron Jacqueline S, Wang Jian, Cao Henian, McIntyre Adam D, Iacocca Michael A, Menard Jyler R, Movsesyan Irina, Malloy Mary J, Pullinger Clive R, Kane John P, Hegele Robert |
Intensive genetic analysis for Chinese patients with very high triglyceride levels: Relations of mutations to triglyceride levels and acute pancreatitis. EBioMedicine 2018 Dec 38 171-177. Jin Jing-Lu, Sun Di, Cao Ye-Xuan, Zhang Hui-Wen, Guo Yuan-Lin, Wu Na-Qiong, Zhu Cheng-Gang, Gao Ying, Dong Qiu-Ting, Liu Geng, Dong Qian, Li Jian-J |
Severe Combined Dyslipidemia With a Complex Genetic Basis. Journal of investigative medicine high impact case reports 2019 9 7 2324709619877050. Le Ryan, Abbas Minan, McIntyre Adam D, Hegele Robert |
Apolipoprotein E-C1-C4-C2 gene cluster region and inter-individual variation in plasma lipoprotein levels: a comprehensive genetic association study in two ethnic groups. PloS one 2019 14 (3): e0214060. Pirim Dilek, Radwan Zaheda H, Wang Xingbin, Niemsiri Vipavee, Hokanson John E, Hamman Richard F, Feingold Eleanor, Bunker Clareann H, Demirci F Yesim, Kamboh M Ily |
Identification of a novel and heterozygous LMF1 nonsense mutation in an acute pancreatitis patient with severe hypertriglyceridemia, severe obesity and heavy smoking. Lipids in health and disease 2019 3 18 (1): 68. Chen Wei-Wei, Yang Qi, Li Xiao-Yao, Shi Xiao-Lei, Pu Na, Lu Guo-Tao, Tong Zhi-Hui, Chen Jian-Min, Li Wei-Q |
Spectrum of Mutations and Long-Term Clinical Outcomes in Genetic Chylomicronemia Syndromes. Arteriosclerosis, thrombosis, and vascular biology 2019 10 39 (12): 2531-2541. D'Erasmo Laura, Di Costanzo Alessia, Cassandra Francesca, Minicocci Ilenia, Polito Luca, Montali Anna, Ceci Fabrizio, Arca Marcel |
The relationship between circulating lipids and breast cancer risk: A Mendelian randomization study. PLoS medicine 2020 9 17 (9): e1003302. Johnson Kelsey E, Siewert Katherine M, Klarin Derek, Damrauer Scott M, , Chang Kyong-Mi, Tsao Philip S, Assimes Themistocles L, Maxwell Kara N, Voight Benjamin |
Genetics of Hypertriglyceridemia. Frontiers in endocrinology 2020 8 11 455. Dron Jacqueline S, Hegele Robert |
Variants of Lipid-Related Genes in Adult Japanese Patients with Severe Hypertriglyceridemia. Journal of atherosclerosis and thrombosis 2020 3 27 (12): 1264-1277. Matsunaga Akira, Nagashima Mariko, Yamagishi Hideko, Saku Keiji |
Ancestry-specific profiles of genetic determinants of severe hypertriglyceridemia. Journal of clinical lipidology 2020 Nov . Gill Praneet K, Dron Jacqueline S, Dilliott Allison A, McIntyre Adam D, Cao Henian, Wang Jian, Movsesyan Irina G, Malloy Mary J, Pullinger Clive R, Kane John P, Hegele Robert |
Sequence analysis of the coding regions of the apolipoprotein C2 (APOC2) gene in Miniature Schnauzers with idiopathic hypertriglyceridemia. Veterinary journal (London, England : 1997) 2020 11 265 105559. Xenoulis Panagiotis G, Tate Nicole M, Bishop Micah A, Steiner Jörg M, Suchodolski Jan S, Furrow E |
Characterization of the Cerebrospinal Fluid Proteome in Patients with Fragile X-Associated Tremor/Ataxia Syndrome. Cerebellum (London, England) 2021 5 21 (1): 86-98. Abbasi Diana A, Nguyen Thu T A, Hall Deborah A, Robertson-Dick Erin, Berry-Kravis Elizabeth, Cologna Stephanie |
Rare Variants in Triglycerides-Related Genes Increase Pancreatitis Risk in Multifactorial Chylomicronemia Syndrome. The Journal of clinical endocrinology and metabolism 2021 5 106 (9): e3473-e3482. Paquette Martine, Amyot Julie, Fantino Manon, Baass Alexis, Bernard Soph |
Novel PPARG mutation in multiple family members with chylomicronemia. Journal of clinical lipidology 2021 4 15 (3): 431-434. Glodowski Michele, Christen Shannon, Saxon David R, Hegele Robert A, Eckel Robert |
Familial hypertriglyceridemia: an entity with distinguishable features from other causes of hypertriglyceridemia. Lipids in health and disease 2021 2 20 (1): 14. Cruz-Bautista Ivette, Huerta-Chagoya Alicia, Moreno-Macías Hortensia, Rodríguez-Guillén Rosario, Ordóñez-Sánchez María Luisa, Segura-Kato Yayoi, Mehta Roopa, Almeda-Valdés Paloma, Gómez-Munguía Lizeth, Ruiz-De Chávez Ximena, Rosas-Flota Ximena, Andrade-Amado Arali, Bernal-Barroeta Bárbara, López-Carrasco María Guadalupe, Guillén-Pineda Luz Elizabeth, López-Estrada Angelina, Elías-López Daniel, Martagón-Rosado Alexandro J, Gómez-Velasco Donají, Lam-Chung Cesar Ernesto, Bello-Chavolla Omar Yaxmehen, Del Razo-Olvera Fabiola, Cetina-Pérez Lucely D, Acosta-Rodríguez José Luis, Tusié-Luna María Teresa, Aguilar-Salinas Carlos |
Identification of genetic variants related to metabolic syndrome by next-generation sequencing. Diabetology & metabolic syndrome 2022 Aug 14 (1): 119. Lee Sanghoo, Kim Seol-A, Hong Jeonghoon, Kim Yejin, Hong Gayeon, Baik SaeYun, Choi Kyeonghwan, Lee Mi-Kyeong, Lee Kyoung-Ry |
Chromosomally Unstable Gastric Cancers Overexpressing Claudin-6 Disclose Cross-Talk between HNF1A and HNF4A, and Upregulated Cholesterol Metabolism. International journal of molecular sciences 2022 11 23 (22): . Dwivedi Sanyog, Hernández-Montes Georgina, Montaño Luis Felipe, Rendón-Huerta Erika Patric |
Clinical heterogeneity in monogenic chylomicronaemia. BMJ case reports 2022 11 15 (11): . Heidemann Britt E, Bemelmans Remy H H, Marais A David, Visseren Frank L J, Koopal Charlot |
Genetic Variants Associated with Severe Hypertriglyceridemia: LPL, APOC2, APOA5, GPIHBP1, LMF1, and APOE. Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir 2023 1 51 (1): 10-21. Abedi Amir Hossein, Y?ld?r?m ?im?ir Ilg?n, Bayram Fahri, Onay Huseyin, Özgür Su, Mcintyre Adam, Toth Peter, Hegele Robe |
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