Human Genome Epidemiology Literature Finder
Records 1 - 29 (of 29 Records) |
Query Trace: LMF1[original query] |
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Two novel rare variants of APOA5 gene found in subjects with severe hypertriglyceridemia. Clinica chimica acta; international journal of clinical chemistry 2011 Nov 412 (23-24): 2194-8. Pisciotta Livia, Fresa Raffaele, Bellocchio Antonella, Guido Virgilia, Priore Oliva Claudio, Calandra Sebastiano, Bertolini Stefa |
Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemia. Circulation. Cardiovascular genetics 2012 Feb 5 (1): 66-72. Johansen Christopher T, Wang Jian, McIntyre Adam D, Martins Rebecca A, Ban Matthew R, Lanktree Matthew B, Huff Murray W, Péterfy Miklós, Mehrabian Margarete, Lusis Aldons J, Kathiresan Sekar, Anand Sonia S, Yusuf Salim, Lee Ann-Hwee, Glimcher Laurie H, Cao Henian, Hegele Robert |
Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia. Journal of internal medicine 2012 Aug 272 (2): 185-96. Surendran R P, Visser M E, Heemelaar S, Wang J, Peter J, Defesche J C, Kuivenhoven J A, Hosseini M, Péterfy M, Kastelein J J P, Johansen C T, Hegele R A, Stroes E S G, Dallinga-Thie G |
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 |
[Identification of variants in LMF1 gene associated with primary hypertriglyceridemia]. Cli?nica e investigacio?n en arteriosclerosis : publicacio?n oficial de la Sociedad Espan?ola de Arteriosclerosis 0 27 (5): 246-52. Lamiquiz-Moneo Itziar, Bea Ana M, Mateo-Gallego Rocío, Baila-Rueda Lucía, Cenarro Ana, Pocoví Miguel, Civeira Fernando, de Castro-Orós Isab |
Rare genetic variants with large effect on triglycerides in subjects with a clinical diagnosis of familial vs nonfamilial hypertriglyceridemia. Journal of clinical lipidology 0 10 (4): 790-7. De Castro-Orós Isabel, Civeira Fernando, Pueyo María Jesús, Mateo-Gallego Rocío, Bolado-Carrancio Alfonso, Lamíquiz-Moneo Itziar, Álvarez-Sala Luis, Fabiani Fernando, Cofán Montserrat, Cenarro Ana, Rodríguez-Rey José Carlos, Ros Emilio, Pocoví Migu |
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 |
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 |
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 |
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 |
Genetic and functional studies of the LMF1 gene in Thai patients with severe hypertriglyceridemia. Molecular genetics and metabolism reports 2020 3 23 100576. Plengpanich Wanee, Muanpetch Suwanna, Charoen Supannika, Kiateprungvej Arunrat, Khovidhunkit Weerap |
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 |
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 |
Genome-Wide Association Study Identifies Multiple Susceptibility Loci for Malignant Neoplasms of the Brain in Taiwan. Journal of personalized medicine 2022 Jul 12 (7): . Lin Jang-Chun, Wu Yi-Chieh, Yang Fu-Chi, Tsai Jo-Ting, Huang David Yc, Liu Wei-Hs |
Australian genome-wide association study confirms higher female risk for adult glioma associated with variants in the region of CCDC26. Neuro-oncology 2022 12 . Alpen Karen, Vajdic Claire M, MacInnis Robert J, Milne Roger L, Koh Eng-Siew, Hovey Elizabeth, Harrup Rosemary, Bruinsma Fiona, Nguyen Tuong L, Li Shuai, Joseph David, Benke Geza, Dugué Pierre-Antoine, Southey Melissa C, Giles Graham G, Rosenthal Mark, Drummond Katharine J, Nowak Anna K, Hopper John L, Kapuscinski Miroslaw, Makalic En |
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 |
Association of LIPC polymorphisms with stroke risk in the Chinese population. Frontiers in neurology 2023 6 14 1095282. Jiaxing Pan, Qingqing Zhuo, Xu Chen, Xuehong Huang, Shiqiang Shen, Qiu Yang, Jiawen Luo, Suiyan Wang, Tianbo J |
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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