HuGE Literature Finder
Records
1
-
30
| 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 |
| Genetic Variants Associated With Increased Plasma Levels of Triglycerides, via Effects on the Lipoprotein Lipase Pathway, Increase Risk of Acute Pancreatitis. Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 2020 Aug . Hansen Signe E J, Madsen Christian M, Varbo Anette, Tybjærg-Hansen Anne, Nordestgaard Børge |
| Gender-related relation between metabolic syndrome and S447X and HindIII polymorphisms of lipoprotein lipase gene in northern Iran. Gene 2019 Apr 706 13-18. Alinaghian Nazila, Abdollahi Elaheh, Torab Mansour, Khodaparast Maral, Zamani Farhad, Rahimi-Moghaddam Parvan |
| 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 |
| 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 |
| LPL gene Pvu II polymorphism and hypertriglyceridemia: a meta-analysis involving 1,640 subjects. The Korean journal of internal medicine 2017 May . Li Yan-Yan, Zhou Yan-Hong, Gong Ge, Geng Hong-Yu, Yang Xin-Xing, Wang Xiang-Ming, Zhou Chuan-Wei, Xu Jian, Qian Y |
| Study of Common Genetic Variant S447X in Lipoprotein Lipase and Its Association with Lipids and Lipoproteins in Type 2 Diabetic Patients. Indian journal of clinical biochemistry : IJCB 2016 Jul 31 (3): 286-93. Momin A A, Bankar M P, Bhoite G |
| 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 |
| Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia. Atherosclerosis 2015 Jul 241 (1): 79-86. Rabacchi Claudio, Pisciotta Livia, Cefalù Angelo B, Noto Davide, Fresa Raffaele, Tarugi Patrizia, Averna Maurizio, Bertolini Stefano, Calandra Sebastia |
| The -93T/G LPL Promoter Polymorphism Is Associated With Lower Third-Trimester Triglycerides in Pregnant African American Women. Biological research for nursing 2015 Jul 17 (4): 429-37. Schmella Mandy J, Ferrell Robert E, Gallaher Marcia J, Lykins David L, Althouse Andrew D, Roberts James M, Hubel Carl |
| 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 |
| Polymorphisms in LPL, CETP, and HL protect HIV-infected patients from atherogenic dyslipidemia in an allele-dose-dependent manner. Journal of the International AIDS Society 2014 17 (4 Suppl 3): 19557. Echeverría Patricia, Guardiola Montse, González Marta, Vallvé Joan Carles, Puig Jordi, Bonjoch Anna, Clotet Bonaventura, Ribalta Josep, Negredo Eugen |
| Resequencing the untranslated regions of the lipoprotein lipase (LPL) gene reveals that variants in microRNA target sequences are associated with triglyceride levels. Journal of clinical lipidology 2013 7 (6): 6. Evans D, Beil FU, Aberle J |
| A lipoprotein lipase gene polymorphism interacts with consumption of alcohol and unsaturated fat to modulate serum HDL-cholesterol concentrations. The Journal of nutrition 2013 Oct 143 (10): 1618-25. Baik Inkyung, Lee Seungku, Kim Seong Hwan, Shin Ch |
| [Hypertriglyceridemia-induced pancreatitis]. Nihon rinsho. Japanese journal of clinical medicine 2013 Sep 71 (9): 1602-5. Nagayama Daiji, Shirai Koh |
Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.
Journal of medical genetics 2013 May 50 (5): 298-308. Weissglas-Volkov Daphna, Aguilar-Salinas Carlos A, Nikkola Elina, Deere Kerry A, Cruz-Bautista Ivette, Arellano-Campos Olimpia, Muñoz-Hernandez Linda Liliana, Gomez-Munguia Lizeth, Ordoñez-Sánchez Maria Luisa, Reddy Prasad M V Linga, Lusis Aldons J, Matikainen Niina, Taskinen Marja-Riitta, Riba Laura, Cantor Rita M, Sinsheimer Janet S, Tusie-Luna Teresa, Pajukanta Päi |
| The g.-469G>A polymorphism in the GPIHBP1 gene promoter is associated with hypertriglyceridemia and has an additive effect on the risk conferred by LPL defective alleles. Nutrition, metabolism, and cardiovascular diseases : NMCD 2013 Apr 23 (4): 358-65. Guay S P, Gaudet D, Brisson |
| 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 |
| Rare variants in the lipoprotein lipase (LPL) gene are common in hypertriglyceridemia but rare in Type III hyperlipidemia. Atherosclerosis 2010 Nov . Evans D, Arzer J, Aberle J, Beil FU |
| Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.
Nature genetics 2010 Aug 42 (8): 684-7. Johansen Christopher T, Wang Jian, Lanktree Matthew B, Cao Henian, McIntyre Adam D, Ban Matthew R, Martins Rebecca A, Kennedy Brooke A, Hassell Reina G, Visser Maartje E, Schwartz Stephen M, Voight Benjamin F, Elosua Roberto, Salomaa Veikko, O'Donnell Christopher J, Dallinga-Thie Geesje M, Anand Sonia S, Yusuf Salim, Huff Murray W, Kathiresan Sekar, Hegele Robert |
| Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples. Circulation. Cardiovascular genetics 2010 Feb 3 (1): 31-8. Weissglas-Volkov Daphna, Aguilar-Salinas Carlos A, Sinsheimer Janet S, Riba Laura, Huertas-Vazquez Adriana, Ordoñez-Sánchez Maria L, Rodriguez-Guillen Rosario, Cantor Rita M, Tusie-Luna Teresa, Pajukanta Päi |
| Additive effects of LPL, APOA5 and APOE variant combinations on triglyceride levels and hypertriglyceridemia: results of the ICARIA genetic sub-study. BMC medical genetics 2010 11 (1): 66. Ariza María-José, Sánchez-Chaparro Miguel-Angel, Barón Francisco-Javier, Hornos Ana-María, Calvo-Bonacho Eva, Rioja José, Valdivielso Pedro, Gelpi José-Antonio, González-Santos Ped |
| Lipoprotein lipase mutation S447X associated with pancreatic calcification and steatorrhea in hyperlipidemic pancreatitis. Journal of clinical gastroenterology 2009 Jul 43 (6): 591-6. Chang Yu-Ting, Chang Ming-Chu, Su Ta-Chen, Liang Po-Chin, Su Yi-Ning, Kuo Chun-Hung, Wei Shu-Chen, Wong Jau-M |
| Common sequence variant in lipoprotein lipase gene conferring triglyceride response to fibrate treatment. Pharmacogenomics 2009 Feb 10 (2): 267-76. Chien Kuo-Liong, Lin Yen-Lin, Wen Hui-Chin, Lin Hsing-Pei, Yen Ching-Tzu, Lin Shu-Wha, Kao Jau-Tsu |
| Effects of six APOA5 variants, identified in patients with severe hypertriglyceridemia, on in vitro lipoprotein lipase activity and receptor binding. Arteriosclerosis, thrombosis, and vascular biology 2008 Oct 28 (10): 1866-71. Dorfmeister B, Zeng W W, Dichlberger A, Nilsson S K, Schaap F G, Hubacek J A, Merkel M, Cooper J A, Lookene A, Putt W, Whittall R, Lee P J, Lins L, Delsaux N, Nierman M, Kuivenhoven J A, Kastelein J J P, Vrablik M, Olivecrona G, Schneider W J, Heeren J, Humphries S E, Talmud P |
| [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 |
| Pathogenic classification of LPL gene variants reported to be associated with LPL deficiency. Journal of clinical lipidology 0 10 (2): 394-409. Rodrigues Rute, Artieda Marta, Tejedor Diego, Martínez Antonio, Konstantinova Pavlina, Petry Harald, Meyer Christian, Corzo Deyanira, Sundgreen Claus, Klor Hans U, Gouni-Berthold Ioanna, Westphal Sabine, Steinhagen-Thiessen Elisabeth, Julius Ulrich, Winkler Karl, Stroes Erik, Vogt Anja, Hardt Phillip, Prophet Heinrich, Otte Britta, Nordestgaard Borge G, Deeb Samir S, Brunzell John |
| 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 |
| Relationship of lipoprotein lipase gene variants and fasting triglyceride levels in a pediatric population: The CASPIAN-III study. Advances in clinical and experimental medicine : official organ Wroclaw Medical University 0 26 (1): 77-82. Kelishadi Roya, Hashemipour Mahin, Esteki Behnoosh, Tajadini Mohammad Hasan, Rafiei Laleh, Motlagh Mohammad Esmaeil, Vaseghi Golnaz, Ardalan Gelayol, Javanmard Shaghayegh Haghjo |
| 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 |
- Page last reviewed:Jul 25, 2022
- Page last updated:Dec 02, 2022
- Content source: