Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 61 Records) |
Query Trace: Syndrome and LPL[original query] |
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Zinc Finger 259 Gene Polymorphism rs964184 is Associated with Serum Triglyceride Levels and Metabolic Syndrome. International journal of molecular and cellular medicine 2016 5 (1): 8-18. Mirhafez Seyed Reza, Avan Amir, Pasdar Alireza, Khatamianfar Sara, Hosseinzadeh Leila, Ganjali Shiva, Movahedi Ali, Pirhoushiaran Maryam, Mellado Valentina Gómez, Rosace Domenico, van Krieken Anne, Nohtani Mahdi, Ferns Gordon A, Ghayour-Mobarhan Maj |
Association and interaction of APOA5, BUD13, CETP, LIPA and health-related behavior with metabolic syndrome in a Taiwanese population. Scientific reports 2016 Nov 6 36830. Lin Eugene, Kuo Po-Hsiu, Liu Yu-Li, Yang Albert C, Kao Chung-Feng, Tsai Shih-J |
Relationship Between Two Common Lipoprotein Lipase Variants and the Metabolic Syndrome and Its Individual Components. Metabolic syndrome and related disorders 2016 Sep . Vishram Julie K K, Hansen Tine W, Torp-Pedersen Christian, Madsbad Sten, Jørgensen Torben, Fenger Mogens, Lyngbæk Stig, Jeppesen Jørg |
Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib.
PloS one 2017 12 (7): e0182115. Yeo Astrid, Li Li, Warren Liling, Aponte Jennifer, Fraser Dana, King Karen, Johansson Kelley, Barnes Allison, MacPhee Colin, Davies Richard, Chissoe Stephanie, Tarka Elizabeth, O'Donoghue Michelle L, White Harvey D, Wallentin Lars, Waterworth Da |
Molecular and functional characterization of familial chylomicronemia syndrome. Atherosclerosis 2017 11 269 272-278. Teramoto Ryota, Tada Hayato, Kawashiri Masa-Aki, Nohara Atsushi, Nakahashi Takuya, Konno Tetsuo, Inazu Akihiro, Mabuchi Hiroshi, Yamagishi Masakazu, Hayashi Kens |
Genome-Wide Association Study Reveals Four Loci for Lipid Ratios in the Korean Population and the Constitutional Subgroup.
PloS one 2017 12 (1): e0168137. Kim Taehyeung, Park Ah Yeon, Baek Younghwa, Cha Seongw |
Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an "FCS score". Atherosclerosis 2018 7 275 265-272. Moulin Philippe, Dufour Robert, Averna Maurizio, Arca Marcello, Cefalù Angelo B, Noto Davide, D'Erasmo Laura, Di Costanzo Alessia, Marçais Christophe, Alvarez-Sala Walther Luis Antonio, Banach Maciej, Borén Jan, Cramb Robert, Gouni-Berthold Ioanna, Hughes Elizabeth, Johnson Colin, Pintó Xavier, Reiner Ċ½eljko, van Lennep Jeanine Roeters, Soran Handrean, Stefanutti Claudia, Stroes Erik, Bruckert Er |
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 |
Association of Multiple Genetic Variants with the Extension and Severity of Coronary Artery Disease. Arquivos brasileiros de cardiologia 2018 Jan 110 (1): 16-23. Fischer Simone Cristina Pinto Matheus, Pinto Simone Pires, Lins Lívia Campos do Amaral Silva, Bianco Henrique Tria, Monteiro Carlos Manoel de Castro, Pinheiro Luiz Fernando Muniz, Fonseca Francisco Antonio Helfenstein, Izar Maria Cristina de Olivei |
Candidate gene polymorphisms related to lipid metabolism in Asian Indians living in Durban, South Africa. The Indian journal of medical research 2018 Aug 148 (2): 169-179. Maistry Tanya, Gordon Michelle, Sartorius Benn, Naidoo Datshana |
Characterizing familial chylomicronemia syndrome: Baseline data of the APPROACH study. Journal of clinical lipidology 2018 10 12 (5): 1234-1243.e5. Blom Dirk J, O'Dea Louis, Digenio Andres, Alexander Veronica J, Karwatowska-Prokopczuk Ewa, Williams Karren R, Hemphill Linda, Muñiz-Grijalvo Ovidio, Santos Raul D, Baum Seth, Witztum Joseph |
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 |
A 3-SNP gene risk score and a metabolic risk score both predict hypertriglyceridemia and cardiovascular disease risk. Journal of clinical lipidology 2019 Feb . Verbeek Rutger, Oldoni Federico, Surendran R Preethi, Zwinderman Ailko H, Khaw Kay T, Stroes Erik S G, Wareham Nick J, Boekholdt S Matthijs, Dallinga-Thie Geesje |
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 |
Association of Candidate Gene Polymorphism with Metabolic Syndrome among Mongolian Subjects: A Case-Control Study. Medical sciences (Basel, Switzerland) 2020 Sep 8 (3): . Chuluun-Erdene Ariunbold, Sengeragchaa Orgil, Altangerel Tsend-Ayush, Sanjmyatav Purevjal, Dagdan Batnaran, Battulga Solongo, Enkhbat Lundiamaa, Byambasuren Nyamjav, Malchinkhuu Munkhzol, Janlav Munkhtstets |
Association of polymorphism genes null , null , null and null with risk of hyperinsulinism and insulin resistance in the Kazakh population. Biomedical reports 2020 Nov 13 (5): 35. Shakhanova Aizhan, Aukenov Nurlan, Nurtazina Alma, Massabayeva Meruyert, Babenko Dmitriy, Adiyeva Madina, Shaimardonov Nurl |
Genetics of Hypertriglyceridemia. Frontiers in endocrinology 2020 8 11 455. Dron Jacqueline S, Hegele Robert |
Age Stratification in Genetic Variation of Lipoprotein Lipase in Metabolic Syndrome Javanese Ethnics of Indonesia. Open access Macedonian journal of medical sciences 2019 Nov 7 (21): 3540-3545. Mus Rosdiana, Sadewa Ahmad Hamim, Hastuti Pramudji, Puspasari Anggelia, Maharani Citra, Setyawati I |
Association of Metabolic Syndrome with Aerobic Exercise and LPL rs3779788 Polymorphism in Taiwan Biobank Individuals. Diabetes, metabolic syndrome and obesity : targets and therapy 2021 14 3997-4004. Hsu Chun-Sheng, Chang Shin-Tsu, Nfor Oswald Ndi, Lee Kuan-Jung, Ho Chien-Chang, Liu Chuan-Ching, Lee Shiuan-Shinn, Liaw Yung- |
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 |
Polymorphism rs10105606 of LPL as a Novel Risk Factor for Microalbuminuria.
Journal of inflammation research 2021 12 14 6833-6844. Lim Zhu Wei, Chen Wei Lia |
Frameshift coding sequence variants in the LPL gene: identification of two novel events and exploration of the genotype-phenotype relationship for variants reported to date. Lipids in health and disease 2023 8 22 (1): 128. Guofu Zhang, Yuepeng Hu, Qi Yang, Na Pu, Gang Li, Jingzhu Zhang, Zhihui Tong, Emmanuelle Masson, David N Cooper, Jian-Min Chen, Weiqin |
A bidirectional link between metabolic syndrome and elevation in alanine aminotransferase in elderly female: a longitudinal community study. Frontiers in cardiovascular medicine 2023 7 10 1156123. Na Wu, Mofan Feng, Hanhua Zhao, Nan Tang, Yalan Xiong, Xinyu Shi, Dong Li, Hualing Song, Shengfu You, Jianying Wang, Lei Zhang, Guang Ji, Baocheng L |
Effect of the Interaction between Seaweed Intake and LPL Polymorphisms on Metabolic Syndrome in Middle-Aged Korean Adults. Nutrients 2023 7 15 (9): . Junkyung Kwak, Gayeon Hong, Kyung Ju Lee, Choong-Gon Kim, Dayeon Sh |
Post-prandial analysis of fluctuations in the platelet count and platelet function in patients with the familial chylomicronemia syndrome. Orphanet journal of rare diseases 2023 6 18 (1): 167. Miriam Larouche, Diane Brisson, Marie-Claude Morissette, Daniel Gaud |
Evinacumab in severe hypertriglyceridemia with or without lipoprotein lipase pathway mutations: a phase 2 randomized trial. Nature medicine 2023 3 . Rosenson Robert S, Gaudet Daniel, Ballantyne Christie M, Baum Seth J, Bergeron Jean, Kershaw Erin E, Moriarty Patrick M, Rubba Paolo, Whitcomb David C, Banerjee Poulabi, Gewitz Andrew, Gonzaga-Jauregui Claudia, McGinniss Jennifer, Ponda Manish P, Pordy Robert, Zhao Jian, Rader Daniel |
Role of lipoprotein lipase activity measurement in the diagnosis of familial chylomicronemia syndrome. Journal of clinical lipidology 2023 2 . Rioja José, Ariza María José, Benítez-Toledo María José, Espíldora-Hernández Javier, Coca-Prieto Inmaculada, Arrobas-Velilla Teresa, Camacho Ana, Olivecrona Gunilla, Sánchez-Chaparro Miguel Ángel, Valdivielso Ped |
Loss-of-Function Homozygous Variant in LPL Causes Type I Hyperlipoproteinemia and Renal Lipidosis. Kidney international reports 2023 11 8 (11): 2428-2438. Hongyan Wu, Huan Xu, Song Lei, Zhi Yang, Shan Yang, Jingxue Du, Yi Zhou, Yunqiang Liu, Yuan Yang, Zhangxue |
Molecular genetic testing and measurement of levels of GPIHBP1 autoantibodies in patients with severe hypertriglyceridemia: The importance of identifying the underlying cause of hypertriglyceridemia. Journal of clinical lipidology 2023 11 . Thea Bismo Strøm, Anders Aune Tveita, Martin Prøven Bogsrud, Trond P Ler |
A Genome-Wide Association Study of Metabolic Syndrome in the Taiwanese Population. Nutrients 2024 1 16 (1): . Chih-Yi Ho, Jia-In Lee, Shu-Pin Huang, Szu-Chia Chen, Jiun-Hung Ge |
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- Page last updated:Apr 22, 2024
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