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Journal Abstract Search

300 related items for PubMed ID: 27108409

  • 1. Frequency of rare mutations and common genetic variations in severe hypertriglyceridemia in the general population of Spain.
    Lamiquiz-Moneo I, Blanco-Torrecilla C, Bea AM, Mateo-Gallego R, Pérez-Calahorra S, Baila-Rueda L, Cenarro A, Civeira F, de Castro-Orós I.
    Lipids Health Dis; 2016 Apr 23; 15():82. PubMed ID: 27108409
    [Abstract] [Full Text] [Related]

  • 2. Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia.
    Surendran RP, Visser ME, Heemelaar S, Wang J, Peter J, Defesche JC, Kuivenhoven JA, Hosseini M, Péterfy M, Kastelein JJ, Johansen CT, Hegele RA, Stroes ES, Dallinga-Thie GM.
    J Intern Med; 2012 Aug 23; 272(2):185-96. PubMed ID: 22239554
    [Abstract] [Full Text] [Related]

  • 3. Genetic Variants Associated with Severe Hypertriglyceridemia: LPL, APOC2, APOA5, GPIHBP1, LMF1, and APOE.
    Abedi AH, Yıldırım Şimşir I, Bayram F, Onay H, Özgür S, Mcintyre AD, Toth PP, Hegele RA.
    Turk Kardiyol Dern Ars; 2023 Jan 23; 51(1):10-21. PubMed ID: 36689289
    [Abstract] [Full Text] [Related]

  • 4. Severe hypertriglyceridemia is primarily polygenic.
    Dron JS, Wang J, Cao H, McIntyre AD, Iacocca MA, Menard JR, Movsesyan I, Malloy MJ, Pullinger CR, Kane JP, Hegele RA.
    J Clin Lipidol; 2019 Jan 23; 13(1):80-88. PubMed ID: 30466821
    [Abstract] [Full Text] [Related]

  • 5. Ancestry-specific profiles of genetic determinants of severe hypertriglyceridemia.
    Gill PK, Dron JS, Dilliott AA, McIntyre AD, Cao H, Wang J, Movsesyan IG, Malloy MJ, Pullinger CR, Kane JP, Hegele RA.
    J Clin Lipidol; 2021 Jan 23; 15(1):88-96. PubMed ID: 33303403
    [Abstract] [Full Text] [Related]

  • 6. Rare and common variants in LPL and APOA5 in Thai subjects with severe hypertriglyceridemia: A resequencing approach.
    Khovidhunkit W, Charoen S, Kiateprungvej A, Chartyingcharoen P, Muanpetch S, Plengpanich W.
    J Clin Lipidol; 2016 Jan 23; 10(3):505-511.e1. PubMed ID: 27206937
    [Abstract] [Full Text] [Related]

  • 7. Rare genetic variants with large effect on triglycerides in subjects with a clinical diagnosis of familial vs nonfamilial hypertriglyceridemia.
    De Castro-Orós I, Civeira F, Pueyo MJ, Mateo-Gallego R, Bolado-Carrancio A, Lamíquiz-Moneo I, Álvarez-Sala L, Fabiani F, Cofán M, Cenarro A, Rodríguez-Rey JC, Ros E, Pocoví M.
    J Clin Lipidol; 2016 Jan 23; 10(4):790-797. PubMed ID: 27578109
    [Abstract] [Full Text] [Related]

  • 8. [Identification of variants in LMF1 gene associated with primary hypertriglyceridemia].
    Lamiquiz-Moneo I, Bea AM, Mateo-Gallego R, Baila-Rueda L, Cenarro A, Pocoví M, Civeira F, de Castro-Orós I.
    Clin Investig Arterioscler; 2015 Jan 23; 27(5):246-52. PubMed ID: 25817768
    [Abstract] [Full Text] [Related]

  • 9. Extreme hypertriglyceridemia: Genetic diversity, pancreatitis, pregnancy, and prevalence.
    Chyzhyk V, Kozmic S, Brown AS, Hudgins LC, Starc TJ, Davila AD, Blevins TC, Diffenderfer MR, He L, Geller AS, Rush C, Hegele RA, Schaefer EJ.
    J Clin Lipidol; 2019 Jan 23; 13(1):89-99. PubMed ID: 30352774
    [Abstract] [Full Text] [Related]

  • 10. Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceride.
    Buonuomo PS, Rabacchi C, Macchiaiolo M, Trenti C, Fasano T, Tarugi P, Bartuli A, Bertolini S, Calandra S.
    J Clin Lipidol; 2017 Jan 23; 11(6):1329-1337.e3. PubMed ID: 28951076
    [Abstract] [Full Text] [Related]

  • 11. Genotype-phenotype relationships in patients with type I hyperlipoproteinemia.
    Chokshi N, Blumenschein SD, Ahmad Z, Garg A.
    J Clin Lipidol; 2014 Jan 23; 8(3):287-95. PubMed ID: 24793350
    [Abstract] [Full Text] [Related]

  • 12. Two novel rare variants of APOA5 gene found in subjects with severe hypertriglyceridemia.
    Pisciotta L, Fresa R, Bellocchio A, Guido V, Priore Oliva C, Calandra S, Bertolini S.
    Clin Chim Acta; 2011 Nov 20; 412(23-24):2194-8. PubMed ID: 21846464
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  • 14. Additive effects of LPL, APOA5 and APOE variant combinations on triglyceride levels and hypertriglyceridemia: results of the ICARIA genetic sub-study.
    Ariza MJ, Sánchez-Chaparro MA, Barón FJ, Hornos AM, Calvo-Bonacho E, Rioja J, Valdivielso P, Gelpi JA, González-Santos P.
    BMC Med Genet; 2010 Apr 29; 11():66. PubMed ID: 20429872
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  • 16. Resequencing genomic DNA of patients with severe hypertriglyceridemia (MIM 144650).
    Wang J, Cao H, Ban MR, Kennedy BA, Zhu S, Anand S, Yusuf S, Pollex RL, Hegele RA.
    Arterioscler Thromb Vasc Biol; 2007 Nov 29; 27(11):2450-5. PubMed ID: 17717288
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  • 18. Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia.
    Rabacchi C, Pisciotta L, Cefalù AB, Noto D, Fresa R, Tarugi P, Averna M, Bertolini S, Calandra S.
    Atherosclerosis; 2015 Jul 29; 241(1):79-86. PubMed ID: 25966443
    [Abstract] [Full Text] [Related]

  • 19. Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemia.
    Johansen CT, Wang J, McIntyre AD, Martins RA, Ban MR, Lanktree MB, Huff MW, Péterfy M, Mehrabian M, Lusis AJ, Kathiresan S, Anand SS, Yusuf S, Lee AH, Glimcher LH, Cao H, Hegele RA.
    Circ Cardiovasc Genet; 2012 Feb 01; 5(1):66-72. PubMed ID: 22135386
    [Abstract] [Full Text] [Related]

  • 20. Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing.
    Cefalù AB, Spina R, Noto D, Ingrassia V, Valenti V, Giammanco A, Fayer F, Misiano G, Cocorullo G, Scrimali C, Palesano O, Altieri GI, Ganci A, Barbagallo CM, Averna MR.
    J Clin Lipidol; 2017 Feb 01; 11(1):272-281.e8. PubMed ID: 28391895
    [Abstract] [Full Text] [Related]

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