1 | FADS3, FCHL1, USF1
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| A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia.
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| Plaisier CL, Horvath S, Huertas-Vazquez A, Cruz-Bautista I, Herrera MF, Tusie-Luna T, Aguilar-Salinas C, Pajukanta P.
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| PLoS Genet 5(9):e1000642. Epub 2009 Sep 11.PMID: 19750004 2009
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2 | FCHL1, USF1
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| Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides.
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| Coon H, Xin Y, Hopkins PN, Cawthon RM, Hasstedt SJ, Hunt SC.
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| Hum Genet 117(5):444-51. Epub 2005 Jun 16. 2005
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3 | FCHL1, FCHL2, LCAT
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| Genetics of familial combined hyperlipidemia and risk of coronary heart disease.
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| Shoulders CC, Jones EL, Naoumova RP.
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| Hum Mol Genet 13 Spec No 1:R149-60. Epub 2004 Feb 05. 2004
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4 | FCHL1, USF1
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| Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).
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| Pajukanta P, Lilja HE, Sinsheimer JS, Cantor RM, Lusis AJ, Gentile M, Duan XJ, Soro-Paavonen A, Naukkarinen J, Saarela J, Laakso M, Ehnholm C, Taskinen MR, Peltonen L.
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| Nat Genet 36(4):371-6. Epub 2004 Feb 29. 2004
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5 | FCHL1
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| Contribution of Chromosome 1q21-q23 to Familial Combined Hyperlipidemia in Mexican Families.
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| Huertas-Vazquez A, Del Rincon JP, Canizales-Quinteros S, Riba L, Vega-Hernandez G, Ramirez-Jimenez S, Auron-Gomez M, Gomez-Perez FJ, Aguilar-Salinas CA, Tusie-Luna MT.
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| Ann Hum Genet 68(Pt 5):419-27. 2004
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6 | FCHL1
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| Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL.
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| Pajukanta P, Bodnar JS, Sallinen R, Chu M, Airaksinen T, Xiao Q, Castellani LW, Sheth SS, Wessman M, Palotie A, Sinsheimer JS, Demant P, Lusis AJ, Peltonen L.
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| Mamm Genome 12(3):238-45. 2001
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7 | FCHL1
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| Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families.
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| Pei W, Baron H, MŸller-Myhsok B, Knoblauch H, Al-Yahyaee SA, Hui R, Wu X, Liu L, Busjahn A, Luft FC, Schuster H.
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| Clin Genet 57:29-34 2000
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8 | FCHL1
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| Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23.
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| Pajukanta P, Nuotio I, Terwilliger JD, Porkka KV, Ylitalo K, Pihlajamaki J, Suomalainen AJ, Syvanen AC, Lehtimaki T, Viikari JS, Laakso M, Taskinen MR, Ehnholm C, Peltonen L.
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| Nat Genet 18(4):369-73. 1998
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9 | FCHL1, SELP
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| The P-selectin gene is highly polymorphic : reduced frequency of the Pro715 allele carriers in patients with myocardial infarction.
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| Herrmann SM, et al.
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| Hum Mol Genet 7 : 1277-1284. 1998
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10 | FCHL1, FCHL2
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| Lack of association of the apolipoprotein AI-CIII-AIV gene XmnI and SstI polymorphisms and of the lipoprotein lipase gene mutations in familial combined hyperlipoproteinemia in French Canadian subjects.
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| Marcil M, et al.
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| J Lipid Res 37 : 309-319. 1996
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