Citations for
1FADS3, FCHL1, USF1
A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia.
Plaisier CL, Horvath S, Huertas-Vazquez A, Cruz-Bautista I, Herrera MF, Tusie-Luna T, Aguilar-Salinas C, Pajukanta P.
PLoS Genet 5(9):e1000642. Epub 2009 Sep 11.PMID: 19750004 2009
2FCHL1, USF1
Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides.
Coon H, Xin Y, Hopkins PN, Cawthon RM, Hasstedt SJ, Hunt SC.
Hum Genet 117(5):444-51. Epub 2005 Jun 16. 2005
3FCHL1, FCHL2, LCAT
Genetics of familial combined hyperlipidemia and risk of coronary heart disease.
Shoulders CC, Jones EL, Naoumova RP.
Hum Mol Genet 13 Spec No 1:R149-60. Epub 2004 Feb 05. 2004
4FCHL1, USF1
Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).
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.
Nat Genet 36(4):371-6. Epub 2004 Feb 29. 2004
5FCHL1
Contribution of Chromosome 1q21-q23 to Familial Combined Hyperlipidemia in Mexican Families.
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.
Ann Hum Genet 68(Pt 5):419-27. 2004
6FCHL1
Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL.
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.
Mamm Genome 12(3):238-45. 2001
7FCHL1
Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families.
Pei W, Baron H, MŸller-Myhsok B, Knoblauch H, Al-Yahyaee SA, Hui R, Wu X, Liu L, Busjahn A, Luft FC, Schuster H.
Clin Genet 57:29-34 2000
8FCHL1
Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23.
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.
Nat Genet 18(4):369-73. 1998
9FCHL1, SELP
The P-selectin gene is highly polymorphic : reduced frequency of the Pro715 allele carriers in patients with myocardial infarction.
Herrmann SM, et al.
Hum Mol Genet 7 : 1277-1284. 1998
10FCHL1, FCHL2
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.
Marcil M, et al.
J Lipid Res 37 : 309-319. 1996