-
1
-
-
63849198178
-
Hypertriglyceridemia and its pharmacologic treatment among US adults
-
Ford ES, Li C, Zhao G, Pearson WS, Mokdad AH. Hypertriglyceridemia and its pharmacologic treatment among US adults. Arch Intern Med. 2009;169:572-578
-
(2009)
Arch Intern Med
, vol.169
, pp. 572-578
-
-
Ford, E.S.1
Li, C.2
Zhao, G.3
Pearson, W.S.4
Mokdad, A.H.5
-
2
-
-
84862302879
-
Aragon workers' health study-design and cohort description
-
Casasnovas JA, Alcaide V, Civeira F, Guallar E, Ibañez B, Borreguero JJ, et al. Aragon workers' health study-design and cohort description. BMC Cardiovasc Disord. 2012;12:45
-
(2012)
BMC Cardiovasc Disord
, vol.12
, pp. 45
-
-
Casasnovas, J.A.1
Alcaide, V.2
Civeira, F.3
Guallar, E.4
Ibañez, B.5
Borreguero, J.J.6
-
3
-
-
77951875017
-
Triglyceride-mediated pathways and coronary disease: Collaborative analysis of 101 studies
-
Triglyceride Coronary Disease Genetics Consortium and Emerging Risk Factors Collaboration, Sarwar N, Sandhu MS Ricketts SL, Butterworth AS, Di Angelantonio E, et al
-
Triglyceride Coronary Disease Genetics Consortium and Emerging Risk Factors Collaboration, Sarwar N, Sandhu MS Ricketts SL, Butterworth AS, Di Angelantonio E, et al. Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies. Lancet. 2010;375:1634-1639
-
(2010)
Lancet
, vol.375
, pp. 1634-1639
-
-
-
4
-
-
84859049036
-
The association of hypertriglyceridemia with cardiovascular events and pancreatitis: A systematic review and meta-analysis
-
Murad MH, Hazem A, Coto-Yglesias F, Dzyubak S, Gupta S, Bancos I, Lane MA, et al. The association of hypertriglyceridemia with cardiovascular events and pancreatitis: a systematic review and meta-analysis. BMC Endocr Disord. 2012;12:2
-
(2012)
BMC Endocr Disord
, vol.12
, pp. 2
-
-
Murad, M.H.1
Hazem, A.2
Coto-Yglesias, F.3
Dzyubak, S.4
Gupta, S.5
Bancos, I.6
Lane, M.A.7
-
5
-
-
84866042826
-
Body mass index, triglycerides, glucose, and blood pressure as predictors of type 2 diabetes in a middle-aged Norwegian cohort of men and women
-
Hjellvik V, Sakshaug S, Strøm H. Body mass index, triglycerides, glucose, and blood pressure as predictors of type 2 diabetes in a middle-aged Norwegian cohort of men and women. Clin Epidemiol. 2012;4:213-224
-
(2012)
Clin Epidemiol
, vol.4
, pp. 213-224
-
-
Hjellvik, V.1
Sakshaug, S.2
Strøm, H.3
-
6
-
-
78649303807
-
Incidence of and risk factors for type-2 diabetes in a general population: The Tromsø Study
-
Joseph J, Svartberg J, Njølstad I, Schirmer H. Incidence of and risk factors for type-2 diabetes in a general population: the Tromsø Study. Scand J Public Health. 2010;38:768-775
-
(2010)
Scand J Public Health
, vol.38
, pp. 768-775
-
-
Joseph, J.1
Svartberg, J.2
Njølstad, I.3
Schirmer, H.4
-
7
-
-
70450081001
-
Major lipids, apolipoproteins, and risk of vascular disease
-
Di Angelantonio E, Sarwar N, Perry P, Kaptoge S, Ray KK, Thompson A, et al. Major lipids, apolipoproteins, and risk of vascular disease. JAMA. 2009;302:1993-2000
-
(2009)
JAMA
, vol.302
, pp. 1993-2000
-
-
Di Angelantonio, E.1
Sarwar, N.2
Perry, P.3
Kaptoge, S.4
Ray, K.K.5
Thompson, A.6
-
8
-
-
84866146620
-
Evaluation and treatment of hypertriglyceridemia: An Endocrine Society clinical practice guideline
-
Endocrine Society
-
Berglund L, Brunzell JD, Goldberg AC, Goldberg IJ, Sacks F, Murad MH, et al.; Endocrine Society. Evaluation and treatment of hypertriglyceridemia: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2012;97:2969-2989
-
(2012)
J Clin Endocrinol Metab
, vol.97
, pp. 2969-2989
-
-
Berglund, L.1
Brunzell, J.D.2
Goldberg, A.C.3
Goldberg, I.J.4
Sacks, F.5
Murad, M.H.6
-
9
-
-
84861347255
-
Apolipoprotein e gene mutations in subjects with mixed hyperlipidemia and a clinical diagnosis of familial combined hyperlipidemia
-
Solanas-Barca M, de Castro-Orós I, Mateo-Gallego R, Cofán M, Plana N, Puzo J, Burillo E, et al. Apolipoprotein E gene mutations in subjects with mixed hyperlipidemia and a clinical diagnosis of familial combined hyperlipidemia. Atherosclerosis. 2012;222:449-455
-
(2012)
Atherosclerosis
, vol.222
, pp. 449-455
-
-
Solanas-Barca, M.1
De Castro-Orós, I.2
Mateo-Gallego, R.3
Cofán, M.4
Plana, N.5
Puzo, J.6
Burillo, E.7
-
11
-
-
0042074140
-
Coronary artery disease risk in familial combined hyperlipidemia and familial hypertriglyceridemia: A case-control comparison from the National Heart, Lung, and Blood Institute Family Heart Study
-
Hopkins PN, Heiss G, Ellison RC, Province MA, Pankow JS, Eckfeldt JH, et al. Coronary artery disease risk in familial combined hyperlipidemia and familial hypertriglyceridemia: a case-control comparison from the National Heart, Lung, and Blood Institute Family Heart Study. Circulation. 2003;108:519-523
-
(2003)
Circulation
, vol.108
, pp. 519-523
-
-
Hopkins, P.N.1
Heiss, G.2
Ellison, R.C.3
Province, M.A.4
Pankow, J.S.5
Eckfeldt, J.H.6
-
12
-
-
84858783318
-
Finding genes and variants for lipid levels after genome-wide association analysis
-
Willer CJ, Mohlke KL. Finding genes and variants for lipid levels after genome-wide association analysis. Curr Opin Lipidol. 2012;23: 98-103
-
(2012)
Curr Opin Lipidol
, vol.23
, pp. 98-103
-
-
Willer, C.J.1
Mohlke, K.L.2
-
13
-
-
77955505564
-
Biological, clinical and population relevance of 95 loci for blood lipids
-
Teslovich TM, Musunuru K, Smith AV, Edmondson AC, Stylianou IM, Koseki M, et al. Biological, clinical and population relevance of 95 loci for blood lipids. Nature. 2010;466:707-713
-
(2010)
Nature
, vol.466
, pp. 707-713
-
-
Teslovich, T.M.1
Musunuru, K.2
Smith, A.V.3
Edmondson, A.C.4
Stylianou, I.M.5
Koseki, M.6
-
14
-
-
84887058576
-
Common variants associated with plasma triglycerides and risk for coronary artery disease
-
Do R, Willer CJ, Schmidt EM, Sengupta S, Gao C, Peloso GM, et al. Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat Genet. 2013;45:1345-1352
-
(2013)
Nat Genet
, vol.45
, pp. 1345-1352
-
-
Do, R.1
Willer, C.J.2
Schmidt, E.M.3
Sengupta, S.4
Gao, C.5
Peloso, G.M.6
-
15
-
-
84859163245
-
Allelic and phenotypic spectrum of plasma triglycerides
-
Johansen CT, Hegele RA. Allelic and phenotypic spectrum of plasma triglycerides. Biochim Biophys Acta. 2012;1821:833-842
-
(2012)
Biochim Biophys Acta
, vol.1821
, pp. 833-842
-
-
Johansen, C.T.1
Hegele, R.A.2
-
16
-
-
0037126526
-
Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report
-
National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III)
-
National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III). Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report. Circulation. 2002;106:3143-3421
-
(2002)
Circulation
, vol.106
, pp. 3143-3421
-
-
-
17
-
-
18844477352
-
Lipid profile of the Spanish population: The DRECE (diet and risk of cardiovascular disease in Spain) study
-
Gómez-Gerique JA, Gutiérrez-Fuentes JA, Montoya MT, Porres A, Rueda A, Avellaneda A, et al. Lipid profile of the Spanish population: the DRECE (diet and risk of cardiovascular disease in Spain) study. DRECE study group. Med Clin (Barc). 1999;113:730-735
-
(1999)
DRECE Study Group. Med Clin (Barc)
, vol.113
, pp. 730-735
-
-
Gómez-Gerique, J.A.1
Gutiérrez-Fuentes, J.A.2
Montoya, M.T.3
Porres, A.4
Rueda, A.5
Avellaneda, A.6
-
18
-
-
70449086254
-
Mutations in HFE causing hemochromatosis are associated with primary hypertriglyceridemia
-
Solanas-Barca M, Mateo-Gallego R, Calmarza P, Jarauta E, Bea AM, Cenarro A, et al. Mutations in HFE causing hemochromatosis are associated with primary hypertriglyceridemia. J Clin Endocrinol Metab. 2009;94:4391-4397
-
(2009)
J Clin Endocrinol Metab
, vol.94
, pp. 4391-4397
-
-
Solanas-Barca, M.1
Mateo-Gallego, R.2
Calmarza, P.3
Jarauta, E.4
Bea, A.M.5
Cenarro, A.6
-
19
-
-
76749163188
-
Carotid intima-media thickness in subjects with no cardiovascular risk factors
-
Jarauta E, Mateo-Gallego R, Bea A, Burillo E, Calmarza P, Civeira F. Carotid intima-media thickness in subjects with no cardiovascular risk factors. Rev Esp Cardiol. 2010;63:97-102
-
(2010)
Rev Esp Cardiol
, vol.63
, pp. 97-102
-
-
Jarauta, E.1
Mateo-Gallego, R.2
Bea, A.3
Burillo, E.4
Calmarza, P.5
Civeira, F.6
-
20
-
-
0036597746
-
Genetic association studies: Design, analysis and interpretation
-
Lewis CM. Genetic association studies: design, analysis and interpretation. Brief Bioinform. 2002;3:146-153
-
(2002)
Brief Bioinform
, vol.3
, pp. 146-153
-
-
Lewis, C.M.1
-
21
-
-
0029966556
-
Adjusting for multiple testing when reporting research results: The Bonferroni vs Holm methods
-
Aickin M, Gensler H. Adjusting for multiple testing when reporting research results: the Bonferroni vs Holm methods. Am J Public Health. 1996;86:726-728
-
(1996)
Am J Public Health
, vol.86
, pp. 726-728
-
-
Aickin, M.1
Gensler, H.2
-
22
-
-
84975795680
-
An integrated map of genetic variation from 1,092 human genomes
-
The 1000 Genomes Project Consortium
-
The 1000 Genomes Project Consortium. An integrated map of genetic variation from 1,092 human genomes. Nature. 2012;491:56-65
-
(2012)
Nature
, vol.491
, pp. 56-65
-
-
-
23
-
-
77955070766
-
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
-
Johansen CT, Wang J, Lanktree MB, et al. Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia. Nat Genet. 2010;42:684-687
-
(2010)
Nat Genet
, vol.42
, pp. 684-687
-
-
Johansen, C.T.1
Wang, J.2
Lanktree, M.B.3
-
24
-
-
84861329705
-
The genetics of familial combined hyperlipidaemia
-
Brouwers MC, van Greevenbroek MM, Stehouwer CD, de Graaf J, Stalenhoef AF. The genetics of familial combined hyperlipidaemia. Nat Rev Endocrinol. 2012;8:352-362
-
(2012)
Nat Rev Endocrinol
, vol.8
, pp. 352-362
-
-
Brouwers, M.C.1
Van Greevenbroek, M.M.2
Stehouwer, C.D.3
De Graaf, J.4
Stalenhoef, A.F.5
-
25
-
-
49649099805
-
Glucokinase and molecular aspects of liver glycogen metabolism
-
Agius L. Glucokinase and molecular aspects of liver glycogen metabolism. Biochem J. 2008;414:1-18
-
(2008)
Biochem J
, vol.414
, pp. 1-18
-
-
Agius, L.1
-
26
-
-
84887099827
-
Discovery and refinement of loci associated with lipid levels
-
Global Lipids Genetics Consortium, Willer CJ, Schmidt EM et al. Discovery and refinement of loci associated with lipid levels. Nat Genet. 2013;45:1274-1283
-
(2013)
Nat Genet
, vol.45
, pp. 1274-1283
-
-
Willer, C.J.1
Schmidt, E.M.2
-
27
-
-
70349656509
-
A systems Genetics Approach Implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia
-
Plaisier CL, Horvacth S, Huertas-Vazquz A, et al. A systems Genetics Approach Implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia. PLoS Gen. 2009;5:e1000642
-
(2009)
PLoS Gen
, vol.5
, pp. e1000642
-
-
Plaisier, C.L.1
Horvacth, S.2
Huertas-Vazquz, A.3
-
28
-
-
57149112963
-
Seven lipoprotein lipase gene polymorphisms, lipid fractions, and coronary disease: A HuGE Association Review and Meta-Analysis
-
Sagos GS, Tatt I, Salanti G, et al. Seven lipoprotein lipase gene polymorphisms, lipid fractions, and coronary disease: A HuGE Association Review and Meta-Analysis. Am J Epidemiol. 2008;168:1233-1246
-
(2008)
Am J Epidemiol
, vol.168
, pp. 1233-1246
-
-
Sagos, G.S.1
Tatt, I.2
Salanti, G.3
-
29
-
-
80051551063
-
An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemia
-
Johansen CT, Wang J, Lanktree MB, et al. An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemia. Arterioscler Thromb Vasc Biol. 2011;31:1916-1926
-
(2011)
Arterioscler Thromb Vasc Biol
, vol.31
, pp. 1916-1926
-
-
Johansen, C.T.1
Wang, J.2
Lanktree, M.B.3
-
30
-
-
84861227604
-
The complex genetic basis of plasma triglycerides
-
Johansen CT, Hegele RA. The complex genetic basis of plasma triglycerides. Curr Atheroscler Rep. 2012;14:227-234
-
(2012)
Curr Atheroscler Rep
, vol.14
, pp. 227-234
-
-
Johansen, C.T.1
Hegele, R.A.2
-
31
-
-
0035812707
-
An apolipoprotein influencing triglycerides in humans and mice revealed by comparative sequencing
-
Pennacchio LA, Olivier M, Hubacek JA, Cohen JC, Cox DR, Fruchart JC, Krauss RM, et al. An apolipoprotein influencing triglycerides in humans and mice revealed by comparative sequencing. Science. 2001;294:169-173
-
(2001)
Science
, vol.294
, pp. 169-173
-
-
Pennacchio, L.A.1
Olivier, M.2
Hubacek, J.A.3
Cohen, J.C.4
Cox, D.R.5
Fruchart, J.C.6
Krauss, R.M.7
-
33
-
-
70349980881
-
The P446L variant in GCKR associated with fasting plasma glucose and triglyceride levels exerts its effect through increased glucokinase activity in liver
-
Beer NL, Tribble ND, McCulloch LJ, Roos C, Johnson PR, Orho-Melander M, et al. The P446L variant in GCKR associated with fasting plasma glucose and triglyceride levels exerts its effect through increased glucokinase activity in liver. Hum Mol Genet. 2009;18:4081-4088.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 4081-4088
-
-
Beer, N.L.1
Tribble, N.D.2
McCulloch, L.J.3
Roos, C.4
Johnson, P.R.5
Orho-Melander, M.6
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