-
1
-
-
0023807047
-
Low-density lipoprotein subclass patterns and risk of myocardial infarction
-
Austin MA, Breslow JL, Hennekens CH, Buring JE, Willett WC, et al. (1988) Low-density lipoprotein subclass patterns and risk of myocardial infarction. JAMA 260(13): 1917-1921.
-
(1988)
JAMA
, vol.260
, Issue.13
, pp. 1917-1921
-
-
Austin, M.A.1
Breslow, J.L.2
Hennekens, C.H.3
Buring, J.E.4
Willett, W.C.5
-
2
-
-
0029741921
-
A prospective study of triglyceride level, low-density lipoprotein particle diameter, and risk of myocardial infarction
-
Stampfer MJ, Krauss RM, Ma J, Blanche PJ, Holl LG, et al. (1996) A prospective study of triglyceride level, low-density lipoprotein particle diameter, and risk of myocardial infarction. JAMA 276(11): 882-888.
-
(1996)
JAMA
, vol.276
, Issue.11
, pp. 882-888
-
-
Stampfer, M.J.1
Krauss, R.M.2
Ma, J.3
Blanche, P.J.4
Holl, L.G.5
-
3
-
-
33644861577
-
Increased small low-density lipoprotein particle number: A prominent feature of the metabolic syndrome in the Framingham Heart Study
-
Kathiresan S, Otvos JD, Sullivan LM, Keyes MJ, Schaefer EJ, et al. (2006) Increased small low-density lipoprotein particle number: a prominent feature of the metabolic syndrome in the Framingham Heart Study. Circulation 113(1): 20-29.
-
(2006)
Circulation
, vol.113
, Issue.1
, pp. 20-29
-
-
Kathiresan, S.1
Otvos, J.D.2
Sullivan, L.M.3
Keyes, M.J.4
Schaefer, E.J.5
-
4
-
-
61849110301
-
Lipoprotein particle profiles by nuclear magnetic resonance compared with standard lipids and apolipoproteins in predicting incident cardiovascular disease in women
-
Mora S, Otvos JD, Rifai N, Rosenson RS, Buring JE, et al. (2009) Lipoprotein particle profiles by nuclear magnetic resonance compared with standard lipids and apolipoproteins in predicting incident cardiovascular disease in women. Circulation 119(7): 931-939.
-
(2009)
Circulation
, vol.119
, Issue.7
, pp. 931-939
-
-
Mora, S.1
Otvos, J.D.2
Rifai, N.3
Rosenson, R.S.4
Buring, J.E.5
-
5
-
-
38649132270
-
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
-
Kathiresan S, Melander O, Guiducci C, Surti A, Burtt NP, et al. (2008) Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. Nat Genet 40(2): 189-197.
-
(2008)
Nat Genet
, vol.40
, Issue.2
, pp. 189-197
-
-
Kathiresan, S.1
Melander, O.2
Guiducci, C.3
Surti, A.4
Burtt, N.P.5
-
6
-
-
38649125868
-
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
-
Willer CJ, Sanna S, Jackson AU, Scuteri A, Bonnycastle LL, et al. (2008) Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nat Genet 40(2): 161-169.
-
(2008)
Nat Genet
, vol.40
, Issue.2
, pp. 161-169
-
-
Willer, C.J.1
Sanna, S.2
Jackson, A.U.3
Scuteri, A.4
Bonnycastle, L.L.5
-
7
-
-
38649084407
-
Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides
-
Kooner JS, Chambers JC, Aguilar-Salinas CA, Hinds DA, Hyde CL, et al. (2008) Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. Nat Genet 40(2): 149-151.
-
(2008)
Nat Genet
, vol.40
, Issue.2
, pp. 149-151
-
-
Kooner, J.S.1
Chambers, J.C.2
Aguilar-Salinas, C.A.3
Hinds, D.A.4
Hyde, C.L.5
-
8
-
-
38849166666
-
LDL-cholesterol concentrations: A genome-wide association study
-
Sandhu MS, Waterworth DM, Debenham SL, Wheeler E, Papadakis K, et al. (2008) LDL-cholesterol concentrations: a genome-wide association study. Lancet 371(9611): 483-491.
-
(2008)
Lancet
, vol.371
, Issue.9611
, pp. 483-491
-
-
Sandhu, M.S.1
Waterworth, D.M.2
Debenham, S.L.3
Wheeler, E.4
Papadakis, K.5
-
9
-
-
58149214774
-
Genetic Loci Associated With Plasma Concentration of Low-Density Lipoprotein Cholesterol, High-Density Lipoprotein Cholesterol, Triglycerides, Apolipoprotein A1, and Apolipoprotein B Among 6382 White Women in Genome-Wide Analysis With Replication
-
Chasman DI, ParéG, Zee RYL, Parker AN, Cook NR, et al. (2008) Genetic Loci Associated With Plasma Concentration of Low-Density Lipoprotein Cholesterol, High-Density Lipoprotein Cholesterol, Triglycerides, Apolipoprotein A1, and Apolipoprotein B Among 6382 White Women in Genome-Wide Analysis With Replication. Circ: Cardio Genet 1: 21-30.
-
(2008)
Circ: Cardio Genet
, vol.1
, pp. 21-30
-
-
Chasman, D.I.1
Paré, G.2
Zee, R.Y.L.3
Parker, A.N.4
Cook, N.R.5
-
10
-
-
58149163149
-
Common variants at 30 loci contribute to polygenic dyslipidemia
-
Kathiresan S, Willer CJ, Peloso GM, Demissie S, Musunuru K, et al. (2009) Common variants at 30 loci contribute to polygenic dyslipidemia. Nat Genet 41(1): 56-65.
-
(2009)
Nat Genet
, vol.41
, Issue.1
, pp. 56-65
-
-
Kathiresan, S.1
Willer, C.J.2
Peloso, G.M.3
Demissie, S.4
Musunuru, K.5
-
11
-
-
58149161560
-
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
-
Aulchenko YS, Ripatti S, Lindqvist I, Boomsma D, Heid IM, et al. (2009) Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat Genet 41(1): 47-55.
-
(2009)
Nat Genet
, vol.41
, Issue.1
, pp. 47-55
-
-
Aulchenko, Y.S.1
Ripatti, S.2
Lindqvist, I.3
Boomsma, D.4
Heid, I.M.5
-
12
-
-
58149159573
-
-
Sabatti C, Service SK, Hartikainen AL, Pouta A, Ripatti S, et al. (2009) Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. Nat Genet 41(1): 35-46.
-
Sabatti C, Service SK, Hartikainen AL, Pouta A, Ripatti S, et al. (2009) Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. Nat Genet 41(1): 35-46.
-
-
-
-
13
-
-
59249096217
-
-
Tanaka T, Shen J, Abecasis GR, Kisialiou A, Ordovas JM, et al. (2009) Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI Study. PLoS Genet 5: e1000338. doi:10.1371/journal.pgen.1000338.
-
Tanaka T, Shen J, Abecasis GR, Kisialiou A, Ordovas JM, et al. (2009) Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI Study. PLoS Genet 5: e1000338. doi:10.1371/journal.pgen.1000338.
-
-
-
-
14
-
-
0014685537
-
Serum-cholesterol and ABO and rhesus blood-groups
-
Oliver MF, Geizerova H, Cumming RA, Heady JA (1969) Serum-cholesterol and ABO and rhesus blood-groups. Lancet 2(7621): 605-606.
-
(1969)
Lancet
, vol.2
, Issue.7621
, pp. 605-606
-
-
Oliver, M.F.1
Geizerova, H.2
Cumming, R.A.3
Heady, J.A.4
-
15
-
-
0014685464
-
ABO and Lewis blood-groups and serum-cholesterol
-
Langman MJ, Elwood PC, Foote J, Ryrie DR (1969) ABO and Lewis blood-groups and serum-cholesterol. Lancet 2(7621): 607-609.
-
(1969)
Lancet
, vol.2
, Issue.7621
, pp. 607-609
-
-
Langman, M.J.1
Elwood, P.C.2
Foote, J.3
Ryrie, D.R.4
-
16
-
-
67649367650
-
Polymorphism in the CETP Gene Region, HDL Cholesterol, and Risk of Future Myocardial Infarction: Genome-wide Analysis Among 18 245 Initially Healthy Women From the Women's Genome Health Study Circ
-
Ridker PM, Pare G, Parker AN, Zee RYL, Miletich JP, et al. (2009) Polymorphism in the CETP Gene Region, HDL Cholesterol, and Risk of Future Myocardial Infarction: Genome-wide Analysis Among 18 245 Initially Healthy Women From the Women's Genome Health Study Circ. Cardio Genet 2(1): 26-33.
-
(2009)
Cardio Genet
, vol.2
, Issue.1
, pp. 26-33
-
-
Ridker, P.M.1
Pare, G.2
Parker, A.N.3
Zee, R.Y.L.4
Miletich, J.P.5
-
17
-
-
17544378927
-
Cloning and characterization of GRB14, a novel member of the GRB7 gene family
-
Daly RJ, Sanderson GM, Janes PW, Sutherland RL (1996) Cloning and characterization of GRB14, a novel member of the GRB7 gene family. J Biol Chem 271(21): 12502-12510.
-
(1996)
J Biol Chem
, vol.271
, Issue.21
, pp. 12502-12510
-
-
Daly, R.J.1
Sanderson, G.M.2
Janes, P.W.3
Sutherland, R.L.4
-
18
-
-
26944466110
-
Structural basis for inhibition of the insulin receptor by the adaptor protein Grb14
-
Depetris RS, Hu J, Gimpelevich I, Holt LJ, Daly RJ, et al. (2005) Structural basis for inhibition of the insulin receptor by the adaptor protein Grb14. Mol Cell 20(2): 325-333.
-
(2005)
Mol Cell
, vol.20
, Issue.2
, pp. 325-333
-
-
Depetris, R.S.1
Hu, J.2
Gimpelevich, I.3
Holt, L.J.4
Daly, R.J.5
-
19
-
-
3042608653
-
Comparison of ultracentrifugation and nuclear magnetic resonance spectroscopy in the quantification of triglyceride-rich lipoproteins after an oral fat load
-
Tsai MY, Georgopoulos A, Otvos JD, Ordovas JM, Hanson NQ, et al. (2004) Comparison of ultracentrifugation and nuclear magnetic resonance spectroscopy in the quantification of triglyceride-rich lipoproteins after an oral fat load. Clin Chem 50(7): 1201-1204.
-
(2004)
Clin Chem
, vol.50
, Issue.7
, pp. 1201-1204
-
-
Tsai, M.Y.1
Georgopoulos, A.2
Otvos, J.D.3
Ordovas, J.M.4
Hanson, N.Q.5
-
20
-
-
0034766696
-
-
Barlera S, Chiodini BD, Franzosi MG, Tognoni G (2001) [PROCARDIS: A current approach to the study of the genetics of myocardial infarct]. Ital Heart J Suppl 2(9): 997-1004.
-
Barlera S, Chiodini BD, Franzosi MG, Tognoni G (2001) [PROCARDIS: A current approach to the study of the genetics of myocardial infarct]. Ital Heart J Suppl 2(9): 997-1004.
-
-
-
-
21
-
-
42749092252
-
Loci related to metabolic-syndrome pathways including LEPR, HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: The Women's Genome Health Study
-
Ridker PM, Pare G, Parker A, Zee RY, Danik JS, et al. (2008) Loci related to metabolic-syndrome pathways including LEPR, HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study. Am J Hum Genet 82(5): 1185-1192.
-
(2008)
Am J Hum Genet
, vol.82
, Issue.5
, pp. 1185-1192
-
-
Ridker, P.M.1
Pare, G.2
Parker, A.3
Zee, R.Y.4
Danik, J.S.5
-
22
-
-
33748796075
-
Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves' disease appears to be secondary to DRB1 exon 2 position beta74
-
Simmonds MJ, Heward JM, Barrett JC, Franklyn JA, Gough SC (2006) Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves' disease appears to be secondary to DRB1 exon 2 position beta74. Clin Endocrinol (Oxf) 65(4): 429-432.
-
(2006)
Clin Endocrinol (Oxf)
, vol.65
, Issue.4
, pp. 429-432
-
-
Simmonds, M.J.1
Heward, J.M.2
Barrett, J.C.3
Franklyn, J.A.4
Gough, S.C.5
-
23
-
-
29644442440
-
Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15
-
Traherne JA, Barcellos LF, Sawcer SJ, Compston A, Ramsay PP, et al. (2006) Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15. Hum Mol Genet 15(1): 155-161.
-
(2006)
Hum Mol Genet
, vol.15
, Issue.1
, pp. 155-161
-
-
Traherne, J.A.1
Barcellos, L.F.2
Sawcer, S.J.3
Compston, A.4
Ramsay, P.P.5
-
24
-
-
20144388906
-
Sarcoidosis is associated with a truncating splice site mutation in BTNL2
-
Valentonyte R, Hampe J, Huse K, Rosenstiel P, Albrecht M, et al. (2005) Sarcoidosis is associated with a truncating splice site mutation in BTNL2. Nat Genet 37(4): 357-364.
-
(2005)
Nat Genet
, vol.37
, Issue.4
, pp. 357-364
-
-
Valentonyte, R.1
Hampe, J.2
Huse, K.3
Rosenstiel, P.4
Albrecht, M.5
-
25
-
-
0033939624
-
High incidence of propionic acidemia in greenland is due to a prevalent mutation, 1540insCCC, in the gene for the beta-subunit of propionyl CoA carboxylase
-
Ravn K, Chloupkova M, Christensen E, Brandt NJ, Simonsen H, et al. (2000) High incidence of propionic acidemia in greenland is due to a prevalent mutation, 1540insCCC, in the gene for the beta-subunit of propionyl CoA carboxylase. Am J Hum Genet 67(1): 203-206.
-
(2000)
Am J Hum Genet
, vol.67
, Issue.1
, pp. 203-206
-
-
Ravn, K.1
Chloupkova, M.2
Christensen, E.3
Brandt, N.J.4
Simonsen, H.5
-
26
-
-
11244289333
-
WIPI-1alpha (WIPI49), a member of the novel 7-bladed WIPI protein family, is aberrantly expressed in human cancer and is linked to starvation-induced autophagy
-
Proikas-Cezanne T, Waddell S, Gaugel A, Frickey T, Lupas A, et al. (2004) WIPI-1alpha (WIPI49), a member of the novel 7-bladed WIPI protein family, is aberrantly expressed in human cancer and is linked to starvation-induced autophagy. Oncogene 23(58): 9314-9325.
-
(2004)
Oncogene
, vol.23
, Issue.58
, pp. 9314-9325
-
-
Proikas-Cezanne, T.1
Waddell, S.2
Gaugel, A.3
Frickey, T.4
Lupas, A.5
-
27
-
-
0031054567
-
Identification of structural mutations in the fifth domain of apolipoprotein H (beta 2-glycoprotein I) which affect phospholipid binding
-
Sanghera DK, Wagenknecht DR, McIntyre JA, Kamboh MI (1997) Identification of structural mutations in the fifth domain of apolipoprotein H (beta 2-glycoprotein I) which affect phospholipid binding. Hum Mol Genet 6(2): 311-316.
-
(1997)
Hum Mol Genet
, vol.6
, Issue.2
, pp. 311-316
-
-
Sanghera, D.K.1
Wagenknecht, D.R.2
McIntyre, J.A.3
Kamboh, M.I.4
-
28
-
-
56749106312
-
Rosuvastatin to prevent vascular events in men and women with elevated C-reactive protein
-
Ridker PM, Danielson E, Fonseca FA, Genest J, Gotto AM Jr, et al. (2008) Rosuvastatin to prevent vascular events in men and women with elevated C-reactive protein. N Engl J Med 359(21): 2195-2207.
-
(2008)
N Engl J Med
, vol.359
, Issue.21
, pp. 2195-2207
-
-
Ridker, P.M.1
Danielson, E.2
Fonseca, F.A.3
Genest, J.4
Gotto Jr, A.M.5
-
29
-
-
39749089905
-
Rationale, design, and methodology of the Women's Genome Health Study: A genomewide association study of more than 25,000 initially healthy american women
-
Ridker PM, Chasman DI, Zee RY, Parker A, Rose L, et al. (2008) Rationale, design, and methodology of the Women's Genome Health Study: a genomewide association study of more than 25,000 initially healthy american women. Clin Chem 54(2): 249-255.
-
(2008)
Clin Chem
, vol.54
, Issue.2
, pp. 249-255
-
-
Ridker, P.M.1
Chasman, D.I.2
Zee, R.Y.3
Parker, A.4
Rose, L.5
-
30
-
-
40549109924
-
Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p
-
Broadbent HM, Peden JF, Lorkowski S, Goel A, Ongen H, et al. (2008) Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p. Hum Mol Genet 17(6): 806-814.
-
(2008)
Hum Mol Genet
, vol.17
, Issue.6
, pp. 806-814
-
-
Broadbent, H.M.1
Peden, J.F.2
Lorkowski, S.3
Goel, A.4
Ongen, H.5
-
31
-
-
33744900610
-
-
Farrall M, Green FR, Peden JF, Olsson Clarke R, et al. (2006) Genomewide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17. PLoS Genet 2: e72. doi:10.1371/journal. pgen.0020072.
-
Farrall M, Green FR, Peden JF, Olsson PG, Clarke R, et al. (2006) Genomewide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17. PLoS Genet 2: e72. doi:10.1371/journal. pgen.0020072.
-
-
-
-
32
-
-
34247579476
-
The Third Generation Cohort of the National Heart, Lung, and Blood Institute's Framingham Heart Study: Design, recruitment, and initial examination
-
Splansky GL, Corey D, Yang Q, Atwood LD, Cupples LA, et al. (2007) The Third Generation Cohort of the National Heart, Lung, and Blood Institute's Framingham Heart Study: design, recruitment, and initial examination. Am J Epidemiol 165(11): 1328-1335.
-
(2007)
Am J Epidemiol
, vol.165
, Issue.11
, pp. 1328-1335
-
-
Splansky, G.L.1
Corey, D.2
Yang, Q.3
Atwood, L.D.4
Cupples, L.A.5
-
33
-
-
33750804460
-
Lipoprotein particle analysis by nuclear magnetic resonance spectroscopy
-
Jeyarajah EJ, Cromwell WC, Otvos JD (2006) Lipoprotein particle analysis by nuclear magnetic resonance spectroscopy. Clin Lab Med 26(4): 847-870.
-
(2006)
Clin Lab Med
, vol.26
, Issue.4
, pp. 847-870
-
-
Jeyarajah, E.J.1
Cromwell, W.C.2
Otvos, J.D.3
-
34
-
-
37549058754
-
Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study
-
Shiffman D, O'Meara ES, Bare LA, Rowland CM, Louie JZ, et al. (2008) Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study. Arterioscler Thromb Vasc Biol 28(1): 173-179.
-
(2008)
Arterioscler Thromb Vasc Biol
, vol.28
, Issue.1
, pp. 173-179
-
-
Shiffman, D.1
O'Meara, E.S.2
Bare, L.A.3
Rowland, C.M.4
Louie, J.Z.5
-
35
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, et al. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81(3): 559-575.
-
(2007)
Am J Hum Genet
, vol.81
, Issue.3
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
-
36
-
-
13144306071
-
Genome-wide association studies for common diseases and complex traits
-
Hirschhorn JN, Daly MJ (2005) Genome-wide association studies for common diseases and complex traits. Nat Rev Genet 6(2): 95-108.
-
(2005)
Nat Rev Genet
, vol.6
, Issue.2
, pp. 95-108
-
-
Hirschhorn, J.N.1
Daly, M.J.2
-
37
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, et al. (2007) A second generation human haplotype map of over 3.1 million SNPs. Nature 449(7164): 851-861.
-
(2007)
Nature
, vol.449
, Issue.7164
, pp. 851-861
-
-
Frazer, K.A.1
Ballinger, D.G.2
Cox, D.R.3
Hinds, D.A.4
Stuve, L.L.5
-
38
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, et al. (2006) Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 38(8): 904-909.
-
(2006)
Nat Genet
, vol.38
, Issue.8
, pp. 904-909
-
-
Price, A.L.1
Patterson, N.J.2
Plenge, R.M.3
Weinblatt, M.E.4
Shadick, N.A.5
-
39
-
-
73649130028
-
-
R Core Development Team (2008) R: A language and environment for statistical computing. In: R-Foundation-for-Statistical-Computing, editor. 2.6.1 ed. Vienna, Austria.
-
R Core Development Team (2008) R: A language and environment for statistical computing. In: R-Foundation-for-Statistical-Computing, editor. 2.6.1 ed. Vienna, Austria.
-
-
-
-
40
-
-
0042424602
-
Statistical significance for genome-wide studies
-
Storey JD, Tibshirani R (2003) Statistical significance for genome-wide studies. Proc Natl Acad Sci U S A 100(16): 9440-9445.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, Issue.16
, pp. 9440-9445
-
-
Storey, J.D.1
Tibshirani, R.2
-
41
-
-
2142773942
-
The fine-scale structure of recombination rate variation in the human genome
-
McVean GA, Myers SR, Hunt S, Deloukas P, Bentley DR, et al. (2004) The fine-scale structure of recombination rate variation in the human genome. Science 304(5670): 581-584.
-
(2004)
Science
, vol.304
, Issue.5670
, pp. 581-584
-
-
McVean, G.A.1
Myers, S.R.2
Hunt, S.3
Deloukas, P.4
Bentley, D.R.5
|