-
1
-
-
84856061348
-
Thirty-five common variants for coronary artery disease: The fruits of much collaborative labour
-
Peden JF, Farrall M. Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour. Hum Mol Genet. 2011; 20:R198-R205.
-
(2011)
Hum Mol Genet
, vol.20
-
-
Peden, J.F.1
Farrall, M.2
-
2
-
-
78651323379
-
Genetics of myocardial infarction: A progress report
-
Schunkert H, Erdmann J, Samani NJ. Genetics of myocardial infarction: a progress report. Eur Heart J. 2010;31:918-925.
-
(2010)
Eur Heart J
, vol.31
, pp. 918-925
-
-
Schunkert, H.1
Erdmann, J.2
Samani, N.J.3
-
3
-
-
77955505564
-
Biological, clinical and population relevance of 95 loci for blood lipids
-
Teslovich TM, Musunuru K, Smith AV, Edmondson AC, Stylianou IM, Koseki M, Pirruccello JP, Ripatti S, Chasman DI, Willer CJ, Johansen CT, Fouchier SW, Isaacs A, Peloso GM, Barbalic M, Ricketts SL, Bis JC, Aulchenko YS, Thorleifsson G, Feitosa MF, Chambers J, Orho-Melander M, Melander O, Johnson T, Li X, Guo X, Li M, Shin Cho Y, Jin Go M, Jin Kim Y, Lee JY, Park T, Kim K, Sim X, Twee-Hee Ong R, Croteau-Chonka DC, Lange LA, Smith JD, Song K, Hua Zhao J, Yuan X, Luan J, Lamina C, Ziegler A, Zhang W, Zee RY, Wright AF, Witteman JC, Wilson JF, Willemsen G, Wichmann HE, Whitfield JB, Waterworth DM, Wareham NJ, Waeber G, Vollenweider P, Voight BF, Vitart V, Uitterlinden AG, Uda M, Tuomilehto J, Thompson JR, Tanaka T, Surakka I, Stringham HM, Spector TD, Soranzo N, Smit JH, Sinisalo J, Silander K, Sijbrands EJ, Scuteri A, Scott J, Schlessinger D, Sanna S, Salomaa V, Saharinen J, Sabatti C, Ruokonen A, Rudan I, Rose LM, Roberts R, Rieder M, Psaty BM, Pramstaller PP, Pichler I, Perola M, Penninx BW, Pedersen NL, Pattaro C, Parker AN, Pare G, Oostra BA, O'Donnell CJ, Nieminen MS, Nickerson DA, Montgomery GW, Meitinger T, McPherson R, McCarthy MI, McArdle W, Masson D, Martin NG, Marroni F, Mangino M, Magnusson PK, Lucas G, Luben R, Loos RJ, Lokki ML, Lettre G, Langenberg C, Launer LJ, Lakatta EG, Laaksonen R, Kyvik KO, Kronenberg F, Konig IR, Khaw KT, Kaprio J, Kaplan LM, Johansson A, Jarvelin MR, Janssens AC, Ingelsson E, Igl W, Kees Hovingh G, Hottenga JJ, Hofman A, Hicks AA, Hengstenberg C, Heid IM, Hayward C, Havulinna AS, Hastie ND, Harris TB, Haritunians T, Hall AS, Gyllensten U, Guiducci C, Groop LC, Gonzalez E, Gieger C, Freimer NB, Ferrucci L, Erdmann J, Elliott P, Ejebe KG, Doring A, Dominiczak AF, Demissie S, Deloukas P, de Geus EJ, de Faire U, Crawford G, Collins FS, Chen YD, Caulfield MJ, Campbell H, Burtt NP, Bonnycastle LL, Boomsma DI, Boekholdt SM, Bergman RN, Barroso I, Bandinelli S, Ballantyne CM, Assimes TL, Quertermous T, Altshuler D, Seielstad M, Wong TY, Tai ES, Feranil AB, Kuzawa CW, Adair LS, Taylor HA Jr, Borecki IB, Gabriel SB, Wilson JG, Holm H, Thorsteinsdottir U, Gudnason V, Krauss RM, Mohlke KL, Ordovas JM, Munroe PB, Kooner JS, Tall AR, Hegele RA, Kastelein JJ, Schadt EE, Rotter JI, Boerwinkle E, Strachan DP, Mooser V, Stefansson K, Reilly MP, Samani NJ, Schunkert H, Cupples LA, Sandhu MS, Ridker PM, Rader DJ, van Duijn CM, Peltonen L, Abecasis GR, Boehnke M, Kathiresan S. 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
Pirruccello, J.P.7
Ripatti, S.8
Chasman, D.I.9
Willer, C.J.10
Johansen, C.T.11
Fouchier, S.W.12
Isaacs, A.13
Peloso, G.M.14
Barbalic, M.15
Ricketts, S.L.16
Bis, J.C.17
Aulchenko, Y.S.18
Thorleifsson, G.19
Feitosa, M.F.20
Chambers, J.21
Orho-Melander, M.22
Melander, O.23
Johnson, T.24
Li, X.25
Guo, X.26
Li, M.27
Shin Cho, Y.28
Jin Go, M.29
Jin Kim, Y.30
Lee, J.Y.31
Park, T.32
Kim, K.33
Sim, X.34
Twee-Hee Ong, R.35
Croteau-Chonka, D.C.36
Lange, L.A.37
Smith, J.D.38
Song, K.39
Hua Zhao, J.40
Yuan, X.41
Luan, J.42
Lamina, C.43
Ziegler, A.44
Zhang, W.45
Zee, R.Y.46
Wright, A.F.47
Witteman, J.C.48
Wilson, J.F.49
Willemsen, G.50
Wichmann, H.E.51
Whitfield, J.B.52
Waterworth, D.M.53
Wareham, N.J.54
Waeber, G.55
Vollenweider, P.56
Voight, B.F.57
Vitart, V.58
Uitterlinden, A.G.59
Uda, M.60
Tuomilehto, J.61
Thompson, J.R.62
Tanaka, T.63
Surakka, I.64
Stringham, H.M.65
Spector, T.D.66
Soranzo, N.67
Smit, J.H.68
Sinisalo, J.69
Silander, K.70
Sijbrands, E.J.71
Scuteri, A.72
Scott, J.73
Schlessinger, D.74
Sanna, S.75
Salomaa, V.76
Saharinen, J.77
Sabatti, C.78
Ruokonen, A.79
Rudan, I.80
Rose, L.M.81
Roberts, R.82
Rieder, M.83
Psaty, B.M.84
Pramstaller, P.P.85
Pichler, I.86
Perola, M.87
Penninx, B.W.88
Pedersen, N.L.89
Pattaro, C.90
Parker, A.N.91
Pare, G.92
Oostra, B.A.93
O'Donnell, C.J.94
Nieminen, M.S.95
Nickerson, D.A.96
Montgomery, G.W.97
Meitinger, T.98
McPherson, R.99
more..
-
4
-
-
77956812723
-
Genetic causes of high and low serum HDL-cholesterol
-
Weissglas-Volkov D, Pajukanta P. Genetic causes of high and low serum HDL-cholesterol. J Lipid Res. 2010;51:2032-2057.
-
(2010)
J Lipid Res
, vol.51
, pp. 2032-2057
-
-
Weissglas-Volkov, D.1
Pajukanta, P.2
-
6
-
-
79956266403
-
Genetics of obesity: What have we learned?
-
Choquet H, Meyre D. Genetics of obesity: what have we learned? Curr Genomics. 2011;12:169-179.
-
(2011)
Curr Genomics
, vol.12
, pp. 169-179
-
-
Choquet, H.1
Meyre, D.2
-
7
-
-
79952987360
-
Recent findings in the genetics of blood pressure and hypertension traits
-
Franceschini N, Reiner AP, Heiss G. Recent findings in the genetics of blood pressure and hypertension traits. Am J Hypertens. 2011;24: 392-400.
-
(2011)
Am J Hypertens
, vol.24
, pp. 392-400
-
-
Franceschini, N.1
Reiner, A.P.2
Heiss, G.3
-
8
-
-
79953204259
-
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
-
Schunkert H, Konig IR, Kathiresan S, Reilly MP, Assimes TL, Holm H, Preuss M, Stewart AF, Barbalic M, Gieger C, Absher D, Aherrahrou Z, Allayee H, Altshuler D, Anand SS, Andersen K, Anderson JL, Ardissino D, Ball SG, Balmforth AJ, Barnes TA, Becker DM, Becker LC, Berger K, Bis JC, Boekholdt SM, Boerwinkle E, Braund PS, Brown MJ, Burnett MS, Buysschaert I, Carlquist JF, Chen L, Cichon S, Codd V, Davies RW, Dedoussis G, Dehghan A, Demissie S, Devaney JM, Diemert P, Do R, Doering A, Eifert S, Mokhtari NE, Ellis SG, Elosua R, Engert JC, Epstein SE, de Faire U, Fischer M, Folsom AR, Freyer J, Gigante B, Girelli D, Gretarsdottir S, Gudnason V, Gulcher JR, Halperin E, Hammond N, Hazen SL, Hofman A, Horne BD, Illig T, Iribarren C, Jones GT, Jukema JW, Kaiser MA, Kaplan LM, Kastelein JJ, Khaw KT, Knowles JW, Kolovou G, Kong A, Laaksonen R, Lambrechts D, Leander K, Lettre G, Li M, Lieb W, Loley C, Lotery AJ, Mannucci PM, Maouche S, Martinelli N, McKeown PP, Meisinger C, Meitinger T, Melander O, Merlini PA, Mooser V, Morgan T, Muhleisen TW, Muhlestein JB, Munzel T, Musunuru K, Nahrstaedt J, Nelson CP, Nothen MM, Olivieri O, Patel RS, Patterson CC, Peters A, Peyvandi F, Qu L, Quyyumi AA, Rader DJ, Rallidis LS, Rice C, Rosendaal FR, Rubin D, Salomaa V, Sampietro ML, Sandhu MS, Schadt E, Schafer A, Schillert A, Schreiber S, Schrezenmeir J, Schwartz SM, Siscovick DS, Sivananthan M, Sivapalaratnam S, Smith A, Smith TB, Snoep JD, Soranzo N, Spertus JA, Stark K, Stirrups K, Stoll M, Tang WH, Tennstedt S, Thorgeirsson G, Thorleifsson G, Tomaszewski M, Uitterlinden AG, van Rij AM, Voight BF, Wareham NJ, Wells GA, Wichmann HE, Wild PS, Willenborg C, Witteman JC, Wright BJ, Ye S, Zeller T, Ziegler A, Cambien F, Goodall AH, Cupples LA, Quertermous T, Marz W, Hengstenberg C, Blankenberg S, Ouwehand WH, Hall AS, Deloukas P, Thompson JR, Stefansson K, Roberts R, Thorsteinsdottir U, O'Donnell CJ, McPherson R, Erdmann J, Samani NJ. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet. 2011;43:333-338.
-
(2011)
Nat Genet
, vol.43
, pp. 333-338
-
-
Schunkert, H.1
Konig, I.R.2
Kathiresan, S.3
Reilly, M.P.4
Assimes, T.L.5
Holm, H.6
Preuss, M.7
Stewart, A.F.8
Barbalic, M.9
Gieger, C.10
Absher, D.11
Aherrahrou, Z.12
Allayee, H.13
Altshuler, D.14
Anand, S.S.15
Andersen, K.16
Anderson, J.L.17
Ardissino, D.18
Ball, S.G.19
Balmforth, A.J.20
Barnes, T.A.21
Becker, D.M.22
Becker, L.C.23
Berger, K.24
Bis, J.C.25
Boekholdt, S.M.26
Boerwinkle, E.27
Braund, P.S.28
Brown, M.J.29
Burnett, M.S.30
Buysschaert, I.31
Carlquist, J.F.32
Chen, L.33
Cichon, S.34
Codd, V.35
Davies, R.W.36
Dedoussis, G.37
Dehghan, A.38
Demissie, S.39
Devaney, J.M.40
Diemert, P.41
Do, R.42
Doering, A.43
Eifert, S.44
Mokhtari, N.E.45
Ellis, S.G.46
Elosua, R.47
Engert, J.C.48
Epstein, S.E.49
De Faire, U.50
Fischer, M.51
Folsom, A.R.52
Freyer, J.53
Gigante, B.54
Girelli, D.55
Gretarsdottir, S.56
Gudnason, V.57
Gulcher, J.R.58
Halperin, E.59
Hammond, N.60
Hazen, S.L.61
Hofman, A.62
Horne, B.D.63
Illig, T.64
Iribarren, C.65
Jones, G.T.66
Jukema, J.W.67
Kaiser, M.A.68
Kaplan, L.M.69
Kastelein, J.J.70
Khaw, K.T.71
Knowles, J.W.72
Kolovou, G.73
Kong, A.74
Laaksonen, R.75
Lambrechts, D.76
Leander, K.77
Lettre, G.78
Li, M.79
Lieb, W.80
Loley, C.81
Lotery, A.J.82
Mannucci, P.M.83
Maouche, S.84
Martinelli, N.85
McKeown, P.P.86
Meisinger, C.87
Meitinger, T.88
Melander, O.89
Merlini, P.A.90
Mooser, V.91
Morgan, T.92
Muhleisen, T.W.93
Muhlestein, J.B.94
Munzel, T.95
Musunuru, K.96
Nahrstaedt, J.97
Nelson, C.P.98
Nothen, M.M.99
more..
-
9
-
-
79953221100
-
A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
-
Peden J, Hopewell JC, Saleheen D, Chambers JC, Hager J, Soranzo N, Collins R, Danesh J, Elliott P, Farrall M. A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. Nat Genet. 2011;43:339-344.
-
(2011)
Nat Genet
, vol.43
, pp. 339-344
-
-
Peden, J.1
Hopewell, J.C.2
Saleheen, D.3
Chambers, J.C.4
Hager, J.5
Soranzo, N.6
Collins, R.7
Danesh, J.8
Elliott, P.9
Farrall, M.10
-
10
-
-
77955070766
-
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
-
Johansen CT, Wang J, Lanktree MB, Cao H, McIntyre AD, Ban MR, Martins RA, Kennedy BA, Hassell RG, Visser ME, Schwartz SM, Voight BF, Elosua R, Salomaa V, O'Donnell CJ, Dallinga-Thie GM, Anand SS, Yusuf S, Huff MW, Kathiresan S, Hegele RA. 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
Cao, H.4
McIntyre, A.D.5
Ban, M.R.6
Martins, R.A.7
Kennedy, B.A.8
Hassell, R.G.9
Visser, M.E.10
Schwartz, S.M.11
Voight, B.F.12
Elosua, R.13
Salomaa, V.14
O'Donnell, C.J.15
Dallinga-Thie, G.M.16
Anand, S.S.17
Yusuf, S.18
Huff, M.W.19
Kathiresan, S.20
Hegele, R.A.21
more..
-
11
-
-
79958863532
-
Dash. A method for identicalby-descent haplotype mapping uncovers association with recent variation
-
Gusev A, Kenny EE, Lowe JK, Salit J, Saxena R, Kathiresan S, Altshuler DM, Friedman JM, Breslow JL, Pe'er I. Dash. A method for identicalby-descent haplotype mapping uncovers association with recent variation. Am J Hum Genet. 2011;88:706-717.
-
(2011)
Am J Hum Genet
, vol.88
, pp. 706-717
-
-
Gusev, A.1
Kenny, E.E.2
Lowe, J.K.3
Salit, J.4
Saxena, R.5
Kathiresan, S.6
Altshuler, D.M.7
Friedman, J.M.8
Breslow, J.L.9
Pe'Er, I.10
-
12
-
-
78649745154
-
Genome-wide analysis of copy number variation in type 1 diabetes
-
Grayson BL, Smith ME, Thomas JW, Wang L, Dexheimer P, Jeffrey J, Fain PR, Nanduri P, Eisenbarth GS, Aune TM. Genome-wide analysis of copy number variation in type 1 diabetes. PLoS One. 2010;5:e15393.
-
(2010)
PLoS One
, vol.5
-
-
Grayson, B.L.1
Smith, M.E.2
Thomas, J.W.3
Wang, L.4
Dexheimer, P.5
Jeffrey, J.6
Fain, P.R.7
Nanduri, P.8
Eisenbarth, G.S.9
Aune, T.M.10
-
13
-
-
79959210305
-
A conditional knockout resource for the genome-wide study of mouse gene function
-
Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, Mujica AO, Thomas M, Harrow J, Cox T, Jackson D, Severin J, Biggs P, Fu J, Nefedov M, de Jong PJ, Stewart AF, Bradley A. A conditional knockout resource for the genome-wide study of mouse gene function. Nature. 2011;474:337-342.
-
(2011)
Nature
, vol.474
, pp. 337-342
-
-
Skarnes, W.C.1
Rosen, B.2
West, A.P.3
Koutsourakis, M.4
Bushell, W.5
Iyer, V.6
Mujica, A.O.7
Thomas, M.8
Harrow, J.9
Cox, T.10
Jackson, D.11
Severin, J.12
Biggs, P.13
Fu, J.14
Nefedov, M.15
De Jong, P.J.16
Stewart, A.F.17
Bradley, A.18
-
14
-
-
80053421469
-
Apoe regulates hematopoietic stem cell proliferation, monocytosis, and monocyte accumulation in atherosclerotic lesions in mice
-
Murphy AJ, Akhtari M, Tolani S, Pagler T, Bijl N, Kuo CL, Wang M, Sanson M, Abramowicz S, Welch C, Bochem AE, Kuivenhoven JA, Yvan-Charvet L, Tall AR. Apoe regulates hematopoietic stem cell proliferation, monocytosis, and monocyte accumulation in atherosclerotic lesions in mice. J Clin Invest. 2011;121:4138-4149.
-
(2011)
J Clin Invest
, vol.121
, pp. 4138-4149
-
-
Murphy, A.J.1
Akhtari, M.2
Tolani, S.3
Pagler, T.4
Bijl, N.5
Kuo, C.L.6
Wang, M.7
Sanson, M.8
Abramowicz, S.9
Welch, C.10
Bochem, A.E.11
Kuivenhoven, J.A.12
Yvan-Charvet, L.13
Tall, A.R.14
-
15
-
-
84856211610
-
ApoE suppresses atherosclerosis by reducing lipid accumulation in circulating monocytes and the expression of inflammatory molecules on monocytes and vascular endothelium
-
[Epub ahead of print]
-
Gaudreault N, Kumar N, Posada JM, Stephens KB, de Mochel NS, Eberle D, Olivas VR, Kim RY, Harms MJ, Johnson A, Messina LM, Rapp JH, Raffai RL. ApoE suppresses atherosclerosis by reducing lipid accumulation in circulating monocytes and the expression of inflammatory molecules on monocytes and vascular endothelium. Arterioscler Thromb Vasc Biol. 2011 [Epub ahead of print].
-
(2011)
Arterioscler Thromb Vasc Biol
-
-
Gaudreault, N.1
Kumar, N.2
Posada, J.M.3
Stephens, K.B.4
De Mochel, N.S.5
Eberle, D.6
Olivas, V.R.7
Kim, R.Y.8
Harms, M.J.9
Johnson, A.10
Messina, L.M.11
Rapp, J.H.12
Raffai, R.L.13
-
16
-
-
77953958749
-
Increased secretion of lipoproteins in transgenic mice expressing human D374Y PCSK9 under physiological genetic control
-
Herbert B, Patel D, Waddington SN, Eden ER, McAleenan A, Sun XM, Soutar AK. Increased secretion of lipoproteins in transgenic mice expressing human D374Y PCSK9 under physiological genetic control. Arterioscler Thromb Vasc Biol. 2010;30:1333-1339.
-
(2010)
Arterioscler Thromb Vasc Biol
, vol.30
, pp. 1333-1339
-
-
Herbert, B.1
Patel, D.2
Waddington, S.N.3
Eden, E.R.4
McAleenan, A.5
Sun, X.M.6
Soutar, A.K.7
-
17
-
-
80053452394
-
Large-scale gene-centric analysis identifies novel variants for coronary artery disease
-
IBC 50K CAD Consortium
-
Butterworth AS, Braund PS, Farrall M, Hardwick RJ, Saleheen D, Peden JF, Soranzo N, Chambers JC, Sivapalaratnam S, Kleber ME, et al; IBC 50K CAD Consortium. Large-scale gene-centric analysis identifies novel variants for coronary artery disease. PLoS Genet. 2011;7:e1002260.
-
(2011)
PLoS Genet
, vol.7
-
-
Butterworth, A.S.1
Braund, P.S.2
Farrall, M.3
Hardwick, R.J.4
Saleheen, D.5
Peden, J.F.6
Soranzo, N.7
Chambers, J.C.8
Sivapalaratnam, S.9
Kleber, M.E.10
-
18
-
-
79953220143
-
Sequences in the nonconsensus nucleotide-binding domain of ABCG5/ABCG8 required for sterol transport
-
Wang J, Grishin N, Kinch L, Cohen JC, Hobbs HH, Xie XS. Sequences in the nonconsensus nucleotide-binding domain of ABCG5/ABCG8 required for sterol transport. J Biol Chem. 2011;286:7308-7314.
-
(2011)
J Biol Chem
, vol.286
, pp. 7308-7314
-
-
Wang, J.1
Grishin, N.2
Kinch, L.3
Cohen, J.C.4
Hobbs, H.H.5
Xie, X.S.6
-
19
-
-
79959747253
-
A reappraisal of the mechanism by which plant sterols promote neutral sterol loss in mice
-
Brufau G, Kuipers F, Lin Y, Trautwein EA, Groen AK. A reappraisal of the mechanism by which plant sterols promote neutral sterol loss in mice. PLoS One. 2011;6:e21576.
-
(2011)
PLoS One
, vol.6
-
-
Brufau, G.1
Kuipers, F.2
Lin, Y.3
Trautwein, E.A.4
Groen, A.K.5
-
20
-
-
77955499945
-
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus
-
Musunuru K, Strong A, Frank-Kamenetsky M, Lee NE, Ahfeldt T, Sachs KV, Li X, Li H, Kuperwasser N, Ruda VM, Pirruccello JP, Muchmore B, Prokunina-Olsson L, Hall JL, Schadt EE, Morales CR, Lund-Katz S, Phillips MC, Wong J, Cantley W, Racie T, Ejebe KG, Orho-Melander M, Melander O, Koteliansky V, Fitzgerald K, Krauss RM, Cowan CA, Kathiresan S, Rader DJ. From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus. Nature. 2010;466:714-719.
-
(2010)
Nature
, vol.466
, pp. 714-719
-
-
Musunuru, K.1
Strong, A.2
Frank-Kamenetsky, M.3
Lee, N.E.4
Ahfeldt, T.5
Sachs, K.V.6
Li, X.7
Li, H.8
Kuperwasser, N.9
Ruda, V.M.10
Pirruccello, J.P.11
Muchmore, B.12
Prokunina-Olsson, L.13
Hall, J.L.14
Schadt, E.E.15
Morales, C.R.16
Lund-Katz, S.17
Phillips, M.C.18
Wong, J.19
Cantley, W.20
Racie, T.21
Ejebe, K.G.22
Orho-Melander, M.23
Melander, O.24
Koteliansky, V.25
Fitzgerald, K.26
Krauss, R.M.27
Cowan, C.A.28
Kathiresan, S.29
Rader, D.J.30
more..
-
21
-
-
78649874589
-
Trib1 is a lipid-and myocardial infarction-associated gene that regulates hepatic lipogenesis and VLDL production in mice
-
Burkhardt R, Toh SA, Lagor WR, Birkeland A, Levin M, Li X, Robblee M, Fedorov VD, Yamamoto M, Satoh T, Akira S, Kathiresan S, Breslow JL, Rader DJ. Trib1 is a lipid-and myocardial infarction-associated gene that regulates hepatic lipogenesis and VLDL production in mice. J Clin Invest. 2010;120:4410-4414.
-
(2010)
J Clin Invest
, vol.120
, pp. 4410-4414
-
-
Burkhardt, R.1
Toh, S.A.2
Lagor, W.R.3
Birkeland, A.4
Levin, M.5
Li, X.6
Robblee, M.7
Fedorov, V.D.8
Yamamoto, M.9
Satoh, T.10
Akira, S.11
Kathiresan, S.12
Breslow, J.L.13
Rader, D.J.14
-
22
-
-
79251619566
-
Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: Two genome-wide association studies
-
Reilly MP, Li M, He J, Ferguson JF, Stylianou IM, Mehta NN, Burnett MS, Devaney JM, Knouff CW, Thompson JR, Horne BD, Stewart AF, Assimes TL, Wild PS, Allayee H, Nitschke PL, Patel RS, Martinelli N, Girelli D, Quyyumi AA, Anderson JL, Erdmann J, Hall AS, Schunkert H, Quertermous T, Blankenberg S, Hazen SL, Roberts R, Kathiresan S, Samani NJ, Epstein SE, Rader DJ. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. Lancet. 2011;377:383-392.
-
(2011)
Lancet
, vol.377
, pp. 383-392
-
-
Reilly, M.P.1
Li, M.2
He, J.3
Ferguson, J.F.4
Stylianou, I.M.5
Mehta, N.N.6
Burnett, M.S.7
Devaney, J.M.8
Knouff, C.W.9
Thompson, J.R.10
Horne, B.D.11
Stewart, A.F.12
Assimes, T.L.13
Wild, P.S.14
Allayee, H.15
Nitschke, P.L.16
Patel, R.S.17
Martinelli, N.18
Girelli, D.19
Quyyumi, A.A.20
Anderson, J.L.21
Erdmann, J.22
Hall, A.S.23
Schunkert, H.24
Quertermous, T.25
Blankenberg, S.26
Hazen, S.L.27
Roberts, R.28
Kathiresan, S.29
Samani, N.J.30
Epstein, S.E.31
Rader, D.J.32
more..
-
23
-
-
77956824626
-
Genetic regulation of serum phytosterol levels and risk of coronary artery disease
-
Teupser D, Baber R, Ceglarek U, Scholz M, Illig T, Gieger C, Holdt LM, Leichtle A, Greiser KH, Huster D, Linsel-Nitschke P, Schafer A, Braund PS, Tiret L, Stark K, Raaz-Schrauder D, Fiedler GM, Wilfert W, Beutner F, Gielen S, Grosshennig A, Konig IR, Lichtner P, Heid IM, Kluttig A, El Mokhtari NE, Rubin D, Ekici AB, Reis A, Garlichs CD, Hall AS, Matthes G, Wittekind C, Hengstenberg C, Cambien F, Schreiber S, Werdan K, Meitinger T, Loeffler M, Samani NJ, Erdmann J, Wichmann HE, Schunkert H, Thiery J. Genetic regulation of serum phytosterol levels and risk of coronary artery disease. Circ Cardiovasc Genet. 2010;3: 331-339.
-
(2010)
Circ Cardiovasc Genet
, vol.3
, pp. 331-339
-
-
Teupser, D.1
Baber, R.2
Ceglarek, U.3
Scholz, M.4
Illig, T.5
Gieger, C.6
Holdt, L.M.7
Leichtle, A.8
Greiser, K.H.9
Huster, D.10
Linsel-Nitschke, P.11
Schafer, A.12
Braund, P.S.13
Tiret, L.14
Stark, K.15
Raaz-Schrauder, D.16
Fiedler, G.M.17
Wilfert, W.18
Beutner, F.19
Gielen, S.20
Grosshennig, A.21
Konig, I.R.22
Lichtner, P.23
Heid, I.M.24
Kluttig, A.25
El Mokhtari, N.E.26
Rubin, D.27
Ekici, A.B.28
Reis, A.29
Garlichs, C.D.30
Hall, A.S.31
Matthes, G.32
Wittekind, C.33
Hengstenberg, C.34
Cambien, F.35
Schreiber, S.36
Werdan, K.37
Meitinger, T.38
Loeffler, M.39
Samani, N.J.40
Erdmann, J.41
Wichmann, H.E.42
Schunkert, H.43
Thiery, J.44
more..
-
24
-
-
80054951104
-
Cdkn2a is an atherosclerosis modifier locus that regulates monocyte/macrophage proliferation
-
Kuo CL, Murphy AJ, Sayers S, Li R, Yvan-Charvet L, Davis JZ, Krishnamurthy J, Liu Y, Puig O, Sharpless NE, Tall AR, Welch CL. Cdkn2a is an atherosclerosis modifier locus that regulates monocyte/macrophage proliferation. Arterioscler Thromb Vasc Biol. 2011;31:2483-2492.
-
(2011)
Arterioscler Thromb Vasc Biol
, vol.31
, pp. 2483-2492
-
-
Kuo, C.L.1
Murphy, A.J.2
Sayers, S.3
Li, R.4
Yvan-Charvet, L.5
Davis, J.Z.6
Krishnamurthy, J.7
Liu, Y.8
Puig, O.9
Sharpless, N.E.10
Tall, A.R.11
Welch, C.L.12
-
25
-
-
57549107877
-
Athsq1 is an atherosclerosis modifier locus with dramatic effects on lesion area and prominent accumulation of versican
-
Seidelmann SB, Kuo C, Pleskac N, Molina J, Sayers S, Li R, Zhou J, Johnson P, Braun K, Chan C, Teupser D, Breslow JL, Wight TN, Tall AR, Welch CL. Athsq1 is an atherosclerosis modifier locus with dramatic effects on lesion area and prominent accumulation of versican. Arterioscler Thromb Vasc Biol. 2008;28:2180-2186.
-
(2008)
Arterioscler Thromb Vasc Biol
, vol.28
, pp. 2180-2186
-
-
Seidelmann, S.B.1
Kuo, C.2
Pleskac, N.3
Molina, J.4
Sayers, S.5
Li, R.6
Zhou, J.7
Johnson, P.8
Braun, K.9
Chan, C.10
Teupser, D.11
Breslow, J.L.12
Wight, T.N.13
Tall, A.R.14
Welch, C.L.15
-
26
-
-
70349569056
-
Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus
-
Jarinova O, Stewart AF, Roberts R, Wells G, Lau P, Naing T, Buerki C, McLean BW, Cook RC, Parker JS, McPherson R. Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus. Arterioscler Thromb Vasc Biol. 2009;29:1671-1677.
-
(2009)
Arterioscler Thromb Vasc Biol
, vol.29
, pp. 1671-1677
-
-
Jarinova, O.1
Stewart, A.F.2
Roberts, R.3
Wells, G.4
Lau, P.5
Naing, T.6
Buerki, C.7
McLean, B.W.8
Cook, R.C.9
Parker, J.S.10
McPherson, R.11
-
27
-
-
70449555143
-
Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression: Identification of eight new ANRIL splice variants
-
Folkersen L, Kyriakou T, Goel A, Peden J, Malarstig A, Paulsson-Berne G, Hamsten A, Hugh W, Franco-Cereceda A, Gabrielsen A, Eriksson P. Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression: identification of eight new ANRIL splice variants. PLoS One. 2009;4:e7677.
-
(2009)
PLoS One
, vol.4
-
-
Folkersen, L.1
Kyriakou, T.2
Goel, A.3
Peden, J.4
Malarstig, A.5
Paulsson-Berne, G.6
Hamsten, A.7
Hugh, W.8
Franco-Cereceda, A.9
Gabrielsen, A.10
Eriksson, P.11
-
28
-
-
64549083268
-
INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis
-
Liu Y, Sanoff HK, Cho H, Burd CE, Torrice C, Mohlke KL, Ibrahim JG, Thomas NE, Sharpless NE. INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis. PLoS One. 2009;4:e5027.
-
(2009)
PLoS One
, vol.4
-
-
Liu, Y.1
Sanoff, H.K.2
Cho, H.3
Burd, C.E.4
Torrice, C.5
Mohlke, K.L.6
Ibrahim, J.G.7
Thomas, N.E.8
Sharpless, N.E.9
-
29
-
-
79955902153
-
Genetic mechanisms mediating atherosclerosis susceptibility at the chromosome 9p21 locus
-
Cunnington MS, Keavney B. Genetic mechanisms mediating atherosclerosis susceptibility at the chromosome 9p21 locus. Curr Atheroscler Rep. 2011;13:193-201.
-
(2011)
Curr Atheroscler Rep
, vol.13
, pp. 193-201
-
-
Cunnington, M.S.1
Keavney, B.2
-
30
-
-
77949775636
-
Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice
-
Visel A, Zhu Y, May D, Afzal V, Gong E, Attanasio C, Blow MJ, Cohen JC, Rubin EM, Pennacchio LA. Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice. Nature. 2010;464:409-412.
-
(2010)
Nature
, vol.464
, pp. 409-412
-
-
Visel, A.1
Zhu, Y.2
May, D.3
Afzal, V.4
Gong, E.5
Attanasio, C.6
Blow, M.J.7
Cohen, J.C.8
Rubin, E.M.9
Pennacchio, L.A.10
-
31
-
-
79953207296
-
Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population
-
Wang F, Xu CQ, He Q, Cai JP, Li XC, Wang D, Xiong X, Liao YH, Zeng QT, Yang YZ, Cheng X, Li C, Yang R, Wang CC, Wu G, Lu QL, Bai Y, Huang YF, Yin D, Yang Q, Wang XJ, Dai DP, Zhang RF, Wan J, Ren JH, Li SS, Zhao YY, Fu FF, Huang Y, Li QX, Shi SW, Lin N, Pan ZW, Li Y, Yu B, Wu YX, Ke YH, Lei J, Wang N, Luo CY, Ji LY, Gao LJ, Li L, Liu H, Huang EW, Cui J, Jia N, Ren X, Li H, Ke T, Zhang XQ, Liu JY, Liu MG, Xia H, Yang B, Shi LS, Xia YL, Tu X, Wang QK. Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population. Nat Genet. 2011;43:345-349.
-
(2011)
Nat Genet
, vol.43
, pp. 345-349
-
-
Wang, F.1
Xu, C.Q.2
He, Q.3
Cai, J.P.4
Li, X.C.5
Wang, D.6
Xiong, X.7
Liao, Y.H.8
Zeng, Q.T.9
Yang, Y.Z.10
Cheng, X.11
Li, C.12
Yang, R.13
Wang, C.C.14
Wu, G.15
Lu, Q.L.16
Bai, Y.17
Huang, Y.F.18
Yin, D.19
Yang, Q.20
Wang, X.J.21
Dai, D.P.22
Zhang, R.F.23
Wan, J.24
Ren, J.H.25
Li, S.S.26
Zhao, Y.Y.27
Fu, F.F.28
Huang, Y.29
Li, Q.X.30
Shi, S.W.31
Lin, N.32
Pan, Z.W.33
Li, Y.34
Yu, B.35
Wu, Y.X.36
Ke, Y.H.37
Lei, J.38
Wang, N.39
Luo, C.Y.40
Ji, L.Y.41
Gao, L.J.42
Li, L.43
Liu, H.44
Huang, E.W.45
Cui, J.46
Jia, N.47
Ren, X.48
Li, H.49
Ke, T.50
Zhang, X.Q.51
Liu, J.Y.52
Liu, M.G.53
Xia, H.54
Yang, B.55
Shi, L.S.56
Xia, Y.L.57
Tu, X.58
Wang, Q.K.59
more..
-
32
-
-
0037432295
-
Eliminating atherogenesis in mice by switching off hepatic lipoprotein secretion
-
Lieu HD, Withycombe SK, Walker Q, Rong JX, Walzem RL, Wong JS, Hamilton RL, Fisher EA, Young SG. Eliminating atherogenesis in mice by switching off hepatic lipoprotein secretion. Circulation. 2003;107: 1315-1321.
-
(2003)
Circulation
, vol.107
, pp. 1315-1321
-
-
Lieu, H.D.1
Withycombe, S.K.2
Walker, Q.3
Rong, J.X.4
Walzem, R.L.5
Wong, J.S.6
Hamilton, R.L.7
Fisher, E.A.8
Young, S.G.9
-
33
-
-
79952736069
-
Reversal of hyperlipidemia with a genetic switch favorably affects the content and inflammatory state of macrophages in atherosclerotic plaques
-
Feig JE, Parathath S, Rong JX, Mick SL, Vengrenyuk Y, Grauer L, Young SG, Fisher EA. Reversal of hyperlipidemia with a genetic switch favorably affects the content and inflammatory state of macrophages in atherosclerotic plaques. Circulation. 2011;123:989-998.
-
(2011)
Circulation
, vol.123
, pp. 989-998
-
-
Feig, J.E.1
Parathath, S.2
Rong, J.X.3
Mick, S.L.4
Vengrenyuk, Y.5
Grauer, L.6
Young, S.G.7
Fisher, E.A.8
-
34
-
-
77955174769
-
The mouse atherosclerosis locus at chromosome 10 (Ath11) acts early in lesion formation with subcongenic strains delineating 2 narrowed regions
-
Wolfrum S, Rodriguez JM, Tan M, Chen KY, Teupser D, Breslow JL. The mouse atherosclerosis locus at chromosome 10 (Ath11) acts early in lesion formation with subcongenic strains delineating 2 narrowed regions. Arterioscler Thromb Vasc Biol. 2010;30:1583-1590.
-
(2010)
Arterioscler Thromb Vasc Biol
, vol.30
, pp. 1583-1590
-
-
Wolfrum, S.1
Rodriguez, J.M.2
Tan, M.3
Chen, K.Y.4
Teupser, D.5
Breslow, J.L.6
-
35
-
-
77952530954
-
Quantitative trait locus mapping and identification of Zhx2 as a novel regulator of plasma lipid metabolism
-
Gargalovic PS, Erbilgin A, Kohannim O, Pagnon J, Wang X, Castellani L, LeBoeuf R, Peterson ML, Spear BT, Lusis AJ. Quantitative trait locus mapping and identification of Zhx2 as a novel regulator of plasma lipid metabolism. Circ Cardiovasc Genet. 2010;3:60-67.
-
(2010)
Circ Cardiovasc Genet
, vol.3
, pp. 60-67
-
-
Gargalovic, P.S.1
Erbilgin, A.2
Kohannim, O.3
Pagnon, J.4
Wang, X.5
Castellani, L.6
Leboeuf, R.7
Peterson, M.L.8
Spear, B.T.9
Lusis, A.J.10
-
36
-
-
70349985243
-
Copy number variation influences gene expression and metabolic traits in mice
-
Orozco LD, Cokus SJ, Ghazalpour A, Ingram-Drake L, Wang S, van Nas A, Che N, Araujo JA, Pellegrini M, Lusis AJ. Copy number variation influences gene expression and metabolic traits in mice. Hum Mol Genet. 2009;18:4118-4129.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 4118-4129
-
-
Orozco, L.D.1
Cokus, S.J.2
Ghazalpour, A.3
Ingram-Drake, L.4
Wang, S.5
Van Nas, A.6
Che, N.7
Araujo, J.A.8
Pellegrini, M.9
Lusis, A.J.10
-
37
-
-
36349014273
-
Spontaneous atherothrombosis and medial degradation in Apoe-/-Npc1-/-mice
-
Welch CL, Sun Y, Arey BJ, Lemaitre V, Sharma N, Ishibashi M, Sayers S, Li R, Gorelik A, Pleskac N, Collins-Fletcher K, Yasuda Y, Bromme D, D'Armiento JM, Ogletree ML, Tall AR. Spontaneous atherothrombosis and medial degradation in Apoe-/-, Npc1-/-mice. Circulation. 2007; 116:2444-2452.
-
(2007)
Circulation
, vol.116
, pp. 2444-2452
-
-
Welch, C.L.1
Sun, Y.2
Arey, B.J.3
Lemaitre, V.4
Sharma, N.5
Ishibashi, M.6
Sayers, S.7
Li, R.8
Gorelik, A.9
Pleskac, N.10
Collins-Fletcher, K.11
Yasuda, Y.12
Bromme, D.13
D'Armiento, J.M.14
Ogletree, M.L.15
Tall, A.R.16
-
38
-
-
52049116691
-
Control of atherosclerotic plaque vulnerability: Insights from transgenic mice
-
Heeneman S, Lutgens E, Schapira KB, Daemen MJ, Biessen EA. Control of atherosclerotic plaque vulnerability: insights from transgenic mice. Front Biosci. 2008;13:6289-6313.
-
(2008)
Front Biosci
, vol.13
, pp. 6289-6313
-
-
Heeneman, S.1
Lutgens, E.2
Schapira, K.B.3
Daemen, M.J.4
Biessen, E.A.5
-
39
-
-
70350731272
-
Mechanisms and consequences of efferocytosis in advanced atherosclerosis
-
Thorp E, Tabas I. Mechanisms and consequences of efferocytosis in advanced atherosclerosis. J Leukoc Biol. 2009;86:1089-1095.
-
(2009)
J Leukoc Biol
, vol.86
, pp. 1089-1095
-
-
Thorp, E.1
Tabas, I.2
-
40
-
-
78149245489
-
Genetic variants influencing circulating lipid levels and risk of coronary artery disease
-
Waterworth DM, Ricketts SL, Song K, Chen L, Zhao JH, Ripatti S, Aulchenko YS, Zhang W, Yuan X, Lim N, Luan J, Ashford S, Wheeler E, Young EH, Hadley D, Thompson JR, Braund PS, Johnson T, Struchalin M, Surakka I, Luben R, Khaw KT, Rodwell SA, Loos RJ, Boekholdt SM, Inouye M, Deloukas P, Elliott P, Schlessinger D, Sanna S, Scuteri A, Jackson A, Mohlke KL, Tuomilehto J, Roberts R, Stewart A, Kesaniemi YA, Mahley RW, Grundy SM, McArdle W, Cardon L, Waeber G, Vollenweider P, Chambers JC, Boehnke M, Abecasis GR, Salomaa V, Jarvelin MR, Ruokonen A, Barroso I, Epstein SE, Hakonarson HH, Rader DJ, Reilly MP, Witteman JC, Hall AS, Samani NJ, Strachan DP, Barter P, van Duijn CM, Kooner JS, Peltonen L, Wareham NJ, McPherson R, Mooser V, Sandhu MS. Genetic variants influencing circulating lipid levels and risk of coronary artery disease. Arterioscler Thromb Vasc Biol. 2010;30:2264-2276.
-
(2010)
Arterioscler Thromb Vasc Biol
, vol.30
, pp. 2264-2276
-
-
Waterworth, D.M.1
Ricketts, S.L.2
Song, K.3
Chen, L.4
Zhao, J.H.5
Ripatti, S.6
Aulchenko, Y.S.7
Zhang, W.8
Yuan, X.9
Lim, N.10
Luan, J.11
Ashford, S.12
Wheeler, E.13
Young, E.H.14
Hadley, D.15
Thompson, J.R.16
Braund, P.S.17
Johnson, T.18
Struchalin, M.19
Surakka, I.20
Luben, R.21
Khaw, K.T.22
Rodwell, S.A.23
Loos, R.J.24
Boekholdt, S.M.25
Inouye, M.26
Deloukas, P.27
Elliott, P.28
Schlessinger, D.29
Sanna, S.30
Scuteri, A.31
Jackson, A.32
Mohlke, K.L.33
Tuomilehto, J.34
Roberts, R.35
Stewart, A.36
Kesaniemi, Y.A.37
Mahley, R.W.38
Grundy, S.M.39
McArdle, W.40
Cardon, L.41
Waeber, G.42
Vollenweider, P.43
Chambers, J.C.44
Boehnke, M.45
Abecasis, G.R.46
Salomaa, V.47
Jarvelin, M.R.48
Ruokonen, A.49
Barroso, I.50
Epstein, S.E.51
Hakonarson, H.H.52
Rader, D.J.53
Reilly, M.P.54
Witteman, J.C.55
Hall, A.S.56
Samani, N.J.57
Strachan, D.P.58
Barter, P.59
Van Duijn, C.M.60
Kooner, J.S.61
Peltonen, L.62
Wareham, N.J.63
McPherson, R.64
Mooser, V.65
Sandhu, M.S.66
more..
-
41
-
-
70749096913
-
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
-
Kathiresan S, Voight BF, Purcell S, Musunuru K, Ardissino D, Mannucci PM, Anand S, Engert JC, Samani NJ, Schunkert H, Erdmann J, Reilly MP, Rader DJ, Morgan T, Spertus JA, Stoll M, Girelli D, McKeown PP, Patterson CC, Siscovick DS, O'Donnell CJ, Elosua R, Peltonen L, Salomaa V, Schwartz SM, Melander O, Altshuler D, Merlini PA, Berzuini C, Bernardinelli L, Peyvandi F, Tubaro M, Celli P, Ferrario M, Fetiveau R, Marziliano N, Casari G, Galli M, Ribichini F, Rossi M, Bernardi F, Zonzin P, Piazza A, Yee J, Friedlander Y, Marrugat J, Lucas G, Subirana I, Sala J, Ramos R, Meigs JB, Williams G, Nathan DM, MacRae CA, Havulinna AS, Berglund G, Hirschhorn JN, Asselta R, Duga S, Spreafico M, Daly MJ, Nemesh J, Korn JM, McCarroll SA, Surti A, Guiducci C, Gianniny L, Mirel D, Parkin M, Burtt N, Gabriel SB, Thompson JR, Braund PS, Wright BJ, Balmforth AJ, Ball SG, Hall AS, Linsel-Nitschke P, Lieb W, Ziegler A, Konig I, Hengstenberg C, Fischer M, Stark K, Grosshennig A, Preuss M, Wichmann HE, Schreiber S, Ouwehand W, Deloukas P, Scholz M, Cambien F, Li M, Chen Z, Wilensky R, Matthai W, Qasim A, Hakonarson HH, Devaney J, Burnett MS, Pichard AD, Kent KM, Satler L, Lindsay JM, Waksman R, Knouff CW, Waterworth DM, Walker MC, Mooser V, Epstein SE, Scheffold T, Berger K, Huge A, Martinelli N, Olivieri O, Corrocher R, McKeown P, Erdmann E, Konig IR, Holm H, Thorleifsson G, Thorsteinsdottir U, Stefansson K, Do R, Xie C, Siscovick D. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet. 2009;41:334-341.
-
(2009)
Nat Genet
, vol.41
, pp. 334-341
-
-
Kathiresan, S.1
Voight, B.F.2
Purcell, S.3
Musunuru, K.4
Ardissino, D.5
Mannucci, P.M.6
Anand, S.7
Engert, J.C.8
Samani, N.J.9
Schunkert, H.10
Erdmann, J.11
Reilly, M.P.12
Rader, D.J.13
Morgan, T.14
Spertus, J.A.15
Stoll, M.16
Girelli, D.17
McKeown, P.P.18
Patterson, C.C.19
Siscovick, D.S.20
O'Donnell, C.J.21
Elosua, R.22
Peltonen, L.23
Salomaa, V.24
Schwartz, S.M.25
Melander, O.26
Altshuler, D.27
Merlini, P.A.28
Berzuini, C.29
Bernardinelli, L.30
Peyvandi, F.31
Tubaro, M.32
Celli, P.33
Ferrario, M.34
Fetiveau, R.35
Marziliano, N.36
Casari, G.37
Galli, M.38
Ribichini, F.39
Rossi, M.40
Bernardi, F.41
Zonzin, P.42
Piazza, A.43
Yee, J.44
Friedlander, Y.45
Marrugat, J.46
Lucas, G.47
Subirana, I.48
Sala, J.49
Ramos, R.50
Meigs, J.B.51
Williams, G.52
Nathan, D.M.53
MacRae, C.A.54
Havulinna, A.S.55
Berglund, G.56
Hirschhorn, J.N.57
Asselta, R.58
Duga, S.59
Spreafico, M.60
Daly, M.J.61
Nemesh, J.62
Korn, J.M.63
McCarroll, S.A.64
Surti, A.65
Guiducci, C.66
Gianniny, L.67
Mirel, D.68
Parkin, M.69
Burtt, N.70
Gabriel, S.B.71
Thompson, J.R.72
Braund, P.S.73
Wright, B.J.74
Balmforth, A.J.75
Ball, S.G.76
Hall, A.S.77
Linsel-Nitschke, P.78
Lieb, W.79
Ziegler, A.80
Konig, I.81
Hengstenberg, C.82
Fischer, M.83
Stark, K.84
Grosshennig, A.85
Preuss, M.86
Wichmann, H.E.87
Schreiber, S.88
Ouwehand, W.89
Deloukas, P.90
Scholz, M.91
Cambien, F.92
Li, M.93
Chen, Z.94
Wilensky, R.95
Matthai, W.96
Qasim, A.97
Hakonarson, H.H.98
Devaney, J.99
more..
-
42
-
-
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, Rieder MJ, Cooper GM, Roos C, Voight BF, Havulinna AS, Wahlstrand B, Hedner T, Corella D, Tai ES, Ordovas JM, Berglund G, Vartiainen E, Jousilahti P, Hedblad B, Taskinen MR, Newton-Cheh C, Salomaa V, Peltonen L, Groop L, Altshuler DM, Orho-Melander M. Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. Nat Genet. 2008;40:189-197.
-
(2008)
Nat Genet
, vol.40
, pp. 189-197
-
-
Kathiresan, S.1
Melander, O.2
Guiducci, C.3
Surti, A.4
Burtt, N.P.5
Rieder, M.J.6
Cooper, G.M.7
Roos, C.8
Voight, B.F.9
Havulinna, A.S.10
Wahlstrand, B.11
Hedner, T.12
Corella, D.13
Tai, E.S.14
Ordovas, J.M.15
Berglund, G.16
Vartiainen, E.17
Jousilahti, P.18
Hedblad, B.19
Taskinen, M.R.20
Newton-Cheh, C.21
Salomaa, V.22
Peltonen, L.23
Groop, L.24
Altshuler, D.M.25
Orho-Melander, M.26
more..
-
43
-
-
13944265645
-
Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9
-
Cohen J, Pertsemlidis A, Kotowski IK, Graham R, Garcia CK, Hobbs HH. Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9. Nat Genet. 2005;37: 161-165.
-
(2005)
Nat Genet
, vol.37
, pp. 161-165
-
-
Cohen, J.1
Pertsemlidis, A.2
Kotowski, I.K.3
Graham, R.4
Garcia, C.K.5
Hobbs, H.H.6
-
44
-
-
17244377696
-
Decreased plasma cholesterol and hypersensitivity to statins in mice lacking Pcsk9
-
Rashid S, Curtis DE, Garuti R, Anderson NN, Bashmakov Y, Ho YK, Hammer RE, Moon YA, Horton JD. Decreased plasma cholesterol and hypersensitivity to statins in mice lacking Pcsk9. Proc Natl Acad Sci USA. 2005;102:5374-5379.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 5374-5379
-
-
Rashid, S.1
Curtis, D.E.2
Garuti, R.3
Anderson, N.N.4
Bashmakov, Y.5
Ho, Y.K.6
Hammer, R.E.7
Moon, Y.A.8
Horton, J.D.9
-
45
-
-
50149101511
-
Therapeutic RNAi targeting PCSK9 acutely lowers plasma cholesterol in rodents and LDL cholesterol in nonhuman primates
-
Frank-Kamenetsky M, Grefhorst A, Anderson NN, Racie TS, Bramlage B, Akinc A, Butler D, Charisse K, Dorkin R, Fan Y, Gamba-Vitalo C, Hadwiger P, Jayaraman M, John M, Jayaprakash KN, Maier M, Nechev L, Rajeev KG, Read T, Rohl I, Soutschek J, Tan P, Wong J, Wang G, Zimmermann T, de Fougerolles A, Vornlocher HP, Langer R, Anderson DG, Manoharan M, Koteliansky V, Horton JD, Fitzgerald K. Therapeutic RNAi targeting PCSK9 acutely lowers plasma cholesterol in rodents and LDL cholesterol in nonhuman primates. Proc Natl Acad Sci USA. 2008;105:11915-11920.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 11915-11920
-
-
Frank-Kamenetsky, M.1
Grefhorst, A.2
Anderson, N.N.3
Racie, T.S.4
Bramlage, B.5
Akinc, A.6
Butler, D.7
Charisse, K.8
Dorkin, R.9
Fan, Y.10
Gamba-Vitalo, C.11
Hadwiger, P.12
Jayaraman, M.13
John, M.14
Jayaprakash, K.N.15
Maier, M.16
Nechev, L.17
Rajeev, K.G.18
Read, T.19
Rohl, I.20
Soutschek, J.21
Tan, P.22
Wong, J.23
Wang, G.24
Zimmermann, T.25
De Fougerolles, A.26
Vornlocher, H.P.27
Langer, R.28
Anderson, D.G.29
Manoharan, M.30
Koteliansky, V.31
Horton, J.D.32
Fitzgerald, K.33
more..
-
46
-
-
34547623750
-
Genomewide association analysis of coronary artery disease
-
Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, Dixon RJ, Meitinger T, Braund P, Wichmann HE, Barrett JH, Konig IR, Stevens SE, Szymczak S, Tregouet DA, Iles MM, Pahlke F, Pollard H, Lieb W, Cambien F, Fischer M, Ouwehand W, Blankenberg S, Balmforth AJ, Baessler A, Ball SG, Strom TM, Braenne I, Gieger C, Deloukas P, Tobin MD, Ziegler A, Thompson JR, Schunkert H. Genomewide association analysis of coronary artery disease. N Engl J Med. 2007;357: 443-453.
-
(2007)
N Engl J Med
, vol.357
, pp. 443-453
-
-
Samani, N.J.1
Erdmann, J.2
Hall, A.S.3
Hengstenberg, C.4
Mangino, M.5
Mayer, B.6
Dixon, R.J.7
Meitinger, T.8
Braund, P.9
Wichmann, H.E.10
Barrett, J.H.11
Konig, I.R.12
Stevens, S.E.13
Szymczak, S.14
Tregouet, D.A.15
Iles, M.M.16
Pahlke, F.17
Pollard, H.18
Lieb, W.19
Cambien, F.20
Fischer, M.21
Ouwehand, W.22
Blankenberg, S.23
Balmforth, A.J.24
Baessler, A.25
Ball, S.G.26
Strom, T.M.27
Braenne, I.28
Gieger, C.29
Deloukas, P.30
Tobin, M.D.31
Ziegler, A.32
Thompson, J.R.33
Schunkert, H.34
more..
-
47
-
-
77956327982
-
Sort1, encoded by the cardiovascular risk locus 1p13.3, is a regulator of hepatic lipoprotein export
-
Kjolby M, Andersen OM, Breiderhoff T, Fjorback AW, Pedersen KM, Madsen P, Jansen P, Heeren J, Willnow TE, Nykjaer A. Sort1, encoded by the cardiovascular risk locus 1p13.3, is a regulator of hepatic lipoprotein export. Cell Metab. 2010;12:213-223.
-
(2010)
Cell Metab
, vol.12
, pp. 213-223
-
-
Kjolby, M.1
Andersen, O.M.2
Breiderhoff, T.3
Fjorback, A.W.4
Pedersen, K.M.5
Madsen, P.6
Jansen, P.7
Heeren, J.8
Willnow, T.E.9
Nykjaer, A.10
-
48
-
-
17744390348
-
Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent abc transporters
-
Berge KE, Tian H, Graf GA, Yu L, Grishin NV, Schultz J, Kwiterovich P, Shan B, Barnes R, Hobbs HH. Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent abc transporters. Science. 2000;290:1771-1775.
-
(2000)
Science
, vol.290
, pp. 1771-1775
-
-
Berge, K.E.1
Tian, H.2
Graf, G.A.3
Yu, L.4
Grishin, N.V.5
Schultz, J.6
Kwiterovich, P.7
Shan, B.8
Barnes, R.9
Hobbs, H.H.10
-
49
-
-
3442902180
-
High-level expression of ABCG5 and ABCG8 attenuates diet-induced hypercholesterolemia and atherosclerosis in LDLr-/-mice
-
Wilund KR, Yu L, Xu F, Hobbs HH, Cohen JC. High-level expression of ABCG5 and ABCG8 attenuates diet-induced hypercholesterolemia and atherosclerosis in LDLr-/-mice. J Lipid Res. 2004;45:1429-1436.
-
(2004)
J Lipid Res
, vol.45
, pp. 1429-1436
-
-
Wilund, K.R.1
Yu, L.2
Xu, F.3
Hobbs, H.H.4
Cohen, J.C.5
-
50
-
-
2542427448
-
Hepatic ABCG5 and ABCG8 overexpression increases hepatobiliary sterol transport but does not alter aortic atherosclerosis in transgenic mice
-
Wu JE, Basso F, Shamburek RD, Amar MJ, Vaisman B, Szakacs G, Joyce C, Tansey T, Freeman L, Paigen BJ, Thomas F, Brewer HB Jr, Santamarina-Fojo S. Hepatic ABCG5 and ABCG8 overexpression increases hepatobiliary sterol transport but does not alter aortic atherosclerosis in transgenic mice. J Biol Chem. 2004;279:22913-22925.
-
(2004)
J Biol Chem
, vol.279
, pp. 22913-22925
-
-
Wu, J.E.1
Basso, F.2
Shamburek, R.D.3
Amar, M.J.4
Vaisman, B.5
Szakacs, G.6
Joyce, C.7
Tansey, T.8
Freeman, L.9
Paigen, B.J.10
Thomas, F.11
Brewer Jr., H.B.12
Santamarina-Fojo, S.13
-
51
-
-
33845993219
-
Hepatic ABCG5/G8 overexpression reduces apoB-lipoproteins and atherosclerosis when cholesterol absorption is inhibited
-
Basso F, Freeman LA, Ko C, Joyce C, Amar MJ, Shamburek RD, Tansey T, Thomas F, Wu J, Paigen B, Remaley AT, Santamarina-Fojo S, Brewer HB Jr. Hepatic ABCG5/G8 overexpression reduces apoB-lipoproteins and atherosclerosis when cholesterol absorption is inhibited. J Lipid Res. 2007;48:114-126.
-
(2007)
J Lipid Res
, vol.48
, pp. 114-126
-
-
Basso, F.1
Freeman, L.A.2
Ko, C.3
Joyce, C.4
Amar, M.J.5
Shamburek, R.D.6
Tansey, T.7
Thomas, F.8
Wu, J.9
Paigen, B.10
Remaley, A.T.11
Santamarina-Fojo, S.12
Brewer Jr., H.B.13
-
52
-
-
1242342236
-
Selective sterol accumulation in ABCG5/ABCG8-deficient mice
-
Yu L, von Bergmann K, Lutjohann D, Hobbs HH, Cohen JC. Selective sterol accumulation in ABCG5/ABCG8-deficient mice. J Lipid Res. 2004;45:301-307.
-
(2004)
J Lipid Res
, vol.45
, pp. 301-307
-
-
Yu, L.1
Von Bergmann, K.2
Lutjohann, D.3
Hobbs, H.H.4
Cohen, J.C.5
-
53
-
-
61349177857
-
New susceptibility locus for coronary artery disease on chromosome 3q22.3
-
Erdmann J, Grosshennig A, Braund PS, Konig IR, Hengstenberg C, Hall AS, Linsel-Nitschke P, Kathiresan S, Wright B, Tregouet DA, Cambien F, Bruse P, Aherrahrou Z, Wagner AK, Stark K, Schwartz SM, Salomaa V, Elosua R, Melander O, Voight BF, O'Donnell CJ, Peltonen L, Siscovick DS, Altshuler D, Merlini PA, Peyvandi F, Bernardinelli L, Ardissino D, Schillert A, Blankenberg S, Zeller T, Wild P, Schwarz DF, Tiret L, Perret C, Schreiber S, El Mokhtari NE, Schafer A, Marz W, Renner W, Bugert P, Kluter H, Schrezenmeir J, Rubin D, Ball SG, Balmforth AJ, Wichmann HE, Meitinger T, Fischer M, Meisinger C, Baumert J, Peters A, Ouwehand WH, Deloukas P, Thompson JR, Ziegler A, Samani NJ, Schunkert H. New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat Genet. 2009;41:280-282.
-
(2009)
Nat Genet
, vol.41
, pp. 280-282
-
-
Erdmann, J.1
Grosshennig, A.2
Braund, P.S.3
Konig, I.R.4
Hengstenberg, C.5
Hall, A.S.6
Linsel-Nitschke, P.7
Kathiresan, S.8
Wright, B.9
Tregouet, D.A.10
Cambien, F.11
Bruse, P.12
Aherrahrou, Z.13
Wagner, A.K.14
Stark, K.15
Schwartz, S.M.16
Salomaa, V.17
Elosua, R.18
Melander, O.19
Voight, B.F.20
O'Donnell, C.J.21
Peltonen, L.22
Siscovick, D.S.23
Altshuler, D.24
Merlini, P.A.25
Peyvandi, F.26
Bernardinelli, L.27
Ardissino, D.28
Schillert, A.29
Blankenberg, S.30
Zeller, T.31
Wild, P.32
Schwarz, D.F.33
Tiret, L.34
Perret, C.35
Schreiber, S.36
El Mokhtari, N.E.37
Schafer, A.38
Marz, W.39
Renner, W.40
Bugert, P.41
Kluter, H.42
Schrezenmeir, J.43
Rubin, D.44
Ball, S.G.45
Balmforth, A.J.46
Wichmann, H.E.47
Meitinger, T.48
Fischer, M.49
Meisinger, C.50
Baumert, J.51
Peters, A.52
Ouwehand, W.H.53
Deloukas, P.54
Thompson, J.R.55
Ziegler, A.56
Samani, N.J.57
Schunkert, H.58
more..
-
54
-
-
73549097512
-
Genetic variants associated with Lp(a) lipoprotein level and coronary disease
-
Clarke R, Peden JF, Hopewell JC, Kyriakou T, Goel A, Heath SC, Parish S, Barlera S, Franzosi MG, Rust S, Bennett D, Silveira A, Malarstig A, Green FR, Lathrop M, Gigante B, Leander K, de Faire U, Seedorf U, Hamsten A, Collins R, Watkins H, Farrall M. Genetic variants associated with Lp(a) lipoprotein level and coronary disease. N Engl J Med. 2009; 361:2518-2528.
-
(2009)
N Engl J Med
, vol.361
, pp. 2518-2528
-
-
Clarke, R.1
Peden, J.F.2
Hopewell, J.C.3
Kyriakou, T.4
Goel, A.5
Heath, S.C.6
Parish, S.7
Barlera, S.8
Franzosi, M.G.9
Rust, S.10
Bennett, D.11
Silveira, A.12
Malarstig, A.13
Green, F.R.14
Lathrop, M.15
Gigante, B.16
Leander, K.17
De Faire, U.18
Seedorf, U.19
Hamsten, A.20
Collins, R.21
Watkins, H.22
Farrall, M.23
more..
-
55
-
-
0026677342
-
Atherogenesis in transgenic mice expressing human apolipoprotein(a)
-
Lawn RM, Wade DP, Hammer RE, Chiesa G, Verstuyft JG, Rubin EM. Atherogenesis in transgenic mice expressing human apolipoprotein(a). Nature. 1992;360:670-672.
-
(1992)
Nature
, vol.360
, pp. 670-672
-
-
Lawn, R.M.1
Wade, D.P.2
Hammer, R.E.3
Chiesa, G.4
Verstuyft, J.G.5
Rubin, E.M.6
-
56
-
-
77956808027
-
Lipoprotein(a) accelerates atherosclerosis in uremic mice
-
Pedersen TX, McCormick SP, Tsimikas S, Bro S, Nielsen LB. Lipoprotein( a) accelerates atherosclerosis in uremic mice. J Lipid Res. 2010; 51:2967-2975.
-
(2010)
J Lipid Res
, vol.51
, pp. 2967-2975
-
-
Pedersen, T.X.1
McCormick, S.P.2
Tsimikas, S.3
Bro, S.4
Nielsen, L.B.5
-
57
-
-
0032516054
-
Low density lipoprotein receptor-negative mice expressing human apolipoprotein B-100 develop complex atherosclerotic lesions on a chow diet: No accentuation by apolipoprotein(a)
-
Sanan DA, Newland DL, Tao R, Marcovina S, Wang J, Mooser V, Hammer RE, Hobbs HH. Low density lipoprotein receptor-negative mice expressing human apolipoprotein B-100 develop complex atherosclerotic lesions on a chow diet: no accentuation by apolipoprotein(a). Proc Natl Acad Sci USA. 1998;95:4544-4549.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 4544-4549
-
-
Sanan, D.A.1
Newland, D.L.2
Tao, R.3
Marcovina, S.4
Wang, J.5
Mooser, V.6
Hammer, R.E.7
Hobbs, H.H.8
-
58
-
-
0028293315
-
Expression of human apolipoprotein B and assembly of lipoprotein(a) in transgenic mice
-
Callow MJ, Stoltzfus LJ, Lawn RM, Rubin EM. Expression of human apolipoprotein B and assembly of lipoprotein(a) in transgenic mice. Proc Natl Acad Sci USA. 1994;91:2130-2134.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 2130-2134
-
-
Callow, M.J.1
Stoltzfus, L.J.2
Lawn, R.M.3
Rubin, E.M.4
-
59
-
-
0029737861
-
Genetically lean mice result from targeted disruption of the RIIβ subunit of protein kinase A
-
Cummings DE, Brandon EP, Planas JV, Motamed K, Idzerda RL, McKnight GS. Genetically lean mice result from targeted disruption of the RIIβ subunit of protein kinase A. Nature. 1996;382:622-626.
-
(1996)
Nature
, vol.382
, pp. 622-626
-
-
Cummings, D.E.1
Brandon, E.P.2
Planas, J.V.3
Motamed, K.4
Idzerda, R.L.5
McKnight, G.S.6
-
60
-
-
0035516189
-
Mutation of the RIIβ subunit of protein kinase a prevents diet-induced insulin resistance and dyslipidemia in mice
-
Schreyer SA, Cummings DE, McKnight GS, LeBoeuf RC. Mutation of the RIIβ subunit of protein kinase a prevents diet-induced insulin resistance and dyslipidemia in mice. Diabetes. 2001;50:2555-2562.
-
(2001)
Diabetes
, vol.50
, pp. 2555-2562
-
-
Schreyer, S.A.1
Cummings, D.E.2
McKnight, G.S.3
Leboeuf, R.C.4
-
61
-
-
52449102485
-
Myocardial expression, signaling, and function of GPR22: A protective role for an orphan G protein-coupled receptor
-
Adams JW, Wang J, Davis JR, Liaw C, Gaidarov I, Gatlin J, Dalton ND, Gu Y, Ross J Jr, Behan D, Chien K, Connolly D. Myocardial expression, signaling, and function of GPR22: a protective role for an orphan G protein-coupled receptor. Am J Physiol Heart Circ Physiol. 2008;295: H509-H521.
-
(2008)
Am J Physiol Heart Circ Physiol
, vol.295
-
-
Adams, J.W.1
Wang, J.2
Davis, J.R.3
Liaw, C.4
Gaidarov, I.5
Gatlin, J.6
Dalton, N.D.7
Gu, Y.8
Ross Jr., J.9
Behan, D.10
Chien, K.11
Connolly, D.12
-
62
-
-
34249996115
-
A common allele on chromosome 9 associated with coronary heart disease
-
McPherson R, Pertsemlidis A, Kavaslar N, Stewart A, Roberts R, Cox DR, Hinds DA, Pennacchio LA, Tybjaerg-Hansen A, Folsom AR, Boerwinkle E, Hobbs HH, Cohen JC. A common allele on chromosome 9 associated with coronary heart disease. Science. 2007;316:1488-1491.
-
(2007)
Science
, vol.316
, pp. 1488-1491
-
-
McPherson, R.1
Pertsemlidis, A.2
Kavaslar, N.3
Stewart, A.4
Roberts, R.5
Cox, D.R.6
Hinds, D.A.7
Pennacchio, L.A.8
Tybjaerg-Hansen, A.9
Folsom, A.R.10
Boerwinkle, E.11
Hobbs, H.H.12
Cohen, J.C.13
-
63
-
-
34250010480
-
A common variant on chromosome 9p21 affects the risk of myocardial infarction
-
Helgadottir A, Thorleifsson G, Manolescu A, Gretarsdottir S, Blondal T, Jonasdottir A, Sigurdsson A, Baker A, Palsson A, Masson G, Gudbjartsson DF, Magnusson KP, Andersen K, Levey AI, Backman VM, Matthiasdottir S, Jonsdottir T, Palsson S, Einarsdottir H, Gunnarsdottir S, Gylfason A, Vaccarino V, Hooper WC, Reilly MP, Granger CB, Austin H, Rader DJ, Shah SH, Quyyumi AA, Gulcher JR, Thorgeirsson G, Thorsteinsdottir U, Kong A, Stefansson K. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science. 2007; 316:1491-1493.
-
(2007)
Science
, vol.316
, pp. 1491-1493
-
-
Helgadottir, A.1
Thorleifsson, G.2
Manolescu, A.3
Gretarsdottir, S.4
Blondal, T.5
Jonasdottir, A.6
Sigurdsson, A.7
Baker, A.8
Palsson, A.9
Masson, G.10
Gudbjartsson, D.F.11
Magnusson, K.P.12
Andersen, K.13
Levey, A.I.14
Backman, V.M.15
Matthiasdottir, S.16
Jonsdottir, T.17
Palsson, S.18
Einarsdottir, H.19
Gunnarsdottir, S.20
Gylfason, A.21
Vaccarino, V.22
Hooper, W.C.23
Reilly, M.P.24
Granger, C.B.25
Austin, H.26
Rader, D.J.27
Shah, S.H.28
Quyyumi, A.A.29
Gulcher, J.R.30
Thorgeirsson, G.31
Thorsteinsdottir, U.32
Kong, A.33
Stefansson, K.34
more..
-
64
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Wellcome Trust Case Control Consortium
-
Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature. 2007;447:661-678.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
65
-
-
77951888636
-
P19(ARF) deficiency reduces macrophage and vascular smooth muscle cell apoptosis and aggravates atherosclerosis
-
Gonzalez-Navarro H, Abu Nabah YN, Vinue A, Andres-Manzano MJ, Collado M, Serrano M, Andres V. p19(ARF) deficiency reduces macrophage and vascular smooth muscle cell apoptosis and aggravates atherosclerosis. J Am Coll Cardiol. 2010;55:2258-2268.
-
(2010)
J Am Coll Cardiol
, vol.55
, pp. 2258-2268
-
-
Gonzalez-Navarro, H.1
Abu Nabah, Y.N.2
Vinue, A.3
Andres-Manzano, M.J.4
Collado, M.5
Serrano, M.6
Andres, V.7
-
66
-
-
0023252392
-
Association between polymorphic blood markers and risk factors for cardiovascular disease in a large pedigree
-
George VT, Elston RC, Amos CI, Ward LJ, Berenson GS. Association between polymorphic blood markers and risk factors for cardiovascular disease in a large pedigree. Genet Epidemiol. 1987;4:267-275.
-
(1987)
Genet Epidemiol
, vol.4
, pp. 267-275
-
-
George, V.T.1
Elston, R.C.2
Amos, C.I.3
Ward, L.J.4
Berenson, G.S.5
-
67
-
-
80053224243
-
Genetics of venous thrombosis: Insights from a new genome wide association study
-
Germain M, Saut N, Greliche N, Dina C, Lambert JC, Perret C, Cohen W, Oudot-Mellakh T, Antoni G, Alessi MC, Zelenika D, Cambien F, Tiret L, Bertrand M, Dupuy AM, Letenneur L, Lathrop M, Emmerich J, Amouyel P, Tregouet DA, Morange PE. Genetics of venous thrombosis: insights from a new genome wide association study. PLoS One. 2011;6:e25581.
-
(2011)
PLoS One
, vol.6
-
-
Germain, M.1
Saut, N.2
Greliche, N.3
Dina, C.4
Lambert, J.C.5
Perret, C.6
Cohen, W.7
Oudot-Mellakh, T.8
Antoni, G.9
Alessi, M.C.10
Zelenika, D.11
Cambien, F.12
Tiret, L.13
Bertrand, M.14
Dupuy, A.M.15
Letenneur, L.16
Lathrop, M.17
Emmerich, J.18
Amouyel, P.19
Tregouet, D.A.20
Morange, P.E.21
more..
-
68
-
-
77952534219
-
Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels
-
Barbalic M, Dupuis J, Dehghan A, Bis JC, Hoogeveen RC, Schnabel RB, Nambi V, Bretler M, Smith NL, Peters A, Lu C, Tracy RP, Aleksic N, Heeriga J, Keaney JF Jr, Rice K, Lip GY, Vasan RS, Glazer NL, Larson MG, Uitterlinden AG, Yamamoto J, Durda P, Haritunians T, Psaty BM, Boerwinkle E, Hofman A, Koenig W, Jenny NS, Witteman JC, Ballantyne C, Benjamin EJ. Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. Hum Mol Genet. 2010;19: 1863-1872.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 1863-1872
-
-
Barbalic, M.1
Dupuis, J.2
Dehghan, A.3
Bis, J.C.4
Hoogeveen, R.C.5
Schnabel, R.B.6
Nambi, V.7
Bretler, M.8
Smith, N.L.9
Peters, A.10
Lu, C.11
Tracy, R.P.12
Aleksic, N.13
Heeriga, J.14
Keaney Jr., J.F.15
Rice, K.16
Lip, G.Y.17
Vasan, R.S.18
Glazer, N.L.19
Larson, M.G.20
Uitterlinden, A.G.21
Yamamoto, J.22
Durda, P.23
Haritunians, T.24
Psaty, B.M.25
Boerwinkle, E.26
Hofman, A.27
Koenig, W.28
Jenny, N.S.29
Witteman, J.C.30
Ballantyne, C.31
Benjamin, E.J.32
more..
-
69
-
-
79955618781
-
Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci
-
Pare G, Ridker PM, Rose L, Barbalic M, Dupuis J, Dehghan A, Bis JC, Benjamin EJ, Shiffman D, Parker AN, Chasman DI. Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci. PLoS Genet. 2011;7:e1001374.
-
(2011)
PLoS Genet
, vol.7
-
-
Pare, G.1
Ridker, P.M.2
Rose, L.3
Barbalic, M.4
Dupuis, J.5
Dehghan, A.6
Bis, J.C.7
Benjamin, E.J.8
Shiffman, D.9
Parker, A.N.10
Chasman, D.I.11
-
70
-
-
84856169845
-
Association of variation at the ABO locus with circulating levels of sICAM-1, sP-selectin and sE-selectin: A meta-analysis
-
Kiechl S, Pare G, Barbalic M, Qi L, Dupuis J, Dehghan A, Bis JC, Laxton RC, Xiao Q, Bonora E, Willeit J, Xu Q, Witteman JC, Chasman D, Tracy RP, Ballantyne CM, Ridker PM, Benjamin EJ, Ye S. Association of variation at the ABO locus with circulating levels of sICAM-1, sP-selectin and sE-selectin: a meta-analysis. Circ Cardiovasc Genet. 2011.
-
(2011)
Circ Cardiovasc Genet
-
-
Kiechl, S.1
Pare, G.2
Barbalic, M.3
Qi, L.4
Dupuis, J.5
Dehghan, A.6
Bis, J.C.7
Laxton, R.C.8
Xiao, Q.9
Bonora, E.10
Willeit, J.11
Xu, Q.12
Witteman, J.C.13
Chasman, D.14
Tracy, R.P.15
Ballantyne, C.M.16
Ridker, P.M.17
Benjamin, E.J.18
Ye, S.19
-
71
-
-
73949157547
-
Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin
-
Paterson AD, Lopes-Virella MF, Waggott D, Boright AP, Hosseini SM, Carter RE, Shen E, Mirea L, Bharaj B, Sun L, Bull SB. Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin. Arterioscler Thromb Vasc Biol. 2009;29:1958-1967.
-
(2009)
Arterioscler Thromb Vasc Biol
, vol.29
, pp. 1958-1967
-
-
Paterson, A.D.1
Lopes-Virella, M.F.2
Waggott, D.3
Boright, A.P.4
Hosseini, S.M.5
Carter, R.E.6
Shen, E.7
Mirea, L.8
Bharaj, B.9
Sun, L.10
Bull, S.B.11
-
72
-
-
67349085063
-
Genome-wide association study identifies eight loci associated with blood pressure
-
Newton-Cheh C, Johnson T, Gateva V, Tobin MD, Bochud M, Coin L, Najjar SS, Zhao JH, Heath SC, Eyheramendy S, Papadakis K, Voight BF, Scott LJ, Zhang F, Farrall M, Tanaka T, Wallace C, Chambers JC, Khaw KT, Nilsson P, van der Harst P, Polidoro S, Grobbee DE, Onland-Moret NC, Bots ML, Wain LV, Elliott KS, Teumer A, Luan J, Lucas G, Kuusisto J, Burton PR, Hadley D, McArdle WL, Brown M, Dominiczak A, Newhouse SJ, Samani NJ, Webster J, Zeggini E, Beckmann JS, Bergmann S, Lim N, Song K, Vollenweider P, Waeber G, Waterworth DM, Yuan X, Groop L, Orho-Melander M, Allione A, Di Gregorio A, Guarrera S, Panico S, Ricceri F, Romanazzi V, Sacerdote C, Vineis P, Barroso I, Sandhu MS, Luben RN, Crawford GJ, Jousilahti P, Perola M, Boehnke M, Bonnycastle LL, Collins FS, Jackson AU, Mohlke KL, Stringham HM, Valle TT, Willer CJ, Bergman RN, Morken MA, Doring A, Gieger C, Illig T, Meitinger T, Org E, Pfeufer A, Wichmann HE, Kathiresan S, Marrugat J, O'Donnell CJ, Schwartz SM, Siscovick DS, Subirana I, Freimer NB, Hartikainen AL, McCarthy MI, O'Reilly PF, Peltonen L, Pouta A, de Jong PE, Snieder H, van Gilst WH, Clarke R, Goel A, Hamsten A, Peden JF, Seedorf U, Syvanen AC, Tognoni G, Lakatta EG, Sanna S, Scheet P, Schlessinger D, Scuteri A, Dorr M, Ernst F, Felix SB, Homuth G, Lorbeer R, Reffelmann T, Rettig R, Volker U, Galan P, Gut IG, Hercberg S, Lathrop GM, Zelenika D, Deloukas P, Soranzo N, Williams FM, Zhai G, Salomaa V, Laakso M, Elosua R, Forouhi NG, Volzke H, Uiterwaal CS, van der Schouw YT, Numans ME, Matullo G, Navis G, Berglund G, Bingham SA, Kooner JS, Connell JM, Bandinelli S, Ferrucci L, Watkins H, Spector TD, Tuomilehto J, Altshuler D, Strachan DP, Laan M, Meneton P, Wareham NJ, Uda M, Jarvelin MR, Mooser V, Melander O, Loos RJ, Elliott P, Abecasis GR, Caulfield M, Munroe PB. Genome-wide association study identifies eight loci associated with blood pressure. Nat Genet. 2009;41:666-676.
-
(2009)
Nat Genet
, vol.41
, pp. 666-676
-
-
Newton-Cheh, C.1
Johnson, T.2
Gateva, V.3
Tobin, M.D.4
Bochud, M.5
Coin, L.6
Najjar, S.S.7
Zhao, J.H.8
Heath, S.C.9
Eyheramendy, S.10
Papadakis, K.11
Voight, B.F.12
Scott, L.J.13
Zhang, F.14
Farrall, M.15
Tanaka, T.16
Wallace, C.17
Chambers, J.C.18
Khaw, K.T.19
Nilsson, P.20
Van Der Harst, P.21
Polidoro, S.22
Grobbee, D.E.23
Onland-Moret, N.C.24
Bots, M.L.25
Wain, L.V.26
Elliott, K.S.27
Teumer, A.28
Luan, J.29
Lucas, G.30
Kuusisto, J.31
Burton, P.R.32
Hadley, D.33
McArdle, W.L.34
Brown, M.35
Dominiczak, A.36
Newhouse, S.J.37
Samani, N.J.38
Webster, J.39
Zeggini, E.40
Beckmann, J.S.41
Bergmann, S.42
Lim, N.43
Song, K.44
Vollenweider, P.45
Waeber, G.46
Waterworth, D.M.47
Yuan, X.48
Groop, L.49
Orho-Melander, M.50
Allione, A.51
Di Gregorio, A.52
Guarrera, S.53
Panico, S.54
Ricceri, F.55
Romanazzi, V.56
Sacerdote, C.57
Vineis, P.58
Barroso, I.59
Sandhu, M.S.60
Luben, R.N.61
Crawford, G.J.62
Jousilahti, P.63
Perola, M.64
Boehnke, M.65
Bonnycastle, L.L.66
Collins, F.S.67
Jackson, A.U.68
Mohlke, K.L.69
Stringham, H.M.70
Valle, T.T.71
Willer, C.J.72
Bergman, R.N.73
Morken, M.A.74
Doring, A.75
Gieger, C.76
Illig, T.77
Meitinger, T.78
Org, E.79
Pfeufer, A.80
Wichmann, H.E.81
Kathiresan, S.82
Marrugat, J.83
O'Donnell, C.J.84
Schwartz, S.M.85
Siscovick, D.S.86
Subirana, I.87
Freimer, N.B.88
Hartikainen, A.L.89
McCarthy, M.I.90
O'Reilly, P.F.91
Peltonen, L.92
Pouta, A.93
De Jong, P.E.94
Snieder, H.95
Van Gilst, W.H.96
Clarke, R.97
Goel, A.98
Hamsten, A.99
more..
-
73
-
-
0025902231
-
Inhibition of early atherogenesis in transgenic mice by human apolipoprotein AI
-
Rubin EM, Krauss RM, Spangler EA, Verstuyft JG, Clift SM. Inhibition of early atherogenesis in transgenic mice by human apolipoprotein AI. Nature. 1991;353:265-267.
-
(1991)
Nature
, vol.353
, pp. 265-267
-
-
Rubin, E.M.1
Krauss, R.M.2
Spangler, E.A.3
Verstuyft, J.G.4
Clift, S.M.5
-
74
-
-
0028167663
-
Apolipoprotein AI transgene corrects apolipoprotein e deficiency-induced atherosclerosis in mice
-
Paszty C, Maeda N, Verstuyft J, Rubin EM. Apolipoprotein AI transgene corrects apolipoprotein E deficiency-induced atherosclerosis in mice. J Clin Invest. 1994;94:899-903.
-
(1994)
J Clin Invest
, vol.94
, pp. 899-903
-
-
Paszty, C.1
Maeda, N.2
Verstuyft, J.3
Rubin, E.M.4
-
75
-
-
0031910099
-
ApoA-I deficiency causes both hypertriglyceridemia and increased atherosclerosis in human apoB transgenic mice
-
Voyiaziakis E, Goldberg IJ, Plump AS, Rubin EM, Breslow JL, Huang LS. ApoA-I deficiency causes both hypertriglyceridemia and increased atherosclerosis in human apoB transgenic mice. J Lipid Res. 1998;39: 313-321.
-
(1998)
J Lipid Res
, vol.39
, pp. 313-321
-
-
Voyiaziakis, E.1
Goldberg, I.J.2
Plump, A.S.3
Rubin, E.M.4
Breslow, J.L.5
Huang, L.S.6
-
76
-
-
54049125406
-
Atheroprotective effect of human apolipoprotein A5 in a mouse model of mixed dyslipidemia
-
Mansouri RM, Bauge E, Gervois P, Fruchart-Najib J, Fievet C, Staels B, Fruchart JC. Atheroprotective effect of human apolipoprotein A5 in a mouse model of mixed dyslipidemia. Circ Res. 2008;103:450-453.
-
(2008)
Circ Res
, vol.103
, pp. 450-453
-
-
Mansouri, R.M.1
Bauge, E.2
Gervois, P.3
Fruchart-Najib, J.4
Fievet, C.5
Staels, B.6
Fruchart, J.C.7
-
77
-
-
33646798747
-
Characterization of a new mouse model for human apolipoprotein A-I/C-III/A-IV deficiency
-
Mezdour H, Larigauderie G, Castro G, Torpier G, Fruchart J, Nowak M, Fruchart JC, Rouis M, Maeda N. Characterization of a new mouse model for human apolipoprotein A-I/C-III/A-IV deficiency. J Lipid Res. 2006; 47:912-920.
-
(2006)
J Lipid Res
, vol.47
, pp. 912-920
-
-
Mezdour, H.1
Larigauderie, G.2
Castro, G.3
Torpier, G.4
Fruchart, J.5
Nowak, M.6
Fruchart, J.C.7
Rouis, M.8
Maeda, N.9
-
78
-
-
0037389235
-
Apolipoprotein A5, a newly identified gene that affects plasma triglyceride levels in humans and mice
-
Pennacchio LA, Rubin EM. Apolipoprotein A5, a newly identified gene that affects plasma triglyceride levels in humans and mice. Arterioscler Thromb Vasc Biol. 2003;23:529-534.
-
(2003)
Arterioscler Thromb Vasc Biol
, vol.23
, pp. 529-534
-
-
Pennacchio, L.A.1
Rubin, E.M.2
-
79
-
-
3042817124
-
Analysis of apolipoprotein A5, c3, and plasma triglyceride concentrations in genetically engineered mice
-
Baroukh N, Bauge E, Akiyama J, Chang J, Afzal V, Fruchart JC, Rubin EM, Fruchart-Najib J, Pennacchio LA. Analysis of apolipoprotein A5, c3, and plasma triglyceride concentrations in genetically engineered mice. Arterioscler Thromb Vasc Biol. 2004;24:1297-1302.
-
(2004)
Arterioscler Thromb Vasc Biol
, vol.24
, pp. 1297-1302
-
-
Baroukh, N.1
Bauge, E.2
Akiyama, J.3
Chang, J.4
Afzal, V.5
Fruchart, J.C.6
Rubin, E.M.7
Fruchart-Najib, J.8
Pennacchio, L.A.9
-
80
-
-
70350644759
-
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
-
Soranzo N, Spector TD, Mangino M, Kuhnel B, Rendon A, Teumer A, Willenborg C, Wright B, Chen L, Li M, Salo P, Voight BF, Burns P, Laskowski RA, Xue Y, Menzel S, Altshuler D, Bradley JR, Bumpstead S, Burnett MS, Devaney J, Doring A, Elosua R, Epstein SE, Erber W, Falchi M, Garner SF, Ghori MJ, Goodall AH, Gwilliam R, Hakonarson HH, Hall AS, Hammond N, Hengstenberg C, Illig T, Konig IR, Knouff CW, McPherson R, Melander O, Mooser V, Nauck M, Nieminen MS, O'Donnell CJ, Peltonen L, Potter SC, Prokisch H, Rader DJ, Rice CM, Roberts R, Salomaa V, Sambrook J, Schreiber S, Schunkert H, Schwartz SM, Serbanovic-Canic J, Sinisalo J, Siscovick DS, Stark K, Surakka I, Stephens J, Thompson JR, Volker U, Volzke H, Watkins NA, Wells GA, Wichmann HE, Van Heel DA, Tyler-Smith C, Thein SL, Kathiresan S, Perola M, Reilly MP, Stewart AF, Erdmann J, Samani NJ, Meisinger C, Greinacher A, Deloukas P, Ouwehand WH, Gieger C. A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. Nat Genet. 2009;41:1182-1190.
-
(2009)
Nat Genet
, vol.41
, pp. 1182-1190
-
-
Soranzo, N.1
Spector, T.D.2
Mangino, M.3
Kuhnel, B.4
Rendon, A.5
Teumer, A.6
Willenborg, C.7
Wright, B.8
Chen, L.9
Li, M.10
Salo, P.11
Voight, B.F.12
Burns, P.13
Laskowski, R.A.14
Xue, Y.15
Menzel, S.16
Altshuler, D.17
Bradley, J.R.18
Bumpstead, S.19
Burnett, M.S.20
Devaney, J.21
Doring, A.22
Elosua, R.23
Epstein, S.E.24
Erber, W.25
Falchi, M.26
Garner, S.F.27
Ghori, M.J.28
Goodall, A.H.29
Gwilliam, R.30
Hakonarson, H.H.31
Hall, A.S.32
Hammond, N.33
Hengstenberg, C.34
Illig, T.35
Konig, I.R.36
Knouff, C.W.37
McPherson, R.38
Melander, O.39
Mooser, V.40
Nauck, M.41
Nieminen, M.S.42
O'Donnell, C.J.43
Peltonen, L.44
Potter, S.C.45
Prokisch, H.46
Rader, D.J.47
Rice, C.M.48
Roberts, R.49
Salomaa, V.50
Sambrook, J.51
Schreiber, S.52
Schunkert, H.53
Schwartz, S.M.54
Serbanovic-Canic, J.55
Sinisalo, J.56
Siscovick, D.S.57
Stark, K.58
Surakka, I.59
Stephens, J.60
Thompson, J.R.61
Volker, U.62
Volzke, H.63
Watkins, N.A.64
Wells, G.A.65
Wichmann, H.E.66
Van Heel, D.A.67
Tyler-Smith, C.68
Thein, S.L.69
Kathiresan, S.70
Perola, M.71
Reilly, M.P.72
Stewart, A.F.73
Erdmann, J.74
Samani, N.J.75
Meisinger, C.76
Greinacher, A.77
Deloukas, P.78
Ouwehand, W.H.79
Gieger, C.80
more..
-
81
-
-
67349208839
-
Genome-wide association study of blood pressure and hypertension
-
Levy D, Ehret GB, Rice K, Verwoert GC, Launer LJ, Dehghan A, Glazer NL, Morrison AC, Johnson AD, Aspelund T, Aulchenko Y, Lumley T, Kottgen A, Vasan RS, Rivadeneira F, Eiriksdottir G, Guo X, Arking DE, Mitchell GF, Mattace-Raso FU, Smith AV, Taylor K, Scharpf RB, Hwang SJ, Sijbrands EJ, Bis J, Harris TB, Ganesh SK, O'Donnell CJ, Hofman A, Rotter JI, Coresh J, Benjamin EJ, Uitterlinden AG, Heiss G, Fox CS, Witteman JC, Boerwinkle E, Wang TJ, Gudnason V, Larson MG, Chakravarti A, Psaty BM, van Duijn CM. Genome-wide association study of blood pressure and hypertension. Nat Genet. 2009;41:677-687.
-
(2009)
Nat Genet
, vol.41
, pp. 677-687
-
-
Levy, D.1
Ehret, G.B.2
Rice, K.3
Verwoert, G.C.4
Launer, L.J.5
Dehghan, A.6
Glazer, N.L.7
Morrison, A.C.8
Johnson, A.D.9
Aspelund, T.10
Aulchenko, Y.11
Lumley, T.12
Kottgen, A.13
Vasan, R.S.14
Rivadeneira, F.15
Eiriksdottir, G.16
Guo, X.17
Arking, D.E.18
Mitchell, G.F.19
Mattace-Raso, F.U.20
Smith, A.V.21
Taylor, K.22
Scharpf, R.B.23
Hwang, S.J.24
Sijbrands, E.J.25
Bis, J.26
Harris, T.B.27
Ganesh, S.K.28
O'Donnell, C.J.29
Hofman, A.30
Rotter, J.I.31
Coresh, J.32
Benjamin, E.J.33
Uitterlinden, A.G.34
Heiss, G.35
Fox, C.S.36
Witteman, J.C.37
Boerwinkle, E.38
Wang, T.J.39
Gudnason, V.40
Larson, M.G.41
Chakravarti, A.42
Psaty, B.M.43
Van Duijn, C.M.44
more..
-
82
-
-
69849104511
-
Lack of phosphatidylethanolamine n-methyltransferase alters plasma VLDL phospholipids and attenuates atherosclerosis in mice
-
Zhao Y, Su B, Jacobs RL, Kennedy B, Francis GA, Waddington E, Brosnan JT, Vance JE, Vance DE. Lack of phosphatidylethanolamine n-methyltransferase alters plasma VLDL phospholipids and attenuates atherosclerosis in mice. Arterioscler Thromb Vasc Biol. 2009;29: 1349-1355.
-
(2009)
Arterioscler Thromb Vasc Biol
, vol.29
, pp. 1349-1355
-
-
Zhao, Y.1
Su, B.2
Jacobs, R.L.3
Kennedy, B.4
Francis, G.A.5
Waddington, E.6
Brosnan, J.T.7
Vance, J.E.8
Vance, D.E.9
-
83
-
-
79953064630
-
Impaired phosphatidylcholine biosynthesis reduces atherosclerosis and prevents lipotoxic cardiac dysfunction in apoe-/-mice
-
Cole LK, Dolinsky VW, Dyck JR, Vance DE. Impaired phosphatidylcholine biosynthesis reduces atherosclerosis and prevents lipotoxic cardiac dysfunction in apoe-/-mice. Circ Res. 2011;108:686-694.
-
(2011)
Circ Res
, vol.108
, pp. 686-694
-
-
Cole, L.K.1
Dolinsky, V.W.2
Dyck, J.R.3
Vance, D.E.4
-
84
-
-
79951783421
-
The role of phosphatidylethanolamine methyltransferase in a mouse model of intrahepatic cholestasis
-
Li Z, Agellon LB, Vance DE. The role of phosphatidylethanolamine methyltransferase in a mouse model of intrahepatic cholestasis. Biochim Biophys Acta. 2011;1811:278-283.
-
(2011)
Biochim Biophys Acta
, vol.1811
, pp. 278-283
-
-
Li, Z.1
Agellon, L.B.2
Vance, D.E.3
-
85
-
-
4444328790
-
Familial hypercholesterolemia and coronary heart disease: A huge association review
-
Austin MA, Hutter CM, Zimmern RL, Humphries SE. Familial hypercholesterolemia and coronary heart disease: a huge association review. Am J Epidemiol. 2004;160:421-429.
-
(2004)
Am J Epidemiol
, vol.160
, pp. 421-429
-
-
Austin, M.A.1
Hutter, C.M.2
Zimmern, R.L.3
Humphries, S.E.4
-
86
-
-
0028345073
-
Massive xanthomatosis and atherosclerosis in cholesterol-fed low density lipoprotein receptor-negative mice
-
Ishibashi S, Goldstein JL, Brown MS, Herz J, Burns DK. Massive xanthomatosis and atherosclerosis in cholesterol-fed low density lipoprotein receptor-negative mice. J Clin Invest. 1994;93:1885-1893.
-
(1994)
J Clin Invest
, vol.93
, pp. 1885-1893
-
-
Ishibashi, S.1
Goldstein, J.L.2
Brown, M.S.3
Herz, J.4
Burns, D.K.5
-
87
-
-
0027258140
-
Hypercholesterolemia in low density lipoprotein receptor knockout mice and its reversal by adenovirus-mediated gene delivery
-
Ishibashi S, Brown MS, Goldstein JL, Gerard RD, Hammer RE, Herz J. Hypercholesterolemia in low density lipoprotein receptor knockout mice and its reversal by adenovirus-mediated gene delivery. J Clin Invest. 1993;92:883-893.
-
(1993)
J Clin Invest
, vol.92
, pp. 883-893
-
-
Ishibashi, S.1
Brown, M.S.2
Goldstein, J.L.3
Gerard, R.D.4
Hammer, R.E.5
Herz, J.6
-
88
-
-
70350189803
-
Common haplotypes in five genes influence genetic variance of LDL and HDL cholesterol in the general population
-
Knoblauch H, Bauerfeind A, Krahenbuhl C, Daury A, Rohde K, Bejanin S, Essioux L, Schuster H, Luft FC, Reich JG. Common haplotypes in five genes influence genetic variance of LDL and HDL cholesterol in the general population. Hum Mol Genet. 2002;11:1477-1485.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1477-1485
-
-
Knoblauch, H.1
Bauerfeind, A.2
Krahenbuhl, C.3
Daury, A.4
Rohde, K.5
Bejanin, S.6
Essioux, L.7
Schuster, H.8
Luft, F.C.9
Reich, J.G.10
-
89
-
-
0026592806
-
Spontaneous hypercholesterolemia and arterial lesions in mice lacking apolipoprotein e
-
Zhang SH, Reddick RL, Piedrahita JA, Maeda N. Spontaneous hypercholesterolemia and arterial lesions in mice lacking apolipoprotein E. Science. 1992;258:468-471.
-
(1992)
Science
, vol.258
, pp. 468-471
-
-
Zhang, S.H.1
Reddick, R.L.2
Piedrahita, J.A.3
Maeda, N.4
-
90
-
-
0026725757
-
Severe hypercholesterolemia and atherosclerosis in apolipoprotein E-deficient mice created by homologous recombination in ES cells
-
Plump AS, Smith JD, Hayek T, Aalto-Setala K, Walsh A, Verstuyft JG, Rubin EM, Breslow JL. Severe hypercholesterolemia and atherosclerosis in apolipoprotein E-deficient mice created by homologous recombination in ES cells. Cell. 1992;71:343-353.
-
(1992)
Cell
, vol.71
, pp. 343-353
-
-
Plump, A.S.1
Smith, J.D.2
Hayek, T.3
Aalto-Setala, K.4
Walsh, A.5
Verstuyft, J.G.6
Rubin, E.M.7
Breslow, J.L.8
-
91
-
-
0027958084
-
ApoEdeficient mice develop lesions of all phases of atherosclerosis throughout the arterial tree
-
Nakashima Y, Plump AS, Raines EW, Breslow JL, Ross R. ApoEdeficient mice develop lesions of all phases of atherosclerosis throughout the arterial tree. Arterioscler Thromb. 1994;14:133-140.
-
(1994)
Arterioscler Thromb
, vol.14
, pp. 133-140
-
-
Nakashima, Y.1
Plump, A.S.2
Raines, E.W.3
Breslow, J.L.4
Ross, R.5
|