-
1
-
-
84888317489
-
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
-
European Alzheimer's Disease Initiative (EADI), Genetic and Environmental Risk in Alzheimer's Disease (GERAD), Alzheimer's Disease Genetic Consortium (ADGC), Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE), doi: 10.1038/ng.2802
-
Lambert JC, Ibrahim-Verbaas CA, Harold D, Naj AC, Sims R, Bellenguez C, Jun G, Destefano AL, Bis JC, Beecham GW, Grenier-Boley B, Russo G, Thornton-Wells TA, Jones N, Smith AV, Chouraki V, Thomas C, Ikram MA, Zelenika D, Vardarajan BN, Kamatani Y, Lin CF, Gerrish A, Schmidt H, Kunkle B, Dunstan ML, Ruiz A, Bihoreau MT, Choi SH, Reitz C, Pasquier F, Hollingworth P, Ramirez A, Hanon O, Fitzpatrick AL, Buxbaum JD, Campion D, Crane PK, Baldwin C, Becker T, Gudnason V, Cruchaga C, Craig D, Amin N, Berr C, Lopez OL, De Jager PL, Deramecourt V, Johnston JA, Evans D, Lovestone S, Letenneur L, Morón FJ, Rubinsztein DC, Eiriksdottir G, Sleegers K, Goate AM, Fiévet N, Huentelman MJ, Gill M, Brown K, Kamboh MI, Keller L, Barberger-Gateau P, McGuinness B, Larson EB, Green R, Myers AJ, Dufouil C, Todd S, Wallon D, Love S, Rogaeva E, Gallacher J, St George-Hyslop P, Clarimon J, Lleo A, Bayer A, Tsuang DW, Yu L, Tsolaki M, Bossù P, Spalletta G, Proitsi P, Collinge J, Sorbi S, Sanchez-Garcia F, Fox NC, Hardy J, Naranjo MC, Bosco P, Clarke R, Brayne C, Galimberti D, Mancuso M, Matthews F, European Alzheimer's Disease Initiative (EADI), Genetic and Environmental Risk in Alzheimer's Disease (GERAD), Alzheimer's Disease Genetic Consortium (ADGC), Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE), Moebus S, Mecocci P, Del Zompo M, Maier W, Hampel H, Pilotto A, Bullido M, Panza F, Caffarra P, Nacmias B, Gilbert JR, Mayhaus M, Lannfelt L, Hakonarson H, Pichler S, Carrasquillo MM, Ingelsson M, Beekly D, Alvarez V, Zou F, Valladares O, Younkin SG, Coto E, Hamilton-Nelson KL, Gu W, Razquin C, Pastor P, Mateo I, Owen MJ, Faber KM, Jonsson PV, Combarros O, O'Donovan MC, Cantwell LB, Soininen H, Blacker D, Mead S, Mosley TH Jr, Bennett DA, Harris TB, Fratiglioni L, Holmes C, de Bruijn RF, Passmore P, Montine TJ, Bettens K, Rotter JI, Brice A, Morgan K, Foroud TM, Kukull WA, Hannequin D, Powell JF, Nalls MA, Ritchie K, Lunetta KL, Kauwe JS, Boerwinkle E, Riemenschneider M, Boada M, Hiltunen M, Martin ER, Schmidt R, Rujescu D, Wang LS, Dartigues JF, Mayeux R, Tzourio C, Hofman A, Nöthen MM, Graff C, Psaty BM, Jones L, Haines JL, Holmans PA, Lathrop M, Pericak-Vance MA, Launer LJ, Farrer LA, van Duijn CM, Van Broeckhoven C, Moskvina V, Seshadri S, Williams J, Schellenberg GD, Amouyel P. Meta-analysis of 74, 046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nat Genet 2013; 45: 1452-1458. doi: 10.1038/ng.2802
-
(2013)
Nat Genet
, vol.45
, pp. 1452-1458
-
-
Lambert, J.C.1
Ibrahim-Verbaas, C.A.2
Harold, D.3
Naj, A.C.4
Sims, R.5
Bellenguez, C.6
Jun, G.7
Destefano, A.L.8
Bis, J.C.9
Beecham, G.W.10
Grenier-Boley, B.11
Russo, G.12
Thornton-Wells, T.A.13
Jones, N.14
Smith, A.V.15
Chouraki, V.16
Thomas, C.17
Ikram, M.A.18
Zelenika, D.19
Vardarajan, B.N.20
Kamatani, Y.21
Lin, C.F.22
Gerrish, A.23
Schmidt, H.24
Kunkle, B.25
Dunstan, M.L.26
Ruiz, A.27
Bihoreau, M.T.28
Choi, S.H.29
Reitz, C.30
Pasquier, F.31
Hollingworth, P.32
Ramirez, A.33
Hanon, O.34
Fitzpatrick, A.L.35
Buxbaum, J.D.36
Campion, D.37
Crane, P.K.38
Baldwin, C.39
Becker, T.40
Gudnason, V.41
Cruchaga, C.42
Craig, D.43
Amin, N.44
Berr, C.45
Lopez, O.L.46
De Jager, P.L.47
Deramecourt, V.48
Johnston, J.A.49
Evans, D.50
Lovestone, S.51
Letenneur, L.52
Morón, F.J.53
Rubinsztein, D.C.54
Eiriksdottir, G.55
Sleegers, K.56
Goate, A.M.57
Fiévet, N.58
Huentelman, M.J.59
Gill, M.60
Brown, K.61
Kamboh, M.I.62
Keller, L.63
Barberger-Gateau, P.64
McGuinness, B.65
Larson, E.B.66
Green, R.67
Myers, A.J.68
Dufouil, C.69
Todd, S.70
Wallon, D.71
Love, S.72
Rogaeva, E.73
Gallacher, J.74
St George-Hyslop, P.75
Clarimon, J.76
Lleo, A.77
Bayer, A.78
Tsuang, D.W.79
Yu, L.80
Tsolaki, M.81
Bossù, P.82
Spalletta, G.83
Proitsi, P.84
Collinge, J.85
Sorbi, S.86
Sanchez-Garcia, F.87
Fox, N.C.88
Hardy, J.89
Naranjo, M.C.90
Bosco, P.91
Clarke, R.92
Brayne, C.93
Galimberti, D.94
Mancuso, M.95
Matthews, F.96
Moebus, S.97
Mecocci, P.98
Del Zompo, M.99
Maier, W.100
Hampel, H.101
Pilotto, A.102
Bullido, M.103
Panza, F.104
Caffarra, P.105
Nacmias, B.106
Gilbert, J.R.107
Mayhaus, M.108
Lannfelt, L.109
Hakonarson, H.110
Pichler, S.111
Carrasquillo, M.M.112
Ingelsson, M.113
Beekly, D.114
Alvarez, V.115
Zou, F.116
Valladares, O.117
Younkin, S.G.118
Coto, E.119
Hamilton-Nelson, K.L.120
Gu, W.121
Razquin, C.122
Pastor, P.123
Mateo, I.124
Owen, M.J.125
Faber, K.M.126
Jonsson, P.V.127
Combarros, O.128
O'Donovan, M.C.129
Cantwell, L.B.130
Soininen, H.131
Blacker, D.132
Mead, S.133
Mosley Jr, T.H.134
Bennett, D.A.135
Harris, T.B.136
Fratiglioni, L.137
Holmes, C.138
de Bruijn, R.F.139
Passmore, P.140
Montine, T.J.141
Bettens, K.142
Rotter, J.I.143
Brice, A.144
Morgan, K.145
Foroud, T.M.146
Kukull, W.A.147
Hannequin, D.148
Powell, J.F.149
Nalls, M.A.150
Ritchie, K.151
Lunetta, K.L.152
Kauwe, J.S.153
Boerwinkle, E.154
Riemenschneider, M.155
Boada, M.156
Hiltunen, M.157
Martin, E.R.158
Schmidt, R.159
Rujescu, D.160
Wang, L.S.161
Dartigues, J.F.162
Mayeux, R.163
Tzourio, C.164
Hofman, A.165
Nöthen, M.M.166
Graff, C.167
Psaty, B.M.168
Jones, L.169
Haines, J.L.170
Holmans, P.A.171
Lathrop, M.172
Pericak-Vance, M.A.173
Launer, L.J.174
Farrer, L.A.175
van Duijn, C.M.176
Van Broeckhoven, C.177
Moskvina, V.178
Seshadri, S.179
Williams, J.180
Schellenberg, G.D.181
Amouyel, P.182
more..
-
2
-
-
84872057940
-
TREM2 variants in Alzheimer's disease
-
Guerreiro R, Wojtas A, Bras J, Carrasquillo M, Rogaeva E, Majounie E, Cruchaga C, Sassi C, Kauwe JSK, Younkin S, Hazrati L, Collinge J, Pocock J, Lashley T, Williams J, Lambert J-C, Amouyel P, Goate A, Rademakers R, Morgan K, Powell J, St. George-Hyslop P, Singleton A, Hardy J. TREM2 variants in Alzheimer's disease. N Engl J Med 2013; 368: 117-127
-
(2013)
N Engl J Med
, vol.368
, pp. 117-127
-
-
Guerreiro, R.1
Wojtas, A.2
Bras, J.3
Carrasquillo, M.4
Rogaeva, E.5
Majounie, E.6
Cruchaga, C.7
Sassi, C.8
Kauwe, J.S.K.9
Younkin, S.10
Hazrati, L.11
Collinge, J.12
Pocock, J.13
Lashley, T.14
Williams, J.15
Lambert, J.-C.16
Amouyel, P.17
Goate, A.18
Rademakers, R.19
Morgan, K.20
Powell, J.21
St George-Hyslop, P.22
Singleton, A.23
Hardy, J.24
more..
-
3
-
-
79955464911
-
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onsheimer's disease
-
Naj AC, Jun G, Beecham GW, Wang L-S, Vardarajan BN, Buros J, Gallins PJ, Buxbaum JD, Jarvik GP, Crane PK, Larson EB, Bird TD, Boeve BF, Graff-Radford NR, De Jager PL, Evans D, Schneider JA, Carrasquillo MM, Ertekin-Taner N, Younkin SG, Cruchaga C, Kauwe JSK, Nowotny P, Kramer P, Hardy J, Huentelman MJ, Myers AJ, Barmada MM, Demirci FY, Baldwin CT, Green RC, Rogaeva E, St George-Hyslop P, Arnold SE, Barber R, Beach T, Bigio EH, Bowen JD, Boxer A, Burke JR, Cairns NJ, Carlson CS, Carney RM, Carroll SL, Chui HC, Clark DG, Corneveaux J, Cotman CW, Cummings JL, DeCarli C, DeKosky ST, Diaz-Arrastia R, Dick M, Dickson DW, Ellis WG, Faber KM, Fallon KB, Farlow MR, Ferris S, Frosch MP, Galasko DR, Ganguli M, Gearing M, Geschwind DH, Ghetti B, Gilbert JR, Gilman S, Giordani B, Glass JD, Growdon JH, Hamilton RL, Harrell LE, Head E, Honig LS, Hulette CM, Hyman BT, Jicha GA, Jin L-W, Johnson N, Karlawish J, Karydas A, Kaye JA, Kim R, Koo EH, Kowall NW, Lah JJ, Levey AI, Lieberman AP, Lopez OL, Mack WJ, Marson DC, Martiniuk F, Mash DC, Masliah E, McCormick WC, McCurry SM, McDavid AN, McKee AC, Mesulam M, Miller BL, Miller CA, Miller JW, Parisi JE, Perl DP, Peskind E, Petersen RC, Poon WW, Quinn JF, Rajbhandary RA, Raskind M, Reisberg B, Ringman JM, Roberson ED, Rosenberg RN, Sano M, Schneider LS, Seeley W, Shelanski ML, Slifer MA, Smith CD, Sonnen JA, Spina S, Stern RA, Tanzi RE, Trojanowski JQ, Troncoso JC, Van Deerlin VM, Vinters HV, Vonsattel JP, Weintraub S, Welsh-Bohmer KA, Williamson J, Woltjer RL, Cantwell LB, Dombroski BA, Beekly D, Lunetta KL, Martin ER, Kamboh MI, Saykin AJ, Reiman EM, Bennett DA, Morris JC, Montine TJ, Goate AM, Blacker D, Tsuang DW, Hakonarson H, Kukull WA, Foroud TM, Haines JL, Mayeux R, Pericak-Vance MA, Farrer LA, Schellenberg GD. Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nat Genet 2011; 43: 436-441
-
(2011)
Nat Genet
, vol.43
, pp. 436-441
-
-
Naj, A.C.1
Jun, G.2
Beecham, G.W.3
Wang, L.-S.4
Vardarajan, B.N.5
Buros, J.6
Gallins, P.J.7
Buxbaum, J.D.8
Jarvik, G.P.9
Crane, P.K.10
Larson, E.B.11
Bird, T.D.12
Boeve, B.F.13
Graff-Radford, N.R.14
De Jager, P.L.15
Evans, D.16
Schneider, J.A.17
Carrasquillo, M.M.18
Ertekin-Taner, N.19
Younkin, S.G.20
Cruchaga, C.21
Kauwe, J.S.K.22
Nowotny, P.23
Kramer, P.24
Hardy, J.25
Huentelman, M.J.26
Myers, A.J.27
Barmada, M.M.28
Demirci, F.Y.29
Baldwin, C.T.30
Green, R.C.31
Rogaeva, E.32
St George-Hyslop, P.33
Arnold, S.E.34
Barber, R.35
Beach, T.36
Bigio, E.H.37
Bowen, J.D.38
Boxer, A.39
Burke, J.R.40
Cairns, N.J.41
Carlson, C.S.42
Carney, R.M.43
Carroll, S.L.44
Chui, H.C.45
Clark, D.G.46
Corneveaux, J.47
Cotman, C.W.48
Cummings, J.L.49
DeCarli, C.50
DeKosky, S.T.51
Diaz-Arrastia, R.52
Dick, M.53
Dickson, D.W.54
Ellis, W.G.55
Faber, K.M.56
Fallon, K.B.57
Farlow, M.R.58
Ferris, S.59
Frosch, M.P.60
Galasko, D.R.61
Ganguli, M.62
Gearing, M.63
Geschwind, D.H.64
Ghetti, B.65
Gilbert, J.R.66
Gilman, S.67
Giordani, B.68
Glass, J.D.69
Growdon, J.H.70
Hamilton, R.L.71
Harrell, L.E.72
Head, E.73
Honig, L.S.74
Hulette, C.M.75
Hyman, B.T.76
Jicha, G.A.77
Jin, L.-W.78
Johnson, N.79
Karlawish, J.80
Karydas, A.81
Kaye, J.A.82
Kim, R.83
Koo, E.H.84
Kowall, N.W.85
Lah, J.J.86
Levey, A.I.87
Lieberman, A.P.88
Lopez, O.L.89
Mack, W.J.90
Marson, D.C.91
Martiniuk, F.92
Mash, D.C.93
Masliah, E.94
McCormick, W.C.95
McCurry, S.M.96
McDavid, A.N.97
McKee, A.C.98
Mesulam, M.99
Miller, B.L.100
Miller, C.A.101
Miller, J.W.102
Parisi, J.E.103
Perl, D.P.104
Peskind, E.105
Petersen, R.C.106
Poon, W.W.107
Quinn, J.F.108
Rajbhandary, R.A.109
Raskind, M.110
Reisberg, B.111
Ringman, J.M.112
Roberson, E.D.113
Rosenberg, R.N.114
Sano, M.115
Schneider, L.S.116
Seeley, W.117
Shelanski, M.L.118
Slifer, M.A.119
Smith, C.D.120
Sonnen, J.A.121
Spina, S.122
Stern, R.A.123
Tanzi, R.E.124
Trojanowski, J.Q.125
Troncoso, J.C.126
Van Deerlin, V.M.127
Vinters, H.V.128
Vonsattel, J.P.129
Weintraub, S.130
Welsh-Bohmer, K.A.131
Williamson, J.132
Woltjer, R.L.133
Cantwell, L.B.134
Dombroski, B.A.135
Beekly, D.136
Lunetta, K.L.137
Martin, E.R.138
Kamboh, M.I.139
Saykin, A.J.140
Reiman, E.M.141
Bennett, D.A.142
Morris, J.C.143
Montine, T.J.144
Goate, A.M.145
Blacker, D.146
Tsuang, D.W.147
Hakonarson, H.148
Kukull, W.A.149
Foroud, T.M.150
Haines, J.L.151
Mayeux, R.152
Pericak-Vance, M.A.153
Farrer, L.A.154
Schellenberg, G.D.155
more..
-
4
-
-
84855925920
-
Rare and common variants: twenty arguments
-
Gibson G. Rare and common variants: twenty arguments. Nat Rev Genet 2011; 13: 135-145
-
(2011)
Nat Rev Genet
, vol.13
, pp. 135-145
-
-
Gibson, G.1
-
5
-
-
79955484414
-
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
-
Hollingworth P, Harold D, Sims R, Gerrish A, Lambert J-C, Carrasquillo MM, Abraham R, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Jones N, Stretton A, Thomas C, Richards A, Ivanov D, Widdowson C, Chapman J, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Holmes C, Mann D, Smith AD, Beaumont H, Warden D, Wilcock G, Love S, Kehoe PG, Hooper NM, Vardy ERLC, Hardy J, Mead S, Fox NC, Rossor M, Collinge J, Maier W, Jessen F, Rüther E, Schürmann B, Heun R, Kölsch H, van den Bussche H, Heuser I, Kornhuber J, Wiltfang J, Dichgans M, Frölich L, Hampel H, Gallacher J, Hüll M, Rujescu D, Giegling I, Goate AM, Kauwe JSK, Cruchaga C, Nowotny P, Morris JC, Mayo K, Sleegers K, Bettens K, Engelborghs S, De Deyn PP, Van Broeckhoven C, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Tsolaki M, Singleton AB, Guerreiro R, Mühleisen TW, Nöthen MM, Moebus S, Jöckel K-H, Klopp N, Wichmann H-E, Pankratz VS, Sando SB, Aasly JO, Barcikowska M, Wszolek ZK, Dickson DW, Graff-Radford NR, Petersen RC, van Duijn CM, Breteler MMB, Ikram MA, DeStefano AL, Fitzpatrick AL, Lopez O, Launer LJ, Seshadri S, Berr C, Campion D, Epelbaum J, Dartigues J-F, Tzourio C, Alpérovitch A, Lathrop M, Feulner TM, Friedrich P, Riehle C, Krawczak M, Schreiber S, Mayhaus M, Nicolhaus S, Wagenpfeil S, Steinberg S, Stefansson H, Stefansson K, Snaedal J, Björnsson S, Jonsson PV, Chouraki V, Genier-Boley B, Hiltunen M, Soininen H, Combarros O, Zelenika D, Delepine M, Bullido MJ, Pasquier F, Mateo I, Frank-Garcia A, Porcellini E, Hanon O, Coto E, Alvarez V, Bosco P, Siciliano G, Mancuso M, Panza F, Solfrizzi V, Nacmias B, Sorbi S, Bossù P, Piccardi P, Arosio B, Annoni G, Seripa D, Pilotto A, Scarpini E, Galimberti D, Brice A, Hannequin D, Licastro F, Jones L, Holmans PA, Jonsson T, Riemenschneider M, Morgan K, Younkin SG, Owen MJ, O'Donovan M, Amouyel P, Williams J. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nat Genet 2011; 43: 429-435
-
(2011)
Nat Genet
, vol.43
, pp. 429-435
-
-
Hollingworth, P.1
Harold, D.2
Sims, R.3
Gerrish, A.4
Lambert, J.-C.5
Carrasquillo, M.M.6
Abraham, R.7
Hamshere, M.L.8
Pahwa, J.S.9
Moskvina, V.10
Dowzell, K.11
Jones, N.12
Stretton, A.13
Thomas, C.14
Richards, A.15
Ivanov, D.16
Widdowson, C.17
Chapman, J.18
Lovestone, S.19
Powell, J.20
Proitsi, P.21
Lupton, M.K.22
Brayne, C.23
Rubinsztein, D.C.24
Gill, M.25
Lawlor, B.26
Lynch, A.27
Brown, K.S.28
Passmore, P.A.29
Craig, D.30
McGuinness, B.31
Todd, S.32
Holmes, C.33
Mann, D.34
Smith, A.D.35
Beaumont, H.36
Warden, D.37
Wilcock, G.38
Love, S.39
Kehoe, P.G.40
Hooper, N.M.41
Vardy, E.R.L.C.42
Hardy, J.43
Mead, S.44
Fox, N.C.45
Rossor, M.46
Collinge, J.47
Maier, W.48
Jessen, F.49
Rüther, E.50
Schürmann, B.51
Heun, R.52
Kölsch, H.53
van den Bussche, H.54
Heuser, I.55
Kornhuber, J.56
Wiltfang, J.57
Dichgans, M.58
Frölich, L.59
Hampel, H.60
Gallacher, J.61
Hüll, M.62
Rujescu, D.63
Giegling, I.64
Goate, A.M.65
Kauwe, J.S.K.66
Cruchaga, C.67
Nowotny, P.68
Morris, J.C.69
Mayo, K.70
Sleegers, K.71
Bettens, K.72
Engelborghs, S.73
De Deyn, P.P.74
Van Broeckhoven, C.75
Livingston, G.76
Bass, N.J.77
Gurling, H.78
McQuillin, A.79
Gwilliam, R.80
Deloukas, P.81
Al-Chalabi, A.82
Shaw, C.E.83
Tsolaki, M.84
Singleton, A.B.85
Guerreiro, R.86
Mühleisen, T.W.87
Nöthen, M.M.88
Moebus, S.89
Jöckel, K.-H.90
Klopp, N.91
Wichmann, H.-E.92
Pankratz, V.S.93
Sando, S.B.94
Aasly, J.O.95
Barcikowska, M.96
Wszolek, Z.K.97
Dickson, D.W.98
Graff-Radford, N.R.99
Petersen, R.C.100
van Duijn, C.M.101
Breteler, M.M.B.102
Ikram, M.A.103
DeStefano, A.L.104
Fitzpatrick, A.L.105
Lopez, O.106
Launer, L.J.107
Seshadri, S.108
Berr, C.109
Campion, D.110
Epelbaum, J.111
Dartigues, J.-F.112
Tzourio, C.113
Alpérovitch, A.114
Lathrop, M.115
Feulner, T.M.116
Friedrich, P.117
Riehle, C.118
Krawczak, M.119
Schreiber, S.120
Mayhaus, M.121
Nicolhaus, S.122
Wagenpfeil, S.123
Steinberg, S.124
Stefansson, H.125
Stefansson, K.126
Snaedal, J.127
Björnsson, S.128
Jonsson, P.V.129
Chouraki, V.130
Genier-Boley, B.131
Hiltunen, M.132
Soininen, H.133
Combarros, O.134
Zelenika, D.135
Delepine, M.136
Bullido, M.J.137
Pasquier, F.138
Mateo, I.139
Frank-Garcia, A.140
Porcellini, E.141
Hanon, O.142
Coto, E.143
Alvarez, V.144
Bosco, P.145
Siciliano, G.146
Mancuso, M.147
Panza, F.148
Solfrizzi, V.149
Nacmias, B.150
Sorbi, S.151
Bossù, P.152
Piccardi, P.153
Arosio, B.154
Annoni, G.155
Seripa, D.156
Pilotto, A.157
Scarpini, E.158
Galimberti, D.159
Brice, A.160
Hannequin, D.161
Licastro, F.162
Jones, L.163
Holmans, P.A.164
Jonsson, T.165
Riemenschneider, M.166
Morgan, K.167
Younkin, S.G.168
Owen, M.J.169
O'Donovan, M.170
Amouyel, P.171
Williams, J.172
more..
-
6
-
-
70349558522
-
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
-
Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Morgan K, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Holmes C, Mann D, Smith AD, Love S, Kehoe PG, Hardy J, Mead S, Fox N, Rossor M, Collinge J, Maier W, Jessen F, Schürmann B, van den Bussche H, Heuser I, Kornhuber J, Wiltfang J, Dichgans M, Frölich L, Hampel H, Hüll M, Rujescu D, Goate AM, Kauwe JSK, Cruchaga C, Nowotny P, Morris JC, Mayo K, Sleegers K, Bettens K, Engelborghs S, De Deyn PP, Van Broeckhoven C, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Tsolaki M, Singleton AB, Guerreiro R, Mühleisen TW, Nöthen MM, Moebus S, Jöckel K-H, Klopp N, Wichmann H-E, Carrasquillo MM, Pankratz VS, Younkin SG, Holmans PA, O'Donovan M, Owen MJ, Williams J. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Nat Genet 2009; 41: 1088-1093
-
(2009)
Nat Genet
, vol.41
, pp. 1088-1093
-
-
Harold, D.1
Abraham, R.2
Hollingworth, P.3
Sims, R.4
Gerrish, A.5
Hamshere, M.L.6
Pahwa, J.S.7
Moskvina, V.8
Dowzell, K.9
Williams, A.10
Jones, N.11
Thomas, C.12
Stretton, A.13
Morgan, A.R.14
Lovestone, S.15
Powell, J.16
Proitsi, P.17
Lupton, M.K.18
Brayne, C.19
Rubinsztein, D.C.20
Gill, M.21
Lawlor, B.22
Lynch, A.23
Morgan, K.24
Brown, K.S.25
Passmore, P.A.26
Craig, D.27
McGuinness, B.28
Todd, S.29
Holmes, C.30
Mann, D.31
Smith, A.D.32
Love, S.33
Kehoe, P.G.34
Hardy, J.35
Mead, S.36
Fox, N.37
Rossor, M.38
Collinge, J.39
Maier, W.40
Jessen, F.41
Schürmann, B.42
van den Bussche, H.43
Heuser, I.44
Kornhuber, J.45
Wiltfang, J.46
Dichgans, M.47
Frölich, L.48
Hampel, H.49
Hüll, M.50
Rujescu, D.51
Goate, A.M.52
Kauwe, J.S.K.53
Cruchaga, C.54
Nowotny, P.55
Morris, J.C.56
Mayo, K.57
Sleegers, K.58
Bettens, K.59
Engelborghs, S.60
De Deyn, P.P.61
Van Broeckhoven, C.62
Livingston, G.63
Bass, N.J.64
Gurling, H.65
McQuillin, A.66
Gwilliam, R.67
Deloukas, P.68
Al-Chalabi, A.69
Shaw, C.E.70
Tsolaki, M.71
Singleton, A.B.72
Guerreiro, R.73
Mühleisen, T.W.74
Nöthen, M.M.75
Moebus, S.76
Jöckel, K.-H.77
Klopp, N.78
Wichmann, H.-E.79
Carrasquillo, M.M.80
Pankratz, V.S.81
Younkin, S.G.82
Holmans, P.A.83
O'Donovan, M.84
Owen, M.J.85
Williams, J.86
more..
-
7
-
-
78549264026
-
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
-
Lambert J-C, Heath S, Even G, Campion D, Sleegers K, Hiltunen M, Combarros O, Zelenika D, Bullido MJ, Tavernier B, Letenneur L, Bettens K, Berr C, Pasquier F, Fiévet N, Barberger-Gateau P, Engelborghs S, De Deyn P, Mateo I, Franck A, Helisalmi S, Porcellini E, Hanon O, de Pancorbo MM, Lendon C, Dufouil C, Jaillard C, Leveillard T, Alvarez V, Bosco P, Mancuso M, Panza F, Nacmias B, Bossù P, Piccardi P, Annoni G, Seripa D, Galimberti D, Hannequin D, Licastro F, Soininen H, Ritchie K, Blanché H, Dartigues J-F, Tzourio C, Gut I, Van Broeckhoven C, Alpérovitch A, Lathrop M, Amouyel P. Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. Nat Genet 2009; 41: 1094-1099
-
(2009)
Nat Genet
, vol.41
, pp. 1094-1099
-
-
Lambert, J.-C.1
Heath, S.2
Even, G.3
Campion, D.4
Sleegers, K.5
Hiltunen, M.6
Combarros, O.7
Zelenika, D.8
Bullido, M.J.9
Tavernier, B.10
Letenneur, L.11
Bettens, K.12
Berr, C.13
Pasquier, F.14
Fiévet, N.15
Barberger-Gateau, P.16
Engelborghs, S.17
De Deyn, P.18
Mateo, I.19
Franck, A.20
Helisalmi, S.21
Porcellini, E.22
Hanon, O.23
de Pancorbo, M.M.24
Lendon, C.25
Dufouil, C.26
Jaillard, C.27
Leveillard, T.28
Alvarez, V.29
Bosco, P.30
Mancuso, M.31
Panza, F.32
Nacmias, B.33
Bossù, P.34
Piccardi, P.35
Annoni, G.36
Seripa, D.37
Galimberti, D.38
Hannequin, D.39
Licastro, F.40
Soininen, H.41
Ritchie, K.42
Blanché, H.43
Dartigues, J.-F.44
Tzourio, C.45
Gut, I.46
Van Broeckhoven, C.47
Alpérovitch, A.48
Lathrop, M.49
Amouyel, P.50
more..
-
8
-
-
77952307991
-
Genome-wide analysis of genetic loci associated with Alzheimer disease
-
Seshadri S, Fitzpatrick AL, Ikram MA, DeStefano AL, Gudnason V, Boada M, Bis JC, Smith A V, Carassquillo MM, Lambert JC, Harold D, Schrijvers EMC, Ramirez-Lorca R, Debette S, Longstreth WT, Janssens ACJW, Pankratz VS, Dartigues JF, Hollingworth P, Aspelund T, Hernandez I, Beiser A, Kuller LH, Koudstaal PJ, Dickson DW, Tzourio C, Abraham R, Antunez C, Du Y, Rotter JI, Aulchenko YS, Harris TB, Petersen RC, Berr C, Owen MJ, Lopez-Arrieta J, Varadarajan BN, Becker JT, Rivadeneira F, Nalls MA, Graff-Radford NR, Campion D, Auerbach S, Rice K, Hofman A, Jonsson P V, Schmidt H, Lathrop M, Mosley TH, Au R, Psaty BM, Uitterlinden AG, Farrer LA, Lumley T, Ruiz A, Williams J, Amouyel P, Younkin SG, Wolf PA, Launer LJ, Lopez OL, van Duijn CM, Breteler MMB. Genome-wide analysis of genetic loci associated with Alzheimer disease. JAMA 2010; 303: 1832-1840
-
(2010)
JAMA
, vol.303
, pp. 1832-1840
-
-
Seshadri, S.1
Fitzpatrick, A.L.2
Ikram, M.A.3
DeStefano, A.L.4
Gudnason, V.5
Boada, M.6
Bis, J.C.7
Smith, V.A.8
Carassquillo, M.M.9
Lambert, J.C.10
Harold, D.11
Schrijvers, E.M.C.12
Ramirez-Lorca, R.13
Debette, S.14
Longstreth, W.T.15
Janssens, A.C.J.W.16
Pankratz, V.S.17
Dartigues, J.F.18
Hollingworth, P.19
Aspelund, T.20
Hernandez, I.21
Beiser, A.22
Kuller, L.H.23
Koudstaal, P.J.24
Dickson, D.W.25
Tzourio, C.26
Abraham, R.27
Antunez, C.28
Du, Y.29
Rotter, J.I.30
Aulchenko, Y.S.31
Harris, T.B.32
Petersen, R.C.33
Berr, C.34
Owen, M.J.35
Lopez-Arrieta, J.36
Varadarajan, B.N.37
Becker, J.T.38
Rivadeneira, F.39
Nalls, M.A.40
Graff-Radford, N.R.41
Campion, D.42
Auerbach, S.43
Rice, K.44
Hofman, A.45
Jonsson, V.P.46
Schmidt, H.47
Lathrop, M.48
Mosley, T.H.49
Au, R.50
Psaty, B.M.51
Uitterlinden, A.G.52
Farrer, L.A.53
Lumley, T.54
Ruiz, A.55
Williams, J.56
Amouyel, P.57
Younkin, S.G.58
Wolf, P.A.59
Launer, L.J.60
Lopez, O.L.61
van Duijn, C.M.62
Breteler, M.M.B.63
more..
-
9
-
-
78649573450
-
Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease
-
Jones L, Holmans PA, Hamshere ML, Harold D, Moskvina V, Ivanov D, Pocklington A, Abraham R, Hollingworth P, Sims R, Gerrish A, Pahwa JS, Jones N, Stretton A, Morgan AR, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Morgan K, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Holmes C, Mann D, Smith AD, Love S, Kehoe PG, Mead S, Fox N, Rossor M, Collinge J, Maier W, Jessen F, Schürmann B, Heun R, Kölsch H, van den Bussche H, Heuser I, Peters O, Kornhuber J, Wiltfang J, Dichgans M, Frölich L, Hampel H, Hüll M, Rujescu D, Goate AM, Kauwe JSK, Cruchaga C, Nowotny P, Morris JC, Mayo K, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Singleton AB, Guerreiro R, Mühleisen TW, Nöthen MM, Moebus S, Jöckel K-H, Klopp N, Wichmann H-E, Rüther E, Carrasquillo MM, Pankratz VS, Younkin SG, Hardy J, O'Donovan MC, Owen MJ, Williams J. Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease. PLoS ONE 2010; 5: e13950
-
(2010)
PLoS ONE
, vol.5
-
-
Jones, L.1
Holmans, P.A.2
Hamshere, M.L.3
Harold, D.4
Moskvina, V.5
Ivanov, D.6
Pocklington, A.7
Abraham, R.8
Hollingworth, P.9
Sims, R.10
Gerrish, A.11
Pahwa, J.S.12
Jones, N.13
Stretton, A.14
Morgan, A.R.15
Lovestone, S.16
Powell, J.17
Proitsi, P.18
Lupton, M.K.19
Brayne, C.20
Rubinsztein, D.C.21
Gill, M.22
Lawlor, B.23
Lynch, A.24
Morgan, K.25
Brown, K.S.26
Passmore, P.A.27
Craig, D.28
McGuinness, B.29
Todd, S.30
Holmes, C.31
Mann, D.32
Smith, A.D.33
Love, S.34
Kehoe, P.G.35
Mead, S.36
Fox, N.37
Rossor, M.38
Collinge, J.39
Maier, W.40
Jessen, F.41
Schürmann, B.42
Heun, R.43
Kölsch, H.44
van den Bussche, H.45
Heuser, I.46
Peters, O.47
Kornhuber, J.48
Wiltfang, J.49
Dichgans, M.50
Frölich, L.51
Hampel, H.52
Hüll, M.53
Rujescu, D.54
Goate, A.M.55
Kauwe, J.S.K.56
Cruchaga, C.57
Nowotny, P.58
Morris, J.C.59
Mayo, K.60
Livingston, G.61
Bass, N.J.62
Gurling, H.63
McQuillin, A.64
Gwilliam, R.65
Deloukas, P.66
Al-Chalabi, A.67
Shaw, C.E.68
Singleton, A.B.69
Guerreiro, R.70
Mühleisen, T.W.71
Nöthen, M.M.72
Moebus, S.73
Jöckel, K.-H.74
Klopp, N.75
Wichmann, H.-E.76
Rüther, E.77
Carrasquillo, M.M.78
Pankratz, V.S.79
Younkin, S.G.80
Hardy, J.81
O'Donovan, M.C.82
Owen, M.J.83
Williams, J.84
more..
-
10
-
-
79959396151
-
The three new pathways leading to Alzheimer's disease
-
Morgan K. The three new pathways leading to Alzheimer's disease. Neuropathol Appl Neurobiol 2011; 37: 353-357
-
(2011)
Neuropathol Appl Neurobiol
, vol.37
, pp. 353-357
-
-
Morgan, K.1
-
11
-
-
79957604912
-
Genetics of Alzheimer's disease: new evidences for an old hypothesis?
-
Lambert J-C, Amouyel P. Genetics of Alzheimer's disease: new evidences for an old hypothesis? Curr Opin Genet Dev 2011; 21: 295-301
-
(2011)
Curr Opin Genet Dev
, vol.21
, pp. 295-301
-
-
Lambert, J.-C.1
Amouyel, P.2
-
12
-
-
77957927865
-
The genetics of Alzheimer disease: back to the future
-
Bertram L, Lill CM, Tanzi RE. The genetics of Alzheimer disease: back to the future. Neuron 2010; 68: 270-281
-
(2010)
Neuron
, vol.68
, pp. 270-281
-
-
Bertram, L.1
Lill, C.M.2
Tanzi, R.E.3
-
13
-
-
78651297619
-
Meta-analysis of the association between variants in SORL1 and Alzheimer disease
-
Reitz C, Cheng R, Rogaeva E, Lee JH, Tokuhiro S, Zou F, Bettens K, Sleegers K, Tan EK, Kimura R, Shibata N, Arai H, Kamboh MI, Prince JA, Maier W, Riemenschneider M, Owen M, Harold D, Hollingworth P, Cellini E, Sorbi S, Nacmias B, Takeda M, Pericak-Vance MA, Haines JL, Younkin S, Williams J, van Broeckhoven C, Farrer LA, St George-Hyslop PH, Mayeux R. Meta-analysis of the association between variants in SORL1 and Alzheimer disease. Arch Neurol 2011; 68: 99-106
-
(2011)
Arch Neurol
, vol.68
, pp. 99-106
-
-
Reitz, C.1
Cheng, R.2
Rogaeva, E.3
Lee, J.H.4
Tokuhiro, S.5
Zou, F.6
Bettens, K.7
Sleegers, K.8
Tan, E.K.9
Kimura, R.10
Shibata, N.11
Arai, H.12
Kamboh, M.I.13
Prince, J.A.14
Maier, W.15
Riemenschneider, M.16
Owen, M.17
Harold, D.18
Hollingworth, P.19
Cellini, E.20
Sorbi, S.21
Nacmias, B.22
Takeda, M.23
Pericak-Vance, M.A.24
Haines, J.L.25
Younkin, S.26
Williams, J.27
van Broeckhoven, C.28
Farrer, L.A.29
St George-Hyslop, P.H.30
Mayeux, R.31
more..
-
14
-
-
33846613222
-
The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease
-
Rogaeva E, Meng Y, Lee JH, Gu Y, Kawarai T, Zou F, Katayama T, Baldwin CT, Cheng R, Hasegawa H, Chen F, Shibata N, Lunetta KL, Pardossi-Piquard R, Bohm C, Wakutani Y, Cupples LA, Cuenco KT, Green RC, Pinessi L, Rainero I, Sorbi S, Bruni A, Duara R, Friedland RP, Inzelberg R, Hampe W, Bujo H, Song Y-Q, Andersen OM, Willnow TE, Graff-Radford N, Petersen RC, Dickson D, Der SD, Fraser PE, Schmitt-Ulms G, Younkin S, Mayeux R, Farrer LA, St George-Hyslop P. The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease. Nat Genet 2007; 39: 168-177
-
(2007)
Nat Genet
, vol.39
, pp. 168-177
-
-
Rogaeva, E.1
Meng, Y.2
Lee, J.H.3
Gu, Y.4
Kawarai, T.5
Zou, F.6
Katayama, T.7
Baldwin, C.T.8
Cheng, R.9
Hasegawa, H.10
Chen, F.11
Shibata, N.12
Lunetta, K.L.13
Pardossi-Piquard, R.14
Bohm, C.15
Wakutani, Y.16
Cupples, L.A.17
Cuenco, K.T.18
Green, R.C.19
Pinessi, L.20
Rainero, I.21
Sorbi, S.22
Bruni, A.23
Duara, R.24
Friedland, R.P.25
Inzelberg, R.26
Hampe, W.27
Bujo, H.28
Song, Y.-Q.29
Andersen, O.M.30
Willnow, T.E.31
Graff-Radford, N.32
Petersen, R.C.33
Dickson, D.34
Der, S.D.35
Fraser, P.E.36
Schmitt-Ulms, G.37
Younkin, S.38
Mayeux, R.39
Farrer, L.A.40
St George-Hyslop, P.41
more..
-
15
-
-
84864770092
-
Association between Parkinson's disease and the HLA-DRB1 locus
-
Ahmed I, Tamouza R, Delord M, Krishnamoorthy R, Tzourio C, Mulot C, Nacfer M, Lambert J-C, Beaune P, Laurent-Puig P, Loriot M-A, Charron D, Elbaz A. Association between Parkinson's disease and the HLA-DRB1 locus. Mov Disord 2012; 27: 1104-1110
-
(2012)
Mov Disord
, vol.27
, pp. 1104-1110
-
-
Ahmed, I.1
Tamouza, R.2
Delord, M.3
Krishnamoorthy, R.4
Tzourio, C.5
Mulot, C.6
Nacfer, M.7
Lambert, J.-C.8
Beaune, P.9
Laurent-Puig, P.10
Loriot, M.-A.11
Charron, D.12
Elbaz, A.13
-
16
-
-
80051684615
-
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
-
Sawcer S, Hellenthal G, Pirinen M, Spencer CCA, Patsopoulos NA, Moutsianas L, Dilthey A, Su Z, Freeman C, Hunt SE, Edkins S, Gray E, Booth DR, Potter SC, Goris A, Band G, Oturai AB, Strange A, Saarela J, Bellenguez C, Fontaine B, Gillman M, Hemmer B, Gwilliam R, Zipp F, Jayakumar A, Martin R, Leslie S, Hawkins S, Giannoulatou E, D'alfonso S, Blackburn H, Martinelli Boneschi F, Liddle J, Harbo HF, Perez ML, Spurkland A, Waller MJ, Mycko MP, Ricketts M, Comabella M, Hammond N, Kockum I, McCann OT, Ban M, Whittaker P, Kemppinen A, Weston P, Hawkins C, Widaa S, Zajicek J, Dronov S, Robertson N, Bumpstead SJ, Barcellos LF, Ravindrarajah R, Abraham R, Alfredsson L, Ardlie K, Aubin C, Baker A, Baker K, Baranzini SE, Bergamaschi L, Bergamaschi R, Bernstein A, Berthele A, Boggild M, Bradfield JP, Brassat D, Broadley SA, Buck D, Butzkueven H, Capra R, Carroll WM, Cavalla P, Celius EG, Cepok S, Chiavacci R, Clerget-Darpoux F, Clysters K, Comi G, Cossburn M, Cournu-Rebeix I, Cox MB, Cozen W, Cree BAC, Cross AH, Cusi D, Daly MJ, Davis E, de Bakker PIW, Debouverie M, D'hooghe MB, Dixon K, Dobosi R, Dubois B, Ellinghaus D, Elovaara I, Esposito F, Fontenille C, Foote S, Franke A, Galimberti D, Ghezzi A, Glessner J, Gomez R, Gout O, Graham C, Grant SFA, Guerini FR, Hakonarson H, Hall P, Hamsten A, Hartung H-P, Heard RN, Heath S, Hobart J, Hoshi M, Infante-Duarte C, Ingram G, Ingram W, Islam T, Jagodic M, Kabesch M, Kermode AG, Kilpatrick TJ, Kim C, Klopp N, Koivisto K, Larsson M, Lathrop M, Lechner-Scott JS, Leone MA, Leppä V, Liljedahl U, Bomfim IL, Lincoln RR, Link J, Liu J, Lorentzen AR, Lupoli S, Macciardi F, Mack T, Marriott M, Martinelli V, Mason D, McCauley JL, Mentch F, Mero I-L, Mihalova T, Montalban X, Mottershead J, Myhr K-M, Naldi P, Ollier W, Page A, Palotie A, Pelletier J, Piccio L, Pickersgill T, Piehl F, Pobywajlo S, Quach HL, Ramsay PP, Reunanen M, Reynolds R, Rioux JD, Rodegher M, Roesner S, Rubio JP, Rückert I-M, Salvetti M, Salvi E, Santaniello A, Schaefer CA, Schreiber S, Schulze C, Scott RJ, Sellebjerg F, Selmaj KW, Sexton D, Shen L, Simms-Acuna B, Skidmore S, Sleiman PMA, Smestad C, Sørensen PS, Søndergaard HB, Stankovich J, Strange RC, Sulonen A-M, Sundqvist E, Syvänen A-C, Taddeo F, Taylor B, Blackwell JM, Tienari P, Bramon E, Tourbah A, Brown MA, Tronczynska E, Casas JP, Tubridy N, Corvin A, Vickery J, Jankowski J, Villoslada P, Markus HS, Wang K, Mathew CG, Wason J, Palmer CNA, Wichmann H-E, Plomin R, Willoughby E, Rautanen A, Winkelmann J, Wittig M, Trembath RC, Yaouanq J, Viswanathan AC, Zhang H, Wood NW, Zuvich R, Deloukas P, Langford C, Duncanson A, Oksenberg JR, Pericak-Vance MA, Haines JL, Olsson T, Hillert J, Ivinson AJ, De Jager PL, Peltonen L, Stewart GJ, Hafler DA, Hauser SL, McVean G, Donnelly P, Compston A. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature 2011; 476: 214-219
-
(2011)
Nature
, vol.476
, pp. 214-219
-
-
Sawcer, S.1
Hellenthal, G.2
Pirinen, M.3
Spencer, C.C.A.4
Patsopoulos, N.A.5
Moutsianas, L.6
Dilthey, A.7
Su, Z.8
Freeman, C.9
Hunt, S.E.10
Edkins, S.11
Gray, E.12
Booth, D.R.13
Potter, S.C.14
Goris, A.15
Band, G.16
Oturai, A.B.17
Strange, A.18
Saarela, J.19
Bellenguez, C.20
Fontaine, B.21
Gillman, M.22
Hemmer, B.23
Gwilliam, R.24
Zipp, F.25
Jayakumar, A.26
Martin, R.27
Leslie, S.28
Hawkins, S.29
Giannoulatou, E.30
D'alfonso, S.31
Blackburn, H.32
Martinelli Boneschi, F.33
Liddle, J.34
Harbo, H.F.35
Perez, M.L.36
Spurkland, A.37
Waller, M.J.38
Mycko, M.P.39
Ricketts, M.40
Comabella, M.41
Hammond, N.42
Kockum, I.43
McCann, O.T.44
Ban, M.45
Whittaker, P.46
Kemppinen, A.47
Weston, P.48
Hawkins, C.49
Widaa, S.50
Zajicek, J.51
Dronov, S.52
Robertson, N.53
Bumpstead, S.J.54
Barcellos, L.F.55
Ravindrarajah, R.56
Abraham, R.57
Alfredsson, L.58
Ardlie, K.59
Aubin, C.60
Baker, A.61
Baker, K.62
Baranzini, S.E.63
Bergamaschi, L.64
Bergamaschi, R.65
Bernstein, A.66
Berthele, A.67
Boggild, M.68
Bradfield, J.P.69
Brassat, D.70
Broadley, S.A.71
Buck, D.72
Butzkueven, H.73
Capra, R.74
Carroll, W.M.75
Cavalla, P.76
Celius, E.G.77
Cepok, S.78
Chiavacci, R.79
Clerget-Darpoux, F.80
Clysters, K.81
Comi, G.82
Cossburn, M.83
Cournu-Rebeix, I.84
Cox, M.B.85
Cozen, W.86
Cree, B.A.C.87
Cross, A.H.88
Cusi, D.89
Daly, M.J.90
Davis, E.91
de Bakker, P.I.W.92
Debouverie, M.93
D'hooghe, M.B.94
Dixon, K.95
Dobosi, R.96
Dubois, B.97
Ellinghaus, D.98
Elovaara, I.99
Esposito, F.100
Fontenille, C.101
Foote, S.102
Franke, A.103
Galimberti, D.104
Ghezzi, A.105
Glessner, J.106
Gomez, R.107
Gout, O.108
Graham, C.109
Grant, S.F.A.110
Guerini, F.R.111
Hakonarson, H.112
Hall, P.113
Hamsten, A.114
Hartung, H.-P.115
Heard, R.N.116
Heath, S.117
Hobart, J.118
Hoshi, M.119
Infante-Duarte, C.120
Ingram, G.121
Ingram, W.122
Islam, T.123
Jagodic, M.124
Kabesch, M.125
Kermode, A.G.126
Kilpatrick, T.J.127
Kim, C.128
Klopp, N.129
Koivisto, K.130
Larsson, M.131
Lathrop, M.132
Lechner-Scott, J.S.133
Leone, M.A.134
Leppä, V.135
Liljedahl, U.136
Bomfim, I.L.137
Lincoln, R.R.138
Link, J.139
Liu, J.140
Lorentzen, A.R.141
Lupoli, S.142
Macciardi, F.143
Mack, T.144
Marriott, M.145
Martinelli, V.146
Mason, D.147
McCauley, J.L.148
Mentch, F.149
Mero, I.-L.150
Mihalova, T.151
Montalban, X.152
Mottershead, J.153
Myhr, K.-M.154
Naldi, P.155
Ollier, W.156
Page, A.157
Palotie, A.158
Pelletier, J.159
Piccio, L.160
Pickersgill, T.161
Piehl, F.162
Pobywajlo, S.163
Quach, H.L.164
Ramsay, P.P.165
Reunanen, M.166
Reynolds, R.167
Rioux, J.D.168
Rodegher, M.169
Roesner, S.170
Rubio, J.P.171
Rückert, I.-M.172
Salvetti, M.173
Salvi, E.174
Santaniello, A.175
Schaefer, C.A.176
Schreiber, S.177
Schulze, C.178
Scott, R.J.179
Sellebjerg, F.180
Selmaj, K.W.181
Sexton, D.182
Shen, L.183
Simms-Acuna, B.184
Skidmore, S.185
Sleiman, P.M.A.186
Smestad, C.187
Sørensen, P.S.188
Søndergaard, H.B.189
Stankovich, J.190
Strange, R.C.191
Sulonen, A.-M.192
Sundqvist, E.193
Syvänen, A.-C.194
Taddeo, F.195
Taylor, B.196
Blackwell, J.M.197
Tienari, P.198
Bramon, E.199
Tourbah, A.200
Brown, M.A.201
Tronczynska, E.202
Casas, J.P.203
Tubridy, N.204
Corvin, A.205
Vickery, J.206
Jankowski, J.207
Villoslada, P.208
Markus, H.S.209
Wang, K.210
Mathew, C.G.211
Wason, J.212
Palmer, C.N.A.213
Wichmann, H.-E.214
Plomin, R.215
Willoughby, E.216
Rautanen, A.217
Winkelmann, J.218
Wittig, M.219
Trembath, R.C.220
Yaouanq, J.221
Viswanathan, A.C.222
Zhang, H.223
Wood, N.W.224
Zuvich, R.225
Deloukas, P.226
Langford, C.227
Duncanson, A.228
Oksenberg, J.R.229
Pericak-Vance, M.A.230
Haines, J.L.231
Olsson, T.232
Hillert, J.233
Ivinson, A.J.234
De Jager, P.L.235
Peltonen, L.236
Stewart, G.J.237
Hafler, D.A.238
Hauser, S.L.239
McVean, G.240
Donnelly, P.241
Compston, A.242
more..
-
17
-
-
0029859565
-
Cloning and characterization of human SHIP, the 145-kD inositol 5-phosphatase that associates with SHC after cytokine stimulation
-
Ware MD, Rosten P, Damen JE, Liu L, Humphries RK, Krystal G. Cloning and characterization of human SHIP, the 145-kD inositol 5-phosphatase that associates with SHC after cytokine stimulation. Blood 1996; 88: 2833-2840
-
(1996)
Blood
, vol.88
, pp. 2833-2840
-
-
Ware, M.D.1
Rosten, P.2
Damen, J.E.3
Liu, L.4
Humphries, R.K.5
Krystal, G.6
-
18
-
-
17744380787
-
CAKbeta/Pyk2 kinase is a signaling link for induction of long-term potentiation in CA1 hippocampus
-
Huang Y, Lu W, Ali DW, Pelkey KA, Pitcher GM, Lu YM, Aoto H, Roder JC, Sasaki T, Salter MW, MacDonald JF. CAKbeta/Pyk2 kinase is a signaling link for induction of long-term potentiation in CA1 hippocampus. Neuron 2001; 29: 485-496
-
(2001)
Neuron
, vol.29
, pp. 485-496
-
-
Huang, Y.1
Lu, W.2
Ali, D.W.3
Pelkey, K.A.4
Pitcher, G.M.5
Lu, Y.M.6
Aoto, H.7
Roder, J.C.8
Sasaki, T.9
Salter, M.W.10
MacDonald, J.F.11
-
19
-
-
0033595764
-
Neuronal activity-dependent cell survival mediated by transcription factor MEF2
-
Mao Z, Bonni A, Xia F, Nadal-Vicens M, Greenberg ME. Neuronal activity-dependent cell survival mediated by transcription factor MEF2. Science 1999; 286: 785-790
-
(1999)
Science
, vol.286
, pp. 785-790
-
-
Mao, Z.1
Bonni, A.2
Xia, F.3
Nadal-Vicens, M.4
Greenberg, M.E.5
-
20
-
-
77952715676
-
Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression
-
Zweier M, Gregor A, Zweier C, Engels H, Sticht H, Wohlleber E, Bijlsma EK, Holder SE, Zenker M, Rossier E, Grasshoff U, Johnson DS, Robertson L, Firth H V, Ekici AB, Reis A, Rauch A. Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression. Hum Mutat 2010; 31: 722-733
-
(2010)
Hum Mutat
, vol.31
, pp. 722-733
-
-
Zweier, M.1
Gregor, A.2
Zweier, C.3
Engels, H.4
Sticht, H.5
Wohlleber, E.6
Bijlsma, E.K.7
Holder, S.E.8
Zenker, M.9
Rossier, E.10
Grasshoff, U.11
Johnson, D.S.12
Robertson, L.13
Firth, V.H.14
Ekici, A.B.15
Reis, A.16
Rauch, A.17
-
21
-
-
48249087704
-
MEF2C, a transcription factor that facilitates learning and memory by negative regulation of synapse numbers and function
-
Barbosa AC, Kim M-S, Ertunc M, Adachi M, Nelson ED, McAnally J, Richardson JA, Kavalali ET, Monteggia LM, Bassel-Duby R, Olson EN. MEF2C, a transcription factor that facilitates learning and memory by negative regulation of synapse numbers and function. Proc Natl Acad Sci U S A 2008; 105: 9391-9396
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 9391-9396
-
-
Barbosa, A.C.1
Kim, M.-S.2
Ertunc, M.3
Adachi, M.4
Nelson, E.D.5
McAnally, J.6
Richardson, J.A.7
Kavalali, E.T.8
Monteggia, L.M.9
Bassel-Duby, R.10
Olson, E.N.11
-
22
-
-
74549139226
-
MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations
-
Le Meur N, Holder-Espinasse M, Jaillard S, Goldenberg A, Joriot S, Amati-Bonneau P, Guichet A, Barth M, Charollais A, Journel H, Auvin S, Boucher C, Kerckaert J-P, David V, Manouvrier-Hanu S, Saugier-Veber P, Frébourg T, Dubourg C, Andrieux J, Bonneau D. MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations. J Med Genet 2010; 47: 22-29
-
(2010)
J Med Genet
, vol.47
, pp. 22-29
-
-
Le Meur, N.1
Holder-Espinasse, M.2
Jaillard, S.3
Goldenberg, A.4
Joriot, S.5
Amati-Bonneau, P.6
Guichet, A.7
Barth, M.8
Charollais, A.9
Journel, H.10
Auvin, S.11
Boucher, C.12
Kerckaert, J.-P.13
David, V.14
Manouvrier-Hanu, S.15
Saugier-Veber, P.16
Frébourg, T.17
Dubourg, C.18
Andrieux, J.19
Bonneau, D.20
more..
-
23
-
-
77950605242
-
CAS proteins in normal and pathological cell growth control
-
Tikhmyanova N, Little JL, Golemis EA. CAS proteins in normal and pathological cell growth control. Cell Mol Life Sci 2010; 67: 1025-1048
-
(2010)
Cell Mol Life Sci
, vol.67
, pp. 1025-1048
-
-
Tikhmyanova, N.1
Little, J.L.2
Golemis, E.A.3
-
24
-
-
39749165788
-
Evidence that common variation in NEDD9 is associated with susceptibility to late-onsheimer's and Parkinson's disease
-
Li Y, Grupe A, Rowland C, Holmans P, Segurado R, Abraham R, Jones L, Catanese J, Ross D, Mayo K, Martinez M, Hollingworth P, Goate A, Cairns NJ, Racette BA, Perlmutter JS, O'Donovan MC, Morris JC, Brayne C, Rubinsztein DC, Lovestone S, Thal LJ, Owen MJ, Williams J. Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease. Hum Mol Genet 2008; 17: 759-767
-
(2008)
Hum Mol Genet
, vol.17
, pp. 759-767
-
-
Li, Y.1
Grupe, A.2
Rowland, C.3
Holmans, P.4
Segurado, R.5
Abraham, R.6
Jones, L.7
Catanese, J.8
Ross, D.9
Mayo, K.10
Martinez, M.11
Hollingworth, P.12
Goate, A.13
Cairns, N.J.14
Racette, B.A.15
Perlmutter, J.S.16
O'Donovan, M.C.17
Morris, J.C.18
Brayne, C.19
Rubinsztein, D.C.20
Lovestone, S.21
Thal, L.J.22
Owen, M.J.23
Williams, J.24
more..
-
25
-
-
50849091905
-
Association study of the NEDD9 gene with the risk of developing Alzheimer's and Parkinson's disease
-
Chapuis J, Moisan F, Mellick G, Elbaz A, Silburn P, Pasquier F, Hannequin D, Lendon C, Campion D, Amouyel P, Lambert J-C. Association study of the NEDD9 gene with the risk of developing Alzheimer's and Parkinson's disease. Hum Mol Genet 2008; 17: 2863-2867
-
(2008)
Hum Mol Genet
, vol.17
, pp. 2863-2867
-
-
Chapuis, J.1
Moisan, F.2
Mellick, G.3
Elbaz, A.4
Silburn, P.5
Pasquier, F.6
Hannequin, D.7
Lendon, C.8
Campion, D.9
Amouyel, P.10
Lambert, J.-C.11
-
27
-
-
84864884471
-
Kindlin 2 forms a transcriptional complex with β-catenin and TCF4 to enhance Wnt signalling
-
Yu Y, Wu J, Wang Y, Zhao T, Ma B, Liu Y, Fang W, Zhu W-G, Zhang H. Kindlin 2 forms a transcriptional complex with β-catenin and TCF4 to enhance Wnt signalling. EMBO Rep 2012; 13: 750-758
-
(2012)
EMBO Rep
, vol.13
, pp. 750-758
-
-
Yu, Y.1
Wu, J.2
Wang, Y.3
Zhao, T.4
Ma, B.5
Liu, Y.6
Fang, W.7
Zhu, W.-G.8
Zhang, H.9
-
28
-
-
0036150827
-
Alzheimer's disease - do tauists and baptists finally shake hands?
-
Mudher A, Lovestone S. Alzheimer's disease - do tauists and baptists finally shake hands? Trends Neurosci 2002; 25: 22-26
-
(2002)
Trends Neurosci
, vol.25
, pp. 22-26
-
-
Mudher, A.1
Lovestone, S.2
-
29
-
-
77956334087
-
Structural insight into the zinc finger CW domain as a histone modification reader
-
He F, Umehara T, Saito K, Harada T, Watanabe S, Yabuki T, Kigawa T, Takahashi M, Kuwasako K, Tsuda K, Matsuda T, Aoki M, Seki E, Kobayashi N, Güntert P, Yokoyama S, Muto Y. Structural insight into the zinc finger CW domain as a histone modification reader. Structure 2010; 18: 1127-1139
-
(2010)
Structure
, vol.18
, pp. 1127-1139
-
-
He, F.1
Umehara, T.2
Saito, K.3
Harada, T.4
Watanabe, S.5
Yabuki, T.6
Kigawa, T.7
Takahashi, M.8
Kuwasako, K.9
Tsuda, K.10
Matsuda, T.11
Aoki, M.12
Seki, E.13
Kobayashi, N.14
Güntert, P.15
Yokoyama, S.16
Muto, Y.17
-
30
-
-
2242451442
-
Molecular cloning of a fourth member of the potassium-dependent sodium-calcium exchanger gene family, NCKX4
-
Li X-F, Kraev AS, Lytton J. Molecular cloning of a fourth member of the potassium-dependent sodium-calcium exchanger gene family, NCKX4. J Biol Chem 2002; 277: 48410-48417
-
(2002)
J Biol Chem
, vol.277
, pp. 48410-48417
-
-
Li, X.-F.1
Kraev, A.S.2
Lytton, J.3
-
31
-
-
36549071998
-
Genetic determinants of hair, eye and skin pigmentation in Europeans
-
Sulem P, Gudbjartsson DF, Stacey SN, Helgason A, Rafnar T, Magnusson KP, Manolescu A, Karason A, Palsson A, Thorleifsson G, Jakobsdottir M, Steinberg S, Pálsson S, Jonasson F, Sigurgeirsson B, Thorisdottir K, Ragnarsson R, Benediktsdottir KR, Aben KK, Kiemeney LA, Olafsson JH, Gulcher J, Kong A, Thorsteinsdottir U, Stefansson K. Genetic determinants of hair, eye and skin pigmentation in Europeans. Nat Genet 2007; 39: 1443-1452
-
(2007)
Nat Genet
, vol.39
, pp. 1443-1452
-
-
Sulem, P.1
Gudbjartsson, D.F.2
Stacey, S.N.3
Helgason, A.4
Rafnar, T.5
Magnusson, K.P.6
Manolescu, A.7
Karason, A.8
Palsson, A.9
Thorleifsson, G.10
Jakobsdottir, M.11
Steinberg, S.12
Pálsson, S.13
Jonasson, F.14
Sigurgeirsson, B.15
Thorisdottir, K.16
Ragnarsson, R.17
Benediktsdottir, K.R.18
Aben, K.K.19
Kiemeney, L.A.20
Olafsson, J.H.21
Gulcher, J.22
Kong, A.23
Thorsteinsdottir, U.24
Stefansson, K.25
more..
-
32
-
-
84878359274
-
Genetic analysis of 16 NMR-lipoprotein fractions in humans, the GOLDN study
-
Kraja AT, Borecki IB, Tsai MY, Ordovas JM, Hopkins PN, Lai C-Q, Frazier-Wood AC, Straka RJ, Hixson JE, Province MA, Arnett DK. Genetic analysis of 16 NMR-lipoprotein fractions in humans, the GOLDN study. Lipids 2013; 48: 155-165
-
(2013)
Lipids
, vol.48
, pp. 155-165
-
-
Kraja, A.T.1
Borecki, I.B.2
Tsai, M.Y.3
Ordovas, J.M.4
Hopkins, P.N.5
Lai, C.-Q.6
Frazier-Wood, A.C.7
Straka, R.J.8
Hixson, J.E.9
Province, M.A.10
Arnett, D.K.11
-
33
-
-
0242351052
-
RIN3: a novel Rab5 GEF interacting with amphiphysin II involved in the early endocytic pathway
-
Kajiho H, Saito K, Tsujita K, Kontani K, Araki Y, Kurosu H, Katada T. RIN3: a novel Rab5 GEF interacting with amphiphysin II involved in the early endocytic pathway. J Cell Sci 2003; 116: 4159-4168
-
(2003)
J Cell Sci
, vol.116
, pp. 4159-4168
-
-
Kajiho, H.1
Saito, K.2
Tsujita, K.3
Kontani, K.4
Araki, Y.5
Kurosu, H.6
Katada, T.7
-
34
-
-
33847678960
-
A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia
-
Duriez B, Duquesnoy P, Escudier E, Bridoux A-M, Escalier D, Rayet I, Marcos E, Vojtek A-M, Bercher J-F, Amselem S. A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia. Proc Natl Acad Sci U S A 2007; 104: 3336-3341
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, pp. 3336-3341
-
-
Duriez, B.1
Duquesnoy, P.2
Escudier, E.3
Bridoux, A.-M.4
Escalier, D.5
Rayet, I.6
Marcos, E.7
Vojtek, A.-M.8
Bercher, J.-F.9
Amselem, S.10
-
35
-
-
84892640123
-
Why it is time to sequence
-
author reply 353-5
-
McClellan J, King M-C. Why it is time to sequence. Cell 2010; 142: 351-353. author reply 353-5
-
(2010)
Cell
, vol.142
, pp. 351-353
-
-
McClellan, J.1
King, M.-C.2
-
36
-
-
77249134594
-
Rare variants create synthetic genome-wide associations
-
Dickson SP, Wang K, Krantz I, Hakonarson H, Goldstein DB. Rare variants create synthetic genome-wide associations. PLoS Biol 2010; 8: e1000294
-
(2010)
PLoS Biol
, vol.8
-
-
Dickson, S.P.1
Wang, K.2
Krantz, I.3
Hakonarson, H.4
Goldstein, D.B.5
-
37
-
-
79851487367
-
Synthetic associations created by rare variants do not explain most GWAS results
-
Wray NR, Purcell SM, Visscher PM. Synthetic associations created by rare variants do not explain most GWAS results. PLoS Biol 2011; 9: e1000579
-
(2011)
PLoS Biol
, vol.9
-
-
Wray, N.R.1
Purcell, S.M.2
Visscher, P.M.3
-
38
-
-
84872088087
-
Variant of TREM2 associated with the risk of Alzheimer's disease
-
Jonsson T, Stefansson H, Steinberg S, Jonsdottir I, Jonsson PV, Snaedal J, Bjornsson S, Huttenlocher J, Levey AI, Lah JJ, Rujescu D, Hampel H, Giegling I, Andreassen OA, Engedal K, Ulstein I, Djurovic S, Ibrahim-Verbaas C, Hofman A, Ikram MA, van Duijn CM, Thorsteinsdottir U, Kong A, Stefansson K. Variant of TREM2 associated with the risk of Alzheimer's disease. N Engl J Med 2013; 368: 107-116
-
(2013)
N Engl J Med
, vol.368
, pp. 107-116
-
-
Jonsson, T.1
Stefansson, H.2
Steinberg, S.3
Jonsdottir, I.4
Jonsson, P.V.5
Snaedal, J.6
Bjornsson, S.7
Huttenlocher, J.8
Levey, A.I.9
Lah, J.J.10
Rujescu, D.11
Hampel, H.12
Giegling, I.13
Andreassen, O.A.14
Engedal, K.15
Ulstein, I.16
Djurovic, S.17
Ibrahim-Verbaas, C.18
Hofman, A.19
Ikram, M.A.20
van Duijn, C.M.21
Thorsteinsdottir, U.22
Kong, A.23
Stefansson, K.24
more..
-
39
-
-
18544390923
-
Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype
-
Paloneva J, Manninen T, Christman G, Hovanes K, Mandelin J, Adolfsson R, Bianchin M, Bird T, Miranda R, Salmaggi A, Tranebjaerg L, Konttinen Y, Peltonen L. Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype. Am J Hum Genet 2002; 71: 656-662
-
(2002)
Am J Hum Genet
, vol.71
, pp. 656-662
-
-
Paloneva, J.1
Manninen, T.2
Christman, G.3
Hovanes, K.4
Mandelin, J.5
Adolfsson, R.6
Bianchin, M.7
Bird, T.8
Miranda, R.9
Salmaggi, A.10
Tranebjaerg, L.11
Konttinen, Y.12
Peltonen, L.13
-
40
-
-
73549110158
-
Mutations in TREM2 lead to pure early-onset dementia without bone cysts
-
Chouery E, Delague V, Bergougnoux A, Koussa S, Serre J-L. Mégarbané A. Mutations in TREM2 lead to pure early-onset dementia without bone cysts. Hum Mutat 2008; 29: E194-204
-
(2008)
Hum Mutat
, vol.29
-
-
Chouery, E.1
Delague, V.2
Bergougnoux, A.3
Koussa, S.4
Serre, J.-L.5
Mégarbané, A.6
-
41
-
-
84872586508
-
Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement
-
Guerreiro RJ, Lohmann E, Brás JM, Gibbs JR, Rohrer JD, Gurunlian N, Dursun B, Bilgic B, Hanagasi H, Gurvit H, Emre M, Singleton A, Hardy J. Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement. JAMA Neurol 2013; 70: 78-84
-
(2013)
JAMA Neurol
, vol.70
, pp. 78-84
-
-
Guerreiro, R.J.1
Lohmann, E.2
Brás, J.M.3
Gibbs, J.R.4
Rohrer, J.D.5
Gurunlian, N.6
Dursun, B.7
Bilgic, B.8
Hanagasi, H.9
Gurvit, H.10
Emre, M.11
Singleton, A.12
Hardy, J.13
-
42
-
-
67349127527
-
Meta-analysis of linkage studies for Alzheimer's disease-a web resource
-
Butler AW, Ng MYM, Hamshere ML, Forabosco P, Wroe R, Al-Chalabi A, Lewis CM, Powell JF. Meta-analysis of linkage studies for Alzheimer's disease-a web resource. Neurobiol Aging 2009; 30: 1037-1047
-
(2009)
Neurobiol Aging
, vol.30
, pp. 1037-1047
-
-
Butler, A.W.1
Ng, M.Y.M.2
Hamshere, M.L.3
Forabosco, P.4
Wroe, R.5
Al-Chalabi, A.6
Lewis, C.M.7
Powell, J.F.8
-
43
-
-
84872143942
-
Analysis of 6515 exomes reveals the recent origin of most human protein-coding variants
-
Fu W, O'Connor TD, Jun G, Kang HM, Abecasis G, Leal SM, Gabriel S, Altshuler D, Shendure J, Nickerson DA, Bamshad MJ, Akey JM. Analysis of 6515 exomes reveals the recent origin of most human protein-coding variants. Nature 2013; 493: 216-220
-
(2013)
Nature
, vol.493
, pp. 216-220
-
-
Fu, W.1
O'Connor, T.D.2
Jun, G.3
Kang, H.M.4
Abecasis, G.5
Leal, S.M.6
Gabriel, S.7
Altshuler, D.8
Shendure, J.9
Nickerson, D.A.10
Bamshad, M.J.11
Akey, J.M.12
-
44
-
-
84863239847
-
TREM2 and β-catenin regulate bone homeostasis by controlling the rate of osteoclastogenesis
-
Otero K, Shinohara M, Zhao H, Cella M, Gilfillan S, Colucci A, Faccio R, Ross FP, Teitelbaum SL, Takayanagi H, Colonna M. TREM2 and β-catenin regulate bone homeostasis by controlling the rate of osteoclastogenesis. J Immunol 2012; 188: 2612-2621
-
(2012)
J Immunol
, vol.188
, pp. 2612-2621
-
-
Otero, K.1
Shinohara, M.2
Zhao, H.3
Cella, M.4
Gilfillan, S.5
Colucci, A.6
Faccio, R.7
Ross, F.P.8
Teitelbaum, S.L.9
Takayanagi, H.10
Colonna, M.11
-
45
-
-
0036732410
-
SHIP-deficient mice are severely osteoporotic due to increased numbers of hyper-resorptive osteoclasts
-
Takeshita S, Namba N, Zhao JJ, Jiang Y, Genant HK, Silva MJ, Brodt MD, Helgason CD, Kalesnikoff J, Rauh MJ, Humphries RK, Krystal G, Teitelbaum SL, Ross FP. SHIP-deficient mice are severely osteoporotic due to increased numbers of hyper-resorptive osteoclasts. Nat Med 2002; 8: 943-949
-
(2002)
Nat Med
, vol.8
, pp. 943-949
-
-
Takeshita, S.1
Namba, N.2
Zhao, J.J.3
Jiang, Y.4
Genant, H.K.5
Silva, M.J.6
Brodt, M.D.7
Helgason, C.D.8
Kalesnikoff, J.9
Rauh, M.J.10
Humphries, R.K.11
Krystal, G.12
Teitelbaum, S.L.13
Ross, F.P.14
-
46
-
-
77953819536
-
TREM2- and DAP12-dependent activation of PI3K requires DAP10 and is inhibited by SHIP1
-
Peng Q, Malhotra S, Torchia JA, Kerr WG, Coggeshall KM, Humphrey MB. TREM2- and DAP12-dependent activation of PI3K requires DAP10 and is inhibited by SHIP1. Sci Signal 2010; 3: ra38
-
(2010)
Sci Signal
, vol.3
-
-
Peng, Q.1
Malhotra, S.2
Torchia, J.A.3
Kerr, W.G.4
Coggeshall, K.M.5
Humphrey, M.B.6
-
47
-
-
0037805700
-
TREMs in the immune system and beyond
-
Colonna M. TREMs in the immune system and beyond. Nat Rev Immunol 2003; 3: 445-453
-
(2003)
Nat Rev Immunol
, vol.3
, pp. 445-453
-
-
Colonna, M.1
-
48
-
-
84876907931
-
Integrated systems approach identifies genetic nodes and networks in late-onsheimer's disease
-
Zhang B, Gaiteri C, Bodea L-G, Wang Z, McElwee J, Podtelezhnikov AA, Zhang C, Xie T, Tran L, Dobrin R, Fluder E, Clurman B, Melquist S, Narayanan M, Suver C, Shah H, Mahajan M, Gillis T, Mysore J, MacDonald ME, Lamb JR, Bennett DA, Molony C, Stone DJ, Gudnason V, Myers AJ, Schadt EE, Neumann H, Zhu J, Emilsson V. Integrated systems approach identifies genetic nodes and networks in late-onset Alzheimer's disease. Cell 2013; 153: 707-720
-
(2013)
Cell
, vol.153
, pp. 707-720
-
-
Zhang, B.1
Gaiteri, C.2
Bodea, L.-G.3
Wang, Z.4
McElwee, J.5
Podtelezhnikov, A.A.6
Zhang, C.7
Xie, T.8
Tran, L.9
Dobrin, R.10
Fluder, E.11
Clurman, B.12
Melquist, S.13
Narayanan, M.14
Suver, C.15
Shah, H.16
Mahajan, M.17
Gillis, T.18
Mysore, J.19
MacDonald, M.E.20
Lamb, J.R.21
Bennett, D.A.22
Molony, C.23
Stone, D.J.24
Gudnason, V.25
Myers, A.J.26
Schadt, E.E.27
Neumann, H.28
Zhu, J.29
Emilsson, V.30
more..
-
49
-
-
79955641534
-
APPswe/Aβ regulation of osteoclast activation and RAGE expression in an age-dependent manner
-
Cui S, Xiong F, Hong Y, Jung J-U, Li X-S, Liu J-Z, Yan R, Mei L, Feng X, Xiong W-C. APPswe/Aβ regulation of osteoclast activation and RAGE expression in an age-dependent manner. J Bone Miner Res 2011; 26: 1084-1098
-
(2011)
J Bone Miner Res
, vol.26
, pp. 1084-1098
-
-
Cui, S.1
Xiong, F.2
Hong, Y.3
Jung, J.-U.4
Li, X.-S.5
Liu, J.-Z.6
Yan, R.7
Mei, L.8
Feng, X.9
Xiong, W.-C.10
-
50
-
-
68449086236
-
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
-
Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan PF, Sklar P. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 2009; 460: 748-752
-
(2009)
Nature
, vol.460
, pp. 748-752
-
-
Purcell, S.M.1
Wray, N.R.2
Stone, J.L.3
Visscher, P.M.4
O'Donovan, M.C.5
Sullivan, P.F.6
Sklar, P.7
|