-
1
-
-
11844257540
-
Complete ascertainment of dementia in the Swedish Twin Registry: The HARMONY study
-
Gatz M, Fratiglioni L, Johansson B, Berg S, Mortimer JA, Reynolds CA, Fiske A, Pedersen NL (2005) Complete ascertainment of dementia in the Swedish Twin Registry: The HARMONY study. Neurobiol Aging 26, 439-447.
-
(2005)
Neurobiol Aging
, vol.26
, pp. 439-447
-
-
Gatz, M.1
Fratiglioni, L.2
Johansson, B.3
Berg, S.4
Mortimer, J.A.5
Reynolds, C.A.6
Fiske, A.7
Pedersen, N.L.8
-
2
-
-
32244435907
-
Role of genes and environments for explaining Alzheimer disease
-
Gatz M, Reynolds CA, Fratiglioni L, Johansson B, Mortimer JA, Berg S, Fiske A, Pedersen NL (2006) Role of genes and environments for explaining Alzheimer disease. Arch Gen Psychiatry 63, 168-174.
-
(2006)
Arch Gen Psychiatry
, vol.63
, pp. 168-174
-
-
Gatz, M.1
Reynolds, C.A.2
Fratiglioni, L.3
Johansson, B.4
Mortimer, J.A.5
Berg, S.6
Fiske, A.7
Pedersen, N.L.8
-
3
-
-
0030823158
-
Effects of age, sex, and ethnicity on the association between apolipoprotein e genotype and Alzheimer disease
-
Farrer LA, Cupples LA, Haines JL, Hyman B, Kukull WA, Mayeux R, Myers RH, Pericak-Vance MA, Risch N, van DuijnCM(1997) Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease.Ameta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium. JAMA 278, 1349-1356.
-
(1997)
Ameta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium. JAMA
, vol.278
, pp. 1349-1356
-
-
Farrer, L.A.1
Cupples, L.A.2
Haines, J.L.3
Hyman, B.4
Kukull, W.A.5
Mayeux, R.6
Myers, R.H.7
Pericak-Vance, M.A.8
Risch, N.9
Van Duijn, C.M.10
-
4
-
-
77955463899
-
Replication of CLU, CR1, and PICALM associations with Alzheimer disease
-
Carrasquillo MM, Belbin O, Hunter TA, Ma L, Bisceglio GD, Zou F, Crook JE, Pankratz VS, Dickson DW, Graff-Radford NR, Petersen RC, Morgan K, Younkin SG (2010) Replication of CLU, CR1, and PICALM associations with Alzheimer disease. Arch Neurol 67, 961-964.
-
(2010)
Arch Neurol
, vol.67
, pp. 961-964
-
-
Carrasquillo, M.M.1
Belbin, O.2
Hunter, T.A.3
Ma, L.4
Bisceglio, G.D.5
Zou, F.6
Crook, J.E.7
Pankratz, V.S.8
Dickson, D.W.9
Graff-Radford, N.R.10
Petersen, R.C.11
Morgan, K.12
Younkin, S.G.13
-
5
-
-
77955036445
-
Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals
-
Corneveaux JJ, Myers AJ, Allen AN, Pruzin JJ, Ramirez M, Engel A, Nalls MA, Chen K, Lee W, Chewning K, Villa SE, Meechoovet HB, Gerber JD, Frost D, Benson HL, O'Reilly S, Chibnik LB, Shulman JM, Singleton AB, Craig DW, Van Keuren-Jensen KR, Dunckley T, Bennett DA, De Jager PL, Heward C, Hardy J, Reiman EM, Huentelman MJ (2010) Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals. Hum Mol Genet 19, 3295-3301.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 3295-3301
-
-
Corneveaux, J.J.1
Myers, A.J.2
Allen, A.N.3
Pruzin, J.J.4
Ramirez, M.5
Engel, A.6
Nalls, M.A.7
Chen, K.8
Lee, W.9
Chewning, K.10
Villa, S.E.11
Meechoovet, H.B.12
Gerber, J.D.13
Frost, D.14
Benson, H.L.15
O'Reilly, S.16
Chibnik, L.B.17
Shulman, J.M.18
Singleton, A.B.19
Craig, D.W.20
Van Keuren-Jensen, K.R.21
Dunckley, T.22
Bennett, D.A.23
De Jager, P.L.24
Heward, C.25
Hardy, J.26
Reiman, E.M.27
Huentelman, M.J.28
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, Schurmann B, van den BH, Heuser I, Kornhuber J, Wiltfang J, Dichgans M, Frolich L, Hampel H, Hull M, Rujescu D, Goate AM, Kauwe JS, Cruchaga C, Nowotny P, Morris JC, Mayo K, Sleegers K, Bettens K, Engelborghs S, De Deyn PP, Van BC, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Tsolaki M, Singleton AB, Guerreiro R, MuhleisenTW, Nothen MM, Moebus S, Jockel KH, Klopp N, Wichmann HE, Carrasquillo MM, Pankratz VS, Younkin SG, Holmans PA, O'Donovan M, Owen MJ, Williams J (2009) Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Nat Genet 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
Schurmann, B.42
Van Den, B.H.43
Heuser, I.44
Kornhuber, J.45
Wiltfang, J.46
Dichgans, M.47
Frolich, L.48
Hampel, H.49
Hull, M.50
Rujescu, D.51
Goate, A.M.52
Kauwe, J.S.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, B.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
Muhleisen, T.W.74
Nothen, M.M.75
Moebus, S.76
Jockel, 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
-
-
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 JC, 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, BrownKS, 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 ER, Hardy J, Mead S, Fox NC, Rossor M, Collinge J, MaierW, Jessen F, Ruther E, Schurmann B, Heun R, Kolsch H, van den BH, Heuser I, Kornhuber J, Wiltfang J, Dichgans M, Frolich L, Hampel H, Gallacher J, Hull M, Rujescu D, Giegling I, Goate AM, Kauwe JS, Cruchaga C, Nowotny P, Morris JC, Mayo K, Sleegers K, Bettens K, Engelborghs S, De Deyn PP, Van BC, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Tsolaki M, Singleton AB, Guerreiro R, Muhleisen TW, Nothen MM, Moebus S, Jockel KH, Klopp N, Wichmann HE, Pankratz VS, Sando SB, Aasly JO, Barcikowska M, Wszolek ZK, Dickson DW, Graff-Radford NR, Petersen RC, van Duijn CM, BretelerMM, IkramMA, DeStefano AL, Fitzpatrick AL, Lopez O, Launer LJ, Seshadri S, Berr C, Campion D, Epelbaum J, Dartigues JF, Tzourio C, Alperovitch 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, Bjornsson 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, Bossu 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 (2011) Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nat Genet 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.42
Hardy, J.43
Mead, S.44
Fox, N.C.45
Rossor, M.46
Collinge, J.47
Maierw Jessen, F.48
Ruther, E.49
Schurmann, B.50
Heun, R.51
Kolsch, H.52
Van Den, B.H.53
Heuser, I.54
Kornhuber, J.55
Wiltfang, J.56
Dichgans, M.57
Frolich, L.58
Hampel, H.59
Gallacher, J.60
Hull, M.61
Rujescu, D.62
Giegling, I.63
more..
-
8
-
-
78549264026
-
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
-
Lambert JC, 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, FievetN, Barberger-Gateau P, Engelborghs S, De DP, 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, Bossu P, Piccardi P, Annoni G, Seripa D, Galimberti D, Hannequin D, Licastro F, Soininen H, Ritchie K, Blanche H, Dartigues JF, Tzourio C, Gut I, Van BC, Alperovitch A, Lathrop M, Amouyel P (2009) Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. Nat Genet 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
Fievet, N.15
Barberger-Gateau, P.16
Engelborghs, S.17
De, D.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
Bossu, 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
Blanche, H.43
Dartigues, J.F.44
Tzourio, C.45
Gut, I.46
Van, B.C.47
Alperovitch, A.48
Lathrop, M.49
Amouyel, P.50
more..
-
9
-
-
79955464911
-
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
-
Naj AC, Jun G, Beecham GW, Wang LS, 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 JS, 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 LW, 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 (2011) Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nat Genet 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.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
more..
-
10
-
-
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 AV, Carassquillo MM, Lambert JC, Harold D, Schrijvers EM, Ramirez-Lorca R, Debette S, LongstrethWTJr, JanssensAC, 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 PV, 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 MM (2010) Genome-wide analysis of genetic loci associated with Alzheimer disease. JAMA 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, A.V.8
Carassquillo, M.M.9
Lambert, J.C.10
Harold, D.11
Schrijvers, E.M.12
Ramirez-Lorca, R.13
Debette, S.14
Longstreth Jr., W.T.15
Janssens, A.C.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, P.V.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.63
more..
-
11
-
-
46849083940
-
Dietary fatty acids, age-related cognitive decline, and mild cognitive impairment
-
Solfrizzi V, Capurso C, D'Introno A, Colacicco AM, Frisardi V, Santamato A, Ranieri M, Fiore P, Vendemiale G, Seripa D, Pilotto A, Capurso A, Panza F (2008) Dietary fatty acids, age-related cognitive decline, and mild cognitive impairment. J Nutr Health Aging 12, 382-386.
-
(2008)
J Nutr Health Aging
, vol.12
, pp. 382-386
-
-
Solfrizzi, V.1
Capurso, C.2
D'Introno, A.3
Colacicco, A.M.4
Frisardi, V.5
Santamato, A.6
Ranieri, M.7
Fiore, P.8
Vendemiale, G.9
Seripa, D.10
Pilotto, A.11
Capurso, A.12
Panza, F.13
-
12
-
-
33746565284
-
Apolipoprotein E, cholesterol metabolism, diabetes, and the convergence of risk factors for Alzheimer's disease and cardiovascular disease
-
Martins IJ, Hone E, Foster JK, Sunram-Lea SI, Gnjec A, Fuller SJ, Nolan D, Gandy SE, MartinsRN(2006) Apolipoprotein E, cholesterol metabolism, diabetes, and the convergence of risk factors for Alzheimer's disease and cardiovascular disease. Mol Psychiatry 11, 721-736.
-
(2006)
Mol Psychiatry
, vol.11
, pp. 721-736
-
-
Martins, I.J.1
Hone, E.2
Foster, J.K.3
Sunram-Lea, S.I.4
Gnjec, A.5
Fuller, S.J.6
Nolan, D.7
Gandy, S.E.8
Martins, R.N.9
-
13
-
-
0034638746
-
Statins and the risk of dementia
-
Jick H, Zornberg GL, Jick SS, Seshadri S, Drachman DA (2000) Statins and the risk of dementia. Lancet 356, 1627-1631.
-
(2000)
Lancet
, vol.356
, pp. 1627-1631
-
-
Jick, H.1
Zornberg, G.L.2
Jick, S.S.3
Seshadri, S.4
Drachman, D.A.5
-
14
-
-
77954556989
-
Can statins prevent or help treat Alzheimer's disease?
-
McGuinness B, Passmore P (2010) Can statins prevent or help treat Alzheimer's disease? J Alzheimers Dis 20, 925-933.
-
(2010)
J Alzheimers Dis
, vol.20
, pp. 925-933
-
-
McGuinness, B.1
Passmore, P.2
-
15
-
-
30044442937
-
Deletion of Abca1 increases Abeta deposition in the PDAPP transgenic mouse model of Alzheimer disease
-
Wahrle SE, Jiang H, Parsadanian M, Hartman RE, Bales KR, Paul SM, Holtzman DM (2005) Deletion of Abca1 increases Abeta deposition in the PDAPP transgenic mouse model of Alzheimer disease. J Biol Chem 280, 43236-43242.
-
(2005)
J Biol Chem
, vol.280
, pp. 43236-43242
-
-
Wahrle, S.E.1
Jiang, H.2
Parsadanian, M.3
Hartman, R.E.4
Bales, K.R.5
Paul, S.M.6
Holtzman, D.M.7
-
16
-
-
38849086036
-
Overexpression of ABCA1 reduces amyloid deposition in the PDAPP mouse model of Alzheimer disease
-
Wahrle SE, Jiang H, Parsadanian M, Kim J, Li A, Knoten A, Jain S, Hirsch-Reinshagen V, Wellington CL, Bales KR, Paul SM, Holtzman DM (2008) Overexpression of ABCA1 reduces amyloid deposition in the PDAPP mouse model of Alzheimer disease. J Clin Invest 118, 671-682.
-
(2008)
J Clin Invest
, vol.118
, pp. 671-682
-
-
Wahrle, S.E.1
Jiang, H.2
Parsadanian, M.3
Kim, J.4
Li, A.5
Knoten, A.6
Jain, S.7
Hirsch-Reinshagen, V.8
Wellington, C.L.9
Bales, K.R.10
Paul, S.M.11
Holtzman, D.M.12
-
17
-
-
36749014486
-
A novel intronic polymorphism of ABCA1 gene reveals risk for sporadic Alzheimer's disease in Chinese
-
Chu LW, Li Y, Li Z, Tang AY, Cheung BM, Leung RY, Yik PY, Jin DY, Song YQ (2007) A novel intronic polymorphism of ABCA1 gene reveals risk for sporadic Alzheimer's disease in Chinese. Am J Med Genet B Neuropsychiatr Genet 144B, 1007-1013.
-
(2007)
Am J Med Genet B Neuropsychiatr Genet
, vol.144 B
, pp. 1007-1013
-
-
Chu, L.W.1
Li, Y.2
Li, Z.3
Tang, A.Y.4
Cheung, B.M.5
Leung, R.Y.6
Yik, P.Y.7
Jin, D.Y.8
Song, Y.Q.9
-
18
-
-
11144357626
-
Genetic variants of ABCA1 modify Alzheimer disease risk and quantitative traits related to beta-amyloid metabolism
-
Katzov H, Chalmers K, Palmgren J, And reasen N, Johansson B, Cairns NJ, Gatz M, Wilcock GK, Love S, Pedersen NL, Brookes AJ, BlennowK, Kehoe PG, Prince JA(2004) Genetic variants of ABCA1 modify Alzheimer disease risk and quantitative traits related to beta-amyloid metabolism. Hum Mutat 23, 358-367.
-
(2004)
Hum Mutat
, vol.23
, pp. 358-367
-
-
Katzov, H.1
Chalmers, K.2
Palmgren, J.3
Andreasen, N.4
Johansson, B.5
Cairns, N.J.6
Gatz, M.7
Wilcock, G.K.8
Love, S.9
Pedersen, N.L.10
Brookes, A.J.11
Blennow, K.12
Kehoe, P.G.13
Prince, J.A.14
-
19
-
-
69549130702
-
Asurvey of ABCA1 sequence variation confirms association with dementia
-
Reynolds CA, Hong MG, Eriksson UK, Blennow K, Bennet AM, Johansson B, Malmberg B, Berg S, Wiklund F, Gatz M, Pedersen NL, Prince JA(2009)Asurvey of ABCA1 sequence variation confirms association with dementia. Hum Mutat 30, 1348-1354.
-
(2009)
Hum Mutat
, vol.30
, pp. 1348-1354
-
-
Reynolds, C.A.1
Hong, M.G.2
Eriksson, U.K.3
Blennow, K.4
Bennet, A.M.5
Johansson, B.6
Malmberg, B.7
Berg, S.8
Wiklund, F.9
Gatz, M.10
Pedersen, N.L.11
Prince, J.A.12
-
20
-
-
34247120141
-
Gender-specific association of ATP-binding cassette transporter 1 (ABCA1) polymorphisms with the risk of late-onset Alzheimer's disease
-
Sundar PD, Feingold E, Minster RL, DeKosky ST, Kamboh MI (2007) Gender-specific association of ATP-binding cassette transporter 1 (ABCA1) polymorphisms with the risk of late-onset Alzheimer's disease. Neurobiol Aging 28, 856-862.
-
(2007)
Neurobiol Aging
, vol.28
, pp. 856-862
-
-
Sundar, P.D.1
Feingold, E.2
Minster, R.L.3
Dekosky, S.T.4
Kamboh, M.I.5
-
21
-
-
34147158749
-
Polymorphisms of cholesterol metabolism genes CYP46 and ABCA1 and the risk of sporadic Alzheimer's disease in Chinese
-
Wang F, Jia J (2007) Polymorphisms of cholesterol metabolism genes CYP46 and ABCA1 and the risk of sporadic Alzheimer's disease in Chinese. Brain Res 1147, 34-38.
-
(2007)
Brain Res
, vol.1147
, pp. 34-38
-
-
Wang, F.1
Jia, J.2
-
22
-
-
33947329031
-
ABCA1 polymorphisms and Alzheimer's disease
-
Wavrant-De VF, Compton D, Womick M, Arepalli S, Adighibe O, Li L, Perez-Tur J, Hardy J (2007) ABCA1 polymorphisms and Alzheimer's disease. Neurosci Lett 416, 180-183.
-
(2007)
Neurosci Lett
, vol.416
, pp. 180-183
-
-
Wavrant-De, V.F.1
Compton, D.2
Womick, M.3
Arepalli, S.4
Adighibe, O.5
Li, L.6
Perez-Tur, J.7
Hardy, J.8
-
23
-
-
12244255799
-
ABCA1 modulates CSF cholesterol levels and influences the age at onset of Alzheimer's disease
-
Wollmer MA, Streffer JR, Lutjohann D, Tsolaki M, Iakovidou V, Hegi T, Pasch T, Jung HH, Bergmann K, Nitsch RM, Hock C, Papassotiropoulos A (2003) ABCA1 modulates CSF cholesterol levels and influences the age at onset of Alzheimer's disease. Neurobiol Aging 24, 421-426.
-
(2003)
Neurobiol Aging
, vol.24
, pp. 421-426
-
-
Wollmer, M.A.1
Streffer, J.R.2
Lutjohann, D.3
Tsolaki, M.4
Iakovidou, V.5
Hegi, T.6
Pasch, T.7
Jung, H.H.8
Bergmann, K.9
Nitsch, R.M.10
Hock, C.11
Papassotiropoulos, A.12
-
24
-
-
33750591113
-
Polymorphism in ABCA1 influences CSF 24S-hydroxycholesterol levels but is not a major risk factor of Alzheimer's disease
-
Kolsch H, Lutjohann D, Jessen F, von BK, Schmitz S, Urbach H, Maier W, Heun R (2006) Polymorphism in ABCA1 influences CSF 24S-hydroxycholesterol levels but is not a major risk factor of Alzheimer's disease. Int J Mol Med 17, 791-794.
-
(2006)
Int J Mol Med
, vol.17
, pp. 791-794
-
-
Kolsch, H.1
Lutjohann, D.2
Jessen, F.3
Von Bk Schmitz, S.4
Urbach, H.5
Maier, W.6
Heun, R.7
-
25
-
-
38349038412
-
Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease
-
Li H, Wetten S, Li L, St Jean PL, Upmanyu R, Surh L, Hosford D, Barnes MR, Briley JD, Borrie M, Coletta N, Delisle R, Dhalla D, Ehm MG, Feldman HH, Fornazzari L, Gauthier S, Goodgame N, Guzman D, Hammond S, Hollingworth P, Hsiung GY, Johnson J, Kelly DD, Keren R, Kertesz A, King KS, Lovestone S, Loy-English I, Matthews PM, Owen MJ, Plumpton M, Pryse-Phillips W, Prinjha RK, Richardson JC, Saunders A, Slater AJ, St George-Hyslop PH, Stinnett SW, Swartz JE, Taylor RL, Wherrett J, Williams J, Yarnall DP, Gibson RA, Irizarry MC, Middleton LT, Roses AD (2008) Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease. Arch Neurol 65, 45-53.
-
(2008)
Arch Neurol
, vol.65
, pp. 45-53
-
-
Li, H.1
Wetten, S.2
Li, L.3
St Jean, P.L.4
Upmanyu, R.5
Surh, L.6
Hosford, D.7
Barnes, M.R.8
Briley, J.D.9
Borrie, M.10
Coletta, N.11
Delisle, R.12
Dhalla, D.13
Ehm, M.G.14
Feldman, H.H.15
Fornazzari, L.16
Gauthier, S.17
Goodgame, N.18
Guzman, D.19
Hammond, S.20
Hollingworth, P.21
Hsiung, G.Y.22
Johnson, J.23
Kelly, D.D.24
Keren, R.25
Kertesz, A.26
King, K.S.27
Lovestone, S.28
Loy-English, I.29
Matthews, P.M.30
Owen, M.J.31
Plumpton, M.32
Pryse-Phillips, W.33
Prinjha, R.K.34
Richardson, J.C.35
Saunders, A.36
Slater, A.J.37
St George-Hyslop, P.H.38
Stinnett, S.W.39
Swartz, J.E.40
Taylor, R.L.41
Wherrett, J.42
Williams, J.43
Yarnall, D.P.44
Gibson, R.A.45
Irizarry, M.C.46
Middleton, L.T.47
Roses, A.D.48
more..
-
26
-
-
3543119039
-
Association of ABCA1 with late-onset Alzheimer's disease is not observed in a casecontrol study
-
Li Y, Tacey K, Doil L, van LR, Garcia V, Rowland C, Schrodi S, Leong D, Lau K, Catanese J, Sninsky J, Nowotny P, Holmans P, Hardy J, Powell J, Lovestone S, Thal L, Owen M, Williams J, Goate A, Grupe A (2004) Association of ABCA1 with late-onset Alzheimer's disease is not observed in a casecontrol study. Neurosci Lett 366, 268-271.
-
(2004)
Neurosci Lett
, vol.366
, pp. 268-271
-
-
Li, Y.1
Tacey, K.2
Doil, L.3
Van Lr Garcia, V.4
Rowland, C.5
Schrodi, S.6
Leong, D.7
Lau, K.8
Catanese, J.9
Sninsky, J.10
Nowotny, P.11
Holmans, P.12
Hardy, J.13
Powell, J.14
Lovestone, S.15
Thal, L.16
Owen, M.17
Williams, J.18
Goate, A.19
Grupe, A.20
more..
-
27
-
-
34249745769
-
GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers
-
Reiman EM, Webster JA, Myers AJ, Hardy J, Dunckley T, Zismann VL, Joshipura KD, Pearson JV, Hu-Lince D, Huentelman MJ, Craig DW, Coon KD, Liang WS, Herbert RH, Beach T, Rohrer KC, Zhao AS, Leung D, Bryden L, Marlowe L, Kaleem M, Mastroeni D, Grover A, Heward CB, Ravid R, Rogers J, Hutton ML, Melquist S, Petersen RC, Alexander GE, Caselli RJ, Kukull W, Papassotiropoulos A, Stephan DA (2007) GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers. Neuron 54, 713-720.
-
(2007)
Neuron
, vol.54
, pp. 713-720
-
-
Reiman, E.M.1
Webster, J.A.2
Myers, A.J.3
Hardy, J.4
Dunckley, T.5
Zismann, V.L.6
Joshipura, K.D.7
Pearson, J.V.8
Hu-Lince, D.9
Huentelman, M.J.10
Craig, D.W.11
Coon, K.D.12
Liang, W.S.13
Herbert, R.H.14
Beach, T.15
Rohrer, K.C.16
Zhao, A.S.17
Leung, D.18
Bryden, L.19
Marlowe, L.20
Kaleem, M.21
Mastroeni, D.22
Grover, A.23
Heward, C.B.24
Ravid, R.25
Rogers, J.26
Hutton, M.L.27
Melquist, S.28
Petersen, R.C.29
Alexander, G.E.30
Caselli, R.J.31
Kukull, W.32
Papassotiropoulos, A.33
Stephan, D.A.34
more..
-
28
-
-
35148898726
-
Association of genetic variants of ABCA1 with Alzheimer's disease risk
-
Rodriguez-Rodriguez E, Mateo I, Llorca J, Sanchez-Quintana C, Infante J, Garcia-Gorostiaga I, Sanchez-Juan P, Berciano J, Combarros O (2007) Association of genetic variants of ABCA1 with Alzheimer's disease risk. Am J Med Genet B Neuropsychiatr Genet 144B 964-968.
-
(2007)
Am J Med Genet B Neuropsychiatr Genet
, vol.144 B
, pp. 964-968
-
-
Rodriguez-Rodriguez, E.1
Mateo, I.2
Llorca, J.3
Sanchez-Quintana, C.4
Infante, J.5
Garcia-Gorostiaga, I.6
Sanchez-Juan, P.7
Berciano, J.8
Combarros, O.9
-
29
-
-
28444470503
-
Association studies of cholesterol metabolism genes (CH25H, ABCA1 and CH24H) in Alzheimer's disease
-
Shibata N, Kawarai T, Lee JH, Lee HS, Shibata E, Sato C, Liang Y, Duara R, Mayeux RP, St George-Hyslop PH, Rogaeva E (2006) Association studies of cholesterol metabolism genes (CH25H, ABCA1 and CH24H) in Alzheimer's disease. Neurosci Lett 391, 142-146.
-
(2006)
Neurosci Lett
, vol.391
, pp. 142-146
-
-
Shibata, N.1
Kawarai, T.2
Lee, J.H.3
Lee, H.S.4
Shibata, E.5
Sato, C.6
Liang, Y.7
Duara, R.8
Mayeux, R.P.9
St George-Hyslop, P.H.10
Rogaeva, E.11
-
30
-
-
34247880309
-
ApolipoproteinElevels in cerebrospinal fluid and the effects ofABCA1polymorphisms
-
Wahrle SE, Shah AR, FaganAM, Smemo S, Kauwe JS, Grupe A, Hinrichs A, Mayo K, Jiang H, Thal LJ, Goate AM, HoltzmanDM (2007) ApolipoproteinElevels in cerebrospinal fluid and the effects ofABCA1polymorphisms. Mol Neurodegener 2, 7.
-
(2007)
Mol Neurodegener
, vol.2
, pp. 7
-
-
Wahrle, S.E.1
Shah, A.R.2
Fagan, A.M.3
Smemo, S.4
Kauwe, J.S.5
Grupe, A.6
Hinrichs, A.7
Mayo, K.8
Jiang, H.9
Thal, L.J.10
Goate, A.M.11
Holtzman, D.M.12
-
31
-
-
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, Schurmann B, Heun R, Kolsch H, van den BH, Heuser I, Peters O, Kornhuber J, Wiltfang J, Dichgans M, Frolich L, Hampel H, Hull M, Rujescu D, Goate AM, Kauwe JS, 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, Muhleisen TW, Nothen MM, Moebus S, Jockel KH, Klopp N, Wichmann HE, Ruther E, Carrasquillo MM, Pankratz VS, Younkin SG, Hardy J, O'Donovan MC, Owen MJ, Williams J (2010) Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease. PLoS One 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
Schurmann, B.42
Heun, R.43
Kolsch, H.44
Van Den Heuser, B.H.I.45
Peters, O.46
Kornhuber, J.47
Wiltfang, J.48
Dichgans, M.49
Frolich, L.50
Hampel, H.51
Hull, M.52
Rujescu, D.53
Goate, A.M.54
Kauwe, J.S.55
Cruchaga, C.56
Nowotny, P.57
Morris, J.C.58
Mayo, K.59
Livingston, G.60
Bass, N.J.61
Gurling, H.62
McQuillin, A.63
Gwilliam, R.64
Deloukas, P.65
Al- Chalabi, A.66
Shaw, C.E.67
Singleton, A.B.68
Guerreiro, R.69
Muhleisen, T.W.70
Nothen, M.M.71
Moebus, S.72
Jockel, K.H.73
Klopp, N.74
Wichmann, H.E.75
Ruther, E.76
Carrasquillo, M.M.77
Pankratz, V.S.78
Younkin, S.G.79
Hardy, J.80
O'Donovan, M.C.81
Owen, M.J.82
Williams, J.83
more..
-
32
-
-
3843056691
-
Multiple rare alleles contribute to low plasma levels of HDL cholesterol
-
Cohen JC, Kiss RS, Pertsemlidis A, Marcel YL, McPherson R, Hobbs HH (2004) Multiple rare alleles contribute to low plasma levels of HDL cholesterol. Science 305, 869-872.
-
(2004)
Science
, vol.305
, pp. 869-872
-
-
Cohen, J.C.1
Kiss, R.S.2
Pertsemlidis, A.3
Marcel, Y.L.4
McPherson, R.5
Hobbs, H.H.6
-
33
-
-
84876106048
-
Cognitive impairment and dietary habits among elders: The Velestino Study
-
Katsiardanis K, Diamantaras AA, Dessypris N, Michelakos T, Anastasiou A, Katsiardani KP, Kanavidis P, Papadopoulos FC, Stefanadis C, Panagiotakos DB, Petridou ET (2013) Cognitive impairment and dietary habits among elders: The Velestino Study. J Med Food 16, 343-350.
-
(2013)
J Med Food
, vol.16
, pp. 343-350
-
-
Katsiardanis, K.1
Diamantaras, A.A.2
Dessypris, N.3
Michelakos, T.4
Anastasiou, A.5
Katsiardani, K.P.6
Kanavidis, P.7
Papadopoulos, F.C.8
Stefanadis, C.9
Panagiotakos, D.B.10
Petridou, E.T.11
-
34
-
-
0016823810
-
Mini-mental state". A practical method for grading the cognitive state of patients for the clinician
-
Folstein MF, Folstein SE, McHugh PR (1975) "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res 12, 189-198.
-
(1975)
J Psychiatr Res
, vol.12
, pp. 189-198
-
-
Folstein, M.F.1
Folstein, S.E.2
McHugh, P.R.3
-
35
-
-
0021271971
-
Clinical diagnosis of Alzheimer's disease: Report of the NINCDS-ADRDAWork Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease
-
McKhann G, Drachman D, Folstein M, Katzman R, Price D, Stadlan EM (1984) Clinical diagnosis of Alzheimer's disease: Report of the NINCDS-ADRDAWork Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease. Neurology 34, 939-944.
-
(1984)
Neurology
, vol.34
, pp. 939-944
-
-
McKhann, G.1
Drachman, D.2
Folstein, M.3
Katzman, R.4
Price, D.5
Stadlan, E.M.6
-
36
-
-
79952141389
-
Deep sequencing of the nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's disease
-
Lupton MK, Proitsi P, Danillidou M, Tsolaki M, Hamilton G, Wroe R, Pritchard M, Lord K, Martin BM, Kloszewska I, Soininen H, Mecocci P, Vellas B, Harold D, Hollingworth P, Lovestone S, Powell JF (2011) Deep sequencing of the nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's disease. PLoS One 6, e17298.
-
(2011)
PLoS One
, vol.6
-
-
Lupton, M.K.1
Proitsi, P.2
Danillidou, M.3
Tsolaki, M.4
Hamilton, G.5
Wroe, R.6
Pritchard, M.7
Lord, K.8
Martin, B.M.9
Kloszewska, I.10
Soininen, H.11
Mecocci, P.12
Vellas, B.13
Harold, D.14
Hollingworth, P.15
Lovestone, S.16
Powell, J.F.17
-
37
-
-
55549097836
-
Mapping short DNA sequencing reads and calling variants using mapping quality scores
-
Li H, Ruan J, Durbin R (2008) Mapping short DNA sequencing reads and calling variants using mapping quality scores. Genome Res 18, 1851-1858.
-
(2008)
Genome Res
, vol.18
, pp. 1851-1858
-
-
Li, H.1
Ruan, J.2
Durbin, R.3
-
38
-
-
71749099456
-
Deep sequencing to reveal new variants in pooled DNA samples
-
Out AA, van MI, Goeman JJ, Ariyurek Y, Ossowski S, Schneeberger K, Weigel D, van GM, Taschner PE, Tops CM, BreuningMH, vanOmmenGJ, den Dunnen JT, Devilee P, Hes FJ (2009) Deep sequencing to reveal new variants in pooled DNA samples. Hum Mutat 30, 1703-1712.
-
(2009)
Hum Mutat
, vol.30
, pp. 1703-1712
-
-
Out, A.A.1
Van Mi Goeman, J.J.2
Ariyurek, Y.3
Ossowski, S.4
Schneeberger, K.5
Weigel, D.6
Van Gm Taschner, P.E.7
Tops, C.M.8
Breuning, M.H.9
Van Ommen, G.J.10
Den Dunnen, J.T.11
Devilee, P.12
Hes, F.J.13
-
39
-
-
77958067631
-
CCRaVAT and QuTie-enabling analysis of rare variants in large-scale case control and quantitative trait association studies
-
Lawrence R, Day-Williams AG, Elliott KS, Morris AP, Zeggini E (2010) CCRaVAT and QuTie-enabling analysis of rare variants in large-scale case control and quantitative trait association studies. BMC Bioinformatics 11, 527.
-
(2010)
BMC Bioinformatics
, vol.11
, pp. 527
-
-
Lawrence, R.1
Day-Williams, A.G.2
Elliott, K.S.3
Morris, A.P.4
Zeggini, E.5
-
40
-
-
84864942403
-
Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies
-
NHLBIGOExome Sequencing Project - ESP Lung Project Team
-
Lee S, Emond MJ, Bamshad MJ, Barnes KC, Rieder MJ, NickersonDA, NHLBIGOExome Sequencing Project - ESP Lung Project Team, Christiani DC, Wurfel MM, Lin X (2012) Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies. Am J Hum Genet 91, 224-237.
-
(2012)
Am J Hum Genet
, vol.91
, pp. 224-237
-
-
Lee, S.1
Emond, M.J.2
Bamshad, M.J.3
Barnes, K.C.4
Rieder, M.J.5
Nickerson, D.A.6
Christiani, D.C.7
Wurfel, M.M.8
Lin, X.9
-
41
-
-
68149165614
-
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
-
Kumar P, Henikoff S, Ng PC (2009) Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm. Nat Protoc 4, 1073-1081.
-
(2009)
Nat Protoc
, vol.4
, pp. 1073-1081
-
-
Kumar, P.1
Henikoff, S.2
Ng, P.C.3
-
42
-
-
44349132708
-
Common and rare variants in multifactorial susceptibility to common diseases
-
Bodmer W, Bonilla C (2008) Common and rare variants in multifactorial susceptibility to common diseases. Nat Genet 40, 695-701.
-
(2008)
Nat Genet
, vol.40
, pp. 695-701
-
-
Bodmer, W.1
Bonilla, C.2
-
43
-
-
38749145596
-
Shifting paradigm of association studies: Value of rare single-nucleotide polymorphisms
-
Gorlov IP, Gorlova OY, Sunyaev SR, Spitz MR, Amos CI (2008) Shifting paradigm of association studies: Value of rare single-nucleotide polymorphisms. Am J Hum Genet 82, 100-112.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 100-112
-
-
Gorlov, I.P.1
Gorlova, O.Y.2
Sunyaev, S.R.3
Spitz, M.R.4
Amos, C.I.5
-
44
-
-
84872057940
-
TREM2 variants in Alzheimer's disease
-
Guerreiro R, Wojtas A, Bras J, Carrasquillo M, Rogaeva E, Majounie E, Cruchaga C, Sassi C, Kauwe JS, Younkin S, Hazrati L, Collinge J, Pocock J, Lashley T, Williams J, Lambert JC, Amouyel P, Goate A, Rademakers R, Morgan K, Powell J, St George-Hyslop P, Singleton A, Hardy J (2012) TREM2 variants in Alzheimer's disease. N Engl J Med 368, 117-127.
-
(2012)
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.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..
-
45
-
-
63949086651
-
Quantification of rare allelic variants from pooled genomic DNA
-
Druley TE, Vallania FL, Wegner DJ, Varley KE, Knowles OL, Bonds JA, Robison SW, Doniger SW, Hamvas A, Cole FS, Fay JC, MitraRD(2009) Quantification of rare allelic variants from pooled genomic DNA. Nat Methods 6, 263-265.
-
(2009)
Nat Methods
, vol.6
, pp. 263-265
-
-
Druley, T.E.1
Vallania, F.L.2
Wegner, D.J.3
Varley, K.E.4
Knowles, O.L.5
Bonds, J.A.6
Robison, S.W.7
Doniger, S.W.8
Hamvas, A.9
Cole, F.S.10
Fay, J.C.11
Mitra, R.D.12
-
46
-
-
84869769984
-
Next generation sequencing of CLU, PICALM and CR1: Pitfalls and potential solutions
-
Lord J, Turton J, Medway C, Shi H, Brown K, Lowe J, Mann D, Pickering-Brown S, Kalsheker N, Passmore P, Morgan K (2012) Next generation sequencing of CLU, PICALM and CR1: Pitfalls and potential solutions. Int J Mol Epidemiol Genet 3, 262-275.
-
(2012)
Int J Mol Epidemiol Genet
, vol.3
, pp. 262-275
-
-
Lord, J.1
Turton, J.2
Medway, C.3
Shi, H.4
Brown, K.5
Lowe, J.6
Mann, D.7
Pickering-Brown, S.8
Kalsheker, N.9
Passmore, P.10
Morgan, K.11
-
47
-
-
65249131713
-
Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes
-
Nejentsev S, Walker N, Riches D, Egholm M, Todd JA (2009) Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes. Science 324, 387-389.
-
(2009)
Science
, vol.324
, pp. 387-389
-
-
Nejentsev, S.1
Walker, N.2
Riches, D.3
Egholm, M.4
Todd, J.A.5
-
48
-
-
0037421206
-
Amyloidogenic processing of the Alzheimer beta-amyloid precursor protein depends on lipid rafts
-
Ehehalt R, Keller P, Haass C, Thiele C, Simons K (2003) Amyloidogenic processing of the Alzheimer beta-amyloid precursor protein depends on lipid rafts. J Cell Biol 160, 113-123.
-
(2003)
J Cell Biol
, vol.160
, pp. 113-123
-
-
Ehehalt, R.1
Keller, P.2
Haass, C.3
Thiele, C.4
Simons, K.5
-
49
-
-
79960044932
-
96-plex molecular barcoding for the Illumina Genome Analyzer
-
Kozarewa I, Turner DJ (2011) 96-plex molecular barcoding for the Illumina Genome Analyzer. Methods Mol Biol 733, 279-298.
-
(2011)
Methods Mol Biol
, vol.733
, pp. 279-298
-
-
Kozarewa, I.1
Turner, D.J.2
-
50
-
-
79952024137
-
Serum lipid levels in patients with Alzheimer's disease
-
Presecki P, Muck-Seler D, Mimica N, Pivac N, Mustapic M, Stipcevic T, Smalc VF (2011) Serum lipid levels in patients with Alzheimer's disease. Coll Antropol 35(Suppl 1), 115-120.
-
(2011)
Coll Antropol
, vol.35
, Issue.SUPPL. 1
, pp. 115-120
-
-
Presecki, P.1
Muck-Seler, D.2
Mimica, N.3
Pivac, N.4
Mustapic, M.5
Stipcevic, T.6
Smalc, V.F.7
-
51
-
-
14644420598
-
Genetic variation in ABC transporter A1 contributes to HDL cholesterol in the general population
-
Frikke-Schmidt R, Nordestgaard BG, Jensen GB, Tybjaerg- Hansen A (2004) Genetic variation in ABC transporter A1 contributes to HDL cholesterol in the general population. J Clin Invest 114, 1343-1353.
-
(2004)
J Clin Invest
, vol.114
, pp. 1343-1353
-
-
Frikke-Schmidt, R.1
Nordestgaard, B.G.2
Jensen, G.B.3
Tybjaerg- Hansen, A.4
-
52
-
-
84869748975
-
Role of abc transporters in the pathogenesis of Alzheimer's disease
-
Abuznait AH, Kaddoumi A (2012) Role of abc transporters in the pathogenesis of Alzheimer's disease. ACS Chem Neurosci 3, 820-831.
-
(2012)
ACS Chem Neurosci
, vol.3
, pp. 820-831
-
-
Abuznait, A.H.1
Kaddoumi, A.2
-
53
-
-
84862221167
-
SMART 7: Recent updates to the protein domain annotation resource
-
Letunic I, Doerks T, Bork P (2012)SMART 7: Recent updates to the protein domain annotation resource. Nucleic Acids Res 40(Database issue), D302-D305.
-
(2012)
Nucleic Acids Res
, vol.40
, Issue.DATABASE ISSUE
-
-
Letunic, I.1
Doerks, T.2
Bork, P.3
|