-
1
-
-
83855165649
-
Cell adhesion molecules contribute to Alzheimer’s disease: multiple pathway analyses of two genome-wide association studies
-
COI: 1:CAS:528:DC%2BC38XhsFygurk%3D, PID: 22017384
-
Liu G, Jiang Y, Wang P, Feng R, Jiang N, Chen X, Song H, Chen Z (2012) Cell adhesion molecules contribute to Alzheimer’s disease: multiple pathway analyses of two genome-wide association studies. J Neurochem 120:190–198
-
(2012)
J Neurochem
, vol.120
, pp. 190-198
-
-
Liu, G.1
Jiang, Y.2
Wang, P.3
Feng, R.4
Jiang, N.5
Chen, X.6
Song, H.7
Chen, Z.8
-
2
-
-
84891371879
-
Cardiovascular disease contributes to Alzheimer’s disease: evidence from large-scale genome-wide association studies
-
PID: 24231519
-
Liu G, Yao L, Liu J, Jiang Y, Ma G, Chen Z, Zhao B, Li K (2014) Cardiovascular disease contributes to Alzheimer’s disease: evidence from large-scale genome-wide association studies. Neurobiol Aging 35:786–792
-
(2014)
Neurobiol Aging
, vol.35
, pp. 786-792
-
-
Liu, G.1
Yao, L.2
Liu, J.3
Jiang, Y.4
Ma, G.5
Chen, Z.6
Zhao, B.7
Li, K.8
-
3
-
-
77954558670
-
Implication of the immune system in Alzheimer’s disease: evidence from genome-wide pathway analysis
-
COI: 1:CAS:528:DC%2BC3cXovFKgtrY%3D, PID: 20413860
-
Lambert JC, Grenier-Boley B, Chouraki V, Heath S, Zelenika D, Fievet N, Hannequin D, Pasquier F, Hanon O, Brice A, Epelbaum J, Berr C, Dartigues JF, Tzourio C, Campion D, Lathrop M, Amouyel P (2010) Implication of the immune system in Alzheimer’s disease: evidence from genome-wide pathway analysis. J Alzheimers Dis 20:1107–1118
-
(2010)
J Alzheimers Dis
, vol.20
, pp. 1107-1118
-
-
Lambert, J.C.1
Grenier-Boley, B.2
Chouraki, V.3
Heath, S.4
Zelenika, D.5
Fievet, N.6
Hannequin, D.7
Pasquier, F.8
Hanon, O.9
Brice, A.10
Epelbaum, J.11
Berr, C.12
Dartigues, J.F.13
Tzourio, C.14
Campion, D.15
Lathrop, M.16
Amouyel, P.17
-
4
-
-
84894227333
-
The CLU gene rs11136000 variant is significantly associated with Alzheimer’s disease in Caucasian and Asian populations
-
COI: 1:CAS:528:DC%2BC3sXhtFOnsbnI
-
Liu G, Wang H, Liu J, Li J, Li H, Ma G, Jiang Y, Chen Z, Zhao B, Li K (2014) The CLU gene rs11136000 variant is significantly associated with Alzheimer’s disease in Caucasian and Asian populations. Neuromol Med 16:52–60
-
(2014)
Neuromol Med
, vol.16
, pp. 52-60
-
-
Liu, G.1
Wang, H.2
Liu, J.3
Li, J.4
Li, H.5
Ma, G.6
Jiang, Y.7
Chen, Z.8
Zhao, B.9
Li, K.10
-
5
-
-
65549105080
-
Differences between subacute and chronic MPTP mice models: investigation of dopaminergic neuronal degeneration and alpha-synuclein inclusions
-
COI: 1:CAS:528:DC%2BD1MXntVCis7g%3D, PID: 19457163
-
Gibrat C, Saint-Pierre M, Bousquet M, Levesque D, Rouillard C, Cicchetti F (2009) Differences between subacute and chronic MPTP mice models: investigation of dopaminergic neuronal degeneration and alpha-synuclein inclusions. J Neurochem 109:1469–1482
-
(2009)
J Neurochem
, vol.109
, pp. 1469-1482
-
-
Gibrat, C.1
Saint-Pierre, M.2
Bousquet, M.3
Levesque, D.4
Rouillard, C.5
Cicchetti, F.6
-
6
-
-
78651110778
-
Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson’s disease in the European population
-
PID: 21084426
-
Saad M, Lesage S, Saint-Pierre A, Corvol JC, Zelenika D, Lambert JC, Vidailhet M, Mellick GD, Lohmann E, Durif F, Pollak P, Damier P, Tison F, Silburn PA, Tzourio C, Forlani S, Loriot MA, Giroud M, Helmer C, Portet F, Amouyel P, Lathrop M, Elbaz A, Durr A, Martinez M, Brice A (2011) Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson’s disease in the European population. Hum Mol Genet 20:615–627
-
(2011)
Hum Mol Genet
, vol.20
, pp. 615-627
-
-
Saad, M.1
Lesage, S.2
Saint-Pierre, A.3
Corvol, J.C.4
Zelenika, D.5
Lambert, J.C.6
Vidailhet, M.7
Mellick, G.D.8
Lohmann, E.9
Durif, F.10
Pollak, P.11
Damier, P.12
Tison, F.13
Silburn, P.A.14
Tzourio, C.15
Forlani, S.16
Loriot, M.A.17
Giroud, M.18
Helmer, C.19
Portet, F.20
Amouyel, P.21
Lathrop, M.22
Elbaz, A.23
Durr, A.24
Martinez, M.25
Brice, A.26
more..
-
7
-
-
38549156140
-
Out foxing Parkinson disease: where development meets neurodegeneration
-
PID: 18092892
-
Wexler EM, Geschwind DH (2007) Out foxing Parkinson disease: where development meets neurodegeneration. PLoS Biol 5:e334
-
(2007)
PLoS Biol
, vol.5
, pp. e334
-
-
Wexler, E.M.1
Geschwind, D.H.2
-
8
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
COI: 1:CAS:528:DC%2BD1MXot1Cgur4%3D, PID: 19474294
-
Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA (2009) Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci U S A 106:9362–9367
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 9362-9367
-
-
Hindorff, L.A.1
Sethupathy, P.2
Junkins, H.A.3
Ramos, E.M.4
Mehta, J.P.5
Collins, F.S.6
Manolio, T.A.7
-
9
-
-
77952298384
-
Reaching the limits of genome-wide significance in Alzheimer disease: back to the environment
-
COI: 1:CAS:528:DC%2BC3cXmtVOrt7Y%3D, PID: 20460629
-
Pedersen NL (2010) Reaching the limits of genome-wide significance in Alzheimer disease: back to the environment. JAMA 303:1864–1865
-
(2010)
JAMA
, vol.303
, pp. 1864-1865
-
-
Pedersen, N.L.1
-
10
-
-
80052284860
-
An exploratory study on CLU, CR1 and PICALM and Parkinson disease
-
COI: 1:CAS:528:DC%2BC3MXht1Wrt7%2FI, PID: 21912625
-
Gao J, Huang X, Park Y, Hollenbeck A, Chen H (2011) An exploratory study on CLU, CR1 and PICALM and Parkinson disease. PLoS One 6:e24211
-
(2011)
PLoS One
, vol.6
, pp. e24211
-
-
Gao, J.1
Huang, X.2
Park, Y.3
Hollenbeck, A.4
Chen, H.5
-
11
-
-
84881548720
-
Alzheimer’s disease and Parkinson’s disease genome-wide association study top hits and risk of Parkinson’s disease in Korean population
-
Chung SJ, Jung Y, Hong M, Kim MJ, You S, Kim YJ, Kim J, Song K (2013) Alzheimer’s disease and Parkinson’s disease genome-wide association study top hits and risk of Parkinson’s disease in Korean population. Neurobiol Aging
-
(2013)
Neurobiol Aging
-
-
Chung, S.J.1
Jung, Y.2
Hong, M.3
Kim, M.J.4
You, S.5
Kim, Y.J.6
Kim, J.7
Song, K.8
-
12
-
-
84885781056
-
Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk
-
PID: 23921447
-
Moskvina V, Harold D, Russo G, Vedernikov A, Sharma M, Saad M, Holmans P, Bras JM, Bettella F, Keller MF, Nicolaou N, Simon-Sanchez J, Gibbs JR, Schulte C, Durr A, Guerreiro R, Hernandez D, Brice A, Stefansson H, Majamaa K, Gasser T, Heutink P, Wood N, Martinez M, Singleton AB, Nalls MA, Hardy J, Owen MJ, O’Donovan MC, Williams J, Morris HR, Williams NM (2013) Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk. JAMA Neurol 70:1268–1276
-
(2013)
JAMA Neurol
, vol.70
, pp. 1268-1276
-
-
Moskvina, V.1
Harold, D.2
Russo, G.3
Vedernikov, A.4
Sharma, M.5
Saad, M.6
Holmans, P.7
Bras, J.M.8
Bettella, F.9
Keller, M.F.10
Nicolaou, N.11
Simon-Sanchez, J.12
Gibbs, J.R.13
Schulte, C.14
Durr, A.15
Guerreiro, R.16
Hernandez, D.17
Brice, A.18
Stefansson, H.19
Majamaa, K.20
Gasser, T.21
Heutink, P.22
Wood, N.23
Martinez, M.24
Singleton, A.B.25
Nalls, M.A.26
Hardy, J.27
Owen, M.J.28
O’Donovan, M.C.29
Williams, J.30
Morris, H.R.31
Williams, N.M.32
more..
-
13
-
-
84878682420
-
The genotype-tissue expression (GTEx) project
-
COI: 1:CAS:528:DC%2BC3sXotlGls74%3D
-
Lonsdale J, Thomas J, Salvatore M, Phillips R, Lo E, Shad S, Hasz R, Walters G, Garcia F, Young N, Foster B, Moser M, Karasik E, Gillard B, Ramsey K, Sullivan S, Bridge J, Magazine H, Syron J, Fleming J, Siminoff L, Traino H, Mosavel M, Barker L, Jewell S, Rohrer D, Maxim D, Filkins D, Harbach P, Cortadillo E, Berghuis B, Turner L, Hudson E, Feenstra K, Sobin L, Robb J, Branton P, Korzeniewski G, Shive C, Tabor D, Qi L, Groch K, Nampally S, Buia S, Zimmerman A, Smith A, Burges R, Robinson K, Valentino K, Bradbury D, Cosentino M, Diaz-Mayoral N, Kennedy M, Engel T, Williams P, Erickson K, Ardlie K, Winckler W, Getz G, Deluca D, Macarthur D, Kellis M, Thomson A, Young T, Gelfand E, Donovan M, Meng Y, Grant G, Mash D, Marcus Y, Basile M, Liu J, Zhu J, Tu Z, Cox NJ, Nicolae DL, Gamazon ER, Im HK, Konkashbaev A, Pritchard J, Stevens M, Flutre T, Wen X, Dermitzakis ET, Lappalainen T, Guigo R, Monlong J, Sammeth M, Koller D, Battle A, Mostafavi S, McCarthy M, Rivas M, Maller J, Rusyn I, Nobel A, Wright F, Shabalin A, Feolo M, Sharopova N, Sturcke A, Paschal J, Anderson JM, Wilder EL, Derr LK, Green ED, Struewing JP, Temple G, Volpi S, Boyer JT, Thomson EJ, Guyer MS, Ng C, Abdallah A, Colantuoni D, Insel TR, Koester SE, Little AR, Bender PK, Lehner T, Yao Y, Compton CC, Vaught JB, Sawyer S, Lockhart NC, Demchok J, Moore HF (2013) The genotype-tissue expression (GTEx) project. Nat Genet 45:580–585
-
(2013)
Nat Genet
, vol.45
, pp. 580-585
-
-
Lonsdale, J.1
Thomas, J.2
Salvatore, M.3
Phillips, R.4
Lo, E.5
Shad, S.6
Hasz, R.7
Walters, G.8
Garcia, F.9
Young, N.10
Foster, B.11
Moser, M.12
Karasik, E.13
Gillard, B.14
Ramsey, K.15
Sullivan, S.16
Bridge, J.17
Magazine, H.18
Syron, J.19
Fleming, J.20
Siminoff, L.21
Traino, H.22
Mosavel, M.23
Barker, L.24
Jewell, S.25
Rohrer, D.26
Maxim, D.27
Filkins, D.28
Harbach, P.29
Cortadillo, E.30
Berghuis, B.31
Turner, L.32
Hudson, E.33
Feenstra, K.34
Sobin, L.35
Robb, J.36
Branton, P.37
Korzeniewski, G.38
Shive, C.39
Tabor, D.40
Qi, L.41
Groch, K.42
Nampally, S.43
Buia, S.44
Zimmerman, A.45
Smith, A.46
Burges, R.47
Robinson, K.48
Valentino, K.49
Bradbury, D.50
Cosentino, M.51
Diaz-Mayoral, N.52
Kennedy, M.53
Engel, T.54
Williams, P.55
Erickson, K.56
Ardlie, K.57
Winckler, W.58
Getz, G.59
Deluca, D.60
Macarthur, D.61
Kellis, M.62
Thomson, A.63
Young, T.64
Gelfand, E.65
Donovan, M.66
Meng, Y.67
Grant, G.68
Mash, D.69
Marcus, Y.70
Basile, M.71
Liu, J.72
Zhu, J.73
Tu, Z.74
Cox, N.J.75
Nicolae, D.L.76
Gamazon, E.R.77
Im, H.K.78
Konkashbaev, A.79
Pritchard, J.80
Stevens, M.81
Flutre, T.82
Wen, X.83
Dermitzakis, E.T.84
Lappalainen, T.85
Guigo, R.86
Monlong, J.87
Sammeth, M.88
Koller, D.89
Battle, A.90
Mostafavi, S.91
McCarthy, M.92
Rivas, M.93
Maller, J.94
Rusyn, I.95
Nobel, A.96
Wright, F.97
Shabalin, A.98
Feolo, M.99
Sharopova, N.100
Sturcke, A.101
Paschal, J.102
Anderson, J.M.103
Wilder, E.L.104
Derr, L.K.105
Green, E.D.106
Struewing, J.P.107
Temple, G.108
Volpi, S.109
Boyer, J.T.110
Thomson, E.J.111
Guyer, M.S.112
Ng, C.113
Abdallah, A.114
Colantuoni, D.115
Insel, T.R.116
Koester, S.E.117
Little, A.R.118
Bender, P.K.119
Lehner, T.120
Yao, Y.121
Compton, C.C.122
Vaught, J.B.123
Sawyer, S.124
Lockhart, N.C.125
Demchok, J.126
Moore, H.F.127
more..
-
14
-
-
79959841853
-
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson’s disease
-
COI: 1:CAS:528:DC%2BC3MXotF2nsLc%3D, PID: 21738487
-
Do CB, Tung JY, Dorfman E, Kiefer AK, Drabant EM, Francke U, Mountain JL, Goldman SM, Tanner CM, Langston JW, Wojcicki A, Eriksson N (2011) Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson’s disease. PLoS Genet 7:e1002141
-
(2011)
PLoS Genet
, vol.7
, pp. e1002141
-
-
Do, C.B.1
Tung, J.Y.2
Dorfman, E.3
Kiefer, A.K.4
Drabant, E.M.5
Francke, U.6
Mountain, J.L.7
Goldman, S.M.8
Tanner, C.M.9
Langston, J.W.10
Wojcicki, A.11
Eriksson, N.12
-
15
-
-
84859199353
-
Meta-analysis of Parkinson’s disease: identification of a novel locus, RIT2
-
COI: 1:CAS:528:DC%2BC38XksFaisrw%3D, PID: 22451204
-
Pankratz N, Beecham GW, DeStefano AL, Dawson TM, Doheny KF, Factor SA, Hamza TH, Hung AY, Hyman BT, Ivinson AJ, Krainc D, Latourelle JC, Clark LN, Marder K, Martin ER, Mayeux R, Ross OA, Scherzer CR, Simon DK, Tanner C, Vance JM, Wszolek ZK, Zabetian CP, Myers RH, Payami H, Scott WK, Foroud T (2012) Meta-analysis of Parkinson’s disease: identification of a novel locus, RIT2. Ann Neurol 71:370–384
-
(2012)
Ann Neurol
, vol.71
, pp. 370-384
-
-
Pankratz, N.1
Beecham, G.W.2
DeStefano, A.L.3
Dawson, T.M.4
Doheny, K.F.5
Factor, S.A.6
Hamza, T.H.7
Hung, A.Y.8
Hyman, B.T.9
Ivinson, A.J.10
Krainc, D.11
Latourelle, J.C.12
Clark, L.N.13
Marder, K.14
Martin, E.R.15
Mayeux, R.16
Ross, O.A.17
Scherzer, C.R.18
Simon, D.K.19
Tanner, C.20
Vance, J.M.21
Wszolek, Z.K.22
Zabetian, C.P.23
Myers, R.H.24
Payami, H.25
Scott, W.K.26
Foroud, T.27
more..
-
16
-
-
84939599004
-
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease
-
COI: 1:CAS:528:DC%2BC2cXht1ait7%2FP, PID: 25064009
-
Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG, Saad M, DeStefano AL, Kara E, Bras J, Sharma M, Schulte C, Keller MF, Arepalli S, Letson C, Edsall C, Stefansson H, Liu X, Pliner H, Lee JH, Cheng R, Ikram MA, Ioannidis JP, Hadjigeorgiou GM, Bis JC, Martinez M, Perlmutter JS, Goate A, Marder K, Fiske B, Sutherland M, Xiromerisiou G, Myers RH, Clark LN, Stefansson K, Hardy JA, Heutink P, Chen H, Wood NW, Houlden H, Payami H, Brice A, Scott WK, Gasser T, Bertram L, Eriksson N, Foroud T, Singleton AB (2014) Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease. Nat Genet 46:989–993
-
(2014)
Nat Genet
, vol.46
, pp. 989-993
-
-
Nalls, M.A.1
Pankratz, N.2
Lill, C.M.3
Do, C.B.4
Hernandez, D.G.5
Saad, M.6
DeStefano, A.L.7
Kara, E.8
Bras, J.9
Sharma, M.10
Schulte, C.11
Keller, M.F.12
Arepalli, S.13
Letson, C.14
Edsall, C.15
Stefansson, H.16
Liu, X.17
Pliner, H.18
Lee, J.H.19
Cheng, R.20
Ikram, M.A.21
Ioannidis, J.P.22
Hadjigeorgiou, G.M.23
Bis, J.C.24
Martinez, M.25
Perlmutter, J.S.26
Goate, A.27
Marder, K.28
Fiske, B.29
Sutherland, M.30
Xiromerisiou, G.31
Myers, R.H.32
Clark, L.N.33
Stefansson, K.34
Hardy, J.A.35
Heutink, P.36
Chen, H.37
Wood, N.W.38
Houlden, H.39
Payami, H.40
Brice, A.41
Scott, W.K.42
Gasser, T.43
Bertram, L.44
Eriksson, N.45
Foroud, T.46
Singleton, A.B.47
more..
-
17
-
-
84888317489
-
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer’s disease
-
COI: 1:CAS:528:DC%2BC3sXhs1yiu7vJ, PID: 24162737
-
Lambert JC, Ibrahim-Verbaas CA, Harold D, Naj AC, Sims R, Bellenguez C, DeStafano AL, Bis JC, Beecham GW, Grenier-Boley B, Russo G, Thorton-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, Cruchaga C, Craig D, Amin N, Berr C, Lopez OL, De Jager PL, Deramecourt V, Johnston JA, Evans D, Lovestone S, Letenneur L, Moron FJ, Rubinsztein DC, Eiriksdottir G, Sleegers K, Goate AM, Fievet N, Huentelman MW, Gill M, Brown K, Kamboh MI, Keller L, Barberger-Gateau P, McGuiness 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, Bossu P, Spalletta G, Proitsi P, Collinge J, Sorbi S, Sanchez-Garcia F, Fox NC, Hardy J, Deniz Naranjo MC, Bosco P, Clarke R, Brayne C, Galimberti D, Mancuso M, Matthews F, 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, Lannefelt 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, Hiltuenen M, Martin ER, Schmidt R, Rujescu D, Wang LS, Dartigues JF, Mayeux R, Tzourio C, Hofman A, Nothen 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 (2013) Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer’s disease. Nat Genet 45:1452–1458
-
(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
DeStafano, A.L.7
Bis, J.C.8
Beecham, G.W.9
Grenier-Boley, B.10
Russo, G.11
Thorton-Wells, T.A.12
Jones, N.13
Smith, A.V.14
Chouraki, V.15
Thomas, C.16
Ikram, M.A.17
Zelenika, D.18
Vardarajan, B.N.19
Kamatani, Y.20
Lin, C.F.21
Gerrish, A.22
Schmidt, H.23
Kunkle, B.24
Dunstan, M.L.25
Ruiz, A.26
Bihoreau, M.T.27
Choi, S.H.28
Reitz, C.29
Pasquier, F.30
Cruchaga, C.31
Craig, D.32
Amin, N.33
Berr, C.34
Lopez, O.L.35
De Jager, P.L.36
Deramecourt, V.37
Johnston, J.A.38
Evans, D.39
Lovestone, S.40
Letenneur, L.41
Moron, F.J.42
Rubinsztein, D.C.43
Eiriksdottir, G.44
Sleegers, K.45
Goate, A.M.46
Fievet, N.47
Huentelman, M.W.48
Gill, M.49
Brown, K.50
Kamboh, M.I.51
Keller, L.52
Barberger-Gateau, P.53
McGuiness, B.54
Larson, E.B.55
Green, R.56
Myers, A.J.57
Dufouil, C.58
Todd, S.59
Wallon, D.60
Love, S.61
Rogaeva, E.62
Gallacher, J.63
St George-Hyslop, P.64
Clarimon, J.65
Lleo, A.66
Bayer, A.67
Tsuang, D.W.68
Yu, L.69
Tsolaki, M.70
Bossu, P.71
Spalletta, G.72
Proitsi, P.73
Collinge, J.74
Sorbi, S.75
Sanchez-Garcia, F.76
Fox, N.C.77
Hardy, J.78
Deniz Naranjo, M.C.79
Bosco, P.80
Clarke, R.81
Brayne, C.82
Galimberti, D.83
Mancuso, M.84
Matthews, F.85
Moebus, S.86
Mecocci, P.87
Del Zompo, M.88
Maier, W.89
Hampel, H.90
Pilotto, A.91
Bullido, M.92
Panza, F.93
Caffarra, P.94
Nacmias, B.95
Gilbert, J.R.96
Mayhaus, M.97
Lannefelt, L.98
Hakonarson, H.99
Pichler, S.100
Carrasquillo, M.M.101
Ingelsson, M.102
Beekly, D.103
Alvarez, V.104
Zou, F.105
Valladares, O.106
Younkin, S.G.107
Coto, E.108
Hamilton-Nelson, K.L.109
Gu, W.110
Razquin, C.111
Pastor, P.112
Mateo, I.113
Owen, M.J.114
Faber, K.M.115
Jonsson, P.V.116
Combarros, O.117
O’Donovan, M.C.118
Cantwell, L.B.119
Soininen, H.120
Blacker, D.121
Mead, S.122
Mosley, T.H.123
Bennett, D.A.124
Harris, T.B.125
Fratiglioni, L.126
Holmes, C.127
de Bruijn, R.F.128
Passmore, P.129
Montine, T.J.130
Bettens, K.131
Rotter, J.I.132
Brice, A.133
Morgan, K.134
Foroud, T.M.135
Kukull, W.A.136
Hannequin, D.137
Powell, J.F.138
Nalls, M.A.139
Ritchie, K.140
Lunetta, K.L.141
Kauwe, J.S.142
Boerwinkle, E.143
Riemenschneider, M.144
Boada, M.145
Hiltuenen, M.146
Martin, E.R.147
Schmidt, R.148
Rujescu, D.149
Wang, L.S.150
Dartigues, J.F.151
Mayeux, R.152
Tzourio, C.153
Hofman, A.154
Nothen, M.M.155
Graff, C.156
Psaty, B.M.157
Jones, L.158
Haines, J.L.159
Holmans, P.A.160
Lathrop, M.161
Pericak-Vance, M.A.162
Launer, L.J.163
Farrer, L.A.164
van Duijn, C.M.165
Van Broeckhoven, C.166
Moskvina, V.167
Seshadri, S.168
Williams, J.169
Schellenberg, G.D.170
Amouyel, P.171
more..
-
18
-
-
84864066707
-
Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants
-
COI: 1:CAS:528:DC%2BC38XovFSqs7s%3D, PID: 22685416
-
Zou F, Chai HS, Younkin CS, Allen M, Crook J, Pankratz VS, Carrasquillo MM, Rowley CN, Nair AA, Middha S, Maharjan S, Nguyen T, Ma L, Malphrus KG, Palusak R, Lincoln S, Bisceglio G, Georgescu C, Kouri N, Kolbert CP, Jen J, Haines JL, Mayeux R, Pericak-Vance MA, Farrer LA, Schellenberg GD, Petersen RC, Graff-Radford NR, Dickson DW, Younkin SG, Ertekin-Taner N (2012) Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants. PLoS Genet 8:e1002707
-
(2012)
PLoS Genet
, vol.8
, pp. e1002707
-
-
Zou, F.1
Chai, H.S.2
Younkin, C.S.3
Allen, M.4
Crook, J.5
Pankratz, V.S.6
Carrasquillo, M.M.7
Rowley, C.N.8
Nair, A.A.9
Middha, S.10
Maharjan, S.11
Nguyen, T.12
Ma, L.13
Malphrus, K.G.14
Palusak, R.15
Lincoln, S.16
Bisceglio, G.17
Georgescu, C.18
Kouri, N.19
Kolbert, C.P.20
Jen, J.21
Haines, J.L.22
Mayeux, R.23
Pericak-Vance, M.A.24
Farrer, L.A.25
Schellenberg, G.D.26
Petersen, R.C.27
Graff-Radford, N.R.28
Dickson, D.W.29
Younkin, S.G.30
Ertekin-Taner, N.31
more..
-
19
-
-
68949204302
-
Strategies and issues in the detection of pathway enrichment in genome-wide association studies
-
COI: 1:CAS:528:DC%2BD1MXhtVWit7%2FI, PID: 19408013
-
Hong MG, Pawitan Y, Magnusson PK, Prince JA (2009) Strategies and issues in the detection of pathway enrichment in genome-wide association studies. Hum Genet 126:289–301
-
(2009)
Hum Genet
, vol.126
, pp. 289-301
-
-
Hong, M.G.1
Pawitan, Y.2
Magnusson, P.K.3
Prince, J.A.4
-
20
-
-
78049236574
-
Genome-wide pathway analysis implicates intracellular transmembrane protein transport in Alzheimer disease
-
COI: 1:CAS:528:DC%2BC3cXhtlaitb3M, PID: 20668461
-
Hong MG, Alexeyenko A, Lambert JC, Amouyel P, Prince JA (2010) Genome-wide pathway analysis implicates intracellular transmembrane protein transport in Alzheimer disease. J Hum Genet 55:707–709
-
(2010)
J Hum Genet
, vol.55
, pp. 707-709
-
-
Hong, M.G.1
Alexeyenko, A.2
Lambert, J.C.3
Amouyel, P.4
Prince, J.A.5
-
21
-
-
79851502150
-
Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology
-
COI: 1:CAS:528:DC%2BC3MXhtFOgsrg%3D, PID: 21249183
-
Rossin EJ, Lage K, Raychaudhuri S, Xavier RJ, Tatar D, Benita Y, Cotsapas C, Daly MJ (2011) Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology. PLoS Genet 7:e1001273
-
(2011)
PLoS Genet
, vol.7
, pp. e1001273
-
-
Rossin, E.J.1
Lage, K.2
Raychaudhuri, S.3
Xavier, R.J.4
Tatar, D.5
Benita, Y.6
Cotsapas, C.7
Daly, M.J.8
-
22
-
-
84864599004
-
Guidelines for genome-wide association studies
-
COI: 1:CAS:528:DC%2BC38XhtVars7zO, PID: 22792080
-
Barsh GS, Copenhaver GP, Gibson G, Williams SM (2012) Guidelines for genome-wide association studies. PLoS Genet 8:e1002812
-
(2012)
PLoS Genet
, vol.8
, pp. e1002812
-
-
Barsh, G.S.1
Copenhaver, G.P.2
Gibson, G.3
Williams, S.M.4
-
23
-
-
84865804544
-
Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner
-
PID: 22950410
-
de Jong S, Chepelev I, Janson E, Strengman E, van den Berg LH, Veldink JH, Ophoff RA (2012) Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner. BMC Genomics 13:458
-
(2012)
BMC Genomics
, vol.13
, pp. 458
-
-
de Jong, S.1
Chepelev, I.2
Janson, E.3
Strengman, E.4
van den Berg, L.H.5
Veldink, J.H.6
Ophoff, R.A.7
-
24
-
-
81255127582
-
Do interactions between SNCA, MAPT, and LRRK2 genes contribute to Parkinson’s disease susceptibility?
-
PID: 21816655
-
Biernacka JM, Armasu SM, Cunningham JM, Ahlskog JE, Chung SJ, Maraganore DM (2011) Do interactions between SNCA, MAPT, and LRRK2 genes contribute to Parkinson’s disease susceptibility? Parkinsonism Relat Disord 17:730–736
-
(2011)
Parkinsonism Relat Disord
, vol.17
, pp. 730-736
-
-
Biernacka, J.M.1
Armasu, S.M.2
Cunningham, J.M.3
Ahlskog, J.E.4
Chung, S.J.5
Maraganore, D.M.6
-
25
-
-
79955389000
-
Independent and joint effects of the MAPT and SNCA genes in Parkinson disease
-
COI: 1:CAS:528:DC%2BC3MXltVyhtLg%3D, PID: 21391235
-
Elbaz A, Ross OA, Ioannidis JP, Soto-Ortolaza AI, Moisan F, Aasly J, Annesi G, Bozi M, Brighina L, Chartier-Harlin MC, Destee A, Ferrarese C, Ferraris A, Gibson JM, Gispert S, Hadjigeorgiou GM, Jasinska-Myga B, Klein C, Kruger R, Lambert JC, Lohmann K, van de Loo S, Loriot MA, Lynch T, Mellick GD, Mutez E, Nilsson C, Opala G, Puschmann A, Quattrone A, Sharma M, Silburn PA, Stefanis L, Uitti RJ, Valente EM, Vilarino-Guell C, Wirdefeldt K, Wszolek ZK, Xiromerisiou G, Maraganore DM, Farrer MJ (2011) Independent and joint effects of the MAPT and SNCA genes in Parkinson disease. Ann Neurol 69:778–792
-
(2011)
Ann Neurol
, vol.69
, pp. 778-792
-
-
Elbaz, A.1
Ross, O.A.2
Ioannidis, J.P.3
Soto-Ortolaza, A.I.4
Moisan, F.5
Aasly, J.6
Annesi, G.7
Bozi, M.8
Brighina, L.9
Chartier-Harlin, M.C.10
Destee, A.11
Ferrarese, C.12
Ferraris, A.13
Gibson, J.M.14
Gispert, S.15
Hadjigeorgiou, G.M.16
Jasinska-Myga, B.17
Klein, C.18
Kruger, R.19
Lambert, J.C.20
Lohmann, K.21
van de Loo, S.22
Loriot, M.A.23
Lynch, T.24
Mellick, G.D.25
Mutez, E.26
Nilsson, C.27
Opala, G.28
Puschmann, A.29
Quattrone, A.30
Sharma, M.31
Silburn, P.A.32
Stefanis, L.33
Uitti, R.J.34
Valente, E.M.35
Vilarino-Guell, C.36
Wirdefeldt, K.37
Wszolek, Z.K.38
Xiromerisiou, G.39
Maraganore, D.M.40
Farrer, M.J.41
more..
-
26
-
-
84857442897
-
SNCA and MAPT genes: independent and joint effects in Parkinson disease in the Italian population
-
PID: 22104010
-
Trotta L, Guella I, Solda G, Sironi F, Tesei S, Canesi M, Pezzoli G, Goldwurm S, Duga S, Asselta R (2012) SNCA and MAPT genes: independent and joint effects in Parkinson disease in the Italian population. Parkinsonism Relat Disord 18:257–262
-
(2012)
Parkinsonism Relat Disord
, vol.18
, pp. 257-262
-
-
Trotta, L.1
Guella, I.2
Solda, G.3
Sironi, F.4
Tesei, S.5
Canesi, M.6
Pezzoli, G.7
Goldwurm, S.8
Duga, S.9
Asselta, R.10
|