-
1
-
-
0036338150
-
Rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis, G. R., Cherny, S. S., Cookson, W. O. & Cardon, L. R. (2002) Rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30, 97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
2
-
-
0042319240
-
Anabaptist genealogy database
-
Agarwala, R., Biesecker, L. G. & Schäffer, A. A. (2003) Anabaptist genealogy database. Am J Med Genet C Semin Med Genet 121, 32-37.
-
(2003)
Am J Med Genet C Semin Med Genet
, vol.121
, pp. 32-37
-
-
Agarwala, R.1
Biesecker, L.G.2
Schäffer, A.A.3
-
3
-
-
0033543468
-
Towards a complete North American Anabaptist genealogy: A systematic approach to merging partially overlapping genealogy resources
-
Agarwala, R., Biesecker, L. G., Tomlin, J. F. & Schäffer, A. A. (1999) Towards a complete North American Anabaptist genealogy: A systematic approach to merging partially overlapping genealogy resources. Am J Med Genet 86, 156-161.
-
(1999)
Am J Med Genet
, vol.86
, pp. 156-161
-
-
Agarwala, R.1
Biesecker, L.G.2
Tomlin, J.F.3
Schäffer, A.A.4
-
6
-
-
77957927865
-
The genetics of Alzheimer disease: Back to the future
-
Bertram, L., Lill, C. M. & Tanzi, R. E. (2010) The genetics of Alzheimer disease: Back to the future. Neuron 68, 270-281.
-
(2010)
Neuron
, vol.68
, pp. 270-281
-
-
Bertram, L.1
Lill, C.M.2
Tanzi, R.E.3
-
7
-
-
23844506823
-
Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing
-
Boyles, A. L., Scott, W. K., Martin, E. R., Schmidt, S., Li, Y. J., Ashley-Koch, A., Bass, M. P., Schmidt, M., Pericak-Vance, M. A., Speer, M. C. & Hauser, E. R.(2005) Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing. Hum Hered 59, 220-227.
-
(2005)
Hum Hered
, vol.59
, pp. 220-227
-
-
Boyles, A.L.1
Scott, W.K.2
Martin, E.R.3
Schmidt, S.4
Li, Y.J.5
Ashley-Koch, A.6
Bass, M.P.7
Schmidt, M.8
Pericak-Vance, M.A.9
Speer, M.C.10
Hauser, E.R.11
-
8
-
-
79958859806
-
Successful aging shows linkage to chromosomes 6, 7, and 14 in the amish
-
Edwards, D. R., Gilbert, J. R, Jiang, L., Gallins, P. J., Caywood, L., Creason, M., Fuzzell, D., Knebusch, C., Jackson, C. E., Pericak-Vance, M. A., Haines, J. L. & Scott, W. K.(2011) Successful aging shows linkage to chromosomes 6, 7, and 14 in the amish. Ann Hum Genet 75, 516-528.
-
(2011)
Ann Hum Genet
, vol.75
, pp. 516-528
-
-
Edwards, D.R.1
Gilbert, J.R.2
Jiang, L.3
Gallins, P.J.4
Caywood, L.5
Creason, M.6
Fuzzell, D.7
Knebusch, C.8
Jackson, C.E.9
Pericak-Vance, M.A.10
Haines, J.L.11
Scott, W.K.12
-
9
-
-
32244436670
-
A genome-wide linkage analysis of dementia in the Amish.
-
Hahs, D. W., McCauley, J. L., Crunk, A. E., McFarland, L. L., Gaskell, P. C., Jiang, L., Slifer, S. H., Vance, J. M., Scott, W. K., Welsh-Bohmer, K. A., Johnson, S. R., Jackson, C. E., Pericak-Vance, M. A. & Haines, J. L. (2006) A genome-wide linkage analysis of dementia in the Amish. Am J Med Genet B Neuropsychiatr Genet 141, 160-166.
-
(2006)
Am J Med Genet B Neuropsychiatr Genet
, vol.141
, pp. 160-166
-
-
Hahs, D.W.1
McCauley, J.L.2
Crunk, A.E.3
McFarland, L.L.4
Gaskell, P.C.5
Jiang, L.6
Slifer, S.H.7
Vance, J.M.8
Scott, W.K.9
Welsh-Bohmer, K.A.10
Johnson, S.R.11
Jackson, C.E.12
Pericak-Vance, M.A.13
Haines, J.L.14
-
10
-
-
35548976654
-
Genome-wide linkage analysis of 723 affected relative pairs with late-onsheimer's disease
-
Hamshere, M. L., Holmans, P. A., Avramopoulos, D., Bassett, S. S., Blacker, D., Bertram, L., Wiener, H., Rochberg, N., Tanzi, R. E., Myers, A., Wavrant-De Vrièze, F., Go, R., Fallin, D., Lovestone, S., Hardy, J., Goate, A., O'Donovan, M., Williams, J. & Owen, M. J. (2007) Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease. Hum Mol Genet 16, 2703-2712.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 2703-2712
-
-
Hamshere, M.L.1
Holmans, P.A.2
Avramopoulos, D.3
Bassett, S.S.4
Blacker, D.5
Bertram, L.6
Wiener, H.7
Rochberg, N.8
Tanzi, R.E.9
Myers, A.10
Wavrant-De Vrièze, F.11
Go, R.12
Fallin, D.13
Lovestone, S.14
Hardy, J.15
Goate, A.16
O'Donovan, M.17
Williams, J.18
Owen, M.J.19
-
11
-
-
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, M. L., Pahwa, J. S., Moskvina, V., Dowzell, K., Williams, A., Jones, N., Thomas, C., Stretton, A., Morgan, A. R., Lovestone, S., Powell, J., Proitsi, P., Lupton, M. K., Brayne, C., Rubinsztein, D. C., Gill, M., Lawlor, B., Lynch, A., Morgan, K., Brown, K. S., Passmore, P. A., Craig, D., McGuinness, B., Todd, S., Holmes, C., Mann, D., Smith, A. D., Love, S., Kehoe, P. G., 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, A. M., Kauwe, J. S., Cruchaga, C., Nowotny, P., Morris, J. C., Mayo, K., Sleegers, K., Bettens, K., Engelborghs, S., De Deyn, P. P., Van Broeckhoven, C., Livingston, G., Bass, N. J., Gurling, H., McQuillin, A., Gwilliam, R., Deloukas, P., Al-Chalabi, A., Shaw, C. E., Tsolaki, M., Singleton, A. B., Guerreiro, R., Mühleisen, T. W., Nöthen, M. M., Moebus, S., Jöckel, K. H., Klopp, N., Wichmann, H. E., Carrasquillo, M. M., Pankratz, V. S., Younkin, S. G., Holmans, P. A., O'Donovan, M., Owen, M. J. & 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
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.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..
-
12
-
-
79955484414
-
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
-
Petersen RC; Alzheimer's Disease Neuroimaging Initiative, CHARGE consortium, EADI1 consortium, amp; () .
-
Hollingworth, P., Harold, D., Sims, R., Gerrish, A., Lambert, J. C., Carrasquillo, M. M., Abraham, R., Hamshere, M. L., Pahwa, J. S., 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, M. K., Brayne, C., Rubinsztein, D. C., Gill, M., Lawlor, B., Lynch, A., Brown, K. S., Passmore, P. A., Craig, D., McGuinness, B., Todd, S., Holmes, C., Mann, D., Smith, A. D., Beaumont, H., Warden, D., Wilcock, G., Love, S., Kehoe, P. G., Hooper, N. M., Vardy, E. R., Hardy, J., Mead, S., Fox, N. C., 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, A. M., Kauwe, J. S., Cruchaga, C., Nowotny, P., Morris, J. C., Mayo, K., Sleegers, K., Bettens, K., Engelborghs, S., De Deyn, P. P., Van Broeckhoven, C., Livingston, G., Bass, N. J., Gurling, H., McQuillin, A., Gwilliam, R., Deloukas, P., Al-Chalabi, A., Shaw, C. E., Tsolaki, M., Singleton, A. B., Guerreiro, R., Mühleisen, T. W., Nöthen, M. M., Moebus, S., Jöckel, K. H., Klopp, N., Wichmann, H. E., Pankratz, V. S., Sando, S. B., Aasly, J. O., Barcikowska, M., Wszolek, Z. K., Dickson, D. W., Graff-Radford, N. R., Petersen RC; Alzheimer's Disease Neuroimaging Initiative, van Duijn, C. M., Breteler, M. M., Ikram, M. A., DeStefano, A. L., Fitzpatrick, A. L., Lopez, O., Launer, L. J., Seshadri, S., CHARGE consortium, Berr, C., Campion, D., Epelbaum, J., Dartigues, J. F., Tzourio, C., Alpérovitch, A., Lathrop, M.; EADI1 consortium, Feulner, T. M., 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, P. V., Chouraki, V., Genier-Boley, B., Hiltunen, M., Soininen, H., Combarros, O., Zelenika, D., Delepine, M., Bullido, M. J., 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, P. A., Jonsson, T., Riemenschneider, M., Morgan, K., Younkin, S. G., Owen, M. J., 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
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.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
van Duijn, C.M.100
Breteler, M.M.101
Ikram, M.A.102
DeStefano, A.L.103
Fitzpatrick, A.L.104
Lopez, O.105
Launer, L.J.106
Seshadri, S.107
Berr, C.108
Campion, D.109
Epelbaum, J.110
Dartigues, J.F.111
Tzourio, C.112
Alpérovitch, A.113
Lathrop, M.114
Feulner, T.M.115
Friedrich, P.116
Riehle, C.117
Krawczak, M.118
Schreiber, S.119
Mayhaus, M.120
Nicolhaus, S.121
Wagenpfeil, S.122
Steinberg, S.123
Stefansson, H.124
Stefansson, K.125
Snaedal, J.126
Björnsson, S.127
Jonsson, P.V.128
Chouraki, V.129
Genier-Boley, B.130
Hiltunen, M.131
Soininen, H.132
Combarros, O.133
Zelenika, D.134
Delepine, M.135
Bullido, M.J.136
Pasquier, F.137
Mateo, I.138
Frank-Garcia, A.139
Porcellini, E.140
Hanon, O.141
Coto, E.142
Alvarez, V.143
Bosco, P.144
Siciliano, G.145
Mancuso, M.146
Panza, F.147
Solfrizzi, V.148
Nacmias, B.149
Sorbi, S.150
Bossù, P.151
Piccardi, P.152
Arosio, B.153
Annoni, G.154
Seripa, D.155
Pilotto, A.156
Scarpini, E.157
Galimberti, D.158
Brice, A.159
Hannequin, D.160
Licastro, F.161
Jones, L.162
Holmans, P.A.163
Jonsson, T.164
Riemenschneider, M.165
Morgan, K.166
Younkin, S.G.167
Owen, M.J.168
O'Donovan, M.169
Amouyel, P.170
Williams, J.171
more..
-
13
-
-
0003879233
-
-
4th ed. Baltimore, MD: Johns Hopkins University Press.
-
Hostetler, J. (1993) Amish Society, 4th ed. Baltimore, MD: Johns Hopkins University Press.
-
(1993)
Amish Society
-
-
Hostetler, J.1
-
14
-
-
52949085789
-
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
-
Korn, J. M., Kuruvilla, F. G., McCarroll, S. A., Wysoker, A., Nemesh, J., Cawley, S., Hubbell, E., Veitch, J., Collins, P. J., Darvishi, K., Lee, C., Nizzari, M. M., Gabriel, S. B., Purcell, S., Daly, M. J. & Altshuler, D. (2008) Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. Nat Genet 40, 1253-1260.
-
(2008)
Nat Genet
, vol.40
, pp. 1253-1260
-
-
Korn, J.M.1
Kuruvilla, F.G.2
McCarroll, S.A.3
Wysoker, A.4
Nemesh, J.5
Cawley, S.6
Hubbell, E.7
Veitch, J.8
Collins, P.J.9
Darvishi, K.10
Lee, C.11
Nizzari, M.M.12
Gabriel, S.B.13
Purcell, S.14
Daly, M.J.15
Altshuler, D.16
-
15
-
-
78549264026
-
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
-
European Alzheimer's Disease Initiative Investigators, amp; () .
-
Lambert, J. C., Heath, S., Even, G., Campion, D., Sleegers, K., Hiltunen, M., Combarros, O., Zelenika, D., Bullido, M. J., 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.; European Alzheimer's Disease Initiative Investigators, de Pancorbo, M. M., 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. (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
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..
-
16
-
-
34347239326
-
A genomewide screen for late-onsheimer disease in a genetically isolated Dutch population.
-
Liu, F., Arias-Vásquez, A., Sleegers, K., Aulchenko, Y. S., Kayser, M., Sanchez-Juan, P., Feng, B. J., Bertoli-Avella, A. M., van Swieten, J., Axenovich, T. I., Heutink, P., van Broeckhoven, C., Oostra, B. A. & van Duijn, C. M. (2007) A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch population. Am J Hum Genet 81, 17-31.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 17-31
-
-
Liu, F.1
Arias-Vásquez, A.2
Sleegers, K.3
Aulchenko, Y.S.4
Kayser, M.5
Sanchez-Juan, P.6
Feng, B.J.7
Bertoli-Avella, A.M.8
van Swieten, J.9
Axenovich, T.I.10
Heutink, P.11
van Broeckhoven, C.12
Oostra, B.A.13
van Duijn, C.M.14
-
17
-
-
33749556680
-
Ignoring distant genealogic loops leads to false-positives in homozygosity mapping
-
Liu, F., Elefante, S., van Duijn, C. M. & Aulchenko, Y. S. (2006) Ignoring distant genealogic loops leads to false-positives in homozygosity mapping. Ann Hum Genet 70, 965-970.
-
(2006)
Ann Hum Genet
, vol.70
, pp. 965-970
-
-
Liu, F.1
Elefante, S.2
van Duijn, C.M.3
Aulchenko, Y.S.4
-
18
-
-
45749129812
-
An approach for cutting large and complex pedigrees for linkage analysis
-
Liu, F., Kirichenko, A., Axenovich, T. I., van Duijn, C. M. & Aulchenko, Y. S. (2008) An approach for cutting large and complex pedigrees for linkage analysis. Eur J Hum Genet 16, 854-860.
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 854-860
-
-
Liu, F.1
Kirichenko, A.2
Axenovich, T.I.3
van Duijn, C.M.4
Aulchenko, Y.S.5
-
19
-
-
33646123529
-
Combinatorial Mismatch Scan (CMS) for loci associated with dementia in the Amish. BMC
-
McCauley, J. L., Hahs, D. W., Jiang, L., Scott, W. K., Welsh-Bohmer, K. A., Jackson, C. E., Vance, J. M., Pericak-Vance, M. A. & Haines, J. L. (2006) Combinatorial Mismatch Scan (CMS) for loci associated with dementia in the Amish. BMC Med Genet 7, 19.
-
(2006)
Med Genet
, vol.7
, pp. 19
-
-
McCauley, J.L.1
Hahs, D.W.2
Jiang, L.3
Scott, W.K.4
Welsh-Bohmer, K.A.5
Jackson, C.E.6
Vance, J.M.7
Pericak-Vance, M.A.8
Haines, J.L.9
-
20
-
-
0021271971
-
Clinical diagnosis of Alzheimer's disease: Report of the NINCDS-ADRDA Work 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, E. M. (1984) Clinical diagnosis of Alzheimer's disease: Report of the NINCDS-ADRDA Work 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
-
21
-
-
0024453856
-
The Consortium to establish a Registry for Alzheimer's Disease (CERAD). Part I. Clinical and neuropsychological assessment of Alzheimer's disease
-
Morris, J. C., Heyman, A., Mohs, R. C., Hughes, J. P., van Belle, G., Fillenbaum, G., Mellits, E. D. & Clark, C. (1989) The Consortium to establish a Registry for Alzheimer's Disease (CERAD). Part I. Clinical and neuropsychological assessment of Alzheimer's disease. Neurology 39, 1159-1165.
-
(1989)
Neurology
, vol.39
, pp. 1159-1165
-
-
Morris, J.C.1
Heyman, A.2
Mohs, R.C.3
Hughes, J.P.4
van Belle, G.5
Fillenbaum, G.6
Mellits, E.D.7
Clark, C.8
-
22
-
-
79955464911
-
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onsheimer's disease
-
Naj, A. C., Jun, G., Beecham, G. W., Wang, L. S., Vardarajan, B. N., Buros, J., Gallins, P. J., Buxbaum, J. D., Jarvik, G. P., Crane, P. K., Larson, E. B., Bird, T. D., Boeve, B. F., Graff-Radford, N. R., De Jager, P. L., Evans, D., Schneider, J. A., Carrasquillo, M. M., Ertekin-Taner, N., Younkin, S. G., Cruchaga, C., Kauwe, J. S., Nowotny, P., Kramer, P., Hardy, J., Huentelman, M. J., Myers, A. J., Barmada, M. M., Demirci, F. Y., Baldwin, C. T., Green, R. C., Rogaeva, E., St George-Hyslop, P., Arnold, S. E., Barber, R., Beach, T., Bigio, E. H., Bowen, J. D., Boxer, A., Burke, J. R., Cairns, N. J., Carlson, C. S., Carney, R. M., Carroll, S. L., Chui, H. C., Clark, D. G., Corneveaux, J., Cotman, C. W., Cummings, J. L., DeCarli, C., DeKosky, S. T., Diaz-Arrastia, R., Dick, M., Dickson, D. W., Ellis, W. G., Faber, K. M., Fallon, K. B., Farlow, M. R., Ferris, S., Frosch, M. P., Galasko, D. R., Ganguli, M., Gearing, M., Geschwind, D. H., Ghetti, B., Gilbert, J. R., Gilman, S., Giordani, B., Glass, J. D., Growdon, J. H., Hamilton, R. L., Harrell, L. E., Head, E., Honig, L. S., Hulette, C. M., Hyman, B. T., Jicha, G. A., Jin, L. W., Johnson, N., Karlawish, J., Karydas, A., Kaye, J. A., Kim, R., Koo, E. H., Kowall, N. W., Lah, J. J., Levey, A. I., Lieberman, A. P., Lopez, O. L., Mack, W. J., Marson, D. C., Martiniuk, F., Mash, D. C., Masliah, E., McCormick, W. C., McCurry, S. M., McDavid, A. N., McKee, A. C., Mesulam, M., Miller, B. L., Miller, C. A., Miller, J. W., Parisi, J. E., Perl, D. P., Peskind, E., Petersen, R. C., Poon, W. W., Quinn, J. F., Rajbhandary, R. A., Raskind, M., Reisberg, B., Ringman, J. M., Roberson, E. D., Rosenberg, R. N., Sano, M., Schneider, L. S., Seeley, W., Shelanski, M. L., Slifer, M. A., Smith, C. D., Sonnen, J. A., Spina, S., Stern, R. A., Tanzi, R. E., Trojanowski, J. Q., Troncoso, J. C., Van Deerlin, V. M., Vinters, H. V., Vonsattel, J. P., Weintraub, S., Welsh-Bohmer, K. A., Williamson, J., Woltjer, R. L., Cantwell, L. B., Dombroski, B. A., Beekly, D., Lunetta, K. L., Martin, E. R., Kamboh, M. I., Saykin, A. J., Reiman, E. M., Bennett, D. A., Morris, J. C., Montine, T. J., Goate, A. M., Blacker, D., Tsuang, D. W., Hakonarson, H., Kukull, W. A., Foroud, T. M., Haines, J. L., Mayeux, R., Pericak-Vance, M. A., Farrer, L. A., & Schellenberg, G. D. (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
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..
-
23
-
-
0036648277
-
Deletion in Catna2, encoding alpha N-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation
-
Park, C., Falls, W., Finger, J. H., Longo-Guess, C. M., & Ackerman, S. L. (2002) Deletion in Catna2, encoding alpha N-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation. Nat Genet 31, 279-284.
-
(2002)
Nat Genet
, vol.31
, pp. 279-284
-
-
Park, C.1
Falls, W.2
Finger, J.H.3
Longo-Guess, C.M.4
Ackerman, S.L.5
-
24
-
-
0029899993
-
Alzheimer's disease and apolipoprotein E-4 allele in an Amish population
-
Pericak-Vance, M. A., Johnson, C. C., Rimmler, J. B., Saunders, A. M., Robinson, L. C., D'Hondt, E. G., Jackson, C. E., & Haines, J. L. (1996) Alzheimer's disease and apolipoprotein E-4 allele in an Amish population. Ann Neurol 39, 700-704.
-
(1996)
Ann Neurol
, vol.39
, pp. 700-704
-
-
Pericak-Vance, M.A.1
Johnson, C.C.2
Rimmler, J.B.3
Saunders, A.M.4
Robinson, L.C.5
D'Hondt, E.G.6
Jackson, C.E.7
Haines, J.L.8
-
25
-
-
77952307991
-
Genome-wide analysis of genetic loci associated with Alzheimer disease
-
CHARGE Consortium; GERAD1 Consortium; EADI1 Consortium. () .
-
Seshadri, S., Fitzpatrick, A. L., Ikram, M. A., DeStefano, A. L., Gudnason, V., Boada, M., Bis, J. C., Smith, A. V., Carassquillo, M. M., Lambert, J. C., Harold, D., Schrijvers, E. M., Ramirez-Lorca, R., Debette, S., Longstreth, W. T. Jr., Janssens, A. C., Pankratz, V. S., Dartigues, J. F., Hollingworth, P., Aspelund, T., Hernandez, I., Beiser, A., Kuller, L. H., Koudstaal, P. J., Dickson, D. W., Tzourio, C., Abraham, R., Antunez, C., Du, Y., Rotter, J. I., Aulchenko, Y. S., Harris, T. B., Petersen, R. C., Berr, C., Owen, M. J., Lopez-Arrieta, J., Varadarajan, B. N., Becker, J. T., Rivadeneira, F., Nalls, M. A., Graff-Radford, N. R., Campion, D., Auerbach, S., Rice, K., Hofman, A., Jonsson, P. V., Schmidt, H., Lathrop, M., Mosley, T. H., Au, R., Psaty, B. M., Uitterlinden, A. G., Farrer, L. A., Lumley, T., Ruiz, A., Williams, J., Amouyel, P., Younkin, S. G., Wolf, P. A., Launer, L. J., Lopez, O. L., van Duijn, C. M. & Breteler, M. M; CHARGE Consortium; GERAD1 Consortium; EADI1 Consortium. (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..
-
26
-
-
0023194048
-
The modified mini-mental state (3MS) examination
-
Teng, E. L. & Chui, H. C. (1987). The modified mini-mental state (3MS) examination. J Clin Psychiatry 48, 314-318.
-
(1987)
J Clin Psychiatry
, vol.48
, pp. 314-318
-
-
Teng, E.L.1
Chui, H.C.2
-
27
-
-
34547756415
-
Case-control association testing with related individuals: a more powerful quasi-likelihood score test
-
Thornton, T. & McPeek, M. S. (2007) Case-control association testing with related individuals: a more powerful quasi-likelihood score test. Am J Hum Genet 81, 321-337.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 321-337
-
-
Thornton, T.1
McPeek, M.S.2
-
28
-
-
0036199591
-
An adaptation of the modified mini-mental state examination: analysis of demographic influences and normative data: the cache county study. Neuropsychiatry Neuropsychol
-
Cache County Study Group. ()
-
Tschanz, J. T., Welsh-Bohmer, K. A., Plassman, B. L., Norton, M. C., Wyse, B. W. & Breitner, J.C; Cache County Study Group. (2002) An adaptation of the modified mini-mental state examination: analysis of demographic influences and normative data: the cache county study. Neuropsychiatry Neuropsychol Behav Neurol 15, 28-38.
-
(2002)
Behav Neurol
, vol.15
, pp. 28-38
-
-
Tschanz, J.T.1
Welsh-Bohmer, K.A.2
Plassman, B.L.3
Norton, M.C.4
Wyse, B.W.5
Breitner, J.C.6
-
29
-
-
0032531793
-
Destabilization of beta-catenin by mutations in presenilin-1 potentiates neuronal apoptosis
-
Zhang, Z., Hartmann, H., Do, V. M., Abramowski, D., Sturchler-Pierrat, C., Staufenbiel, M., Sommer, B., van de Wetering, M., Clevers, H., Saftig, P., De Strooper, B., He, X. & Yankner, B. A. (1998) Destabilization of beta-catenin by mutations in presenilin-1 potentiates neuronal apoptosis. Nature 395, 698-702.
-
(1998)
Nature
, vol.395
, pp. 698-702
-
-
Zhang, Z.1
Hartmann, H.2
Do, V.M.3
Abramowski, D.4
Sturchler-Pierrat, C.5
Staufenbiel, M.6
Sommer, B.7
van de Wetering, M.8
Clevers, H.9
Saftig, P.10
De Strooper, B.11
He, X.12
Yankner, B.A.13
|