-
1
-
-
79959503826
-
The international HapMap project
-
10.1038/nature02168 14685227
-
The international HapMap project. Tanaka T, Nature 2003 426 789 796 10.1038/nature02168 14685227
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
Tanaka, T.1
-
2
-
-
32244435907
-
Role of genes and environments for explaining Alzheimer disease
-
10.1001/archpsyc.63.2.168 16461860
-
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, Arch Gen Psychiatry 2006 63 168 174 10.1001/archpsyc.63.2.168 16461860
-
(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
-
-
84872088087
-
Variant of TREM2 associated with the risk of Alzheimer's disease
-
10.1056/NEJMoa1211103 23150908
-
Variant of TREM2 associated with the risk of Alzheimer's disease. Jonsson T, Stefansson H, Ph.D SS, Jonsdottir I, Jonsson PV, Snaedal J, Bjornsson S, Huttenlocher J, Levey AI, Lah JJ, Rujescu D, Hampel H, Giegling I, Andreassen O a, Engedal K, Ulstein I, Djurovic S, Ibrahim-Verbaas C, Hofman A, Ikram MA, van Duijn CM, Thorsteinsdottir U, Kong A, Stefansson K, N Engl J Med 2013 368 107 116 10.1056/NEJMoa1211103 23150908
-
(2013)
N Engl J Med
, vol.368
, pp. 107-116
-
-
Jonsson, T.1
Stefansson, H.2
Jonsdottir, I.3
Jonsson, P.V.4
Snaedal, J.5
Bjornsson, S.6
Huttenlocher, J.7
Levey, A.I.8
Lah, J.J.9
Rujescu, D.10
Hampel, H.11
Giegling, I.12
Andreassen, O.A.13
Engedal, K.14
Ulstein, I.15
Djurovic, S.16
Ibrahim-Verbaas, C.17
Hofman, A.18
Ikram, M.A.19
Van Duijn, C.M.20
Thorsteinsdottir, U.21
Kong, A.22
Stefansson, K.23
more..
-
4
-
-
84872057940
-
TREM2 Variants in Alzheimer's disease
-
10.1056/NEJMoa1211851 23150934
-
TREM2 Variants in Alzheimer's disease. Guerreiro R, Wojtas A, Bras J, Carrasquillo M, Rogaeva E, Majounie E, Cruchaga C, Sassi C, Kauwe JSK, Younkin S, Hazrati L, Collinge J, Pocock J, Lashley T, Williams J, Lambert J-C, Amouyel P, Goate A, Rademakers R, Morgan K, Powell J, St. George-Hyslop P, Singleton A, Hardy J, N Engl J Med 2013 368 117 127 10.1056/NEJMoa1211851 23150934
-
(2013)
N Engl J Med
, vol.368
, pp. 117-127
-
-
Guerreiro, R.1
Wojtas, A.2
Bras, J.3
Carrasquillo, M.4
Rogaeva, E.5
Majounie, E.6
Cruchaga, C.7
Sassi, C.8
Kauwe, J.S.K.9
Younkin, S.10
Hazrati, L.11
Collinge, J.12
Pocock, J.13
Lashley, T.14
Williams, J.15
Lambert, J.-C.16
Amouyel, P.17
Goate, A.18
Rademakers, R.19
Morgan, K.20
Powell, J.21
St. George-Hyslop, P.22
Singleton, A.23
Hardy, J.24
more..
-
5
-
-
0033605611
-
A novel mutation in the apolipoprotein e gene (APOE*4 Pittsburgh) is associated with the risk of late-onset Alzheimer's disease
-
10.1016/S0304-3940(99)00129-9 10213152
-
A novel mutation in the apolipoprotein E gene (APOE*4 Pittsburgh) is associated with the risk of late-onset Alzheimer's disease. Kamboh MI, Aston CE, Perez-Tur J, Kokmen E, Ferrell RE, Hardy J, DeKosky ST, Neurosci Lett 1999 263 129 132 10.1016/S0304-3940(99)00129-9 10213152
-
(1999)
Neurosci Lett
, vol.263
, pp. 129-132
-
-
Kamboh, M.I.1
Aston, C.E.2
Perez-Tur, J.3
Kokmen, E.4
Ferrell, R.E.5
Hardy, J.6
Dekosky, S.T.7
-
6
-
-
0041321068
-
Apolipoprotein e Pittsburgh variant is not associated with the risk of late-onset Alzheimer's disease in a Spanish population
-
10.1002/ajmg.b.20028 12815750
-
Apolipoprotein E Pittsburgh variant is not associated with the risk of late-onset Alzheimer's disease in a Spanish population. Baron M, Jimenez-Escrig A, Orensanz L, Simon J, Perez-Tur J, Am J Med Genet B Neuropsychiatr Genet 2003 120B 121 124 10.1002/ajmg.b.20028 12815750
-
(2003)
Am J Med Genet B Neuropsychiatr Genet
, vol.120
, pp. 121-124
-
-
Baron, M.1
Jimenez-Escrig, A.2
Orensanz, L.3
Simon, J.4
Perez-Tur, J.5
-
7
-
-
0037333645
-
Screening of two mutations at exon 3 of the apolipoprotein e gene (sites 28 and 42) in a sample of patients with sporadic late-onset Alzheimer's disease
-
10.1016/S0197-4580(02)00089-1 12498968
-
Screening of two mutations at exon 3 of the apolipoprotein E gene (sites 28 and 42) in a sample of patients with sporadic late-onset Alzheimer's disease. Scacchi R, Gambina G, Ferrari G, Corbo RM, Neurobiol Aging 2003 24 339 343 10.1016/S0197-4580(02)00089-1 12498968
-
(2003)
Neurobiol Aging
, vol.24
, pp. 339-343
-
-
Scacchi, R.1
Gambina, G.2
Ferrari, G.3
Corbo, R.M.4
-
8
-
-
80052604940
-
Topology of human apolipoprotein E3 uniquely regulates its diverse biological functions
-
10.1073/pnas.1106420108 21873229
-
Topology of human apolipoprotein E3 uniquely regulates its diverse biological functions. Chen J, Li Q, Wang J, Proc Natl Acad Sci USA 2011 108 14813 14818 10.1073/pnas.1106420108 21873229
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 14813-14818
-
-
Chen, J.1
Li, Q.2
Wang, J.3
-
9
-
-
67349270965
-
Apolipoprotein e and its receptors in Alzheimer's disease: Pathways, pathogenesis and therapy
-
10.1038/nrn2620 19339974
-
Apolipoprotein E and its receptors in Alzheimer's disease: pathways, pathogenesis and therapy. Bu G, Nat Rev Neurosci 2009 10 333 344 10.1038/nrn2620 19339974
-
(2009)
Nat Rev Neurosci
, vol.10
, pp. 333-344
-
-
Bu, G.1
-
10
-
-
0027524456
-
Characterization of five new mutants in the carboxyl-terminal domain of human apolipoprotein E: No cosegregation with severe hyperlipidemia
-
8488843
-
Characterization of five new mutants in the carboxyl-terminal domain of human apolipoprotein E: no cosegregation with severe hyperlipidemia. van den Maagdenberg a M, Weng W, de Bruijn IH, de Knijff P, Funke H, Smelt a H, Gevers Leuven J a, van't Hooft FM, Assmann G, Hofker MH, Am J Hum Genet 1993 52 937 946 8488843
-
(1993)
Am J Hum Genet
, vol.52
, pp. 937-946
-
-
Van Den Maagdenberg, A.M.1
Weng, W.2
De Bruijn, I.H.3
De Knijff, P.4
Funke, H.5
Smelt, A.H.6
Gevers Leuven, J.A.7
Van'T Hooft, F.M.8
Assmann, G.9
Hofker, M.H.10
-
11
-
-
0028354059
-
Lipoprotein profiles in a family with two mutants of apolipoprotein E: Possible association with hypertriglyceridaemia but not with dysbetalipoproteinaemia
-
8156744
-
Lipoprotein profiles in a family with two mutants of apolipoprotein E: possible association with hypertriglyceridaemia but not with dysbetalipoproteinaemia. Zhao SP, van den Maagdenberg AM, Vroom TF, van 't Hooft FM, Gevers Leuvens JA, Havekes LM, Frants RR, Van der Laarse A, Smelt AH, Clin Sci (Lond) 1994 86 323 329 8156744
-
(1994)
Clin Sci (Lond)
, vol.86
, pp. 323-329
-
-
Zhao, S.P.1
Van Den Maagdenberg, A.M.2
Vroom, T.F.3
Van 'T Hooft, F.M.4
Gevers Leuvens, J.A.5
Havekes, L.M.6
Frants, R.R.7
Van Der Laarse, A.8
Smelt, A.H.9
-
12
-
-
84861903643
-
Structural differences between apoE3 and apoE4 may be useful in developing therapeutic agents for Alzheimer's disease
-
10.1073/pnas.1207022109 22615372
-
Structural differences between apoE3 and apoE4 may be useful in developing therapeutic agents for Alzheimer's disease. Frieden C, Garai K, Proc Natl Acad Sci USA 2012 109 8913 8918 10.1073/pnas.1207022109 22615372
-
(2012)
Proc Natl Acad Sci USA
, vol.109
, pp. 8913-8918
-
-
Frieden, C.1
Garai, K.2
-
13
-
-
43549116348
-
APOE epsilon 4 lowers age at onset and is a high risk factor for Alzheimer's disease; A case control study from central Norway
-
10.1186/1471-2377-8-9 18416843
-
APOE epsilon 4 lowers age at onset and is a high risk factor for Alzheimer's disease; a case control study from central Norway. Sando SB, Melquist S, Cannon A, Hutton ML, Sletvold O, Saltvedt I, White LR, Lydersen S, Aasly JO, BMC Neurol 2008 8 9 10.1186/1471-2377-8-9 18416843
-
(2008)
BMC Neurol
, vol.8
, pp. 9
-
-
Sando, S.B.1
Melquist, S.2
Cannon, A.3
Hutton, M.L.4
Sletvold, O.5
Saltvedt, I.6
White, L.R.7
Lydersen, S.8
Aasly, J.O.9
-
14
-
-
80155135295
-
The impact of mitochondrial and nuclear DNA variants on late-onset Alzheimer's disease risk
-
21799244
-
The impact of mitochondrial and nuclear DNA variants on late-onset Alzheimer's disease risk. Maruszak A, Safranow K, Branicki W, Gawȩda-Walerych K, Pośpiech E, Gabryelewicz T, Canter JA, Barcikowska M, Zekanowski C, J Alzheimers Dis 2011 27 197 210 21799244
-
(2011)
J Alzheimers Dis
, vol.27
, pp. 197-210
-
-
Maruszak, A.1
Safranow, K.2
Branicki, W.3
Gawȩda-Walerych, K.4
Pośpiech, E.5
Gabryelewicz, T.6
Canter, J.A.7
Barcikowska, M.8
Zekanowski, C.9
-
15
-
-
70450162929
-
Interleukin-1 gene -511 CT polymorphism and the risk of Alzheimer's disease in a Polish population
-
10.1159/000259460 19940477
-
Interleukin-1 gene -511 CT polymorphism and the risk of Alzheimer's disease in a Polish population. Klimkowicz-Mrowiec A, Marona M, Wołkow P, Maruszak A, Styczynska M, Barcikowska M, Zekanowski C, Szczudlik A, Slowik A, Dement Geriatr Cogn Disord 2009 28 461 464 10.1159/000259460 19940477
-
(2009)
Dement Geriatr Cogn Disord
, vol.28
, pp. 461-464
-
-
Klimkowicz-Mrowiec, A.1
Marona, M.2
Wołkow, P.3
Maruszak, A.4
Styczynska, M.5
Barcikowska, M.6
Zekanowski, C.7
Szczudlik, A.8
Slowik, A.9
-
16
-
-
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
-
10.1212/WNL.34.7.939 6610841
-
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 EM, Neurology 1984 34 939 944 10.1212/WNL.34.7.939 6610841
-
(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
-
18
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
10.1086/519795 17701901
-
PLINK: a tool set for whole-genome association and population-based linkage analyses. Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MAR, Bender D, Maller J, Sklar P, de Bakker PIW, Daly MJ, Sham PC, Am J Hum Genet 2007 81 559 575 10.1086/519795 17701901
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.R.5
Bender, D.6
Maller, J.7
Sklar, P.8
De Bakker, P.I.W.9
Daly, M.J.10
Sham, P.C.11
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