-
2
-
-
0042023711
-
Alzheimer disease in the US population: Prevalence estimates using the 2000 census
-
Hebert LE, Scherr PA, Bienias JL, Bennett DA, Evans DA (2003) Alzheimer disease in the US population: prevalence estimates using the 2000 census. Arch Neurol 60: 1119-1122.
-
(2003)
Arch Neurol
, vol.60
, pp. 1119-1122
-
-
Hebert, L.E.1
Scherr, P.A.2
Bienias, J.L.3
Bennett, D.A.4
Evans, D.A.5
-
3
-
-
0026088977
-
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
-
Goate A, Chartier-Harlin MC, Mullan M, Brown J, Crawford F, et al. (1991) Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. Nature 349: 704-706.
-
(1991)
Nature
, vol.349
, pp. 704-706
-
-
Goate, A.1
Chartier-Harlin, M.C.2
Mullan, M.3
Brown, J.4
Crawford, F.5
-
4
-
-
0029004341
-
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
-
Sherrington R, Rogaev EI, Liang Y, Rogaeva EA, Levesque G, et al. (1995) Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. Nature 375: 754-760.
-
(1995)
Nature
, vol.375
, pp. 754-760
-
-
Sherrington, R.1
Rogaev, E.I.2
Liang, Y.3
Rogaeva, E.A.4
Levesque, G.5
-
5
-
-
0029166112
-
Apolipoprotein E genotypes and age of onset in early-onset familial Alzheimer's disease
-
Levy-Lahad E, Lahad A, Wijsman EM, Bird TD, Schellenberg GD (1995) Apolipoprotein E genotypes and age of onset in early-onset familial Alzheimer's disease. Ann Neurol 38: 678-680.
-
(1995)
Ann Neurol
, vol.38
, pp. 678-680
-
-
Levy-Lahad, E.1
Lahad, A.2
Wijsman, E.M.3
Bird, T.D.4
Schellenberg, G.D.5
-
6
-
-
0029087026
-
Candidate gene for the chromosome 1 familial Alzheimer's disease locus
-
Levy-Lahad E, Wasco W, Poorkaj P, Romano DM, Oshima J, et al. (1995) Candidate gene for the chromosome 1 familial Alzheimer's disease locus. Science 269: 973-977.
-
(1995)
Science
, vol.269
, pp. 973-977
-
-
Levy-Lahad, E.1
Wasco, W.2
Poorkaj, P.3
Romano, D.M.4
Oshima, J.5
-
7
-
-
0029101491
-
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
-
Rogaev EI, Sherrington R, Rogaeva EA, Levesque G, Ikeda M, et al. (1995) Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene. Nature 376: 775-778.
-
(1995)
Nature
, vol.376
, pp. 775-778
-
-
Rogaev, E.I.1
Sherrington, R.2
Rogaeva, E.A.3
Levesque, G.4
Ikeda, M.5
-
8
-
-
0027327267
-
Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease
-
Saunders AM, Strittmatter WJ, Schmechel D, George-Hyslop PH, Pericak-Vance MA, et al. (1993) Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease. Neurology 43: 1467-1472.
-
(1993)
Neurology
, vol.43
, pp. 1467-1472
-
-
Saunders, A.M.1
Strittmatter, W.J.2
Schmechel, D.3
George-Hyslop, P.H.4
Pericak-Vance, M.A.5
-
9
-
-
0027194791
-
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
-
Corder EH, Saunders AM, Strittmatter WJ, Schmechel DE, Gaskell PC, et al. (1993) Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. Science 261: 921-923.
-
(1993)
Science
, vol.261
, pp. 921-923
-
-
Corder, E.H.1
Saunders, A.M.2
Strittmatter, W.J.3
Schmechel, D.E.4
Gaskell, P.C.5
-
10
-
-
0027407565
-
Apolipoprotein E: High-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease
-
Strittmatter WJ, Saunders AM, Schmechel D, Pericak-Vance M, Enghild J, et al. (1993) Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease. Proc Natl Acad Sci U S A 90: 1977-1981.
-
(1993)
Proc Natl Acad Sci U S A
, vol.90
, pp. 1977-1981
-
-
Strittmatter, W.J.1
Saunders, A.M.2
Schmechel, D.3
Pericak-Vance, M.4
Enghild, J.5
-
11
-
-
18844479720
-
Heritability for Alzheimer's disease: The study of dementia in Swedish twins
-
Gatz M, Pedersen NL, Berg S, Johansson B, Johansson K, et al. (1997) Heritability for Alzheimer's disease: the study of dementia in Swedish twins. J Gerontol A Biol Sci Med Sci 52: M117-125.
-
(1997)
J Gerontol A Biol Sci Med Sci
, vol.52
-
-
Gatz, M.1
Pedersen, N.L.2
Berg, S.3
Johansson, B.4
Johansson, K.5
-
12
-
-
10044274396
-
APOE genotype, family history of dementia, and Alzheimer disease risk: A 6-year follow-up study
-
Huang W, Qiu C, von Strauss E, Winblad B, Fratiglioni L (2004) APOE genotype, family history of dementia, and Alzheimer disease risk: a 6-year follow-up study. Arch Neurol 61: 1930-1934.
-
(2004)
Arch Neurol
, vol.61
, pp. 1930-1934
-
-
Huang, W.1
Qiu, C.2
von Strauss, E.3
Winblad, B.4
Fratiglioni, L.5
-
13
-
-
34447559923
-
Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genomewide association study of putative functional variants
-
Grupe A, Abraham R, Li Y, Rowland C, Hollingworth P, et al. (2007) Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genomewide association study of putative functional variants. Hum Mol Genet 16: 865-873.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 865-873
-
-
Grupe, A.1
Abraham, R.2
Li, Y.3
Rowland, C.4
Hollingworth, P.5
-
14
-
-
34047272692
-
A highdensity whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease
-
Coon KD, Myers AJ, Craig DW, Webster JA, Pearson JV, et al. (2007) A highdensity whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease. J Clin Psychiatry 68: 613-618.
-
(2007)
J Clin Psychiatry
, vol.68
, pp. 613-618
-
-
Coon, K.D.1
Myers, A.J.2
Craig, D.W.3
Webster, J.A.4
Pearson, J.V.5
-
15
-
-
34249745769
-
GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers
-
Reiman EM, Webster JA, Myers AJ, Hardy J, Dunckley T, et al. (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
-
16
-
-
68049148052
-
A genome-wide association study for late-onset Alzheimer's disease using DNA pooling
-
Abraham R, Moskvina V, Sims R, Hollingworth P, Morgan A, et al. (2008) A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. BMC Med Genomics 1: 44.
-
(2008)
BMC Med Genomics
, vol.1
, pp. 44
-
-
Abraham, R.1
Moskvina, V.2
Sims, R.3
Hollingworth, P.4
Morgan, A.5
-
17
-
-
55049142500
-
Genomewide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE
-
Bertram L, Lange C, Mullin K, Parkinson M, Hsiao M, et al. (2008) Genomewide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE. Am J Hum Genet 83: 623-632.
-
(2008)
Am J Hum Genet
, vol.83
, pp. 623-632
-
-
Bertram, L.1
Lange, C.2
Mullin, K.3
Parkinson, M.4
Hsiao, M.5
-
18
-
-
58049200536
-
Genomewide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease
-
Beecham GW, Martin ER, Li YJ, Slifer MA, Gilbert JR, et al. (2009) Genomewide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. Am J Hum Genet 84: 35-43.
-
(2009)
Am J Hum Genet
, vol.84
, pp. 35-43
-
-
Beecham, G.W.1
Martin, E.R.2
Li, Y.J.3
Slifer, M.A.4
Gilbert, J.R.5
-
19
-
-
59149084048
-
Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease
-
Carrasquillo MM, Zou F, Pankratz VS, Wilcox SL, Ma L, et al. (2009) Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease. Nat Genet 41: 192-198.
-
(2009)
Nat Genet
, vol.41
, pp. 192-198
-
-
Carrasquillo, M.M.1
Zou, F.2
Pankratz, V.S.3
Wilcox, S.L.4
Ma, L.5
-
20
-
-
78549264026
-
Genomewide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
-
Lambert JC, Heath S, Even G, Campion D, Sleegers K, et al. (2009) Genomewide 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
-
21
-
-
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, et al. (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
-
22
-
-
77952307991
-
Genome-wide analysis of genetic loci associated with Alzheimer disease
-
Seshadri S, Fitzpatrick AL, Ikram MA, DeStefano AL, Gudnason V, et al. (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
-
23
-
-
38349038412
-
Candidate singlenucleotide polymorphisms from a genomewide association study of Alzheimer disease
-
Li H, Wetten S, Li L, St Jean PL, Upmanyu R, et al. (2008) Candidate singlenucleotide 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
-
25
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Welcome Trust Case Control Consortium
-
Welcome Trust Case Control Consortium (2007) Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447: 661-678.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
26
-
-
77951170478
-
Mitochondrial C1- Tetrahydrofolate Synthase (MTHFD1L) Supports the Flow of Mitochondrial One-carbon Units into the Methyl Cycle in Embryos
-
Pike ST, Rajendra R, Artzt K, Appling DR (2010) Mitochondrial C1- Tetrahydrofolate Synthase (MTHFD1L) Supports the Flow of Mitochondrial One-carbon Units into the Methyl Cycle in Embryos. J Biol Chem 285: 4612-4620.
-
(2010)
J Biol Chem
, vol.285
, pp. 4612-4620
-
-
Pike, S.T.1
Rajendra, R.2
Artzt, K.3
Appling, D.R.4
-
27
-
-
62949129136
-
Hyperhomocysteinemia and Alzheimer's disease: A systematic review
-
Van Dam F, Van Gool WA (2009) Hyperhomocysteinemia and Alzheimer's disease: A systematic review. Arch Gerontol Geriatr 48: 425-430.
-
(2009)
Arch Gerontol Geriatr
, vol.48
, pp. 425-430
-
-
Van Dam, F.1
Van Gool, W.A.2
-
28
-
-
0038387939
-
Homocysteine and Alzheimer's disease
-
Morris MS (2003) Homocysteine and Alzheimer's disease. Lancet Neurol 2: 425-428.
-
(2003)
Lancet Neurol
, vol.2
, pp. 425-428
-
-
Morris, M.S.1
-
29
-
-
0036398629
-
Hyperhomocysteinemia: A new risk factor for degenerative diseases
-
Herrmann W, Knapp JP (2002) Hyperhomocysteinemia: a new risk factor for degenerative diseases. Clin Lab 48: 471-481.
-
(2002)
Clin Lab
, vol.48
, pp. 471-481
-
-
Herrmann, W.1
Knapp, J.P.2
-
30
-
-
0035814640
-
Pathogenesis and genetics of pre-eclampsia
-
Roberts JM, Cooper DW (2001) Pathogenesis and genetics of pre-eclampsia. Lancet 357: 53-56.
-
(2001)
Lancet
, vol.357
, pp. 53-56
-
-
Roberts, J.M.1
Cooper, D.W.2
-
31
-
-
11844286368
-
Total homocysteine levels relation with chronic complications of diabetes, body composition, and other cardiovascular risk factors in a population of patients with diabetes mellitus type 2
-
de Luis DA, Fernandez N, Arranz ML, Aller R, Izaola O, et al. (2005) Total homocysteine levels relation with chronic complications of diabetes, body composition, and other cardiovascular risk factors in a population of patients with diabetes mellitus type 2. J Diabetes Complications 19: 42-46.
-
(2005)
J Diabetes Complications
, vol.19
, pp. 42-46
-
-
de Luis, D.A.1
Fernandez, N.2
Arranz, M.L.3
Aller, R.4
Izaola, O.5
-
32
-
-
0029084552
-
Serum total homocysteine and coronary heart disease
-
Arnesen E, Refsum H, Bonaa KH, Ueland PM, Forde OH, et al. (1995) Serum total homocysteine and coronary heart disease. Int J Epidemiol 24: 704-709.
-
(1995)
Int J Epidemiol
, vol.24
, pp. 704-709
-
-
Arnesen, E.1
Refsum, H.2
Bonaa, K.H.3
Ueland, P.M.4
Forde, O.H.5
-
33
-
-
34547623750
-
Genomewide association analysis of coronary artery disease
-
Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, et al. (2007) Genomewide association analysis of coronary artery disease. N Engl J Med 357: 443-453.
-
(2007)
N Engl J Med
, vol.357
, pp. 443-453
-
-
Samani, N.J.1
Erdmann, J.2
Hall, A.S.3
Hengstenberg, C.4
Mangino, M.5
-
34
-
-
0031054674
-
Brain infarction and the clinical expression of Alzheimer disease. The nun study
-
Snowdon DA, Greiner LH, Mortimer JA, Riley KP, Greiner PA, et al. (1997) Brain infarction and the clinical expression of Alzheimer disease. The Nun Study. Jama 277: 813-817.
-
(1997)
Jama
, vol.277
, pp. 813-817
-
-
Snowdon, D.A.1
Greiner, L.H.2
Mortimer, J.A.3
Riley, K.P.4
Greiner, P.A.5
-
35
-
-
0036892748
-
Multiple aspects of homocysteine neurotoxicity: Glutamate excitotoxicity, kinase hyperactivation and DNA damage
-
Ho PI, Ortiz D, Rogers E, Shea TB (2002) Multiple aspects of homocysteine neurotoxicity: glutamate excitotoxicity, kinase hyperactivation and DNA damage. J Neurosci Res 70: 694-702.
-
(2002)
J Neurosci Res
, vol.70
, pp. 694-702
-
-
Ho, P.I.1
Ortiz, D.2
Rogers, E.3
Shea, T.B.4
-
36
-
-
0037076486
-
Functional vitamin B(12) deficiency and Alzheimer disease
-
McCaddon A, Regland B, Hudson P, Davies G (2002) Functional vitamin B(12) deficiency and Alzheimer disease. Neurology 58: 1395-1399.
-
(2002)
Neurology
, vol.58
, pp. 1395-1399
-
-
McCaddon, A.1
Regland, B.2
Hudson, P.3
Davies, G.4
-
37
-
-
0037305028
-
Alzheimer's disease and total plasma aminothiols
-
McCaddon A, Hudson P, Hill D, Barber J, Lloyd A, et al. (2003) Alzheimer's disease and total plasma aminothiols. Biol Psychiatry 53: 254-260.
-
(2003)
Biol Psychiatry
, vol.53
, pp. 254-260
-
-
McCaddon, A.1
Hudson, P.2
Hill, D.3
Barber, J.4
Lloyd, A.5
-
38
-
-
0037364417
-
Folate and homocysteine metabolism in neural plasticity and neurodegenerative disorders
-
Mattson MP, Shea TB (2003) Folate and homocysteine metabolism in neural plasticity and neurodegenerative disorders. Trends Neurosci 26: 137-146.
-
(2003)
Trends Neurosci
, vol.26
, pp. 137-146
-
-
Mattson, M.P.1
Shea, T.B.2
-
39
-
-
50249099760
-
iTRAQ analysis of complex proteome alterations in 3xTgAD Alzheimer's mice: Understanding the interface between physiology and disease
-
doi:10.1371/journal.pone.0002750
-
Martin B, Brenneman R, Becker KG, Gucek M, Cole RN, et al. (2008) iTRAQ analysis of complex proteome alterations in 3xTgAD Alzheimer's mice: understanding the interface between physiology and disease. PLoS One 3: e2750. doi:10.1371/journal.pone.0002750.
-
(2008)
PLoS One
, vol.3
-
-
Martin, B.1
Brenneman, R.2
Becker, K.G.3
Gucek, M.4
Cole, R.N.5
-
40
-
-
77649314768
-
Treatment of Alzheimer's disease with anti-homocysteic acid antibody in 3xTg-AD male mice
-
doi:10.1371/journal.pone.0008593
-
Hasegawa T, Mikoda N, Kitazawa M, LaFerla FM (2010) Treatment of Alzheimer's disease with anti-homocysteic acid antibody in 3xTg-AD male mice. PLoS One 5: e8593. doi:10.1371/journal.pone.0008593.
-
(2010)
PLoS One
, vol.5
-
-
Hasegawa, T.1
Mikoda, N.2
Kitazawa, M.3
LaFerla, F.M.4
-
41
-
-
0036301635
-
A second locus for very-late-onset Alzheimer disease: A genome scan reveals linkage to 20p and epistasis between 20p and the amyloid precursor protein region
-
Olson JM, Goddard KA, Dudek DM (2002) A second locus for very-late-onset Alzheimer disease: a genome scan reveals linkage to 20p and epistasis between 20p and the amyloid precursor protein region. Am J Hum Genet 71: 154-161.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 154-161
-
-
Olson, J.M.1
Goddard, K.A.2
Dudek, D.M.3
-
42
-
-
12244296117
-
Results of a high-resolution genome screen of 437 Alzheimer's disease families
-
Blacker D, Bertram L, Saunders AJ, Moscarillo TJ, Albert MS, et al. (2003) Results of a high-resolution genome screen of 437 Alzheimer's disease families. Hum Mol Genet 12: 23-32.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 23-32
-
-
Blacker, D.1
Bertram, L.2
Saunders, A.J.3
Moscarillo, T.J.4
Albert, M.S.5
-
43
-
-
78049531016
-
PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility
-
In press
-
Beecham GW, Naj AC, Gilbert JR, Haines JL, Buxbaum JD, et al. (2010) PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility. Psychiatr Genet, In press.
-
(2010)
Psychiatr Genet
-
-
Beecham, G.W.1
Naj, A.C.2
Gilbert, J.R.3
Haines, J.L.4
Buxbaum, J.D.5
-
45
-
-
33750977267
-
Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease
-
Lee JH, Cheng R, Santana V, Williamson J, Lantigua R, et al. (2006) Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease. Arch Neurol 63: 1591-1598.
-
(2006)
Arch Neurol
, vol.63
, pp. 1591-1598
-
-
Lee, J.H.1
Cheng, R.2
Santana, V.3
Williamson, J.4
Lantigua, R.5
-
46
-
-
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
-
47
-
-
0031781988
-
Regional distribution of neuritic plaques in the nondemented elderly and subjects with very mild Alzheimer disease
-
Haroutunian V, Perl DP, Purohit DP, Marin D, Khan K, et al. (1998) Regional distribution of neuritic plaques in the nondemented elderly and subjects with very mild Alzheimer disease. Arch Neurol 55: 1185-1191.
-
(1998)
Arch Neurol
, vol.55
, pp. 1185-1191
-
-
Haroutunian, V.1
Perl, D.P.2
Purohit, D.P.3
Marin, D.4
Khan, K.5
-
48
-
-
77951185469
-
Genomewide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease
-
Edwards TL, Scott WK, Almonte C, Burt A, Powell EH, et al. (2010) Genomewide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. Ann Hum Genet 74: 97-109.
-
(2010)
Ann Hum Genet
, vol.74
, pp. 97-109
-
-
Edwards, T.L.1
Scott, W.K.2
Almonte, C.3
Burt, A.4
Powell, E.H.5
-
49
-
-
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, et al. (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
-
50
-
-
0027534657
-
Vascular dementia: Diagnostic criteria for research studies. Report of the NINDS-AIREN international workshop
-
Roman GC, Tatemichi TK, Erkinjuntti T, Cummings JL, Masdeu JC, et al. (1993) Vascular dementia: diagnostic criteria for research studies. Report of the NINDS-AIREN International Workshop. Neurology 43: 250-260.
-
(1993)
Neurology
, vol.43
, pp. 250-260
-
-
Roman, G.C.1
Tatemichi, T.K.2
Erkinjuntti, T.3
Cummings, J.L.4
Masdeu, J.C.5
-
51
-
-
33645992747
-
Lack of association between UBQLN1 and Alzheimer disease
-
Slifer MA, Martin ER, Bronson PG, Browning-Large C, Doraiswamy PM, et al. (2006) Lack of association between UBQLN1 and Alzheimer disease. Am J Med Genet B Neuropsychiatr Genet 141B: 208-213.
-
(2006)
Am J Med Genet B Neuropsychiatr Genet
, vol.141 B
, pp. 208-213
-
-
Slifer, M.A.1
Martin, E.R.2
Bronson, P.G.3
Browning-Large, C.4
Doraiswamy, P.M.5
-
53
-
-
0034118493
-
Inference of population structure using multilocus genotype data
-
Pritchard JK, Stephens M, Donnelly P (2000) Inference of population structure using multilocus genotype data. Genetics 155: 945-959.
-
(2000)
Genetics
, vol.155
, pp. 945-959
-
-
Pritchard, J.K.1
Stephens, M.2
Donnelly, P.3
-
55
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, et al. (2006) Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 38: 904-909.
-
(2006)
Nat Genet
, vol.38
, pp. 904-909
-
-
Price, A.L.1
Patterson, N.J.2
Plenge, R.M.3
Weinblatt, M.E.4
Shadick, N.A.5
-
56
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, et al. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81: 559-575.
-
(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.5
-
57
-
-
34347344976
-
A new multipoint method for genome-wide association studies by imputation of genotypes
-
Marchini J, Howie B, Myers S, McVean G, Donnelly P (2007) A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet 39: 906-913.
-
(2007)
Nat Genet
, vol.39
, pp. 906-913
-
-
Marchini, J.1
Howie, B.2
Myers, S.3
McVean, G.4
Donnelly, P.5
-
58
-
-
71449096845
-
Genome-wide association studies: Quality control and population-based measures
-
Ziegler A (2009) Genome-wide association studies: quality control and population-based measures. Genet Epidemiol 33: S45-S50.
-
(2009)
Genet Epidemiol
, vol.33
-
-
Ziegler, A.1
-
60
-
-
0037411512
-
Biological markers for therapeutic trials in Alzheimer's disease. Proceedings of the biological markers working group; NIA initiative on neuroimaging in Alzheimer's disease
-
Frank RA, Galasko D, Hampel H, Hardy J, de Leon MJ, et al. (2003) Biological markers for therapeutic trials in Alzheimer's disease. Proceedings of the biological markers working group; NIA initiative on neuroimaging in Alzheimer's disease. Neurobiol Aging 24: 521-536.
-
(2003)
Neurobiol Aging
, vol.24
, pp. 521-536
-
-
Frank, R.A.1
Galasko, D.2
Hampel, H.3
Hardy, J.4
de Leon, M.J.5
-
61
-
-
0026508937
-
Prevalence of dementia and probable senile dementia of the Alzheimer type in the Framingham Study
-
Bachman DL, Wolf PA, Linn R, Knoefel JE, Cobb J, et al. (1992) Prevalence of dementia and probable senile dementia of the Alzheimer type in the Framingham Study. Neurology 42: 115-119.
-
(1992)
Neurology
, vol.42
, pp. 115-119
-
-
Bachman, D.L.1
Wolf, P.A.2
Linn, R.3
Knoefel, J.E.4
Cobb, J.5
-
62
-
-
0036948098
-
SNPper: Retrieval and analysis of human SNPs
-
Riva A, Kohane IS (2002) SNPper: retrieval and analysis of human SNPs. Bioinformatics 18: 1681-1685.
-
(2002)
Bioinformatics
, vol.18
, pp. 1681-1685
-
-
Riva, A.1
Kohane, I.S.2
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