-
1
-
-
52449089987
-
Thirty years of Alzheimer's disease genetics: The implications of systematic meta-analyses
-
Bertram L, Tanzi RE (2008) Thirty years of Alzheimer's disease genetics: the implications of systematic meta-analyses. Nat Rev Neurosci 9:768-778
-
(2008)
Nat Rev Neurosci
, vol.9
, pp. 768-778
-
-
Bertram, L.1
Tanzi, R.E.2
-
2
-
-
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, Georgieva L, Dowzell K, Cichon S, Hillmer AM, O'Donovan MC 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
Georgieva, L.6
Dowzell, K.7
Cichon, S.8
Hillmer, A.M.9
O'Donovan, M.C.10
-
3
-
-
34047272692
-
A high-density 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, Lince DH, Zismann VL, Beach TG, Leung D, Bryden L et al (2007) A high-density 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
Lince, D.H.6
Zismann, V.L.7
Beach, T.G.8
Leung, D.9
Bryden, L.10
-
4
-
-
38349038412
-
Candidate singlenucleotide 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 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
Surh, L.6
Hosford, D.7
Barnes, M.R.8
Briley, J.D.9
Borrie, M.10
-
6
-
-
59149084048
-
Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease
-
CarrasquilloMM, Zou F, Pankratz VS,Wilcox SL,Ma L,Walker LP, Younkin SG, Younkin CS, Younkin LH, Bisceglio GD 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
Walker, L.P.6
Younkin, S.G.7
Younkin, C.S.8
Younkin, L.H.9
Bisceglio, G.D.10
-
7
-
-
58049200536
-
Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease
-
Beecham GW, Martin ER, Li YJ, Slifer MA, Gilbert JR, Haines JL, Pericak-Vance MA (2009) Genome-wide 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
Haines, J.L.6
Pericak-Vance, M.A.7
-
8
-
-
55049142500
-
Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE
-
Bertram L, Lange C, Mullin K, Parkinson M, Hsiao M, Hogan MF, Schjeide BM, Hooli B, Divito J, Ionita I et al (2008) Genome-wide 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
Hogan, M.F.6
Schjeide, B.M.7
Hooli, B.8
Divito, J.9
Ionita, I.10
-
9
-
-
34447559923
-
Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants
-
Grupe A, Abraham R, Li Y, Rowland C, Hollingworth P, Morgan A, Jehu L, Segurado R, Stone D, Schadt E et al (2007) Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide 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
Morgan, A.6
Jehu, L.7
Segurado, R.8
Stone, D.9
Schadt, E.10
-
10
-
-
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 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
Hamshere, M.L.6
Pahwa, J.S.7
Moskvina, V.8
Dowzell, K.9
Williams, A.10
-
11
-
-
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 et al (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
-
12
-
-
68449089420
-
Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease
-
Potkin SG, Guffanti G, Lakatos A, Turner JA, Kruggel F, Fallon JH, Saykin AJ, Orro A, Lupoli S, Salvi E et al (2009) Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. PLoS ONE 4:e6501
-
(2009)
PLoS ONE
, vol.4
-
-
Potkin, S.G.1
Guffanti, G.2
Lakatos, A.3
Turner, J.A.4
Kruggel, F.5
Fallon, J.H.6
Saykin, A.J.7
Orro, A.8
Lupoli, S.9
Salvi, E.10
-
13
-
-
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 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
Zismann, V.L.6
Joshipura, K.D.7
Pearson, J.V.8
Hu-Lince, D.9
Huentelman, M.J.10
-
14
-
-
0037043838
-
Evidence for parent of origin effect in late-onset Alzheimer disease
-
Bassett SS, Avramopoulos D, Fallin D (2002) Evidence for parent of origin effect in late-onset Alzheimer disease. Am J Med Genet 114:679-686
-
(2002)
Am J Med Genet
, vol.114
, pp. 679-686
-
-
Bassett, S.S.1
Avramopoulos, D.2
Fallin, D.3
-
15
-
-
33745794924
-
Further evidence of a maternal parentof- origin effect on chromosome 10 in late-onset Alzheimer's disease
-
Bassett SS, Avramopoulos D, Perry RT, Wiener H, Watson B Jr, Go RC, Fallin MD (2006) Further evidence of a maternal parentof- origin effect on chromosome 10 in late-onset Alzheimer's disease. Am J Med Genet B Neuropsychiatr Genet 141B:537-540
-
(2006)
Am J Med Genet B Neuropsychiatr Genet 141B
, pp. 537-540
-
-
Bassett, S.S.1
Avramopoulos, D.2
Perry, R.T.3
Wiener, H.4
Watson Jr., B.5
Go, R.C.6
Fallin, M.D.7
-
16
-
-
12244296117
-
Results of a high-resolution genome screen of 437 Alzheimer's disease families
-
Blacker D, Bertram L, Saunders AJ, Moscarillo TJ, Albert MS, Wiener H, Perry RT, Collins JS, Harrell LE, Go RC 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
Wiener, H.6
Perry, R.T.7
Collins, J.S.8
Harrell, L.E.9
Go, R.C.10
-
17
-
-
35548976654
-
Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease
-
Hamshere ML, Holmans PA, Avramopoulos D, Bassett SS, Blacker D, Bertram L, Wiener H, Rochberg N, Tanzi RE, Myers A et al (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
-
18
-
-
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, Fidani L, Giuffra L, Haynes A, Irving N, James L et al (1991) Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. Nature 349:704-706 (Pubitemid 21912142)
-
(1991)
Nature
, vol.349
, Issue.6311
, pp. 704-706
-
-
Goate, A.1
Chartier-Harlin, M.-C.2
Mullan, M.3
Brown, J.4
Crawford, F.5
Fldani, L.6
Giuffra, L.7
Haynes, A.8
Irving, N.9
James, L.10
Mant, R.11
Newton, P.12
Rooke, K.13
Roques, P.14
Talbot, C.15
Pericak-Vance, M.16
Roses, A.17
Williamson, R.18
Rossor, M.19
Owen, M.20
Hardy, J.21
more..
-
19
-
-
0034704197
-
Susceptibility locus for Alzheimer's disease on chromosome 10
-
Myers A, Holmans P, Marshall H, Kwon J, Meyer D, Ramic D, Shears S, Booth J, DeVrieze FW, Crook R et al (2000) Susceptibility locus for Alzheimer's disease on chromosome 10. Science 290:2304-2305
-
(2000)
Science
, vol.290
, pp. 2304-2305
-
-
Myers, A.1
Holmans, P.2
Marshall, H.3
Kwon, J.4
Meyer, D.5
Ramic, D.6
Shears, S.7
Booth, J.8
DeVrieze, F.W.9
Crook, R.10
-
20
-
-
0034704198
-
Evidence for genetic linkage of Alzheimer's disease to chromosome 10q
-
Bertram L, Blacker D, Mullin K, Keeney D, Jones J, Basu S, Yhu S, McInnis MG, Go RC, Vekrellis K et al (2000) Evidence for genetic linkage of Alzheimer's disease to chromosome 10q. Science 290:2302-2303
-
(2000)
Science
, vol.290
, pp. 2302-2303
-
-
Bertram, L.1
Blacker, D.2
Mullin, K.3
Keeney, D.4
Jones, J.5
Basu, S.6
Yhu, S.7
McInnis, M.G.8
Go, R.C.9
Vekrellis, K.10
-
21
-
-
0034703979
-
Linkage of plasma Abeta42 to a quantitative locus on chromosome 10 in late-onset Alzheimer's disease pedigrees
-
Ertekin-Taner N, Graff-Radford N, Younkin LH, Eckman C, Baker M, Adamson J, Ronald J, Blangero J, Hutton M, Younkin SG (2000) Linkage of plasma Abeta42 to a quantitative locus on chromosome 10 in late-onset Alzheimer's disease pedigrees. Science 290:2303-2304
-
(2000)
Science
, vol.290
, pp. 2303-2304
-
-
Ertekin-Taner, N.1
Graff-Radford, N.2
Younkin, L.H.3
Eckman, C.4
Baker, M.5
Adamson, J.6
Ronald, J.7
Blangero, J.8
Hutton, M.9
Younkin, S.G.10
-
22
-
-
4143140828
-
Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2
-
DOI 10.1086/423393
-
Wijsman EM, Daw EW, Yu CE, Payami H, Steinbart EJ, Nochlin D, Conlon EM, Bird TD, Schellenberg GD (2004) Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2. Am J Hum Genet 75:398-409 (Pubitemid 39095816)
-
(2004)
American Journal of Human Genetics
, vol.75
, Issue.3
, pp. 398-409
-
-
Wijsman, E.M.1
Daw, E.W.2
Yu, C.-E.3
Payami, H.4
Steinbart, E.J.5
Nochlin, D.6
Conlon, E.M.7
Bird, T.D.8
Schellenberg, G.D.9
-
23
-
-
21844451120
-
Brain activation in offspring of AD cases corresponds to 10q linkage
-
Bassett SS, Kusevic I, Cristinzio C, Yassa MA, Avramopoulos D, Yousem DM, Fallin MD (2005) Brain activation in offspring of AD cases corresponds to 10q linkage. Ann Neurol 58:142-146
-
(2005)
Ann Neurol
, vol.58
, pp. 142-146
-
-
Bassett, S.S.1
Kusevic, I.2
Cristinzio, C.3
Yassa, M.A.4
Avramopoulos, D.5
Yousem, D.M.6
Fallin, M.D.7
-
24
-
-
17744410836
-
ApoE-4 and age at onset of Alzheimer's disease: The NIMH genetics initiative
-
Blacker D, Haines JL, Rodes L, Terwedow H, Go RC, Harrell LE, Perry RT, Bassett SS, Chase G, Meyers D et al (1997) ApoE-4 and age at onset of Alzheimer's disease: the NIMH genetics initiative. Neurology 48:139-147
-
(1997)
Neurology
, vol.48
, pp. 139-147
-
-
Blacker, D.1
Haines, J.L.2
Rodes, L.3
Terwedow, H.4
Go, R.C.5
Harrell, L.E.6
Perry, R.T.7
Bassett, S.S.8
Chase, G.9
Meyers, D.10
-
25
-
-
2342597140
-
A high-density admixture map for disease gene discovery in african americans
-
Smith MW, Patterson N, Lautenberger JA, Truelove AL, McDonald GJ, Waliszewska A, Kessing BD, Malasky MJ, Scafe C, Le E et al (2004) A high-density admixture map for disease gene discovery in african americans. Am J Hum Genet 74:1001-1013
-
(2004)
Am J Hum Genet
, vol.74
, pp. 1001-1013
-
-
Smith, M.W.1
Patterson, N.2
Lautenberger, J.A.3
Truelove, A.L.4
McDonald, G.J.5
Waliszewska, A.6
Kessing, B.D.7
Malasky, M.J.8
Scafe, C.9
Le, E.10
-
26
-
-
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
-
27
-
-
34548292504
-
PLINK: A tool set for whole-genome association and populationbased linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ et al (2007) PLINK: a tool set for whole-genome association and populationbased 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
Bender, D.6
Maller, J.7
Sklar, P.8
De Bakker, P.I.9
Daly, M.J.10
-
28
-
-
62649155943
-
A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals
-
Browning BL, Browning SR (2009) A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals. Am J Hum Genet 84:210-223
-
(2009)
Am J Hum Genet
, vol.84
, pp. 210-223
-
-
Browning, B.L.1
Browning, S.R.2
-
31
-
-
0036634250
-
Involvement of cyclic GMP and protein kinase G in the regulation of apoptosis and survival in neural cells
-
Fiscus RR (2002) Involvement of cyclic GMP and protein kinase G in the regulation of apoptosis and survival in neural cells. Neurosignals 11:175-190
-
(2002)
Neurosignals
, vol.11
, pp. 175-190
-
-
Fiscus, R.R.1
-
32
-
-
0034968358
-
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
-
Ahmed ZM, Riazuddin S, Bernstein SL, Ahmed Z, Khan S, Griffith AJ, Morell RJ, Friedman TB, Wilcox ER (2001) Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F. Am J Hum Genet 69:25-34
-
(2001)
Am J Hum Genet
, vol.69
, pp. 25-34
-
-
Ahmed, Z.M.1
Riazuddin, S.2
Bernstein, S.L.3
Ahmed, Z.4
Khan, S.5
Griffith, A.J.6
Morell, R.J.7
Friedman, T.B.8
Wilcox, E.R.9
-
33
-
-
33645002056
-
Inactivation status of PCDH11X: Sexual dimorphisms in gene expression levels in brain
-
Lopes AM, Ross N, Close J, Dagnall A, Amorim A, Crow TJ (2006) Inactivation status of PCDH11X: sexual dimorphisms in gene expression levels in brain. Hum Genet 119:267-275
-
(2006)
Hum Genet
, vol.119
, pp. 267-275
-
-
Lopes, A.M.1
Ross, N.2
Close, J.3
Dagnall, A.4
Amorim, A.5
Crow, T.J.6
-
34
-
-
9144268889
-
Characterization of the pufferfish Otx2 cis-regulators reveals evolutionarily conserved genetic mechanisms for vertebrate head specification
-
Kimura-Yoshida C, Kitajima K, Oda-Ishii I, Tian E, Suzuki M, Yamamoto M, Suzuki T, Kobayashi M, Aizawa S, Matsuo I (2004) Characterization of the pufferfish Otx2 cis-regulators reveals evolutionarily conserved genetic mechanisms for vertebrate head specification. Development 131:57-71
-
(2004)
Development
, vol.131
, pp. 57-71
-
-
Kimura-Yoshida, C.1
Kitajima, K.2
Oda-Ishii, I.3
Tian, E.4
Suzuki, M.5
Yamamoto, M.6
Suzuki, T.7
Kobayashi, M.8
Aizawa, S.9
Matsuo, I.10
-
36
-
-
3543060533
-
Efficient identification of regulatory sequences in the chicken genome by a powerful combination of embryo electroporation and genome comparison
-
Uchikawa M, Takemoto T, Kamachi Y, Kondoh H (2004) Efficient identification of regulatory sequences in the chicken genome by a powerful combination of embryo electroporation and genome comparison. Mech Dev 121:1145-1158
-
(2004)
Mech Dev
, vol.121
, pp. 1145-1158
-
-
Uchikawa, M.1
Takemoto, T.2
Kamachi, Y.3
Kondoh, H.4
-
37
-
-
0029030017
-
Localized Bicaudal-C RNA encodes a protein containing a KH domain, the RNA binding motif of FMR1
-
Mahone M, Saffman EE, Lasko PF (1995) Localized Bicaudal-C RNA encodes a protein containing a KH domain, the RNA binding motif of FMR1. Embo J 14:2043-2055
-
(1995)
Embo J
, vol.14
, pp. 2043-2055
-
-
Mahone, M.1
Saffman, E.E.2
Lasko, P.F.3
-
38
-
-
0031877789
-
Premature translation of oskar in oocytes lacking the RNAbinding protein bicaudal-C
-
Saffman EE, Styhler S, Rother K, Li W, Richard S, Lasko P (1998) Premature translation of oskar in oocytes lacking the RNAbinding protein bicaudal-C. Mol Cell Biol 18:4855-4862
-
(1998)
Mol Cell Biol
, vol.18
, pp. 4855-4862
-
-
Saffman, E.E.1
Styhler, S.2
Rother, K.3
Li, W.4
Richard, S.5
Lasko, P.6
-
39
-
-
69049097145
-
Bicaudal C, a novel regulator of Dvl signaling abutting RNA-processing bodies, controls cilia orientation and leftward flow
-
Maisonneuve C, Guilleret I, Vick P, Weber T, Andre P, Beyer T, Blum M, Constam DB (2009) Bicaudal C, a novel regulator of Dvl signaling abutting RNA-processing bodies, controls cilia orientation and leftward flow. Development 136:3019-3030
-
(2009)
Development
, vol.136
, pp. 3019-3030
-
-
Maisonneuve, C.1
Guilleret, I.2
Vick, P.3
Weber, T.4
Andre, P.5
Beyer, T.6
Blum, M.7
Constam, D.B.8
-
40
-
-
0037385521
-
Positional cloning of jcpk/bpk locus of the mouse
-
Cogswell C, Price SJ, Hou X, Guay-Woodford LM, Flaherty L, Bryda EC (2003) Positional cloning of jcpk/bpk locus of the mouse. Mamm Genome 14:242-249
-
(2003)
Mamm Genome
, vol.14
, pp. 242-249
-
-
Cogswell, C.1
Price, S.J.2
Hou, X.3
Guay-Woodford, L.M.4
Flaherty, L.5
Bryda, E.C.6
-
41
-
-
63749094517
-
Bicaudal is a conserved substrate for Drosophila and mammalian caspases and is essential for cell survival
-
Creagh EM, Brumatti G, Sheridan C, Duriez PJ, Taylor RC, Cullen SP, Adrain C, Martin SJ (2009) Bicaudal is a conserved substrate for Drosophila and mammalian caspases and is essential for cell survival. PLoS ONE 4:e5055
-
(2009)
PLoS ONE
, vol.4
-
-
Creagh, E.M.1
Brumatti, G.2
Sheridan, C.3
Duriez, P.J.4
Taylor, R.C.5
Cullen, S.P.6
Adrain, C.7
Martin, S.J.8
-
42
-
-
4644224016
-
Association analysis of genes involved in cholesterol metabolism located within the linkage region on chromosome 10 and Alzheimer's disease
-
Riemenschneider M, Mahmoodzadeh S, Eisele T, Klopp N, Schwarz S, Wagenpfeil S, Diehl J, Mueller U, Foerstl H, Illig T et al (2004) Association analysis of genes involved in cholesterol metabolism located within the linkage region on chromosome 10 and Alzheimer's disease. Neurobiol Aging 25:1305-1308
-
(2004)
Neurobiol Aging
, vol.25
, pp. 1305-1308
-
-
Riemenschneider, M.1
Mahmoodzadeh, S.2
Eisele, T.3
Klopp, N.4
Schwarz, S.5
Wagenpfeil, S.6
Diehl, J.7
Mueller, U.8
Foerstl, H.9
Illig, T.10
-
43
-
-
33847689055
-
A novel gene derived from a segmental duplication shows perturbed expression in Alzheimer's disease
-
Avramopoulos D, Wang R, Valle D, Fallin MD, Bassett SS (2007) A novel gene derived from a segmental duplication shows perturbed expression in Alzheimer's disease. Neurogenetics 8:111-120
-
(2007)
Neurogenetics
, vol.8
, pp. 111-120
-
-
Avramopoulos, D.1
Wang, R.2
Valle, D.3
Fallin, M.D.4
Bassett, S.S.5
|