-
1
-
-
33746919083
-
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
-
DOI 10.1038/nature05016, PII NATURE05016
-
Baker M, Mackenzie IR, Pickering-Brown SM, et al: Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 2006; 442: 916-919. (Pubitemid 44285946)
-
(2006)
Nature
, vol.442
, Issue.7105
, pp. 916-919
-
-
Baker, M.1
Mackenzie, I.R.2
Pickering-Brown, S.M.3
Gass, J.4
Rademakers, R.5
Lindholm, C.6
Snowden, J.7
Adamson, J.8
Sadovnick, A.D.9
Rollinson, S.10
Cannon, A.11
Dwosh, E.12
Neary, D.13
Melquist, S.14
Richardson, A.15
Dickson, D.16
Berger, Z.17
Eriksen, J.18
Robinson, T.19
Zehr, C.20
Dickey, C.A.21
Crook, R.22
McGowan, E.23
Mann, D.24
Boeve, B.25
Feldman, H.26
Hutton, M.27
more..
-
2
-
-
33746910649
-
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
-
DOI 10.1038/nature05017, PII NATURE05017
-
Cruts M, Gijselinck I, van der Zee J, et al: Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 2006; 442: 920-924. (Pubitemid 44285947)
-
(2006)
Nature
, vol.442
, Issue.7105
, pp. 920-924
-
-
Cruts, M.1
Gijselinck, I.2
Van Der Zee, J.3
Engelborghs, S.4
Wils, H.5
Pirici, D.6
Rademakers, R.7
Vandenberghe, R.8
Dermaut, B.9
Martin, J.-J.10
Van Duijn, C.11
Peeters, K.12
Sciot, R.13
Santens, P.14
De Pooter, T.15
Mattheijssens, M.16
Van Den Broeck, M.17
Cuijt, I.18
Vennekens, K.19
De Deyn, P.P.20
Kumar-Singh, S.21
Van Broeckhoven, C.22
more..
-
3
-
-
56049083010
-
Common variation in the miR-659 bindingsite of GRN is a major risk factor for TDP43-positive frontotemporal dementia
-
Rademakers R, Eriksen JL, Baker M, et al: Common variation in the miR-659 bindingsite of GRN is a major risk factor for TDP43-positive frontotemporal dementia. Hum Mol Genet 2008; 17: 3631-3642.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 3631-3642
-
-
Rademakers, R.1
Eriksen, J.L.2
Baker, M.3
-
4
-
-
70449564311
-
Variation at GRN-3′ UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population
-
Simón-Sànchez J, Seelaar H, Bochdanvoits Z, Deeg DJH, van Swieten JC, Heutink P: Variation at GRN-3′ UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population. PLoS ONE 2009; 4:e7494.
-
(2009)
PLoS ONE
, vol.4
-
-
Simón-Sànchez, J.1
Seelaar, H.2
Bochdanvoits, Z.3
Djh, D.4
Van Swieten, J.C.5
Heutink, P.6
-
5
-
-
75149192605
-
Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease
-
Fenoglio C, Galimberti D, Cortini F, et al: rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease. J Alzheimers Dis 2009; 18: 603-612.
-
(2009)
J Alzheimers Dis
, vol.18
, pp. 603-612
-
-
Fenoglio, C.1
Galimberti, D.2
Cortini, F.3
-
6
-
-
52449110477
-
Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease
-
Brouwers N, Sleegers K, Engelborghs S, et al: Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease. Neurology 2008; 71: 656-664.
-
(2008)
Neurology
, vol.71
, pp. 656-664
-
-
Brouwers, N.1
Sleegers, K.2
Engelborghs, S.3
-
7
-
-
67649435606
-
An association study between granulin gene polymorphisms and Alzheimer's disease in Finnish population
-
Viswanathan J, Mäkinen P, Helisalmi S, et al: An association study between granulin gene polymorphisms and Alzheimer's disease in Finnish population. Am J Med Genet Part A 2008; 150B:747-750.
-
(2008)
Am J Med Genet Part A
, vol.150 B
, pp. 747-750
-
-
Viswanathan, J.1
Mäkinen, P.2
Helisalmi, S.3
-
8
-
-
60149090387
-
Hardy-Weinberg equilibrium testing of biological ascertainment for mendelian randomization studies
-
Rodriguez S, Gaunt TR, Day INM: Hardy-Weinberg equilibrium testing of biological ascertainment for mendelian randomization studies. Am J Epidemol 2009; 169: 505-514.
-
(2009)
Am J Epidemol
, vol.169
, pp. 505-514
-
-
Rodriguez, S.1
Gaunt, T.R.2
Day, I.N.M.3
-
9
-
-
1842859051
-
Power and sample size calculations for case-control genetic association tests when errors are present: Application to single nucleotide polymorphisms
-
DOI 10.1159/000066696
-
Gordon D, Finch SJ, Nothnagel M, Ott J: Power and sample size calculations for casecontrol genetic association tests when errors present: application to single nucleotide polymorphisms. Hum Hered 2002; 54: 22-33. (Pubitemid 35404246)
-
(2002)
Human Heredity
, vol.54
, Issue.1
, pp. 22-33
-
-
Gordon, D.1
Finch, S.J.2
Nothnagel, M.3
Ott, J.4
-
10
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
DOI 10.1093/bioinformatics/bth457
-
Barrett JC, Fry B, Maller J, Daly MJ: Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 2005; 21: 263-265. (Pubitemid 40202029)
-
(2005)
Bioinformatics
, vol.21
, Issue.2
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
11
-
-
70349091081
-
Progranulin expression correlates with densecore amyloid plaque burden in Alzheimer's disease mouse models
-
Pereson S, Wils H, Kleinberger G, et al: Progranulin expression correlates with densecore amyloid plaque burden in Alzheimer's disease mouse models. J Pathol 2009; 219: 173-181.
-
(2009)
J Pathol
, vol.219
, pp. 173-181
-
-
Pereson, S.1
Wils, H.2
Kleinberger, G.3
-
12
-
-
77449111778
-
Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly
-
Dickson DW, Baker M, Rademakers R: Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly. Neurodegener Dis 2010; 7: 170-174.
-
(2010)
Neurodegener Dis
, vol.7
, pp. 170-174
-
-
Dickson, D.W.1
Baker, M.2
Rademakers, R.3
-
13
-
-
71249139954
-
Different models and single-nucleotide polymorphisms signal the simulated weak gene-gene interaction for a quantitative trait using haplotype-based and mixed models testing
-
Kovac IP, Dubé MP: Different models and single-nucleotide polymorphisms signal the simulated weak gene-gene interaction for a quantitative trait using haplotype-based and mixed models testing. BMC Proc 2009; 3(suppl 7):S77.
-
(2009)
BMC Proc
, vol.3
, Issue.SUPPL. 7
-
-
Kovac, I.P.1
Dubé, M.P.2
|