-
1
-
-
25844524877
-
Neurodegenerative diseases: an overview of environmental risk factors
-
COI: 1:CAS:528:DC%2BD2MXht1agu7nJ, PID: 16140637
-
Brown RC, Lockwood AH, Sonawane BR (2005) Neurodegenerative diseases: an overview of environmental risk factors. Environ Health Perspect 113:1250–1256
-
(2005)
Environ Health Perspect
, vol.113
, pp. 1250-1256
-
-
Brown, R.C.1
Lockwood, A.H.2
Sonawane, B.R.3
-
2
-
-
84856200093
-
Towards unveiling the genetics of neurodegenerative diseases
-
PID: 22266890
-
Lill CM, Bertram L (2011) Towards unveiling the genetics of neurodegenerative diseases. Semin Neurol 31:531–541
-
(2011)
Semin Neurol
, vol.31
, pp. 531-541
-
-
Lill, C.M.1
Bertram, L.2
-
3
-
-
62149141328
-
Rethinking ALS: the FUS about TDP-43
-
COI: 1:CAS:528:DC%2BD1MXltFSntr0%3D, PID: 19303844
-
Lagier-Tourenne C, Cleveland DW (2009) Rethinking ALS: the FUS about TDP-43. Cell 136:1001–1004
-
(2009)
Cell
, vol.136
, pp. 1001-1004
-
-
Lagier-Tourenne, C.1
Cleveland, D.W.2
-
4
-
-
70449365115
-
The heritability and genetics of frontotemporal lobar degeneration
-
COI: 1:CAS:528:DC%2BD1MXhtlCmsrjP, PID: 19884572
-
Rohrer JD, Guerreiro R, Vandrovcova J, Uphill J, Reiman D et al (2009) The heritability and genetics of frontotemporal lobar degeneration. Neurology 73:1451–1456
-
(2009)
Neurology
, vol.73
, pp. 1451-1456
-
-
Rohrer, J.D.1
Guerreiro, R.2
Vandrovcova, J.3
Uphill, J.4
Reiman, D.5
-
5
-
-
33746919083
-
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
-
COI: 1:CAS:528:DC%2BD28XosVOgurc%3D, PID: 16862116
-
Baker M, Mackenzie IR, Pickering-Brown SM, Gass J, Rademakers R et al (2006) Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 442:916–919
-
(2006)
Nature
, vol.442
, pp. 916-919
-
-
Baker, M.1
Mackenzie, I.R.2
Pickering-Brown, S.M.3
Gass, J.4
Rademakers, R.5
-
6
-
-
33746910649
-
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
-
COI: 1:CAS:528:DC%2BD28XosVOgu74%3D, PID: 16862115
-
Cruts M, Gijselinck I, van der Zee J, Engelborghs S, Wils H et al (2006) Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 442:920–924
-
(2006)
Nature
, vol.442
, pp. 920-924
-
-
Cruts, M.1
Gijselinck, I.2
van der Zee, J.3
Engelborghs, S.4
Wils, H.5
-
7
-
-
34347245619
-
Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes
-
COI: 1:STN:280:DC%2BD2szlsFekuw%3D%3D, PID: 17371905
-
Schymick JC, Yang Y, Andersen PM, Vonsattel JP, Greenway M et al (2007) Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes. J Neurol Neurosurg Psychiatry 78:754–756
-
(2007)
J Neurol Neurosurg Psychiatry
, vol.78
, pp. 754-756
-
-
Schymick, J.C.1
Yang, Y.2
Andersen, P.M.3
Vonsattel, J.P.4
Greenway, M.5
-
8
-
-
35348872039
-
Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family
-
PID: 17923627
-
Brouwers N, Nuytemans K, van der Zee J, Gijselinck I, Engelborghs S et al (2007) Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family. Arch Neurol 64:1436–1446
-
(2007)
Arch Neurol
, vol.64
, pp. 1436-1446
-
-
Brouwers, N.1
Nuytemans, K.2
van der Zee, J.3
Gijselinck, I.4
Engelborghs, S.5
-
9
-
-
80855130704
-
Potential mechanisms of progranulin-deficient FTLD
-
COI: 1:CAS:528:DC%2BC3MXhsVWit7bO, PID: 21892758
-
Ward ME, Miller BL (2011) Potential mechanisms of progranulin-deficient FTLD. J Mol Neurosci 45:574–582
-
(2011)
J Mol Neurosci
, vol.45
, pp. 574-582
-
-
Ward, M.E.1
Miller, B.L.2
-
10
-
-
84878797585
-
Progranulin mutations as risk factors for Alzheimer disease
-
PID: 23609919
-
Perry DC, Lehmann M, Yokoyama JS, Karydas A, Lee JJ et al (2013) Progranulin mutations as risk factors for Alzheimer disease. JAMA Neurol 70:774–778
-
(2013)
JAMA Neurol
, vol.70
, pp. 774-778
-
-
Perry, D.C.1
Lehmann, M.2
Yokoyama, J.S.3
Karydas, A.4
Lee, J.J.5
-
11
-
-
84879092067
-
Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BC3sXnt1Wmsbk%3D, PID: 23596077
-
Cannon A, Fujioka S, Rutherford NJ, Ferman TJ, Broderick DF et al (2013) Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis. Neurology 80:1771–1777
-
(2013)
Neurology
, vol.80
, pp. 1771-1777
-
-
Cannon, A.1
Fujioka, S.2
Rutherford, N.J.3
Ferman, T.J.4
Broderick, D.F.5
-
12
-
-
45049084534
-
Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease
-
COI: 1:CAS:528:DC%2BD1cXnsF2lt7o%3D, PID: 18479928
-
Rovelet-Lecrux A, Deramecourt V, Legallic S, Maurage CA, Le Ber I et al (2008) Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease. Neurobiol Dis 31:41–45
-
(2008)
Neurobiol Dis
, vol.31
, pp. 41-45
-
-
Rovelet-Lecrux, A.1
Deramecourt, V.2
Legallic, S.3
Maurage, C.A.4
Le Ber, I.5
-
13
-
-
33749568019
-
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
-
COI: 1:CAS:528:DC%2BD28XhtVOgt77J, PID: 16950801
-
Gass J, Cannon A, Mackenzie IR, Boeve B, Baker M et al (2006) Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. Hum Mol Genet 15:2988–3001
-
(2006)
Hum Mol Genet
, vol.15
, pp. 2988-3001
-
-
Gass, J.1
Cannon, A.2
Mackenzie, I.R.3
Boeve, B.4
Baker, M.5
-
14
-
-
41249089087
-
Loss of progranulin function in frontotemporal lobar degeneration
-
COI: 1:CAS:528:DC%2BD1cXktVKhtbs%3D, PID: 18328591
-
Cruts M, Van Broeckhoven C (2008) Loss of progranulin function in frontotemporal lobar degeneration. Trends Genet 24:186–194
-
(2008)
Trends Genet
, vol.24
, pp. 186-194
-
-
Cruts, M.1
Van Broeckhoven, C.2
-
15
-
-
56049083010
-
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia
-
COI: 1:CAS:528:DC%2BD1cXhtlGis7%2FM, PID: 18723524
-
Rademakers R, Eriksen JL, Baker M, Robinson T, Ahmed Z et al (2008) Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia. Hum Mol Genet 17:3631–3642
-
(2008)
Hum Mol Genet
, vol.17
, pp. 3631-3642
-
-
Rademakers, R.1
Eriksen, J.L.2
Baker, M.3
Robinson, T.4
Ahmed, Z.5
-
16
-
-
84872463000
-
Association between GRN rs5848 polymorphism and Parkinson’s disease in Taiwanese population
-
COI: 1:CAS:528:DC%2BC3sXhs1ylsL4%3D, PID: 23342160
-
Chang KH, Chen CM, Chen YC, Hsiao YC, Huang CC et al (2013) Association between GRN rs5848 polymorphism and Parkinson’s disease in Taiwanese population. PLoS One 8:e54448
-
(2013)
PLoS One
, vol.8
, pp. e54448
-
-
Chang, K.H.1
Chen, C.M.2
Chen, Y.C.3
Hsiao, Y.C.4
Huang, C.C.5
-
17
-
-
79953058497
-
No association of PGRN 3′UTR rs5848 in frontotemporal lobar degeneration
-
COI: 1:CAS:528:DC%2BC3MXktFKgu7c%3D, PID: 19446372
-
Rollinson S, Rohrer JD, van der Zee J, Sleegers K, Mead S et al (2011) No association of PGRN 3′UTR rs5848 in frontotemporal lobar degeneration. Neurobiol Aging 32:754–755
-
(2011)
Neurobiol Aging
, vol.32
, pp. 754-755
-
-
Rollinson, S.1
Rohrer, J.D.2
van der Zee, J.3
Sleegers, K.4
Mead, S.5
-
18
-
-
75149192605
-
Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer’s disease
-
COI: 1:CAS:528:DC%2BD1MXhsFCitLnI, PID: 19625741
-
Fenoglio C, Galimberti D, Cortini F, Kauwe JS, Cruchaga C et al (2009) Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer’s disease. J Alzheimers Dis 18:603–612
-
(2009)
J Alzheimers Dis
, vol.18
, pp. 603-612
-
-
Fenoglio, C.1
Galimberti, D.2
Cortini, F.3
Kauwe, J.S.4
Cruchaga, C.5
-
19
-
-
67651250941
-
GRN 3′UTR+ 78 C>T is not associated with risk for Parkinson’s disease
-
COI: 1:STN:280:DC%2BD1Mrgsl2itw%3D%3D, PID: 19473366
-
Jasinska-Myga B, Wider C, Opala G, Krygowska-Wajs A, Barcikowska M et al (2009) GRN 3′UTR+ 78 C>T is not associated with risk for Parkinson’s disease. Eur J Neurol 16:909–911
-
(2009)
Eur J Neurol
, vol.16
, pp. 909-911
-
-
Jasinska-Myga, B.1
Wider, C.2
Opala, G.3
Krygowska-Wajs, A.4
Barcikowska, M.5
-
20
-
-
79955952980
-
No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort
-
PID: 19632744
-
Del Bo R, Corti S, Santoro D, Ghione I, Fenoglio C et al (2011) No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort. Neurobiol Aging 32:1157–1158
-
(2011)
Neurobiol Aging
, vol.32
, pp. 1157-1158
-
-
Del Bo, R.1
Corti, S.2
Santoro, D.3
Ghione, I.4
Fenoglio, C.5
-
21
-
-
28344452460
-
Systematic evaluation and comparison of statistical tests for publication bias
-
PID: 16276033
-
Hayashino Y, Noguchi Y, Fukui T (2005) Systematic evaluation and comparison of statistical tests for publication bias. J Epidemiol 15:235–243
-
(2005)
J Epidemiol
, vol.15
, pp. 235-243
-
-
Hayashino, Y.1
Noguchi, Y.2
Fukui, T.3
-
22
-
-
0028659004
-
Operating characteristics of a rank correlation test for publication bias
-
COI: 1:STN:280:DyaK2Mzgs1GrtQ%3D%3D, PID: 7786990
-
Begg CB, Mazumdar M (1994) Operating characteristics of a rank correlation test for publication bias. Biometrics 50:1088–1101
-
(1994)
Biometrics
, vol.50
, pp. 1088-1101
-
-
Begg, C.B.1
Mazumdar, M.2
-
23
-
-
84977788952
-
Controlling the false discovery rate: a practical and powerful approach to multiple testing
-
Benjamini Y, Hochberg Y (1995) Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc Ser B57:289–300
-
(1995)
J R Stat Soc Ser
, vol.B57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
24
-
-
79955830791
-
rs5848 variant of progranulin gene is a risk of Alzheimer’s disease in the Taiwanese population
-
COI: 1:CAS:528:DC%2BC3MXlslKmtrk%3D, PID: 21212639
-
Lee MJ, Chen TF, Cheng TW, Chiu MJ (2011) rs5848 variant of progranulin gene is a risk of Alzheimer’s disease in the Taiwanese population. Neurodegener Dis 8:216–220
-
(2011)
Neurodegener Dis
, vol.8
, pp. 216-220
-
-
Lee, M.J.1
Chen, T.F.2
Cheng, T.W.3
Chiu, M.J.4
-
25
-
-
75149197665
-
GRN variability contributes to sporadic frontotemporal lobar degeneration
-
PID: 20061636
-
Galimberti D, Fenoglio C, Cortini F, Serpente M, Venturelli E et al (2010) GRN variability contributes to sporadic frontotemporal lobar degeneration. J Alzheimers Dis 19:171–177
-
(2010)
J Alzheimers Dis
, vol.19
, pp. 171-177
-
-
Galimberti, D.1
Fenoglio, C.2
Cortini, F.3
Serpente, M.4
Venturelli, E.5
-
26
-
-
42049120518
-
Progranulin genetic variability contributes to amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BD1cXosFSku70%3D, PID: 18184915
-
Sleegers K, Brouwers N, Maurer-Stroh S, van Es MA, Van Damme P et al (2008) Progranulin genetic variability contributes to amyotrophic lateral sclerosis. Neurology 71:253–259
-
(2008)
Neurology
, vol.71
, pp. 253-259
-
-
Sleegers, K.1
Brouwers, N.2
Maurer-Stroh, S.3
van Es, M.A.4
Van Damme, P.5
-
27
-
-
55249086715
-
Progranulin variability has no major role in Parkinson disease genetic etiology
-
COI: 1:STN:280:DC%2BD1cnksF2ksw%3D%3D, PID: 18838661
-
Nuytemans K, Pals P, Sleegers K, Engelborghs S, Corsmit E et al (2008) Progranulin variability has no major role in Parkinson disease genetic etiology. Neurology 71:1147–1151
-
(2008)
Neurology
, vol.71
, pp. 1147-1151
-
-
Nuytemans, K.1
Pals, P.2
Sleegers, K.3
Engelborghs, S.4
Corsmit, E.5
-
28
-
-
84872442945
-
GRN variant rs5848 reduces plasma and brain levels of granulin in Alzheimer’s disease patients
-
COI: 1:CAS:528:DC%2BC38XhslGrurnM, PID: 22890097
-
Kamalainen A, Viswanathan J, Natunen T, Helisalmi S, Kauppinen T et al (2013) GRN variant rs5848 reduces plasma and brain levels of granulin in Alzheimer’s disease patients. J Alzheimers Dis 33:23–27
-
(2013)
J Alzheimers Dis
, vol.33
, pp. 23-27
-
-
Kamalainen, A.1
Viswanathan, J.2
Natunen, T.3
Helisalmi, S.4
Kauppinen, T.5
-
29
-
-
67649435606
-
An association study between granulin gene polymorphisms and Alzheimer’s disease in Finnish population
-
COI: 1:CAS:528:DC%2BD1MXovFaqtro%3D, PID: 19016491
-
Viswanathan J, Makinen P, Helisalmi S, Haapasalo A, Soininen H et al (2009) An association study between granulin gene polymorphisms and Alzheimer’s disease in Finnish population. Am J Med Genet B Neuropsychiatr Genet 150B:747–750
-
(2009)
Am J Med Genet B Neuropsychiatr Genet
, vol.150B
, pp. 747-750
-
-
Viswanathan, J.1
Makinen, P.2
Helisalmi, S.3
Haapasalo, A.4
Soininen, H.5
-
30
-
-
70449564311
-
Variation at GRN 3′-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population
-
PID: 19847305
-
Simon-Sanchez J, Seelaar H, Bochdanovits Z, Deeg DJ, van Swieten JC et al (2009) Variation at GRN 3′-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population. PLoS One 4:e7494
-
(2009)
PLoS One
, vol.4
, pp. e7494
-
-
Simon-Sanchez, J.1
Seelaar, H.2
Bochdanovits, Z.3
Deeg, D.J.4
van Swieten, J.C.5
-
31
-
-
44949215794
-
Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BD1cXnsF2ltro%3D, PID: 17383054
-
Xiao S, Sato C, Kawarai T, Goodall EF, Pall HS et al (2008) Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis. Neurobiol Aging 29:1279–1282
-
(2008)
Neurobiol Aging
, vol.29
, pp. 1279-1282
-
-
Xiao, S.1
Sato, C.2
Kawarai, T.3
Goodall, E.F.4
Pall, H.S.5
-
32
-
-
52449110477
-
Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease
-
COI: 1:CAS:528:DC%2BD1cXpvFygtb8%3D, PID: 18565828
-
Brouwers N, Sleegers K, Engelborghs S, Maurer-Stroh S, Gijselinck I et al (2008) Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease. Neurology 71:656–664
-
(2008)
Neurology
, vol.71
, pp. 656-664
-
-
Brouwers, N.1
Sleegers, K.2
Engelborghs, S.3
Maurer-Stroh, S.4
Gijselinck, I.5
-
33
-
-
34247868937
-
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia
-
PID: 17345602
-
van der Zee J, Le Ber I, Maurer-Stroh S, Engelborghs S, Gijselinck I et al (2007) Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia. Hum Mutat 28:416
-
(2007)
Hum Mutat
, vol.28
, pp. 416
-
-
van der Zee, J.1
Le Ber, I.2
Maurer-Stroh, S.3
Engelborghs, S.4
Gijselinck, I.5
-
34
-
-
0031839545
-
Risk estimates of dementia by apolipoprotein E genotypes from a population-based incidence study: the Rotterdam Study
-
COI: 1:STN:280:DyaK1czktFCmtg%3D%3D, PID: 9678314
-
Slooter AJ, Cruts M, Kalmijn S, Hofman A, Breteler MM et al (1998) Risk estimates of dementia by apolipoprotein E genotypes from a population-based incidence study: the Rotterdam Study. Arch Neurol 55:964–968
-
(1998)
Arch Neurol
, vol.55
, pp. 964-968
-
-
Slooter, A.J.1
Cruts, M.2
Kalmijn, S.3
Hofman, A.4
Breteler, M.M.5
-
35
-
-
70349091081
-
Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models
-
COI: 1:CAS:528:DC%2BD1MXhtlSksb3M, PID: 19557827
-
Pereson S, Wils H, Kleinberger G, McGowan E, Vandewoestyne M et al (2009) Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models. J Pathol 219:173–181
-
(2009)
J Pathol
, vol.219
, pp. 173-181
-
-
Pereson, S.1
Wils, H.2
Kleinberger, G.3
McGowan, E.4
Vandewoestyne, M.5
-
36
-
-
77449111778
-
Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly
-
COI: 1:CAS:528:DC%2BC3cXks1KjtLg%3D, PID: 20197700
-
Dickson DW, Baker M, Rademakers R (2010) Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly. Neurodegener Dis 7:170–174
-
(2010)
Neurodegener Dis
, vol.7
, pp. 170-174
-
-
Dickson, D.W.1
Baker, M.2
Rademakers, R.3
-
37
-
-
0242320195
-
Progranulin (granulin-epithelin precursor, PC-cell-derived growth factor, acrogranin) mediates tissue repair and tumorigenesis
-
COI: 1:CAS:528:DC%2BD3sXotVars7o%3D
-
He Z, Bateman A (2003) Progranulin (granulin-epithelin precursor, PC-cell-derived growth factor, acrogranin) mediates tissue repair and tumorigenesis. J Mol Med (Berl) 81:600–612
-
(2003)
J Mol Med (Berl)
, vol.81
, pp. 600-612
-
-
He, Z.1
Bateman, A.2
-
38
-
-
70549109118
-
The granulin gene family: from cancer to dementia
-
COI: 1:CAS:528:DC%2BD1MXhsFSqurnP, PID: 19795409
-
Bateman A, Bennett HP (2009) The granulin gene family: from cancer to dementia. Bioessays 31:1245–1254
-
(2009)
Bioessays
, vol.31
, pp. 1245-1254
-
-
Bateman, A.1
Bennett, H.P.2
-
39
-
-
84860859794
-
Progranulin: an emerging target for FTLD therapies
-
COI: 1:CAS:528:DC%2BC38Xot1yntbc%3D, PID: 22338605
-
Gass J, Prudencio M, Stetler C, Petrucelli L (2012) Progranulin: an emerging target for FTLD therapies. Brain Res 1462:118–128
-
(2012)
Brain Res
, vol.1462
, pp. 118-128
-
-
Gass, J.1
Prudencio, M.2
Stetler, C.3
Petrucelli, L.4
|