-
1
-
-
84872088087
-
Variant of TREM2 associated with the risk of Alzheimer's disease
-
COI: 1:CAS:528:DC%2BC3sXovVyiug%3D%3D, PID: 23150908
-
Jonsson T, Stefansson H, Steinberg S, Jonsdottir I, Jonsson PV, Snaedal J, Bjornsson S, Huttenlocher J et al (2013) Variant of TREM2 associated with the risk of Alzheimer's disease. N Engl J Med 368:107–116
-
(2013)
N Engl J Med
, vol.368
, pp. 107-116
-
-
Jonsson, T.1
Stefansson, H.2
Steinberg, S.3
Jonsdottir, I.4
Jonsson, P.V.5
Snaedal, J.6
Bjornsson, S.7
Huttenlocher, J.8
-
2
-
-
84952631227
-
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease
-
Lill CM, Rengmark A, Pihlstrom L, Fogh I, Shatunov A, Sleiman PM, Wang LS, Liu T et al (2015) The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease. Alzheimers Dement
-
(2015)
Alzheimers Dement
-
-
Lill, C.M.1
Rengmark, A.2
Pihlstrom, L.3
Fogh, I.4
Shatunov, A.5
Sleiman, P.M.6
Wang, L.S.7
Liu, T.8
-
3
-
-
84879113935
-
TREM2 in neurodegeneration: evidence for association of the p.R47h variant with frontotemporal dementia and Parkinson's disease
-
COI: 1:CAS:528:DC%2BC3sXhtVyhtLfF, PID: 23800361
-
Rayaprolu S, Mullen B, Baker M, Lynch T, Finger E, Seeley WW, Hatanpaa KJ, Lomen-Hoerth C et al (2013) TREM2 in neurodegeneration: evidence for association of the p.R47h variant with frontotemporal dementia and Parkinson's disease. Mol Neurodegener 8:19
-
(2013)
Mol Neurodegener
, vol.8
, pp. 19
-
-
Rayaprolu, S.1
Mullen, B.2
Baker, M.3
Lynch, T.4
Finger, E.5
Seeley, W.W.6
Hatanpaa, K.J.7
Lomen-Hoerth, C.8
-
4
-
-
84885821412
-
TREM2 and neurodegenerative disease
-
PID: 24131187
-
Benitez BA, Cruchaga C (2013) TREM2 and neurodegenerative disease. N Engl J Med 369:1567–1568
-
(2013)
N Engl J Med
, vol.369
, pp. 1567-1568
-
-
Benitez, B.A.1
Cruchaga, C.2
-
5
-
-
84885828745
-
TREM2 and neurodegenerative disease
-
COI: 1:CAS:528:DC%2BC3sXhs1CgsbjE, PID: 24131183
-
Jonsson T, Stefansson K (2013) TREM2 and neurodegenerative disease. N Engl J Med 369:1568–1569
-
(2013)
N Engl J Med
, vol.369
, pp. 1568-1569
-
-
Jonsson, T.1
Stefansson, K.2
-
6
-
-
11844302840
-
Treating individuals 2. Subgroup analysis in randomised controlled trials: importance, indications, and interpretation
-
PID: 15639301
-
Rothwell PM (2005) Treating individuals 2. Subgroup analysis in randomised controlled trials: importance, indications, and interpretation. Lancet 365:176–186
-
(2005)
Lancet
, vol.365
, pp. 176-186
-
-
Rothwell, P.M.1
-
7
-
-
84896417597
-
Analyzing large-scale samples confirms the association between the abca7 rs3764650 polymorphism and alzheimer's disease susceptibility
-
Liu G, Li F, Zhang S, Jiang Y, Ma G, Shang H, Liu J, Feng R et al. Analyzing large-scale samples confirms the association between the abca7 rs3764650 polymorphism and alzheimer's disease susceptibility. Mol Neurobiol 2014
-
(2014)
Mol Neurobiol
-
-
Liu, G.1
Li, F.2
Zhang, S.3
Jiang, Y.4
Ma, G.5
Shang, H.6
Liu, J.7
Feng, R.8
-
8
-
-
85018091239
-
Analyzing 54,936 samples supports the association between cd2ap rs9349407 polymorphism and Alzheimer's disease susceptibility
-
Chen H, Wu G, Jiang Y, Feng R, Liao M, Zhang L, Ma G, Chen Z et al (2014) Analyzing 54,936 samples supports the association between cd2ap rs9349407 polymorphism and Alzheimer's disease susceptibility. Mol Neurobiol
-
(2014)
Mol Neurobiol
-
-
Chen, H.1
Wu, G.2
Jiang, Y.3
Feng, R.4
Liao, M.5
Zhang, L.6
Ma, G.7
Chen, Z.8
-
9
-
-
84877762031
-
PICALM gene rs3851179 polymorphism contributes to Alzheimer's disease in an Asian population
-
COI: 1:CAS:528:DC%2BC3sXnsVWmt7g%3D, PID: 23572399
-
Liu G, Zhang S, Cai Z, Ma G, Zhang L, Jiang Y, Feng R, Liao M et al (2013) PICALM gene rs3851179 polymorphism contributes to Alzheimer's disease in an Asian population. Neuromolecular Med 15:384–388
-
(2013)
Neuromolecular Med
, vol.15
, pp. 384-388
-
-
Liu, G.1
Zhang, S.2
Cai, Z.3
Ma, G.4
Zhang, L.5
Jiang, Y.6
Feng, R.7
Liao, M.8
-
11
-
-
0030922816
-
Bias in meta-analysis detected by a simple, graphical test
-
COI: 1:STN:280:DyaK2svls1KjtA%3D%3D, PID: 9310563
-
Egger M, Davey Smith G, Schneider M, Minder C (1997) Bias in meta-analysis detected by a simple, graphical test. BMJ 315:629–634
-
(1997)
BMJ
, vol.315
, pp. 629-634
-
-
Egger, M.1
Davey Smith, G.2
Schneider, M.3
Minder, C.4
-
12
-
-
0034823867
-
Funnel plots for detecting bias in meta-analysis: guidelines on choice of axis
-
COI: 1:STN:280:DC%2BD3MrivFWisA%3D%3D, PID: 11576817
-
Sterne JA, Egger M (2001) Funnel plots for detecting bias in meta-analysis: guidelines on choice of axis. J Clin Epidemiol 54:1046–1055
-
(2001)
J Clin Epidemiol
, vol.54
, pp. 1046-1055
-
-
Sterne, J.A.1
Egger, M.2
-
13
-
-
0036208313
-
Asymmetric funnel plots and publication bias in meta-analyses of diagnostic accuracy
-
PID: 11914301
-
Song F, Khan KS, Dinnes J, Sutton AJ (2002) Asymmetric funnel plots and publication bias in meta-analyses of diagnostic accuracy. Int J Epidemiol 31:88–95
-
(2002)
Int J Epidemiol
, vol.31
, pp. 88-95
-
-
Song, F.1
Khan, K.S.2
Dinnes, J.3
Sutton, A.J.4
-
14
-
-
84939599004
-
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
-
COI: 1:CAS:528:DC%2BC2cXht1ait7%2FP, PID: 25064009
-
Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG, Saad M, DeStefano AL, Kara E et al (2014) Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nat Genet 46:989–993
-
(2014)
Nat Genet
, vol.46
, pp. 989-993
-
-
Nalls, M.A.1
Pankratz, N.2
Lill, C.M.3
Do, C.B.4
Hernandez, D.G.5
Saad, M.6
DeStefano, A.L.7
Kara, E.8
-
15
-
-
84859339977
-
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: the PDGene database
-
COI: 1:CAS:528:DC%2BC38Xkslagsbg%3D, PID: 22438815
-
Lill CM, Roehr JT, McQueen MB, Kavvoura FK, Bagade S, Schjeide BM, Schjeide LM, Meissner E et al (2012) Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: the PDGene database. PLoS Genet 8:e1002548
-
(2012)
PLoS Genet
, vol.8
, pp. 1002548
-
-
Lill, C.M.1
Roehr, J.T.2
McQueen, M.B.3
Kavvoura, F.K.4
Bagade, S.5
Schjeide, B.M.6
Schjeide, L.M.7
Meissner, E.8
-
16
-
-
84864066707
-
Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants
-
COI: 1:CAS:528:DC%2BC38XovFSqs7s%3D, PID: 22685416
-
Zou F, Chai HS, Younkin CS, Allen M, Crook J, Pankratz VS, Carrasquillo MM, Rowley CN et al (2012) Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants. PLoS Genet 8:e1002707
-
(2012)
PLoS Genet
, vol.8
, pp. 1002707
-
-
Zou, F.1
Chai, H.S.2
Younkin, C.S.3
Allen, M.4
Crook, J.5
Pankratz, V.S.6
Carrasquillo, M.M.7
Rowley, C.N.8
-
17
-
-
84864026404
-
Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation
-
COI: 1:CAS:528:DC%2BC38XpvVWrtbc%3D, PID: 22761592
-
Dumitriu A, Latourelle JC, Hadzi TC, Pankratz N, Garza D, Miller JP, Vance JM, Foroud T et al (2012) Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation. PLoS Genet 8:e1002794
-
(2012)
PLoS Genet
, vol.8
, pp. 1002794
-
-
Dumitriu, A.1
Latourelle, J.C.2
Hadzi, T.C.3
Pankratz, N.4
Garza, D.5
Miller, J.P.6
Vance, J.M.7
Foroud, T.8
-
18
-
-
84903366979
-
Missense variant in TREML2 protects against Alzheimer's disease
-
Benitez BA, Jin SC, Guerreiro R, Graham R, Lord J, Harold D, Sims R, Lambert JC et al (2014) Missense variant in TREML2 protects against Alzheimer's disease. Neurobiol Aging 35:1510 e1519–1526
-
(2014)
Neurobiol Aging
, vol.35
, pp. 1510 e1519-1526
-
-
Benitez, B.A.1
Jin, S.C.2
Guerreiro, R.3
Graham, R.4
Lord, J.5
Harold, D.6
Sims, R.7
Lambert, J.C.8
-
19
-
-
84923666918
-
A TREM1 variant alters the accumulation of Alzheimer-related amyloid pathology
-
COI: 1:CAS:528:DC%2BC2MXjtlSltLw%3D, PID: 25545807
-
Replogle JM, Chan G, White CC, Raj T, Winn PA, Evans DA, Sperling RA, Chibnik LB et al (2015) A TREM1 variant alters the accumulation of Alzheimer-related amyloid pathology. Ann Neurol 77:469–477
-
(2015)
Ann Neurol
, vol.77
, pp. 469-477
-
-
Replogle, J.M.1
Chan, G.2
White, C.C.3
Raj, T.4
Winn, P.A.5
Evans, D.A.6
Sperling, R.A.7
Chibnik, L.B.8
-
20
-
-
84888317489
-
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
-
COI: 1:CAS:528:DC%2BC3sXhs1yiu7vJ, PID: 24162737
-
Lambert JC, Ibrahim-Verbaas CA, Harold D, Naj AC, Sims R, Bellenguez C, DeStafano AL, Bis JC et al (2013) Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nat Genet 45:1452–1458
-
(2013)
Nat Genet
, vol.45
, pp. 1452-1458
-
-
Lambert, J.C.1
Ibrahim-Verbaas, C.A.2
Harold, D.3
Naj, A.C.4
Sims, R.5
Bellenguez, C.6
DeStafano, A.L.7
Bis, J.C.8
-
21
-
-
84952065620
-
The triggering receptor expressed on myeloid cells 2 (TREM2) is associated with enhanced inflammation, neuropathological lesions and increased risk for Alzheimer's dementia
-
Roussos P, Katsel P, Fam P, Tan W, Purohit DP, Haroutunian V (2014) The triggering receptor expressed on myeloid cells 2 (TREM2) is associated with enhanced inflammation, neuropathological lesions and increased risk for Alzheimer's dementia. Alzheimers Dement
-
(2014)
Alzheimers Dement
-
-
Roussos, P.1
Katsel, P.2
Fam, P.3
Tan, W.4
Purohit, D.P.5
Haroutunian, V.6
-
22
-
-
84979865800
-
Trem2 protein expression changes correlate with Alzheimer's disease neurodegenerative pathologies in post-mortem temporal cortices
-
Lue LF, Schmitz CT, Serrano G, Sue LI, Beach TG, Walker DG (2014) Trem2 protein expression changes correlate with Alzheimer's disease neurodegenerative pathologies in post-mortem temporal cortices. Brain Pathol
-
(2014)
Bra
-
-
Lue, L.F.1
Schmitz, C.T.2
Serrano, G.3
Sue, L.I.4
Beach, T.G.5
Walker, D.G.6
-
23
-
-
84889650344
-
Increased expression of TREM2 in peripheral blood of Alzheimer's disease patients
-
COI: 1:CAS:528:DC%2BC3sXhvVGrs7fP, PID: 24002183
-
Hu N, Tan MS, Yu JT, Sun L, Tan L, Wang YL, Jiang T (2014) Increased expression of TREM2 in peripheral blood of Alzheimer's disease patients. J Alzheimers Dis 38:497–501
-
(2014)
J Alzheimers Dis
, vol.38
, pp. 497-501
-
-
Hu, N.1
Tan, M.S.2
Yu, J.T.3
Sun, L.4
Tan, L.5
Wang, Y.L.6
Jiang, T.7
-
24
-
-
84937468720
-
Changes in the expression of genes related to neuroinflammation over the course of sporadic Alzheimer's disease progression: CX3CL1, TREM2, and PPARgamma
-
Strobel S, Grunblatt E, Riederer P, Heinsen H, Arzberger T, Al-Sarraj S, Troakes C, Ferrer I et al (2015) Changes in the expression of genes related to neuroinflammation over the course of sporadic Alzheimer's disease progression: CX3CL1, TREM2, and PPARgamma. J Neural Transm
-
(2015)
J Neural Transm
-
-
Strobel, S.1
Grunblatt, E.2
Riederer, P.3
Heinsen, H.4
Arzberger, T.5
Al-Sarraj, S.6
Troakes, C.7
Ferrer, I.8
-
25
-
-
84897398469
-
TREM2 variant p.R47H as a risk factor for sporadic amyotrophic lateral sclerosis
-
PID: 24535663
-
Cady J, Koval ED, Benitez BA, Zaidman C, Jockel-Balsarotti J, Allred P, Baloh RH, Ravits J et al (2014) TREM2 variant p.R47H as a risk factor for sporadic amyotrophic lateral sclerosis. JAMA Neurol 71:449–453
-
(2014)
JAMA Neurol
, vol.71
, pp. 449-453
-
-
Cady, J.1
Koval, E.D.2
Benitez, B.A.3
Zaidman, C.4
Jockel-Balsarotti, J.5
Allred, P.6
Baloh, R.H.7
Ravits, J.8
-
26
-
-
84976462403
-
Triggering receptor expressed on myeloid cells 2 variants are rare in Parkinson's disease in a Han Chinese cohort
-
Feng SJ, Nie K, Gan R, Huang J, Zhang YW, Wang LM, Zhao JH, Tang HM et al (1780) Triggering receptor expressed on myeloid cells 2 variants are rare in Parkinson's disease in a Han Chinese cohort. Neurobiol Aging 2014(35):e1711–1782
-
(1780)
Neurobiol Aging
, vol.2014
, Issue.35
, pp. 1711-e1782
-
-
Feng, S.J.1
Nie, K.2
Gan, R.3
Huang, J.4
Zhang, Y.W.5
Wang, L.M.6
Zhao, J.H.7
Tang, H.M.8
-
27
-
-
84942502247
-
Assessment of TREM2 rs75932628 association with Parkinson's disease and multiple system atrophy in a Chinese population
-
Chen Y, Chen X, Guo X, Song W, Cao B, Wei Q, Ou R, Zhao B et al (2015) Assessment of TREM2 rs75932628 association with Parkinson's disease and multiple system atrophy in a Chinese population. Neurol Sci
-
(2015)
Neurol Sci
-
-
Chen, Y.1
Chen, X.2
Guo, X.3
Song, W.4
Cao, B.5
Wei, Q.6
Ou, R.7
Zhao, B.8
-
28
-
-
84898618563
-
Rare variant association testing by adaptive combination of p-values
-
PID: 24454922
-
Lin WY, Lou XY, Gao G, Liu N (2014) Rare variant association testing by adaptive combination of p-values. PLoS One 9:e85728
-
(2014)
PLoS One
, vol.9
, pp. 85728
-
-
Lin, W.Y.1
Lou, X.Y.2
Gao, G.3
Liu, N.4
-
29
-
-
84884635946
-
A flexible approach for the analysis of rare variants allowing for a mixture of effects on binary or quantitative traits
-
COI: 1:CAS:528:DC%2BC3sXhsVagtLnO, PID: 23966874
-
Clarke GM, Rivas MA, Morris AP (2013) A flexible approach for the analysis of rare variants allowing for a mixture of effects on binary or quantitative traits. PLoS Genet 9:e1003694
-
(2013)
PLoS Genet
, vol.9
, pp. 1003694
-
-
Clarke, G.M.1
Rivas, M.A.2
Morris, A.P.3
-
30
-
-
80051499915
-
Rare-variant association testing for sequencing data with the sequence kernel association test
-
COI: 1:CAS:528:DC%2BC3MXovF2mtLc%3D, PID: 21737059
-
Wu MC, Lee S, Cai T, Li Y, Boehnke M, Lin X (2011) Rare-variant association testing for sequencing data with the sequence kernel association test. Am J Hum Genet 89:82–93
-
(2011)
Am J Hum Genet
, vol.89
, pp. 82-93
-
-
Wu, M.C.1
Lee, S.2
Cai, T.3
Li, Y.4
Boehnke, M.5
Lin, X.6
-
31
-
-
78650856517
-
GCTA: a tool for genome-wide complex trait analysis
-
COI: 1:CAS:528:DC%2BC3MXktVejtg%3D%3D, PID: 21167468
-
Yang J, Lee SH, Goddard ME, Visscher PM (2011) GCTA: a tool for genome-wide complex trait analysis. Am J Hum Genet 88:76–82
-
(2011)
Am J Hum Genet
, vol.88
, pp. 76-82
-
-
Yang, J.1
Lee, S.H.2
Goddard, M.E.3
Visscher, P.M.4
|