-
1
-
-
33750285158
-
Nongenetic causes of Parkinson's disease
-
Chade A.R., Kasten M., Tanner C.M. Nongenetic causes of Parkinson's disease. J Neural Transm 2006, 70(suppl):147-151.
-
(2006)
J Neural Transm
, vol.70
, Issue.SUPPL.
, pp. 147-151
-
-
Chade, A.R.1
Kasten, M.2
Tanner, C.M.3
-
2
-
-
33749667345
-
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data
-
Fung H.C., Scholz S., Matarin M., Simon-Sanchez J., Hernandez D., Britton A., et al. Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. Lancet Neurol 2006, 5:911-916.
-
(2006)
Lancet Neurol
, vol.5
, pp. 911-916
-
-
Fung, H.C.1
Scholz, S.2
Matarin, M.3
Simon-Sanchez, J.4
Hernandez, D.5
Britton, A.6
-
3
-
-
58149100151
-
Genomewide association study for susceptibility genes contributing to familial Parkinson disease
-
Pankratz N., Wilk J.B., Latourelle J.C., DeStefano A.L., Halter C., Pugh E.W., et al. Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Hum Genet 2009, 124:593-605.
-
(2009)
Hum Genet
, vol.124
, pp. 593-605
-
-
Pankratz, N.1
Wilk, J.B.2
Latourelle, J.C.3
DeStefano, A.L.4
Halter, C.5
Pugh, E.W.6
-
4
-
-
70549084415
-
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
-
Satake W., Nakabayashi Y., Mizuta I., Hirota Y., Ito C., Kubo M., et al. Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nat Genet 2009, 41:1303-1307.
-
(2009)
Nat Genet
, vol.41
, pp. 1303-1307
-
-
Satake, W.1
Nakabayashi, Y.2
Mizuta, I.3
Hirota, Y.4
Ito, C.5
Kubo, M.6
-
5
-
-
70549088602
-
Genome-wide association study reveals genetic risk underlying Parkinson's disease
-
Simon-Sanchez J., Schulte C., Bras J.M., Sharma M., Gibbs J.R., Berg D., et al. Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat Genet 2009, 41:1308-1312.
-
(2009)
Nat Genet
, vol.41
, pp. 1308-1312
-
-
Simon-Sanchez, J.1
Schulte, C.2
Bras, J.M.3
Sharma, M.4
Gibbs, J.R.5
Berg, D.6
-
6
-
-
77951185469
-
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease
-
Edwards T.L., Scott W.K., Almonte C., Burt A., Powell E.H., Beecham G.W., et al. Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. Ann Hum Genet 2010, 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
Beecham, G.W.6
-
7
-
-
77956646167
-
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease
-
Hamza T.H., Zabetian C.P., Tenesa A., Laederach A., Montimurro J., Yearout D., et al. Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. Nat Genet 2010, 42:781-785.
-
(2010)
Nat Genet
, vol.42
, pp. 781-785
-
-
Hamza, T.H.1
Zabetian, C.P.2
Tenesa, A.3
Laederach, A.4
Montimurro, J.5
Yearout, D.6
-
8
-
-
79960981876
-
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population
-
Liu X., Cheng R., Verbitsky M., Kisselev S., Browne A., Mejia-Sanatana H., et al. Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population. BMC Med Genet 2011, 12:104.
-
(2011)
BMC Med Genet
, vol.12
, pp. 104
-
-
Liu, X.1
Cheng, R.2
Verbitsky, M.3
Kisselev, S.4
Browne, A.5
Mejia-Sanatana, H.6
-
9
-
-
78651110778
-
Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population
-
Saad M., Lesage S., Saint-Pierre A., Corvol J.C., Zelenika D., Lambert J.C., et al. Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. Hum Mol Genet 2011, 20:615-627.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 615-627
-
-
Saad, M.1
Lesage, S.2
Saint-Pierre, A.3
Corvol, J.C.4
Zelenika, D.5
Lambert, J.C.6
-
10
-
-
78650550275
-
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
-
Spencer C.C., Plagnol V., Strange A., Gardner M., Paisan-Ruiz C., Band G., et al. Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. Hum Mol Genet 2011, 20:345-353.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 345-353
-
-
Spencer, C.C.1
Plagnol, V.2
Strange, A.3
Gardner, M.4
Paisan-Ruiz, C.5
Band, G.6
-
11
-
-
77953501722
-
The role of neuroinflammation on the pathogenesis of Parkinson's disease
-
Chung Y.C., Ko H.W., Bok E., Park E.S., Huh S.H., Nam J.H., et al. The role of neuroinflammation on the pathogenesis of Parkinson's disease. BMB Rep 2010, 43:225-232.
-
(2010)
BMB Rep
, vol.43
, pp. 225-232
-
-
Chung, Y.C.1
Ko, H.W.2
Bok, E.3
Park, E.S.4
Huh, S.H.5
Nam, J.H.6
-
12
-
-
0026514953
-
Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases
-
Hughes A.J., Daniel S.E., Kilford L., Lees A.J. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. J Neurol Neurosurg Psychiatry 1992, 55:181-184.
-
(1992)
J Neurol Neurosurg Psychiatry
, vol.55
, pp. 181-184
-
-
Hughes, A.J.1
Daniel, S.E.2
Kilford, L.3
Lees, A.J.4
-
13
-
-
0023789193
-
Reactive microglia are positive for HLA-DR in the substantia nigra of Parkinson's and Alzheimer's disease brains
-
McGeer P.L., Itagaki S., Boyes B.E., McGeer E.G. Reactive microglia are positive for HLA-DR in the substantia nigra of Parkinson's and Alzheimer's disease brains. Neurology 1988, 38:1285-1291.
-
(1988)
Neurology
, vol.38
, pp. 1285-1291
-
-
McGeer, P.L.1
Itagaki, S.2
Boyes, B.E.3
McGeer, E.G.4
-
14
-
-
35348966882
-
Neuroinflammatory mechanisms in Parkinson's disease: potential environmental triggers, pathways, and targets for early therapeutic intervention
-
Tansey M.G., McCoy M.K., Frank-Cannon T.C. Neuroinflammatory mechanisms in Parkinson's disease: potential environmental triggers, pathways, and targets for early therapeutic intervention. Exp Neurol 2007, 208:1-25.
-
(2007)
Exp Neurol
, vol.208
, pp. 1-25
-
-
Tansey, M.G.1
McCoy, M.K.2
Frank-Cannon, T.C.3
-
15
-
-
77949899236
-
Anti-inflammatory drugs and risk of Parkinson disease: a meta-analysis
-
Gagne J.J., Power M.C. Anti-inflammatory drugs and risk of Parkinson disease: a meta-analysis. Neurology 2010, 74:995-1002.
-
(2010)
Neurology
, vol.74
, pp. 995-1002
-
-
Gagne, J.J.1
Power, M.C.2
-
16
-
-
77955759020
-
Association of the human leucocyte antigen region with susceptibility to Parkinson's disease
-
Saiki M., Baker A., Williams-Gray C.H., Foltynie T., Goodman R.S., Taylor C.J., et al. Association of the human leucocyte antigen region with susceptibility to Parkinson's disease. J Neurol Neurosurg Psychiatry 2010, 81:890-891.
-
(2010)
J Neurol Neurosurg Psychiatry
, vol.81
, pp. 890-891
-
-
Saiki, M.1
Baker, A.2
Williams-Gray, C.H.3
Foltynie, T.4
Goodman, R.S.5
Taylor, C.J.6
-
17
-
-
0141792772
-
HLA typing and Parkinson's disease
-
Lampe J.B., Gossrau G., Herting B., Kempe A., Sommer U., Fussel M., et al. HLA typing and Parkinson's disease. Eur Neurol 2003, 50:64-68.
-
(2003)
Eur Neurol
, vol.50
, pp. 64-68
-
-
Lampe, J.B.1
Gossrau, G.2
Herting, B.3
Kempe, A.4
Sommer, U.5
Fussel, M.6
-
18
-
-
79951811351
-
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
-
Nalls M.A., Plagnol V., Hernandez D.G., Sharma M., Sheerin U.M., Saad M., et al. Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. Lancet 2011, 377:641-649.
-
(2011)
Lancet
, vol.377
, pp. 641-649
-
-
Nalls, M.A.1
Plagnol, V.2
Hernandez, D.G.3
Sharma, M.4
Sheerin, U.M.5
Saad, M.6
-
19
-
-
77950458649
-
Transcriptome genetics using second generation sequencing in a Caucasian population
-
Montgomery S.B., Sammeth M., Gutierrez-Arcelus M., Lach R.P., Ingle C., Nisbett J., et al. Transcriptome genetics using second generation sequencing in a Caucasian population. Nature 2010, 464:773-777.
-
(2010)
Nature
, vol.464
, pp. 773-777
-
-
Montgomery, S.B.1
Sammeth, M.2
Gutierrez-Arcelus, M.3
Lach, R.P.4
Ingle, C.5
Nisbett, J.6
-
20
-
-
34548738566
-
Population genomics of human gene expression
-
Stranger B.E., Nica A.C., Forrest M.S., Dimas A., Bird C.P., Beazley C., et al. Population genomics of human gene expression. Nat Genet 2007, 39:1217-1224.
-
(2007)
Nat Genet
, vol.39
, pp. 1217-1224
-
-
Stranger, B.E.1
Nica, A.C.2
Forrest, M.S.3
Dimas, A.4
Bird, C.P.5
Beazley, C.6
-
21
-
-
79955113404
-
Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson's disease
-
Mata I.F., Yearout D., Alvarez V., Coto E., de Mena L., Ribacoba R., et al. Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson's disease. Mov Disord 2010, 26:819-823.
-
(2010)
Mov Disord
, vol.26
, pp. 819-823
-
-
Mata, I.F.1
Yearout, D.2
Alvarez, V.3
Coto, E.4
de Mena, L.5
Ribacoba, R.6
-
22
-
-
79956321752
-
Genome-wide association study confirms extant PD risk loci among the Dutch
-
Simon-Sanchez J., van Hilten J.J., van de Warrenburg B., Post B., Berendse H.W., Arepalli S., et al. Genome-wide association study confirms extant PD risk loci among the Dutch. Eur J Hum Genet 2011, 19:655-661.
-
(2011)
Eur J Hum Genet
, vol.19
, pp. 655-661
-
-
Simon-Sanchez, J.1
van Hilten, J.J.2
van de Warrenburg, B.3
Post, B.4
Berendse, H.W.5
Arepalli, S.6
-
23
-
-
79959965866
-
The PDGene Database
-
Available at: Accessed [09/15/2011].
-
Lill C, Roehr J, McQueen M, Kavvoura F, Bagade S, Schjeide B, et al. The PDGene Database. Alzheimer Research Forum. Available at: Accessed [09/15/2011]. http://www.pdgene.org/.
-
Alzheimer Research Forum
-
-
Lill, C.1
Roehr, J.2
McQueen, M.3
Kavvoura, F.4
Bagade, S.5
Schjeide, B.6
-
24
-
-
79957935283
-
Human leukocyte antigen variation and Parkinson's disease
-
Puschmann A., Verbeeck C., Heckman M.G., Soto-Ortolaza A.I., Lynch T., Jasinska-Myga B., et al. Human leukocyte antigen variation and Parkinson's disease. Parkinsonism Relat Disord 2011, 17:376-378.
-
(2011)
Parkinsonism Relat Disord
, vol.17
, pp. 376-378
-
-
Puschmann, A.1
Verbeeck, C.2
Heckman, M.G.3
Soto-Ortolaza, A.I.4
Lynch, T.5
Jasinska-Myga, B.6
-
25
-
-
79961211173
-
HLA rs3129882 variant in Chinese Han patients with late-onset sporadic Parkinson disease
-
Guo Y., Deng X., Zheng W., Xu H., Song Z., Liang H., et al. HLA rs3129882 variant in Chinese Han patients with late-onset sporadic Parkinson disease. Neurosci Lett 2011, 501:185-187.
-
(2011)
Neurosci Lett
, vol.501
, pp. 185-187
-
-
Guo, Y.1
Deng, X.2
Zheng, W.3
Xu, H.4
Song, Z.5
Liang, H.6
-
26
-
-
0034851739
-
Genetic link between Asians and native Americans: evidence from HLA genes and haplotypes
-
Tokunaga K., Ohashi J., Bannai M., Juji T. Genetic link between Asians and native Americans: evidence from HLA genes and haplotypes. Hum Immunol 2001, 62:1001-1008.
-
(2001)
Hum Immunol
, vol.62
, pp. 1001-1008
-
-
Tokunaga, K.1
Ohashi, J.2
Bannai, M.3
Juji, T.4
-
27
-
-
0034149934
-
Both the HLA-CPB1 and -DRB1 alleles correlate with risk for multiple sclerosis in Japanese: clinical phenotypes and gender as important factors
-
Fukazawa T., Yamasaki K., Ito H., Kikuchi S., Minohara M., Horiuchi I., et al. Both the HLA-CPB1 and -DRB1 alleles correlate with risk for multiple sclerosis in Japanese: clinical phenotypes and gender as important factors. Tissue Antigens 2000, 55:199-205.
-
(2000)
Tissue Antigens
, vol.55
, pp. 199-205
-
-
Fukazawa, T.1
Yamasaki, K.2
Ito, H.3
Kikuchi, S.4
Minohara, M.5
Horiuchi, I.6
-
28
-
-
0022628406
-
Ethnic and HLA patterns related to multiple sclerosis in Wellington, New Zealand
-
Miller D.H., Hornabrook R.W., Dagger J., Fong R. Ethnic and HLA patterns related to multiple sclerosis in Wellington, New Zealand. J Neurol Neurosurg Psychiatry 1986, 49:43-46.
-
(1986)
J Neurol Neurosurg Psychiatry
, vol.49
, pp. 43-46
-
-
Miller, D.H.1
Hornabrook, R.W.2
Dagger, J.3
Fong, R.4
-
29
-
-
0025091114
-
HLA antigens in Japanese patients with myasthenia gravis
-
Matsuki K., Juji T., Tokunaga K., Takamizawa M., Maeda H., Soda M., et al. HLA antigens in Japanese patients with myasthenia gravis. J Clin Invest 1990, 86:392-399.
-
(1990)
J Clin Invest
, vol.86
, pp. 392-399
-
-
Matsuki, K.1
Juji, T.2
Tokunaga, K.3
Takamizawa, M.4
Maeda, H.5
Soda, M.6
-
30
-
-
80052832240
-
Ethnicity and route of HCV infection can influence the associations of HLA with viral clearance in an ethnically heterogeneous population
-
de Almeida B.S., Silva G.M., da Silva P.M., Perez Rde M., Figueiredo F.A., Porto L.C. Ethnicity and route of HCV infection can influence the associations of HLA with viral clearance in an ethnically heterogeneous population. J Viral Hepat 2011, 18:692-699.
-
(2011)
J Viral Hepat
, vol.18
, pp. 692-699
-
-
de Almeida, B.S.1
Silva, G.M.2
da Silva, P.M.3
Perez Rde, M.4
Figueiredo, F.A.5
Porto, L.C.6
-
31
-
-
79952093148
-
Ethnoepidemiology of HTLV-1 related diseases: ethnic determinants of HTLV-1 susceptibility and its worldwide dispersal
-
Sonoda S., Li H.C., Tajima K. Ethnoepidemiology of HTLV-1 related diseases: ethnic determinants of HTLV-1 susceptibility and its worldwide dispersal. Cancer Sci 2010, 102:295-301.
-
(2010)
Cancer Sci
, vol.102
, pp. 295-301
-
-
Sonoda, S.1
Li, H.C.2
Tajima, K.3
-
32
-
-
16244368430
-
Further evidence for an HLA-related recessive mutation in nasopharyngeal carcinoma among the Chinese
-
Hu S.P., Day N.E., Li D.R., Luben R.N., Cai K.L., Ou-Yang T., et al. Further evidence for an HLA-related recessive mutation in nasopharyngeal carcinoma among the Chinese. Br J Cancer 2005, 92:967-970.
-
(2005)
Br J Cancer
, vol.92
, pp. 967-970
-
-
Hu, S.P.1
Day, N.E.2
Li, D.R.3
Luben, R.N.4
Cai, K.L.5
Ou-Yang, T.6
-
33
-
-
0035093475
-
Genetic susceptibility factors of Type 1 diabetes in Asians
-
Park Y., Eisenbarth G.S. Genetic susceptibility factors of Type 1 diabetes in Asians. Diabetes Metab Res Rev 2001, 17:2-11.
-
(2001)
Diabetes Metab Res Rev
, vol.17
, pp. 2-11
-
-
Park, Y.1
Eisenbarth, G.S.2
-
34
-
-
33845693567
-
Genetics of type 1 diabetes: similarities and differences between Asian and Caucasian populations
-
Ikegami H., Fujisawa T., Kawabata Y., Noso S., Ogihara T. Genetics of type 1 diabetes: similarities and differences between Asian and Caucasian populations. Ann N Y Acad Sci 2006, 1079:51-59.
-
(2006)
Ann N Y Acad Sci
, vol.1079
, pp. 51-59
-
-
Ikegami, H.1
Fujisawa, T.2
Kawabata, Y.3
Noso, S.4
Ogihara, T.5
-
35
-
-
38949149289
-
Modifying effect of HLA haplotypes located trans to DQB1*02-DRB1*03 in celiac patients of Southern Europe
-
Hernandez-Charro B., Donat E., Miner I., Aranburu E., Sanchez-Valverde F., Ramos-Arroyo M.A. Modifying effect of HLA haplotypes located trans to DQB1*02-DRB1*03 in celiac patients of Southern Europe. Tissue Antigens 2008, 71:213-218.
-
(2008)
Tissue Antigens
, vol.71
, pp. 213-218
-
-
Hernandez-Charro, B.1
Donat, E.2
Miner, I.3
Aranburu, E.4
Sanchez-Valverde, F.5
Ramos-Arroyo, M.A.6
|