-
1
-
-
0030744876
-
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
-
10.1126/science.276.5321.2045, 9197268
-
Polymeropoulos MH, Lavedan C, Leroy E, Ide SE, Dehejia A, Dutra A, Pike B, Root H, Rubenstein J, Boyer R, Stenroos ES, Chandrasekharappa S, Athanassiadou A, Papapetropoulos T, Johnson WG, Lazzarini AM, Duvoisin RC, Di Iorio G, Golbe LI, Nussbaum RL. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science 1997, 276(5321):2045-2047. 10.1126/science.276.5321.2045, 9197268.
-
(1997)
Science
, vol.276
, Issue.5321
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
Lavedan, C.2
Leroy, E.3
Ide, S.E.4
Dehejia, A.5
Dutra, A.6
Pike, B.7
Root, H.8
Rubenstein, J.9
Boyer, R.10
Stenroos, E.S.11
Chandrasekharappa, S.12
Athanassiadou, A.13
Papapetropoulos, T.14
Johnson, W.G.15
Lazzarini, A.M.16
Duvoisin, R.C.17
Di Iorio, G.18
Golbe, L.I.19
Nussbaum, R.L.20
more..
-
2
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
10.1038/33416, 9560156
-
Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, Yokochi M, Mizuno Y, Shimizu N. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 1998, 392(6676):605-608. 10.1038/33416, 9560156.
-
(1998)
Nature
, vol.392
, Issue.6676
, pp. 605-608
-
-
Kitada, T.1
Asakawa, S.2
Hattori, N.3
Matsumine, H.4
Yamamura, Y.5
Minoshima, S.6
Yokochi, M.7
Mizuno, Y.8
Shimizu, N.9
-
3
-
-
2442668926
-
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
-
10.1126/science.1096284, 15087508
-
Valente EM, Abou-Sleiman PM, Caputo V, Muqit MM, Harvey K, Gispert S, Ali Z, Del Turco D, Bentivoglio AR, Healy DG, Albanese A, Nussbaum R, Gonzalez-Maldonado R, Deller T, Salvi S, Cortelli P, Gilks WP, Latchman DS, Harvey RJ, Dallapiccola B, Auburger G, Wood NW. Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science 2004, 304(5674):1158-1160. 10.1126/science.1096284, 15087508.
-
(2004)
Science
, vol.304
, Issue.5674
, pp. 1158-1160
-
-
Valente, E.M.1
Abou-Sleiman, P.M.2
Caputo, V.3
Muqit, M.M.4
Harvey, K.5
Gispert, S.6
Ali, Z.7
Del Turco, D.8
Bentivoglio, A.R.9
Healy, D.G.10
Albanese, A.11
Nussbaum, R.12
Gonzalez-Maldonado, R.13
Deller, T.14
Salvi, S.15
Cortelli, P.16
Gilks, W.P.17
Latchman, D.S.18
Harvey, R.J.19
Dallapiccola, B.20
Auburger, G.21
Wood, N.W.22
more..
-
4
-
-
0037428241
-
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
-
10.1126/science.1077209, 12446870
-
Bonifati V, Rizzu P, van Baren MJ, Schaap O, Breedveld GJ, Krieger E, Dekker MC, Squitieri F, Ibanez P, Joosse M, van Dongen JW, Vanacore N, van Swieten JC, Brice A, Meco G, van Duijn CM, Oostra BA, Heutink P. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Science 2003, 299(5604):256-259. 10.1126/science.1077209, 12446870.
-
(2003)
Science
, vol.299
, Issue.5604
, pp. 256-259
-
-
Bonifati, V.1
Rizzu, P.2
van Baren, M.J.3
Schaap, O.4
Breedveld, G.J.5
Krieger, E.6
Dekker, M.C.7
Squitieri, F.8
Ibanez, P.9
Joosse, M.10
van Dongen, J.W.11
Vanacore, N.12
van Swieten, J.C.13
Brice, A.14
Meco, G.15
van Duijn, C.M.16
Oostra, B.A.17
Heutink, P.18
-
5
-
-
8844266996
-
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
-
10.1016/j.neuron.2004.10.023, 15541308
-
Paisan-Ruiz C, Jain S, Evans EW, Gilks WP, Simon J, van der Brug M, Lopez de Munain A, Aparicio S, Gil AM, Khan N, Johnson J, Martinez JR, Nicholl D, Carrera IM, Pena AS, de Silva R, Lees A, Marti-Masso JF, Perez-Tur J, Wood NW, Singleton AB. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron 2004, 44(4):595-600. 10.1016/j.neuron.2004.10.023, 15541308.
-
(2004)
Neuron
, vol.44
, Issue.4
, pp. 595-600
-
-
Paisan-Ruiz, C.1
Jain, S.2
Evans, E.W.3
Gilks, W.P.4
Simon, J.5
van der Brug, M.6
Lopez de Munain, A.7
Aparicio, S.8
Gil, A.M.9
Khan, N.10
Johnson, J.11
Martinez, J.R.12
Nicholl, D.13
Carrera, I.M.14
Pena, A.S.15
de Silva, R.16
Lees, A.17
Marti-Masso, J.F.18
Perez-Tur, J.19
Wood, N.W.20
Singleton, A.B.21
more..
-
6
-
-
66949152096
-
Parkinson's disease
-
10.1016/S0140-6736(09)60492-X, 19524782
-
Lees AJ, Hardy J, Revesz T. Parkinson's disease. Lancet 2009, 373(9680):2055-2066. 10.1016/S0140-6736(09)60492-X, 19524782.
-
(2009)
Lancet
, vol.373
, Issue.9680
, pp. 2055-2066
-
-
Lees, A.J.1
Hardy, J.2
Revesz, T.3
-
7
-
-
77954104112
-
Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update
-
10.1002/humu.21277, 3056147, 20506312
-
Nuytemans K, Theuns J, Cruts M, Van Broeckhoven C. Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update. Hum Mutat 2010, 31(7):763-780. 10.1002/humu.21277, 3056147, 20506312.
-
(2010)
Hum Mutat
, vol.31
, Issue.7
, pp. 763-780
-
-
Nuytemans, K.1
Theuns, J.2
Cruts, M.3
Van Broeckhoven, C.4
-
8
-
-
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
-
10.1093/hmg/ddq497, 21084426
-
Saad M, Lesage S, Saint-Pierre A, Corvol JC, Zelenika D, Lambert JC, Vidailhet M, Mellick GD, Lohmann E, Durif F, Pollak P, Damier P, Tison F, Silburn PA, Tzourio C, Forlani S, Loriot MA, Giroud M, Helmer C, Portet F, Amouyel P, Lathrop M, Elbaz A, Durr A, Martinez M, Brice A. 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(3):615-627. 10.1093/hmg/ddq497, 21084426.
-
(2011)
Hum Mol Genet
, vol.20
, Issue.3
, pp. 615-627
-
-
Saad, M.1
Lesage, S.2
Saint-Pierre, A.3
Corvol, J.C.4
Zelenika, D.5
Lambert, J.C.6
Vidailhet, M.7
Mellick, G.D.8
Lohmann, E.9
Durif, F.10
Pollak, P.11
Damier, P.12
Tison, F.13
Silburn, P.A.14
Tzourio, C.15
Forlani, S.16
Loriot, M.A.17
Giroud, M.18
Helmer, C.19
Portet, F.20
Amouyel, P.21
Lathrop, M.22
Elbaz, A.23
Durr, A.24
Martinez, M.25
Brice, A.26
more..
-
9
-
-
78650550275
-
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
-
3005904, 21044948
-
Spencer CC, Plagnol V, Strange A, Gardner M, Paisan-Ruiz C, Band G, Barker RA, Bellenguez C, Bhatia K, Blackburn H, Blackwell JM, Bramon E, Brown MA, Burn D, Casas JP, Chinnery PF, Clarke CE, Corvin A, Craddock N, Deloukas P, Edkins S, Evans J, Freeman C, Gray E, Hardy J, Hudson G, Hunt S, Jankowski J, Langford C, Lees AJ, 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(2):345-353. 3005904, 21044948.
-
(2011)
Hum Mol Genet
, vol.20
, Issue.2
, pp. 345-353
-
-
Spencer, C.C.1
Plagnol, V.2
Strange, A.3
Gardner, M.4
Paisan-Ruiz, C.5
Band, G.6
Barker, R.A.7
Bellenguez, C.8
Bhatia, K.9
Blackburn, H.10
Blackwell, J.M.11
Bramon, E.12
Brown, M.A.13
Burn, D.14
Casas, J.P.15
Chinnery, P.F.16
Clarke, C.E.17
Corvin, A.18
Craddock, N.19
Deloukas, P.20
Edkins, S.21
Evans, J.22
Freeman, C.23
Gray, E.24
Hardy, J.25
Hudson, G.26
Hunt, S.27
Jankowski, J.28
Langford, C.29
Lees, A.J.30
more..
-
10
-
-
27244451809
-
High-resolution whole-genome association study of Parkinson disease
-
10.1086/496902, 1271381, 16252231
-
Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, Pant PV, Frazer KA, Cox DR, Ballinger DG. High-resolution whole-genome association study of Parkinson disease. Am J Hum Genet 2005, 77(5):685-693. 10.1086/496902, 1271381, 16252231.
-
(2005)
Am J Hum Genet
, vol.77
, Issue.5
, pp. 685-693
-
-
Maraganore, D.M.1
de Andrade, M.2
Lesnick, T.G.3
Strain, K.J.4
Farrer, M.J.5
Rocca, W.A.6
Pant, P.V.7
Frazer, K.A.8
Cox, D.R.9
Ballinger, D.G.10
-
11
-
-
33749667345
-
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data
-
10.1016/S1474-4422(06)70578-6, 17052657
-
Fung HC, Scholz S, Matarin M, Simon-Sanchez J, Hernandez D, Britton A, Gibbs JR, Langefeld C, Stiegert ML, Schymick J, Okun MS, Mandel RJ, Fernandez HH, Foote KD, Rodriguez RL, Peckham E, De Vrieze FW, Gwinn-Hardy K, Hardy JA, Singleton A. Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. Lancet Neurol 2006, 5(11):911-916. 10.1016/S1474-4422(06)70578-6, 17052657.
-
(2006)
Lancet Neurol
, vol.5
, Issue.11
, pp. 911-916
-
-
Fung, H.C.1
Scholz, S.2
Matarin, M.3
Simon-Sanchez, J.4
Hernandez, D.5
Britton, A.6
Gibbs, J.R.7
Langefeld, C.8
Stiegert, M.L.9
Schymick, J.10
Okun, M.S.11
Mandel, R.J.12
Fernandez, H.H.13
Foote, K.D.14
Rodriguez, R.L.15
Peckham, E.16
De Vrieze, F.W.17
Gwinn-Hardy, K.18
Hardy, J.A.19
Singleton, A.20
more..
-
12
-
-
70349771038
-
Genomewide association study for onset age in Parkinson disease
-
10.1186/1471-2350-10-98, 2758866, 19772629
-
Latourelle JC, Pankratz N, Dumitriu A, Wilk JB, Goldwurm S, Pezzoli G, Mariani CB, DeStefano AL, Halter C, Gusella JF, Nichols WC, Myers RH, Foroud T. Genomewide association study for onset age in Parkinson disease. BMC Med Genet 2009, 10:98. 10.1186/1471-2350-10-98, 2758866, 19772629.
-
(2009)
BMC Med Genet
, vol.10
, pp. 98
-
-
Latourelle, J.C.1
Pankratz, N.2
Dumitriu, A.3
Wilk, J.B.4
Goldwurm, S.5
Pezzoli, G.6
Mariani, C.B.7
DeStefano, A.L.8
Halter, C.9
Gusella, J.F.10
Nichols, W.C.11
Myers, R.H.12
Foroud, T.13
-
13
-
-
70549084415
-
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
-
10.1038/ng.485, 19915576
-
Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, Kubo M, Kawaguchi T, Tsunoda T, Watanabe M, Takeda A, Tomiyama H, Nakashima K, Hasegawa K, Obata F, Yoshikawa T, Kawakami H, Sakoda S, Yamamoto M, Hattori N, Murata M, Nakamura Y, Toda T. Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nat Genet 2009, 41(12):1303-1307. 10.1038/ng.485, 19915576.
-
(2009)
Nat Genet
, vol.41
, Issue.12
, pp. 1303-1307
-
-
Satake, W.1
Nakabayashi, Y.2
Mizuta, I.3
Hirota, Y.4
Ito, C.5
Kubo, M.6
Kawaguchi, T.7
Tsunoda, T.8
Watanabe, M.9
Takeda, A.10
Tomiyama, H.11
Nakashima, K.12
Hasegawa, K.13
Obata, F.14
Yoshikawa, T.15
Kawakami, H.16
Sakoda, S.17
Yamamoto, M.18
Hattori, N.19
Murata, M.20
Nakamura, Y.21
Toda, T.22
more..
-
14
-
-
70549088602
-
Genome-wide association study reveals genetic risk underlying Parkinson's disease
-
10.1038/ng.487, 2787725, 19915575
-
Simon-Sanchez J, Schulte C, Bras JM, Sharma M, Gibbs JR, Berg D, Paisan-Ruiz C, Lichtner P, Scholz SW, Hernandez DG, Kruger R, Federoff M, Klein C, Goate A, Perlmutter J, Bonin M, Nalls MA, Illig T, Gieger C, Houlden H, Steffens M, Okun MS, Racette BA, Cookson MR, Foote KD, Fernandez HH, Traynor BJ, Schreiber S, Arepalli S, Zonozi R, et al. Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat Genet 2009, 41(12):1308-1312. 10.1038/ng.487, 2787725, 19915575.
-
(2009)
Nat Genet
, vol.41
, Issue.12
, pp. 1308-1312
-
-
Simon-Sanchez, J.1
Schulte, C.2
Bras, J.M.3
Sharma, M.4
Gibbs, J.R.5
Berg, D.6
Paisan-Ruiz, C.7
Lichtner, P.8
Scholz, S.W.9
Hernandez, D.G.10
Kruger, R.11
Federoff, M.12
Klein, C.13
Goate, A.14
Perlmutter, J.15
Bonin, M.16
Nalls, M.A.17
Illig, T.18
Gieger, C.19
Houlden, H.20
Steffens, M.21
Okun, M.S.22
Racette, B.A.23
Cookson, M.R.24
Foote, K.D.25
Fernandez, H.H.26
Traynor, B.J.27
Schreiber, S.28
Arepalli, S.29
Zonozi, R.30
more..
-
15
-
-
77951185469
-
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease
-
10.1111/j.1469-1809.2009.00560.x, 2853717, 20070850
-
Edwards TL, Scott WK, Almonte C, Burt A, Powell EH, Beecham GW, Wang L, Zuchner S, Konidari I, Wang G, Singer C, Nahab F, Scott B, Stajich JM, Pericak-Vance M, Haines J, Vance JM, Martin ER. Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. Ann Hum Genet 2010, 74(2):97-109. 10.1111/j.1469-1809.2009.00560.x, 2853717, 20070850.
-
(2010)
Ann Hum Genet
, vol.74
, Issue.2
, 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
Wang, L.7
Zuchner, S.8
Konidari, I.9
Wang, G.10
Singer, C.11
Nahab, F.12
Scott, B.13
Stajich, J.M.14
Pericak-Vance, M.15
Haines, J.16
Vance, J.M.17
Martin, E.R.18
-
16
-
-
77956646167
-
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease
-
10.1038/ng.642, 2930111, 20711177
-
Hamza TH, Zabetian CP, Tenesa A, Laederach A, Montimurro J, Yearout D, Kay DM, Doheny KF, Paschall J, Pugh E, Kusel VI, Collura R, Roberts J, Griffith A, Samii A, Scott WK, Nutt J, Factor SA, Payami H. Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. Nat Genet 2010, 42(9):781-785. 10.1038/ng.642, 2930111, 20711177.
-
(2010)
Nat Genet
, vol.42
, Issue.9
, pp. 781-785
-
-
Hamza, T.H.1
Zabetian, C.P.2
Tenesa, A.3
Laederach, A.4
Montimurro, J.5
Yearout, D.6
Kay, D.M.7
Doheny, K.F.8
Paschall, J.9
Pugh, E.10
Kusel, V.I.11
Collura, R.12
Roberts, J.13
Griffith, A.14
Samii, A.15
Scott, W.K.16
Nutt, J.17
Factor, S.A.18
Payami, H.19
-
17
-
-
79951811351
-
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
-
Consortium IPDG. Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. The Lancet 2011, 377(9766):641-649.
-
(2011)
The Lancet
, vol.377
, Issue.9766
, pp. 641-649
-
-
Consortium, I.P.D.G.1
-
18
-
-
0035514049
-
A genetic profile of contemporary Jewish populations
-
10.1038/35098506, 11715044
-
Ostrer H. A genetic profile of contemporary Jewish populations. Nat Rev Genet 2001, 2(11):891-898. 10.1038/35098506, 11715044.
-
(2001)
Nat Rev Genet
, vol.2
, Issue.11
, pp. 891-898
-
-
Ostrer, H.1
-
19
-
-
77953231974
-
Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry
-
10.1016/j.ajhg.2010.04.015, 3032072, 20560205
-
Atzmon G, Hao L, Pe'er I, Velez C, Pearlman A, Palamara PF, Morrow B, Friedman E, Oddoux C, Burns E, Ostrer H. Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry. Am J Hum Genet 2010, 86(6):850-859. 10.1016/j.ajhg.2010.04.015, 3032072, 20560205.
-
(2010)
Am J Hum Genet
, vol.86
, Issue.6
, pp. 850-859
-
-
Atzmon, G.1
Hao, L.2
Pe'er, I.3
Velez, C.4
Pearlman, A.5
Palamara, P.F.6
Morrow, B.7
Friedman, E.8
Oddoux, C.9
Burns, E.10
Ostrer, H.11
-
20
-
-
31344439221
-
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews
-
10.1056/NEJMc055509, 16436782
-
Ozelius LJ, Senthil G, Saunders-Pullman R, Ohmann E, Deligtisch A, Tagliati M, Hunt AL, Klein C, Henick B, Hailpern SM, Lipton RB, Soto-Valencia J, Risch N, Bressman SB. LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews. N Engl J Med 2006, 354(4):424-425. 10.1056/NEJMc055509, 16436782.
-
(2006)
N Engl J Med
, vol.354
, Issue.4
, pp. 424-425
-
-
Ozelius, L.J.1
Senthil, G.2
Saunders-Pullman, R.3
Ohmann, E.4
Deligtisch, A.5
Tagliati, M.6
Hunt, A.L.7
Klein, C.8
Henick, B.9
Hailpern, S.M.10
Lipton, R.B.11
Soto-Valencia, J.12
Risch, N.13
Bressman, S.B.14
-
21
-
-
79958116682
-
Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries
-
10.1007/s10048-009-0186-0, 19283415
-
Bar-Shira A, Hutter CM, Giladi N, Zabetian CP, Orr-Urtreger A. Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries. Neurogenetics 2009, 10(4):355-358. 10.1007/s10048-009-0186-0, 19283415.
-
(2009)
Neurogenetics
, vol.10
, Issue.4
, pp. 355-358
-
-
Bar-Shira, A.1
Hutter, C.M.2
Giladi, N.3
Zabetian, C.P.4
Orr-Urtreger, A.5
-
22
-
-
34548726339
-
Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease
-
10.1212/01.wnl.0000276989.17578.02, 17875915
-
Clark LN, Ross BM, Wang Y, Mejia-Santana H, Harris J, Louis ED, Cote LJ, Andrews H, Fahn S, Waters C, Ford B, Frucht S, Ottman R, Marder K. Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease. Neurology 2007, 69(12):1270-1277. 10.1212/01.wnl.0000276989.17578.02, 17875915.
-
(2007)
Neurology
, vol.69
, Issue.12
, pp. 1270-1277
-
-
Clark, L.N.1
Ross, B.M.2
Wang, Y.3
Mejia-Santana, H.4
Harris, J.5
Louis, E.D.6
Cote, L.J.7
Andrews, H.8
Fahn, S.9
Waters, C.10
Ford, B.11
Frucht, S.12
Ottman, R.13
Marder, K.14
-
23
-
-
70350319531
-
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
-
10.1056/NEJMoa0901281, 2856322, 19846850
-
Sidransky E, Nalls MA, Aasly JO, Aharon-Peretz J, Annesi G, Barbosa ER, Bar-Shira A, Berg D, Bras J, Brice A, Chen CM, Clark LN, Condroyer C, De Marco EV, Durr A, Eblan MJ, Fahn S, Farrer MJ, Fung HC, Gan-Or Z, Gasser T, Gershoni-Baruch R, Giladi N, Griffith A, Gurevich T, Januario C, Kropp P, Lang AE, Lee-Chen GJ, Lesage S, et al. Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. N Engl J Med 2009, 361(17):1651-1661. 10.1056/NEJMoa0901281, 2856322, 19846850.
-
(2009)
N Engl J Med
, vol.361
, Issue.17
, pp. 1651-1661
-
-
Sidransky, E.1
Nalls, M.A.2
Aasly, J.O.3
Aharon-Peretz, J.4
Annesi, G.5
Barbosa, E.R.6
Bar-Shira, A.7
Berg, D.8
Bras, J.9
Brice, A.10
Chen, C.M.11
Clark, L.N.12
Condroyer, C.13
De Marco, E.V.14
Durr, A.15
Eblan, M.J.16
Fahn, S.17
Farrer, M.J.18
Fung, H.C.19
Gan-Or, Z.20
Gasser, T.21
Gershoni-Baruch, R.22
Giladi, N.23
Griffith, A.24
Gurevich, T.25
Januario, C.26
Kropp, P.27
Lang, A.E.28
Lee-Chen, G.J.29
Lesage, S.30
more..
-
24
-
-
58149100151
-
Genomewide association study for susceptibility genes contributing to familial Parkinson disease
-
10.1007/s00439-008-0582-9, 2627511, 18985386
-
Pankratz N, Wilk JB, Latourelle JC, DeStefano AL, Halter C, Pugh EW, Doheny KF, Gusella JF, Nichols WC, Foroud T, Myers RH. Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Hum Genet 2009, 124(6):593-605. 10.1007/s00439-008-0582-9, 2627511, 18985386.
-
(2009)
Hum Genet
, vol.124
, Issue.6
, 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
Doheny, K.F.7
Gusella, J.F.8
Nichols, W.C.9
Foroud, T.10
Myers, R.H.11
-
25
-
-
0141535355
-
Familial aggregation of early- and late-onset Parkinson's disease
-
10.1002/ana.10711, 14520664
-
Marder K, Levy G, Louis ED, Mejia-Santana H, Cote L, Andrews H, Harris J, Waters C, Ford B, Frucht S, Fahn S, Ottman R. Familial aggregation of early- and late-onset Parkinson's disease. Ann Neurol 2003, 54(4):507-513. 10.1002/ana.10711, 14520664.
-
(2003)
Ann Neurol
, vol.54
, Issue.4
, pp. 507-513
-
-
Marder, K.1
Levy, G.2
Louis, E.D.3
Mejia-Santana, H.4
Cote, L.5
Andrews, H.6
Harris, J.7
Waters, C.8
Ford, B.9
Frucht, S.10
Fahn, S.11
Ottman, R.12
-
26
-
-
34548292504
-
PLINK: a tool set for whole-genome association and population-based linkage analyses
-
10.1086/519795, 1950838, 17701901
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007, 81(3):559-575. 10.1086/519795, 1950838, 17701901.
-
(2007)
Am J Hum Genet
, vol.81
, Issue.3
, 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
Sham, P.C.11
-
27
-
-
0004226825
-
Principles of population genetics
-
Sunderland, Mass.: Sinauer Associates, 4
-
Hartl DL, Clark AG. Principles of population genetics. 2007, Sunderland, Mass.: Sinauer Associates, 4.
-
(2007)
-
-
Hartl, D.L.1
Clark, A.G.2
-
28
-
-
41649083448
-
WGAViewer: software for genomic annotation of whole genome association studies
-
10.1101/gr.071571.107, 2279251, 18256235
-
Ge D, Zhang K, Need AC, Martin O, Fellay J, Urban TJ, Telenti A, Goldstein DB. WGAViewer: software for genomic annotation of whole genome association studies. Genome Res 2008, 18(4):640-643. 10.1101/gr.071571.107, 2279251, 18256235.
-
(2008)
Genome Res
, vol.18
, Issue.4
, pp. 640-643
-
-
Ge, D.1
Zhang, K.2
Need, A.C.3
Martin, O.4
Fellay, J.5
Urban, T.J.6
Telenti, A.7
Goldstein, D.B.8
-
29
-
-
57249114505
-
SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap
-
10.1093/bioinformatics/btn564, 2720775, 18974171
-
Johnson AD, Handsaker RE, Pulit SL, Nizzari MM, O'Donnell CJ, de Bakker PI. SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap. Bioinformatics 2008, 24(24):2938-2939. 10.1093/bioinformatics/btn564, 2720775, 18974171.
-
(2008)
Bioinformatics
, vol.24
, Issue.24
, pp. 2938-2939
-
-
Johnson, A.D.1
Handsaker, R.E.2
Pulit, S.L.3
Nizzari, M.M.4
O'Donnell, C.J.5
de Bakker, P.I.6
-
30
-
-
33845453622
-
Frequency of LRRK2 mutations in early- and late-onset Parkinson disease
-
10.1212/01.wnl.0000244345.49809.36, 17050822
-
Clark LN, Wang Y, Karlins E, Saito L, Mejia-Santana H, Harris J, Louis ED, Cote LJ, Andrews H, Fahn S, Waters C, Ford B, Frucht S, Ottman R, Marder K. Frequency of LRRK2 mutations in early- and late-onset Parkinson disease. Neurology 2006, 67(10):1786-1791. 10.1212/01.wnl.0000244345.49809.36, 17050822.
-
(2006)
Neurology
, vol.67
, Issue.10
, pp. 1786-1791
-
-
Clark, L.N.1
Wang, Y.2
Karlins, E.3
Saito, L.4
Mejia-Santana, H.5
Harris, J.6
Louis, E.D.7
Cote, L.J.8
Andrews, H.9
Fahn, S.10
Waters, C.11
Ford, B.12
Frucht, S.13
Ottman, R.14
Marder, K.15
-
31
-
-
13944278863
-
A common inversion under selection in Europeans
-
10.1038/ng1508, 15654335
-
Stefansson H, Helgason A, Thorleifsson G, Steinthorsdottir V, Masson G, Barnard J, Baker A, Jonasdottir A, Ingason A, Gudnadottir VG, Desnica N, Hicks A, Gylfason A, Gudbjartsson DF, Jonsdottir GM, Sainz J, Agnarsson K, Birgisdottir B, Ghosh S, Olafsdottir A, Cazier JB, Kristjansson K, Frigge ML, Thorgeirsson TE, Gulcher JR, Kong A, Stefansson K. A common inversion under selection in Europeans. Nat Genet 2005, 37(2):129-137. 10.1038/ng1508, 15654335.
-
(2005)
Nat Genet
, vol.37
, Issue.2
, pp. 129-137
-
-
Stefansson, H.1
Helgason, A.2
Thorleifsson, G.3
Steinthorsdottir, V.4
Masson, G.5
Barnard, J.6
Baker, A.7
Jonasdottir, A.8
Ingason, A.9
Gudnadottir, V.G.10
Desnica, N.11
Hicks, A.12
Gylfason, A.13
Gudbjartsson, D.F.14
Jonsdottir, G.M.15
Sainz, J.16
Agnarsson, K.17
Birgisdottir, B.18
Ghosh, S.19
Olafsdottir, A.20
Cazier, J.B.21
Kristjansson, K.22
Frigge, M.L.23
Thorgeirsson, T.E.24
Gulcher, J.R.25
Kong, A.26
Stefansson, K.27
more..
-
32
-
-
33750952513
-
Fourteen novel human members of mitochondrial solute carrier family 25 (SLC25) widely expressed in the central nervous system
-
10.1016/j.ygeno.2006.06.016, 16949250
-
Haitina T, Lindblom J, Renstrom T, Fredriksson R. Fourteen novel human members of mitochondrial solute carrier family 25 (SLC25) widely expressed in the central nervous system. Genomics 2006, 88(6):779-790. 10.1016/j.ygeno.2006.06.016, 16949250.
-
(2006)
Genomics
, vol.88
, Issue.6
, pp. 779-790
-
-
Haitina, T.1
Lindblom, J.2
Renstrom, T.3
Fredriksson, R.4
-
33
-
-
1242317666
-
The mitochondrial transporter family (SLC25): physiological and pathological implications
-
10.1007/s00424-003-1099-7, 14598172
-
Palmieri F. The mitochondrial transporter family (SLC25): physiological and pathological implications. Pflugers Arch 2004, 447(5):689-709. 10.1007/s00424-003-1099-7, 14598172.
-
(2004)
Pflugers Arch
, vol.447
, Issue.5
, pp. 689-709
-
-
Palmieri, F.1
-
34
-
-
0035214180
-
Uncoupling protein 2 in the brain: distribution and function
-
Richard D, Clavel S, Huang Q, Sanchis D, Ricquier D. Uncoupling protein 2 in the brain: distribution and function. Biochem Soc Trans 2001, 29:(Pt 6):812-817.
-
(2001)
Biochem Soc Trans
, vol.29
, Issue.PART 6
, pp. 812-817
-
-
Richard, D.1
Clavel, S.2
Huang, Q.3
Sanchis, D.4
Ricquier, D.5
-
35
-
-
67650215189
-
A network of G-protein signaling pathways control neuronal activity in C. elegans
-
Perez-Mansilla B, Nurrish S. A network of G-protein signaling pathways control neuronal activity in C. elegans. Adv Genet 2009, 65:145-192.
-
(2009)
Adv Genet
, vol.65
, pp. 145-192
-
-
Perez-Mansilla, B.1
Nurrish, S.2
-
36
-
-
0031794650
-
NSF--fusion and beyond
-
10.1016/S0962-8924(98)01388-9, 9861668
-
Haas A. NSF--fusion and beyond. Trends Cell Biol 1998, 8(12):471-473. 10.1016/S0962-8924(98)01388-9, 9861668.
-
(1998)
Trends Cell Biol
, vol.8
, Issue.12
, pp. 471-473
-
-
Haas, A.1
-
37
-
-
77955380970
-
Interaction of dopamine D1 receptor with N-ethylmaleimide-sensitive factor is important for the membrane localization of the receptor
-
Chen S, Liu F. Interaction of dopamine D1 receptor with N-ethylmaleimide-sensitive factor is important for the membrane localization of the receptor. J Neurosci Res 2010, 88(11):2504-2512.
-
(2010)
J Neurosci Res
, vol.88
, Issue.11
, pp. 2504-2512
-
-
Chen, S.1
Liu, F.2
-
38
-
-
72449165994
-
Dimerization of dopamine D1 and D3 receptors in the regulation of striatal function
-
10.1016/j.coph.2009.09.008, 19837631
-
Fiorentini C, Busi C, Spano P, Missale C. Dimerization of dopamine D1 and D3 receptors in the regulation of striatal function. Curr Opin Pharmacol 2010, 10(1):87-92. 10.1016/j.coph.2009.09.008, 19837631.
-
(2010)
Curr Opin Pharmacol
, vol.10
, Issue.1
, pp. 87-92
-
-
Fiorentini, C.1
Busi, C.2
Spano, P.3
Missale, C.4
-
39
-
-
78549251699
-
Genetic variability at the PARK16 locus
-
10.1038/ejhg.2010.125, 20683486
-
Tucci A, Nalls MA, Houlden H, Revesz T, Singleton AB, Wood NW, Hardy J, Paisan-Ruiz C. Genetic variability at the PARK16 locus. Eur J Hum Genet 2010, 18(12):1356-1359. 10.1038/ejhg.2010.125, 20683486.
-
(2010)
Eur J Hum Genet
, vol.18
, Issue.12
, pp. 1356-1359
-
-
Tucci, A.1
Nalls, M.A.2
Houlden, H.3
Revesz, T.4
Singleton, A.B.5
Wood, N.W.6
Hardy, J.7
Paisan-Ruiz, C.8
|