-
1
-
-
17644365438
-
Mutations in PTEN-induced putative kinase 1 associated with recessive parkinsonism have differential effects on protein stability
-
Beilina A., Van Der Brug M., Ahmad R.S., Kesavapany, Miller D.W., Petsko G.A., and Cookson M.R. Mutations in PTEN-induced putative kinase 1 associated with recessive parkinsonism have differential effects on protein stability. Proc. Natl. Acad. Sci. USA 102 (2005) 5703-5708
-
(2005)
Proc. Natl. Acad. Sci. USA
, vol.102
, pp. 5703-5708
-
-
Beilina, A.1
Van Der Brug, M.2
Ahmad, R.S.3
Kesavapany4
Miller, D.W.5
Petsko, G.A.6
Cookson, M.R.7
-
2
-
-
0037428241
-
Mutations in the DJ-1 gene associated with autosomal recessive earlyonset parkinsonism
-
Bonifati V., Rizzu P., van Baren M.J., Schaap O., Breedveld G.J., Krieger E., Dekker M.C., Squitieri F., Ibanez P., oosse M.J., van Dongen J.W., Vanacore N., van Swieten J.C., Brice A., Meco G., van Duijn C.M., Oostra B.A., and Heutink P. Mutations in the DJ-1 gene associated with autosomal recessive earlyonset parkinsonism. Science 299 (2003) 256-259
-
(2003)
Science
, vol.299
, 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
oosse, M.J.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
-
3
-
-
22044432781
-
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes
-
Bonifati V., Rohe C.F., Breedveld G.J., Fabrizio E., De M.C., Tassorelli M., Tavella A., Marconi R., Nicholl D.J., Chien H.F., Fincati E., Abbruzzese G., Marini P., De Gaetano A., Horstink M.W., Maat-Kievit J.A., Sampaio C., Antonini A., Stocchi F., Montagna P., Toni V., Guidi M., Dalla Libera A., Tinazzi M., De Pandis F., Fabbrini G., Goldwurm S., de Klein A., Barbosa E., Lopiano L., Martignoni E., Lamberti P., Vanacore N., Meco G., and Oostra B.A. Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes. Neurology 65 (2005) 87-95
-
(2005)
Neurology
, vol.65
, pp. 87-95
-
-
Bonifati, V.1
Rohe, C.F.2
Breedveld, G.J.3
Fabrizio, E.4
De, M.C.5
Tassorelli, M.6
Tavella, A.7
Marconi, R.8
Nicholl, D.J.9
Chien, H.F.10
Fincati, E.11
Abbruzzese, G.12
Marini, P.13
De Gaetano, A.14
Horstink, M.W.15
Maat-Kievit, J.A.16
Sampaio, C.17
Antonini, A.18
Stocchi, F.19
Montagna, P.20
Toni, V.21
Guidi, M.22
Dalla Libera, A.23
Tinazzi, M.24
De Pandis, F.25
Fabbrini, G.26
Goldwurm, S.27
de Klein, A.28
Barbosa, E.29
Lopiano, L.30
Martignoni, E.31
Lamberti, P.32
Vanacore, N.33
Meco, G.34
Oostra, B.A.35
more..
-
4
-
-
0026695663
-
Criteria for diagnosing Parkinson's disease
-
Calne D.B., Snowx B.J., and Lee C. Criteria for diagnosing Parkinson's disease. Ann. Neurol. 32 (1992) S125-S127
-
(1992)
Ann. Neurol.
, vol.32
-
-
Calne, D.B.1
Snowx, B.J.2
Lee, C.3
-
5
-
-
33646483185
-
Assessment of PINK1 (PARK6) polymorphisms in Finnish PD
-
Clarimon J., Eerola J., Hellstrom O., Peuralinna T., Tienari P.J., and Singleton A.B. Assessment of PINK1 (PARK6) polymorphisms in Finnish PD. Neurobiol. Aging 27 (2006) 906-907
-
(2006)
Neurobiol. Aging
, vol.27
, pp. 906-907
-
-
Clarimon, J.1
Eerola, J.2
Hellstrom, O.3
Peuralinna, T.4
Tienari, P.J.5
Singleton, A.B.6
-
6
-
-
12244262766
-
Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson's disease
-
Foroud T., Uniacke S.K., Liu L., Pankratz N., Rudolph A., Halter C., Shults C., Marder K., Conneally P.M., and Nichols W.C. Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson's disease. Neurology 60 (2003) 796-801
-
(2003)
Neurology
, vol.60
, pp. 796-801
-
-
Foroud, T.1
Uniacke, S.K.2
Liu, L.3
Pankratz, N.4
Rudolph, A.5
Halter, C.6
Shults, C.7
Marder, K.8
Conneally, P.M.9
Nichols, W.C.10
-
7
-
-
30144445796
-
Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in Taiwan
-
Fung H.C., Chen C.M., Hardy J., Singleton A.B., Lee-Chen G.J., and Wu Y.R. Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in Taiwan. Neurosci. Lett. 394 (2006) 33-36
-
(2006)
Neurosci. Lett.
, vol.394
, pp. 33-36
-
-
Fung, H.C.1
Chen, C.M.2
Hardy, J.3
Singleton, A.B.4
Lee-Chen, G.J.5
Wu, Y.R.6
-
8
-
-
19944432921
-
A common LRRK2 mutation in idiopathic Parkinson's disease
-
Gilks W.P., Abou-Sleiman P.M., Gandhi S., Jain S., Singleton A., Lees A.J., Shaw K., Bhatia K.P., Bonifati V., Quinn N.P., Lynch J., Healy D.G., Holton J.L., Revesz T., and Wood N.W. A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet 365 (2005) 415-416
-
(2005)
Lancet
, vol.365
, pp. 415-416
-
-
Gilks, W.P.1
Abou-Sleiman, P.M.2
Gandhi, S.3
Jain, S.4
Singleton, A.5
Lees, A.J.6
Shaw, K.7
Bhatia, K.P.8
Bonifati, V.9
Quinn, N.P.10
Lynch, J.11
Healy, D.G.12
Holton, J.L.13
Revesz, T.14
Wood, N.W.15
-
9
-
-
7944221966
-
Genetic association study of PINK1 coding polymorphisms in Parkinson's disease
-
Groen J.L., Kawarai T., Toulina A., Rivoiro C., Salehi-Rad S., Sato C., Morgan A., Liang Y., Postuma R.B., St George-Hyslop P., Lang A.E., and Rogaeva E. Genetic association study of PINK1 coding polymorphisms in Parkinson's disease. Neurosci. Lett. 372 (2004) 226-229
-
(2004)
Neurosci. Lett.
, vol.372
, pp. 226-229
-
-
Groen, J.L.1
Kawarai, T.2
Toulina, A.3
Rivoiro, C.4
Salehi-Rad, S.5
Sato, C.6
Morgan, A.7
Liang, Y.8
Postuma, R.B.9
St George-Hyslop, P.10
Lang, A.E.11
Rogaeva, E.12
-
10
-
-
4444237208
-
Novel PINK1 mutations in early-onset parkinsonism
-
Hatano Y., Li Y., Sato K., Asakawa S., Yamamura Y., Tomiyama H., Yoshino H., Asahina M., Kobayashi S., Hassin-Baer S., Lu C.S., Ng A.R., Rosales R.L., Shimizu N., Toda T., Mizuno Y., and Hattori N. Novel PINK1 mutations in early-onset parkinsonism. Ann. Neurol. 56 (2004) 424-427
-
(2004)
Ann. Neurol.
, vol.56
, pp. 424-427
-
-
Hatano, Y.1
Li, Y.2
Sato, K.3
Asakawa, S.4
Yamamura, Y.5
Tomiyama, H.6
Yoshino, H.7
Asahina, M.8
Kobayashi, S.9
Hassin-Baer, S.10
Lu, C.S.11
Ng, A.R.12
Rosales, R.L.13
Shimizu, N.14
Toda, T.15
Mizuno, Y.16
Hattori, N.17
-
11
-
-
0032433332
-
Genetic linkage analysis of complex genetic traits by using affected sibling pairs
-
Hauser E.R., and Boehnke M. Genetic linkage analysis of complex genetic traits by using affected sibling pairs. Biometrics 54 (1998) 1238-1246
-
(1998)
Biometrics
, vol.54
, pp. 1238-1246
-
-
Hauser, E.R.1
Boehnke, M.2
-
12
-
-
0036830525
-
A susceptibility gene for late onset idiopathic Parkinson's disease
-
Hicks A.A., Petursson H., Jonsson T., Stefansson H., Johannsdottir H.S., Sainz J., Frigge M.L., Kong A., Gulcher J.R., Stefansson K., and Sveinbjornsdottir S. A susceptibility gene for late onset idiopathic Parkinson's disease. Ann. Neurol. 52 (2002) 549-555
-
(2002)
Ann. Neurol.
, vol.52
, pp. 549-555
-
-
Hicks, A.A.1
Petursson, H.2
Jonsson, T.3
Stefansson, H.4
Johannsdottir, H.S.5
Sainz, J.6
Frigge, M.L.7
Kong, A.8
Gulcher, J.R.9
Stefansson, K.10
Sveinbjornsdottir, S.11
-
13
-
-
33244482539
-
Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa
-
Ibanez P., Lesage S., Lohmann E., Thobois S., De Michele G., Borg M., Agid Y., Durr A., and Brice A. Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa. Brain 129 Pt 3 (2006) 686-694
-
(2006)
Brain
, vol.129
, Issue.PART 3
, pp. 686-694
-
-
Ibanez, P.1
Lesage, S.2
Lohmann, E.3
Thobois, S.4
De Michele, G.5
Borg, M.6
Agid, Y.7
Durr, A.8
Brice, A.9
-
14
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
Kitada T., Asakawa S., Hattori N., Matsumine H., Yamamura Y., Minoshima S., Yokochi M., Mizuno Y., and Shimizu N. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 392 (1998) 605-608
-
(1998)
Nature
, vol.392
, 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
-
15
-
-
0037131567
-
The UCH-L1 gene encodes two opposing enzymatic activities that affect alpha-synuclein degradation and Parkinson's disease susceptibility
-
Liu Y., Fallon L., Lashuel H.A., Liu Z., and Lansbury Jr. P.T. The UCH-L1 gene encodes two opposing enzymatic activities that affect alpha-synuclein degradation and Parkinson's disease susceptibility. Cell 111 (2002) 209-218
-
(2002)
Cell
, vol.111
, pp. 209-218
-
-
Liu, Y.1
Fallon, L.2
Lashuel, H.A.3
Liu, Z.4
Lansbury Jr., P.T.5
-
16
-
-
12144289221
-
UCHL1 Global Genetics Consortium, UCHL1 is a Parkinson's disease susceptibility gene
-
Maraganore D.M., Lesnick T.G., Elbaz A., Chartier-Harlin M.C., Gasser T., Kruger R., Hattori N., Mellick G.D., Quattrone A., Satoh J., Toda T., Wang J., Ioannidis J.P., de Andrade M., and Rocca W.A. UCHL1 Global Genetics Consortium, UCHL1 is a Parkinson's disease susceptibility gene. Ann. Neurol. 55 (2004) 512-521
-
(2004)
Ann. Neurol.
, vol.55
, pp. 512-521
-
-
Maraganore, D.M.1
Lesnick, T.G.2
Elbaz, A.3
Chartier-Harlin, M.C.4
Gasser, T.5
Kruger, R.6
Hattori, N.7
Mellick, G.D.8
Quattrone, A.9
Satoh, J.10
Toda, T.11
Wang, J.12
Ioannidis, J.P.13
de Andrade, M.14
Rocca, W.A.15
-
17
-
-
1842455356
-
Parkin genetics: one model for Parkinson's disease
-
Mata I.F., Lockhart P.J., and Farrer M.J. Parkin genetics: one model for Parkinson's disease. Hum. Mol. Genet. 13 (2004) 127-133
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 127-133
-
-
Mata, I.F.1
Lockhart, P.J.2
Farrer, M.J.3
-
18
-
-
17044419163
-
Genetic association studies of complex traits: design and analysis issues
-
Newton-Cheh C., and Hirschhorn J.N. Genetic association studies of complex traits: design and analysis issues. Mutat. Res. 573 (2005) 54-69
-
(2005)
Mutat. Res.
, vol.573
, pp. 54-69
-
-
Newton-Cheh, C.1
Hirschhorn, J.N.2
-
19
-
-
0038754178
-
Parkin mutations and susceptibility alleles in late onset Parkinson's disease
-
Oliveira S.A., Scott W.K., Martin E.R., Nance M.A., Watts R.L., Hubble J.P., Koller W.C., Pahwa R., Stern M.B., Hiner B.C., Ondo W.G., Allen Jr. F.H., Scott B.L., Goetz C.G., Small G.W., Mastaglia F., Stajich J.M., Zhang F., Booze M.W., Winn M.P., Middleton L.T., Haines J.L., Pericak-Vance M.A., and Vance J.M. Parkin mutations and susceptibility alleles in late onset Parkinson's disease. Ann. Neurol. 53 (2003) 624-629
-
(2003)
Ann. Neurol.
, vol.53
, pp. 624-629
-
-
Oliveira, S.A.1
Scott, W.K.2
Martin, E.R.3
Nance, M.A.4
Watts, R.L.5
Hubble, J.P.6
Koller, W.C.7
Pahwa, R.8
Stern, M.B.9
Hiner, B.C.10
Ondo, W.G.11
Allen Jr., F.H.12
Scott, B.L.13
Goetz, C.G.14
Small, G.W.15
Mastaglia, F.16
Stajich, J.M.17
Zhang, F.18
Booze, M.W.19
Winn, M.P.20
Middleton, L.T.21
Haines, J.L.22
Pericak-Vance, M.A.23
Vance, J.M.24
more..
-
20
-
-
8844266996
-
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
-
Paisan-Ruiz C., Jain S., Evans E.W., Gilks W.P., Simon J., van der Brug M., de Munain A.L., Aparicio S., Gil A.M., Khan N., Johnson J., Martinez J.R., Nicholl D., Carrera I.M., Pena A.S., de Silva R., Lees A., Marti-Masso J.F., Perez-Tur J., Wood N.W., and Singleton A.B. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron 44 (2004) 595-600
-
(2004)
Neuron
, vol.44
, 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
de Munain, A.L.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..
-
21
-
-
4844222408
-
Alpha-Synuclein promoter confers susceptibility to Parkinson's disease
-
Pals P., Lincoln S., Manning J., Heckman M., Skipper L., Hulihan M., Van Den Broeck M., De Pooter T., Cras P., and Crook J. Alpha-Synuclein promoter confers susceptibility to Parkinson's disease. Ann. Neurol. 56 (2004) 591-595
-
(2004)
Ann. Neurol.
, vol.56
, pp. 591-595
-
-
Pals, P.1
Lincoln, S.2
Manning, J.3
Heckman, M.4
Skipper, L.5
Hulihan, M.6
Van Den Broeck, M.7
De Pooter, T.8
Cras, P.9
Crook, J.10
-
22
-
-
26644440926
-
Wild-type PINK1 prevents basal and induced neuronal apoptosis, a protective effect abrogated by Parkinson disease-related mutations
-
Petit A., Kawarai T., Paitel E., Sanjo N., Maj M., Scheid M., Chen F., Gu Y., Hasegawa H., Salehi-Rad S., Wang L., Rogaeva E., Fraser P., Robinson B., St George-Hyslop P., and Tandon A. Wild-type PINK1 prevents basal and induced neuronal apoptosis, a protective effect abrogated by Parkinson disease-related mutations. J. Biol. Chem. 280 (2005) 34025-34032
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 34025-34032
-
-
Petit, A.1
Kawarai, T.2
Paitel, E.3
Sanjo, N.4
Maj, M.5
Scheid, M.6
Chen, F.7
Gu, Y.8
Hasegawa, H.9
Salehi-Rad, S.10
Wang, L.11
Rogaeva, E.12
Fraser, P.13
Robinson, B.14
St George-Hyslop, P.15
Tandon, A.16
-
23
-
-
0030744876
-
Mutation in the a-synuclein gene identified in families with Parkinson's disease
-
Polymeropoulos M.H., Lavedan C., Leroy E., Ide S.E., Dehejia A., Dutra A., Pike B., Root H., Rubenstein J., Boyer R., Stenroos E.S., Chandrasekharappa S., Athanassiadou A., Papapetropoulos T., Johnson W.G., Lazzarini A.M., Duvoisin R.C., Di Iorio G., Golbe L.I., and Nussbaum R.L. Mutation in the a-synuclein gene identified in families with Parkinson's disease. Science 276 (1997) 2045-2047
-
(1997)
Science
, vol.276
, 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..
-
24
-
-
12244264435
-
Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits
-
Purcell S., Cherny S.S., and Sham P.C. Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits. Bioinformatics 19 (2003) 149-150
-
(2003)
Bioinformatics
, vol.19
, pp. 149-150
-
-
Purcell, S.1
Cherny, S.S.2
Sham, P.C.3
-
25
-
-
10044275502
-
Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease
-
Rogaeva E., Johnson J., Lang A.E., Gulick C., Gwinn-Hardy K., Kawarai T., Sato C., Morgan A., Werner J., Nussbaum R., Petit A., Okun M.S., McInerney A., Mandel R., Groen J.L., Fernandez H.H., Postuma R., Foote K.D., Salehi-Rad S., Liang Y., Reimsnider S., Tandon A., Hardy J., St George-Hyslop P., and Singleton A.B. Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease. Arch. Neurol. 61 (2004) 1898-1904
-
(2004)
Arch. Neurol.
, vol.61
, pp. 1898-1904
-
-
Rogaeva, E.1
Johnson, J.2
Lang, A.E.3
Gulick, C.4
Gwinn-Hardy, K.5
Kawarai, T.6
Sato, C.7
Morgan, A.8
Werner, J.9
Nussbaum, R.10
Petit, A.11
Okun, M.S.12
McInerney, A.13
Mandel, R.14
Groen, J.L.15
Fernandez, H.H.16
Postuma, R.17
Foote, K.D.18
Salehi-Rad, S.19
Liang, Y.20
Reimsnider, S.21
Tandon, A.22
Hardy, J.23
St George-Hyslop, P.24
Singleton, A.B.25
more..
-
26
-
-
30344483246
-
Exclusion of PINK1 as candidate gene for the late-onset form of Parkinson's disease in two European populations
-
Schlitter A.M., Kurz M., Larsen J.P., Woitalla D., Mueller T., Epplen J.T., and Dekomien G. Exclusion of PINK1 as candidate gene for the late-onset form of Parkinson's disease in two European populations. J. Negat. Results Biomed. 4 (2005) 10
-
(2005)
J. Negat. Results Biomed.
, vol.4
, pp. 10
-
-
Schlitter, A.M.1
Kurz, M.2
Larsen, J.P.3
Woitalla, D.4
Mueller, T.5
Epplen, J.T.6
Dekomien, G.7
-
27
-
-
27944444154
-
Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism
-
Silvestri L., Caputo V., Bellacchio E., Atorino L., Dallapiccola B., Valente E.M., and Casari G. Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism. Hum. Mol. Genet. 14 (2005) 3477-3492
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 3477-3492
-
-
Silvestri, L.1
Caputo, V.2
Bellacchio, E.3
Atorino, L.4
Dallapiccola, B.5
Valente, E.M.6
Casari, G.7
-
28
-
-
20644455323
-
The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients
-
Tan E.K., Shen H., Tan L.C., Farrer M., Yew K., Chua E., Jamora R.D., Puvan K., Puong K.Y., Zhao Y., Pavanni R., Wong M.C., Yih Y., Skipper L., and Liu J.J. The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients. Neurosci. Lett. 384 (2005) 327-329
-
(2005)
Neurosci. Lett.
, vol.384
, pp. 327-329
-
-
Tan, E.K.1
Shen, H.2
Tan, L.C.3
Farrer, M.4
Yew, K.5
Chua, E.6
Jamora, R.D.7
Puvan, K.8
Puong, K.Y.9
Zhao, Y.10
Pavanni, R.11
Wong, M.C.12
Yih, Y.13
Skipper, L.14
Liu, J.J.15
-
29
-
-
33745845523
-
PINK1 mutations in sporadic early-onset Parkinson's disease
-
Tan E.K., Yew K., Chua E., Puvan K., Shen H., Lee E., Puong K.Y., Zhao Y., Pavanni R., Wong M.C., Jamora D., de Silva D., Moe K.T., Woon F.P., Yuen Y., and Tan L. PINK1 mutations in sporadic early-onset Parkinson's disease. Mov. Disord. 21 (2006) 789-793
-
(2006)
Mov. Disord.
, vol.21
, pp. 789-793
-
-
Tan, E.K.1
Yew, K.2
Chua, E.3
Puvan, K.4
Shen, H.5
Lee, E.6
Puong, K.Y.7
Zhao, Y.8
Pavanni, R.9
Wong, M.C.10
Jamora, D.11
de Silva, D.12
Moe, K.T.13
Woon, F.P.14
Yuen, Y.15
Tan, L.16
-
30
-
-
2442668926
-
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
-
Valente E.M., Abou-Sleiman P.M., Caputo V., Muqit M.M.K., Harvey K., Gispert S., Ali Z., Del Turco D., Bentivoglio A.R., Healy D.G., Albanese A., Nussbaum R., Gonźalez-Maldonado R., Deller T., Salvi S., Cortelli P., Gilks W.P., Latchman D.S., Harvey R.J., Dallapiccola B., Auburger G., and Wood N.W. Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science 304 (2004) 1158-1160
-
(2004)
Science
, vol.304
, pp. 1158-1160
-
-
Valente, E.M.1
Abou-Sleiman, P.M.2
Caputo, V.3
Muqit, M.M.K.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
Gonźalez-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..
-
31
-
-
4444274910
-
PINK1 mutations are associated with sporadic early-onset parkinsonism
-
Valente E.M., Salvi S., Ialongo T., Marongiu R., Elia A.E., Caputo V., Romito L., Albanese A., Dallapiccola B., and Bentivoglio A.R. PINK1 mutations are associated with sporadic early-onset parkinsonism. Ann. Neurol. 56 (2004) 336-341
-
(2004)
Ann. Neurol.
, vol.56
, pp. 336-341
-
-
Valente, E.M.1
Salvi, S.2
Ialongo, T.3
Marongiu, R.4
Elia, A.E.5
Caputo, V.6
Romito, L.7
Albanese, A.8
Dallapiccola, B.9
Bentivoglio, A.R.10
-
32
-
-
0037108727
-
Functional association of the parkin gene promoter with idiopathic Parkinson's disease
-
West A.B., Maraganore D., Crook J., Lesnick T., Lockhart P.J., Wilkes K.M., Kapatos G., Hardy J.A., and Farrer M.J. Functional association of the parkin gene promoter with idiopathic Parkinson's disease. Hum. Mol. Genet. 11 (2002) 2787-2792
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 2787-2792
-
-
West, A.B.1
Maraganore, D.2
Crook, J.3
Lesnick, T.4
Lockhart, P.J.5
Wilkes, K.M.6
Kapatos, G.7
Hardy, J.A.8
Farrer, M.J.9
-
33
-
-
12244262772
-
Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach
-
Williams N.M., Spurlock G., Norton N., Williams H.J., Hamshere M.L., Krawczak M., Kirov G., Nikolov I., Georgieva L., Jones S., Cardno A.G., O'Donovan M.C., and Owen M.J. Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach. Mol. Psychiatry 7 (2002) 1092-1100
-
(2002)
Mol. Psychiatry
, vol.7
, pp. 1092-1100
-
-
Williams, N.M.1
Spurlock, G.2
Norton, N.3
Williams, H.J.4
Hamshere, M.L.5
Krawczak, M.6
Kirov, G.7
Nikolov, I.8
Georgieva, L.9
Jones, S.10
Cardno, A.G.11
O'Donovan, M.C.12
Owen, M.J.13
-
34
-
-
0034537609
-
High-throughput SNP detection by using DNA pooling and denaturing high performance liquid chromatography (DHPLC)
-
Wolford J.K., Blunt D., Ballecer C., and Prochazka M. High-throughput SNP detection by using DNA pooling and denaturing high performance liquid chromatography (DHPLC). Hum. Genet. 107 (2000) 483-487
-
(2000)
Hum. Genet.
, vol.107
, pp. 483-487
-
-
Wolford, J.K.1
Blunt, D.2
Ballecer, C.3
Prochazka, M.4
-
35
-
-
13844271853
-
Parkinson's disease in China: prevalence in Beijing, Xian, and Shanghai
-
Zhang Z.X., Roman G.C., Hong Z., Wu C.B., Qu Q.M., Huang J.B., Zhou B., Geng Z.P., Wu J.X., Wen H.B., Zhao H., and Zahner G.E. Parkinson's disease in China: prevalence in Beijing, Xian, and Shanghai. Lancet 365 (2005) 595-597
-
(2005)
Lancet
, vol.365
, pp. 595-597
-
-
Zhang, Z.X.1
Roman, G.C.2
Hong, Z.3
Wu, C.B.4
Qu, Q.M.5
Huang, J.B.6
Zhou, B.7
Geng, Z.P.8
Wu, J.X.9
Wen, H.B.10
Zhao, H.11
Zahner, G.E.12
-
36
-
-
8844233579
-
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
-
Zimprich A., Biskup S., Leitner P., Lichtner P., Farrer M., Lincoln S., Kachergus J., Hulihan M., Uitti R.J., Calne D.B., Stoessl A.J., Pfeiffer R.F., Patenge N., Carbajal I.C., Vieregge P., Asmus F., Mü ller-Myhsok B., Dickson D.W., Meitinger T., Strom T.M., Wszolek Z.K., and Gasser T. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Neuron 44 (2004) 601-607
-
(2004)
Neuron
, vol.44
, pp. 601-607
-
-
Zimprich, A.1
Biskup, S.2
Leitner, P.3
Lichtner, P.4
Farrer, M.5
Lincoln, S.6
Kachergus, J.7
Hulihan, M.8
Uitti, R.J.9
Calne, D.B.10
Stoessl, A.J.11
Pfeiffer, R.F.12
Patenge, N.13
Carbajal, I.C.14
Vieregge, P.15
Asmus, F.16
Mü ller-Myhsok, B.17
Dickson, D.W.18
Meitinger, T.19
Strom, T.M.20
Wszolek, Z.K.21
Gasser, T.22
more..
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