-
1
-
-
0029435462
-
Prevalence of Parkinson's disease in the elderly: the Rotterdam Study
-
de Rijk, M.C., Breteler, M.M., Graveland, G.A., Ott, A., Grobbee, D.E., van der Meche, F.G. and Hofman, A. (1995) Prevalence of Parkinson's disease in the elderly: the Rotterdam Study. Neurology, 45, 2143-2146.
-
(1995)
Neurology
, vol.45
, pp. 2143-2146
-
-
de Rijk, M.C.1
Breteler, M.M.2
Graveland, G.A.3
Ott, A.4
Grobbee, D.E.5
van der Meche, F.G.6
Hofman, A.7
-
2
-
-
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., Lopez de Munain, A., Aparicio, S., Gil, A.M., Khan, N. et al. (2004) Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron, 44, 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
Lopez de Munain, A.7
Aparicio, S.8
Gil, A.M.9
Khan, N.10
-
3
-
-
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. et al. (2004) Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Neuron, 44, 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
-
4
-
-
37349103945
-
Mutations in LRRK2 as a cause of Parkinson's disease
-
Giasson, B.I. and Van Deerlin, V.M. (2008) Mutations in LRRK2 as a cause of Parkinson's disease. Neurosignals, 16, 99-105.
-
(2008)
Neurosignals
, vol.16
, pp. 99-105
-
-
Giasson, B.I.1
Van Deerlin, V.M.2
-
5
-
-
35948952469
-
The roles of kinases in familial Parkinson's disease
-
Cookson, M.R., Dauer, W., Dawson, T., Fon, E.A., Guo, M. and Shen, J. (2007) The roles of kinases in familial Parkinson's disease. J. Neurosci., 27, 11865-11868.
-
(2007)
J. Neurosci.
, vol.27
, pp. 11865-11868
-
-
Cookson, M.R.1
Dauer, W.2
Dawson, T.3
Fon, E.A.4
Guo, M.5
Shen, J.6
-
6
-
-
67650501546
-
Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease
-
Lesage, S., Condroyer, C., Lannuzel, A., Lohmann, E., Troiano, A., Tison, F., Damier, P., Thobois, S., Ouvrard-Hernandez, A.M., Rivaud-Pechoux, S. et al. (2009) Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease. J. Med. Genet., 46, 458-464.
-
(2009)
J. Med. Genet.
, vol.46
, pp. 458-464
-
-
Lesage, S.1
Condroyer, C.2
Lannuzel, A.3
Lohmann, E.4
Troiano, A.5
Tison, F.6
Damier, P.7
Thobois, S.8
Ouvrard-Hernandez, A.M.9
Rivaud-Pechoux, S.10
-
7
-
-
19944431081
-
A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease
-
Di Fonzo, A., Rohe, C.F., Ferreira, J., Chien, H.F., Vacca, L., Stocchi, F., Guedes, L., Fabrizio, E., Manfredi, M., Vanacore, N. et al. (2005) A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease. Lancet, 365, 412-415.
-
(2005)
Lancet
, vol.365
, pp. 412-415
-
-
Di Fonzo, A.1
Rohe, C.F.2
Ferreira, J.3
Chien, H.F.4
Vacca, L.5
Stocchi, F.6
Guedes, L.7
Fabrizio, E.8
Manfredi, M.9
Vanacore, N.10
-
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. et al. (2005) A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet, 365, 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
-
9
-
-
19944432606
-
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease
-
Nichols, W.C., Pankratz, N., Hernandez, D., Paisan-Ruiz, C., Jain, S., Halter, C.A., Michaels, V.E., Reed, T., Rudolph, A., Shults, C.W. et al. (2005) Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease. Lancet, 365, 410-412.
-
(2005)
Lancet
, vol.365
, pp. 410-412
-
-
Nichols, W.C.1
Pankratz, N.2
Hernandez, D.3
Paisan-Ruiz, C.4
Jain, S.5
Halter, C.A.6
Michaels, V.E.7
Reed, T.8
Rudolph, A.9
Shults, C.W.10
-
10
-
-
33646151866
-
LRRK2 in Parkinson's disease: protein domains and functional insights
-
Mata, I.F., Wedemeyer, W.J., Farrer, M.J., Taylor, J.P. and Gallo, K.A. (2006) LRRK2 in Parkinson's disease: protein domains and functional insights. Trends Neurosci., 29, 286-293.
-
(2006)
Trends Neurosci.
, vol.29
, pp. 286-293
-
-
Mata, I.F.1
Wedemeyer, W.J.2
Farrer, M.J.3
Taylor, J.P.4
Gallo, K.A.5
-
11
-
-
33645160640
-
The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor
-
Goldwurm, S., Di Fonzo, A., Simons, E.J., Rohe, C.F., Zini, M., Canesi, M., Tesei, S., Zecchinelli, A., Antonini, A., Mariani, C. et al. (2005) The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor. J. Med. Genet., 42, e65.
-
(2005)
J. Med. Genet.
, vol.42
-
-
Goldwurm, S.1
Di Fonzo, A.2
Simons, E.J.3
Rohe, C.F.4
Zini, M.5
Canesi, M.6
Tesei, S.7
Zecchinelli, A.8
Antonini, A.9
Mariani, C.10
-
12
-
-
20144387207
-
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations
-
Kachergus, J., Mata, I.F., Hulihan, M., Taylor, J.P., Lincoln, S., Aasly, J., Gibson, J.M., Ross, O.A., Lynch, T., Wiley, J. et al. (2005) Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations. Am. J. Hum. Genet., 76, 672-680.
-
(2005)
Am. J. Hum. Genet.
, vol.76
, pp. 672-680
-
-
Kachergus, J.1
Mata, I.F.2
Hulihan, M.3
Taylor, J.P.4
Lincoln, S.5
Aasly, J.6
Gibson, J.M.7
Ross, O.A.8
Lynch, T.9
Wiley, J.10
-
13
-
-
22544465257
-
LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century
-
Lesage, S., Leutenegger, A.L., Ibanez, P., Janin, S., Lohmann, E., Durr, A. and Brice, A. (2005) LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century. Am. J. Hum. Genet., 77, 330-332.
-
(2005)
Am. J. Hum. Genet.
, vol.77
, pp. 330-332
-
-
Lesage, S.1
Leutenegger, A.L.2
Ibanez, P.3
Janin, S.4
Lohmann, E.5
Durr, A.6
Brice, A.7
-
14
-
-
31344432937
-
LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs
-
Lesage, S., Durr, A., Tazir, M., Lohmann, E., Leutenegger, A.L., Janin, S., Pollak, P. and Brice, A. (2006) LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs. N. Engl. J. Med., 354, 422-423.
-
(2006)
N. Engl. J. Med.
, vol.354
, pp. 422-423
-
-
Lesage, S.1
Durr, A.2
Tazir, M.3
Lohmann, E.4
Leutenegger, A.L.5
Janin, S.6
Pollak, P.7
Brice, A.8
-
15
-
-
33749021352
-
LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago
-
Zabetian, C.P., Hutter, C.M., Yearout, D., Lopez, A.N., Factor, S.A., Griffith, A., Leis, B.C., Bird, T.D., Nutt, J.G., Higgins, D.S. et al. (2006) LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago. Am. J. Hum. Genet., 79, 752-758.
-
(2006)
Am. J. Hum. Genet.
, vol.79
, pp. 752-758
-
-
Zabetian, C.P.1
Hutter, C.M.2
Yearout, D.3
Lopez, A.N.4
Factor, S.A.5
Griffith, A.6
Leis, B.C.7
Bird, T.D.8
Nutt, J.G.9
Higgins, D.S.10
-
16
-
-
38349189767
-
A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease
-
Warren, L., Gibson, R., Ishihara, L., Elango, R., Xue, Z., Akkari, A., Ragone, L., Pahwa, R., Jankovic, J., Nance, M. et al. (2008) A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease. Parkinsonism Relat. Disord., 14, 77-80.
-
(2008)
Parkinsonism Relat. Disord.
, vol.14
, pp. 77-80
-
-
Warren, L.1
Gibson, R.2
Ishihara, L.3
Elango, R.4
Xue, Z.5
Akkari, A.6
Ragone, L.7
Pahwa, R.8
Jankovic, J.9
Nance, M.10
-
17
-
-
33645130652
-
Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries
-
Tomiyama, H., Li, Y., Funayama, M., Hasegawa, K., Yoshino, H., Kubo, S., Sato, K., Hattori, T., Lu, C.S., Inzelberg, R. et al. (2006) Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries. Mov. Disord., 21, 1102-1108.
-
(2006)
Mov. Disord.
, vol.21
, pp. 1102-1108
-
-
Tomiyama, H.1
Li, Y.2
Funayama, M.3
Hasegawa, K.4
Yoshino, H.5
Kubo, S.6
Sato, K.7
Hattori, T.8
Lu, C.S.9
Inzelberg, R.10
-
18
-
-
33747701497
-
Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease
-
Zabetian, C.P., Morino, H., Ujike, H., Yamamoto, M., Oda, M., Maruyama, H., Izumi, Y., Kaji, R., Griffith, A., Leis, B.C. et al. (2006) Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease. Neurology, 67, 697-699.
-
(2006)
Neurology
, vol.67
, pp. 697-699
-
-
Zabetian, C.P.1
Morino, H.2
Ujike, H.3
Yamamoto, M.4
Oda, M.5
Maruyama, H.6
Izumi, Y.7
Kaji, R.8
Griffith, A.9
Leis, B.C.10
-
20
-
-
50049104725
-
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
-
Healy, D.G., Falchi, M., O'Sullivan, S.S., Bonifati, V., Durr, A., Bressman, S., Brice, A., Aasly, J., Zabetian, C.P., Goldwurm, S. et al. (2008) Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. Lancet Neurol., 7, 583-590.
-
(2008)
Lancet Neurol
, vol.7
, pp. 583-590
-
-
Healy, D.G.1
Falchi, M.2
O'Sullivan, S.S.3
Bonifati, V.4
Durr, A.5
Bressman, S.6
Brice, A.7
Aasly, J.8
Zabetian, C.P.9
Goldwurm, S.10
-
21
-
-
27744446035
-
The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease
-
Lu, C.S., Simons, E.J., Wu-Chou, Y.H., Fonzo, A.D., Chang, H.C., Chen, R.S., Weng, Y.H., Rohe, C.F., Breedveld, G.J., Hattori, N. et al. (2005) The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease. Parkinsonism Relat. Disord., 11, 521-522.
-
(2005)
Parkinsonism Relat. Disord.
, vol.11
, pp. 521-522
-
-
Lu, C.S.1
Simons, E.J.2
Wu-Chou, Y.H.3
Fonzo, A.D.4
Chang, H.C.5
Chen, R.S.6
Weng, Y.H.7
Rohe, C.F.8
Breedveld, G.J.9
Hattori, N.10
-
22
-
-
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. et al. (2005) The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients. Neurosci. Lett., 384, 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
-
23
-
-
33745862378
-
Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease
-
Fung, H.C., Chen, C.M., Hardy, J., Hernandez, D., Singleton, A. and Wu, Y.R. (2006) Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease. Mov. Disord., 21, 880-881.
-
(2006)
Mov. Disord.
, vol.21
, pp. 880-881
-
-
Fung, H.C.1
Chen, C.M.2
Hardy, J.3
Hernandez, D.4
Singleton, A.5
Wu, Y.R.6
-
24
-
-
31344439221
-
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews
-
Ozelius, L.J., Senthil, G., Saunders-Pullman, R., Ohmann, E., Deligtisch, A., Tagliati, M., Hunt, A.L., Klein, C., Henick, B., Hailpern, S.M. et al. (2006) LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews. N. Engl. J. Med., 354, 424-425.
-
(2006)
N. Engl. J. Med.
, vol.354
, 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
-
25
-
-
33750406222
-
Absence/rarity of commonly reported LRRK2 mutations in Indian Parkinson's disease patients
-
Punia, S., Behari, M., Govindappa, S.T., Swaminath, P.V., Jayaram, S., Goyal, V., Muthane, U.B., Juyal, R.C. and Thelma, B.K. (2006) Absence/rarity of commonly reported LRRK2 mutations in Indian Parkinson's disease patients. Neurosci. Lett., 409, 83-88.
-
(2006)
Neurosci. Lett.
, vol.409
, pp. 83-88
-
-
Punia, S.1
Behari, M.2
Govindappa, S.T.3
Swaminath, P.V.4
Jayaram, S.5
Goyal, V.6
Muthane, U.B.7
Juyal, R.C.8
Thelma, B.K.9
-
26
-
-
35848939603
-
The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect?
-
Orr-Urtreger, A., Shifrin, C., Rozovski, U., Rosner, S., Bercovich, D., Gurevich, T., Yagev-More, H., Bar-Shira, A. and Giladi, N. (2007) The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect? Neurology, 69, 1595-1602.
-
(2007)
Neurology
, vol.69
, pp. 1595-1602
-
-
Orr-Urtreger, A.1
Shifrin, C.2
Rozovski, U.3
Rosner, S.4
Bercovich, D.5
Gurevich, T.6
Yagev-More, H.7
Bar-Shira, A.8
Giladi, N.9
-
27
-
-
48849092336
-
LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study
-
Hulihan, M.M., Ishihara-Paul, L., Kachergus, J., Warren, L., Amouri, R., Elango, R., Prinjha, R.K., Upmanyu, R., Kefi, M., Zouari, M. et al. (2008) LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study. Lancet Neurol., 7, 591-594.
-
(2008)
Lancet Neurol
, vol.7
, pp. 591-594
-
-
Hulihan, M.M.1
Ishihara-Paul, L.2
Kachergus, J.3
Warren, L.4
Amouri, R.5
Elango, R.6
Prinjha, R.K.7
Upmanyu, R.8
Kefi, M.9
Zouari, M.10
-
28
-
-
56149125336
-
Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?
-
Lesage, S., Belarbi, S., Troiano, A., Condroyer, C., Hecham, N., Pollak, P., Lohman, E., Benhassine, T., Ysmail-Dahlouk, F., Durr, A. et al. (2008) Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease? Neurology, 71, 1550-1552.
-
(2008)
Neurology
, vol.71
, pp. 1550-1552
-
-
Lesage, S.1
Belarbi, S.2
Troiano, A.3
Condroyer, C.4
Hecham, N.5
Pollak, P.6
Lohman, E.7
Benhassine, T.8
Ysmail-Dahlouk, F.9
Durr, A.10
-
29
-
-
55449120805
-
Genetic mapping in human disease
-
Altshuler, D., Daly, M.J. and Lander, E.S. (2008) Genetic mapping in human disease. Science, 322, 881-888.
-
(2008)
Science
, vol.322
, pp. 881-888
-
-
Altshuler, D.1
Daly, M.J.2
Lander, E.S.3
-
30
-
-
70249150754
-
A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype
-
Pirkevi, C., Lesage, S., Condroyer, C., Tomiyama, H., Hattori, N., Ertan, S., Brice, A. and Basak, A.N. (2009) A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype. Neurogenetics, 10, 271-273.
-
(2009)
Neurogenetics
, vol.10
, pp. 271-273
-
-
Pirkevi, C.1
Lesage, S.2
Condroyer, C.3
Tomiyama, H.4
Hattori, N.5
Ertan, S.6
Brice, A.7
Basak, A.N.8
-
31
-
-
57149148084
-
The genetic legacy of religious diversity and intolerance: paternal lineages of Christians, Jews, and Muslims in the Iberian Peninsula
-
Adams, S.M., Bosch, E., Balaresque, P.L., Ballereau, S.J., Lee, A.C., Arroyo, E., Lopez-Parra, A.M., Aler, M., Grifo, M.S., Brion, M. et al. (2008) The genetic legacy of religious diversity and intolerance: paternal lineages of Christians, Jews, and Muslims in the Iberian Peninsula. Am. J. Hum. Genet., 83, 725-736.
-
(2008)
Am. J. Hum. Genet.
, vol.83
, pp. 725-736
-
-
Adams, S.M.1
Bosch, E.2
Balaresque, P.L.3
Ballereau, S.J.4
Lee, A.C.5
Arroyo, E.6
Lopez-Parra, A.M.7
Aler, M.8
Grifo, M.S.9
Brion, M.10
-
32
-
-
79958116682
-
Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries
-
Epub 2009 March
-
Bar-Shira, A., Hutter, C.M., Giladi, N., Zabetian, C.P. and Orr-Urtreger, A. (2009) Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries. Neurogenetics, 10, 355-358. Epub 2009 March 13.
-
(2009)
Neurogenetics
, vol.10
-
-
Bar-Shira, A.1
Hutter, C.M.2
Giladi, N.3
Zabetian, C.P.4
Orr-Urtreger, A.5
-
33
-
-
33344474976
-
The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder event
-
Behar, D.M., Metspalu, E., Kivisild, T., Achilli, A., Hadid, Y., Tzur, S., Pereira, L., Amorim, A., Quintana-Murci, L., Majamaa, K. et al. (2006) The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder event. Am. J. Hum. Genet, 78, 487-497.
-
(2006)
Am. J. Hum. Genet
, vol.78
, pp. 487-497
-
-
Behar, D.M.1
Metspalu, E.2
Kivisild, T.3
Achilli, A.4
Hadid, Y.5
Tzur, S.6
Pereira, L.7
Amorim, A.8
Quintana-Murci, L.9
Majamaa, K.10
-
34
-
-
43049175775
-
Counting the founders: the matrilineal genetic ancestry of the Jewish Diaspora
-
Behar, D.M., Metspalu, E., Kivisild, T., Rosset, S., Tzur, S., Hadid, Y., Yudkovsky, G., Rosengarten, D., Pereira, L., Amorim, A. et al. (2008) Counting the founders: the matrilineal genetic ancestry of the Jewish Diaspora. PLoS One, 3, e2062.
-
(2008)
PLoS One
, vol.3
-
-
Behar, D.M.1
Metspalu, E.2
Kivisild, T.3
Rosset, S.4
Tzur, S.5
Hadid, Y.6
Yudkovsky, G.7
Rosengarten, D.8
Pereira, L.9
Amorim, A.10
-
35
-
-
27644455523
-
G2019S LRRK2 mutation in French and North African families with Parkinson's disease
-
Lesage, S., Ibanez, P., Lohmann, E., Pollak, P., Tison, F., Tazir, M., Leutenegger, A.L., Guimaraes, J., Bonnet, A.M., Agid, Y. et al. (2005) G2019S LRRK2 mutation in French and North African families with Parkinson's disease. Ann. Neurol., 58, 784-787.
-
(2005)
Ann. Neurol.
, vol.58
, pp. 784-787
-
-
Lesage, S.1
Ibanez, P.2
Lohmann, E.3
Pollak, P.4
Tison, F.5
Tazir, M.6
Leutenegger, A.L.7
Guimaraes, J.8
Bonnet, A.M.9
Agid, Y.10
-
36
-
-
64549084210
-
A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations
-
French Parkinson's Disease Genetics Studyroup
-
Lohmann, E., Leclere, L., De Anna, F., Lesage, S., Dubois, B., Agid, Y., Dürr, A. and Brice, A. and French Parkinson's Disease Genetics Study Group (2009) A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations. Parkinsonism Relat. Disord., 15, 273-276.
-
(2009)
Parkinsonism Relat. Disord
, vol.15
, pp. 273-276
-
-
Lohmann, E.1
Leclere, L.2
De Anna, F.3
Lesage, S.4
Dubois, B.5
Agid, Y.6
Dürr, A.7
Brice, A.8
-
37
-
-
33947215402
-
LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans
-
Lesage, S., Janin, S., Lohmann, E., Leutenegger, A.L., Leclere, L., Viallet, F., Pollak, P., Durif, F., Thobois, S., Layet, V. et al. (2007) LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans. Arch. Neurol., 64, 425-430.
-
(2007)
Arch. Neurol.
, vol.64
, pp. 425-430
-
-
Lesage, S.1
Janin, S.2
Lohmann, E.3
Leutenegger, A.L.4
Leclere, L.5
Viallet, F.6
Pollak, P.7
Durif, F.8
Thobois, S.9
Layet, V.10
-
38
-
-
34347247284
-
Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease
-
Lesage, S., Leclere, L., Lohmann, E., Borg, M., Ruberg, M., Durr, A. and Brice, A. (2007) Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease. Neurodegener. Dis., 4, 195-198.
-
(2007)
Neurodegener. Dis.
, vol.4
, pp. 195-198
-
-
Lesage, S.1
Leclere, L.2
Lohmann, E.3
Borg, M.4
Ruberg, M.5
Durr, A.6
Brice, A.7
-
39
-
-
0033555906
-
Tandem repeats finder: a program to analyze DNA sequences
-
Benson, G. (1999) Tandem repeats finder: a program to analyze DNA sequences. Nucleic Acids Res., 27, 573-580.
-
(1999)
Nucleic Acids Res.
, vol.27
, pp. 573-580
-
-
Benson, G.1
-
40
-
-
0242691208
-
A comparison of bayesian methods for haplotype reconstruction from population genotype data
-
Stephens, M. and Donnelly, P. (2003) A comparison of bayesian methods for haplotype reconstruction from population genotype data. Am. J. Hum. Genet., 73, 1162-1169.
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 1162-1169
-
-
Stephens, M.1
Donnelly, P.2
-
41
-
-
0032900678
-
Median-joining networks for inferring intraspecific phylogenies
-
Bandelt, H.J., Forster, P. and Rohl, A. (1999) Median-joining networks for inferring intraspecific phylogenies. Mol. Biol. Evol., 16, 37-48.
-
(1999)
Mol. Biol. Evol.
, vol.16
, pp. 37-48
-
-
Bandelt, H.J.1
Forster, P.2
Rohl, A.3
-
42
-
-
0346991739
-
Detecting population growth, selection and inherited fertility from haplotypic data in humans
-
Austerlitz, F., Kalaydjieva, L. and Heyer, E. (2003) Detecting population growth, selection and inherited fertility from haplotypic data in humans. Genetics, 165, 1579-1586.
-
(2003)
Genetics
, vol.165
, pp. 1579-1586
-
-
Austerlitz, F.1
Kalaydjieva, L.2
Heyer, E.3
-
43
-
-
2942726191
-
Estimating the age of rare disease mutations: the example of Triple-A syndrome
-
Genin, E., Tullio-Pelet, A., Begeot, F., Lyonnet, S. and Abel, L. (2004) Estimating the age of rare disease mutations: the example of Triple-A syndrome. J. Med. Genet., 41, 445-449.
-
(2004)
J. Med. Genet.
, vol.41
, pp. 445-449
-
-
Genin, E.1
Tullio-Pelet, A.2
Begeot, F.3
Lyonnet, S.4
Abel, L.5
-
44
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
Frazer, K.A., Ballinger, D.G., Cox, D.R., Hinds, D.A., Stuve, L.L., Gibbs, R.A., Belmont, J.W., Boudreau, A., Hardenbol, P., Leal, S.M. et al. (2007) A second generation human haplotype map of over 3.1 million SNPs. Nature, 449, 851-861.
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
Frazer, K.A.1
Ballinger, D.G.2
Cox, D.R.3
Hinds, D.A.4
Stuve, L.L.5
Gibbs, R.A.6
Belmont, J.W.7
Boudreau, A.8
Hardenbol, P.9
Leal, S.M.10
-
45
-
-
0031778070
-
Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat
-
Brinkmann, B., Klintschar, M., Neuhuber, F., Huhne, J. and Rolf, B. (1998) Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat. Am. J. Hum. Genet., 62, 1408-1415.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 1408-1415
-
-
Brinkmann, B.1
Klintschar, M.2
Neuhuber, F.3
Huhne, J.4
Rolf, B.5
|