-
1
-
-
0037417254
-
Alzheimer's disease and Parkinson's disease
-
Nussbaum, R.L. and Ellis, C.E. (2003) Alzheimer's disease and Parkinson's disease. N. Engl. J. Med., 348, 1356-1364.
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 1356-1364
-
-
Nussbaum, R.L.1
Ellis, C.E.2
-
2
-
-
84868134823
-
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
-
Keller, M.F., Saad, M., Bras, J., Bettella, F., Nicolaou, N., Simon-Sanchez, J., Mittag, F., Buchel, F., Sharma, M., Gibbs, J.R. et al. (2012) Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. Hum. Mol. Genet., 21, 4996-5009.
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 4996-5009
-
-
Keller, M.F.1
Saad, M.2
Bras, J.3
Bettella, F.4
Nicolaou, N.5
Simon-Sanchez, J.6
Mittag, F.7
Buchel, F.8
Sharma, M.9
Gibbs, J.R.10
-
3
-
-
79959841853
-
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease
-
Do, C.B., Tung, J.Y., Dorfman, E., Kiefer, A.K., Drabant, E.M., Francke, U., Mountain, J.L., Goldman, S.M., Tanner, C.M., Langston, J.W. et al. (2011) Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. PLoS Genet., 7, e1002141.
-
(2011)
PLoS Genet
, vol.7
-
-
Do, C.B.1
Tung, J.Y.2
Dorfman, E.3
Kiefer, A.K.4
Drabant, E.M.5
Francke, U.6
Mountain, J.L.7
Goldman, S.M.8
Tanner, C.M.9
Langston, J.W.10
-
4
-
-
63149090431
-
Parkinson's disease: from monogenic forms to genetic susceptibility factors
-
Lesage, S. and Brice, A. (2009) Parkinson's disease: from monogenic forms to genetic susceptibility factors. Hum. Mol. Genet., 18, R48-R59.
-
(2009)
Hum. Mol. Genet.
, vol.18
-
-
Lesage, S.1
Brice, A.2
-
5
-
-
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., Simon-Sanchez, J., Schulte, C., Lesage, S., Sveinbjornsdottir, S. et al. (2011) Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. Lancet, 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
Simon-Sanchez, J.7
Schulte, C.8
Lesage, S.9
Sveinbjornsdottir, S.10
-
6
-
-
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., Kawaguchi, T., Tsunoda, T., Watanabe, M., Takeda, A. et al. (2009) Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nat. Genet., 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
Kawaguchi, T.7
Tsunoda, T.8
Watanabe, M.9
Takeda, A.10
-
7
-
-
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., Paisan-Ruiz, C., Lichtner, P., Scholz, S.W., Hernandez, D.G. et al. (2009) Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat. Genet., 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
Paisan-Ruiz, C.7
Lichtner, P.8
Scholz, S.W.9
Hernandez, D.G.10
-
8
-
-
0029248868
-
Jewish diseases and origins
-
Motulsky, A.G. (1995) Jewish diseases and origins. Nat. Genet., 9, 99-101.
-
(1995)
Nat. Genet.
, vol.9
, pp. 99-101
-
-
Motulsky, A.G.1
-
9
-
-
0035514049
-
Agenetic profile of contemporary Jewish populations
-
Ostrer, H. (2001)Agenetic profile of contemporary Jewish populations. Nat. Rev. Genet., 2, 891-898.
-
(2001)
Nat. Rev. Genet.
, vol.2
, pp. 891-898
-
-
Ostrer, H.1
-
10
-
-
77955568656
-
Microdeletions of 3q29 confer high risk for schizophrenia
-
Mulle, J.G., Dodd, A.F., McGrath, J.A., Wolyniec, P.S., Mitchell, A.A., Shetty, A.C., Sobreira, N.L., Valle, D., Rudd, M.K., Satten, G. et al. (2010) Microdeletions of 3q29 confer high risk for schizophrenia. Am. J. Hum. Genet., 87, 229-236.
-
(2010)
Am. J. Hum. Genet.
, vol.87
, pp. 229-236
-
-
Mulle, J.G.1
Dodd, A.F.2
McGrath, J.A.3
Wolyniec, P.S.4
Mitchell, A.A.5
Shetty, A.C.6
Sobreira, N.L.7
Valle, D.8
Rudd, M.K.9
Satten, G.10
-
11
-
-
0036913209
-
A highly significant association between a COMT haplotype and schizophrenia
-
Shifman, S., Bronstein, M., Sternfeld, M., Pisante-Shalom, A., Lev-Lehman, E., Weizman, A., Reznik, I., Spivak, B., Grisaru, N., Karp, L. et al. (2002)A highly significant association between a COMT haplotype and schizophrenia. Am. J. Hum. Genet., 71, 1296-1302.
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 1296-1302
-
-
Shifman, S.1
Bronstein, M.2
Sternfeld, M.3
Pisante-Shalom, A.4
Lev-Lehman, E.5
Weizman, A.6
Reznik, I.7
Spivak, B.8
Grisaru, N.9
Karp, L.10
-
12
-
-
46049112735
-
Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset
-
Gan-Or, Z., Giladi, N., Rozovski, U., Shifrin, C., Rosner, S., Gurevich, T., Bar-Shira, A. and Orr-Urtreger, A. (2008) Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset. Neurology, 70, 2277-2283.
-
(2008)
Neurology
, vol.70
, pp. 2277-2283
-
-
Gan-Or, Z.1
Giladi, N.2
Rozovski, U.3
Shifrin, C.4
Rosner, S.5
Gurevich, T.6
Bar-Shira, A.7
Orr-Urtreger, A.8
-
13
-
-
33845453622
-
Frequency of LRRK2 mutations in early- and late-onset Parkinson disease
-
Clark, L.N., Wang, Y., Karlins, E., Saito, L., Mejia-Santana, H., Harris, J., Louis, E.D., Cote, L.J., Andrews, H., Fahn, S. et al. (2006) Frequency of LRRK2 mutations in early- and late-onset Parkinson disease. Neurology, 67, 1786-1791.
-
(2006)
Neurology
, vol.67
, 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
-
14
-
-
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
-
15
-
-
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
-
16
-
-
7444237665
-
Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews
-
Aharon-Peretz, J., Rosenbaum, H. and Gershoni-Baruch, R. (2004) Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews. N. Engl. J. Med., 351, 1972-1977.
-
(2004)
N. Engl. J. Med.
, vol.351
, pp. 1972-1977
-
-
Aharon-Peretz, J.1
Rosenbaum, H.2
Gershoni-Baruch, R.3
-
17
-
-
0029773625
-
Occurrence of Parkinson's syndrome in type I Gaucher disease
-
Neudorfer, O., Giladi, N., Elstein, D., Abrahamov, A., Turezkite, T., Aghai, E., Reches, A., Bembi, B. and Zimran, A. (1996) Occurrence of Parkinson's syndrome in type I Gaucher disease. Q. J. Med., 89, 691-694.
-
(1996)
Q. J. Med.
, vol.89
, pp. 691-694
-
-
Neudorfer, O.1
Giladi, N.2
Elstein, D.3
Abrahamov, A.4
Turezkite, T.5
Aghai, E.6
Reches, A.7
Bembi, B.8
Zimran, A.9
-
18
-
-
34548726339
-
Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease
-
Clark, L.N., Ross, B.M., Wang, Y., Mejia-Santana, H., Harris, J., Louis, E.D., Cote, L.J., Andrews, H., Fahn, S., Waters, C. et al. (2007) Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease. Neurology, 69, 1270-1277.
-
(2007)
Neurology
, vol.69
, 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
-
19
-
-
7344232563
-
Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewish population
-
Horowitz, M., Pasmanik-Chor, M., Borochowitz, Z., Falik-Zaccai, T., Heldmann, K., Carmi, R., Parvari, R., Beit-Or, H., Goldman, B., Peleg, L. et al. (1998) Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewish population. Hum. Mutat., 12, 240-244.
-
(1998)
Hum. Mutat.
, vol.12
, pp. 240-244
-
-
Horowitz, M.1
Pasmanik-Chor, M.2
Borochowitz, Z.3
Falik-Zaccai, T.4
Heldmann, K.5
Carmi, R.6
Parvari, R.7
Beit-Or, H.8
Goldman, B.9
Peleg, L.10
-
20
-
-
77953231974
-
Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry
-
Atzmon, G., Hao, L., Pe'er, I., Velez, C., Pearlman, A., Palamara, P.F., Morrow, B., Friedman, E., Oddoux, C., Burns, E. et al. (2010) Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry. Am. J. Hum. Genet., 86, 850-859.
-
(2010)
Am. J. Hum. Genet.
, vol.86
, 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
-
21
-
-
79958863532
-
DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation
-
Gusev, A., Kenny, E.E., Lowe, J.K., Salit, J., Saxena, R., Kathiresan, S., Altshuler, D.M., Friedman, J.M., Breslow, J.L. and Pe'er, I. (2011) DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation. Am. J. Hum. Genet., 88, 706-717.
-
(2011)
Am. J. Hum. Genet.
, vol.88
, pp. 706-717
-
-
Gusev, A.1
Kenny, E.E.2
Lowe, J.K.3
Salit, J.4
Saxena, R.5
Kathiresan, S.6
Altshuler, D.M.7
Friedman, J.M.8
Breslow, J.L.9
Pe'er, I.10
-
22
-
-
84859253322
-
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility Loci
-
Kenny, E.E., Pe'er, I., Karban, A., Ozelius, L., Mitchell, A.A., Ng, S.M., Erazo, M., Ostrer, H., Abraham, C., Abreu, M.T. et al. (2012) A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility Loci. PLoS Genet., 8, e1002559.
-
(2012)
PLoS Genet
, vol.8
-
-
Kenny, E.E.1
Pe'er, I.2
Karban, A.3
Ozelius, L.4
Mitchell, A.A.5
Ng, S.M.6
Erazo, M.7
Ostrer, H.8
Abraham, C.9
Abreu, M.T.10
-
23
-
-
59949088494
-
Whole population, genome-wide mapping of hidden relatedness
-
Gusev, A., Lowe, J.K., Stoffel, M., Daly, M.J., Altshuler, D., Breslow, J.L., Friedman, J.M. and Pe'er, I. (2009) Whole population, genome-wide mapping of hidden relatedness. Genome Res., 19, 318-326.
-
(2009)
Genome Res
, vol.19
, pp. 318-326
-
-
Gusev, A.1
Lowe, J.K.2
Stoffel, M.3
Daly, M.J.4
Altshuler, D.5
Breslow, J.L.6
Friedman, J.M.7
Pe'er, I.8
-
24
-
-
77950301214
-
Variance component model to account for sample structure in genome-wide association studies
-
Kang, H.M., Sul, J.H., Service, S.K., Zaitlen, N.A., Kong, S.Y., Freimer, N.B., Sabatti, C. and Eskin, E. (2010) Variance component model to account for sample structure in genome-wide association studies. Nat. Genet., 42, 348-354.
-
(2010)
Nat. Genet.
, vol.42
, pp. 348-354
-
-
Kang, H.M.1
Sul, J.H.2
Service, S.K.3
Zaitlen, N.A.4
Kong, S.Y.5
Freimer, N.B.6
Sabatti, C.7
Eskin, E.8
-
25
-
-
78751695726
-
Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population
-
Kenny, E.E., Kim, M., Gusev, A., Lowe, J.K., Salit, J., Smith, J.G., Kovvali, S., Kang, H.M., Newton-Cheh, C., Daly, M.J. et al. (2011) Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population. Hum. Mol. Genet., 20, 827-839.
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 827-839
-
-
Kenny, E.E.1
Kim, M.2
Gusev, A.3
Lowe, J.K.4
Salit, J.5
Smith, J.G.6
Kovvali, S.7
Kang, H.M.8
Newton-Cheh, C.9
Daly, M.J.10
-
26
-
-
46149098096
-
Long-range LDcan confoundgenomescans in admixedpopulations
-
author reply 135-139
-
Price, A.L., Weale, M.E., Patterson, N., Myers, S.R., Need, A.C., Shianna, K.V., Ge, D., Rotter, J.I., Torres, E., Taylor, K.D. et al. (2008) Long-range LDcan confoundgenomescans in admixedpopulations.Am. J.Hum.Genet., 83, 132-135; author reply 135-139.
-
(2008)
Am. J. Hum. Genet.
, vol.83
, pp. 132-135
-
-
Price, A.L.1
Weale, M.E.2
Patterson, N.3
Myers, S.R.4
Need, A.C.5
Shianna, K.V.6
Ge, D.7
Rotter, J.I.8
Torres, E.9
Taylor, K.D.10
-
27
-
-
13944278863
-
Acommon inversion under selection in Europeans
-
Stefansson, H., Helgason, A., Thorleifsson, G., Steinthorsdottir, V., Masson, G., Barnard, J., Baker, A., Jonasdottir, A., Ingason, A., Gudnadottir, V.G. et al. (2005)Acommon inversion under selection in Europeans. Nat. Genet., 37, 129-137.
-
(2005)
Nat. Genet.
, vol.37
, 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
-
28
-
-
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., Louis, E.D., Cote, L.J., Andrews, H., Waters, C. et al. (2011) Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population. BMC Med. Genet., 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
Louis, E.D.7
Cote, L.J.8
Andrews, H.9
Waters, C.10
-
29
-
-
76349117214
-
The distribution and most recent common ancestor of the 17q21 inversion in humans
-
Donnelly, M.P., Paschou, P., Grigorenko, E., Gurwitz, D., Mehdi, S.Q., Kajuna, S.L.B., Barta, C., Kungulilo, S., Karoma, N.J., Lu, R.B. et al. (2010) The distribution and most recent common ancestor of the 17q21 inversion in humans. Am. J. Hum. Genet., 86, 161-171.
-
(2010)
Am. J. Hum. Genet.
, vol.86
, pp. 161-171
-
-
Donnelly, M.P.1
Paschou, P.2
Grigorenko, E.3
Gurwitz, D.4
Mehdi, S.Q.5
Kajuna, S.L.B.6
Barta, C.7
Kungulilo, S.8
Karoma, N.J.9
Lu, R.B.10
-
30
-
-
0036727834
-
ALFRED: an allele frequency database for anthropology
-
Osier, M.V., Cheung, K.H., Kidd, J.R., Pakstis, A.J., Miller, P.L. and Kidd, K.K. (2002) ALFRED: an allele frequency database for anthropology. Am. J. Phys. Anthropol., 119, 77-83.
-
(2002)
Am. J. Phys. Anthropol.
, vol.119
, pp. 77-83
-
-
Osier, M.V.1
Cheung, K.H.2
Kidd, J.R.3
Pakstis, A.J.4
Miller, P.L.5
Kidd, K.K.6
-
31
-
-
77955694150
-
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia
-
Pagnamenta, A.T., Bacchelli, E., de Jonge, M.V., Mirza, G., Scerri, T.S., Minopoli, F., Chiocchetti, A., Ludwig, K.U., Hoffmann, P., Paracchini, S. et al. (2010) Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. Biol. Psychiatry, 68, 320-328.
-
(2010)
Biol. Psychiatry
, vol.68
, pp. 320-328
-
-
Pagnamenta, A.T.1
Bacchelli, E.2
De Jonge, M.V.3
Mirza, G.4
Scerri, T.S.5
Minopoli, F.6
Chiocchetti, A.7
Ludwig, K.U.8
Hoffmann, P.9
Paracchini, S.10
-
32
-
-
84855569525
-
Association of sequence alterations in the putative promoter of rab7l1 with a reduced Parkinson disease risk
-
Gan-Or, Z., Bar-Shira, A., Dahary, D., Mirelman, A., Kedmi, M., Gurevich, T., Giladi, N. and Orr-Urtreger, A. (2012) Association of sequence alterations in the putative promoter of rab7l1 with a reduced Parkinson disease risk. Arch. Neurol., 69, 105-110.
-
(2012)
Arch. Neurol.
, vol.69
, pp. 105-110
-
-
Gan-Or, Z.1
Bar-Shira, A.2
Dahary, D.3
Mirelman, A.4
Kedmi, M.5
Gurevich, T.6
Giladi, N.7
Orr-Urtreger, A.8
-
33
-
-
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., Doheny, K.F., Gusella, J.F., Nichols, W.C., Foroud, T. et al. (2009) Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Hum. Genet., 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
Doheny, K.F.7
Gusella, J.F.8
Nichols, W.C.9
Foroud, T.10
-
34
-
-
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., Barker, R.A., Bellenguez, C., Bhatia, K., Blackburn, H. et al. (2011) Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21. Hum. Mol. Genet., 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
Barker, R.A.7
Bellenguez, C.8
Bhatia, K.9
Blackburn, H.10
-
35
-
-
0036138219
-
Cross-sectional study of the prevalence of Parkinson's disease in the Kibbutz movement in Israel
-
Anca, M., Paleacu, D., Shabtai, H. and Giladi, N. (2002) Cross-sectional study of the prevalence of Parkinson's disease in the Kibbutz movement in Israel. Neuroepidemiology, 21, 50-55.
-
(2002)
Neuroepidemiology
, vol.21
, pp. 50-55
-
-
Anca, M.1
Paleacu, D.2
Shabtai, H.3
Giladi, N.4
-
36
-
-
79958232053
-
Use of a refined drug tracer algorithm to estimate prevalence and incidence of Parkinson's disease in a large Israeli population
-
Chillag-Talmora, O., Giladi, N., Linn, S., Gurevich, T., El-Ad, B., Silverman, B., Friedman,N. and Peretz, C. (2011)Use of a refined drug tracer algorithm to estimate prevalence and incidence of Parkinson's disease in a large Israeli population. J. Parkinson's Dis., 1, 35-47.
-
(2011)
J. Parkinson's Dis.
, vol.1
, pp. 35-47
-
-
Chillag-Talmora, O.1
Giladi, N.2
Linn, S.3
Gurevich, T.4
El-Ad, B.5
Silverman, B.6
Friedman, N.7
Peretz, C.8
-
37
-
-
0141535355
-
Familial aggregation of early- and late-onset Parkinson's disease
-
Marder, K., Levy, G., Louis, E.D., Mejia-Santana, H., Cote, L., Andrews, H., Harris, J., Waters, C., Ford, B., Frucht, S. et al. (2003) Familial aggregation of early- and late-onset Parkinson's disease. Ann. Neurol., 54, 507-513.
-
(2003)
Ann. Neurol.
, vol.54
, 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
-
38
-
-
84855900920
-
The architecture of long-range haplotypes shared within and across populations
-
Gusev, A., Palamara, P.F., Aponte, G., Zhuang, Z., Darvasi, A., Gregersen, P. and Pe'er, I. (2012) The architecture of long-range haplotypes shared within and across populations. Mol. Biol. Evol., 29, 473-486.
-
(2012)
Mol. Biol. Evol.
, vol.29
, pp. 473-486
-
-
Gusev, A.1
Palamara, P.F.2
Aponte, G.3
Zhuang, Z.4
Darvasi, A.5
Gregersen, P.6
Pe'er, I.7
-
39
-
-
84856084252
-
Implications for health and disease in the genetic signature of the Ashkenazi Jewish population
-
Guha, S., Rosenfeld, J.A., Malhotra, A.K., Lee, A.T., Gregersen, P.K., Kane, J.M., Pe'er, I., Darvasi, A. and Lencz, T. (2012) Implications for health and disease in the genetic signature of the Ashkenazi Jewish population. Genome Biol., 13, R2.
-
(2012)
Genome Biol
, vol.13
-
-
Guha, S.1
Rosenfeld, J.A.2
Malhotra, A.K.3
Lee, A.T.4
Gregersen, P.K.5
Kane, J.M.6
Pe'er, I.7
Darvasi, A.8
Lencz, T.9
-
40
-
-
0842296490
-
Clinical phenotype of families with longevity
-
Atzmon, G., Schechter, C., Greiner, W., Davidson, D., Rennert, G. and Barzilai, N. (2004) Clinical phenotype of families with longevity. J. Am. Geriatr. Soc., 52, 274-277.
-
(2004)
J. Am. Geriatr. Soc.
, vol.52
, pp. 274-277
-
-
Atzmon, G.1
Schechter, C.2
Greiner, W.3
Davidson, D.4
Rennert, G.5
Barzilai, N.6
-
41
-
-
33846572874
-
Projected number of people with Parkinson disease in the most populous nations 2005 through 2030
-
Dorsey, E.R., Constantinescu, R., Thompson, J.P., Biglan, K.M., Holloway, R.G., Kieburtz, K., Marshall, F.J., Ravina, B.M., Schifitto, G., Siderowf, A. et al. (2007) Projected number of people with Parkinson disease in the most populous nations, 2005 through 2030. Neurology, 68, 384-386.
-
(2007)
Neurology
, vol.68
, pp. 384-386
-
-
Dorsey, E.R.1
Constantinescu, R.2
Thompson, J.P.3
Biglan, K.M.4
Holloway, R.G.5
Kieburtz, K.6
Marshall, F.J.7
Ravina, B.M.8
Schifitto, G.9
Siderowf, A.10
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