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Genetics of Parkinson's disease: LRRK2 on the rise.

Brice A.

Brain · 2005-12-01

DOI: 10.1093/brain/awh676PMID: 16311269

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[LRRK2: a gene belonging to the ROCO family is implicated in the Parkinson's disease].

Lesage S, Leutenegger AL, Brice A.

Med Sci (Paris) · 2005-12-01

DOI: 10.1051/medsci/200521121015PMID: 16324633

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The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity.

Gloeckner CJ, Kinkl N, Schumacher A, Braun RJ, O'Neill E, Meitinger T, Kolch W, Prokisch H, Ueffing M.

Hum Mol Genet · 2005-12-01

DOI: 10.1093/hmg/ddi439PMID: 16321986

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LRRK2 G2019S is a common mutation in Spanish patients with late-onset Parkinson's disease.

Infante J, Rodríguez E, Combarros O, Mateo I, Fontalba A, Pascual J, Oterino A, Polo JM, Leno C, Berciano J.

Neurosci Lett · 2005-11-18

DOI: 10.1016/j.neulet.2005.10.083PMID: 16298482

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Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data.

Khan NL, Jain S, Lynch JM, Pavese N, Abou-Sleiman P, Holton JL, Healy DG, Gilks WP, Sweeney MG, Ganguly M, Gibbons V, Gandhi S, Vaughan J, Eunson LH, Katzenschlager R, Gayton J, Lennox G, Revesz T, Nicholl D, Bhatia KP, Quinn N, Brooks D, Lees AJ, Davis MB, Piccini P, Singleton AB, Wood NW.

Brain · 2005-11-04

DOI: 10.1093/brain/awh667PMID: 16272164

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Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease.

Skipper L, Li Y, Bonnard C, Pavanni R, Yih Y, Chua E, Sung WK, Tan L, Wong MC, Tan EK, Liu J.

Hum Mol Genet · 2005-11-03

DOI: 10.1093/hmg/ddi376PMID: 16269443

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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 AL, Guimaraes J, Bonnet AM, Agid Y, Dürr A, Brice A, French Parkinson's Disease Genetics Study Group.

Ann Neurol · 2005-11-01

DOI: 10.1002/ana.20636PMID: 16240353

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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 EJ, Rohé CF, Zini M, Canesi M, Tesei S, Zecchinelli A, Antonini A, Mariani C, Meucci N, Sacilotto G, Sironi F, Salani G, Ferreira J, Chien HF, Fabrizio E, Vanacore N, Dalla Libera A, Stocchi F, Diroma C, Lamberti P, Sampaio C, Meco G, Barbosa E, Bertoli-Avella AM, Breedveld GJ, Oostra BA, Pezzoli G, Bonifati V.

J Med Genet · 2005-11-01

DOI: 10.1136/jmg.2005.035568PMID: 16272257

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The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease.

Lu CS, Simons EJ, Wu-Chou YH, Fonzo AD, Chang HC, Chen RS, Weng YH, Rohé CF, Breedveld GJ, Hattori N, Gasser T, Oostra BA, Bonifati V.

Parkinsonism Relat Disord · 2005-10-26

DOI: 10.1016/j.parkreldis.2005.09.003PMID: 16256409

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Analysis of LRRK2 functional domains in nondominant Parkinson disease.

Skipper L, Shen H, Chua E, Bonnard C, Kolatkar P, Tan LC, Jamora RD, Puvan K, Puong KY, Zhao Y, Pavanni R, Wong MC, Yuen Y, Farrer M, Liu JJ, Tan EK.

Neurology · 2005-10-01

DOI: 10.1212/01.wnl.0000180517.70572.37PMID: 16247070

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Lrrk2 pathogenic substitutions in Parkinson's disease.

Mata IF, Kachergus JM, Taylor JP, Lincoln S, Aasly J, Lynch T, Hulihan MM, Cobb SA, Wu RM, Lu CS, Lahoz C, Wszolek ZK, Farrer MJ.

Neurogenetics · 2005-09-17

DOI: 10.1007/s10048-005-0005-1PMID: 16172858

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Clinical traits of LRRK2-associated Parkinson's disease in Ireland: a link between familial and idiopathic PD.

Gosal D, Ross OA, Wiley J, Irvine GB, Johnston JA, Toft M, Mata IF, Kachergus J, Hulihan M, Taylor JP, Lincoln SJ, Farrer MJ, Lynch T, Mark Gibson J.

Parkinsonism Relat Disord · 2005-09-01

DOI: 10.1016/j.parkreldis.2005.05.004PMID: 16102999

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Records come from scientific sources. Bibliographic counts do not represent completed translations or editorial approvals.

1.220 articles found

Genetics of Parkinson's disease: LRRK2 on the rise.

[LRRK2: a gene belonging to the ROCO family is implicated in the Parkinson's disease].

The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity.

LRRK2 G2019S is a common mutation in Spanish patients with late-onset Parkinson's disease.

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data.

Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease.

G2019S LRRK2 mutation in French and North African families with Parkinson's disease.

The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor.

The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease.

Analysis of LRRK2 functional domains in nondominant Parkinson disease.

Lrrk2 pathogenic substitutions in Parkinson's disease.

Clinical traits of LRRK2-associated Parkinson's disease in Ireland: a link between familial and idiopathic PD.

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