Cited by 81

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Genetic variability at the PARK16 locus

Tucci, Arianna, Nalls, Mike A, Houlden, Henry, Revesz, Tamas, Singleton, Andrew B, Wood, Nicholas W, Hardy, John, Paisán-Ruiz, Coro·2010·European Journal of Human Genetics

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Crossref · 10.1038/ejhg.2010.125

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Research works printed but not linked: 22

  1. Lees AJ, Hardy J, Revesz T : Parkinson's disease. Lancet 2009; 373: 2055–2066. · DOI · Paper page
  2. Hardy J, Lewis P, Revesz T, Lees A, Paisan-Ruiz C : The genetics of Parkinson's syndromes: a critical review. Curr Opin Genet Dev 2009; 19: 254–265. · DOI
  3. Winkler S, Hagenah J, Lincoln S et al: alpha-Synuclein and Parkinson disease susceptibility. Neurology 2007; 69: 1745–1750. · DOI
  4. Skipper L, Li Y, Bonnard C et al: Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease. Hum Mol Genet 2005; 14: 3549–3556. · DOI
  5. Di Fonzo A, Wu-Chou YH, Lu CS et al: A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan. Neurogenetics 2006; 7: 133–138. · DOI
  6. Ross OA, Wu YR, Lee MC et al: Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease. Ann Neurol 2008; 64: 88–92. · DOI
  7. Paisan-Ruiz C, Washecka N, Nath P, Singleton AB, Corder EH : Parkinson's disease and low frequency alleles found together throughout LRRK2. Ann Hum Genet 2009; 73: 391–403. · DOI
  8. Sidransky E, Nalls MA, Aasly JO et al: Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. N Engl J Med 2009; 361: 1651–1661. · DOI · Paper page
  9. Paisan-Ruiz C : LRRK2 gene variation and its contribution to Parkinson disease. Hum Mutat 2009; 30: 1153–1160. · DOI
  10. Hardy J, Singleton A : Genomewide association studies and human disease. N Engl J Med 2009; 360: 1759–1768. · DOI · Paper page
  11. Pankratz N, Wilk JB, Latourelle JC et al: Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Hum Genet 2009; 124: 593–605. · DOI
  12. Satake W, Nakabayashi Y, Mizuta I et al: Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nat Genet 2009; 41: 1303–1307. · DOI
  13. Simon-Sanchez J, Schulte C, Bras JM et al: Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat Genet 2009; 41: 1308–1312. · DOI · Paper page
  14. Edwards TL, Scott WK, Almonte C et al: Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. Ann Hum Genet 2010; 74: 97–109. · DOI
  15. Hughes AJ, Daniel SE, Kilford L, Lees AJ : Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. J Neurol Neurosurg Psychiatry 1992; 55: 181–184. · DOI · Paper page
  16. Edgar RC : MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res 2004; 32: 1792–1797. · DOI · Paper page
  17. Greggio E, Cookson MR : Leucine-rich repeat kinase 2 mutations and Parkinson's disease: three questions. ASN Neuro 2009; 1: e00002. · DOI
  18. Cooper AA, Gitler AD, Cashikar A et al: Alpha-synuclein blocks ER-Golgi traffic and Rab1 rescues neuron loss in Parkinson's models. Science 2006; 313: 324–328. · DOI
  19. Gitler AD, Bevis BJ, Shorter J et al: The Parkinson's disease protein alpha-synuclein disrupts cellular Rab homeostasis. Proc Natl Acad Sci USA 2008; 105: 145–150. · DOI
  20. Bolognin S, Messori L, Zatta P : Metal ion physiopathology in neurodegenerative disorders. Neuromolecular Med 2009; 11: 223–238. · DOI
  21. Kolisek M, Launay P, Beck A et al: SLC41A1 is a novel mammalian Mg2+ carrier. J Biol Chem 2008; 283: 16235–16247. · DOI
  22. Evans W, Fung HC, Steele J et al: The tau H2 haplotype is almost exclusively Caucasian in origin. Neurosci Lett 2004; 369: 183–185. · DOI

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Metadata

Authors
Tucci, A., Nalls, M. A., Houlden, H., Revesz, T., Singleton, A. B., Wood, N. W., Hardy, J., & Paisán-Ruiz, C.
Venue
European Journal of Human Genetics
Published
2010-08-04
Volume
18
Issue
12
Pages
1356-1359
ISSN
  • 1018-4813
  • 1476-5438
Cited by
81
References
1
Language
en

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