Summary of GIGYF2 studies in Parkinson's disease: The burden of proof

European Journal of Neurology

Volumn 17, Issue 2, 2010, Pages 175-176

  Tan, E K ^a,b   Schapira, A H ^c  

^a SINGAPORE GENERAL HOSPITAL   (Singapore)

^b DUKE NUS MEDICAL SCHOOL   (Singapore)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; GIGYF 2 PROTEIN; GROWTH FACTOR RECEPTOR BOUND PROTEIN 10; PROTEIN; UNCLASSIFIED DRUG;

EDITORIAL; ETHNICITY; GENE DELETION; GENE INSERTION; GENE LOCUS; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC RISK; GENETIC VARIABILITY; HUMAN; LINKAGE ANALYSIS; MARKER GENE; MISSENSE MUTATION; PARKINSON DISEASE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

CARRIER PROTEINS; HUMANS; MUTATION; PARKINSON DISEASE;

EID: 74549218759     PISSN: 13515101     EISSN: 14681331     Source Type: Journal    
DOI: 10.1111/j.1468-1331.2009.02834.x     Document Type: Editorial

References (16)

1. Tan EK, Skipper LM. Pathogenic mutations in Parkinson disease. Hum Mutat 2007 28 : 641 653.
2. Harbo HF, Finsterer J, Baets J, et al. EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias. Eur J Neurol 2009 16 : 777 785.
3. Tan EK, Schapira AH. Uniting Chinese across Asia: the LRRK2 Gly2385Arg risk variant. Eur J Neurol 2008 15 : 203 204.
4. Pankratz N, Nichols WC, Uniacke SK, et al. Significant linkage of Parkinson disease to chromosome 2q36-37. Am J Hum Genet 2003 72 : 1053 1057.
5. Lautier C, Goldwurm S, Dürr A, et al. Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease. Am J Hum Genet 2008 82 : 822 833.
6. Bras J, Simón-Sánchez J, Federoff M, et al. Lack of replication of association between GIGYF2 variants and Parkinson disease. Hum Mol Genet 2009 2 : 341 346.
7. Vilariño-Güell C, Ross OA, Soto AI, et al. Reported mutations in GIGYF2 are not a common cause of Parkinson's disease. Mov Disord 2009 24 : 619 620.
8. Bonetti M, Ferraris A, Petracca M, Bentivoglio AR, Dallapiccola B, Valente EM. GIGYF2 variants are not associated with Parkinson's disease in Italy. Mov Disord 2009 24 : 1867 1868.
9. Di Fonzo A, Fabrizio E, Thomas A, et al. GIGYF2 mutations are not a frequent cause of familial Parkinson's disease. Parkinsonism Relat Disord 2009 May 30. [Epub ahead of print].
10. Tan EK, Lin CH, Tai CH, et al. Non-synonymous GIGYF2 variants in Parkinson's disease from two Asian populations. Hum Genet 2009 126 : 425 430.
11. Guo Y, Jankovic J, Zhu S, et al. GIGYF2 Asn56Ser and Asn457Thr mutations in Parkinson disease patients. Neurosci Lett 2009 454 : 209 211.
12. Meeus B, Nuytemans K, Crosiers D, et al. GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population. Neurobiol Aging 2009 March 23. [Epub ahead of print].
13. Nichols WC, Kissell DK, Pankratz N, et al. Variation in GIGYF2 is not associated with Parkinson disease. Neurology 2009 72 : 1886 1892.
14. Zimprich A, Schulte C, Reinthaler E, et al. PARK11 gene (GIGYF2) variants Asn56Ser and Asn457Thr are not pathogenic for Parkinson's disease. Parkinsonism Relat Disord 2009 15 : 532 534.
15. Samaranch L, Lorenzo E, Pastor M, et al. Analysis of the GIGYF2 gene in familial and sporadic Parkinson's disease in the Spanish population. Eur J Neurol 2010 17 : 321 325.
16. Sutherland GT, Siebert GA, Newman JR, et al. Haplotype analysis of the PARK 11 gene, GIGYF2, in sporadic Parkinson's disease. Mov Disord 2009 24 : 449 452.