Response from Maraganore et al. [6]

American Journal of Human Genetics

Volumn 78, Issue 6, 2006, Pages 1092-1094

  Maraganore, Demetrius M ^a   De Andrade, Mariza ^a   Lesnick, Timothy G ^a   Pant, P V Krishna ^b   Cox, David R ^b   Ballinger, Dennis G ^b  

^a Mayo Clinic   (United States)

^b Perlegen Sciences Inc   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENE; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; HUMAN; LETTER; LRRK2 GENE; MANTEL HAENSZEL ANALYSIS; PARKINSON DISEASE; PRIORITY JOURNAL; REPRODUCIBILITY; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL ANALYSIS; STATISTICAL SIGNIFICANCE; TAIWAN;

EID: 33646888629     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/504731     Document Type: Letter

References (8)

1. Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, Pant PVK, Frazer KA, Cox DR, Ballinger DG (2005) High-resolution whole-genome association study of Parkinson disease. Am J Hum Genet 77:685-693
2. Clarimon J, Scholz S, Fung H-C, Hardy J, Eerola J, Hellström O, Chen C-M, Wu Y-R, Tienari PJ, Singleton A (2006) Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease. Am J Hum Genet 78:1082-1084 (in this issue)
3. Li Y, Rowland C, Schrodi S, Laird W, Tacey K, Ross D, Leong D, Catanese J, Sninsky J, Grupe A (2006) A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan. Am J Hum Genet 78: 1090-1092 (in this issue)
4. Farrer MJ, Haugarvoll K, Ross OA, Stone JT, Milkovic NM, Cobb SA, Whittle AJ, Lincoln SJ, Hulihan MM, Heckman MG, White LR, Aasly JO, Gibson JM, Gosal D, Lynch T, Wszolek ZK, Uitti RJ, Toft M (2006) Genomewide association, Parkinson disease, and PARK10. Am J Hum Genet 78:1084-1088 (in this issue)
5. Goris A, Williams-Gray CH, Foltynie T, Compston DAS, Barker RA, Sawcer SJ (2006) No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening. Am J Hum Genet 78:1088-1090 (in this issue)
6. Myers RH (2006) Considerations for genomewide association studies in Parkinson disease. Am J Hum Genet 78:1081-1082 (in this issue)
7. Farrer M, Stone J, Mata IF, Lincoln S, Kachergus J, Hulihan M, Strain KJ, Maraganore MD (2005) LRRK2 mutations in Parkinson disease. Neurology 65:738-740
8. Rocca WA, McDonnell SK, Strain KJ, Bower JH, Ahlskog JE, Elbaz A, Schaid DJ, Maraganore DM (2004) Familial aggregation of Parkinson's disease: the Mayo Clinic Family Study. Ann Neurol 56: 495-502