Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset

Author:

Ramos Eliana Marisa,Latourelle Jeanne C.,Lee Ji-Hyun,Gillis Tammy,Mysore Jayalakshmi S.,Squitieri Ferdinando,Di Pardo Alba,Di Donato Stefano,Hayden Michael R.,Morrison Patrick J.,Nance Martha,Ross Christopher A.,Margolis Russell L.,Gomez-Tortosa Estrella,Ayuso Carmen,Suchowersky Oksana,Trent Ronald J.,McCusker Elizabeth,Novelletto Andrea,Frontali Marina,Jones Randi,Ashizawa Tetsuo,Frank Samuel,Saint-Hilaire Marie-Helene,Hersch Steven M.,Rosas Herminia D.,Lucente Diane,Harrison Madaline B.,Zanko Andrea,Marder Karen,Gusella James F.,Lee Jong-Min,Alonso Isabel,Sequeiros Jorge,Myers Richard H.,MacDonald Marcy E.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference28 articles.

1. Alberch J, Lopez M, Badenas C, Carrasco JL, Mila M, Munoz E, Canals JM (2005) Association between BDNF Val66Met polymorphism and age at onset in Huntington disease. Neurology 65(6):964–965. doi: 10.1212/01.wnl.0000175977.57661.b1

2. Che HV, Metzger S, Portal E, Deyle C, Riess O, Nguyen HP (2011) Localization of sequence variations in PGC-1alpha influence their modifying effect in Huntington disease. Mol Neurodegener 6(1):1. doi: 10.1186/1750-1326-6-1

3. Cui L, Jeong H, Borovecki F, Parkhurst CN, Tanese N, Krainc D (2006) Transcriptional repression of PGC-1alpha by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration. Cell 127(1):59–69. doi: 10.1016/j.cell.2006.09.015

4. Di Maria E, Marasco A, Tartari M, Ciotti P, Abbruzzese G, Novelli G, Bellone E, Cattaneo E, Mandich P (2006) No evidence of association between BDNF gene variants and age-at-onset of Huntington’s disease. Neurobio Dis 24(2):274–279. doi: 10.1016/j.nbd.2006.07.002

5. Duyao M, Ambrose C, Myers R, Novelletto A, Persichetti F, Frontali M, Folstein S, Ross C, Franz M, Abbott M, Gray J, Conneally P, Young A, Penney J, Hollingsworth Z, Shoulson I, Lazzarini A, Falek A, Koroshetz W, Sax D, Bird E, Vonsattel J, Bonilla E, Alvir J, Bickham Conde J, Cha J-H, Dure L, Gomez F, Ramos M, Sanchez-Ramos J, Snodgrass S, de Young M, Wexler N, Moscowitz C, Penchaszadeh G, MacFarlane H, Anderson M, Jenkins B, Srinidhi J, Barnes G, Gusella JF, MacDonald M (1993) Trinucleotide repeat length instability and age of onset in Huntington’s disease. Nat Genet 4(4):387–392. doi: 10.1038/ng0893-387

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