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Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations.
Clark LN, Afridi S, Mejia-Santana H, Harris J, Louis ED, Cote LJ, Andrews H, Singleton A, Wavrant De-Vrieze F, Hardy J, Mayeux R, Fahn S, Waters C, Ford B, Frucht S, Ottman R, Marder K. Clark LN, et al. Mov Disord. 2004 Jul;19(7):796-800. doi: 10.1002/mds.20131. Mov Disord. 2004. PMID: 15254937
Linkage exclusion in French families with probable Parkinson' s disease.
Farrer M, Destée T, Becquet E, Wavrant-De Vrièze F, Mouroux V, Richard F, Defebvre L, Lincoln S, Hardy J, Amouyel P, Chartier-Harlin MC. Farrer M, et al. Mov Disord. 2000 Nov;15(6):1075-83. doi: 10.1002/1531-8257(200011)15:6<1075::aid-mds1004>3.0.co;2-2. Mov Disord. 2000. PMID: 11104189
ABCA1 polymorphisms and Alzheimer's disease.
Wavrant-De Vrièze F, Compton D, Womick M, Arepalli S, Adighibe O, Li L, Pérez-Tur J, Hardy J. Wavrant-De Vrièze F, et al. Neurosci Lett. 2007 Apr 12;416(2):180-3. doi: 10.1016/j.neulet.2007.02.010. Epub 2007 Feb 7. Neurosci Lett. 2007. PMID: 17324514 Free PMC article.
Support for association between ADHD and two candidate genes: NET1 and DRD1.
Bobb AJ, Addington AM, Sidransky E, Gornick MC, Lerch JP, Greenstein DK, Clasen LS, Sharp WS, Inoff-Germain G, Wavrant-De Vrièze F, Arcos-Burgos M, Straub RE, Hardy JA, Castellanos FX, Rapoport JL. Bobb AJ, et al. Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):67-72. doi: 10.1002/ajmg.b.30142. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15717291
IL1RN VNTR polymorphism in ischemic stroke: analysis in 3 populations.
Worrall BB, Brott TG, Brown RD Jr, Brown WM, Rich SS, Arepalli S, Wavrant-De Vrièze F, Duckworth J, Singleton AB, Hardy J, Meschia JF; SWISS, ISGS, and MSGD Investigators. Worrall BB, et al. Among authors: wavrant de vrieze f. Stroke. 2007 Apr;38(4):1189-96. doi: 10.1161/01.STR.0000260099.42744.b0. Epub 2007 Mar 1. Stroke. 2007. PMID: 17332449 Free PMC article.
42 results