A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson’s disease risk in Taiwan Alessio Di FonzoYah-Huei Wu-ChouVincenzo Bonifati Original Article 22 April 2006 Pages: 133 - 138
Transcriptome analysis reveals link between proteasomal and mitochondrial pathways in Parkinson’s disease D. C. DukeL. B. MoranM. B. Graeber Original Article 13 May 2006 Pages: 139 - 148
Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity Giovanni StevaninGiorgia MontagnaFilippo M. Santorelli Original Article 13 May 2006 Pages: 149 - 156
Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis Ping-I LinEden R. MartinMargaret A. Pericak-Vance Original Article 13 June 2006 Pages: 157 - 165
Investigation of autism and GABA receptor subunit genes in multiple ethnic groups Ann L. CollinsDeqiong MaMargaret A. Pericak-Vance Original Article Open access 13 June 2006 Pages: 167 - 174
Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene Yuji OkamotoHiroshi TakashimaKimiyoshi Arimura Original Article 15 June 2006 Pages: 175 - 183
Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL Johanna Annunen-RasilaSaara FinniläKari Majamaa Original Article 29 June 2006 Pages: 185 - 194
Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer’s disease in Mexican families Petra YescasAdriana Huertas-VazquezMaría Elisa Alonso Short Communication 21 April 2006 Pages: 195 - 200