1. A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson’s disease risk in Taiwan

   • Alessio Di Fonzo
   • Yah-Huei Wu-Chou
   • Vincenzo Bonifati

   Original Article 22 April 2006 Pages: 133 - 138

   

2. Transcriptome analysis reveals link between proteasomal and mitochondrial pathways in Parkinson’s disease

   • D. C. Duke
   • L. B. Moran
   • M. B. Graeber

   Original Article 13 May 2006 Pages: 139 - 148

   

3. 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 Stevanin
   • Giorgia Montagna
   • Filippo M. Santorelli

   Original Article 13 May 2006 Pages: 149 - 156

   

4. Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis

   • Ping-I Lin
   • Eden R. Martin
   • Margaret A. Pericak-Vance

   Original Article 13 June 2006 Pages: 157 - 165

   

5. Investigation of autism and GABA receptor subunit genes in multiple ethnic groups

   • Ann L. Collins
   • Deqiong Ma
   • Margaret A. Pericak-Vance

   Original Article Open access 13 June 2006 Pages: 167 - 174

   

6. Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene

   • Yuji Okamoto
   • Hiroshi Takashima
   • Kimiyoshi Arimura

   Original Article 15 June 2006 Pages: 175 - 183

   

7. Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL

   • Johanna Annunen-Rasila
   • Saara Finnilä
   • Kari Majamaa

   Original Article 29 June 2006 Pages: 185 - 194

   

8. Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer’s disease in Mexican families

   • Petra Yescas
   • Adriana Huertas-Vazquez
   • María Elisa Alonso

   Short Communication 21 April 2006 Pages: 195 - 200