1. Whole-genome conditional two-locus analysis identifies novel candidate genes for late-onset Parkinson’s disease

   • A. González-Pérez
   • J. Gayán
   • A. Ruiz

   Original Article 21 January 2009 Pages: 173 - 181

   

2. Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer’s disease

   • M. A. Nalls
   • R. J. Guerreiro
   • A. B. Singleton

   Original Article 07 March 2009 Pages: 183 - 190

   

3. Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred

   • Ester Cuenca-León
   • Roser Corominas
   • Alfons Macaya

   Original Article 20 January 2009 Pages: 191 - 198

   

4. Association between migraine and a functional polymorphism at the dopamine β-hydroxylase locus

   • F. Fernandez
   • N. Colson
   • L. R. Griffiths

   Original Article 14 February 2009 Pages: 199 - 208

   

5. Examination of association of genes in the serotonin system to autism

   • B. M. Anderson
   • N. C. Schnetz-Boutaud
   • J. L. Haines

   Original Article 28 January 2009 Pages: 209 - 216

   

6. Interaction of the SPG21 protein ACP33/maspardin with the aldehyde dehydrogenase ALDH16A1

   • Michael C. Hanna
   • Craig Blackstone

   Original Article 31 January 2009 Pages: 217 - 228

   

7. Molecular analysis of NPC1 and NPC2 gene in 34 Niemann–Pick C Italian Patients: identification and structural modeling of novel mutations

   • Tatiana Fancello
   • Andrea Dardis
   • Mirella Filocamo

   Original Article 28 February 2009 Pages: 229 - 239

   

8. Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes

   • S. Russo
   • M. Marchi
   • L. Larizza

   Original Article 25 February 2009 Pages: 241 - 250

   

9. The spectrum of somatic and germline NF1 mutations in NF1 patients with spinal neurofibromas

   • Meena Upadhyaya
   • Gill Spurlock
   • Victor Mautner

   Original Article 17 February 2009 Pages: 251 - 263

   

10. A new complex homozygous large rearrangement of the PINK1 gene in a Sudanese family with early onset Parkinson’s disease

    • Cécile Cazeneuve
    • Channkanira Sân
    • Mustafa A. Salih

    Short Communication 12 February 2009 Pages: 265 - 270

    

11. A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype

    • C. Pirkevi
    • S. Lesage
    • A. N. Başak

    Short Communication 27 January 2009 Pages: 271 - 273