1. Call for participation in the neurogenetics consortium within the Human Variome Project

   • Andrea Haworth
   • Lars Bertram
   • Maria-Jesus Sobrido

   NEUROGENETICS NEWS 01 June 2011 Pages: 169 - 173

   

2. Pathological mechanisms and parent-of-origin effects in hereditary paraganglioma/pheochromocytoma (PGL/PCC)

   • Ulrich Müller

   REVIEW ARTICLE 09 March 2011 Pages: 175 - 181

   

3. Genotype–phenotype correlations in sepiapterin reductase deficiency. A splicing defect accounts for a new phenotypic variant

   • Luisa Arrabal
   • Libertad Teresa
   • Lourdes R. Desviat

   ORIGINAL ARTICLE 24 March 2011 Pages: 183 - 191

   

4. Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients

   • Barbara Castellotti
   • Caterina Mariotti
   • Cinzia Gellera

   Original Article 05 April 2011 Pages: 193 - 201

   

5. Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson’s disease in Sardinia

   • Marialuisa Quadri
   • Giovanni Cossu
   • Vincenzo Bonifati

   ORIGINAL ARTICLE Open access 11 June 2011 Pages: 203 - 209

   

6. Differentially expressed genes in hypothalamus in relation to genomic regions under selection in two chicken lines resulting from divergent selection for high or low body weight

   • Sojeong Ka
   • Frank W. Albert
   • Finn Hallböök

   ORIGINAL ARTICLE 12 July 2011 Pages: 211 - 221

   

7. A novel mitofusin 2 mutation causes canine fetal-onset neuroaxonal dystrophy

   • John C. Fyfe
   • Rabá A. Al-Tamimi
   • Paula S. Henthorn

   ORIGINAL ARTICLE 04 June 2011 Pages: 223 - 232

   

8. Familial spinal neurofibromatosis due to a multiexonic NF1 gene deletion

   • Antonio Pizzuti
   • Irene Bottillo
   • Bruno Dallapiccola

   SHORT COMMUNICATION 02 March 2011 Pages: 233 - 240

   

9. FGF17, a gene involved in cerebellar development, is downregulated in a patient with Dandy–Walker malformation carrying a de novo 8p deletion

   • Ginevra Zanni
   • Sabina Barresi
   • Enrico Silvio Bertini

   SHORT COMMUNICATION 12 April 2011 Pages: 241 - 245

   

10. Autozygosity mapping of a large consanguineous Pakistani family reveals a novel non-syndromic autosomal recessive mental retardation locus on 11p15-tel

    • Shoaib ur Rehman
    • Shahid Mahmood Baig
    • Lars Hansen

    SHORT COMMUNICATION 04 June 2011 Pages: 247 - 251

    

11. Audiogenic seizure proneness requires the contribution of two susceptibility loci in mice

    • M. Catharine Jawahar
    • Carolina I. Sari
    • Mark Murphy

    SHORT COMMUNICATION 18 June 2011 Pages: 253 - 257

    

12. Adult-onset leukoencephalopathies with vanishing white matter with novel missense mutations in EIF2B2, EIF2B3, and EIF2B5

    • Takashi Matsukawa
    • Xuemin Wang
    • Shoji Tsuji

    Letter to the Editors 12 April 2011 Pages: 259 - 261