1. Circular RNAs—one of the enigmas of the brain

   • Ivan B. Filippenkov
   • Eugene O. Kalinichenko
   • Lyudmila V. Dergunova

   Review Article 23 July 2016 Pages: 1 - 6

   

2. Epigenome-wide DNA methylation analysis in siblings and monozygotic twins discordant for sporadic Parkinson’s disease revealed different epigenetic patterns in peripheral blood mononuclear cells

   • Oliver Kaut
   • Ina Schmitt
   • Ullrich Wüllner

   Original Article 06 October 2016 Pages: 7 - 22

   

3. Mosaicism in ATP1A3-related disorders: not just a theoretical risk

   • Marie Hully
   • Juliette Ropars
   • Nadia Bahi-Buisson

   Original Article 10 October 2016 Pages: 23 - 28

   

4. DRD2 C957T polymorphism is associated with improved 6-month verbal learning following traumatic brain injury

   • John K. Yue
   • Ethan A. Winkler
   • TRACK-TBI Investigators

   Original Article 08 November 2016 Pages: 29 - 38

5. A homozygous PIGN missense mutation in Soft-Coated Wheaten Terriers with a canine paroxysmal dyskinesia

   • Ana L. Kolicheski
   • Gary S. Johnson
   • Dennis P. O’Brien

   Original Article Open access 28 November 2016 Pages: 39 - 47

   

6. Mosaicism for a pathogenic MFN2 mutation causes minimal clinical features of CMT2A in the parent of a severely affected child

   • Katherine Schon
   • Olivera Spasic-Boskovic
   • Ruth Armstrong

   Original Article Open access 06 January 2017 Pages: 49 - 55

   

7. Homozygous mutation, p.Pro304His, in IDH3A, encoding isocitrate dehydrogenase subunit is associated with severe encephalopathy in infancy

   • Aviva Fattal-Valevski
   • Hila Eliyahu
   • Orly Elpeleg

   Original Article 05 January 2017 Pages: 57 - 61

   

8. SBF1 mutations associated with autosomal recessive axonal neuropathy with cranial nerve involvement

   • Andreea Manole
   • Alejandro Horga
   • Henry Houlden

   Short Communication 22 December 2016 Pages: 63 - 67

   

9. Erratum to: Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations

   • Michelangelo Cao
   • Marta Donà
   • Elena Pegoraro

   Erratum 02 December 2016 Pages: 69 - 69

10. Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect

    • Maher Awni Shahrour
    • Claudia M. Nicolae
    • Orly Elpeleg

    Erratum 06 December 2016 Pages: 71 - 71