1. Familial analysis reveals rare risk variants for migraine in regulatory regions

   • Tanya Ramdal Techlo
   • Andreas Høiberg Rasmussen
   • Thomas Folkmann Hansen

   Original Article Open access 19 February 2020 Pages: 149 - 157

   

2. Cognitive decline and depressive symptoms: early non-motor presentations of parkinsonism among Egyptian Gaucher patients

   • Azza Abdel Gawad Tantawy
   • Amira Abdel Moneam Adly
   • Nouran Yousef Salah

   Original Article 26 March 2020 Pages: 159 - 167

   

3. Autosomal dominant hereditary spastic paraplegia caused by mutation of UBAP1

   • Jianda Wang
   • Yanqi Hou
   • Jianhua Feng

   Original Article 28 March 2020 Pages: 169 - 177

   

4. Adult-onset glutaric aciduria type I: rare presentation of a treatable disorder

   • Pınar Gelener
   • Mariasavina Severino
   • Mahmut Cerkez Ergoren

   Original Article 18 April 2020 Pages: 179 - 186

   

5. Loss of mitochondrial ClpP, Lonp1, and Tfam triggers transcriptional induction of Rnf213, a susceptibility factor for moyamoya disease

   • Jana Key
   • Antonia Maletzko
   • Georg Auburger

   Original Article Open access 28 April 2020 Pages: 187 - 203

   

6. Polygenic risk scores indicates genetic overlap between peripheral pain syndromes and chronic postsurgical pain

   • Roel R. I. van Reij
   • Jan Willem Voncken
   • Nynke J. van den Hoogen

   Original Article Open access 06 May 2020 Pages: 205 - 215

   

7. Rare copy number variations of planar cell polarity genes are associated with human neural tube defects

   • Tian Tian
   • Yunping Lei
   • Aiguo Ren

   Original Article 09 May 2020 Pages: 217 - 225

   

8. Oligogenicity, C9orf72 expansion, and variant severity in ALS

   • Jay P. Ross
   • Claire S. Leblond
   • Guy A. Rouleau

   Short Communication 08 May 2020 Pages: 227 - 242