Familial analysis reveals rare risk variants for migraine in regulatory regions Tanya Ramdal TechloAndreas Høiberg RasmussenThomas Folkmann Hansen Original Article Open access 19 February 2020 Pages: 149 - 157
Cognitive decline and depressive symptoms: early non-motor presentations of parkinsonism among Egyptian Gaucher patients Azza Abdel Gawad TantawyAmira Abdel Moneam AdlyNouran Yousef Salah Original Article 26 March 2020 Pages: 159 - 167
Autosomal dominant hereditary spastic paraplegia caused by mutation of UBAP1 Jianda WangYanqi HouJianhua Feng Original Article 28 March 2020 Pages: 169 - 177
Adult-onset glutaric aciduria type I: rare presentation of a treatable disorder Pınar GelenerMariasavina SeverinoMahmut Cerkez Ergoren Original Article 18 April 2020 Pages: 179 - 186
Loss of mitochondrial ClpP, Lonp1, and Tfam triggers transcriptional induction of Rnf213, a susceptibility factor for moyamoya disease Jana KeyAntonia MaletzkoGeorg Auburger Original Article Open access 28 April 2020 Pages: 187 - 203
Polygenic risk scores indicates genetic overlap between peripheral pain syndromes and chronic postsurgical pain Roel R. I. van ReijJan Willem VonckenNynke J. van den Hoogen Original Article Open access 06 May 2020 Pages: 205 - 215
Rare copy number variations of planar cell polarity genes are associated with human neural tube defects Tian TianYunping LeiAiguo Ren Original Article 09 May 2020 Pages: 217 - 225
Oligogenicity, C9orf72 expansion, and variant severity in ALS Jay P. RossClaire S. LeblondGuy A. Rouleau Short Communication 08 May 2020 Pages: 227 - 242