Oliveira LM, Rastin T, Nimmo GAM, Ross JP, Dion PA, Zhang M, Nevay DL, Arkadir D, Gotkine M, Barnett C, Shoesmith CL, Zimran A, Rogaeva EA, Zinman L, Rouleau GA, Gan-Or Z , Amato D and Kalia L. Occurrence of amyotrophic lateral sclerosis in type 1 Gaucher disease. Neurology Genetics. 2021. PubMed
Author: meron
Lack of Causal Relationship or Genetic Correlation between Restless Legs Syndrome and Parkinson’s Disease.
Common and rare variants in HFE are not associated with Parkinson’s disease in Europeans.
Analysis of PTRHD1 common and rare variants in European patients with Parkinson’s disease.
Investigation of Autosomal Genetic Sex Differences in Parkinson’s disease.
Blauwendraat C, Iwaki H, Makarious MB, Bandres-Ciga S, Leonard H, Grenn FP, Lake J, Krohn L, Tan M, Kim JJ, Gibbs JR, Hernandez DG, Ruskey JA, Pihlstrøm L, Toft M, van Hilten JJ, Marinus J, Schulte C, Brockmann K, Sharma M, Siitonen A, Majamaa K, Eerola-Rautio J, Tienari PJ, Grosset D, Lesage S, Corvol JC, Brice A, Wood N, Hardy J, Gan-Or Z, Heutink P, Gasser T, Morris H, Noyce AJ, Nalls and Singleton AB. Investigation of Autosomal Genetic Sex Differences in Parkinson’s disease. Annals of Neurology. 2021. PubMed, Preprint
GCH1 mutations in hereditary spastic paraplegia.
Type 2 diabetes as a determinant of Parkinson’s disease risk and progression.
No evidence for a causal relationship between cancers and Parkinson’s disease.
Evidence for non-Mendelian inheritance in spastic paraplegia 7.
Estiar MA, Yu E, Haj Salem I, Ross JP, Mufti K, Akçimen F, Leveille E, Spiegelman D, Ruskey JA, Asayesh F, Dagher A, Yoon G, Tarnopolsky M, Boycott KM, Dupre N, Dion PA, Suchowersky O, Trempe JF, Rouleau GA and Gan-Or Z. Evidence for non-Mendelian inheritance in spastic paraplegia 7. Movement Disorders. 2021. PubMed, Preprint