Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia

Zhu R, Liu L, Estiar MA, Asayesh F, Ahmad J, Teferra M, Yoon G, Tarnopolsky M, Boycott KM, Dupre N, Dion PA, Suchowersky O, Jordanova A, Lee YC, Stevanin G, Zuchner S, Rouleau GA, Gan-Or Z. Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia. Mov Disord. 2025. Preprint, PubMed.

Lack of Association Between G6PD Variants and Parkinson’s Disease

Chifamba LV, Parlar SC, Liu L, Sokol LL, Yu E, Asayesh F, Ahmad J, Ruskey JA, Spiegelman D, Waters C, Monchi O, Dauvilliers Y, Dupré N, Timofeeva A, Emelyanov A, Pchelina S, Miliukhina I, Greenbaum L, Hassin-Baer S, Alcalay RN, Espay AJ, Gan-Or Z, Senkevich K. Lack of Association Between G6PD Variants and Parkinson’s Disease. HGG Adv. 2025. Preprint, PubMed.

No Evidence for Genetic Role of the Tumor Necrosis Factor Pathway in Parkinson’s Disease.

Shahkhali MG, Liu L, Somerville EN, Noyce AJ, Gan-Or Z, Senkevich K. No Evidence for Genetic Role of the Tumor Necrosis Factor Pathway in Parkinson’s Disease. NPJ Parkinsons Dis. 2025. Preprint, PubMed.

Lack of epistatic interaction of SNCA with APOE in synucleinopathies

Saini P, Yu E, Estiar MA, Krohn L, Mufti K, Rudakou U, Ruskey JA, Asayesh F, Laurent SB, Spiegelman D, Arnulf I, Montplaisir JY, Gagnon JF, Desautels A, Dauvilliers Y, Gigli GL, Valente M, Janes F, Bernardini A, Šonka K, Kemlink D, Oertel WH, Kaivola K, Janzen A, Plazzi G, Antelmi E, Biscarini F, Figorilli M, Puligheddu M, Mollenhauer B, Trenkwalder C, Sixel-Döring F, Cochen De Cock V, Monaca CC, Heidbreder A, Ferini-Strambi L, Dijkstra F, Viaene M, Abril B, Boeve BF, Postuma RB, Rouleau GA, Anselmi V, Ibrahim A, Stefani A, Högl B, Hu MTM, Scholz SW, Gan-Or Z. Lack of epistatic interaction of SNCA with APOE in synucleinopathies. Brain Commun. 2025. Preprint, PubMed