Author
Mayo ClinicORCID 0000-0001-8113-4710Unclaimed ORCID profile · follow to get notified of new preprints
Mutual co-authors in cluster
5 papers
Recent·Most cited
Lara Mariah Lange, Zih‐Hua Fang, Laurel A. Screven…·the Global Parkinson's Genetics Program (GP2)
The paper assesses the frequency of dystonia-linked pathogenic variants in Parkinson's disease patients and finds they are present in 0.57% of cases, with GCH1 being the most common gene affected.
Cyril P. Pottier, Fahri Küçükali, Matt C. Baker…·Edward B. Lee
This study identifies genetic risk factors for FTLD-TDP subtypes using whole-genome sequencing and meta-analysis across multiple cohorts.
Franziska Hopfner, Anja K. Tietz, Viktoria Ruf…·Günter U. Höglinger
Dongbing Lai, Babak Alipanahi, Pierre Fontanillas…·Tatiana Foroud
This study identifies genetic modifiers of LRRK2 mutations in Parkinson's disease, finding a significant variant in CORO1C and a polygenic risk score effect on penetrance.
Rebecca R. Valentino, Nikoleta Tamvaka, Michael G. Heckman…·Owen A. Ross
This study investigates associations between mitochondrial genomic variation and risk of Corticobasal Degeneration (CBD) and Progressive Supranuclear Palsy (PSP), as well as tau pathology measures in PSP.