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Performance of the 12-item WHODAS 2.0 in prodromal Huntington disease.
Kim JI, Long JD, Mills JA, Downing N, Williams JK, Paulsen JS; PREDICT-HD Investigators and Coordinators of the Huntington Study Group. Kim JI, et al. Eur J Hum Genet. 2015 Nov;23(11):1584-7. doi: 10.1038/ejhg.2015.11. Epub 2015 Mar 4. Eur J Hum Genet. 2015. PMID: 25735480 Free PMC article.
Diagnostic accuracy of screening tools for depression and anxiety in cervical dystonia.
Martino D, Ramezani M, Bellows S, Berman BD, Chang FC, Feuerstein J, Fung V, Berkmen GK, Malaty IA, MacIver C, Norris SA, Peall KJ, Perlmutter JS, Richardson SP, Wright LJ, Goodarzi Z, Jinnah HA. Martino D, et al. Among authors: perlmutter js. Parkinsonism Relat Disord. 2025 Jul;136:107891. doi: 10.1016/j.parkreldis.2025.107891. Epub 2025 May 26. Parkinsonism Relat Disord. 2025. PMID: 40446700 Free PMC article.
Impact of Y chromosome loss on the risk of Parkinson's disease and progression.
Wang J, Chen X, Du W, Lin C, Liao Y, Corvol JC, Maple-Grødem J, Campbell MC, Elbaz A, Lesage S, Brice A, Schwarzschild MA, Taba P, Kõks S, Alves G, Tysnes OB, Perlmutter JS, Maiti B, van Hilten JJ, Barker RA, Williams-Gray CH, Scherzer CR, Liu G; International Genetics of Parkinson Disease Progression (IGPP) Consortium. Wang J, et al. Among authors: perlmutter js. EBioMedicine. 2025 Jul;117:105769. doi: 10.1016/j.ebiom.2025.105769. Epub 2025 May 29. EBioMedicine. 2025. PMID: 40446401 Free PMC article.
Genetic Analysis of the X Chromosome Associates Loci with Progression of Parkinson's Disease.
Liao Y, Wu H, Wang J, Corvol JC, Maple-Grødem J, Campbell MC, Elbaz A, Brice A, Schwarzschild MA, Taba P, Kõks S, Beach TG, Alves G, Tysnes OB, Perlmutter JS, Maiti B, van Hilten JJ, Barker RA, Williams-Gray CH, Scherzer CR, Liu G; International Genetics of Parkinson Disease Progression Consortium. Liao Y, et al. Among authors: perlmutter js. Mov Disord. 2025 Sep;40(9):1908-1918. doi: 10.1002/mds.30252. Epub 2025 Jun 3. Mov Disord. 2025. PMID: 40459076
Genetic Risk Factors in Isolated Dystonia Escape Genome-Wide Association Studies.
Laabs BH, Lohmann K, Vollstedt EJ, Reinberger T, Nuxoll LM, Kilic-Berkmen G, Perlmutter JS, Loens S, Cruchaga C, Franke A, Dobricic V, Hinrichs F, Grözinger A, Altenmüller E, Bellows S, Boesch S, Bressman SB, Duque KR, Espay AJ, Ferbert A, Feuerstein JS, Frank S, Gasser T, Haslinger B, Jech R, Kaiser F, Kamm C, Kollewe K, Kühn AA, LeDoux MS, Lohmann E, Mahajan A, Münchau A, Multhaupt-Buell T, Pantelyat A, Pirio Richardson SE, Raymond D, Reich SG, Saunders Pullman R, Schormair B, Sharma N, Sichani AH, Simonyan K, Volkmann J, Wagle Shukla A, Winkelmann J, Wright LJ, Zech M, Zeuner KE, Zittel S, Kasten M, Sun YV, Bäumer T, Brüggemann N, Ozelius LJ, Jinnah HA, Klein C, König IR. Laabs BH, et al. Among authors: perlmutter js. Mov Disord. 2024 Nov;39(11):2110-2116. doi: 10.1002/mds.29968. Epub 2024 Sep 17. Mov Disord. 2024. PMID: 39287592 Free PMC article.
470 results