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Year Number of Results
2002 3
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2004 1
2005 1
2006 1
2007 1
2008 3
2009 4
2010 2
2011 3
2012 5
2013 1
2014 1
2015 1
2016 6
2017 5
2018 2
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2025 0

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46 results

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Page 1
Structures of α-synuclein filaments from human brains with Lewy pathology.
Yang Y, Shi Y, Schweighauser M, Zhang X, Kotecha A, Murzin AG, Garringer HJ, Cullinane PW, Saito Y, Foroud T, Warner TT, Hasegawa K, Vidal R, Murayama S, Revesz T, Ghetti B, Hasegawa M, Lashley T, Scheres SHW, Goedert M. Yang Y, et al. Nature. 2022 Oct;610(7933):791-795. doi: 10.1038/s41586-022-05319-3. Epub 2022 Sep 15. Nature. 2022. PMID: 36108674 Free PMC article.
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease.
Hop PJ, Lai D, Keagle PJ, Baron DM, Kenna BJ, Kooyman M, Shankaracharya, Halter C, Straniero L, Asselta R, Bonvegna S, Soto-Beasley AI; Project MinE ALS Sequencing Consortium; Wszolek ZK, Uitti RJ, Isaias IU, Pezzoli G, Ticozzi N, Ross OA, Veldink JH, Foroud TM, Kenna KP, Landers JE. Hop PJ, et al. Nat Genet. 2024 Jul;56(7):1371-1376. doi: 10.1038/s41588-024-01787-7. Epub 2024 Jun 10. Nat Genet. 2024. PMID: 38858457 Free PMC article.
Genetics of Parkinson disease.
Pankratz N, Foroud T. Pankratz N, et al. NeuroRx. 2004 Apr;1(2):235-42. doi: 10.1602/neurorx.1.2.235. NeuroRx. 2004. PMID: 15717024 Free PMC article. Review.
Coding and Noncoding Variation in LRRK2 and Parkinson's Disease Risk.
Lake J, Reed X, Langston RG, Nalls MA, Gan-Or Z, Cookson MR, Singleton AB, Blauwendraat C, Leonard HL; International Parkinson's Disease Genomics Consortium (IPDGC). Lake J, et al. Mov Disord. 2022 Jan;37(1):95-105. doi: 10.1002/mds.28787. Epub 2021 Sep 20. Mov Disord. 2022. PMID: 34542912 Free PMC article.
Whole-Exome Sequencing in Familial Parkinson Disease.
Farlow JL, Robak LA, Hetrick K, Bowling K, Boerwinkle E, Coban-Akdemir ZH, Gambin T, Gibbs RA, Gu S, Jain P, Jankovic J, Jhangiani S, Kaw K, Lai D, Lin H, Ling H, Liu Y, Lupski JR, Muzny D, Porter P, Pugh E, White J, Doheny K, Myers RM, Shulman JM, Foroud T. Farlow JL, et al. JAMA Neurol. 2016 Jan;73(1):68-75. doi: 10.1001/jamaneurol.2015.3266. JAMA Neurol. 2016. PMID: 26595808 Free PMC article.
Alpha-synuclein and familial Parkinson's disease.
Pankratz N, Nichols WC, Elsaesser VE, Pauciulo MW, Marek DK, Halter CA, Wojcieszek J, Rudolph A, Pfeiffer RF, Foroud T; Parkinson Study Group - PROGENI Investigators. Pankratz N, et al. Mov Disord. 2009 Jun 15;24(8):1125-31. doi: 10.1002/mds.22524. Mov Disord. 2009. PMID: 19412953 Free PMC article.
KTN1 Variants Underlying Putamen Gray Matter Volumes and Parkinson's Disease.
Mao Q, Wang X, Chen B, Fan L, Wang S, Zhang Y, Lin X, Cao Y, Wu YC, Ji J, Xu J, Zheng J, Zhang H, Zheng C, Chen W, Cheng W, Luo X, Wang K, Zuo L, Kang L, Li CR, Luo X. Mao Q, et al. Front Neurosci. 2020 Jun 23;14:651. doi: 10.3389/fnins.2020.00651. eCollection 2020. Front Neurosci. 2020. PMID: 32655362 Free PMC article.
Copy number variation in familial Parkinson disease.
Pankratz N, Dumitriu A, Hetrick KN, Sun M, Latourelle JC, Wilk JB, Halter C, Doheny KF, Gusella JF, Nichols WC, Myers RH, Foroud T, DeStefano AL; PSG-PROGENI and GenePD Investigators, Coordinators and Molecular Genetic Laboratories. Pankratz N, et al. PLoS One. 2011;6(8):e20988. doi: 10.1371/journal.pone.0020988. Epub 2011 Aug 2. PLoS One. 2011. PMID: 21829596 Free PMC article.
46 results