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Association of Mitochondrial DNA Genomic Variation With Risk of Pick Disease.
Valentino RR, Heckman MG, Johnson PW, Baker MC, Soto-Beasley AI, Walton RL, Koga S, Roemer SF, Suh E, Uitti RJ, Trojanowski JQ, Grossman M, Van Deerlin VM, Rademakers R, Wszolek ZK, Dickson DW, Ross OA. Valentino RR, et al. Neurology. 2021 Mar 30;96(13):e1755-e1760. doi: 10.1212/WNL.0000000000011649. Epub 2021 Feb 10. Neurology. 2021. PMID: 33568542 Free PMC article.
Screening non-MAPT genes of the Chr17q21 H1 haplotype in Parkinson's disease.
Soto-Beasley AI, Walton RL, Valentino RR, Hook PW, Labbé C, Heckman MG, Johnson PW, Goff LA, Uitti RJ, McLean PJ, Springer W, McCallion AS, Wszolek ZK, Ross OA. Soto-Beasley AI, et al. Among authors: valentino rr. Parkinsonism Relat Disord. 2020 Sep;78:138-144. doi: 10.1016/j.parkreldis.2020.07.022. Epub 2020 Aug 1. Parkinsonism Relat Disord. 2020. PMID: 32829096 Free PMC article.
Association of mitochondrial genomic background with risk of Multiple System Atrophy.
Valentino RR, Heckman MG, Johnson PW, Soto-Beasley AI, Walton RL, Koga S, Uitti RJ, Wszolek ZK, Dickson DW, Ross OA. Valentino RR, et al. Parkinsonism Relat Disord. 2020 Dec;81:200-204. doi: 10.1016/j.parkreldis.2020.10.040. Epub 2020 Oct 29. Parkinsonism Relat Disord. 2020. PMID: 33189969 Free PMC article.
MAPT subhaplotypes in corticobasal degeneration: assessing associations with disease risk, severity of tau pathology, and clinical features.
Valentino RR, Koga S, Walton RL, Soto-Beasley AI, Kouri N, DeTure MA, Murray ME, Johnson PW, Petersen RC, Boeve BF, Uitti RJ, Wszolek ZK, Dickson DW, Ross OA, Heckman MG. Valentino RR, et al. Acta Neuropathol Commun. 2020 Dec 7;8(1):218. doi: 10.1186/s40478-020-01097-z. Acta Neuropathol Commun. 2020. PMID: 33287913 Free PMC article.
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study.
Jabbari E, Koga S, Valentino RR, Reynolds RH, Ferrari R, Tan MMX, Rowe JB, Dalgard CL, Scholz SW, Dickson DW, Warner TT, Revesz T, Höglinger GU, Ross OA, Ryten M, Hardy J, Shoai M, Morris HR; PSP Genetics Group. Jabbari E, et al. Among authors: valentino rr. Lancet Neurol. 2021 Feb;20(2):107-116. doi: 10.1016/S1474-4422(20)30394-X. Epub 2020 Dec 17. Lancet Neurol. 2021. PMID: 33341150 Free PMC article.
Fine-mapping of the non-coding variation driving the Caucasian LRRK2 GWAS signal in Parkinson's disease.
Heckman MG, Labbé C, Kolicheski AL, Soto-Beasley AI, Walton RL, Valentino RR, Brennan ER, Johnson PW, Baheti S, Sarangi V, Ren Y, Uitti RJ, Wszolek ZK, Ross OA. Heckman MG, et al. Among authors: valentino rr. Parkinsonism Relat Disord. 2021 Feb;83:22-30. doi: 10.1016/j.parkreldis.2020.12.016. Epub 2021 Jan 11. Parkinsonism Relat Disord. 2021. PMID: 33454605 Free PMC article.
Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophy.
Wernick AI, Walton RL, Soto-Beasley AI, Koga S, Heckman MG, Valentino RR, Milanowski LM, Hoffman-Zacharska D, Koziorowski D, Hassan A, Uitti RJ, Cheshire WP, Singer W, Wszolek ZK, Dickson DW, Low PA, Ross OA. Wernick AI, et al. Among authors: valentino rr. Clin Auton Res. 2021 Feb;31(1):117-125. doi: 10.1007/s10286-020-00759-1. Epub 2021 Jan 27. Clin Auton Res. 2021. PMID: 33502644 Free PMC article.
Investigating ELOVL7 coding variants in multiple system atrophy.
Wernick AI, Walton RL, Soto-Beasley AI, Koga S, Ren Y, Heckman MG, Milanowski LM, Valentino RR, Kondru N, Uitti RJ, Cheshire WP, Wszolek ZK, Dickson DW, Ross OA. Wernick AI, et al. Among authors: valentino rr. Neurosci Lett. 2021 Apr 1;749:135723. doi: 10.1016/j.neulet.2021.135723. Epub 2021 Feb 15. Neurosci Lett. 2021. PMID: 33600908 Free PMC article.
16 results