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434 results

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Page 1
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. Among authors: johnson pw. 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: johnson pw. 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.
Associations of mitochondrial genomic variation with corticobasal degeneration, progressive supranuclear palsy, and neuropathological tau measures.
Valentino RR, Tamvaka N, Heckman MG, Johnson PW, Soto-Beasley AI, Walton RL, Koga S, Uitti RJ, Wszolek ZK, Dickson DW, Ross OA. Valentino RR, et al. Among authors: johnson pw. Acta Neuropathol Commun. 2020 Sep 17;8(1):162. doi: 10.1186/s40478-020-01035-z. Acta Neuropathol Commun. 2020. PMID: 32943110 Free PMC article.
Plasma neurofilament light predicts mortality in patients with stroke.
Gendron TF, Badi MK, Heckman MG, Jansen-West KR, Vilanilam GK, Johnson PW, Burch AR, Walton RL, Ross OA, Brott TG, Miller TM, Berry JD, Nicholson KA, Wszolek ZK, Oskarsson BE, Sheth KN, Sansing LH, Falcone GJ, Cucchiara BL, Meschia JF, Petrucelli L. Gendron TF, et al. Among authors: johnson pw. Sci Transl Med. 2020 Nov 11;12(569):eaay1913. doi: 10.1126/scitranslmed.aay1913. Sci Transl Med. 2020. PMID: 33177179 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. Among authors: johnson pw. 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. Among authors: johnson pw. 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.
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: johnson pw. 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.
Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measures.
Valentino RR, Ramnarine C, Heckman MG, Johnson PW, Soto-Beasley AI, Walton RL, Koga S, Kasanuki K, Murray ME, Uitti RJ, Fields JA, Botha H, Ramanan VK, Kantarci K, Lowe VJ, Jack CR, Ertekin-Taner N, Savica R, Graff-Radford J, Petersen RC, Parisi JE, Reichard RR, Graff-Radford NR, Ferman TJ, Boeve BF, Wszolek ZK, Dickson DW, Ross OA. Valentino RR, et al. Among authors: johnson pw. Acta Neuropathol Commun. 2022 Jul 14;10(1):103. doi: 10.1186/s40478-022-01399-4. Acta Neuropathol Commun. 2022. PMID: 35836284 Free PMC article.
434 results