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73 results

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Page 1
Multi-ancestry genome-wide association meta-analysis of Parkinson's disease.
Kim JJ, Vitale D, Otani DV, Lian MM, Heilbron K; 23andMe Research Team; Iwaki H, Lake J, Solsberg CW, Leonard H, Makarious MB, Tan EK, Singleton AB, Bandres-Ciga S, Noyce AJ; Global Parkinson’s Genetics Program (GP2); Blauwendraat C, Nalls MA, Foo JN, Mata I. Kim JJ, et al. Nat Genet. 2024 Jan;56(1):27-36. doi: 10.1038/s41588-023-01584-8. Epub 2023 Dec 28. Nat Genet. 2024. PMID: 38155330 Free PMC article.
Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study.
Rizig M, Bandres-Ciga S, Makarious MB, Ojo OO, Crea PW, Abiodun OV, Levine KS, Abubakar SA, Achoru CO, Vitale D, Adeniji OA, Agabi OP, Koretsky MJ, Agulanna U, Hall DA, Akinyemi RO, Xie T, Ali MW, Shamim EA, Ani-Osheku I, Padmanaban M, Arigbodi OM, Standaert DG, Bello AH, Dean MN, Erameh CO, Elsayed I, Farombi TH, Okunoye O, Fawale MB, Billingsley KJ, Imarhiagbe FA, Jerez PA, Iwuozo EU, Baker B, Komolafe MA, Malik L, Nwani PO, Daida K, Nwazor EO, Miano-Burkhardt A, Nyandaiti YW, Fang ZH, Obiabo YO, Kluss JH, Odeniyi OA, Hernandez DG, Odiase FE, Tayebi N, Ojini FI, Sidranksy E, Onwuegbuzie GA, D'Souza AM, Osaigbovo GO, Berhe B, Osemwegie N, Reed X, Oshinaike OO, Leonard HL, Otubogun FM, Alvarado CX, Oyakhire SI, Ozomma SI, Samuel SC, Taiwo FT, Wahab KW, Zubair YA, Iwaki H, Kim JJ, Morris HR, Hardy J, Nalls MA, Heilbron K, Norcliffe-Kaufmann L; Nigeria Parkinson Disease Research Network; International Parkinson's Disease Genomics Consortium Africa; Black and African American Connections to Parkinson's Disease Study Group; 23andMe Research Team; Blauwendraat C, Houlden H, Singleton A, Okubadejo NU; Global Parkinson's Genetics Program. Rizig M, et al. Lancet Neurol. 2023 Nov;22(11):1015-1025. doi: 10.1016/S1474-4422(23)00283-1. Epub 2023 Aug 23. Lancet Neurol. 2023. PMID: 37633302 Free PMC article.
Accelerating biomedical discoveries in brain health through transformative neuropathology of aging and neurodegeneration.
Murray ME, Smith C, Menon V, Keene CD, Lein E, Hawrylycz M, Aguzzi A, Benedetti B, Brose K, Caetano-Anolles K, Sillero MIC, Crary JF, De Jager PL, Faustin A, Flanagan ME, Gokce O, Grant SGN, Grinberg LT, Gutman DA, Hillman EMC, Huang Z, Irwin DJ, Jones DT, Kapasi A, Karch CM, Kukull WT, Lashley T, Lee EB, Lehner T, Parkkinen L, Pedersen M, Pritchett D, Rutledge MH, Schneider JA, Seeley WW, Shepherd CE, Spires-Jones TL, Steen JA, Sutherland M, Vickovic S, Zhang B, Stewart DJ, Keiser MJ, Vogel JW, Dugger BN, Phatnani H. Murray ME, et al. Among authors: shepherd ce. Neuron. 2025 Jul 15:S0896-6273(25)00472-6. doi: 10.1016/j.neuron.2025.06.014. Online ahead of print. Neuron. 2025. PMID: 40683248 Free article. Review.
Evidence of COMT dysfunction in the olfactory bulb in Parkinson's disease.
Beauchamp LC, Ellett LJ, Juan SMA, Liu XM, Hunt CPJ, Parish CL, Jacobson LH, Shepherd CE, Halliday GM, Bush AI, Vella LJ, Finkelstein DI, Barnham KJ. Beauchamp LC, et al. Among authors: shepherd ce. Acta Neuropathol. 2025 Mar 1;149(1):21. doi: 10.1007/s00401-025-02861-y. Acta Neuropathol. 2025. PMID: 40024917 Free PMC article.
The LRRK2 p.L1795F variant causes Parkinson's disease in the European population.
Lange LM, Levine K, Fox SH, Marras C, Ahmed N, Kuznetsov N, Vitale D, Iwaki H, Lohmann K, Marsili L, Espay AJ, Bauer P, Beetz C, Martin J, Factor SA, Higginbotham LA, Chen H, Leonard H, Nalls MA, Mencacci NE, Morris HR, Singleton AB, Klein C, Blauwendraat C, Fang ZH; Global Parkinson’s Genetics Program (GP2). Lange LM, et al. NPJ Parkinsons Dis. 2025 Mar 25;11(1):58. doi: 10.1038/s41531-025-00896-2. NPJ Parkinsons Dis. 2025. PMID: 40133296 Free PMC article.
73 results