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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1980 1
1987 1
1989 6
1990 1
1991 3
1992 8
1993 5
1994 5
1995 5
1996 4
1997 4
1998 1
1999 5
2000 2
2001 4
2002 3
2003 1
2004 2
2005 2
2007 3
2008 2
2009 1
2018 1
2019 6
2020 5
2021 12
2022 9
2023 16
2024 3

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116 results

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Page 1
Open science in precision medicine for neurodegenerative diseases.
Leonard HL, Nalls MA, Day-Williams A, Esmaeeli S, Jarreau P, Bandres-Ciga S, Heutink P, Sardi SP, Singleton AB. Leonard HL, et al. Nat Rev Drug Discov. 2024 Apr;23(4):233-234. doi: 10.1038/d41573-024-00017-3. Nat Rev Drug Discov. 2024. PMID: 38287165 No abstract available.
Assessing the lack of diversity in genetics research across neurodegenerative diseases: a systematic review of the GWAS Catalog and literature.
Jonson C, Levine KS, Lake J, Hertslet L, Jones L, Patel D, Kim J, Bandres-Ciga S, Terry N, Mata IF, Blauwendraat C, Singleton AB, Nalls MA, Yokoyama JS, Leonard HL. Jonson C, et al. Among authors: leonard hl. medRxiv [Preprint]. 2024 Jan 9:2024.01.08.24301007. doi: 10.1101/2024.01.08.24301007. medRxiv. 2024. PMID: 38260595 Free PMC article. Preprint.
Human brain single nucleus cell type enrichments in neurodegenerative diseases.
Alvarado CX, Weller CA, Johnson N, Leonard HL, Singleton AB, Reed X, Blauewendraat C, Nalls MA. Alvarado CX, et al. Among authors: leonard hl. Res Sq [Preprint]. 2023 Nov 15:rs.3.rs-3390225. doi: 10.21203/rs.3.rs-3390225/v1. Res Sq. 2023. PMID: 38014237 Free PMC article. Preprint.
Sleep disturbances as risk factors for neurodegeneration later in life.
Simmonds E, Levine KS, Han J, Iwaki H, Koretsky MJ, Kuznetsov N, Faghri F, Solsberg CW, Schuh A, Jones L, Bandres-Ciga S, Blauwendraat C, Singleton A, Escott-Price V, Leonard HL, Nalls MA. Simmonds E, et al. Among authors: leonard hl. medRxiv [Preprint]. 2023 Nov 9:2023.11.08.23298037. doi: 10.1101/2023.11.08.23298037. medRxiv. 2023. PMID: 37986827 Free PMC article. Preprint.
Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease.
Daida K, Funayama M, Billingsley KJ, Malik L, Miano-Burkhardt A, Leonard HL, Makarious MB, Iwaki H, Ding J, Gibbs JR, Ishiguro M, Yoshino H, Ogaki K, Oyama G, Nishioka K, Nonaka R, Akamatsu W, Blauwendraat C, Hattori N. Daida K, et al. Among authors: leonard hl. Mov Disord. 2023 Dec;38(12):2249-2257. doi: 10.1002/mds.29610. Epub 2023 Nov 5. Mov Disord. 2023. PMID: 37926948
Long-read sequencing resolves a complex structural variant in PRKN Parkinson's disease.
Daida K, Funayama M, Billingsley KJ, Malik L, Miano-Burkhardt A, Leonard HL, Makarious MB, Iwaki H, Ding J, Gibbs JR, Ishiguro M, Yoshino H, Ogaki K, Oyama G, Nishioka K, Nonaka R, Akamatsu W, Blauwendraat C, Hattori N. Daida K, et al. Among authors: leonard hl. medRxiv [Preprint]. 2023 Aug 21:2023.08.14.23293948. doi: 10.1101/2023.08.14.23293948. medRxiv. 2023. PMID: 37790330 Free PMC article. Updated. Preprint.
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. Among authors: leonard hl. 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
Human brain single nucleus cell type enrichments in neurodegenerative diseases.
Alvarado CX, Weller CA, Johnson N, Leonard HL, Singleton AB, Reed X, Blauewendraat C, Nalls M. Alvarado CX, et al. Among authors: leonard hl. medRxiv [Preprint]. 2023 Jul 1:2023.06.30.23292084. doi: 10.1101/2023.06.30.23292084. medRxiv. 2023. PMID: 37577689 Free PMC article. Preprint.
116 results