Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Edit custom filters

Results by year

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

Year Number of Results
2004 2
2005 2
2006 3
2007 2
2011 2
2012 4
2013 2
2014 5
2015 4
2016 2
2018 2
2019 5
2020 3
2021 7
2022 4
2023 9
2024 6
2025 5
2026 4

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

64 results

Results by year

Filters applied: . Clear all
Page 1
Cerebrospinal fluid proteomics define the natural history of autosomal dominant Alzheimer's disease.
Johnson ECB, Bian S, Haque RU, Carter EK, Watson CM, Gordon BA, Ping L, Duong DM, Epstein MP, McDade E, Barthélemy NR, Karch CM, Xiong C, Cruchaga C, Perrin RJ, Wingo AP, Wingo TS, Chhatwal JP, Day GS, Noble JM, Berman SB, Martins R, Graff-Radford NR, Schofield PR, Ikeuchi T, Mori H, Levin J, Farlow M, Lah JJ, Haass C, Jucker M, Morris JC, Benzinger TLS, Roberts BR, Bateman RJ, Fagan AM, Seyfried NT, Levey AI; Dominantly Inherited Alzheimer Network. Johnson ECB, et al. Nat Med. 2023 Aug;29(8):1979-1988. doi: 10.1038/s41591-023-02476-4. Epub 2023 Aug 7. Nat Med. 2023. PMID: 37550416 Free PMC article.
Etiology of White Matter Hyperintensities in Autosomal Dominant and Sporadic Alzheimer Disease.
Shirzadi Z, Schultz SA, Yau WW, Joseph-Mathurin N, Fitzpatrick CD, Levin R, Kantarci K, Preboske GM, Jack CR Jr, Farlow MR, Hassenstab J, Jucker M, Morris JC, Xiong C, Karch CM, Levey AI, Gordon BA, Schofield PR, Salloway SP, Perrin RJ, McDade E, Levin J, Cruchaga C, Allegri RF, Fox NC, Goate A, Day GS, Koeppe R, Chui HC, Berman S, Mori H, Sanchez-Valle R, Lee JH, Rosa-Neto P, Ruthirakuhan M, Wu CY, Swardfager W, Benzinger TLS, Sohrabi HR, Martins RN, Bateman RJ, Johnson KA, Sperling RA, Greenberg SM, Schultz AP, Chhatwal JP; Dominantly Inherited Alzheimer Network and the Alzheimer’s Disease Neuroimaging Initiative. Shirzadi Z, et al. JAMA Neurol. 2023 Dec 1;80(12):1353-1363. doi: 10.1001/jamaneurol.2023.3618. JAMA Neurol. 2023. PMID: 37843849 Free PMC article.
Parkinson's Disease Gene Screening in Familial Cases from Central and South America.
Lorenzo-Betancor O, Mehta S, Ramchandra J, Mumuney S, Schumacher-Schuh AF, Cornejo-Olivas M, Sarapura-Castro EH, Torres L, Inca-Martinez MA, Mazzetti P, Cosentino C, Micheli F, Tumas V, Dieguez E, Raggio V, Borges V, Ferraz HB, Chana-Cuevas P, Jimenez-Del-Rio M, Velez-Pardo C, Moreno S, Lopera F, Orozco-Velez JL, Muñoz-Ospina B, Rieder CRM, Medina-Escobar A, Yearout D, Zabetian CP, Mata IF; Latin American Research Consortium on the Genetics of PD (LARGE‐PD). Lorenzo-Betancor O, et al. Among authors: moreno s. Mov Disord. 2024 Oct;39(10):1843-1855. doi: 10.1002/mds.29931. Epub 2024 Jul 25. Mov Disord. 2024. PMID: 39051491 Free PMC article.
Genotype-phenotype association study conducted on LARGE-PD reveals novel loci associated with Parkinson's Disease.
Leal TP, Waldo E, Duarte-Zambrano F, Inca-Martinez M, Ramchandra J, Chaparro-Solano HM, Anello AE, Borda V, Gouveia MH, Teixeira-Dos-Santos D, Reyes-Pérez P, Gatto EM, Santos-Lobato BL, Eufraseo G, Letro GH, Arboleda G, Bernal-Pacheco O, Orozco JL, Munoz B, Chana-Cuevas P, Aguillon D, Moreno S, Torrealba-Acosta G, Lobo-Prada T, Muller V, Razquin CML, Braga-Neto P, Durón RM, Rodríguez-Violante M, Hernández-Medrano AJ, Cervantes-Arriaga A, Martinez-Ramirez D, Schuh AFS, de Mello Rieder CR, Cornejo-Olivas M, Rios-Pinto J, Medina AC, Cornejo-Herrera I, Mejia-Rojas K, Vinuela A, Tumas V, Pimentel AV, Borges V, Avila CL, Olguin P, Colombo A, Nuñez JC, Medina-Rivera A, Ruiz-Contreras AE, Alcauter S, Dieguez E, Nuytemans K; Global Parkinson’s Genetics Program; Mata IF. Leal TP, et al. Among authors: moreno s. medRxiv [Preprint]. 2025 Jul 18:2025.07.18.25331793. doi: 10.1101/2025.07.18.25331793. medRxiv. 2025. PMID: 40791673 Free PMC article. Preprint.
Sex differences in the diagnosis latency of Parkinson's disease in Latin America.
Ramchandra J, Inca-Martinez M, Leal TP, Chaparro-Solano HM, Salim A, Gatto EM, Rojas NG, Da Prat G, Micheli F, Santos-Lobato BL, Cardoso FEC, Camargos S, Letro GH, Braga-Neto P, Peixoto VMT, Schuh AFS, Tumas V, Brito MM, Borges V, Candeias da Silva C, Ferraz HB, Chana-Cuevas P, Saffie-Awad P, Olguin P, Colombo A, de la Cerda A, Farías GA, Nuñez JC, Arboleda G, Arboleda H, Fernandez W, Arboleda-Bustos CE, Orozco JL, Muñoz-Ospina B, Velez-Pardo C, Jiménez-Del-Río M, Lopera F, Moreno S, Pineda DA, Buritica O, Torrealba-Acosta G, Medina Escobar A, Rodríguez-Violante M, Hernández-Medrano AJ, Martinez-Ramirez D, González-González M, Rentería ME, Alcauter S, Reyes-Pérez P, Medina-Rivera A, Vazquez-Guevara D, de María Ugalde-Mejía L, Valadez M MJ, Cárdenas-Sáenz O, Rodríguez-Leyva I, Guerra-Galicia CM, Gandarilla-Martínez NA, Matuk-Pérez Y, Morelos-Figaredo E, Salinas-Barboza K, Isais-Millán S, Pérez-Torres T, Deras Gaucin DC, Ruiz-Contreras AE, Estrada-Bellmann I, Rios-Pinto J, Cornejo-Olivas M, Cosentino C, Torres Ramirez L, Mori N, Mejía-Rojas K, Medina ÁC, Cornejo-Herrera I, Ochoa EM, Viñuela Á, Dieguez E, Amorín I, Lescano A, Mata IF. Ramchandra J, et al. Among authors: moreno s. Parkinsonism Relat Disord. 2025 May;134:107344. doi: 10.1016/j.parkreldis.2025.107344. Epub 2025 Feb 25. Parkinsonism Relat Disord. 2025. PMID: 40058072 Free PMC article.
Exploring MAPT-containing H1 and H2 haplotypes in Parkinson's disease across diverse populations.
Reyes-Pérez P, Hor JW, Toh TS, Sanyaolu AO, Pantazis CB, Leal TP, Yeboah S, Bandres-Ciga S, Morris HR, Makarious MB, Senkevich K; Latin American Research Consortium on the Genetics of Parkinson’s Disease (LARGE-PD); Global Parkinson’s Genetics Program (GP2); Leonard H, Atterling Brolin K. Reyes-Pérez P, et al. NPJ Parkinsons Dis. 2026 Jun 24. doi: 10.1038/s41531-026-01394-9. Online ahead of print. NPJ Parkinsons Dis. 2026. PMID: 42342696 Free article.
Symptom onset in autosomal dominant Alzheimer disease: a systematic review and meta-analysis.
Ryman DC, Acosta-Baena N, Aisen PS, Bird T, Danek A, Fox NC, Goate A, Frommelt P, Ghetti B, Langbaum JB, Lopera F, Martins R, Masters CL, Mayeux RP, McDade E, Moreno S, Reiman EM, Ringman JM, Salloway S, Schofield PR, Sperling R, Tariot PN, Xiong C, Morris JC, Bateman RJ; Dominantly Inherited Alzheimer Network. Ryman DC, et al. Among authors: moreno s. Neurology. 2014 Jul 15;83(3):253-60. doi: 10.1212/WNL.0000000000000596. Epub 2014 Jun 13. Neurology. 2014. PMID: 24928124 Free PMC article.
Genetic modifiers of cognitive decline in PSEN1 E280A Alzheimer's disease.
Sepulveda-Falla D, Vélez JI, Acosta-Baena N, Baena A, Moreno S, Krasemann S, Lopera F, Mastronardi CA, Arcos-Burgos M. Sepulveda-Falla D, et al. Among authors: moreno s. Alzheimers Dement. 2024 Apr;20(4):2873-2885. doi: 10.1002/alz.13754. Epub 2024 Mar 7. Alzheimers Dement. 2024. PMID: 38450831 Free PMC article.
X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson's Disease.
Leal TP, Rao SC, French-Kwawu JN, Gouveia MH, Borda V, Bandres-Ciga S, Inca-Martinez M, Mason EA, Horimoto ARVR, Loesch DP, Sarihan EI, Cornejo-Olivas MR, Torres LE, Mazzetti-Soler PE, Cosentino C, Sarapura-Castro EH, Rivera-Valdivia A, Medina AC, Dieguez EM, Raggio VE, Lescano A, Tumas V, Borges V, Ferraz HB, Rieder CR, Schumacher Schuh A, Santos-Lobato BL, Velez-Pardo C, Jimenez-Del-Rio M, Lopera F, Moreno S, Chana-Cuevas P, Fernandez W, Arboleda G, Arboleda H, Arboleda Bustos CE, Yearout D, Barbosa MT, Cardoso FEC, Caramelli P, Cunningham MCQ, Maia DP, Lima-Costa MF, Tarazona-Santos E, Zabetian CP; International Parkinson Disease Genomics Consortium (IPDGC); Thornton TA, O'Connor TD, Mata IF; Latin American Research Consortium on the Genetics of Parkinson's Disease (LARGE-PD). Leal TP, et al. Among authors: moreno s. Mov Disord. 2023 Sep;38(9):1625-1635. doi: 10.1002/mds.29508. Epub 2023 Jul 20. Mov Disord. 2023. PMID: 37469269 Free PMC article.
A neurodegenerative disease landscape of rare mutations in Colombia due to founder effects.
Acosta-Uribe J, Aguillón D, Cochran JN, Giraldo M, Madrigal L, Killingsworth BW, Singhal R, Labib S, Alzate D, Velilla L, Moreno S, García GP, Saldarriaga A, Piedrahita F, Hincapié L, López HE, Perumal N, Morelo L, Vallejo D, Solano JM, Reiman EM, Surace EI, Itzcovich T, Allegri R, Sánchez-Valle R, Villegas-Lanau A, White CL 3rd, Matallana D, Myers RM, Browning SR, Lopera F, Kosik KS. Acosta-Uribe J, et al. Among authors: moreno s. Genome Med. 2022 Mar 8;14(1):27. doi: 10.1186/s13073-022-01035-9. Genome Med. 2022. PMID: 35260199 Free PMC article.
64 results