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51 results

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Page 1
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort.
Vollstedt EJ, Schaake S, Lohmann K, Padmanabhan S, Brice A, Lesage S, Tesson C, Vidailhet M, Wurster I, Hentati F, Mirelman A, Giladi N, Marder K, Waters C, Fahn S, Kasten M, Brüggemann N, Borsche M, Foroud T, Tolosa E, Garrido A, Annesi G, Gagliardi M, Bozi M, Stefanis L, Ferreira JJ, Correia Guedes L, Avenali M, Petrucci S, Clark L, Fedotova EY, Abramycheva NY, Alvarez V, Menéndez-González M, Jesús Maestre S, Gómez-Garre P, Mir P, Belin AC, Ran C, Lin CH, Kuo MC, Crosiers D, Wszolek ZK, Ross OA, Jankovic J, Nishioka K, Funayama M, Clarimon J, Williams-Gray CH, Camacho M, Cornejo-Olivas M, Torres-Ramirez L, Wu YR, Lee-Chen GJ, Morgadinho A, Pulkes T, Termsarasab P, Berg D, Kuhlenbäumer G, Kühn AA, Borngräber F, de Michele G, De Rosa A, Zimprich A, Puschmann A, Mellick GD, Dorszewska J, Carr J, Ferese R, Gambardella S, Chase B, Markopoulou K, Satake W, Toda T, Rossi M, Merello M, Lynch T, Olszewska DA, Lim SY, Ahmad-Annuar A, Tan AH, Al-Mubarak B, Hanagasi H, Koziorowski D, Ertan S, Genç G, de Carvalho Aguiar P, Barkhuizen M, Pimentel MMG, Saunders-Pullman R, van de Warrenburg B, Bressman S, Toft M, Appel-Cresswell S, Lang AE, Skorvanek M, Boon AJW, Krüger R, Sammler EM, Tumas V, … See abstract for full author list ➔ Vollstedt EJ, et al. Mov Disord. 2023 Feb;38(2):286-303. doi: 10.1002/mds.29288. Epub 2023 Jan 24. Mov Disord. 2023. PMID: 36692014 Free 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: dieguez e. 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.
Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas.
Borda V, Loesch DP, Guo B, Laboulaye R, Veliz-Otani D, French JN, Leal TP, Gogarten SM, Ikpe S, Gouveia MH, Mendes M, Abecasis GR, Alvim I, Arboleda-Bustos CE, Arboleda G, Arboleda H, Barreto ML, Barwick L, Bezzera MA, Blangero J, Borges V, Caceres O, Cai J, Chana-Cuevas P, Chen Z, Custer B, Dean M, Dinardo C, Domingos I, Duggirala R, Dieguez E, Fernandez W, Ferraz HB, Gilliland F, Guio H, Horta B, Curran JE, Johnsen JM, Kaplan RC, Kelly S, Kenny EE, Konkle BA, Kooperberg C, Lescano A, Lima-Costa MF, Loos RJF, Manichaikul A, Meyers DA, Naslavsky MS, Nickerson DA, North KE, Padilla C, Preuss M, Raggio V, Reiner AP, Rich SS, Rieder CR, Rienstra M, Rotter JI, Rundek T, Sacco RL, Sanchez C, Sankaran VG, Santos-Lobato BL, Schumacher-Schuh AF, Scliar MO, Silverman EK, Sofer T, Lasky-Su J, Tumas V, Weiss ST; Latin American Research Consortium on the Genetics of Parkinson’s Disease (LARGE-PD); National Institute of Neurological Disorders and Stroke (NINDS) Stroke Genetics Network (SiGN) Consortium; Trans-Omics for Precision Medicine (TOPMed) Population Genetics Working Group; Mata IF, Hernandez RD, Tarazona-Santos E, O'Connor TD. Borda V, et al. Among authors: dieguez e. Cell Genom. 2024 Nov 13;4(11):100692. doi: 10.1016/j.xgen.2024.100692. Epub 2024 Oct 31. Cell Genom. 2024. PMID: 39486408 Free PMC article.
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: dieguez e. 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 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: dieguez e. medRxiv [Preprint]. 2025 Jul 18:2025.07.18.25331793. doi: 10.1101/2025.07.18.25331793. medRxiv. 2025. PMID: 40791673 Free PMC article. Preprint.
51 results