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

Year Number of Results
2004 2
2005 1
2009 3
2013 1
2014 3
2015 6
2016 5
2017 1
2018 3
2019 8
2020 1
2021 1
2024 1

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30 results

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Page 1
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: mastronardi ca. 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.
Impulsive and Omission Errors: Potential Temporal Processing Endophenotypes in ADHD.
Acosta-López JE, Suárez I, Pineda DA, Cervantes-Henríquez ML, Martínez-Banfi ML, Lozano-Gutiérrez SG, Ahmad M, Pineda-Alhucema W, Noguera-Machacón LM, Hoz M, Mejía-Segura E, Jiménez-Figueroa G, Sánchez-Rojas M, Mastronardi CA, Arcos-Burgos M, Vélez JI, Puentes-Rozo PJ. Acosta-López JE, et al. Among authors: mastronardi ca. Brain Sci. 2021 Sep 15;11(9):1218. doi: 10.3390/brainsci11091218. Brain Sci. 2021. PMID: 34573239 Free PMC article.
Familial Alzheimer's Disease and Recessive Modifiers.
Vélez JI, Lopera F, Silva CT, Villegas A, Espinosa LG, Vidal OM, Mastronardi CA, Arcos-Burgos M. Vélez JI, et al. Among authors: mastronardi ca. Mol Neurobiol. 2020 Feb;57(2):1035-1043. doi: 10.1007/s12035-019-01798-0. Epub 2019 Oct 29. Mol Neurobiol. 2020. PMID: 31664702 Free PMC article.
Genetic Variation Underpinning ADHD Risk in a Caribbean Community.
Puentes-Rozo PJ, Acosta-López JE, Cervantes-Henríquez ML, Martínez-Banfi ML, Mejia-Segura E, Sánchez-Rojas M, Anaya-Romero ME, Acosta-Hoyos A, García-Llinás GA, Mastronardi CA, Pineda DA, Castellanos FX, Arcos-Burgos M, Vélez JI. Puentes-Rozo PJ, et al. Among authors: mastronardi ca. Cells. 2019 Aug 16;8(8):907. doi: 10.3390/cells8080907. Cells. 2019. PMID: 31426340 Free PMC article.
Congenital Leptin Deficiency and Leptin Gene Missense Mutation Found in Two Colombian Sisters with Severe Obesity.
Yupanqui-Lozno H, Bastarrachea RA, Yupanqui-Velazco ME, Alvarez-Jaramillo M, Medina-Méndez E, Giraldo-Peña AP, Arias-Serrano A, Torres-Forero C, Garcia-Ordoñez AM, Mastronardi CA, Restrepo CM, Rodriguez-Ayala E, Nava-Gonzalez EJ, Arcos-Burgos M, Kent JW Jr, Cole SA, Licinio J, Celis-Regalado LG. Yupanqui-Lozno H, et al. Among authors: mastronardi ca. Genes (Basel). 2019 May 7;10(5):342. doi: 10.3390/genes10050342. Genes (Basel). 2019. PMID: 31067764 Free PMC article.
Generation of one iPSC line (IMEDEAi006-A) from an early-onset familial Alzheimer's Disease (fAD) patient carrying the E280A mutation in the PSEN1 gene.
Vallejo-Diez S, Fleischer A, Martín-Fernández JM, Sánchez-Gilabert A, Castresana M, Aguillón D, Villegas A, Mastronardi CA, Espinosa LG, Arcos-Burgos M, Del Pozo Á, Herrán E, Gainza E, Isaza-Ruget M, Lopera F, Bachiller D. Vallejo-Diez S, et al. Among authors: mastronardi ca. Stem Cell Res. 2019 May;37:101440. doi: 10.1016/j.scr.2019.101440. Epub 2019 Apr 15. Stem Cell Res. 2019. PMID: 31026686 Free article.
ADGRL3 (LPHN3) variants predict substance use disorder.
Arcos-Burgos M, Vélez JI, Martinez AF, Ribasés M, Ramos-Quiroga JA, Sánchez-Mora C, Richarte V, Roncero C, Cormand B, Fernández-Castillo N, Casas M, Lopera F, Pineda DA, Palacio JD, Acosta-López JE, Cervantes-Henriquez ML, Sánchez-Rojas MG, Puentes-Rozo PJ, Molina BSG; MTA Cooperative Group; Boden MT, Wallis D, Lidbury B, Newman S, Easteal S, Swanson J, Patel H, Volkow N, Acosta MT, Castellanos FX, de Leon J, Mastronardi CA, Muenke M. Arcos-Burgos M, et al. Among authors: mastronardi ca. Transl Psychiatry. 2019 Jan 29;9(1):42. doi: 10.1038/s41398-019-0396-7. Transl Psychiatry. 2019. PMID: 30696812 Free PMC article.
Leptin: role over central nervous system in epilepsy.
Mora-Muñoz L, Guerrero-Naranjo A, Rodríguez-Jimenez EA, Mastronardi CA, Velez-van-Meerbeke A. Mora-Muñoz L, et al. BMC Neurosci. 2018 Sep 5;19(1):51. doi: 10.1186/s12868-018-0453-9. BMC Neurosci. 2018. PMID: 30185147 Free PMC article.
30 results