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Dissecting the role of Amerindian genetic ancestry and the ApoE ε4 allele on Alzheimer disease in an admixed Peruvian population.
Neurobiol Aging. 2021 May;101:298.e11-298.e15. doi: 10.1016/j.neurobiolaging.2020.10.003. Epub 2020 Dec 10.
Neurobiol Aging. 2021.
PMID: 33541779
Free PMC article.
ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population.
Véliz-Otani D, Inca-Martinez M, Bampi GB, Ortega O, Jardim LB, Saraiva-Pereira ML, Mazzetti P, Cornejo-Olivas M.
Véliz-Otani D, et al.
Cerebellum. 2019 Oct;18(5):841-848. doi: 10.1007/s12311-019-01057-x.
Cerebellum. 2019.
PMID: 31342269
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Response to ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population.
Véliz-Otani D, Cubas-Montecino D, Milla-Neyra K, Ashizawa T, Saraiva-Pereira ML, Jardim LB, Cornejo-Olivas M.
Véliz-Otani D, et al.
Cerebellum. 2021 Dec;20(6):946-947. doi: 10.1007/s12311-021-01258-3. Epub 2021 Mar 17.
Cerebellum. 2021.
PMID: 33728569
No abstract available.
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The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin America.
Kay C, Tirado-Hurtado I, Cornejo-Olivas M, Collins JA, Wright G, Inca-Martinez M, Veliz-Otani D, Ketelaar ME, Slama RA, Ross CJ, Mazzetti P, Hayden MR.
Kay C, et al.
Eur J Hum Genet. 2017 Feb;25(3):332-340. doi: 10.1038/ejhg.2016.169. Epub 2016 Dec 21.
Eur J Hum Genet. 2017.
PMID: 28000697
Free PMC article.
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Distribution of the CAG Triplet Repeat in ATXN1, ATXN3, and CACNA1A Loci in Peruvian Population.
Gonzales-Sáenz C, Cruz-Rodriguez C, Espinoza-Huertas K, Véliz-Otani D, Marca V, Ortega O, Milla-Neyra K, Alvarez-Tejada J, Mazzetti P, Cornejo-Olivas M.
Gonzales-Sáenz C, et al.
Cerebellum. 2020 Aug;19(4):527-535. doi: 10.1007/s12311-020-01129-3.
Cerebellum. 2020.
PMID: 32285347
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Clinical and Molecular Features of Late Onset Huntington Disease in a Peruvian Cohort.
Cornejo-Olivas MR, Inca-Martinez MA, Espinoza-Huertas K, Veliz-Otani D, Velit-Salazar MR, Marca V, Ortega O, Cornejo-Herrera IF, Lindo-Samanamud S, Mora-Alferez P, Mazzetti P.
Cornejo-Olivas MR, et al.
J Huntingtons Dis. 2015;4(1):99-105.
J Huntingtons Dis. 2015.
PMID: 26333261
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Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.
Bampi GB, Bisso-Machado R, Hünemeier T, Gheno TC, Furtado GV, Veliz-Otani D, Cornejo-Olivas M, Mazzeti P, Bortolini MC, Jardim LB, Saraiva-Pereira ML; Rede Neurogenetica.
Bampi GB, et al.
Neuromolecular Med. 2017 Dec;19(4):501-509. doi: 10.1007/s12017-017-8464-8. Epub 2017 Sep 13.
Neuromolecular Med. 2017.
PMID: 28905220
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Neurogenetics in Peru: clinical, scientific and ethical perspectives.
Cornejo-Olivas M, Espinoza-Huertas K, Velit-Salazar MR, Veliz-Otani D, Tirado-Hurtado I, Inca-Martinez M, Silva-Paredes G, Milla-Neyra K, Marca V, Ortega O, Mazzetti P.
Cornejo-Olivas M, et al.
J Community Genet. 2015 Jul;6(3):251-7. doi: 10.1007/s12687-015-0239-z. Epub 2015 May 27.
J Community Genet. 2015.
PMID: 26013639
Free PMC article.
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