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Page 1
Clinical genome sequencing in patients with suspected rare genetic disease in Peru.
Bazalar-Montoya J, Cornejo-Olivas M, Duenas-Roque MM, Purizaca-Rosillo N, Rodriguez RS, Milla-Neyra K, De La Torre-Hernandez CA, Sarapura-Castro E, Galarreta Aima CI, Manassero-Morales G, Chávez-Pasco G, Celis-García L, La Serna-Infantes JE; Illumina Laboratory Services Bioinformatics, Software, Interpretation and Customer Support; Chekalin E, Thorpe E, Taft RJ. Bazalar-Montoya J, et al. Among authors: milla neyra k. NPJ Genom Med. 2024 Oct 28;9(1):51. doi: 10.1038/s41525-024-00434-8. NPJ Genom Med. 2024. PMID: 39468051 Free PMC article.
The impact of clinical genome sequencing in a global population with suspected rare genetic disease.
Thorpe E, Williams T, Shaw C, Chekalin E, Ortega J, Robinson K, Button J, Jones MC, Campo MD, Basel D, McCarrier J, Keppen LD, Royer E, Foster-Bonds R, Duenas-Roque MM, Urraca N, Bosfield K, Brown CW, Lydigsen H, Mroczkowski HJ, Ward J, Sirchia F, Giorgio E, Vaux K, Salguero HP, Lumaka A, Mubungu G, Makay P, Ngole M, Lukusa PT, Vanderver A, Muirhead K, Sherbini O, Lah MD, Anderson K, Bazalar-Montoya J, Rodriguez RS, Cornejo-Olivas M, Milla-Neyra K, Shinawi M, Magoulas P, Henry D, Gibson K, Wiafe S, Jayakar P, Salyakina D, Masser-Frye D, Serize A, Perez JE, Taylor A, Shenbagam S, Abou Tayoun A, Malhotra A, Bennett M, Rajan V, Avecilla J, Warren A, Arseneault M, Kalista T, Crawford A, Ajay SS, Perry DL, Belmont J, Taft RJ. Thorpe E, et al. Among authors: milla neyra k. Am J Hum Genet. 2024 Jul 11;111(7):1271-1281. doi: 10.1016/j.ajhg.2024.05.006. Epub 2024 Jun 5. Am J Hum Genet. 2024. PMID: 38843839 Free PMC article.
Juvenile-Onset Huntington's Disease in Peru: A Case Series of 32 Patients.
Vishnevetsky A, Cornejo-Olivas M, Sarapura-Castro E, Inca-Martinez M, Rabinowitz D, Milla-Neyra K, Mazzetti P, Bird T. Vishnevetsky A, et al. Among authors: milla neyra k. Mov Disord Clin Pract. 2022 Dec 2;10(2):238-247. doi: 10.1002/mdc3.13625. eCollection 2023 Feb. Mov Disord Clin Pract. 2022. PMID: 36825038 Free PMC article.
Machado Joseph-Disease Is Rare in the Peruvian Population.
Cornejo-Olivas M, Solis-Ponce L, Araujo-Aliaga I, Milla-Neyra K, Ortega O, Illanes-Manrique M, Mazzetti P, Manrique-Enciso C, Cubas-Montecino D, Saraiva-Pereira ML, Jardim LB, Sarapura-Castro E. Cornejo-Olivas M, et al. Among authors: milla neyra k. Cerebellum. 2023 Dec;22(6):1192-1199. doi: 10.1007/s12311-022-01491-4. Epub 2022 Nov 3. Cerebellum. 2023. PMID: 36323979
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. Among authors: milla neyra k. 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.
The First Report of CADASIL in Peru: Olfactory Dysfunction on Initial Presentation.
Vishnevetsky A, Inca-Martinez M, Milla-Neyra K, Barrientos-Iman DM, Cornejo-Herrera I, Cosentino C, Cornejo-Olivas M. Vishnevetsky A, et al. Among authors: milla neyra k. eNeurologicalSci. 2016 Dec;5:15-19. doi: 10.1016/j.ensci.2016.09.001. Epub 2016 Sep 28. eNeurologicalSci. 2016. PMID: 28534048 Free PMC article.
[Neurogenetics in Peru, example of translational research].
Mazzetti P, Inca-Martínez M, Tirado-Hurtado I, Milla-Neyra K, Silva-Paredes G, Vishnevetsky A, Cornejo-Olivas M. Mazzetti P, et al. Among authors: milla neyra k. Rev Peru Med Exp Salud Publica. 2015 Oct;32(4):787-93. Rev Peru Med Exp Salud Publica. 2015. PMID: 26732930 Free article. Spanish.
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. Among authors: milla neyra k. 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.