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 NCBI Filters

Results by year

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

Year Number of Results
2011 1
2012 2
2014 2
2015 3
2018 1
2019 3
2020 2
2021 1
2022 2
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

15 results

Results by year

Filters applied: . Clear all
Page 1
A Previously Unrecognized Molecular Landscape of Lynch Syndrome in the Mexican Population.
Padua-Bracho A, Velázquez-Aragón JA, Fragoso-Ontiveros V, Nuñez-Martínez PM, Mejía Aguayo ML, Sánchez-Contreras Y, Ramirez-Otero MA, De la Fuente-Hernández MA, Vidal-Millán S, Wegman-Ostrosky T, Pedroza-Torres A, Arriaga-Canon C, Herrera-Montalvo LA, Alvarez-Gómez RM. Padua-Bracho A, et al. Among authors: velazquez aragon ja. Int J Mol Sci. 2022 Sep 30;23(19):11549. doi: 10.3390/ijms231911549. Int J Mol Sci. 2022. PMID: 36232851 Free PMC article.
First comprehensive TSC1/TSC2 mutational analysis in Mexican patients with Tuberous Sclerosis Complex reveals numerous novel pathogenic variants.
Reyna-Fabián ME, Hernández-Martínez NL, Alcántara-Ortigoza MA, Ayala-Sumuano JT, Enríquez-Flores S, Velázquez-Aragón JA, Varela-Echavarría A, Todd-Quiñones CG, González-Del Angel A. Reyna-Fabián ME, et al. Among authors: velazquez aragon ja. Sci Rep. 2020 Apr 20;10(1):6589. doi: 10.1038/s41598-020-62759-5. Sci Rep. 2020. PMID: 32313033 Free PMC article.
Variants in ARID5B gene are associated with the development of acute lymphoblastic leukemia in Mexican children.
Reyes-León A, Ramírez-Martínez M, Fernández-García D, Amaro-Muñoz D, Velázquez-Aragón JA, Salas-Labadía C, Zapata-Tarrés M, Velasco-Hidalgo L, López-Santiago N, López-Ruiz MI, Malavar-Guadarrama MA, Cárdenas-Cardós R, Paredes-Aguilera R, Rivera-Luna R, Dean M, Pérez-Vera P. Reyes-León A, et al. Among authors: velazquez aragon ja. Ann Hematol. 2019 Oct;98(10):2379-2388. doi: 10.1007/s00277-019-03730-x. Epub 2019 Jun 21. Ann Hematol. 2019. PMID: 31227872 Clinical Trial.
Mexican BRCA1 founder mutation: Shortening the gap in genetic assessment for hereditary breast and ovarian cancer patients.
Fragoso-Ontiveros V, Velázquez-Aragón JA, Nuñez-Martínez PM, de la Luz Mejía-Aguayo M, Vidal-Millán S, Pedroza-Torres A, Sánchez-Contreras Y, Ramírez-Otero MA, Muñiz-Mendoza R, Domínguez-Ortíz J, Wegman-Ostrosky T, Bargalló-Rocha JE, Gallardo-Rincón D, Reynoso-Noveron N, Arriaga-Canon C, Meneses-García A, Herrera-Montalvo LA, Alvarez-Gomez RM. Fragoso-Ontiveros V, et al. Among authors: velazquez aragon ja. PLoS One. 2019 Sep 23;14(9):e0222709. doi: 10.1371/journal.pone.0222709. eCollection 2019. PLoS One. 2019. PMID: 31545835 Free PMC article.
Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes.
Barrientos-Rios R, Frias S, Velázquez-Aragón JA, Villaroel CE, Sánchez S, Molina B, Martínez A, Carnevale A, García-de-Teresa B, Bonilla E, Alvarado-Araiza CD, Valderrama-Hernández A, Ríos-Gallardo PT, Calzada-León R, Altamirano-Bustamante N, Torres L. Barrientos-Rios R, et al. Among authors: velazquez aragon ja. Gynecol Endocrinol. 2019 Sep;35(9):772-776. doi: 10.1080/09513590.2019.1582626. Epub 2019 Mar 19. Gynecol Endocrinol. 2019. PMID: 30887870
5,10-Methylenetetrahydrofolate reductase single nucleotide polymorphisms and gene-environment interaction analysis in non-syndromic cleft lip/palate.
Estandia-Ortega B, Velázquez-Aragón JA, Alcántara-Ortigoza MA, Reyna-Fabian ME, Villagómez-Martínez S, González-Del Angel A. Estandia-Ortega B, et al. Among authors: velazquez aragon ja. Eur J Oral Sci. 2014 Apr;122(2):109-13. doi: 10.1111/eos.12114. Epub 2014 Jan 24. Eur J Oral Sci. 2014. PMID: 24460828
Phenotype-Genotype Discrepancy Due to a 5.5-kb Deletion in the GALT Gene.
González-del Angel A, Velázquez-Aragón J, Alcántara-Ortigoza MA, Vela-Amieva M, Hernández-Martínez N. González-del Angel A, et al. Among authors: velazquez aragon j. JIMD Rep. 2012;2:1-5. doi: 10.1007/8904_2011_30. Epub 2011 Sep 6. JIMD Rep. 2012. PMID: 23430845 Free PMC article.
15 results