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Page 1
Unraveling Signatures of Local Adaptation among Indigenous Groups from Mexico.
Genes (Basel). 2022 Nov 30;13(12):2251. doi: 10.3390/genes13122251.
Genes (Basel). 2022.
PMID: 36553518
Free PMC article.
CFTR pathogenic variants spectrum in a cohort of Mexican patients with cystic fibrosis.
Martínez-Hernández A, Mendoza-Caamal EC, Mendiola-Vidal NG, Barajas-Olmos F, Villafan-Bernal JR, Jiménez-Ruiz JL, Monge-Cazares T, García-Ortiz H, Cubas CC, Centeno-Cruz F, Alaez-Verson C, Ortega-Torres S, Luna-Castañeda ADC, Baca V, Lezana JL, Orozco L.
Martínez-Hernández A, et al. Among authors: monge cazares t.
Heliyon. 2024 Mar 29;10(7):e28984. doi: 10.1016/j.heliyon.2024.e28984. eCollection 2024 Apr 15.
Heliyon. 2024.
PMID: 38601560
Free PMC article.
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Association between Apolipoprotein E Variants and Obesity-Related Traits in Mexican School Children.
Rodríguez-Carmona Y, Pérez-Rodríguez M, Gámez-Valdez E, López-Alavez FJ, Hernández-Armenta CI, Vega-Monter N, Leyva-García G, Monge-Cázares T, Barrera Valencia D, Balderas Monroy M, Pfeffer F, Meléndez G, Pérez Lizaur AB, Pardío J, Tejero ME.
Rodríguez-Carmona Y, et al. Among authors: monge cazares t.
J Nutrigenet Nutrigenomics. 2014;7(4-6):243-51. doi: 10.1159/000381345. Epub 2015 May 6.
J Nutrigenet Nutrigenomics. 2014.
PMID: 25968937
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Resequencing, haplotype construction and identification of novel variants of CYP2D6 in Mexican Mestizos.
Contreras AV, Monge-Cazares T, Alfaro-Ruiz L, Hernandez-Morales S, Miranda-Ortiz H, Carrillo-Sanchez K, Jimenez-Sanchez G, Silva-Zolezzi I.
Contreras AV, et al. Among authors: monge cazares t.
Pharmacogenomics. 2011 May;12(5):745-56. doi: 10.2217/pgs.11.8. Epub 2011 Mar 11.
Pharmacogenomics. 2011.
PMID: 21391885
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Rare intronic variants of TCF7L2 arising by selective sweeps in an indigenous population from Mexico.
Acosta JL, Hernández-Mondragón AC, Correa-Acosta LC, Cazañas-Padilla SN, Chávez-Florencio B, Ramírez-Vega EY, Monge-Cázares T, Aguilar-Salinas CA, Tusié-Luna T, Del Bosque-Plata L.
Acosta JL, et al. Among authors: monge cazares t.
BMC Genet. 2016 May 26;17(1):68. doi: 10.1186/s12863-016-0372-7.
BMC Genet. 2016.
PMID: 27230431
Free PMC article.
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A homozygous CEP57 c.915_925dupCAATGTTCAGC mutation in a patient with mosaic variegated aneuploidy syndrome with rhizomelic shortening in the upper and lower limbs and a narrow thorax.
De la Torre-García O, Mar-Aldama R, Salgado-Sangri R, Diaz-Gomez N, Bonilla-Arcaute L, Diaz-Ponce-Medrano J, Guevara-Yañez R, Córdova EJ, Monge-Cazares T, Orozco L, Martínez-Hernández A.
De la Torre-García O, et al. Among authors: monge cazares t.
Eur J Med Genet. 2019 Mar;62(3):195-197. doi: 10.1016/j.ejmg.2018.07.013. Epub 2018 Jul 17.
Eur J Med Genet. 2019.
PMID: 30010053
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