Tulia Monge-Cázares

Unraveling Signatures of Local Adaptation among Indigenous Groups from Mexico

Deborah A. Bolnick, A. Kostic, H. Rangel-Villalobos, 2022, Genes.

Rare intronic variants of TCF7L2 arising by selective sweeps in an indigenous population from Mexico

Alma Cristal Hernández-Mondragón, C. Aguilar-Salinas, T. Tusié-Luna, 2016, BMC Genetics.

Resequencing, haplotype construction and identification of novel variants of CYP2D6 in Mexican Mestizos.

G. Jiménez-Sánchez, I. Silva-Zolezzi, A. Contreras, 2011, Pharmacogenomics.

Association between Apolipoprotein E Variants and Obesity-Related Traits in Mexican School Children

Y. Rodríguez-Carmona, Claudia Hernandez-Armenta, G. Meléndez, 2015, Lifestyle Genomics.

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.

L. Orozco, A. Martinez-Hernandez, R. Guevara-Yáñez, 2019, European journal of medical genetics.

Rare intronic variants of TCF7L2 arising by selective sweeps in an indigenous population from Mexico

C. Aguilar-Salinas, L. del Bosque-Plata, J. L. Acosta, 2016, BMC Genetics.

Effect of the Complex Allele p.[Ile148Thr;Ile1023_Val1024del] in Cystic Fibrosis and Tracing of a Founder Effect in Mexican Families

H. García-Ortiz, A. Martinez-Hernandez, F. Barajas-Olmos, 2024, Life.