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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 2, 2010
Mutation of SDHB is a cause of hypoxia-related high-altitude paragangliomaNidia Y Cerecer-Gil, Luis E Figuera, Francisco J Llamas, et al.American Journal of Human Genetics|June 4, 2011
X-linked congenital hypertrichosis syndrome is associated with interchromosomal insertions mediated by a human-specific palindrome near SOX3Hongwen Zhu, Dandan Shang, Miao Sun, et al.European Review for Medical and Pharmacological Sciences|February 20, 2024
Variants rs2758346, rs5746094, and rs2758331 of SOD2 gene: association study with breast cancer in a Mexican population and their analysis in silicoM P Gallegos-Arreola, A F Garibaldi-Ríos, L E Figuera, et al.Tissue Antigens|July 27, 2006
High-resolution molecular characterization of the HLA class I and class II in the Tarahumara Amerindian populationJ E García-Ortiz, L Sandoval-Ramírez, H Rangel-Villalobos, et al.Diseases (Basel, Switzerland)|August 27, 2025
Regulatory Effects of Endometriosis-Associated Genetic Variants: A Multi-Tissue eQTL AnalysisAsbiel Felipe Garibaldi-Ríos, Perla Graciela Rodríguez-Gutiérrez, Jesús Magdiel García-Díaz, et al.Genetics and Molecular Research : GMR|December 5, 2013
Association of the tumor necrosis factor-alpha -308G>A polymorphism with breast cancer in Mexican womenL Gómez Flores-Ramos, A Escoto-De Dios, A M Puebla-Pérez, et al.Biomedicines|March 28, 2024
Association of the rs1966265 and rs351855 FGFR4 Variants with Colorectal Cancer in a Mexican Population and Their Analysis In SilicoIrving Alejandro Carrillo-Dávila, Asbiel Felipe Garibaldi-Ríos, Luis E Figuera, et al.Clinical Genetics|February 14, 2018
Exome sequencing reveals three homozygous missense variants in SNRPA in two sisters with syndromic intellectual disabilityM M Rangel-Sosa, L E Figuera-Villanueva, I A González-Ramos, et al.European Review for Medical and Pharmacological Sciences|August 2, 2022
Mutational spectrum of the iduronate-2-sulfatase gene in Mexican patients with Hunter syndromeM A Ramírez-Hernández, L E Figuera, L C Rizo-de la Torre, et al.Journal of Molecular Medicine (Berlin, Germany)|August 23, 2000
Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticumB Struk, L Cai, S Zäch, et al.Pageof 12