Perceptions of Knowledge, Disease Impact and Predictive Genetic Testing in Family Members at Risk to Develop Early-Onset Alzheimer’s Disease (EOAD) and Their Levels of Suicidal Ide...

por Reyes-Domínguez, Yesica Arlae, Figuera, Luis E., Brambila-Tapia, Aniel Jessica Leticia
Publicado 2023

Prediction of Regulatory SNPs in Putative Minor Genes of the Neuro-Cardiovascular Variant in Fabry Reveals Insights into Autophagy/Apoptosis and Fibrosis

por Ruiz Ramírez, Andrea Virginia, Prado Montes de Oca, Ernesto, Figuera, Luis E
Publicado 2022

Association of the Alu insertion polymorphism in the progesterone receptor gene with breast cancer in a Mexican population

por Gallegos-Arreola, Martha Patricia, Figuera, Luis E., Flores-Ramos, Liliana Gómez, Puebla-Pérez, Ana María, Zúñiga-González, Guillermo Moisés
Publicado 2015

ESR2 gene variants (rs1256049, rs4986938, and rs1256030) and their association with breast cancer risk

por Gallegos-Arreola, Martha Patricia, Zúñiga-González, Guillermo M., Figuera, Luis E., Puebla-Pérez, Ana María, Márquez-Rosales, María Guadalupe, Gómez-Meda, Belinda Claudia, Rosales-Reynoso, Mónica Alejandra
Publicado 2022

Potential Modifying Effect of the APOEε4 Allele on Age of Onset and Clinical Manifestations in Patients with Early-Onset Alzheimer’s Disease with and without a Pathogenic Variant i...

por Valdez-Gaxiola, César A., Maciel-Cruz, Eric Jonathan, Hernández-Peña, Rubiceli, Dumois-Petersen, Sofía, Rosales-Leycegui, Frida, Gallegos-Arreola, Martha Patricia, Moreno-Ortiz, José Miguel, Figuera, Luis E.
Publicado 2023

SOD2 Gene Variants (rs4880 and rs5746136) and Their Association with Breast Cancer Risk

por Gallegos-Arreola, Martha P., Ramírez-Patiño, Ramiro, Sánchez-López, Josefina Y., Zúñiga-González, Guillermo M., Figuera, Luis E., Delgado-Saucedo, Jorge I., Gómez-Meda, Belinda C., Rosales-Reynoso, Mónica A., Puebla-Pérez, Ana M., Lemus-Varela, María L., Garibaldi-Ríos, Asbiel F., Marín-Domínguez, Nayely A., Pacheco-Verduzco, Diana P., Mohamed-Flores, Emaan A.
Publicado 2022

Clinical and molecular features of 66 patients with musculocontractural Ehlers−Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)

por Minatogawa, Mari, Unzaki, Ai, Morisaki, Hiroko, Syx, Delfien, Sonoda, Tohru, Janecke, Andreas R, Slavotinek, Anne, Voermans, Nicol C, Lacassie, Yves, Mendoza-Londono, Roberto, Wierenga, Klaas J, Jayakar, Parul, Gahl, William A, Tifft, Cynthia J, Figuera, Luis E, Hilhorst-Hofstee, Yvonne, Maugeri, Alessandra, Ishikawa, Ken, Kobayashi, Tomoko, Aoki, Yoko, Ohura, Toshihiro, Kawame, Hiroshi, Kono, Michihiro, Mochida, Kosuke, Tokorodani, Chiho, Kikkawa, Kiyoshi, Morisaki, Takayuki, Kobayashi, Tetsuyuki, Nakane, Takaya, Kubo, Akiharu, Ranells, Judith D, Migita, Ohsuke, Sobey, Glenda, Kaur, Anupriya, Ishikawa, Masumi, Yamaguchi, Tomomi, Matsumoto, Naomichi, Malfait, Fransiska, Miyake, Noriko, Kosho, Tomoki
Publicado 2022