Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes
Florez, J. C, Price, A. L, Campbell, D, Riba, L, Parra, M. V, Yu, F, Duque, C, Saxena, R, Gallego, N, Tello-Ruiz, M, Franco, L, Rodríguez-Torres, M, Villegas, A, Bedoya, G, Aguilar-Salinas, C. A, Tusié-Luna, M. T, Ruiz-Linares, A, Reich, D
Published in Diabetologia (01.08.2009)
Published in Diabetologia (01.08.2009)
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The influence of high-density lipoprotein (HDL) and HDL subfractions on insulin secretion and cholesterol efflux in pancreatic derived β-cells
Ochoa-Guzmán, A., Guillén-Quintero, D., Muñoz-Hernández, L., García, A., Díaz-Díaz, E., Pérez-Méndez, O., Rodríguez-Guillén, R., Mitre-Aguilar, I. B., Zentella-Dehesa, A., Aguilar-Salinas, C. A., Tusié-Luna, M. T.
Published in Journal of endocrinological investigation (01.09.2021)
Published in Journal of endocrinological investigation (01.09.2021)
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R230C but not − 565C/T variant of the ABCA1 gene is associated with type 2 diabetes in Mexicans through an effect on lowering HDL-cholesterol levels
Ochoa-Guzmán, A., Moreno-Macías, H., Guillén-Quintero, D., Chávez-Talavera, O., Ordoñez-Sánchez, M. L., Segura-Kato, Y., Ortíz, V., Díaz-Díaz, E., Muñoz-Hernández, L., García, A., Pérez-Méndez, O., Zentella-Dehesa, A., Aguilar-Salinas, C. A., Tusié-Luna, M. T.
Published in Journal of endocrinological investigation (01.08.2020)
Published in Journal of endocrinological investigation (01.08.2020)
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Journal Article
High frequency of T130I mutation of HNF4A gene in Mexican patients with early-onset type 2 diabetes
Menjívar, M, Granados-Silvestre, MA, Montúfar-Robles, I, Herrera, M, Tusié-Luna, MT, Canizales-Quinteros, S, Aguilar-Salinas, CA, Ortiz-López, MG
Published in Clinical genetics (01.02.2008)
Published in Clinical genetics (01.02.2008)
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HNF-1α G574S is a functional variant with decreased transactivation activity
Navalón-García, K., Mendoza-Alcantar, L., Díaz-Vargas, M. E., Martínez-Godínez, M. A., Reyna-Garfias, H., Aguilar-Salinas, C. A., Riba, L., Canizales-Quinteros, S., Villarreal-Molina, T., González-Chávez, A., Argueta-Villamar, V., Tusié-Luna, M. T., Miliar-García, A.
Published in Diabetic medicine (01.12.2006)
Published in Diabetic medicine (01.12.2006)
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Molecular genetic analysis of patients carrying steroid 21-hydroxylase deficiency in the Mexican population : identification of possible new mutations and high prevalence of apparent germ-line mutations
ORDONEZ-SANCHEZ, M. L, RAMIREZ-JIMENEZ, S, TUSIE-LUNA, M. T, LOPEZ-GUTIERREZ, A. U, RIBA, L, GAMBOA-CARDIEL, S, CERRILLO-HINOJOSA, M, ALTAMIRANO-BUSTAMANTE, N, CALZADA-LEON, R, ROBLES-VALDES, C, MENDOZA-MORFIN, F
Published in Human genetics (01.02.1998)
Published in Human genetics (01.02.1998)
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Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Speiser, P W, Dupont, J, Zhu, D, Serrat, J, Buegeleisen, M, Tusie-Luna, M T, Lesser, M, New, M I, White, P C
Published in The Journal of clinical investigation (01.08.1992)
Published in The Journal of clinical investigation (01.08.1992)
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Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease
López-Gutiérrez, A U, Riba, L, Ordoñez-Sánchez, M L, Ramírez-Jiménez, S, Cerrillo-Hinojosa, M, Tusié-Luna, M T
Published in Journal of medical genetics (01.12.1998)
Published in Journal of medical genetics (01.12.1998)
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Association of PPARG2 Pro12Ala Variant with Larger Body Mass Index in Mestizo and Amerindian Populations of Mexico
Canizales-Quinteros, S., Aguilar-Salinas, C. A., Ortiz-López, M. G., Rodríguez-Cruz, M., Villarreal-Molina, M. T., Coral-Vázquez, R., Huertas-Vázquez, A., Hernández-Caballero, A., López-Alarcón, M., Brito-Zurita, O. R., Domínguez-Banda, A., Martinez-Sánchez, L. R., Canto-De Cetina, T., Vilchis-Dorantes, G., Rosas-Vargas, H., Granados-Silvestre, M. A., Medeiros-Domingo, A., Menjivar, M., Tusié-Luna, M. T.
Published in Human biology (01.02.2007)
Published in Human biology (01.02.2007)
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Contribution of Chromosome 1q21‐q23 to Familial Combined Hyperlipidemia in Mexican Families
Huertas‐Vázquez, A., del Rincón, J. P., Canizales‐Quinteros, S., Riba, L., Vega‐Hernández, G., Ramírez‐Jiménez, S., Aurón‐Gómez, M., Gómez–Pérez, F. J., Aguilar‐Salinas, C. A., Tusié‐Luna, M. T.
Published in Annals of human genetics (01.09.2004)
Published in Annals of human genetics (01.09.2004)
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Journal Article
Low frequency of deletion alleles in patients with steroid 21-hydroxylase deficiency in a Mexican population
Tusié-Luna, M T, Ramírez-Jiménez, S, Ordóñez-Sánchez, M L, Cabello-Villegas, J, Altamirano-Bustamante, N, Calzada-León, R, Robles-Valdés, C, Mendoza-Morfín, F, Méndez, J P, Terán-García, M
Published in Human genetics (01.09.1996)
Published in Human genetics (01.09.1996)
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Journal Article
The -514C>T polymorphism in the LIPC gene modifies type 2 diabetes risk through modulation of HDL-cholesterol levels in Mexicans
Guerra-García, M. T., Moreno-Macías, H., Ochoa-Guzmán, A., Ordoñez-Sánchez, M. L., Rodríguez-Guillen, R., Vázquez-Cárdenas, P., Ortíz-Ortega, V. M., Peimbert-Torres, M., Aguilar-Salinas, C. A., Tusié-Luna, M. T.
Published in Journal of endocrinological investigation (01.03.2021)
Published in Journal of endocrinological investigation (01.03.2021)
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Journal Article
Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population
del Bosque-Plata, Laura, Aguilar-Salinas, Carlos A, Tusié-Luna, Marı́a Teresa, Ramı́rez-Jiménez, Salvador, Rodrı́guez-Torres, Maribel, Aurón-Gómez, Moisés, Ramı́rez, Erika, Velasco-Pérez, Marı́a Luisa, Ramı́rez-Silva, Alfredo, Gómez-Pérez, Francisco, Hanis, Craig L, Tsuchiya, Takafumi, Yoshiuchi, Issei, Cox, Nancy J, Bell, Graeme I
Published in Molecular genetics and metabolism (01.02.2004)
Published in Molecular genetics and metabolism (01.02.2004)
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Early-onset type 2 diabetes : Metabolic and genetic characterization in the Mexican population
AGUILAR-SALINAS, Carlos A, REYES-RODRIGUEZ, Eduardo, GOMEZ-PEREZ, Francisco, RULL, Juan, TUSIE-LUNA, Ma. Teresa, ORDONEZ-SANCHEZ, Ma. Luisa, ARELLANO TORRES, Marcelo, RAMIREZ-JIMENEZ, Salvador, DOMINGUEZ-LOPEZ, Aaron, MARTINEZ-FRANCOIS, Juan Ramon, VELASCO-PEREZ, Ma. Luisa, ALPIZAR, Melchor, GARCIA-GARCIA, Eduardo
Published in The journal of clinical endocrinology and metabolism (2001)
Published in The journal of clinical endocrinology and metabolism (2001)
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Mutation Analysis in Patients with Congenital Adrenal Hyperplasia in the Spanish Population: Identification of Putative Novel Steroid 21-Hydroxylase Deficiency Alleles Associated with the Classic Form of the Disease
Lobato, M. Natividad, Ordóñez-Sánchez, M. Luisa, Tusié-Luna, M. Teresa, Meseguer, Anna
Published in Human heredity (01.01.1999)
Published in Human heredity (01.01.1999)
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