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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Prediction of incident hypertension and arterial stiffness using the non–insulin‐based metabolic score for insulin resistance (METS‐IR) index
Bello‐Chavolla, Omar Yaxmehen, Antonio‐Villa, Neftali E., Vargas‐Vázquez, Arsenio, Martagón, Alexandro J., Mehta, Roopa, Arellano‐Campos, Olimpia, Gómez‐Velasco, Donaji V., Almeda‐Valdés, Paloma, Cruz‐Bautista, Ivette, Melgarejo‐Hernandez, Marco A., Muñoz‐Hernandez, Liliana, Guillén, Luz E., Garduño‐García, José de Jesús, Alvirde, Ulices, Ono‐Yoshikawa, Yukiko, Choza‐Romero, Ricardo, Sauque‐Reyna, Leobardo, Garay‐Sevilla, Ma. Eugenia, Malacara‐Hernandez, Juan M., Tusié‐Luna, María T., Gutierrez‐Robledo, Luis M., Gómez‐Pérez, Francisco J., Rojas, Rosalba, Aguilar‐Salinas, Carlos A.
Published in The journal of clinical hypertension (Greenwich, Conn.) (01.08.2019)
Published in The journal of clinical hypertension (Greenwich, Conn.) (01.08.2019)
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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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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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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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TCF7L2 is associated with high serum triacylglycerol and differentially expressed in adipose tissue in families with familial combined hyperlipidaemia
Huertas-Vazquez, A, Plaisier, C, Weissglas-Volkov, D, Sinsheimer, J, Canizales-Quinteros, S, Cruz-Bautista, I, Nikkola, E, Herrera-Hernandez, M, Davila-Cervantes, A, Tusie-Luna, T, Taskinen, M.-R, Aguilar-Salinas, C, Pajukanta, P
Published in Diabetologia (01.01.2008)
Published in Diabetologia (01.01.2008)
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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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Journal Article
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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Genetic contributions to lupus nephritis in a multi-ethnic cohort of systemic lupus erythematous patients
Lanata, Cristina M, Nititham, Joanne, Taylor, Kimberly E, Chung, Sharon A, Torgerson, Dara G, Seldin, Michael F, Pons-Estel, Bernardo A, Tusié-Luna, Teresa, Tsao, Betty P, Morand, Eric F, Alarcón-Riquelme, Marta E, Criswell, Lindsey A
Published in PloS one (28.06.2018)
Published in PloS one (28.06.2018)
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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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Abstract P2-02-04: Li-Fraumeni syndrome in females with early onset breast cancer in a Mexican population
Gallardo-Alvarado, LN, Cantu-De Leon, DF, Tusie-Luna, T, Tusie-Luna, I, Diaz-Chavez, J, Herrera, EM, Chavez-MacGregor, M, Bargallo-Rocha, E, Villarreal, C, Herrera.Montalvo, LA, Segura-Kato, YX
Published in Cancer research (Chicago, Ill.) (15.02.2017)
Published in Cancer research (Chicago, Ill.) (15.02.2017)
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