Identification of TBX15 as an adipose master trans regulator of abdominal obesity genes von Pan, David Z., Miao, Zong, Comenho, Caroline, Rajkumar, Sandhya, Koka, Amogha, Lee, Seung Hyuk T., Alvarez, Marcus, Kaminska, Dorota, Ko, Arthur, Sinsheimer, Janet S., Mohlke, Karen L., Mancuso, Nicholas, Munoz-Hernandez, Linda Liliana, Herrera-Hernandez, Miguel, Tusie-Luna, Maria Teresa, Aguilar-Salinas, Carlos, Pietilainen, Kirsi H., Pihlajamaki, Jussi, Laakso, Markku, Garske, Kristina M., Pajukanta, Paivi

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LCAT deficiency: a systematic review with the clinical and genetic description of Mexican kindred von Mehta, Roopa, Elias-Lopez, Daniel, Martagon, Alexandro J., Perez-Mendez, Oscar A., Ordonez Sanchez, Maria Luisa, Segura, Yayoi, Teresa Tusie, Maria, Aguilar-Salinas, Carlos A.

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The panorama of familial hypercholesterolemia in Latin America: a systematic review[S] von Mehta, Roopa, Zubirán, Rafael, Martagón, Alexandro J., Vazquez-Cárdenas, Alejandra, Segura-Kato, Yayoi, Tusié-Luna, María Teresa, Aguilar-Salinas, Carlos A.

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Prevalence of germline mutations in the TP53 gene in patients with early-onset breast cancer in the Mexican population von Gallardo-Alvarado, Lenny N, Tusié-Luna, María Teresa, Tussié-Luna, María Isabel, Díaz-Chávez, José, Segura, Yayoi X, Bargallo-Rocha, Enrique, Villarreal, Cynthia, Herrera-Montalvo, Luis A, Herrera-Medina, Enrique M, Cantu-de Leon, David F

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Contribution of Common Genetic Variation to the Risk of Type 2 Diabetes in the Mexican Mestizo Population von GAMBOA-MELENDEZ, Marco Alberto, HUERTA-CHAGOYA, Alicia, CHOUDHRY, Shweta, DEL BOSQUE-PLATA, Laura, CANIZALES-QUINTEROS, Samuel, PEREZ-ORTIZ, Gustavo, ESCOBEDO-AGUIRRE, Fernando, PARRA, Adalberto, LERMAN-GARBER, Israel, AGUILAR-SALINAS, Carlos Alberto, TUSIE-LUNA, Maria Teresa, MORENO-MACIAS, Hortensia, VAZQUEZ-CARDENAS, Paola, ORDONEZ-SANCHEZ, Maria Luisa, RODRIGUEZ-GUILLEN, Rosario, RIBA, Laura, RODRIGUEZ-TORRES, Maribel, GUERRA-GARCIA, Maria Teresa, ELIZABETH GUILLEN-PINEDA, Luz

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Development and validation of a predictive model for incident type 2 diabetes in middle-aged Mexican adults: the metabolic syndrome cohort von Arellano-Campos, Olimpia, Gómez-Velasco, Donaji V, Bello-Chavolla, Omar Yaxmehen, Cruz-Bautista, Ivette, Melgarejo-Hernandez, Marco A, Muñoz-Hernandez, Liliana, Guillén, Luz E, Garduño-Garcia, Jose de Jesus, Alvirde, Ulices, Ono-Yoshikawa, Yukiko, Choza-Romero, Ricardo, Sauque-Reyna, Leobardo, Garay-Sevilla, Maria Eugenia, Malacara-Hernandez, Juan Manuel, Tusie-Luna, Maria Teresa, Gutierrez-Robledo, Luis Miguel, Gómez-Pérez, Francisco J, Rojas, Rosalba, Aguilar-Salinas, Carlos A

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The non-synonymous Arg230Cys variant (R230C) of the ATP-binding cassette transporter A1 is associated with low HDL cholesterol concentrations in Mexican adults: A population based... von Aguilar-Salinas, Carlos A, Canizales-Quinteros, Samuel, Rojas-Martínez, Rosalba, Mehta, Roopa, Rodriguez-Guillén, Rosario, Ordoñez-Sanchez, María Luisa, Riba, Laura, Tusié-Luna, María Teresa

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Use of PCSK9 Inhibitor in a Mexican Boy with Compound Heterozygous Familial Hypercholesterolemia: A Case Report von Ceballos-Macías, José Juan, Madriz-Prado, Ramón, Vázquez Cárdenas, Norma Alejandra, Aguilar-Salinas, Carlos, Tusié-Luna, Maria Teresa, Flores-Real, Jorge Alberto, Ortega-Gutiérrez, Guillermo, Vargas-Sánchez, Joel, Lara-Sánchez, Carolina, Hernández-Moreno, Alfredo

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Critical role of acute hypoxemia on the cognitive impairment after severe COVID-19 pneumonia: a multivariate causality model analysis von García-Grimshaw, Miguel, Chirino-Pérez, Amanda, Flores-Silva, Fernando Daniel, Valdés-Ferrer, Sergio Iván, Vargas-Martínez, María de los Ángeles, Jiménez-Ávila, Ana Itiel, Chávez-Martínez, Oswaldo Alan, Ramos-Galicia, Enrique Manuel, Marché-Fernández, Osvaldo Alexis, Ramírez-Carrillo, Martha Fernanda, Grajeda-González, Samara Lissete, Ramírez-Jiménez, Marco Eduardo, Chávez-Manzanera, Emma Adriana, Tusié-Luna, María Teresa, Ochoa-Guzmán, Ana, Cantú-Brito, Carlos, Fernandez-Ruiz, Juan, Chiquete, Erwin

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DYSLIPIDEMIA IN MEXICO, A CALL FOR ACTION von Rivas-Gomez, Bernardette, Almeda-Valdés, Paloma, Tussié-Luna, María Teresa, Aguilar-Salinas, Carlos A

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Mutations in Steroid 21-Hydroxylase (CYP21) von White, Perrin C., Tusie-Luna, Maria-Teresa, New, Maria I., Speiser, Phyllis W.

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Searching for the Causal Variants of the Association Between Hypertriglyceridemia and the Genome-Wide Association Studies-Derived Signals? Take a Look in the Native American Popula... von Aguilar-Salinas, Carlos A, Sevilla González, Magdalena Del Rocío, Tusie-Luna, María Teresa

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La obesidad y el síndrome metabólico como problema de salud pública: una reflexión von García-García, Eduardo, De la Llata-Romero, Manuel, Kaufer-Horwitz, Martha, Tusié-Luna, María Teresa, Calzada-León, Raúl, Vázquez-Velázquez, Verónica, Barquera-Cervera, Simón, Caballero-Romo, Alejandro de Jesús, Orozco, Lorena, Velásquez-Fernández, David, Rosas-Peralta, Martín, Barriguete-Meléndez, Armando, Zacarías-Castillo, Rogelio, Sotelo-Morales, Julio

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Gene Conversions and Unequal Crossovers Between CYP21 (Steroid 21- Hydroxylase Gene) and CYP21P Involve Different Mechanisms von Tusie-Luna, Maria-Teresa, White, Perrin C.

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Mutations in MODY genes are not common cause of early-onset type 2 diabetes in Mexican families von Domínguez-López, Aarón, Miliar-García, Angel, Segura-Kato, Yayoi X, Riba, Laura, Esparza-López, Riba, Ramírez-Jiménez, Salvador, Rodríguez-Torres, Maribel, Canizales-Quinteros, Samuel, Cabrera-Vásquez, Siraam, Fragoso-Ontiveros, Verónica, Aguilar-Salinas, Carlos A, Altamirano-Bustamante, Nelly, Calzada-León, Raúl, Robles-Valdés, Carlos, Bravo-Ríos, Luz E, Tusié-Luna, Maria Teresa

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Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma von RASMUSSEN, Astrid, NAVA-SALAZAR, Sonia, YESCAS, Petra, ALONSO, Elisa, REVUELTA, Rogelio, ORTIZ, Ivan, CANIZALES-QUINTEROS, Samuel, TUSIE-LUNA, Maria Teresa, LOPEZ-LOPEZ, Marisol

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Increased visceral fat accumulation modifies the effect of insulin resistance on arterial stiffness and hypertension risk von Antonio-Villa, Neftali Eduardo, Bello-Chavolla, Omar Yaxmehen, Vargas-Vázquez, Arsenio, Mehta, Roopa, Fermín-Martínez, Carlos A., Martagón-Rosado, Alexandro J., Barquera-Guevara, Daphne Abigail, Aguilar-Salinas, Carlos A., Arellano-Campos, Olimpia, Gómez-Velasco, Donaji V., Bello-Chavolla, Omar Yaxmehen, Viveros-Ruiz, Tania, Martagón-Rosado, Alexandro J., Cruz-Bautista, Ivette, Melgarejo-Hernandez, Marco A., Almeda-Valdés, Paloma, Muñoz-Hernandez, Liliana, Elias-Lopez, Daniel, Del Razo-Olvera, Fabiola Mabel, Encinas, Bethsabel Rodríguez, Fagoaga Ramírez, Renán Fernando, Guillén, Luz E., de Jesús Garduño-García, José, Alvirde, Ulices, Ono-Yoshikawa, Yukiko, Choza-Romero, Ricardo, Sauque-Reyna, Leobardo, Garay-Sevilla, Ma. Eugenia, Malacara-Hernandez, Juan M., Tusié-Luna, María Teresa, Gutierrez-Robledo, Luis Miguel, Gómez-Pérez, Francisco J., Rojas, Rosalba, Aguilar-Salinas, Carlos A.

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With the finished human genome in hand, what next? von Collado-Vides, Julio, Medrano-Soto, Arturo, Tusié-Luna, Maria Teresa

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GENEHUNTER versus SimWalk2 in the context of an extended kindred and a qualitative trait locus von Romero-Hidalgo, Sandra, Rodrigues, Eliane R, Gutiérrez-Peña, Eduardo, Riba, Laura, Tusié-Luna, María Teresa

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Additional file 1 of LCAT deficiency: a systematic review with the clinical and genetic description of Mexican kindred von Mehta, Roopa, Elías-López, Daniel, Martagón, Alexandro J., Pérez-Méndez, Oscar A, Sánchez, Maria Luisa Ordóñez, Segura, Yayoi, Tusié, Maria Teresa, Aguilar-Salinas, Carlos A.

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