| Analysis of protein-coding genetic variation in 60,706 humans M Lek, KJ Karczewski, EV Minikel, KE Samocha, E Banks, T Fennell, ... Nature 536 (7616), 285-291, 2016 | 10415 | 2016 |
| Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency. PW Speiser, J Dupont, D Zhu, J Serrat, M Buegeleisen, MT Tusie-Luna, ... The Journal of clinical investigation 90 (2), 584-595, 1992 | 690 | 1992 |
| SCN4B-encoded sodium channel β4 subunit in congenital long-QT syndrome A Medeiros-Domingo, T Kaku, DJ Tester, P Iturralde-Torres, A Itty, B Ye, ... Circulation 116 (2), 134, 2007 | 466 | 2007 |
| The product of the CYP11B2 gene is required for aldosterone biosynthesis in the human adrenal cortex KM Curnow, MT Tusie-Luna, L Pascoe, R Natarajan, JL Gu, JL Nadler, ... Molecular Endocrinology 5 (10), 1513-1522, 1991 | 455 | 1991 |
| High adiponectin concentrations are associated with the metabolically healthy obese phenotype CA Aguilar-Salinas, EG García, L Robles, D Riano, DG Ruiz-Gomez, ... The Journal of Clinical Endocrinology & Metabolism 93 (10), 4075-4079, 2008 | 399 | 2008 |
| La obesidad y el síndrome metabólico como problema de salud pública: Una reflexión E García-García, D la Llata-Romero, M Kaufer-Horwitz, MT Tusié-Luna, ... Salud pública de México 50, 530-547, 2008 | 358 | 2008 |
| La obesidad y el síndrome metabólico como problema de salud pública: Una reflexión E García-García, D la Llata-Romero, M Kaufer-Horwitz, MT Tusié-Luna, ... Salud pública de México 50, 530-547, 2008 | 358 | 2008 |
| Determination of functional effects of mutations in the steroid 21-hydroxylase gene (CYP21) using recombinant vaccinia virus. MT Tusie-Luna, P Traktman, PC White Journal of Biological Chemistry 265 (34), 20916-20922, 1990 | 304 | 1990 |
| Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms MT Tusie-Luna, PC White Proceedings of the National Academy of Sciences 92 (23), 10796-10800, 1995 | 219 | 1995 |
| A Mutation (Pro-30 to Leu) in CYP21 Represents a Potential Nonclassic Steroid 21-Hydroxylase Deficiency Allele MT Tusie-Luna, PW Speiser, M Dumic, MI New, PC White Molecular endocrinology 5 (5), 685-692, 1991 | 217 | 1991 |
| Expression of 11β-hydroxysteroid dehydrogenase using recombinant vaccinia virus AK Agarwal, MT Tusie-Luna, C Monder, PC White Molecular Endocrinology 4 (12), 1827-1832, 1990 | 193 | 1990 |
| The FTO Gene Is Associated With Adulthood Obesity in the Mexican Population M Villalobos‐Comparán, MT Flores‐Dorantes, MT Villarreal‐Molina, ... Obesity 16 (10), 2296-2301, 2008 | 187 | 2008 |
| Mutations in steroid 21‐hydroxylase (CYP21) PC White, MT Tusie‐Luna, MI New, PW Speiser Human mutation 3 (4), 373-378, 1994 | 155 | 1994 |
| R339H and P453S: CYP21 mutations associated with nonclassic steroid 21-hydroxylase deficiency that are not apparent gene conversions. A Helmberg, MT Tusie-Luna, M Tabarelli, R Kofler, PC White Molecular endocrinology 6 (8), 1318-1322, 1992 | 154 | 1992 |
| Association of the ATP-binding cassette transporter A1 R230C variant with early-onset type 2 diabetes in a Mexican population MT Villarreal-Molina, MT Flores-Dorantes, O Arellano-Campos, ... Diabetes 57 (2), 509-513, 2008 | 132 | 2008 |
| Contribution of common genetic variation to the risk of type 2 diabetes in the Mexican Mestizo population MA Gamboa-Meléndez, A Huerta-Chagoya, H Moreno-Macías, ... Diabetes 61 (12), 3314-3321, 2012 | 129 | 2012 |
| The ATP-binding cassette transporter A1 R230C variant affects HDL cholesterol levels and BMI in the Mexican population: association with obesity and obesity-related comorbidities MT Villarreal-Molina, CA Aguilar-Salinas, M Rodríguez-Cruz, D Riaño, ... Diabetes 56 (7), 1881-1887, 2007 | 122 | 2007 |
| Strong association of socioeconomic status and genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes JC Florez, AL Price, D Campbell, L Riba, MV Parra, F Yu, C Duque, ... Racial Identities, Genetic Ancestry, and Health in South America, 137-153, 2011 | 121 | 2011 |
| Early-onset type 2 diabetes: metabolic and genetic characterization in the Mexican population CA Aguilar-Salinas, E Reyes-RodrÍguez, ML Ordóñez-Sánchez, ... The Journal of Clinical Endocrinology & Metabolism 86 (1), 220-226, 2001 | 101 | 2001 |
| Molecular genetic analysis of patients carrying steroid 21-hydroxylase deficiency in the Mexican population: identification of possible new mutations and high prevalence of … ML Ordoñez-Sánchez, S Ramírez-Jiménez, AU López-Gutierrez, L Riba, ... Human genetics 102 (2), 170-177, 1998 | 93 | 1998 |
Carlos A. Aguilar SalinasHead of Research. Instituto Nacional de Ciencias Medicas y Nutricion, Mexico在 incmnsz.mx 的电子邮件经过验证
