María Luisa Ordóñez-Sánchez

Association of a Low-Frequency Variant in<i>HNF1A</i>With Type 2 Diabetes in a Latino Population

Karol Estrada, Ingvild Aukrust, Lise Bjørkhaug et al. · JAMA · 2014 · 264 citations · Full text

Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms

Victor Rusu, Eitan Hoch, Josep M. Mercader et al. · Cell · 2017 · 155 citations · Full text

Metabolic Syndrome, Distinct Mechanisms, Signal Transduction +8

Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci

Daphna Weissglas‐Volkov, Carlos A. Aguilar‐Salinas, Elina Nikkola et al. · Journal of Medical Genetics · 2013 · 120 citations · Full text

Contribution of Common Genetic Variation to the Risk of Type 2 Diabetes in the Mexican Mestizo Population

Marco Alberto Gamboa-Meléndez, Alicia Huerta‐Chagoya, Hortensia Moreno-Macías et al. · Diabetes · 2012 · 109 citations · Full text

Mexican Population, Genetics, Genetic Epidemiology +19

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

María Luisa Ordóñez-Sánchez, Salvador Ramı́rez-Jiménez, Antonio Ulises López-Gutierrez et al. · Human Genetics · 1998 · 64 citations

Mexican Population, Mendelian Disorder, Genetic Disorder +10