León Mimila P, Villamil Ramírez H, López Contreras B, Moran Ramos S, Macías Kauffer L, Acuña Alonzo V, et al
. Low Salivary Amylase Gene (AMY1) Copy Number Is Associated with Obesity and Gut Prevotella Abundance in Mexican Children and Adults. Nutrients. 2018;10: pubmed publisher
..To our knowledge, this is the first study to analyze the association of these five CNVs in the Mexican population and to report a correlation between AMY1 CN and gut microbiota in humans. ..
Macías Kauffer L, Villamil Ramírez H, León Mimila P, Jacobo Albavera L, Posadas Romero C, Posadas Sánchez R, et al
. Genetic contributors to serum uric acid levels in Mexicans and their effect on premature coronary artery disease. Int J Cardiol. 2018;: pubmed publisher
..However, a Mendelian randomization approach using the lead SUA-associated SNPs (SLC2A9 and ABCG2) did not support a causal role of elevated SUA levels for premature CAD. ..
Posadas SÃ¡nchez R, Posadas Romero C, Cardoso SaldaÃ±a G, Vargas AlarcÃ³n G, Villarreal Molina M, PÃ©rez HernÃ¡ndez N, et al
. Serum magnesium is inversely associated with coronary artery calcification in the Genetics of Atherosclerotic Disease (GEA) study. Nutr J. 2016;15:22 pubmed publisher
Villarreal Molina T, Posadas Romero C, Romero Hidalgo S, Antúnez Argüelles E, Bautista Grande A, Vargas Alarcon G, et al
. The ABCA1 gene R230C variant is associated with decreased risk of premature coronary artery disease: the genetics of atherosclerotic disease (GEA) study. PLoS ONE. 2012;7:e49285 pubmed publisher
..Although it has been associated with other cardiovascular risk factors such as obesity and type 2 diabetes mellitus, it is not known whether it is associated with coronary artery disease (CAD)...
Antúnez Argüelles E, Rojo Dominguez A, Arregui Mena A, Jacobo Albavera L, Márquez M, Iturralde Torres P, et al
. Compound heterozygous KCNQ1 mutations (A300T/P535T) in a child with sudden unexplained death: Insights into possible molecular mechanisms based on protein modeling. Gene. 2017;627:40-48 pubmed publisher
..Altogether, the evidence strongly suggests that this child was affected with a recessive form of Romano Ward syndrome. ..