Published in Gac Med Mex on May 16, 2005
Reconstructing Native American population history. Nature (2012) 3.49
Slower fibrosis progression in HIV/HCV-coinfected patients with successful HIV suppression using antiretroviral therapy. J Hepatol (2005) 2.27
A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia. PLoS Genet (2009) 2.24
Chronic hepatitis C in patients with persistently normal alanine transaminase levels. Clin Gastroenterol Hepatol (2006) 1.77
The FTO gene is associated with adulthood obesity in the Mexican population. Obesity (Silver Spring) (2008) 1.62
A functional ABCA1 gene variant is associated with low HDL-cholesterol levels and shows evidence of positive selection in Native Americans. Hum Mol Genet (2010) 1.60
Familial combined hyperlipidemia in Mexicans: association with upstream transcription factor 1 and linkage on chromosome 16q24.1. Arterioscler Thromb Vasc Biol (2005) 1.46
Significance of CASP8AP2 and H2AFZ expression in survival and risk of relapse in children with acute lymphoblastic leukemia. Leuk Lymphoma (2014) 1.43
Diabetes in Mexico: cost and management of diabetes and its complications and challenges for health policy. Global Health (2013) 1.42
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. Diabetes (2007) 1.29
Contribution of common genetic variation to the risk of type 2 diabetes in the Mexican Mestizo population. Diabetes (2012) 1.24
Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican families. Neurogenetics (2006) 1.24
Association of the ATP-binding cassette transporter A1 R230C variant with early-onset type 2 diabetes in a Mexican population. Diabetes (2007) 1.16
Common hepatic nuclear factor-4alpha variants are associated with high serum lipid levels and the metabolic syndrome. Diabetes (2006) 1.15
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) 1.08
Tumor necrosis factor-alpha is a common genetic risk factor for asthma, juvenile rheumatoid arthritis, and systemic lupus erythematosus in a Mexican pediatric population. Hum Immunol (2009) 1.03
The epidemiologic burden of hepatitis C virus infection in Latin America . Ann Hepatol (2012) 1.00
Genetic heterogeneity of autosomal dominant hypercholesterolemia in Mexico. Arch Med Res (2006) 0.99
Contribution of common genetic variants to obesity and obesity-related traits in mexican children and adults. PLoS One (2013) 0.96
Systemic lupus erythematosus risk factors for coronary artery calcifications. Rheumatology (Oxford) (2011) 0.96
Potential additional effect of omentectomy on metabolic syndrome, acute-phase reactants, and inflammatory mediators in grade III obese patients undergoing laparoscopic Roux-en-Y gastric bypass: a randomized trial. Diabetes Care (2010) 0.94
Efficacy of glimepiride/metformin combination versus glibenclamide/metformin in patients with uncontrolled type 2 diabetes mellitus. J Diabetes Complications (2008) 0.92
Balapiravir plus peginterferon alfa-2a (40KD)/ribavirin in a randomized trial of hepatitis C genotype 1 patients. Ann Hepatol (2011) 0.90
PCSK1 rs6232 is associated with childhood and adult class III obesity in the Mexican population. PLoS One (2012) 0.89
Locus on chromosome 6p linked to elevated HDL cholesterol serum levels and to protection against premature atherosclerosis in a kindred with familial hypercholesterolemia. Circ Res (2003) 0.88
Galanin preproprotein is associated with elevated plasma triglycerides. Arterioscler Thromb Vasc Biol (2008) 0.88
Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population. Mol Genet Metab (2004) 0.85
Irisin levels before and after physical activity among school-age children with different BMI: a direct relation with leptin. Obesity (Silver Spring) (2015) 0.85
Mutations in MODY genes are not common cause of early-onset type 2 diabetes in Mexican families. JOP (2005) 0.85
Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma. J Neurosurg (2006) 0.83
GENEHUNTER versus SimWalk2 in the context of an extended kindred and a qualitative trait locus. Genetica (2005) 0.82
Transcript levels of Toll-Like Receptors 5, 8 and 9 correlate with inflammatory activity in Ulcerative Colitis. BMC Gastroenterol (2011) 0.82
Estimating ethnic admixture from pedigree data. Am J Hum Genet (2008) 0.82
Identification of influenza A pandemic (H1N1) 2009 variants during the first 2009 influenza outbreak in Mexico City. J Clin Virol (2010) 0.81
Association of the I148M/PNPLA3 variant with elevated alanine transaminase levels in normal-weight and overweight/obese Mexican children. Gene (2013) 0.81
Pharmacokinetics of fosamprenavir plus ritonavir in human immunodeficiency virus type 1-infected adult subjects with hepatic impairment. Antimicrob Agents Chemother (2009) 0.81
Changes in peripheral blood mononuclear cells glutamine synthetase mRNA after exercise in healthy volunteers: exploring an alternative proposal for non hepatic ammonia metabolism. Rev Invest Clin (2012) 0.80
[Early-onset type 2 diabetes mellitus. The experience from a third level medical institution]. Gac Med Mex (2010) 0.80
Founder effect and ancestral origin of the spinocerebellar ataxia type 7 (SCA7) mutation in Mexican families. Neurogenetics (2013) 0.80
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 nation wide study. Atherosclerosis (2011) 0.79
Expression of NLRP3 inflammasome, cytokines and vascular mediators in the skin of systemic sclerosis patients. Isr Med Assoc J (2015) 0.79
Association of R230C ABCA1 gene variant with low HDL-C levels and abnormal HDL subclass distribution in Mexican school-aged children. Clin Chim Acta (2010) 0.79
A novel ARH splice site mutation in a Mexican kindred with autosomal recessive hypercholesterolemia. Hum Genet (2004) 0.79
PNPLA3 I148M polymorphism is associated with elevated alanine transaminase levels in Mexican Indigenous and Mestizo populations. Mol Biol Rep (2014) 0.78
VNN1 gene expression levels and the G-137T polymorphism are associated with HDL-C levels in Mexican prepubertal children. PLoS One (2012) 0.78
Familial hypobetalipoproteinemia in a hospital survey: genetics, metabolism and non-alcoholic fatty liver disease. Ann Hepatol (2011) 0.77
[Fifty years studying hiperlipidemias: the case of familial combined hyperlipidemia]. Invest Clin (2010) 0.77
Normal HDL-apo AI turnover and cholesterol enrichment of HDL subclasses in New Zealand rabbits with partial nephrectomy. Metabolism (2012) 0.77
[Succesful collaborations between three Mexican institutions for research on dislipidemias, obesity and diabetes]. Gac Med Mex (2008) 0.76
Interleukin-18 upregulation is associated with the use of steroids in patients with ulcerative colitis. Inflamm Bowel Dis (2011) 0.76
[Familial homozygous hypercholesterolemia due to the c2271delT mutation in the LDL receptor gene, detected exclusively in Mexicans]. Gac Med Mex (2011) 0.75
[Obesity and metabolic syndrome. A challenge for the Mexican Institutes of Health]. Rev Invest Clin (2009) 0.75
TNFRSF11B gene haplotype and its association with bone mineral density variations in postmenopausal Mexican-Mestizo women. Maturitas (2011) 0.75
Steroid 21-hydroxylase (P450c21) naturally occurring mutants I172N, V281L and I236n/V237E/M239K exert a dominant negative effect on enzymatic activity when co-expressed with the wild-type protein. J Pediatr Endocrinol Metab (2003) 0.75
[Obesity and the metabolic syndrome as a public health problem: a reflection]. Salud Publica Mex (2008) 0.75
Prevalence of abnormal eating behaviors in adolescents in Mexico: Mexican National Health and Nutrition Survey 2006. Salud Publica Mex (2009) 0.75