M. Ordóñez-Sánchez

发表

A panel of 32 AIMs suitable for population stratification correction and global ancestry estimation in Mexican mestizos

A. Hidalgo-Miranda, Andrés Moreno-Estrada, J. Fernández-López, 2019, BMC Genetics.

Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population.

Amy L. Williams, T. Fennell, S. Gabriel, 2014, JAMA.

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

Päivi Pajukanta, Marja-Riitta Taskinen, Rita M Cantor, 2013, Journal of Medical Genetics.

Investigation of Variants Identified in Caucasian Genome-Wide Association Studies for Plasma High-Density Lipoprotein Cholesterol and Triglycerides Levels in Mexican Dyslipidemic Study Samples

R. Cantor, J. Sinsheimer, C. Aguilar-Salinas, 2010, Circulation. Cardiovascular genetics.

Early-onset type 2 diabetes: metabolic and genetic characterization in the mexican population.

C. Aguilar-Salinas, M. Tusié-Luna, M. Ordóñez-Sánchez, 2001, The Journal of clinical endocrinology and metabolism.

Familial hypertriglyceridemia: an entity with distinguishable features from other causes of hypertriglyceridemia

Omar Yaxmehen Bello-Chavolla, C. Aguilar-Salinas, M. Tusié-Luna, 2020, Lipids in Health and Disease.

Molecular characterization of the lipid GWAS signal on chromosome 18q11.2 implicates HNF4A-mediated regulation of the TMEM241 gene

Yash, M. Laakso, C. Aguilar-Salinas, 2016 .

LCAT Deficiency in Amerindian Populations: A Systematic Review With the Clinical and Genetic Description of Mexican Kindred

C. Aguilar-Salinas, D. Elías-López, R. Mehta, 2020 .

A cis-acting element in the promoter of human ether à go-go 1 potassium channel gene mediates repression by calcitriol in human cervical cancer cells.

M. Makishima, F. Larrea, M. Ordóñez-Sánchez, 2015, Biochemistry and cell biology = Biochimie et biologie cellulaire.

Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico

Tanya M. Teslovich, Amy L. Williams, Ian C. Smith, 2013, Nature.

Contribution of Known Genetic Risk Variants to Dyslipidemias and Type 2 Diabetes in Mexico: A Population-Based Nationwide Study

C. Aguilar-Salinas, H. Moreno-Macías, T. Tusié-Luna, 2020, Genes.

Mexican Carriers of the HNF1A p.E508K Variant Do Not Experience an Enhanced Response to Sulfonylureas

J. Florez, Omar Yaxmehen Bello-Chavolla, C. Aguilar-Salinas, 2018, Diabetes Care.

Mutation Analysis in Patients with Congenital Adrenal Hyperplasia in the Spanish Population: Identification of Putative Novel Steroid 21-Hydroxylase Deficiency Alleles Associated with the Classic Form of the Disease

M. Tusié-Luna, A. Meseguer, M. Lobato, 1999, Human Heredity.

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

M. Tusié-Luna, L. Riba, R. Calzada-León, 1998, Human Genetics.

The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humans.

J. Sinsheimer, C. Aguilar-Salinas, P. Pajukanta, 2011, The Journal of clinical investigation.

The -514C>T polymorphism in the LIPC gene modifies type 2 diabetes risk through modulation of HDL-cholesterol levels in Mexicans

C. Aguilar-Salinas, M. Tusié-Luna, H. Moreno-Macías, 2020, Journal of Endocrinological Investigation.

A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes

Rachel G Liao, J. Lane, C. Hartl, 2017, Diabetes.

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

S. Choudhry, C. Aguilar-Salinas, M. Tusié-Luna, 2012, Diabetes.

Primary amenorrhea in two sisters: description of a Mexican family with 17α hydroxylase-17 lyase deficiency caused by arginine – stop mutation

C. Aguilar-Salinas, M. Tusié-Luna, M. Ordóñez-Sánchez, 2012, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Contribution of genetic, biochemical and environmental factors on insulin resistance and obesity in Mexican young adults.

M. Ordóñez-Sánchez, T. García-Gasca, K. L. Flores-Viveros, 2019, Obesity research & clinical practice.

Low frequency of deletion alleles in patients with steroid 21-hydroxylase deficiency in a Mexican population

M. Tusié-Luna, J. Cabello-Villegas, R. Calzada-León, 1996, Human Genetics.

Apolipoprotein E ɛ4, Alzheimer's Disease, and Cognitive Performance in Elderly Mexican Mestizos

C. Aguilar-Salinas, M. Ordóñez-Sánchez, S. Mejia-Arango, 2008, Journal of the American Geriatrics Society.

Familial hypobetalipoproteinemia in a hospital survey: genetics, metabolism and non-alcoholic fatty liver disease.

C. Aguilar-Salinas, M. Tusié-Luna, G. Schonfeld, 2011, Annals of hepatology.

Genome-wide association study of colorectal cancer in Hispanics

C. Haiman, D. Conti, L. Le Marchand, 2016, Carcinogenesis.

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

Nicholette D. Palmer, Yan V. Sun, M. Fornage, 2017, Cell.

A panel of 32 AIMs suitable for population stratification correction and global ancestry estimation in Mexican mestizos

A. Hidalgo-Miranda, J. Fernández-López, C. Aguilar-Salinas, 2019, BMC Genetics.

A novel ARH splice site mutation in a Mexican kindred with autosomal recessive hypercholesterolemia

C. Aguilar-Salinas, M. Tusié-Luna, S. Canizales-Quinteros, 2004, Human Genetics.

R230C but not − 565C/T variant of the ABCA1 gene is associated with type 2 diabetes in Mexicans through an effect on lowering HDL-cholesterol levels

C. Aguilar-Salinas, M. Tusié-Luna, H. Moreno-Macías, 2020, Journal of Endocrinological Investigation.

Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease.

M. Teresa, M. Tusié-Luna, L. Riba, 1998, Journal of medical genetics.

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

M. Tusié-Luna, L. Riba, M. Ordóñez-Sánchez, 2003, Journal of pediatric endocrinology & metabolism : JPEM.

Molecular Characterization of the Lipid Genome-Wide Association Study Signal on Chromosome 18q11.2 Implicates HNF4A-Mediated Regulation of the TMEM241 Gene

M. Laakso, K. Mohlke, C. Aguilar-Salinas, 2016, Arteriosclerosis, thrombosis, and vascular biology.

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.

C. Aguilar-Salinas, M. Tusié-Luna, R. Rojas-Martínez, 2011, Atherosclerosis.

Combined loss of CDH1 and downstream regulatory sequences drive early-onset diffuse gastric cancer and increase penetrance of hereditary diffuse gastric cancer

E. Schröck, C. Caldas, D. Huntsman, 2023, Gastric Cancer.

The R230C variant of the ATP binding cassette protein A1 (ABCA1) gene is associated with a decreased response to glyburide therapy in patients with type 2 diabetes mellitus.

C. Aguilar-Salinas, M. Tusié-Luna, R. Medina‐Santillán, 2013, Metabolism: clinical and experimental.