M. Ordoñez-Sánchez

发表

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.

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.

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.

Genome-wide association study of colorectal cancer in Hispanics

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

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.

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

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

A novel nonsense mutation in the insulin receptor gene in a patient with HAIR-AN syndrome and endometrial cancer

M. Tusié-Luna, P. Almeda-Valdés, J. L. Ventura-Gallegos, 2023, Molecular Genetics and Metabolism Reports.

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.

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.

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.

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.

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.

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.

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.

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.

The SLC16A11 risk haplotype is associated with decreased insulin action, higher transaminases and large-size adipocytes.

J. Florez, Omar Yaxmehen Bello-Chavolla, C. Aguilar-Salinas, 2019, European journal of endocrinology.

Implication of myddosome complex genetic variants in outcome severity of COVID-19 patients

M. M. Mata-Miranda, J. Granados, M. Vela-Amieva, 2023, Journal of Microbiology, Immunology and Infection.

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.

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.

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.

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.

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.

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.

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 second update on mapping the human genetic architecture of COVID-19

M. A. Hakim Newton, Jack D. Sanders, Jonathan H. Morgan, 2022, Nature.

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.

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.

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.

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.

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.

The fatal contribution of serine protease-related genetic variants to COVID-19 outcomes

M. M. Mata-Miranda, J. Fragoso, G. Vargas-Alarcón, 2024, Frontiers in immunology.

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.

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.

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.

Metabolomic Profile Alterations Associated with the SLC16A11 Risk Haplotype Following a Lifestyle Intervention in People with Prediabetes

A. Vargas-Vázquez, C. Clish, P. Almeda-Valdés, 2024, Current Developments in Nutrition.

Familial Hypertriglyceridemia : An entity with distinguishable features from other 1 causes of hypertriglyceridemia 2 3

H. Moreno-Macías, I. Cruz-Bautista, Ximena Rosas-Flota, 2020 .

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.