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SCN4B-encoded sodium channel β4 subunit in congenital long-QT syndrome

Circulation (New York, N.Y.), 2007-07, Vol.116 (2), p.134-142

2007

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Identification of TBX15 as an adipose master trans regulator of abdominal obesity genes

Genome medicine, 2021-08, Vol.13 (1), p.123-123, Article 123

2021

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The panorama of familial hypercholesterolemia in Latin America: a systematic review[S]

Journal of lipid research, 2016-12, Vol.57 (12), p.2115-2129

2016

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Prevalence of germline mutations in the TP53 gene in patients with early-onset breast cancer in the Mexican population

BMC cancer, 2019-02, Vol.19 (1), p.118-118, Article 118

2019

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

European journal of endocrinology, 2019-02, Vol.180 (2), p.99-107

2019

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

Molecular genetics and metabolism reports, 2023-06, Vol.35, p.100965, Article 100965

2023

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Correction to: Identification of TBX15 as an adipose master trans regulator of abdominal obesity genes

Genome medicine, 2021-08, Vol.13 (1), p.1-139, Article 139

2021

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

Annals of hepatology, 2011-04, Vol.10 (2), p.155-164

2011

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

Diabetes care, 2018-08, Vol.41 (8), p.1726-1731

2018

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Mexican Biobank advances population and medical genomics of diverse ancestries

Nature (London), 2023-10, Vol.622 (7984), p.775-783

2023

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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, 2011-05, Vol.216 (1), p.146-150

2011

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The role of SLC16A11 variations in diabetes mellitus

Current opinion in nephrology and hypertension, 2023-09, Vol.32 (5), p.445-450

2023

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Use of PCSK9 Inhibitor in a Mexican Boy with Compound Heterozygous Familial Hypercholesterolemia: A Case Report

Journal of the Endocrine Society, 2020-02, Vol.4 (2), p.bvz018

2020

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Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in mexican families

Neurogenetics, 2006-07, Vol.7 (3), p.195-200

2006

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Differentiating Among Type 1, Type 2 Diabetes, and MODY: Raising Awareness About the Clinical Implementation of Genetic Testing in Latin America

AACE clinical case reports, 2021-03, Vol.7 (2), p.138-140

2021

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DYSLIPIDEMIA IN MEXICO, A CALL FOR ACTION

Revista de investigacion clinica, 2018-09, Vol.70 (5), p.211-216

2018

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Mutations in Steroid 21-Hydroxylase (CYP21)

Human mutation, 1994, Vol.3 (4), p.373-378

1994

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Searching for the Causal Variants of the Association Between Hypertriglyceridemia and the Genome-Wide Association Studies–Derived Signals?: Take a Look in the Native American Populations

Circulation. Cardiovascular genetics, 2017-12, Vol.10 (6)

2017

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The product of the CYP11B2 gene is required for aldosterone biosynthesis in the human adrenal cortex

Molecular endocrinology (Baltimore, Md.), 1991-10, Vol.5 (10), p.1513-1522

1991

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Mutations in MODY genes are not common cause of early-onset type 2 diabetes in Mexican families

Journal of the Pancreas, 2005-05, Vol.6 (3), p.238-245

2005

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Natural course of metabolically healthy phenotype and risk of developing Cardiometabolic diseases: a three years follow-up study

BMC endocrine disorders, 2021-04, Vol.21 (1), p.85-85, Article 85

2021

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SCN4B-encoded sodium channel β4 subunit in congenital long-QT syndrome

Identification of TBX15 as an adipose master trans regulator of abdominal obesity genes

The panorama of familial hypercholesterolemia in Latin America: a systematic review[S]

Prevalence of germline mutations in the TP53 gene in patients with early-onset breast cancer in the Mexican population

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

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

Correction to: Identification of TBX15 as an adipose master trans regulator of abdominal obesity genes

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

Locus on Chromosome 6p Linked to Elevated HDL Cholesterol Serum Levels and to Protection Against Premature Atherosclerosis in a Kindred With Familial Hypercholesterolemia

Development and validation of a predictive model for incident type 2 diabetes in middle-aged Mexican adults: the metabolic syndrome cohort

Critical role of acute hypoxemia on the cognitive impairment after severe COVID-19 pneumonia: a multivariate causality model analysis

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

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

Mexican Biobank advances population and medical genomics of diverse ancestries

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

The role of SLC16A11 variations in diabetes mellitus

Use of PCSK9 Inhibitor in a Mexican Boy with Compound Heterozygous Familial Hypercholesterolemia: A Case Report

Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in mexican families

Differentiating Among Type 1, Type 2 Diabetes, and MODY: Raising Awareness About the Clinical Implementation of Genetic Testing in Latin America

DYSLIPIDEMIA IN MEXICO, A CALL FOR ACTION

Mutations in Steroid 21-Hydroxylase (CYP21)

Searching for the Causal Variants of the Association Between Hypertriglyceridemia and the Genome-Wide Association Studies–Derived Signals?: Take a Look in the Native American Populations

The product of the CYP11B2 gene is required for aldosterone biosynthesis in the human adrenal cortex

Mutations in MODY genes are not common cause of early-onset type 2 diabetes in Mexican families

Natural course of metabolically healthy phenotype and risk of developing Cardiometabolic diseases: a three years follow-up study

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