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Genetic contributions to lupus nephritis in a multi-ethnic cohort of systemic lupus erythematous patients

PloS one, 2018-06, Vol.13 (6), p.e0199003-e0199003

2018

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Frequency of the T307A, N680S, and -29G>A single-nucleotide polymorphisms in the follicle-stimulating hormone receptor in Mexican subjects of Hispanic ancestry

Reproductive biology and endocrinology, 2018-10, Vol.16 (1), p.100-100, Article 100

2018

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Differences in MTHFR and LRRK2 variant's association with sporadic Parkinson's disease in Mexican Mestizos correlated to Native American ancestry

NPJ Parkinson's Disease, 2021-02, Vol.7 (1), p.13-13, Article 13

2021

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

Genes, 2020-01, Vol.11 (1), p.114

2020

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The causal effect of obesity on prediabetes and insulin resistance reveals the important role of adipose tissue in insulin resistance

PLoS genetics, 2020-09, Vol.16 (9), p.e1009018-e1009018

2020

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Familial Hyperkalemic Hypertension Genotype With a Negative Phenotype: A CUL3 Mosaicism

American journal of hypertension, 2020-03, Vol.33 (3), p.278-281

2020

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A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia

PLoS genetics, 2009-09, Vol.5 (9), p.e1000642-e1000642

2009

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Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5A

Heart rhythm, 2009-08, Vol.6 (8), p.1170-1175

2009

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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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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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Local Ancestry at the Major Histocompatibility Complex Region is Not a Major Contributor to Disease Heterogeneity in a Multiethnic Lupus Cohort

Arthritis & rheumatology (Hoboken, N.J.), 2024-04, Vol.76 (4), p.614-619

2024

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

Frontiers in immunology, 2024, Vol.15, p.1335963-1335963

2024

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

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

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Association between APOE-ε4 Carrier Status and Qualitative Neuroimaging Characteristics in Older Adults with Mild Cognitive Impairment

Revista de investigacion clinica, 2022, Vol.74 (2), p.113-120

2022

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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

2023

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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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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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Association of the ATP-Binding Cassette Transporter A1 R230C Variant With Early-Onset Type 2 Diabetes in a Mexican Population

Diabetes (New York, N.Y.), 2008-02, Vol.57 (2), p.509-513

2008

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Genetic contributions to lupus nephritis in a multi-ethnic cohort of systemic lupus erythematous patients

Genetic determinants for gestational diabetes mellitus and related metabolic traits in Mexican women

Frequency of the T307A, N680S, and -29G>A single-nucleotide polymorphisms in the follicle-stimulating hormone receptor in Mexican subjects of Hispanic ancestry

Differences in MTHFR and LRRK2 variant's association with sporadic Parkinson's disease in Mexican Mestizos correlated to Native American ancestry

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

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

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

The causal effect of obesity on prediabetes and insulin resistance reveals the important role of adipose tissue in insulin resistance

Familial Hyperkalemic Hypertension Genotype With a Negative Phenotype: A CUL3 Mosaicism

A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia

Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5A

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

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

Local Ancestry at the Major Histocompatibility Complex Region is Not a Major Contributor to Disease Heterogeneity in a Multiethnic Lupus Cohort

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

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

Mexican Biobank advances population and medical genomics of diverse ancestries

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

Association between APOE-ε4 Carrier Status and Qualitative Neuroimaging Characteristics in Older Adults with Mild Cognitive Impairment

The role of SLC16A11 variations in diabetes mellitus

DYSLIPIDEMIA IN MEXICO, A CALL FOR ACTION

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

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

Association of the ATP-Binding Cassette Transporter A1 R230C Variant With Early-Onset Type 2 Diabetes in a Mexican Population

PCSK1 rs6232 is associated with childhood and adult class III obesity in the Mexican population

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