Maria T. Molina-Villarreal

Mexico City, DIF, Mexico

Last Updated: 09/26/2026

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Found 18 publications

West-Central African Ancestry of the Repeat-Expansion Founder Mutation on the JPH3 Gene in Mexican Patients With Huntington's Disease-Like 2.

West-Central African Ancestry of the Repeat-Expansion Founder Mutation on the JPH3 Gene in Mexican Patients With Huntington's Disease-Like 2.

Journal: Archives of medical research
Published: September 17, 2024

Identification and characterization of short-chain dehydrogenase/reductase 3 (DHRS3) deficiency, a retinoic acid embryopathy of humans.

Identification and characterization of short-chain dehydrogenase/reductase 3 (DHRS3) deficiency, a retinoic acid embryopathy of humans.

Journal: Genetics in medicine open
Published: July 11, 2024

Leukocyte Nuclear Morphology Alterations in Dilated Cardiomyopathy Caused by a Lamin AC Truncating Mutation (LMNA/Ser431*) Are Modified by the Presence of a LAP2 Missense Polymorphism (TMPO/Arg690Cys).

Leukocyte Nuclear Morphology Alterations in Dilated Cardiomyopathy Caused by a Lamin AC Truncating Mutation (LMNA/Ser431*) Are Modified by the Presence of a LAP2 Missense Polymorphism (TMPO/Arg690Cys).

Journal: International journal of molecular sciences
Published: October 01, 2022

Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG.

Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG.

Journal: International journal of molecular sciences
Published: December 24, 2021

Interaction of HLA Class II rs9272219 and TMPO rs17028450 (Arg690Cys) Variants Affects Neuromyelitis Optica Spectrum Disorder Susceptibility in an Admixed Mexican Population.

Interaction of HLA Class II rs9272219 and TMPO rs17028450 (Arg690Cys) Variants Affects Neuromyelitis Optica Spectrum Disorder Susceptibility in an Admixed Mexican Population.

Journal: Frontiers in genetics
Published: December 29, 2020

Genomic study of dilated cardiomyopathy in a group of Mexican patients using site-directed next generation sequencing.

Genomic study of dilated cardiomyopathy in a group of Mexican patients using site-directed next generation sequencing.

Journal: Molecular genetics & genomic medicine
Published: July 13, 2020

Native American ancestry significantly contributes to neuromyelitis optica susceptibility in the admixed Mexican population.

Native American ancestry significantly contributes to neuromyelitis optica susceptibility in the admixed Mexican population.

Journal: Scientific reports
Published: February 14, 2020

Genes frequently associated with sudden death in primary hypertrophic cardiomyopathy.

Genes frequently associated with sudden death in primary hypertrophic cardiomyopathy.

Journal: Archivos de cardiologia de Mexico
Published: January 31, 2020

Host Genetics, Diet, and Microbiome: The Role of AMY1.

Host Genetics, Diet, and Microbiome: The Role of AMY1.

Journal: Trends in microbiology
Published: April 04, 2019

Influence of Genetic and Non-Genetic Risk Factors for Serum Uric Acid Levels and Hyperuricemia in Mexicans.

Influence of Genetic and Non-Genetic Risk Factors for Serum Uric Acid Levels and Hyperuricemia in Mexicans.

Journal: Nutrients
Published: March 31, 2019

Exercise Induces White Adipose Tissue Browning Across the Weight Spectrum in Humans.

Exercise Induces White Adipose Tissue Browning Across the Weight Spectrum in Humans.

Journal: Frontiers in physiology
Published: September 19, 2018

Compound heterozygous KCNQ1 mutations (A300T/P535T) in a child with sudden unexplained death: Insights into possible molecular mechanisms based on protein modeling.

Compound heterozygous KCNQ1 mutations (A300T/P535T) in a child with sudden unexplained death: Insights into possible molecular mechanisms based on protein modeling.

Journal: Gene
Published: April 06, 2017
Showing 1-12 of 18

Last Updated: 09/26/2026