Alessandra Carnevale

Periferico Sur No.4809, Col. Arenal Tepepan, D.F, C.P. 14610
Tlalpan, VER 14610, Mexico

Last Updated: 09/26/2026

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Found 32 publications

Demographic History of Indigenous Populations in Mexico Explored Through Whole Mitogenome Analysis.

Demographic History of Indigenous Populations in Mexico Explored Through Whole Mitogenome Analysis.

Journal: Genome biology and evolution

Published: April 07, 2026

Correlation of MLASA2 Clinical Phenotype and Survival with Mt-TyrRS Protein Damage: Linking Systematic Review, Meta-Analysis and 3D Hotspot Mapping.

Correlation of MLASA2 Clinical Phenotype and Survival with Mt-TyrRS Protein Damage: Linking Systematic Review, Meta-Analysis and 3D Hotspot Mapping.

Journal: Current issues in molecular biology

Published: December 11, 2025

First Latin American Case of MLASA2 Caused by a Pathogenic Variant in the Anticodon-Binding Domain of YARS2.

First Latin American Case of MLASA2 Caused by a Pathogenic Variant in the Anticodon-Binding Domain of YARS2.

Journal: International journal of molecular sciences

Published: November 18, 2025

The peruvian genome project: expanding the global pool of genome diversity from South America.

The peruvian genome project: expanding the global pool of genome diversity from South America.

Journal: Frontiers in genetics

Published: April 18, 2025

Selection scan in Native Americans of Mexico identifies FADS2 rs174616: Evidence of gene-diet interactions affecting lipid levels and Delta-6-desaturase activity.

Selection scan in Native Americans of Mexico identifies FADS2 rs174616: Evidence of gene-diet interactions affecting lipid levels and Delta-6-desaturase activity.

Journal: Heliyon

Published: July 20, 2024

KCNQ1 p.D446E Variant as a Risk Allele for Arrhythmogenic Phenotypes: Electrophysiological Characterization Reveals a Complex Phenotype Affecting the Slow Delayed Rectifier Potassium Current (IKs) Voltage Dependence by Causing a Hyperpolarizing Shift and a Lack of Response to Protein Kinase A Activation.

KCNQ1 p.D446E Variant as a Risk Allele for Arrhythmogenic Phenotypes: Electrophysiological Characterization Reveals a Complex Phenotype Affecting the Slow Delayed Rectifier Potassium Current (IKs) Voltage Dependence by Causing a Hyperpolarizing Shift and a Lack of Response to Protein Kinase A Activation.

Journal: International journal of molecular sciences

Published: November 27, 2023

Frequent copy number variants in a cohort of Mexican-Mestizo individuals.

Frequent copy number variants in a cohort of Mexican-Mestizo individuals.

Journal: Molecular cytogenetics

Published: November 01, 2022

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

Clinical Spectrum of SCN5A Channelopathy in Children with Primary Electrical Disease and Structurally Normal Hearts.

Clinical Spectrum of SCN5A Channelopathy in Children with Primary Electrical Disease and Structurally Normal Hearts.

Journal: Genes

Published: October 30, 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

Compound Heterozygous KCNQ1 Mutations Causing Recessive Romano-Ward Syndrome: Functional Characterization by Mutant Co-expression.

Compound Heterozygous KCNQ1 Mutations Causing Recessive Romano-Ward Syndrome: Functional Characterization by Mutant Co-expression.

Journal: Frontiers in cardiovascular medicine

Published: November 03, 2020

Showing 1-12 of 32

Last Updated: 09/26/2026