Lizbeth J. Herrera-Gonzalez
Merida, YUC, Mexico
Last Updated: 09/26/2026
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Found 22 publications
Late Diagnosis of a 3p26.3p25.2 Microduplication in a Young Adult with Mild Neurodevelopmental Features: A Case Report and Literature Review.
Journal: Molecular syndromology
Published: November 13, 2025
LAMA2 Triple Variant in a Mexican Child with Congenital Muscular Dystrophy.
Journal: Annals of Indian Academy of Neurology
Published: September 19, 2025
The rare in the common: unsuspected Fabry disease in a large family with common diseases.
Journal: Gaceta medica de Mexico
Published: January 01, 2025
Presence of white-nose syndrome in bats from Southern Mexico.
Journal: PloS one
Published: August 07, 2024
Association between personality traits, eating behaviors, and the genetic polymorphisms FTO-rs9939609 and MAO-A 30 bp u-VNTR with obesity in Mexican Mayan children.
Journal: Frontiers in genetics
Published: April 23, 2024
Association of the polymorphisms rs179008 (TLR7), rs2004640 (IRF5), rs1800795 (IL-6) and rs2280788 (CCL5) with systemic lupus erythematosus in women of Mayan ethnicity from Yucatan.
Journal: Nucleosides, nucleotides & nucleic acids
Published: March 09, 2024
L-2 hydroxyglutaric aciduria: report of a Mexican-Mayan patient with the mutation c.569C>T and response to vitamin supplements and levocarnitine.
Journal: Tremor and other hyperkinetic movements (New York, N.Y.)
Published: December 21, 2023
FNDC5/Irisin polymorphisms are associated with osteopenia in postmenopausal Mayan-Mestizo women.
Journal: Climacteric : the journal of the International Menopause Society
Published: July 22, 2022
Copy Number Variation and Frequency of rs179008 in TLR7 Gene Associated with Systemic Lupus Erythematosus in Two Mexican Populations.
Journal: Journal of immunology research
Published: September 18, 2021
Genetic variants of PON1, GSTM1, GSTT1, and locus 9p21.3, and the risk for premature coronary artery disease in Yucatan, Mexico.
Journal: American journal of human biology : the official journal of the Human Biology Council
Published: July 21, 2021
Correction to: A four-step mutation at D22S1045 in one complex paternity case when the brother of the alleged father hypothesis is evaluated.
Journal: International journal of legal medicine
Published: June 07, 2020
Last Updated: 09/26/2026