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José de Jesús Lugo-Trampe

Universidad Autónoma de Nuevo León

17

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55

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Maternal Folic Acid Intake and Methylation Status of Genes Associated with Ventricular Septal Defects in Children: Case-Control Study.

2021 Nutrients
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Molecular Characterization of Associated Pathogens in Febrile Patients during Inter-Epidemic Periods of Urban Arboviral Diseases in Tapachula Southern Mexico

2021 Pathogenetics
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Whole exome sequencing identifies multiple novel candidate genes in familial gastroschisis.

2020 Molecular Genetics & Genomic Medicine
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Analysis of the pathogenic variants of BRCA1 and BRCA2 using next-generation sequencing in women with familial breast cancer: a case–control study

2019 BMC Cancer
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Genetic Variants at the rs4720169 Locus of TBX20 and the rs12921862 Locus of AXIN1 May Increase the Risk of Congenital Heart Defects in the Mexican Population: A Pilot Study

2019 Genetic Testing and Molecular Biomarkers
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Bioinformatic Analysis of Gene Variants from Gastroschisis Recurrence Identifies Multiple Novel Pathogenetic Pathways: Implication for the Closure of the Ventral Body Wall

2019 International Journal of Molecular Sciences
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A Case Series Of Infants With Increased Vamp7 Gene Dosage At Birth And Virilization Defects.

2019 Journal of Pediatric Urology
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Frequency of SMN1 deletion carriers in a Mestizo population of central and northeastern Mexico: A pilot study.

2015 Experimental and Therapeutic Medicine
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Rothmund-thomson syndrome: a 13-year follow-up.

2014 Case Reports in Dermatology
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GJB2 and GJB6 mutations are an infrequent cause of autosomal-recessive nonsyndromic hearing loss in residents of Mexico.

2014 International Journal of Pediatric Otorhinolaryngology
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