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David Eduardo Cervantes-Barragán

Observed names: Cervantes-Barragán, D., D. Cervantes-Barragán, David Cervantes-Barragan, David E Cervantes-Barragán, David E. Cervantes-Barragan, David E. Cervantes-Barragán, David E. Cervantes‐Barragán
Observed institutions: Yamagata University, Kanagawa Children's Medical Center, Instituto Nacional de Pediatria, Universidad La Salle, Hospital Central Sur de Alta Especialidad PEMEX, Universidad Autónoma de Zacatecas "Francisco García Salinas", Pemex (Mexico), Yokohama City University
ORCID: 0000-0002-4789-9581
Observed ORCID: 0000-0002-4789-9581
OpenAlex ID: A5024799217
Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome
2013 · Kazuyuki Nakamura, Mitsuhiro Kato, et al. · Neurology · 204
Newborn screening for six lysosomal storage disorders in a cohort of Mexican patients: Three-year findings from a screening program in a closed Mexican health system
2017 · Juana Inés Navarrete-Martínez, Ana Elena Limón-Rojas, et al. · Molecular Genetics and Metabolism · 63
Sanger sequencing as a first-line approach for molecular diagnosis of Andersen-Tawil syndrome
2017 · Armando Totomoch-Serra, Manlio F. Marquez, et al. · F1000Research · 36
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Setleis syndrome in Mexican-Nahua sibs due to a homozygous TWIST2 frameshift mutation and partial expression in heterozygotes: review of the focal facial dermal dysplasias and subtype reclassification
2011 · David E Cervantes-Barragán, Camilo E Villarroel, et al. · Journal of Medical Genetics · 32
Genetic and clinical characterization of 73 Pigmentary Mosaicism patients: revealing the genetic basis of clinical manifestations
2019 · C. Salas-Labadía, S. Gómez-Carmona, et al. · Orphanet Journal of Rare Diseases · 20
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Genomic chaos in peripheral blood lymphocytes of Hodgkin's lymphoma patients one year after ABVD chemotherapy/radiotherapy
2018 · Sandra Ramos, Pilar Navarrete‐Meneses, et al. · Environmental and Molecular Mutagenesis · 20
Editing the Human Genome with CRISPR/Cas: A Review of its Molecular Basis, Current Clinical Applications, and Bioethical Implications
2023 · Miguel Ahumada-Ayala, Regina Aguilar-Lopez, et al. · Revista de investigaci�n Cl�nica · 15
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Cytogenomic and phenotypic analysis in low‐level monosomy 7 mosaicism with non‐supernumerary ring chromosome 7
2014 · Consuelo Salas‐Labadía, David E. Cervantes‐Barragán, et al. · American Journal of Medical Genetics Part A · 9
Prevalencia de anemias hemolíticas hereditarias detectadas por tamiz metabólico ampliado en los servicios de salud de Petróleos Mexicanos
2023 · Lizbeth Yamilet Hernández-Verdugo, María Fernanda Fernández-Bautista, et al. · Revista Mexicana de Pediatría · 4
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Pediatric Porcelain Aorta Secondary to Gaucher Disease Type 3C With Successful Aortic Replacement Surgery
2022 · Jorge Silva-Estrada, David E. Cervantes-Barragán, et al. · JACC Case Reports · 4
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Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review
2022 · A. Martínez-Hernández, D. Martínez-Anaya, et al. · BMC Medical Genomics · 3
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Clinical heterogeneity in Andersen-Tawil syndrome
2017 · Armando Totomoch-Serra, Manlio F. Márquez, et al. · Neuromuscular Disorders · 3
Unclassified Chromosomal Abnormalities as an Indicator of Genomic Damage in Survivors of Hodgkin’s Lymphoma
2025 · Sandra Ramos, Bertha Molina, et al. · Cancers · 1
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Mitochondrial DNA polymorphisms in Andersen–Tawil syndrome
2020 · Armando Totomoch-Serra, Cesar A. Brito-Carreón, et al. · Kardiologia Polska · 1
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El Rezago Y Abandono Escolar En Ingeniería Química De La Uaz Retos Y Expectativas
2018 · Ricardo Conejo‐Flores, David E. Cervantes‐Barragán, et al. · Journal of Energy, Engineering Optimization and Sustainability. · 1
Biochemical and molecular analysis of MPS III in 6 Mexican patients
2019 · Jose E. Garcia, Esther Lieberman-Hernandez, et al. · Molecular Genetics and Metabolism
Works count: 18
Citation count: 416
H-index: 8
I10-index: 7
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