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Benilde García‐de Teresa

Observed names: B. García‐de Teresa, Benilde García-de Teresa, Benilde Garcia de Teresa, Benilde Garcia-de-Teresa, Benilde García de Teresa, Benilde García-De Teresa, Benilde García-de Teresa, Benilde García-de-Teresa, Benilde García-deTeresa, García-De-Teresa, Benilde
ORCID: 0000-0002-9378-1007
Observed ORCID: 0000-0002-9378-1007
OpenAlex ID: A5016899634
Chromosome Instability in Fanconi Anemia: From Breaks to Phenotypic Consequences
2020 · Benilde García-de-Teresa, Alfredo Rodríguez, et al. · Genes · 86
MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia
2020 · Alfredo Rodríguez, Kaiyang Zhang, et al. · Cell stem cell · 65
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Fanconi anemia and dyskeratosis congenita/telomere biology disorders: Two inherited bone marrow failure syndromes with genomic instability
2022 · Moisés Ó. Fiesco-Roa, Benilde García-de Teresa, et al. · Frontiers in Oncology · 36
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Inhibition of TGFβ1 and TGFβ3 promotes hematopoiesis in Fanconi anemia
2020 · Alfredo Rodríguez, Chunyu Yang, et al. · Experimental Hematology · 26
DNA Damage as a Driver for Growth Delay: Chromosome Instability Syndromes with Intrauterine Growth Retardation
2017 · Benilde García-de Teresa, Mariana Hernández-Gómez, et al. · BioMed Research International · 25
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Germinal Mosaicism in a Sample of Families with Duchenne/Becker Muscular Dystrophy with Partial Deletions in the DMD Gene
2013 · Cesárea Bermúdez-López, Benilde García-de Teresa, et al. · Genetic Testing and Molecular Biomarkers · 23
Fanconi anemia cells with unrepaired DNA damage activate components of the checkpoint recovery process
2015 · Alfredo Rodríguez, Leda Torres, et al. · Theoretical Biology and Medical Modelling · 22
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Wide allelic heterogeneity with predominance of large IDS gene complex rearrangements in a sample of Mexican patients with Hunter syndrome
2016 · M.A. Alcántara‐Ortigoza, B. García‐de Teresa, et al. · Clinical Genetics · 19
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Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG
2022 · Pedro Reyes, Benilde García-deTeresa, et al. · International Journal of Molecular Sciences · 13
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FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México
2019 · Benilde García‐de Teresa, Sara Frias, et al. · Molecular Genetics & Genomic Medicine · 11
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Deletion of Exon 1 of the SLC16A2 Gene: A Common Occurrence in Patients with Allan-Herndon-Dudley Syndrome
2014 · Benilde García-de Teresa, Ariadna González-del Angel, et al. · Thyroid · 9
Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes
2019 · Rehotbevely Barrientos-Rios, Sara Frias, et al. · Gynecological Endocrinology · 8
A Boolean network model of the double-strand break repair pathway choice
2023 · Cecilia Ayala-Zambrano, Mariana Yuste, et al. · Journal of Theoretical Biology · 7
WIP1 Contributes to the Adaptation of Fanconi Anemia Cells to DNA Damage as Determined by the Regulatory Network of the Fanconi Anemia and Checkpoint Recovery Pathways
2019 · Alfredo Rodríguez, J. Jesús Naveja, et al. · Frontiers in Genetics · 7
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BRCA1-, BRCA2-, and PALB2-related Fanconi anemia: Scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes
2025 · Sharon E. Johnatty, Emma Tudini, et al. · The American Journal of Human Genetics · 6
Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics
2018 · Emiy Yokoyama, Victoria Del Castillo, et al. · Molecular Cytogenetics · 6
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The tight bond between Fanconi anemia and aging
2026 · Marco Antonio Mejía-Barrera, Enya Enara Martínez-Torres, et al. · Frontiers in Aging · 3
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High Burden of Non-Clonal Chromosome Aberrations Before Onset of Detectable Neoplasia in Fanconi Anemia Bone Marrow
2025 · Silvia Sánchez, Benilde García-de-Teresa, et al. · Cancers · 3
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Microcefalia: Consideraciones En El Abordaje Diagnóstico
2020 · Gilda Garza-Mayén, Moisés Fiesco-Roa, et al. · Acta Pediátrica de México · 3
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Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico
2024 · Paula Leal-Anaya, Tamara N. Kimball, et al. · Frontiers in Genetics · 2
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Correction: Reversion from basal histone H4 hypoacetylation at the replication fork increases DNA damage in FANCA deficient cells
2024 · Benilde García-de-Teresa, Cecilia Ayala-Zambrano, et al. · PLoS ONE · 1
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Reversion from basal histone H4 hypoacetylation at the replication fork increases DNA damage in FANCA deficient cells
2024 · Benilde García-de Teresa, Cecilia Ayala-Zambrano, et al. · PLoS ONE · 1
Síndromes de falla medular hereditarios: etiología, fisiopatología, diagnóstico y tratamiento
2021 · Moisés Fiesco Roa, Angélica Monsivais Orozco, et al. · Acta Pediátrica de México · 1
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Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes
2019 · Rehotbevely Barrientos-Rios, Frias, Sara, et al. · Figshare · 1
Diagnóstico clínico y de laboratorio de la anemia de Fanconi
2014 · Benilde García‐de Teresa, Victoria del Castillo, et al. · Acta Pediátrica de México · 1
Works count: 32
Citation count: 385
H-index: 10
I10-index: 10
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