FIESCO ROA, MOISES OSCAR
ESPECIALIDAD MÉDICA · Nivel 1
Desde 2021 es Researcher assistant en Instituto Nacional de Pediatría
I am a clinical geneticist with a formal training in clinical and epidemiological research (MD, MSc). Since 2011, I have...
I am a clinical geneticist with a formal training in clinical and epidemiological research (MD, MSc). Since 2011, I have evaluated several patients with a broad kind of diseases, such as: bone dysplasia, familiar cancer and cancer predisposition syndromes, chromosomal abnormalities, neuromuscular disorders, inborn errors of metabolism, intellectual disability, congenital malformations, etcetera.
My main research interests are Clinical and Translational Genetics, particularly focused on genetic, dysmorphological and cancer predisposition syndromes.
Nowadays, I am a research at the National Institute of Pediatrics in Mexico and an associate professor at the Embryology and Genetics department at the National University of Mexico-School of Medicine.
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| Nombre | MOISES OSCAR FIESCO ROA |
|---|---|
| Área | MEDICINA Y CIENCIAS DE LA SALUD |
| Campo | ESPECIALIDAD MÉDICA |
| Disciplina | GENÉTICA MEDICA |
| Especialidad | GENETICA MEDICA |
| CVU | 289206 |
| Institución | |
|---|---|
| Tipo de institución | Pública |
| Dependencia | DIVISION DE INVESTIGACION MEDICA |
| Entidad | CIUDAD DE MEXICO |
| Nivel | 1 |
| Vigencia | Inicio: 01/01/2024 |
| Fin: 31/12/2028 |
Evolución en el SNII
- Nivel I: 2024–2026
Publicaciones ORCID
- 2025
- High Burden of Non-Clonal Chromosome Aberrations Before Onset of Detectable Neoplasia in Fanconi Anemia Bone Marrow Cancers
- High Burden of Non-Clonal Chromosome Aberrations Before Onset of Detectable Neoplasia in Fanconi Anemia Bone Marrow
- Situación epidemiológica de las anomalías congénitas en Paraguay en el periodo 2017-2021 Medicina Clínica y Social
- 2022
- Genotypic spectrum underlying tetrahydrobiopterin metabolism defects: Experience in a single Mexican reference center Frontiers in Genetics · ISSN 1664-8021
- Fanconi anemia and dyskeratosis congenita/telomere biology disorders: Two inherited bone marrow failure syndromes with genomic instability Frontiers in Oncology · ISSN 2234-943X
- La Dismorfología como Herramienta para un Diagnóstico Temprano de la Anemia de Fanconi; Dysmorphology as a Tool for Earlier Diagnosis of Fanconi Anemia Acta Pediátrica de México
- Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG International Journal of Molecular Sciences
- 2021
- Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG
- ALG1-CDG Caused by Non-functional Alternative Splicing Involving a Novel Pathogenic Complex Allele Frontiers in Genetics · ISSN 1664-8021
- 2019
- Genotype-phenotype associations in Fanconi anemia: A literature review Blood Reviews · ISSN 0268-960X
