María
Isidoro García
Profesora Asociada CC. Salud
Hospital Universitario de Salamanca
Salamanca, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario de Salamanca (77)
2024
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PTEN hamartoma tumor syndrome: Clinical and genetic characterization in pediatric patients
Child's Nervous System
2023
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Clinical description, molecular delineation and genotype-phenotype correlation in 340 patients with KBG syndrome: Addition of 67 new patients
Journal of Medical Genetics, Vol. 60, Núm. 7, pp. 644-654
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Interleukin 5 Receptor Subunit Alpha Expression as a Potential Biomarker in Patients with Nasal Polyposis
Biomedicines, Vol. 11, Núm. 7
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Intermediate Molecular Phenotypes to Identify Genetic Markers of Anthracycline-Induced Cardiotoxicity Risk
Cells, Vol. 12, Núm. 15
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RNY3 modulates cell proliferation and IL13 mRNA levels in a T lymphocyte model: a possible new epigenetic mechanism of IL-13 regulation
Journal of Physiology and Biochemistry, Vol. 79, Núm. 1, pp. 59-69
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Transcriptomics reveals new regulatory mechanisms involved in benralizumab response
Allergy: European Journal of Allergy and Clinical Immunology
2022
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Case Report: Pharmacogenetics Applied to Precision Psychiatry Could Explain the Outcome of a Patient With a New CYP2D6 Genotype
Frontiers in Psychiatry, Vol. 12
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Identification of Germinal Neurofibromin Hotspots
Biomedicines, Vol. 10, Núm. 8
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Polymorphisms in Human IL4, IL10, and TNF Genes Are Associated with an Increased Risk of Developing NSAID-Exacerbated Respiratory Disease
Genes, Vol. 13, Núm. 4
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Ten Years of Experience Support Pharmacogenetic Testing to Guide Individualized Drug Therapy
Pharmaceutics, Vol. 14, Núm. 1
2021
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Economic impact of the application of a precision medicine model (5SPM) on psychotic patients
Pharmacogenomics and Personalized Medicine, Vol. 14, pp. 1015-1025
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Genetics and Epigenetics of Nasal Polyposis: A Systematic Review
Journal of investigational allergology & clinical immunology, Vol. 31, Núm. 3, pp. 196-211
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Increased TPSAB1 Copy Number in a Family With Elevated Basal Serum Levels of Tryptase
Frontiers in Medicine, Vol. 8
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Integrated in silico MS-based phosphoproteomics and network enrichment analysis of RASopathy proteins
Orphanet Journal of Rare Diseases, Vol. 16, Núm. 1
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Juvenile myelomonocytic leukemia in CBL syndrome associated with germline splice-site mutations: Two case reports and a literature review
Clinical Case Reports, Vol. 9, Núm. 5
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Review: Influence of the cyp450 genetic variation on the treatment of psychotic disorders
Journal of Clinical Medicine, Vol. 10, Núm. 18
2020
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Application of a pharmacogenetics-based precision medicine model (5SPM) to psychotic patients that presented poor response to neuroleptic therapy
Journal of Personalized Medicine, Vol. 10, Núm. 4, pp. 1-16
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Atopy can be an interfering factor in genetic association studies of ß-lactam allergy
Journal of Investigational Allergology and Clinical Immunology
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Genetics and epigenetics of atopic dermatitis: An updated systematic review
Genes, Vol. 11, Núm. 4
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Molecular Analysis of IL-5 Receptor Subunit Alpha as a Possible Pharmacogenetic Biomarker in Asthma
Frontiers in Medicine, Vol. 7