Juan Luis
García Hernández
Investigador desde null
Publicaciones en las que colabora con Juan Luis García Hernández (128)
2024
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Chromosomal breaks: another differential gap between early-onset and late-onset colorectal cancers
British Journal of Surgery, Vol. 111, Núm. 3
2023
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Adult T-cell leukemia/lymphoma in HTLV-1 non-endemic regions
Journal of Clinical Virology, Vol. 167
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Efficacy and safety of PARP inhibitor in non-small cell lung cancer: a systematic review with meta-analysis
Chinese Clinical Oncology, Vol. 12, Núm. 6
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Improvement of large copy number variant detection by whole genome nanopore sequencing
Journal of Advanced Research, Vol. 50, pp. 145-158
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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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Predominantly Pro-Inflammatory Phenotype with Mixed M1/M2 Polarization of Peripheral Blood Classical Monocytes and Monocyte-Derived Macrophages among Patients with Excessive Ethanol Intake
Antioxidants, Vol. 12, Núm. 9
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Real-world effectiveness and safety of stereotactic body radiotherapy for liver metastases with different respiratory motion management techniques
Strahlentherapie und Onkologie, Vol. 199, Núm. 11, pp. 1000-1010
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Stereotactic body radiation therapy (SBRT) for spinal metastases: 12 years of a single center experience
Clinical and Translational Oncology, Vol. 25, Núm. 12, pp. 3395-3404
2022
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25-Hydroxyvitamin D Serum Levels Linked to Single Nucleotide Polymorphisms (SNPs) (rs2228570, rs2282679, rs10741657) in Skeletal Muscle Aging in Institutionalized Elderly Men Not Supplemented with Vitamin D
International Journal of Molecular Sciences, Vol. 23, Núm. 19
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Intrafraction target shift comparison using two breath-hold systems in lung stereotactic body radiotherapy
Physics and Imaging in Radiation Oncology, Vol. 22, pp. 57-62
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Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency
Thrombosis and Haemostasis, Vol. 122, Núm. 8, pp. 1369-1378
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Molecular Dissection of Structural Variations Involved in Antithrombin Deficiency
Journal of Molecular Diagnostics, Vol. 24, Núm. 5, pp. 462-475
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Recurrent NOMO1 Gene Deletion Is a Potential Clinical Marker in Early-Onset Colorectal Cancer and Is Involved in the Regulation of Cell Migration
Cancers, Vol. 14, Núm. 16
2021
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Copy neutral loss of heterozygosity (cnLOH) patterns in synchronous colorectal cancer
European Journal of Human Genetics, Vol. 29, Núm. 4, pp. 709-713
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Long COVID a new derivative in the chaos of SARS-CoV-2 infection: The emergent pandemic?
Journal of Clinical Medicine, Vol. 10, Núm. 24
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Pathogenic convergence of CNVs in genes functionally associated to a severe neuromotor developmental delay syndrome
Human Genomics, Vol. 15, Núm. 1
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Radiotherapy CT-based contouring atlas for nonmalignant skeletal and soft tissue disorders: a practical proposal from Spanish experience
British Journal of Radiology, Vol. 94, Núm. 1124
2020
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CRISPR/Cas9-generated models uncover therapeutic vulnerabilities of del(11q) CLL cells to dual BCR and PARP inhibition
Leukemia, Vol. 34, Núm. 6, pp. 1599-1612
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Comment on: Clinicopathological features and oncological outcomes of patients with young-onset rectal cancer
British Journal of Surgery
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Novel dominant kcnq2 exon 7 partial in-frame duplication in a complex epileptic and neurodevelopmental delay syndrome
International Journal of Molecular Sciences, Vol. 21, Núm. 12, pp. 1-11