Publicacións (119) Publicacións de Juan Luis García Hernández

2024

  1. Chromosomal breaks: another differential gap between early-onset and late-onset colorectal cancers

    British Journal of Surgery, Vol. 111, Núm. 3

2023

  1. Adult T-cell leukemia/lymphoma in HTLV-1 non-endemic regions

    Journal of Clinical Virology, Vol. 167

  2. 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

  3. Improvement of large copy number variant detection by whole genome nanopore sequencing

    Journal of Advanced Research, Vol. 50, pp. 145-158

  4. Intermediate Molecular Phenotypes to Identify Genetic Markers of Anthracycline-Induced Cardiotoxicity Risk

    Cells, Vol. 12, Núm. 15

  5. 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

  6. 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

  7. 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

  1. 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

  2. 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

  3. 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

  4. Molecular Dissection of Structural Variations Involved in Antithrombin Deficiency

    Journal of Molecular Diagnostics, Vol. 24, Núm. 5, pp. 462-475

  5. 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

  1. Copy neutral loss of heterozygosity (cnLOH) patterns in synchronous colorectal cancer

    European Journal of Human Genetics, Vol. 29, Núm. 4, pp. 709-713

  2. Long COVID a new derivative in the chaos of SARS-CoV-2 infection: The emergent pandemic?

    Journal of Clinical Medicine, Vol. 10, Núm. 24

  3. Pathogenic convergence of CNVs in genes functionally associated to a severe neuromotor developmental delay syndrome

    Human Genomics, Vol. 15, Núm. 1

  4. 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

  1. 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

  2. Comment on: Clinicopathological features and oncological outcomes of patients with young-onset rectal cancer

    British Journal of Surgery

  3. 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