Lorenzo Vaccaro
Naples, Italy
Last Updated: 09/26/2026
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Found 16 publications
A coordinated transcriptional program controls de novo Golgi biogenesis.
Journal: The EMBO journal
Published: November 17, 2025
Modelling severe COVID-19 in TLR3-mutated hiPSCs-derived lung organoids.
Journal: Cell death discovery
Published: September 12, 2025
Deciphering brain metastasis in epithelial ovarian cancer: multimodal analysis and potential biomarkers.
Journal: NPJ precision oncology
Published: April 29, 2025
Whole Blood Multi-OMIC Analysis Is Effective in Clinical Interpretation of Splicing Aberrations in PLOD1 -Related Kyphoscoliotic Ehlers-Danlos Syndrome.
Journal: American journal of medical genetics. Part A
Published: January 31, 2025
Multi-OMICs analysis on tridimensional fibroblast spheroids to model vascular Ehlers-Danlos syndrome pathogenesis.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: January 09, 2025
Excitatory Cortical Neurons from CDKL5 Deficiency Disorder Patient-Derived Organoids Show Early Hyperexcitability Not Identified in Neurogenin2 Induced Neurons.
Journal: bioRxiv : the preprint server for biology
Published: November 28, 2024
Excitatory cortical neurons from CDKL5 deficiency disorder patient-derived organoids show early hyperexcitability not identified in neurogenin2 induced neurons.
Journal: Neurobiology of disease
Published: November 05, 2024
Variant sub-tiering, disease-gene associations and strictness of clinical criteria improves the interpretation of variants of uncertain significance in hereditary cardiomyopathies and rhythm disorders.
Journal: Journal of human genetics
Published: October 10, 2024
Heterozygous variants disrupting the interaction of ERF with activated ERK1/2 cause microcephaly, developmental delay, and skeletal anomalies.
Journal: European journal of human genetics : EJHG
Published: June 18, 2024
Combined biochemical profiling and DNA sequencing in the expanded newborn screening for inherited metabolic diseases: the experience in an Italian reference center.
Journal: Orphanet journal of rare diseases
Published: June 17, 2024
Combined exome and whole transcriptome sequencing identifies a de novo intronic SRCAP variant causing DEHMBA syndrome with severe sleep disorder.
Journal: Journal of human genetics
Published: September 28, 2023
Identification of druggable host dependency factors shared by multiple SARS-CoV-2 variants of concern.
Journal: Journal of molecular cell biology
Published: February 03, 2023
Last Updated: 09/26/2026