Publications

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9
Phenotypical characterization of immune cells associated with histological regression in cutaneous melanoma: which role in daily practice?
Population structure of modern-day Italians reveals patterns of ancient and archaic ancestries in Southern Europe
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new dataset
Prenatal exposure to PM10and changes in DNA methylation and telomere length in cord blood
Prognostic Characterization of Higher-Grade Meningiomas: A Histopathological Score to Predict Progression and Outcome
Prognostic impact of regression in patients with primary cutaneous melanoma >1 mm in thickness
Prognostic role of PD-L1 and immune-related gene expression profiles in giant cell tumors of bone
Prognostic value of blood DNA methylation in Malignant Pleural Mesothelioma
Protein Stability Perturbation Contributes to the Loss of Function in Haploinsufficient Genes
Pursuit of Gene Fusions in Daily Practice: Evidence from Real-World Data in Wild-Type and Microsatellite Instable Patients
Review: Peering through a keyhole: liquid biopsy in primary and metastatic central nervous system tumours
RollFISH achieves robust quantification of single-molecule RNA biomarkers in paraffin-embedded tumor tissue samples
ROR1 targeting with the antibody-drug conjugate VLS-101 is effective in Richter syndrome patient-derived xenograft mouse models
SeqFu: A suite of utilities for the robust and reproducible manipulation of sequence files
Small Non-Coding RNA Profiling in Plasma Extracellular Vesicles of Bladder Cancer Patients by Next-Generation Sequencing: Expression Levels of miR-126-3p and piR-5936 Increase with Higher Histologic Grades
Spontaneous remission in a Diamond-Blackfan anaemia patient due to a revertant uniparental disomy ablating a de novo RPS19 mutation
Synergistic efficacy of the dual PI3K-δ/γ inhibitor duvelisib with the Bcl-2 inhibitor venetoclax in Richter syndrome PDX models
Targeting of the A2A adenosine receptor counteracts immunosuppression in vivo in a mouse model of chronic lymphocytic leukemia.
Temporal transcriptome analysis reveals dynamic gene expression patterns driving β-cell maturation
TERT Promoter Mutations are Associated with Visceral Spreading in Melanoma of the Trunk
The Dilemma of HER2 Double-equivocal Breast Carcinomas: Genomic Profiling and Implications for Treatment
The frequency of rare and monogenic diseases in pediatric organ transplant recipients in Italy
The Impact of Dysmetabolic Sarcopenia Among Insulin Sensitive Tissues: A Narrative Review
The Multifaceted Nature of Tumor Microenvironment in Breast Carcinomas
The NOTCH Pathway and Its Mutations in Mature B Cell Malignancies
Therapeutic application of allele-specific silencing by siRNA for gene duplication disorders: a proof-of-principle in Autosomal Dominant LeukoDystrophy (ADLD)
ThermoScan: Semi-automatic Identification of Protein Stability Data From PubMed
Tissues under-vacuum to overcome suboptimal preservation
Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy.
When the neurodevelopmental disorder has a genetic cause: Kleefstra syndrome
Wilms tumour occurring in a patient with osteopathia striata with cranial sclerosis: A still unsolved biological question.

Pagine

Publications