Meetings
- Utilizzo dell'immunoistochimica in patologia mammaria: i miglior marcatori negli scenari peggiori
- Use of clinical exome sequencing in the diagnostic flow of monogenic kidney diseases: the Piedmont experience
- TILs: the next morphological biomarker for daily practice?
- The impact of the COVID-19 pandemic on head and neck cancer diagnosis in the Piedmont region
- The impact of the COVID-19 pandemic on head and neck cancer diagnosis in the Piedmont region
- The HLA and ABO genetic background impact on SARS-CoV-2 infection and COVID-19 severity
- The HLA and ABO genetic background impact on SARS-CoV-2 infection and COVID-19 severity
- Terapia mediata da RNA di interferenza per malattie neurodegenerative
- Tecniche di Next Generation sequencing per la diagnosi di malattie suscettibili di trapianto
- Rare and monogenic diseases in an Italian pediatric cohort of transplanted patients: numbers in real life
- Rare and monogenic diseases in adult and pediatric transplanted patients: an Italian national survey
- Prognostic value of blood DNA methylation in Malignant Pleural Mesothelioma
- Progetto NeuroWES: studiare le basi genetiche dei disturbi dello spettro autistico
- Progetto NeuroWES: studiare le basi genetiche dei disturbi dello spettro autistico
- Peripheral blood DNA methylation as prognostic tool in Malignant Pleural Mesothelioma
- Pan-cancer evaluation of the association between immune cell infiltration and Necroptosis activity
- Nuovi biomarcatori di malattia renale
- Novità nella genetica delle malattie da espansione di repeat e metodi di analisi in laboratorio. Sviluppo di metodi in NGS per le malattie da espansione.
- Novità nella genetica delle malattie da espansione di repeat e metodi di analisi in laboratorio. Sviluppo di metodi in NGS per le malattie da espansione
- Novel and known potentially causative variants identified by clinical exome sequencing in patients with polycystic kidney disease
- Novel and known mutations identified by clinical exome sequencing for the diagnosis of polycystic kidney
- NGS ed autismo. Exome sequencing ed identificazione di geni coinvolti nei disturbi dello spettro autistico.
- Next generation sequencing in the diagnosis of monogenic diseases leading to organ failure
- Multi-Gene Panel Testing Of Triple Negative Breast Cancer Patients
- Multi-Gene Panel Testing Of Melanoma Patients
- Monitoraggio del rigetto acuto del trapianto cardiaco mediante un nuovo metodo di analisi del DNA libero
- Monitoraggio del rigetto acuto del trapianto cardiaco mediante un nuovo metodo di analisi del DNA libero
- Microambiente e cancro della mammella
- Machine Learning per la genomica clinica
- Increased serum ferritin levels predict long-term mortality in patients with NAFLD
- Improving the prediction of cardiovascular risk with machine-learning and DNA methylation data
- Il carcinoma triplo negativo della mammella
- HLA-DRB1 mismatch-based identification of donor-derived cell free DNA (dd-cfDNA) as a marker of rejection in heart transplant recipients
- Hereditary ataxias
- Hereditary ataxias
- Genomic Approaches to Undiagnosed diseases
- Genomic Approaches to Undiagnosed diseases
- From the edge to the center and back: the Piedmont Transplant Center experience in clinical exome sequencing to diagnose kidney diseases
- Extracellular vesicle-miRNAs as early biomarkers of coronary heart diseases
- Extracellular vesicle-miRNAs as early biomarkers of coronary heart diseases
- Extracellular vesicle-derived microRNAs as possible biomarkers for pleural mesothelioma early detection
- Exploring pathogenic mechanisms in neurodegeneration: the examples of Spinocerebellar Ataxia type 28 (SCA28) and Adult-Onset Autosomal Dominant Leukodystrophy (ADLD)
- Exome sequencing ed identificazione di geni coinvolti nei disturbi dello spettro autistico
- Eterogeneità inter- e intratumorale nell'evoluzione del carcinoma della mammella: implicazioni cliniche
- DNA sequence symmetries from randomness: the origin of the Chargaff’s second parity rule
- Determinazione di HER2 dall’IHC al gene expression: implicazioni nelle scelte terapeutiche
- Damage from fixatives in clinical tissues
- Comprehensive Characterization of 1,400 Breast and/or Ovarian Cancer Cases by Integrating Next Generation Sequencing and Clinical Data
- Comparison of approaches to model sequential multiple mediator
- COLEC10 and 3MC Syndrome: Expanding the Genotypic and Phenotypic Spectrum of a very rare disease
- COLEC10 and 3MC Syndrome: Expanding the Genotypic and Phenotypic Spectrum of a very rare disease
- Characterization of 1,400 Breast and/or Ovarian Cancer Cases by Integrating Next Generation Sequencing and Clinical Data
- Carcinoma della mammella: classificazione molecolare
- CAPRIN1 haploinsufficiency causes a novel neurodevelopmental disorder associated with morphological and functional impairment in hiPSCs-derived cortical neurons
- Calibrating variant-scoring methods for clinical decision making
- Biomarcatori di malattia renale: lo studio PRIORITY
- Basi genetiche dell’autismo
- Association between small non-coding RNAs in serum extracellular vesicles and micro/macrovascular complications of type 1 diabetes
- ASCO/CAP HER2 guidelines update
- An innovative dual-reporter cell line to identify protein level modulators in drug-repositioning for rare genetic diseases: a proof-of-principle in Autosomal Dominant LeukoDystrophy (ADLD)
- Allele-specific silencing as therapeutic strategy for disorders due to gene duplication: a proof of principle in Autosomal Dominant LeukoDystrophy (ADLD)
