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A proposal of a new evaluation framework towards implementation of genetic tests

PloS one, 2019-08, Vol.14 (8), p.e0219755-e0219755

2019

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Genetic variants of the human host influencing the coronavirus-associated phenotypes (SARS, MERS and COVID-19): rapid systematic review and field synopsis

Human genomics, 2020-09, Vol.14 (1), p.30-30, Article 30

2020

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The Anti-Viral Activity of Stem Cells: A Rational Explanation for their Use in Clinical Application

Endocrine, metabolic & immune disorders drug targets, 2023-01, Vol.23 (6), p.739

2023

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Determinants of left ventricular mechanical dyssynchrony in patients submitted to myocardial perfusion imaging: A cardiac CZT study

Journal of nuclear cardiology, 2016-08, Vol.23 (4), p.728-736

2016

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How is genetic testing evaluated? A systematic review of the literature

European journal of human genetics : EJHG, 2018-05, Vol.26 (5), p.605-615

2018

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Life-threatening paradoxical thromboembolism in a patient with patent foramen ovale

Cardiovascular ultrasound, 2022-11, Vol.20 (1), p.28-28, Article 28

2022

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Analysis of Gene Single Nucleotide Polymorphisms in COVID-19 Disease Highlighting the Susceptibility and the Severity towards the Infection

Diagnostics (Basel), 2022-11, Vol.12 (11), p.2824

2022

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The policy of public health genomics in Italy

Health policy (Amsterdam), 2013-05, Vol.110 (2), p.214-219

2013

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External validation of unsupervised COVID-19 clinical phenotypes and their prognostic impact

Annals of medicine (Helsinki), 2023-12, Vol.55 (1), p.2195204-2195204

2023

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New Translational Trends in Personalized Medicine: Autologous Peripheral Blood Stem Cells and Plasma for COVID-19 Patient

Journal of personalized medicine, 2022-01, Vol.12 (1), p.85

2022

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Penetrance of the V203I variant of the PRNP gene: report of a patient with stroke-like onset of Creutzfeld-Jacob Disease and review of published cases

Prion, 2022-12, Vol.16 (1), p.19-22

2022

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The relationship between carotid and coronary calcification in patients with coronary artery disease

Clinical physiology and functional imaging, 2021-05, Vol.41 (3), p.271-280

2021

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Predicting Response to Neoadjuvant Therapy in Colorectal Cancer Patients the Role of Messenger-and Micro-RNA Profiling

Cancers, 2020-06, Vol.12 (6), p.1652

2020

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On personal identity and space: some remarks on Ruth Boeker’s Catharine Trotter Cockburn

British journal for the history of philosophy, 2024-01, p.1-9

De Tommaso, Emilio Maria

2024

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Prognostic value of reverse remodelling criteria in heart failure with reduced or mid‐range ejection fraction

ESC Heart Failure, 2021-08, Vol.8 (4), p.3014-3025

2021

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Reputational Risk for financial institutions: a proposal of quantitative approach

Risk management magazine (Online), 2021-08, Vol.16 (2), p.50-67

2021

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Metastability of Synchronous and Asynchronous Dynamics

Entropy (Basel, Switzerland), 2022-03, Vol.24 (4), p.450

2022

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Genotyping of the Alzheimer's Disease Genome-Wide Association Study Index Single Nucleotide Polymorphisms in the Brains for Dementia Research Cohort

Journal of Alzheimer's disease, 2018-01, Vol.64 (2), p.355

2018

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Genetic counselling and testing for inherited dementia: single-centre evaluation of the consensus Italian DIAfN protocol

Alzheimer's research & therapy, 2020-11, Vol.12 (1), p.152-152, Article 152

2020

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Novel tau biomarkers phosphorylated at T181, T217 or T231 rise in the initial stages of the preclinical Alzheimer’s continuum when only subtle changes in Aβ pathology are detected

EMBO molecular medicine, 2020-12, Vol.12 (12), p.e12921-n/a

2020

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Activating mutations in discoidin domain receptor 2 cause Warburg‐Cinotti syndrome

Acta ophthalmologica (Oxford, England), 2019-12, Vol.97 (S263), p.n/a

2019

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Relationship between electrocardiographic findings and Cardiac Magnetic Resonance phenotypes in patients with Hypertrophic Cardiomyopathy

International journal of cardiology. Heart & vasculature, 2016-06, Vol.11 (C), p.7-11

2016

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Disclosure of Genetic Risk Factors for Alzheimer's Disease to Cognitively Healthy Individuals-From Current Practice towards a Personalised Medicine Scenario

Biomedicines, 2022-12, Vol.10 (12), p.3177

2022

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Naringerin as candidate drug against SARS-CoV-2: The role for TPC2 genomic variants in COVID-19

Pharmacological research, 2021-02, Vol.164, p.105402-105402, Article 105402

2021

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Frontotemporal Dementia due to the Novel GRN Arg161GlyfsX36 Mutation

Journal of Alzheimer's disease, 2017, Vol.57 (4), p.1185

2017

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A proposal of a new evaluation framework towards implementation of genetic tests

Genetic variants of the human host influencing the coronavirus-associated phenotypes (SARS, MERS and COVID-19): rapid systematic review and field synopsis

The Anti-Viral Activity of Stem Cells: A Rational Explanation for their Use in Clinical Application

Determinants of left ventricular mechanical dyssynchrony in patients submitted to myocardial perfusion imaging: A cardiac CZT study

How is genetic testing evaluated? A systematic review of the literature

Life-threatening paradoxical thromboembolism in a patient with patent foramen ovale

Analysis of Gene Single Nucleotide Polymorphisms in COVID-19 Disease Highlighting the Susceptibility and the Severity towards the Infection

The policy of public health genomics in Italy

External validation of unsupervised COVID-19 clinical phenotypes and their prognostic impact

New Translational Trends in Personalized Medicine: Autologous Peripheral Blood Stem Cells and Plasma for COVID-19 Patient

Penetrance of the V203I variant of the PRNP gene: report of a patient with stroke-like onset of Creutzfeld-Jacob Disease and review of published cases

The relationship between carotid and coronary calcification in patients with coronary artery disease

Predicting Response to Neoadjuvant Therapy in Colorectal Cancer Patients the Role of Messenger-and Micro-RNA Profiling

On personal identity and space: some remarks on Ruth Boeker’s Catharine Trotter Cockburn

Prognostic value of reverse remodelling criteria in heart failure with reduced or mid‐range ejection fraction

Reputational Risk for financial institutions: a proposal of quantitative approach

Metastability of Synchronous and Asynchronous Dynamics

Genotyping of the Alzheimer's Disease Genome-Wide Association Study Index Single Nucleotide Polymorphisms in the Brains for Dementia Research Cohort

Genetic counselling and testing for inherited dementia: single-centre evaluation of the consensus Italian DIAfN protocol

Novel tau biomarkers phosphorylated at T181, T217 or T231 rise in the initial stages of the preclinical Alzheimer’s continuum when only subtle changes in Aβ pathology are detected

Activating mutations in discoidin domain receptor 2 cause Warburg‐Cinotti syndrome

Relationship between electrocardiographic findings and Cardiac Magnetic Resonance phenotypes in patients with Hypertrophic Cardiomyopathy

Disclosure of Genetic Risk Factors for Alzheimer's Disease to Cognitively Healthy Individuals-From Current Practice towards a Personalised Medicine Scenario

Naringerin as candidate drug against SARS-CoV-2: The role for TPC2 genomic variants in COVID-19

Frontotemporal Dementia due to the Novel GRN Arg161GlyfsX36 Mutation

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