IRIS
DI RESTA, CHIARA
 Distribuzione geografica
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Continente #
NA - Nord America 406
EU - Europa 383
AS - Asia 45
Continente sconosciuto - Info sul continente non disponibili 4
Totale 838
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Nazione #
US - Stati Uniti d'America 406
SE - Svezia 222
IT - Italia 88
FI - Finlandia 30
CN - Cina 26
DE - Germania 18
IE - Irlanda 9
GR - Grecia 7
IN - India 6
IR - Iran 6
GB - Regno Unito 5
SG - Singapore 4
A1 - Anonimo 2
BE - Belgio 2
EU - Europa 2
PH - Filippine 2
FR - Francia 1
RU - Federazione Russa 1
TR - Turchia 1
Totale 838
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Città #
Ashburn 95
Lawrence 57
Princeton 57
New York 52
Helsinki 30
Shanghai 24
Milan 19
Seattle 14
Rome 11
Dublin 9
Viareggio 5
Ardabil 4
Athens 4
Atlanta 4
Turin 4
Washington 4
Los Angeles 3
Lykovrysi 3
Manchester 3
Pune 3
Antwerp 2
Bitonto 2
Cebu City 2
Chandler 2
Falkenstein 2
Indore 2
Las Vegas 2
Malandriano 2
Modena 2
Naples 2
Nerviano 2
Orta Nova 2
Pistoia 2
Sant'Ambrogio di Valpolicella 2
Seriate 2
Vaprio d'Adda 2
Varedo 2
Beijing 1
Bergamo 1
Boardman 1
Borås 1
Campodolcino 1
Cantù 1
Chennai 1
Cremona 1
Girasole 1
Izmir 1
Kish 1
Mairano 1
Monza 1
Piacenza 1
Portland 1
Rockville 1
Shenzhen 1
Singapore 1
Temple Hills 1
Zanjan 1
Totale 459
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Nome #
Antibody Titer Kinetics and SARS-CoV-2 Infections Six Months after Administration with the BNT162b2 Vaccine 30
Development, evaluation, and validation of machine learning models for COVID-19 detection based on routine blood tests 29
Machine Learning based on laboratory medicine test results in diagnosis and prognosis for COVID-19 patients: A systematic review 27
Cardiac and Neuromuscular Features of Patients with LMNA-Related Cardiomyopathy 24
Electrophysiological properties of mutant alpha2beta4 nAChR linked to a form of Autosomal Dominant Nocturnal Frontal Lobe Epilepsy (ADNFLE) 23
Comparable clinical characteristics in Brugada syndrome patients harboring SCN5A or novel SCN10A variants 23
Erratum: Genetic testing in neurology exploiting next generation sequencing: State of art (Neural Regeneration Research (2020) 15:2 (265-266) DOI: 10.4103/1673-5374.265554) 23
Concealed Substrates in Brugada Syndrome: Isolated Channelopathy or Associated Cardiomyopathy? 22
Cardiac magneti resonance and arrhythmic risk stratification of cardiomyopathy associated with lamin A/C mutations: results from a 5 years study 22
A longitudinal analysis of humoral, T cellular response and influencing factors in a cohort of healthcare workers: Implications for personalized SARS-CoV-2 vaccination strategies 20
Analytical Ancestry: Evolution of the Array in Analysis 19
Long-term antibody persistence and exceptional vaccination response on previously SARS-CoV-2 infected subjects 18
Myocardial Inflammation as a Manifestation of Genetic Cardiomyopathies: From Bedside to the Bench 17
A Brugada Syndrome mutation (p.S216L) and its modulation by p.H558R polymorphism: standard and dynamic characterization 17
Brugada syndrome genetics is associated with phenotype severity 17
Inflammation on Endomyocardial Biopsy Predicts Risk of MACE in Undefined Left Ventricular Arrhythmogenic Cardiomyopathy 16
Current Updates on Expanded Carrier Screening: New Insights in the Omics Era 16
Challenges of the Effectiveness of Traumatic Brain Injuries Biomarkers in the Sports-Related Context 15
Effect of Carbamazepine and Related Compounds on Ligand-Gated Channels: Possible Implications for Synaptic Transmission and Side Effects. 15
A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia 15
Quantitative serological evaluation as a valuable tool in the COVID-19 vaccination campaign 15
Genetic background of mitral valve prolapse 15
Evaluation of antibody titer kinetics and SARS-CoV-2 infections in a large cohort of healthcare professionals ten months after administration of the BNT162b2 vaccine 14
Exploratory assessment of serological tests to determine antibody titer against SARS-CoV-2: Appropriateness and limits 14
Effect of carbamazepine and oxcarbazepine on wild-type and mutant neuronal nicotinic acetylcholine receptors linked to nocturnal frontal lobe epilepsy 14
Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study 14
Impaired turnover of hyperfused mitochondria in severe axonal neuropathy due to a novel DRP1 mutation 14
Current scenario of the genetic testing for rare neurological disorders exploiting next generation sequencing 14
The gender impact assessment among healthcare workers in the sars-cov-2 vaccination—an analysis of serological response and side effects 14
Harmonization of six quantitative SARS-CoV-2 serological assays using sera of vaccinated subjects 14
Functional Characterisation of the Rare SCN5A p.E1225K Variant, Segregating in a Brugada Syndrome Familial Case, in Human Cardiomyocytes from Pluripotent Stem Cells 13
Genetic factors predisposing to bronchopulmonary dysplasia. A pilot study by exome sequencing and pathways analysis 13
Premature cardiac senescence in patients with lamin A/C mutations: at least 5 years gap from electrical to mechanical dysfunction 13
Late gadolinium enhancement role in arrhythmic risk stratification of patients with LMNA cardiomyopathy: results from a long-term follow-up multicentre study 13
Alpha2-I279N human nicotinic acetylcholine receptors, linked to a form of nocturnal epilepsy, present higher sensitivity to agonists 12
Immunosuppressive therapy in childhood‐onset arrhythmogenic inflammatory cardiomyopathy 12
SETBP1 accumulation induces P53 inhibition and genotoxic stress in neural progenitors underlying neurodegeneration in Schinzel-Giedion syndrome 12
Increased sensitivity of the neuronal nicotinic receptor alpha2 subunit causes familial epilepsy with nocturnal wandering and ictal fear 11
P3170Innovative approach for risk stratification of LMNA-related cardiomyopathy: results from an integrated cardiological and neurological 10-year follow-up multicentre study 11
Genotype/Phenotype Relationship in a Consanguineal Family With Brugada Syndrome Harboring the R1632C Missense Variant in the SCN5A Gene 11
Evaluation of three advanced methodologies, COLD-PCR, microarray and ddPCR, for identifying the mutational status by liquid biopsies in metastatic colorectal cancer patients 11
Electrocardiogram Changes in the Postictal Phase of Epileptic Seizure: Results from a Prospective Study 10
Health technology assessment to employ COVID-19 serological tests as companion diagnostics in the vaccination campaign against SARS-CoV-2 10
High-throughput genetic characterization of a cohort of Brugada syndrome patients. 10
Next-generation sequencing approach for the diagnosis of human diseases: open challenges and new opportunities 10
SCN5A nonsense mutation and NF1 frameshift mutation in a family with brugada syndrome and neurofibromatosis 10
Novel scn5a p.V1429m variant segregation in a family with brugada syndrome 10
Molecular diagnostics in the prenatal age: technological evolution and ethical implications in reproductive medicine|La diagnostica molecolare in epoca prenatale: evoluzione tecnologica ed implicazioni etiche in medicina della riproduzione 10
The total testing process harmonization: the case study of SARS-CoV-2 serological tests 9
Evaluation of damaging effects of splicing mutations: validation of an in vitro method for diagnostic laboratories 9
Implementation of companion diagnostics in the clinical laboratories: the BRAF example in Melanoma 9
Transcriptional role of androgen receptor in the expression of long non-coding RNA Sox2OT in neurogenesis 9
Increased sensitivity of the neuronal nicotinic receptor alpha 2 subunit causes familial epilepsy with nocturnal wandering and ictal fear 9
Generation of a triadin KnockOut syndrome zebrafish model 9
Increased sensitivity of the alpha-2 neuronal nicotinic receptor causes familial epilepsy with nocturnal wandering and ictal fear 8
Is laboratory medicine ready for the era of personalized medicine? A survey addressed to laboratory directors of hospitals/academic schools of medicine in Europe. 8
Novel SCN5A Frameshift Mutation in Brugada Syndrome Associated With Complex Arrhythmic Phenotype 8
New molecular approaches to Alzheimer's disease 8
Genetic testing in neurology exploiting next generation sequencing: State of art 8
Next Generation Sequencing: From Research Area to Clinical Practice 8
Editorial: Whole Genome Sequencing for rare diseases 7
Advance in Genomics of Rare Genetic Diseases 7
Is laboratory medicine ready for the era of personalized medicine? A survey addressed to laboratory directors of hospitals/academic schools of medicine in Europe 7
Translating genes into health. 7
Integration of multigene panels for the diagnosis of hereditary retinal disorders using Next Generation Sequencing and bioinformatics approaches 7
Multimodal Detection and Targeting of Biopsy-Proven Myocardial Inflammation in Genetic Cardiomyopathies: A Pilot Report 6
Genetics can contribute to the prognosis of the Brugada syndrome: a pilot model for risk stratification. 6
Human neuronal nicotinic receptors and epilepsy during sleep 6
Personalized laboratory medicine: A patient-centered future approach 6
Novel scn5a p.W697x nonsense mutation segregation in a family with brugada syndrome 6
Evidence of significant difference in key covid-19 biomarkers during the italian lockdown strategy. A retrospective study on patients admitted to a hospital emergency department in northern italy 6
Updated clinical overview on cardiac laminopathies: an electrical and mechanical disease 5
Pharmacogenomics education in medical and pharmacy schools: conclusions of a global survey 5
Introduction to ion channels 4
null 4
Six months SARS-CoV-2 serology in a cohort of mRNA vaccinated subjects over 90 years old 3
Totale 946
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Categoria #
all - tutte 11.952
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 11.952
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202027 20 0 2 1 0 2 0 0 0 2 0 0
2020/202115 4 1 0 5 1 2 0 0 1 0 0 1
2021/202282 0 0 0 16 8 8 33 1 3 4 1 8
2022/2023434 133 85 37 0 14 57 13 29 16 2 25 23
2023/2024378 28 18 58 75 27 99 17 42 1 13 0 0
Totale 946