IRIS
NICORA, GIOVANNA
 Distribuzione geografica
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Continente #
EU - Europa 433
NA - Nord America 328
AS - Asia 109
AF - Africa 1
SA - Sud America 1
Totale 872
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Nazione #
US - Stati Uniti d'America 316
IT - Italia 204
IE - Irlanda 119
CN - Cina 73
SE - Svezia 25
DE - Germania 20
FI - Finlandia 16
BE - Belgio 12
CA - Canada 12
IN - India 11
JP - Giappone 11
FR - Francia 8
CZ - Repubblica Ceca 5
RU - Federazione Russa 5
SG - Singapore 5
PL - Polonia 4
DK - Danimarca 3
IR - Iran 3
AT - Austria 2
GB - Regno Unito 2
RO - Romania 2
SA - Arabia Saudita 2
SI - Slovenia 2
TR - Turchia 2
UA - Ucraina 2
CH - Svizzera 1
CL - Cile 1
HK - Hong Kong 1
LB - Libano 1
NL - Olanda 1
ZA - Sudafrica 1
Totale 872
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Città #
Dublin 118
Chandler 74
Pavia 63
Ashburn 41
Shanghai 35
Boardman 24
Milan 22
Ann Arbor 17
Beijing 17
Helsinki 16
Lawrence 12
Medford 12
Princeton 12
Rome 12
Toronto 12
Tokyo 11
Brussels 10
New York 10
Wilmington 9
Naples 8
Genzano Di Roma 7
Brno 5
Nanjing 5
Bengaluru 4
Brignano Gera D'adda 4
Cagliari 4
Falkenstein 4
Los Angeles 4
Pisa 4
Washington 4
Copenhagen 3
Dearborn 3
Florence 3
Gurgaon 3
Hangzhou 3
Jiaxing 3
Moscow 3
Piscataway 3
Pistoia 3
Redwood City 3
Trontano 3
Caserta 2
Castel del Giudice 2
Corsico 2
Erlangen 2
Fairfield 2
Gottignies 2
Hebei 2
Istanbul 2
Karaj 2
Ljubljana 2
Nanchang 2
Newcastle Upon Tyne 2
Paullo 2
Pesaro 2
Riyadh 2
Salerno 2
Santa Clara 2
Seattle 2
Shenyang 2
Travaco Siccomario 2
Agra 1
Amsterdam 1
Anzano Del Parco 1
Athens 1
Atlanta 1
Bangalore 1
Bareggio 1
Basel 1
Bereguardo 1
Bologna 1
Brivio 1
Chenzhou 1
Chicago 1
Des Moines 1
Ferrara 1
Gavardo 1
Gunzenhausen 1
Hong Kong 1
Jinan 1
Johannesburg 1
Kish 1
Kunming 1
Mammelzen 1
Norwalk 1
Piateda 1
Pune 1
San Francisco 1
San Mateo 1
Serio 1
Tralee 1
Veruno 1
Warsaw 1
Totale 685
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Nome #
An automatic implementation of ACMG/ClinGen guidelines for constitutional Copy Number Variants annotation and interpretation 142
A comparison of eVai, CADD and VVP variant prediction results on the ICR639 hereditary cancer dataset 101
A semi-supervised learning approach for pan-cancer somatic genomic variant classification 61
Time-Lapse imaging combined with artificial neural-network analysis predicts oocytes and preimplantation embryos developmental competence. 53
A rule-based expert system for automatic implementation of somatic variant clinical interpretation guidelines 53
CardioVAI: An automatic implementation of ACMG-AMP variant interpretation guidelines in the diagnosis of cardiovascular diseases 47
Cytoplasmic movements of the early human embryo: imaging and artificial intelligence to predict blastocyst development 47
Artificial intelligence and machine learning: just a hype or a new opportunity for pharmacometrics? 46
Strategie di Intelligenza Artificiale per l'interpretazione delle varianti genomiche nelle neoplasie ematologiche 42
A continuous-time Markov model approach for modeling myelodysplastic syndromes progression from cross-sectional data 41
Integrated Multi-Omics Analyses in Oncology: A Review of Machine Learning Methods and Tools 41
Understanding user needs for robotics assisted cognitive and physical rehabilitation 40
Evaluating pointwise reliability of machine learning prediction 23
Evaluation of XAI on ALS 6-months mortality prediction 22
Correlation between PD-L1 Expression of Non-Small Cell Lung Cancer and Data from IVIM-DWI Acquired during Magnetic Resonance of the Thorax: Preliminary Results 21
MALDI mass spectrometry imaging shows a gradual change in the proteome landscape during mouse ovarian folliculogenesis 17
A machine learning approach for the detection of incidental findings in genetic testing 13
Performance of an AI algorithm during the different phases of the COVID pandemics: what can we learn from the AI and vice versa 11
A machine learning approach based on ACMG/AMP guidelines for genomic variant classification and prioritization 11
SynthCheck: A Dashboard for Synthetic Data Quality Assessment 8
Bayesian Networks in the Management of Hospital Admissions: A Comparison between Explainable AI and Black Box AI during the Pandemic † 8
A machine learning approach for the detection of incidental findings in genetic testing 8
eVai's Suggested Diagnosis feature: a new AI-based method to increase diagnostic yield in Rare Disease Patients 7
An AI-based approach driven by genotypes and phenotypes to uplift the diagnostic yield of genetic diseases 6
A synthetic dataset of liver disorder patients 6
Predicting and Explaining Risk of Disease Worsening Using Temporal Features in Multiple Sclerosis 6
Forecasting dominance of SARS-CoV-2 lineages by anomaly detection using deep AutoEncoders 5
Why did AI get this one wrong? — Tree-based explanations of machine learning model predictions 5
Dynamic Prediction of Non-Neutral SARS-Cov-2 Variants Using Incremental Machine Learning 5
Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project 4
A Reliable Machine Learning Approach applied to Single-Cell Classification in Acute Myeloid Leukemia 4
CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods 3
Predicting emerging SARS-CoV-2 variants of concern through a One Class dynamic anomaly detection algorithm 2
Totale 909
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Categoria #
all - tutte 3.941
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 3.941
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202051 11 14 0 4 1 2 3 5 1 5 5 0
2020/202165 5 0 0 3 1 5 8 12 17 7 2 5
2021/2022149 7 7 15 17 7 10 2 8 15 11 14 36
2022/2023284 26 23 7 12 20 19 6 15 130 4 13 9
2023/2024359 26 38 19 29 11 46 25 36 3 20 22 84
Totale 909