IRIS
IACOVIELLO, MATTEO
 Distribuzione geografica
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Continente #
NA - Nord America 210
EU - Europa 82
AS - Asia 18
Totale 310
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Nazione #
US - Stati Uniti d'America 209
SE - Svezia 32
IT - Italia 27
SG - Singapore 9
CN - Cina 5
BE - Belgio 4
CZ - Repubblica Ceca 4
DE - Germania 4
GB - Regno Unito 4
IN - India 4
FR - Francia 2
RU - Federazione Russa 2
SI - Slovenia 2
CA - Canada 1
FI - Finlandia 1
Totale 310
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Città #
Chandler 46
Nyköping 22
Fairfield 17
Bari 13
Ashburn 12
New York 12
Houston 9
Woodbridge 9
Seattle 8
Lawrence 7
Cambridge 6
Singapore 6
Valenzano 6
Des Moines 5
Ann Arbor 4
Brno 4
Brussels 4
Inglewood 4
Munich 4
Roxbury 4
Wilmington 4
Padova 3
Princeton 3
Grottaglie 2
Kolkata 2
Ljubljana 2
Pune 2
San Diego 2
Altopascio 1
Beijing 1
Boardman 1
Helsinki 1
Paris 1
Quanzhou 1
Santa Marinella 1
Stockholm 1
Toronto 1
Wuhu 1
Yiwu 1
Totale 233
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Nome #
Beyond BRCA1/2: Homologous Recombination Repair Genetic Profile in a Large Cohort of Apulian Ovarian Cancers 57
Metformin: Up to Date 55
Thyroid disorders and prognosis in chronic heart failure: A long-term follow-up study 54
Mineralcorticoid Receptor Antagonist Withdrawal for Hyperkalemia and Mortality in Patients with Heart Failure 52
A new case of Smith-Kingsmore syndrome with somatic MTOR pathogenic variant expands the phenotypic spectrum to lateralized overgrowth 33
Evidence of an interaction between FXR1 and GSK3β polymorphisms on levels of Negative Symptoms of Schizophrenia and their response to antipsychotics 33
Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants 30
Genetic and clinical features of Familial Mediterranean Fever (FMF) in a homogeneous cohort of patients from south-eastern Italy 11
Lateralized overgrowth with vascular malformation caused by a somatic PTPN11 pathogenic variant: another piece added to the puzzle of mosaic RASopathies 7
First report of whole CFTR gene duplication in a healthy newborn carrying R74W and V855I variants on the same allele 3
The somatic p.T81dup variant in AKT3 gene underlies a mild cerebral phenotype and expands the spectrum including capillary malformation and lateralized overgrowth 3
Impact of High-to-Moderate Penetrance Genes on Genetic Testing: Looking over Breast Cancer 2
Missense and Non-Missense Lamin A/C Gene Mutations Are Similarly Associated with Major Arrhythmic Cardiac Events: A 20-Year Single-Centre Experience 2
Work-Up and Treatment Strategies for Individuals with PIK3CA-Related Disorders: A Consensus of Experts from the Scientific Committee of the Italian Macrodactyly and PROS Association 1
Totale 343
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Categoria #
all - tutte 2.851
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 2.851
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202011 0 0 0 0 0 0 0 0 0 0 7 4
2020/202155 3 2 4 10 3 2 12 3 6 3 5 2
2021/202271 3 0 2 0 4 7 0 3 9 13 20 10
2022/2023121 12 20 5 4 10 15 1 18 25 2 3 6
2023/202462 3 8 2 6 8 17 0 3 4 1 2 8
2024/202523 22 1 0 0 0 0 0 0 0 0 0 0
Totale 343