IRIS
BAGNULO, ROSANNA
 Distribuzione geografica
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Continente #
NA - Nord America 760
EU - Europa 252
AS - Asia 95
Totale 1.107
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Nazione #
US - Stati Uniti d'America 757
SE - Svezia 87
IT - Italia 65
CN - Cina 45
SG - Singapore 29
GB - Regno Unito 25
DE - Germania 19
FI - Finlandia 18
BE - Belgio 12
FR - Francia 12
VN - Vietnam 10
IN - India 7
CZ - Repubblica Ceca 5
CA - Canada 2
LT - Lituania 2
RU - Federazione Russa 2
SI - Slovenia 2
TR - Turchia 2
CH - Svizzera 1
CR - Costa Rica 1
IL - Israele 1
IR - Iran 1
MK - Macedonia 1
PL - Polonia 1
Totale 1.107
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Città #
Chandler 107
Fairfield 103
Ashburn 82
Woodbridge 80
Nyköping 68
Ann Arbor 46
Cambridge 45
Houston 36
Seattle 35
Wilmington 32
Bari 26
Singapore 23
Beijing 16
Helsinki 16
Munich 15
Roxbury 14
Brussels 12
Lawrence 12
New York 12
Brooklyn 10
Dong Ket 10
Nanjing 9
Pune 7
Des Moines 6
Paris 6
Brno 5
Redwood City 5
San Diego 4
Santa Clara 4
Valenzano 4
Inglewood 3
Los Angeles 3
Norwalk 3
Padova 3
Shenyang 3
Washington 3
Boardman 2
Frankfurt am Main 2
Grottaglie 2
Kilburn 2
Ljubljana 2
London 2
Modugno 2
Princeton 2
Rome 2
Shanghai 2
Taranto 2
Toronto 2
Wuhan 2
Albenga 1
Altopascio 1
Bisceglie 1
Chicago 1
Chiswick 1
Guangzhou 1
Gunzenhausen 1
Hebei 1
Hefei 1
Jiaxing 1
Jinan 1
Miami Beach 1
Nanchang 1
Napoli 1
New Bedfont 1
Ningbo 1
Quanzhou 1
Sabz 1
San José 1
Santa Marinella 1
Stimigliano 1
Tel Aviv 1
Tianjin 1
Toulouse 1
Turi 1
Wandsworth 1
Zurich 1
Totale 921
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Nome #
Loss of STK11 expression is an early event in prostate carcinogenesis and predicts therapeutic response to targeted therapy against MAPK/p38. 136
636 Genotoxic damage and dna repair gene polymorphisms in workers exposed to low doses of ionising radiation 131
Accurate classification of NF1 gene variants in 84 Italian patients with neurofibromatosis type 1 116
In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS) 97
Association of autoimmune thyroiditis and celiac disease with Juvenile Polyposis due to 10q23.1q23.31 deletion: Potential role of PI3K/Akt pathway dysregulation 93
Influence of polymorphisms of DNA repair and GST genes on genotoxic damage and mutagen sensitivity in workers occupationally exposed to very low doses of ionizing radiation 81
The longevity SNP rs2802292 uncovered: HSF1 activates stress-dependent expression of FOXO3 through an intronic enhancer. 64
null 63
Old treatments for new genetic conditions: Sirolimus therapy in a child affected by mosaic overgrowth with fibroadipose hyperplasia 61
The first case of congenital myasthenic syndrome caused by a large homozygous deletion in the cterminal region of colq (Collagen like tail subunit of asymmetric acetylcholinesterase) protein 60
Beyond BRCA1/2: Homologous Recombination Repair Genetic Profile in a Large Cohort of Apulian Ovarian Cancers 59
Novel scn5a p.W697x nonsense mutation segregation in a family with brugada syndrome 56
Spectrum of germline pathogenic variants in brca1/2 genes in the apulian southern italy population: Geographic distribution and evidence for targeted genetic testing 34
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 32
Clinical presentation and genetic analyses of neurofibromatosis type 1 in independent patients with monoallelic double de novo closely spaced mutations in the NF1 gene 27
Characterization of the rs2802292 SNP identifies FOXO3A as a modifier locus predicting cancer risk in patients with PJS and PHTS hamartomatous polyposis syndromes 27
Genetic and clinical features of Familial Mediterranean Fever (FMF) in a homogeneous cohort of patients from south-eastern Italy 16
Sigma-2 Receptor Ligand Binding Modulates Association between TSPO and TMEM97 12
Lateralized overgrowth with vascular malformation caused by a somatic PTPN11 pathogenic variant: another piece added to the puzzle of mosaic RASopathies 9
Missense and Non-Missense Lamin A/C Gene Mutations Are Similarly Associated with Major Arrhythmic Cardiac Events: A 20-Year Single-Centre Experience 9
Missense and Non-Missense Lamin A/C Gene Mutations Are Similarly Associated with Major Arrhythmic Cardiac Events: A 20-Year Single-Centre Experience 6
Impact of High-to-Moderate Penetrance Genes on Genetic Testing: Looking over Breast Cancer 4
Deep Intronic ETFDH Variants Represent a Recurrent Pathogenic Event in Multiple Acyl-CoA Dehydrogenase Deficiency 4
Coinheritance of germline mutations in APC and MUTYH genes defines the clinical outcome of adenomatous polyposis syndromes 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
Epidemiology of the disorders of the Pik3ca-related overgrowth spectrum (Pros) 2
Totale 1.205
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Categoria #
all - tutte 6.780
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 6.780
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020129 0 0 0 0 13 8 10 15 20 27 20 16
2020/2021232 5 19 7 22 38 9 32 24 8 31 15 22
2021/2022158 7 7 5 4 3 29 6 12 12 17 27 29
2022/2023268 33 41 17 22 30 39 7 29 34 2 12 2
2023/2024131 6 12 7 17 25 34 7 8 4 1 0 10
2024/2025102 29 4 45 22 2 0 0 0 0 0 0 0
Totale 1.205