IRIS
BAGNULO, ROSANNA
 Distribuzione geografica
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Continente #
NA - Nord America 767
EU - Europa 262
AS - Asia 112
Totale 1.141
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Nazione #
US - Stati Uniti d'America 762
SE - Svezia 87
IT - Italia 66
CN - Cina 47
SG - Singapore 44
GB - Regno Unito 27
FI - Finlandia 26
DE - Germania 17
BE - Belgio 13
FR - Francia 12
VN - Vietnam 10
IN - India 7
CZ - Repubblica Ceca 5
CA - Canada 4
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 1.141
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Città #
Chandler 107
Fairfield 103
Ashburn 82
Woodbridge 80
Nyköping 68
Ann Arbor 46
Cambridge 45
Singapore 38
Houston 36
Seattle 35
Wilmington 32
Bari 27
Helsinki 24
Beijing 16
Roxbury 14
Brussels 13
Munich 13
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
Toronto 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
Wuhan 2
Albenga 1
Altopascio 1
Bisceglie 1
Chicago 1
Chiswick 1
Chongqing 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
North Bergen 1
Ottawa 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 948
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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 133
Accurate classification of NF1 gene variants in 84 Italian patients with neurofibromatosis type 1 117
In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS) 98
Association of autoimmune thyroiditis and celiac disease with Juvenile Polyposis due to 10q23.1q23.31 deletion: Potential role of PI3K/Akt pathway dysregulation 95
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 82
The longevity SNP rs2802292 uncovered: HSF1 activates stress-dependent expression of FOXO3 through an intronic enhancer. 64
null 63
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 63
Beyond BRCA1/2: Homologous Recombination Repair Genetic Profile in a Large Cohort of Apulian Ovarian Cancers 63
Old treatments for new genetic conditions: Sirolimus therapy in a child affected by mosaic overgrowth with fibroadipose hyperplasia 61
Novel scn5a p.W697x nonsense mutation segregation in a family with brugada syndrome 58
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 33
Characterization of the rs2802292 SNP identifies FOXO3A as a modifier locus predicting cancer risk in patients with PJS and PHTS hamartomatous polyposis syndromes 29
Clinical presentation and genetic analyses of neurofibromatosis type 1 in independent patients with monoallelic double de novo closely spaced mutations in the NF1 gene 28
Sigma-2 Receptor Ligand Binding Modulates Association between TSPO and TMEM97 17
Genetic and clinical features of Familial Mediterranean Fever (FMF) in a homogeneous cohort of patients from south-eastern Italy 16
Missense and Non-Missense Lamin A/C Gene Mutations Are Similarly Associated with Major Arrhythmic Cardiac Events: A 20-Year Single-Centre Experience 14
Lateralized overgrowth with vascular malformation caused by a somatic PTPN11 pathogenic variant: another piece added to the puzzle of mosaic RASopathies 11
Impact of High-to-Moderate Penetrance Genes on Genetic Testing: Looking over Breast Cancer 7
Deep Intronic ETFDH Variants Represent a Recurrent Pathogenic Event in Multiple Acyl-CoA Dehydrogenase Deficiency 7
Epidemiology of the disorders of the Pik3ca-related overgrowth spectrum (Pros) 6
The somatic p.T81dup variant in AKT3 gene underlies a mild cerebral phenotype and expands the spectrum including capillary malformation and lateralized overgrowth 5
Coinheritance of germline mutations in APC and MUTYH genes defines the clinical outcome of adenomatous polyposis syndromes 4
Totale 1.244
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Categoria #
all - tutte 7.195
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 7.195
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020116 0 0 0 0 0 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
2024/2025141 26 4 42 22 22 25 0 0 0 0 0 0
Totale 1.244