IRIS UniCatt

Tartaglia, Marco
 Distribuzione geografica
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Continente #
NA - Nord America 2.332
EU - Europa 1.660
AS - Asia 1.306
SA - Sud America 263
AF - Africa 43
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 1
Totale 5.607
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Nazione #
US - Stati Uniti d'America 2.294
SG - Singapore 543
PL - Polonia 436
CN - Cina 404
DE - Germania 360
BR - Brasile 220
SE - Svezia 216
UA - Ucraina 160
VN - Vietnam 118
IT - Italia 111
FR - Francia 81
IE - Irlanda 70
GB - Regno Unito 61
FI - Finlandia 43
ID - Indonesia 43
IN - India 42
AT - Austria 36
JP - Giappone 33
RU - Federazione Russa 32
TR - Turchia 23
AR - Argentina 20
IQ - Iraq 20
BD - Bangladesh 14
HK - Hong Kong 14
MX - Messico 14
NL - Olanda 14
CA - Canada 11
ES - Italia 10
IR - Iran 8
CI - Costa d'Avorio 7
SA - Arabia Saudita 7
ZA - Sudafrica 7
BE - Belgio 6
CL - Cile 6
KE - Kenya 6
VE - Venezuela 6
MA - Marocco 5
PK - Pakistan 5
UZ - Uzbekistan 5
CO - Colombia 4
TN - Tunisia 4
AE - Emirati Arabi Uniti 3
BH - Bahrain 3
DO - Repubblica Dominicana 3
DZ - Algeria 3
EC - Ecuador 3
EG - Egitto 3
ET - Etiopia 3
HN - Honduras 3
KR - Corea 3
LT - Lituania 3
PT - Portogallo 3
CH - Svizzera 2
HR - Croazia 2
JM - Giamaica 2
JO - Giordania 2
KZ - Kazakistan 2
MY - Malesia 2
NP - Nepal 2
PA - Panama 2
PY - Paraguay 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
A1 - Anonimo 1
AF - Afghanistan, Repubblica islamica di 1
AL - Albania 1
AM - Armenia 1
AU - Australia 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BO - Bolivia 1
CG - Congo 1
CR - Costa Rica 1
EE - Estonia 1
GR - Grecia 1
GT - Guatemala 1
HU - Ungheria 1
KG - Kirghizistan 1
KW - Kuwait 1
LB - Libano 1
LU - Lussemburgo 1
LV - Lettonia 1
LY - Libia 1
MD - Moldavia 1
MN - Mongolia 1
NG - Nigeria 1
NO - Norvegia 1
PE - Perù 1
QA - Qatar 1
RE - Reunion 1
TT - Trinidad e Tobago 1
XK - ???statistics.table.value.countryCode.XK??? 1
ZW - Zimbabwe 1
Totale 5.607
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Città #
Warsaw 432
Singapore 250
Ashburn 246
Chandler 237
San Jose 169
Fairfield 149
Woodbridge 136
Seattle 108
Jacksonville 101
Nanjing 83
Wilmington 83
San Mateo 71
Dublin 69
Houston 69
Beijing 66
Cambridge 63
Ann Arbor 53
Dearborn 50
Jakarta 40
Lauterbourg 37
Ho Chi Minh City 36
Vienna 34
Boston 32
Redmond 32
Nanchang 30
Hanoi 26
Los Angeles 26
Tokyo 26
Lawrence 25
Frankfurt am Main 23
Hefei 23
New York 23
São Paulo 21
Rome 19
Nürnberg 18
Moscow 17
Buffalo 16
Cattolica 16
Dong Ket 15
Izmir 15
Milan 15
Munich 15
Redwood City 15
Santa Clara 15
Hangzhou 14
London 14
Princeton 14
Chicago 13
Hong Kong 13
Bremen 12
Hebei 11
Jiaxing 11
Brooklyn 10
Council Bluffs 10
Kunming 10
Changsha 9
Guangzhou 9
Helsinki 9
Shanghai 9
Shenyang 9
Baghdad 8
Belo Horizonte 8
Phoenix 8
University Park 8
Abidjan 7
Marseille 7
Norwalk 7
Tianjin 7
Atlanta 6
Brussels 6
Dallas 6
Kent 6
Nairobi 6
Nuremberg 6
Orem 6
Rio de Janeiro 6
Stockholm 6
Amsterdam 5
Boardman 5
Caracas 5
Düsseldorf 5
Lancaster 5
Mountain View 5
Paris 5
Porto Alegre 5
San Diego 5
San Francisco 5
Shahid 5
Tashkent 5
Andover 4
Auburn Hills 4
Chongqing 4
Curitiba 4
Da Nang 4
Dammam 4
Falls Church 4
Johannesburg 4
Newark 4
Ottawa 4
Philadelphia 4
Totale 3.440
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Nome #
CHK1-targeted therapy to deplete DNA replication- stressed, p53-deficient, hyperdiploid colorectal cancer stem cells 438
Tyr1068-phosphorylated epidermal growth factor receptor (EGFR) predicts cancer stem cell targeting by erlotinib in preclinical models of wild-type EGFR lung cancer 332
Tyr1068-phosphorylated epidermal growth factor receptor (EGFR) predicts cancer stem cell targeting by erlotinib in preclinical models of wild-type EGFR lung cancer 305
Noncanonical GLI1 signaling promotes stemness features and in vivo growth in lung adenocarcinoma 292
Noncanonical GLI1 signaling promotes stemness features and in vivo growth in lung adenocarcinoma 280
Enhanced human brain associative plasticity in Costello syndrome 229
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 195
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 182
Long Term Memory Profile of Disorders Associated with Dysregulation of the RAS-MAPK Signaling Cascade. 158
A RESTRICTED SPECTRUM OF NRAS MUTATION CAUSES NOONAN SYNDROME 152
Structural, Functional, and Clinical Characterization of a Novel PTPN11 Mutation Cluster Underlying Noonan Syndrome 140
Dystonia in Costello syndrome 139
Cancer stem cell-based models of colorectal cancer reveal molecular determinants of therapy resistance 137
Novel SEC61G-EGFR fusion gene in pediatric ependymomas discovered by clonal expansion of stem cells in absence of exogenous mitogens 135
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration 132
Diversity parental germline origin, and phenotypic spectrum of de novo HRAS missense changes in Costello syndrome 130
Noonan syndrome: clinical aspects and molecular pathogenesis. 124
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy 120
A Specific Mutational Signature Associated with DNA 8-Oxoguanine Persistence in MUTYH-defective Colorectal Cancer. 118
SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations. 116
Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A 114
GAIN-OF-FUNCTION SOS1 MUTATIONS CAUSE A DISTINCTIVE FORM OF NOONAN SYNDROME. 113
Transcriptional hallmarks of Noonan syndrome and Noonan-like syndrome with loose anagen hair 112
Differential Effects of HRAS Mutation on LTP-Like Activity Induced by Different Protocols of Repetitive Transcranial Magnetic Stimulation 107
Activating PTPN11 mutations play a minor role in pediatric and adult solid tumors 104
Cancer stem cell-based models of colorectal cancer reveal molecular determinants of therapy resistance 103
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome 102
Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype. 100
MUTATION OF SHOC2 PROMOTES ABERRANT PROTEIN N-MYRISTOYLATION AND CAUSES NOONAN-LIKE SUNDROME WITH LOOSE ANAGEN HAIR. 96
Spectrum of MEK1 and MEK2 gene mutations in cardio-facio-cutaneous syndrome and genotype -phenotype correlations. 95
Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotype 94
CRANIOSYNOSTOSIS IN PATIENTS WITH NOONAN SYNDROME CAUSED BY GERMLINE KRAS MUTATIONS 94
NF1 gene mutations represent the major molecular event underlying Neurofibromatosis-Noonan syndrome 92
Exclusion of PTPN1 mutations in Costello syndrome: further evidence for distinct genic etiologies for Noonan, cardio-facio-cutaneous and Costello syndromes 85
GERMLINE BRAF MUTATIONS IN NOONAN, LEOPARD, AND CARDIOFACIOCUTANEOUS SYNDROMES: MOLECULAR DIVERSITY AND ASSOCIATED PHENOTYPIC SPECTRUM 81
Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome 78
DIVERSITY AND FUNCTIONAL CONSEQUENCES OF GERMLINE AND SOMATIC PTPN11 MUTATIONS IN HUMAN DISEASE 78
Proceeding from the 2009 genetic syndromes of the Ras/MAPK pathway: from bedside to bench and back 76
absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome. 76
The italian national genomic strategy: current status, challenges, and future perspectives in clinical practice and public health 4
Multidisciplinary Management of Costello Syndrome: Current Perspectives 2
Totale 5.660
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Categoria #
all - tutte 21.582
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 21.582
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202119 0 0 0 0 0 0 0 0 0 0 0 19
2021/2022319 31 25 5 15 14 17 2 61 13 29 47 60
2022/2023623 84 85 41 87 47 99 21 48 73 12 24 2
2023/2024309 14 103 13 34 6 21 22 8 4 11 31 42
2024/2025560 16 18 49 23 46 19 25 30 74 48 106 106
2025/20261.528 247 45 85 188 237 80 226 89 105 151 48 27
Totale 5.660