IRIS
STELLA, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 4.554
AS - Asia 1.946
EU - Europa 1.584
SA - Sud America 519
AF - Africa 106
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 3
Totale 8.716
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Nazione #
US - Stati Uniti d'America 4.451
SG - Singapore 862
BR - Brasile 431
CN - Cina 395
IT - Italia 328
SE - Svezia 262
RU - Federazione Russa 252
HK - Hong Kong 221
DE - Germania 186
VN - Vietnam 139
FI - Finlandia 114
GB - Regno Unito 101
FR - Francia 98
UA - Ucraina 92
IN - India 81
CA - Canada 53
BD - Bangladesh 52
CI - Costa d'Avorio 44
ID - Indonesia 34
NL - Olanda 29
BE - Belgio 28
MX - Messico 28
AR - Argentina 27
IQ - Iraq 21
TR - Turchia 21
UZ - Uzbekistan 20
ES - Italia 18
JP - Giappone 18
PL - Polonia 16
CO - Colombia 15
SA - Arabia Saudita 15
AT - Austria 14
VE - Venezuela 14
ZA - Sudafrica 14
CZ - Repubblica Ceca 11
IE - Irlanda 11
PK - Pakistan 11
CL - Cile 10
MA - Marocco 10
TN - Tunisia 10
EC - Ecuador 9
KE - Kenya 9
MY - Malesia 9
PH - Filippine 8
AE - Emirati Arabi Uniti 6
JM - Giamaica 6
PS - Palestinian Territory 6
CR - Costa Rica 5
EG - Egitto 5
ET - Etiopia 5
AL - Albania 4
AU - Australia 4
LT - Lituania 4
PE - Perù 4
HU - Ungheria 3
IR - Iran 3
KZ - Kazakistan 3
PY - Paraguay 3
UY - Uruguay 3
XK - ???statistics.table.value.countryCode.XK??? 3
AZ - Azerbaigian 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
HN - Honduras 2
IL - Israele 2
JO - Giordania 2
KW - Kuwait 2
LY - Libia 2
NP - Nepal 2
OM - Oman 2
PT - Portogallo 2
RO - Romania 2
RS - Serbia 2
AM - Armenia 1
BB - Barbados 1
BF - Burkina Faso 1
BG - Bulgaria 1
BO - Bolivia 1
BY - Bielorussia 1
CY - Cipro 1
EE - Estonia 1
GA - Gabon 1
GP - Guadalupe 1
GR - Grecia 1
GT - Guatemala 1
GY - Guiana 1
HR - Croazia 1
KG - Kirghizistan 1
KR - Corea 1
LB - Libano 1
LV - Lettonia 1
MN - Mongolia 1
NG - Nigeria 1
NI - Nicaragua 1
PA - Panama 1
PR - Porto Rico 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
SR - Suriname 1
TH - Thailandia 1
Totale 8.712
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Città #
Fairfield 524
Ashburn 523
Singapore 477
Chandler 345
Woodbridge 321
Houston 238
Hong Kong 220
San Jose 219
Jacksonville 209
Nyköping 203
Cambridge 185
Seattle 183
Wilmington 160
Ann Arbor 143
Beijing 139
Bari 85
New York 80
Lauterbourg 71
Los Angeles 69
Roxbury 68
Munich 65
Lawrence 63
Boardman 51
Nanjing 51
Helsinki 47
São Paulo 46
Abidjan 44
Ho Chi Minh City 44
Dallas 43
Des Moines 40
Council Bluffs 38
Inglewood 34
Princeton 34
London 29
Hanoi 27
Santa Clara 26
Brooklyn 24
Brussels 21
Jakarta 21
Montreal 21
San Diego 21
Buffalo 19
Chennai 19
Tokyo 18
Orem 16
Moscow 15
Nanchang 15
Pune 15
Shenyang 15
Tashkent 15
Turku 15
Dhaka 14
Dong Ket 14
Falkenstein 14
Rome 14
Atlanta 13
Belo Horizonte 13
Frankfurt am Main 13
Jiaxing 13
Nuremberg 13
Paris 12
Toronto 12
Dearborn 11
Dublin 11
Hebei 11
Milan 11
Tianjin 11
Chicago 10
Curitiba 10
San Francisco 10
Baghdad 9
Warsaw 9
Boston 8
Brasília 8
Brno 8
Changsha 8
Guarulhos 8
Kuala Lumpur 8
Mumbai 8
Nairobi 8
Osasco 8
Redwood City 8
Denver 7
Falls Church 7
Haiphong 7
Kingston 7
Manchester 7
The Dalles 7
Waanrode 7
Columbus 6
Foggia 6
Jeddah 6
Johannesburg 6
Mexico City 6
Poplar 6
Rio de Janeiro 6
Santo André 6
Tunis 6
Vienna 6
Washington 6
Totale 5.857
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Nome #
Accurate classification of NF1 gene variants in 84 Italian patients with neurofibromatosis type 1 214
Loss of STK11 expression is an early event in prostate carcinogenesis and predicts therapeutic response to targeted therapy against MAPK/p38. 203
Improvement of MEFV gene variants classification to aid treatment decision making in familial Mediterranean fever 176
Analysis of telomere dynamics in peripheral blood cells from patients with lynch syndrome 174
Beyond BRCA1/2: Homologous Recombination Repair Genetic Profile in a Large Cohort of Apulian Ovarian Cancers 165
Gastric polyposis and desmoid tumours as a new familial adenomatous polyposis clinical variant associated with APC mutation at the extreme 3′-end 163
Anticipation in Lynch Syndrome: Where We Are Where We Go 158
Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: Results of an Italian multicenter study 155
A long diagnostic delay in patients with Hereditary Haemorrhagic Telangiectasia: A questionnaire-based retrospective study 154
Blood-based test for diagnosis and functional subtyping of familial Mediterranean fever 153
Breakpoint determination of 15 large deletions in Peutz-Jeghers subjects 152
Clinical findings in a family with familial adenomatous polyposis and a missense mutation of the adenomatous polyposis coli gene 151
An LKB1 AT-AC intron mutation causes Peutz-Jeghers syndrome via splicing at noncanonical cryptic splice sites 150
Cancer family syndrome: cytogenetic investigations, in vitro tetraploidy, and biomarker studies in a large family 138
A homozygous frameshift mutation in the ESCO2 gene: evidence of intertissue and interindividual variation in NMD efficiency 137
Nine novel APC mutations in Italian FAP patients 135
Establishment and characterization of a highly immunogenic human renal carcinoma cell line 135
A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP family 132
Molecular and Functional Characterization of Three Different Postzygotic Mutations in PIK3CA-Related Overgrowth Spectrum (PROS) Patients: Effects on PI3K/AKT/mTOR Signaling and Sensitivity to PIK3 Inhibitors 131
Familial Mediterranean Fever and COVID-19: Friends or Foes? 125
Colorectal cancer and the Muir-Torre syndrome in a Gypsy family: a review 123
Population data for 17 Y-chromosome STRs in a sample from Apulia (Southern Italy) 122
Alternative splicing in colorectal cancer 119
In-silico analysis of NF1 missense variants in clinvar: Translating variant predictions into variant interpretation and classification 119
Functional analysis of LKB1/STK11 mutants and two aberrant isoforms found in Peutz-Jeghers Syndrome patients 117
DEPRESSED LEVEL OF NATURAL-KILLER CELLS IN CANCER FAMILY SYNDROME 117
Deep Intronic ETFDH Variants Represent a Recurrent Pathogenic Event in Multiple Acyl-CoA Dehydrogenase Deficiency 117
The mechanism of alternative splicing of the X-linked NDUFB11 gene of the respiratory chain complex I, impact of rotenone treatment in neuroblastoma cells 116
Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation 115
Novel Insights into Autophagy and Prostate Cancer: A Comprehensive Review 115
Familial Mediterranean fever: Breaking all the (genetic) rules 114
FAMILIAL ADENOMATOUS POLYPOSIS - IDENTIFICATION OF A NEW FRAMESHIFT MUTATION OF THE APC GENE IN AN ITALIAN FAMILY 113
Neurofibromatosis type 1 and melanoma of the iris arising from a dysplastic nevus: A rare yet casual association? 113
Survey of KRAS, BRAF and PIK3CA mutational status in 209 consecutive Italian colorectal cancer patients 112
Infertility in carriers of two bisatellited marker chromosomes 111
CANCER FAMILY SYNDROME: REPORT ON A GENETIC STUDIES IN A FAMILY 110
The recurrent SETBP1 c.2608G > A, p.(Gly870Ser) variant in a patient with Schinzel-Giedion syndrome: an illustrative case of the utility of whole exome sequencing in a critically ill neonate 110
Germline novel MSH2 deletions and a founder MSH2 deletion associated with anticipation effects in HNPCC 109
The hUPF1-NMD factor controls the cellular transcript levels of different genes of complex I of the respiratory chain. 109
The mechanism of alternative splicing of the X-linked NDUFB11 gene of the respiratory chain complex I, impact of rotenone treatment in neuroblastoma cells 108
The grandfather’s fever 107
Relief of transcriptional polarity by a mutation that creates a promoter in the hisG gene of Salmonella typhimurium LT2 106
Linkage studies in Italian families with familial adenomatous polyposis 106
Comparison of clinical and demographic features between affected pairs of italian Multiple Sclerosis multiplex families; relation to tumour necrosis factor genomic polymorphisms 104
A Nonsense Mutation in MLH1 Causes Exon-Skipping in Three Unrelated HNPCC Families 102
Esiste un’influenza dei polimorfismi dell’enzima epossi-idrolasi microsomiale(mEH) sui marcatori citogenetici di danno genotossico? 102
Gut microbiota between environment and genetic background in familial mediterranean fever (Fmf) 102
Clinical presentation and genetic analyses of neurofibromatosis type 1 in independent patients with monoallelic double de novo closely spaced mutations in the NF1 gene 101
Mutations in the NDUFS4 gene of mitochondrial complex I alter stability of the splice variants 101
EXCLUSION OF THE APC GENE AS THE CAUSE OF A VARIANT FORM OF FAMILIAL ADENOMATOUS POLYPOSIS (FAP) 100
Four novel mutations of the APC (adenomatous polyposis coli) gene in FAP patients 99
Impact of High-to-Moderate Penetrance Genes on Genetic Testing: Looking over Breast Cancer 98
Bioinformatica applicata alla consulenza genetica 98
APC is essential for targeting phosphorylated beta-catenin to the SCFbeta-TrCP ubiquitin ligase 97
Genetic and clinical features of Familial Mediterranean Fever (FMF) in a homogeneous cohort of patients from south-eastern Italy 96
Renal Cell Carcinoma as a Metabolic Disease: An Update on Main Pathways, Potential Biomarkers, and Therapeutic Targets 93
Country-level factors dynamics and ABO/Rh blood groups contribution to COVID-19 mortality 91
Lateralized overgrowth with vascular malformation caused by a somatic PTPN11 pathogenic variant: another piece added to the puzzle of mosaic RASopathies 90
Clinical findings in a family with FAP and a missense mutation of APC gene 89
The familial adenomatous polyposis region exhibits many different haplotypes 87
A RARE MSH2 MUTATION CAUSING DEFECTIVE BINDING TO MSH6 NORMAL MSH2 STAINING AND LOSS OF MSH6 IN ADVANCED CANCER STAGE 86
Metabolomic Approaches for Detection and Identification of Biomarkers and Altered Pathways in Bladder Cancer 85
Intraabdominal sporadic desmoid tumors and inflammation: an updated literature review and presentation and insights on pathogenesis of synchronous sporadic mesenteric desmoid tumors occurring after surgery for necrotizing pancreatitis 84
Laminin alpha2 muscular dystrophy: genotype-phenotype studies of 22 patients 79
LOSS OF LKB1 EXPRESSION IS AN EARLY MOLECULAR EVENT IN PROSTATE CARCINOGENESIS 78
In silico and in vivo analysis of MLH1 and MSH2 missense mutations shows exon- and tissue-specific effects 70
Large expert-curated database for benchmarking document similarity detection in biomedical literature search 65
Comment on: Improvement of MEFV gene variants classification to aid treatment decision making in familial Mediterranean fever—reply 64
FAMILIAL ADENOMATOUS POLYPOSIS - HETEROGENEITY - REPLY 63
Exclusion of the APC gene as a variant form of familial adenomatous polyposis 60
Identification of a new frameshift mutation of the APC gene in an Italian family 59
Oro-dental manifestations in a pediatric patient affected by helsmoortel-van der Aa syndrome 58
Distinguishing between recent balancing selection and incomplete sweep using deep neural networks 57
Histopathological characteristics of synovitis in Familial Mediterranean Fever (FMF) 56
Aftershock prediction for high-frequency financial markets' dynamics 53
Site directed mutagenesis of hMLH1 exonic splicing enhancer does not correlate with splicing disruption 51
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Clinical implications and molecular pathogenesis in colorectal tumors with microsatellite in stability. 50
Metabolic dysfunction-associated gallstone disease: expecting more from critical care manifestations 46
Novel Splice Isoforms of STRADalpha Differentially Affect LKB1 Activity, Complex Assembly and Subcellular Localization 45
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The unsolved mystery of MEFV variants variable expressivity in Familial Mediterranean Fever 40
L'impatto delle mutazioni del DNA sul processo di splicing: un'analisi statistica nel contesto del gene BRCA1 36
Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients 34
Prognostic value of 18q allelic loss and microsatellite instability in colorectal cancer. 34
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Option pricing with non-Gaussian scaling and infinite-state switching volatility 26
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Totale 8.942
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Categoria #
all - tutte 38.984
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 38.984
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202152 0 0 0 0 0 0 0 0 0 0 0 52
2021/2022575 31 87 11 17 16 32 33 31 27 68 104 118
2022/2023920 123 100 74 89 99 135 13 117 138 7 14 11
2023/2024300 25 60 11 26 36 88 8 15 1 4 1 25
2024/20251.483 31 16 102 39 50 125 198 129 70 75 218 430
2025/20262.944 461 146 211 313 371 171 343 116 326 335 119 32
Totale 8.942