IRIS
STELLA, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 3.996
AS - Asia 1.560
EU - Europa 1.307
SA - Sud America 424
AF - Africa 73
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 7.366
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Nazione #
US - Stati Uniti d'America 3.929
SG - Singapore 755
BR - Brasile 383
CN - Cina 350
SE - Svezia 260
RU - Federazione Russa 245
IT - Italia 217
HK - Hong Kong 208
DE - Germania 167
FI - Finlandia 96
GB - Regno Unito 93
VN - Vietnam 93
UA - Ucraina 92
IN - India 50
CI - Costa d'Avorio 44
CA - Canada 36
BE - Belgio 28
ID - Indonesia 26
NL - Olanda 22
FR - Francia 20
MX - Messico 20
AR - Argentina 18
BD - Bangladesh 16
AT - Austria 14
ES - Italia 12
JP - Giappone 12
CZ - Repubblica Ceca 10
IE - Irlanda 10
TR - Turchia 10
PL - Polonia 9
ZA - Sudafrica 9
CO - Colombia 7
UZ - Uzbekistan 6
IQ - Iraq 5
KE - Kenya 5
PK - Pakistan 5
SA - Arabia Saudita 5
MA - Marocco 4
XK - ???statistics.table.value.countryCode.XK??? 4
CL - Cile 3
EC - Ecuador 3
ET - Etiopia 3
IR - Iran 3
JM - Giamaica 3
LT - Lituania 3
MY - Malesia 3
AE - Emirati Arabi Uniti 2
AU - Australia 2
DO - Repubblica Dominicana 2
EG - Egitto 2
HN - Honduras 2
KZ - Kazakistan 2
NP - Nepal 2
PE - Perù 2
PS - Palestinian Territory 2
PY - Paraguay 2
RO - Romania 2
VE - Venezuela 2
AL - Albania 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BO - Bolivia 1
BY - Bielorussia 1
CR - Costa Rica 1
DZ - Algeria 1
EE - Estonia 1
GA - Gabon 1
GR - Grecia 1
GY - Guiana 1
HU - Ungheria 1
IL - Israele 1
JO - Giordania 1
LB - Libano 1
NG - Nigeria 1
NI - Nicaragua 1
OM - Oman 1
PR - Porto Rico 1
PT - Portogallo 1
SN - Senegal 1
SR - Suriname 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
UG - Uganda 1
UY - Uruguay 1
Totale 7.366
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Città #
Fairfield 524
Ashburn 457
Singapore 391
Chandler 345
Woodbridge 321
Houston 235
Jacksonville 209
Hong Kong 207
Nyköping 203
Cambridge 185
Seattle 182
Wilmington 160
Ann Arbor 143
Beijing 133
Bari 82
New York 70
Roxbury 68
Munich 65
Lawrence 64
Los Angeles 58
Nanjing 51
Abidjan 44
Dallas 41
Des Moines 40
São Paulo 38
Boardman 37
Princeton 35
Inglewood 34
Ho Chi Minh City 33
Helsinki 29
Brooklyn 24
London 24
Brussels 21
Jakarta 21
San Diego 21
Nanchang 15
Pune 15
Shenyang 15
Turku 15
Buffalo 14
Dong Ket 14
Hanoi 14
Moscow 14
Santa Clara 14
Chennai 13
Jiaxing 13
Montreal 13
Rome 13
Nuremberg 12
Tokyo 12
Belo Horizonte 11
Dearborn 11
Hebei 11
Tianjin 11
Atlanta 10
Dublin 10
Paris 10
Toronto 10
Orem 9
San Francisco 9
Boston 8
Brno 8
Chicago 8
Curitiba 8
Osasco 8
Redwood City 8
Changsha 7
Falls Church 7
Guarulhos 7
The Dalles 7
Waanrode 7
Brasília 6
Council Bluffs 6
Denver 6
Dhaka 6
Foggia 6
Mexico City 6
Mumbai 6
Poplar 6
Santo André 6
Vienna 6
Warsaw 6
Washington 6
Campinas 5
Columbus 5
Falkenstein 5
Frankfurt am Main 5
Guangzhou 5
Haiphong 5
Manchester 5
Nairobi 5
Querétaro 5
Rio de Janeiro 5
Tashkent 5
Acton 4
Amsterdam 4
Ankara 4
Auburn Hills 4
Bauru 4
Betim 4
Totale 5.137
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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. 184
Accurate classification of NF1 gene variants in 84 Italian patients with neurofibromatosis type 1 183
Gastric polyposis and desmoid tumours as a new familial adenomatous polyposis clinical variant associated with APC mutation at the extreme 3′-end 145
Improvement of MEFV gene variants classification to aid treatment decision making in familial Mediterranean fever 144
Analysis of telomere dynamics in peripheral blood cells from patients with lynch syndrome 140
Breakpoint determination of 15 large deletions in Peutz-Jeghers subjects 139
Clinical findings in a family with familial adenomatous polyposis and a missense mutation of the adenomatous polyposis coli gene 136
Anticipation in Lynch Syndrome: Where We Are Where We Go 135
An LKB1 AT-AC intron mutation causes Peutz-Jeghers syndrome via splicing at noncanonical cryptic splice sites 134
Blood-based test for diagnosis and functional subtyping of familial Mediterranean fever 134
Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: Results of an Italian multicenter study 133
A long diagnostic delay in patients with Hereditary Haemorrhagic Telangiectasia: A questionnaire-based retrospective study 130
Cancer family syndrome: cytogenetic investigations, in vitro tetraploidy, and biomarker studies in a large family 125
Establishment and characterization of a highly immunogenic human renal carcinoma cell line 125
Beyond BRCA1/2: Homologous Recombination Repair Genetic Profile in a Large Cohort of Apulian Ovarian Cancers 124
Nine novel APC mutations in Italian FAP patients 122
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 120
A homozygous frameshift mutation in the ESCO2 gene: evidence of intertissue and interindividual variation in NMD efficiency 116
Familial Mediterranean Fever and COVID-19: Friends or Foes? 116
A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP family 115
Population data for 17 Y-chromosome STRs in a sample from Apulia (Southern Italy) 113
Colorectal cancer and the Muir-Torre syndrome in a Gypsy family: a review 109
DEPRESSED LEVEL OF NATURAL-KILLER CELLS IN CANCER FAMILY SYNDROME 109
Functional analysis of LKB1/STK11 mutants and two aberrant isoforms found in Peutz-Jeghers Syndrome patients 106
FAMILIAL ADENOMATOUS POLYPOSIS - IDENTIFICATION OF A NEW FRAMESHIFT MUTATION OF THE APC GENE IN AN ITALIAN FAMILY 104
Germline novel MSH2 deletions and a founder MSH2 deletion associated with anticipation effects in HNPCC 103
The mechanism of alternative splicing of the X-linked NDUFB11 gene of the respiratory chain complex I, impact of rotenone treatment in neuroblastoma cells 103
Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation 103
The mechanism of alternative splicing of the X-linked NDUFB11 gene of the respiratory chain complex I, impact of rotenone treatment in neuroblastoma cells 102
Familial Mediterranean fever: Breaking all the (genetic) rules 101
Survey of KRAS, BRAF and PIK3CA mutational status in 209 consecutive Italian colorectal cancer patients 101
Alternative splicing in colorectal cancer 100
Infertility in carriers of two bisatellited marker chromosomes 99
Relief of transcriptional polarity by a mutation that creates a promoter in the hisG gene of Salmonella typhimurium LT2 97
Linkage studies in Italian families with familial adenomatous polyposis 97
CANCER FAMILY SYNDROME: REPORT ON A GENETIC STUDIES IN A FAMILY 96
Comparison of clinical and demographic features between affected pairs of italian Multiple Sclerosis multiplex families; relation to tumour necrosis factor genomic polymorphisms 95
The hUPF1-NMD factor controls the cellular transcript levels of different genes of complex I of the respiratory chain. 95
Four novel mutations of the APC (adenomatous polyposis coli) gene in FAP patients 94
In-silico analysis of NF1 missense variants in clinvar: Translating variant predictions into variant interpretation and classification 91
EXCLUSION OF THE APC GENE AS THE CAUSE OF A VARIANT FORM OF FAMILIAL ADENOMATOUS POLYPOSIS (FAP) 89
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 88
A Nonsense Mutation in MLH1 Causes Exon-Skipping in Three Unrelated HNPCC Families 87
Mutations in the NDUFS4 gene of mitochondrial complex I alter stability of the splice variants 84
Novel Insights into Autophagy and Prostate Cancer: A Comprehensive Review 84
APC is essential for targeting phosphorylated beta-catenin to the SCFbeta-TrCP ubiquitin ligase 82
Bioinformatica applicata alla consulenza genetica 82
Neurofibromatosis type 1 and melanoma of the iris arising from a dysplastic nevus: A rare yet casual association? 81
Clinical findings in a family with FAP and a missense mutation of APC gene 80
Gut microbiota between environment and genetic background in familial mediterranean fever (Fmf) 80
Clinical presentation and genetic analyses of neurofibromatosis type 1 in independent patients with monoallelic double de novo closely spaced mutations in the NF1 gene 78
The grandfather’s fever 78
The familial adenomatous polyposis region exhibits many different haplotypes 77
Country-level factors dynamics and ABO/Rh blood groups contribution to COVID-19 mortality 73
Esiste un’influenza dei polimorfismi dell’enzima epossi-idrolasi microsomiale(mEH) sui marcatori citogenetici di danno genotossico? 72
Deep Intronic ETFDH Variants Represent a Recurrent Pathogenic Event in Multiple Acyl-CoA Dehydrogenase Deficiency 71
A RARE MSH2 MUTATION CAUSING DEFECTIVE BINDING TO MSH6 NORMAL MSH2 STAINING AND LOSS OF MSH6 IN ADVANCED CANCER STAGE 70
Impact of High-to-Moderate Penetrance Genes on Genetic Testing: Looking over Breast Cancer 69
Laminin alpha2 muscular dystrophy: genotype-phenotype studies of 22 patients 68
Lateralized overgrowth with vascular malformation caused by a somatic PTPN11 pathogenic variant: another piece added to the puzzle of mosaic RASopathies 67
Genetic and clinical features of Familial Mediterranean Fever (FMF) in a homogeneous cohort of patients from south-eastern Italy 66
Renal Cell Carcinoma as a Metabolic Disease: An Update on Main Pathways, Potential Biomarkers, and Therapeutic Targets 66
Metabolomic Approaches for Detection and Identification of Biomarkers and Altered Pathways in Bladder Cancer 62
In silico and in vivo analysis of MLH1 and MSH2 missense mutations shows exon- and tissue-specific effects 61
LOSS OF LKB1 EXPRESSION IS AN EARLY MOLECULAR EVENT IN PROSTATE CARCINOGENESIS 61
Comment on: Improvement of MEFV gene variants classification to aid treatment decision making in familial Mediterranean fever—reply 59
Identification of a new frameshift mutation of the APC gene in an Italian family 55
Large expert-curated database for benchmarking document similarity detection in biomedical literature search 54
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 54
FAMILIAL ADENOMATOUS POLYPOSIS - HETEROGENEITY - REPLY 54
Exclusion of the APC gene as a variant form of familial adenomatous polyposis 53
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Aftershock prediction for high-frequency financial markets' dynamics 45
Site directed mutagenesis of hMLH1 exonic splicing enhancer does not correlate with splicing disruption 45
Clinical implications and molecular pathogenesis in colorectal tumors with microsatellite in stability. 42
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Histopathological characteristics of synovitis in Familial Mediterranean Fever (FMF) 40
Oro-dental manifestations in a pediatric patient affected by helsmoortel-van der Aa syndrome 40
Distinguishing between recent balancing selection and incomplete sweep using deep neural networks 39
Papillary thyroid carcinoma in Peutz-Jeghers syndrome 37
Novel Splice Isoforms of STRADalpha Differentially Affect LKB1 Activity, Complex Assembly and Subcellular Localization 35
Metabolic dysfunction-associated gallstone disease: expecting more from critical care manifestations 34
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Prognostic value of 18q allelic loss and microsatellite instability in colorectal cancer. 27
Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients 26
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Option pricing with non-Gaussian scaling and infinite-state switching volatility 19
The unsolved mystery of MEFV variants variable expressivity in Familial Mediterranean Fever 17
L'impatto delle mutazioni del DNA sul processo di splicing: un'analisi statistica nel contesto del gene BRCA1 17
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Totale 7.590
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Categoria #
all - tutte 35.357
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 35.357
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021376 0 0 0 0 0 26 51 52 53 104 38 52
2021/2022575 31 87 11 17 16 32 33 31 27 68 104 118
2022/2023922 125 100 74 89 99 135 13 117 138 7 14 11
2023/2024300 25 60 11 26 36 88 8 15 1 4 1 25
2024/20251.496 31 16 103 39 50 126 199 130 71 75 219 437
2025/20261.577 464 147 215 324 373 54 0 0 0 0 0 0
Totale 7.590