IRIS
STELLA, Alessandro
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 5.583
AS - Asia 1.985
EU - Europa 1.975
SA - Sud America 553
Continente sconosciuto - Info sul continente non disponibili 238
AF - Africa 106
OC - Oceania 4
Totale 10.444
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 5.367
SG - Singapore 867
IT - Italia 686
BR - Brasile 452
CN - Cina 402
SE - Svezia 262
RU - Federazione Russa 254
HK - Hong Kong 221
DE - Germania 187
VN - Vietnam 140
FI - Finlandia 114
GB - Regno Unito 114
FR - Francia 101
CA - Canada 100
UA - Ucraina 93
IN - India 81
BD - Bangladesh 67
CI - Costa d'Avorio 44
ID - Indonesia 36
NL - Olanda 35
AR - Argentina 31
MX - Messico 31
BE - Belgio 28
TR - Turchia 22
CO - Colombia 21
IQ - Iraq 21
UZ - Uzbekistan 20
ES - Italia 18
JP - Giappone 18
PL - Polonia 17
VE - Venezuela 16
AT - Austria 15
SA - Arabia Saudita 15
ZA - Sudafrica 14
CR - Costa Rica 12
PK - Pakistan 12
CZ - Repubblica Ceca 11
IE - Irlanda 11
SV - El Salvador 11
CL - Cile 10
EC - Ecuador 10
HN - Honduras 10
MA - Marocco 10
MY - Malesia 10
TN - Tunisia 10
CW - ???statistics.table.value.countryCode.CW??? 9
GP - Guadalupe 9
KE - Kenya 9
TT - Trinidad e Tobago 9
PH - Filippine 8
PR - Porto Rico 8
JM - Giamaica 7
LT - Lituania 7
NI - Nicaragua 7
AE - Emirati Arabi Uniti 6
GT - Guatemala 6
PS - Palestinian Territory 6
EG - Egitto 5
ET - Etiopia 5
IL - Israele 5
AL - Albania 4
AU - Australia 4
PE - Perù 4
HU - Ungheria 3
IR - Iran 3
KG - Kirghizistan 3
KZ - Kazakistan 3
NP - Nepal 3
PY - Paraguay 3
UY - Uruguay 3
XK - ???statistics.table.value.countryCode.XK??? 3
AZ - Azerbaigian 2
BB - Barbados 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
EE - Estonia 2
JO - Giordania 2
KW - Kuwait 2
LY - Libia 2
OM - Oman 2
PT - Portogallo 2
RO - Romania 2
RS - Serbia 2
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BF - Burkina Faso 1
BG - Bulgaria 1
BM - Bermuda 1
BO - Bolivia 1
BY - Bielorussia 1
CY - Cipro 1
GA - Gabon 1
GR - Grecia 1
GY - Guiana 1
HR - Croazia 1
KR - Corea 1
LB - Libano 1
LV - Lettonia 1
MN - Mongolia 1
NG - Nigeria 1
Totale 10.210
Salva come PNG Salva come JPEG
Città #
Ashburn 684
Fairfield 524
Singapore 479
Chandler 345
San Jose 327
Woodbridge 322
Houston 238
Hong Kong 220
Jacksonville 209
Nyköping 203
Cambridge 186
Seattle 184
Milan 183
Wilmington 164
Ann Arbor 143
Beijing 140
Council Bluffs 121
New York 92
Bari 88
Los Angeles 81
Lauterbourg 71
Roxbury 68
Munich 65
Rome 65
Lawrence 63
São Paulo 55
Boardman 53
Nanjing 51
Dallas 50
Helsinki 47
Abidjan 44
Ho Chi Minh City 44
Santa Clara 42
Des Moines 40
Princeton 35
Inglewood 34
Columbus 32
London 31
Hanoi 28
Brooklyn 25
Montreal 24
San Diego 24
Brussels 21
Jakarta 21
Toronto 21
Buffalo 19
Chennai 19
Atlanta 18
Tokyo 18
Orem 16
Moscow 15
Nanchang 15
Pune 15
Shenyang 15
Tashkent 15
Turku 15
Dhaka 14
Dong Ket 14
Falkenstein 14
Figino 14
Belo Horizonte 13
Chicago 13
Frankfurt am Main 13
Jiaxing 13
Nuremberg 13
Paris 12
San Francisco 12
Dearborn 11
Dublin 11
Hebei 11
Tianjin 11
Curitiba 10
North Bergen 10
San Salvador 10
Warsaw 10
Baghdad 9
Denver 9
Guarulhos 9
Kingston 9
Kuala Lumpur 9
Manchester 9
Miami 9
Phoenix 9
San José 9
Willemstad 9
Boston 8
Brasília 8
Brno 8
Changsha 8
Mumbai 8
Nairobi 8
Naples 8
Osasco 8
Redwood City 8
The Dalles 8
Turin 8
Falls Church 7
Haiphong 7
Managua 7
Rio de Janeiro 7
Totale 6.602
Salva come PNG Salva come JPEG
Nome #
Deep Intronic ETFDH Variants Represent a Recurrent Pathogenic Event in Multiple Acyl-CoA Dehydrogenase Deficiency 252
Accurate classification of NF1 gene variants in 84 Italian patients with neurofibromatosis type 1 236
Loss of STK11 expression is an early event in prostate carcinogenesis and predicts therapeutic response to targeted therapy against MAPK/p38. 217
Beyond BRCA1/2: Homologous Recombination Repair Genetic Profile in a Large Cohort of Apulian Ovarian Cancers 198
Improvement of MEFV gene variants classification to aid treatment decision making in familial Mediterranean fever 191
Analysis of telomere dynamics in peripheral blood cells from patients with lynch syndrome 186
Anticipation in Lynch Syndrome: Where We Are Where We Go 185
Gastric polyposis and desmoid tumours as a new familial adenomatous polyposis clinical variant associated with APC mutation at the extreme 3′-end 185
A long diagnostic delay in patients with Hereditary Haemorrhagic Telangiectasia: A questionnaire-based retrospective study 181
Blood-based test for diagnosis and functional subtyping of familial Mediterranean fever 181
Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: Results of an Italian multicenter study 171
Clinical findings in a family with familial adenomatous polyposis and a missense mutation of the adenomatous polyposis coli gene 167
Breakpoint determination of 15 large deletions in Peutz-Jeghers subjects 167
An LKB1 AT-AC intron mutation causes Peutz-Jeghers syndrome via splicing at noncanonical cryptic splice sites 165
Nine novel APC mutations in Italian FAP patients 164
Establishment and characterization of a highly immunogenic human renal carcinoma cell line 151
A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP family 149
A homozygous frameshift mutation in the ESCO2 gene: evidence of intertissue and interindividual variation in NMD efficiency 146
Cancer family syndrome: cytogenetic investigations, in vitro tetraploidy, and biomarker studies in a large family 146
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 142
Colorectal cancer and the Muir-Torre syndrome in a Gypsy family: a review 140
Novel Insights into Autophagy and Prostate Cancer: A Comprehensive Review 140
Familial Mediterranean Fever and COVID-19: Friends or Foes? 136
Bioinformatica applicata alla consulenza genetica 135
Population data for 17 Y-chromosome STRs in a sample from Apulia (Southern Italy) 135
In-silico analysis of NF1 missense variants in clinvar: Translating variant predictions into variant interpretation and classification 134
Germline novel MSH2 deletions and a founder MSH2 deletion associated with anticipation effects in HNPCC 132
Functional analysis of LKB1/STK11 mutants and two aberrant isoforms found in Peutz-Jeghers Syndrome patients 131
Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation 131
The grandfather’s fever 129
Impact of High-to-Moderate Penetrance Genes on Genetic Testing: Looking over Breast Cancer 128
Survey of KRAS, BRAF and PIK3CA mutational status in 209 consecutive Italian colorectal cancer patients 128
Alternative splicing in colorectal cancer 126
The mechanism of alternative splicing of the X-linked NDUFB11 gene of the respiratory chain complex I, impact of rotenone treatment in neuroblastoma cells 126
Esiste un’influenza dei polimorfismi dell’enzima epossi-idrolasi microsomiale(mEH) sui marcatori citogenetici di danno genotossico? 126
Neurofibromatosis type 1 and melanoma of the iris arising from a dysplastic nevus: A rare yet casual association? 125
CANCER FAMILY SYNDROME: REPORT ON A GENETIC STUDIES IN A FAMILY 124
Familial Mediterranean fever: Breaking all the (genetic) rules 124
DEPRESSED LEVEL OF NATURAL-KILLER CELLS IN CANCER FAMILY SYNDROME 123
LOSS OF LKB1 EXPRESSION IS AN EARLY MOLECULAR EVENT IN PROSTATE CARCINOGENESIS 123
EXCLUSION OF THE APC GENE AS THE CAUSE OF A VARIANT FORM OF FAMILIAL ADENOMATOUS POLYPOSIS (FAP) 122
Gut microbiota between environment and genetic background in familial mediterranean fever (Fmf) 122
Comparison of clinical and demographic features between affected pairs of italian Multiple Sclerosis multiplex families; relation to tumour necrosis factor genomic polymorphisms 121
Clinical presentation and genetic analyses of neurofibromatosis type 1 in independent patients with monoallelic double de novo closely spaced mutations in the NF1 gene 120
Relief of transcriptional polarity by a mutation that creates a promoter in the hisG gene of Salmonella typhimurium LT2 120
FAMILIAL ADENOMATOUS POLYPOSIS - IDENTIFICATION OF A NEW FRAMESHIFT MUTATION OF THE APC GENE IN AN ITALIAN FAMILY 120
A Nonsense Mutation in MLH1 Causes Exon-Skipping in Three Unrelated HNPCC Families 120
Infertility in carriers of two bisatellited marker chromosomes 119
The hUPF1-NMD factor controls the cellular transcript levels of different genes of complex I of the respiratory chain. 119
The mechanism of alternative splicing of the X-linked NDUFB11 gene of the respiratory chain complex I, impact of rotenone treatment in neuroblastoma cells 118
Linkage studies in Italian families with familial adenomatous polyposis 117
Mutations in the NDUFS4 gene of mitochondrial complex I alter stability of the splice variants 117
APC is essential for targeting phosphorylated beta-catenin to the SCFbeta-TrCP ubiquitin ligase 117
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 116
Renal Cell Carcinoma as a Metabolic Disease: An Update on Main Pathways, Potential Biomarkers, and Therapeutic Targets 111
Country-level factors dynamics and ABO/Rh blood groups contribution to COVID-19 mortality 111
Genetic and clinical features of Familial Mediterranean Fever (FMF) in a homogeneous cohort of patients from south-eastern Italy 110
Lateralized overgrowth with vascular malformation caused by a somatic PTPN11 pathogenic variant: another piece added to the puzzle of mosaic RASopathies 107
A RARE MSH2 MUTATION CAUSING DEFECTIVE BINDING TO MSH6 NORMAL MSH2 STAINING AND LOSS OF MSH6 IN ADVANCED CANCER STAGE 107
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 106
Four novel mutations of the APC (adenomatous polyposis coli) gene in FAP patients 105
Metabolomic Approaches for Detection and Identification of Biomarkers and Altered Pathways in Bladder Cancer 104
Clinical findings in a family with FAP and a missense mutation of APC gene 102
FAMILIAL ADENOMATOUS POLYPOSIS - HETEROGENEITY - REPLY 101
The familial adenomatous polyposis region exhibits many different haplotypes 96
Laminin alpha2 muscular dystrophy: genotype-phenotype studies of 22 patients 89
Large expert-curated database for benchmarking document similarity detection in biomedical literature search 83
In silico and in vivo analysis of MLH1 and MSH2 missense mutations shows exon- and tissue-specific effects 81
Identification of a new frameshift mutation of the APC gene in an Italian family 80
Distinguishing between recent balancing selection and incomplete sweep using deep neural networks 78
Exclusion of the APC gene as a variant form of familial adenomatous polyposis 74
Histopathological characteristics of synovitis in Familial Mediterranean Fever (FMF) 72
Comment on: Improvement of MEFV gene variants classification to aid treatment decision making in familial Mediterranean fever—reply 70
Oro-dental manifestations in a pediatric patient affected by helsmoortel-van der Aa syndrome 68
Aftershock prediction for high-frequency financial markets' dynamics 66
Clinical implications and molecular pathogenesis in colorectal tumors with microsatellite in stability. 63
Metabolic dysfunction-associated gallstone disease: expecting more from critical care manifestations 60
The unsolved mystery of MEFV variants variable expressivity in Familial Mediterranean Fever 58
Novel Splice Isoforms of STRADalpha Differentially Affect LKB1 Activity, Complex Assembly and Subcellular Localization 57
Site directed mutagenesis of hMLH1 exonic splicing enhancer does not correlate with splicing disruption 56
L'impatto delle mutazioni del DNA sul processo di splicing: un'analisi statistica nel contesto del gene BRCA1 54
null 50
Prognostic value of 18q allelic loss and microsatellite instability in colorectal cancer. 49
Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients 42
null 41
Option pricing with non-Gaussian scaling and infinite-state switching volatility 36
null 30
null 27
null 23
null 17
null 16
Totale 10.444
Salva come PNG Salva come JPEG
Categoria #
all - tutte 44.192
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 44.192
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022429 0 0 0 0 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
2025/20263.252 461 146 211 313 371 171 343 116 326 335 119 340
2026/20271.194 199 134 372 455 34 0 0 0 0 0 0 0
Totale 10.444