IRIS
STELLA, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 4.730
AS - Asia 1.958
EU - Europa 1.888
SA - Sud America 524
Continente sconosciuto - Info sul continente non disponibili 230
AF - Africa 106
OC - Oceania 4
Totale 9.440
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Nazione #
US - Stati Uniti d'America 4.615
SG - Singapore 864
IT - Italia 623
BR - Brasile 435
CN - Cina 399
SE - Svezia 262
RU - Federazione Russa 252
HK - Hong Kong 221
DE - Germania 186
VN - Vietnam 139
FI - Finlandia 114
GB - Regno Unito 105
FR - Francia 100
UA - Ucraina 92
IN - India 81
CA - Canada 60
BD - Bangladesh 57
CI - Costa d'Avorio 44
ID - Indonesia 34
NL - Olanda 32
MX - Messico 29
BE - Belgio 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
VE - Venezuela 15
AT - Austria 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
JM - Giamaica 7
AE - Emirati Arabi Uniti 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
NP - Nepal 3
PY - Paraguay 3
UY - Uruguay 3
XK - ???statistics.table.value.countryCode.XK??? 3
AZ - Azerbaigian 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
GP - Guadalupe 2
GT - Guatemala 2
HN - Honduras 2
IL - Israele 2
JO - Giordania 2
KW - Kuwait 2
LY - Libia 2
NI - Nicaragua 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
CW - ???statistics.table.value.countryCode.CW??? 1
CY - Cipro 1
EE - Estonia 1
GA - Gabon 1
GR - Grecia 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
PA - Panama 1
PR - Porto Rico 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
SR - Suriname 1
Totale 9.209
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Città #
Ashburn 542
Fairfield 524
Singapore 478
Chandler 345
Woodbridge 321
Houston 238
Hong Kong 220
San Jose 219
Jacksonville 209
Nyköping 203
Cambridge 185
Seattle 184
Milan 178
Wilmington 161
Ann Arbor 143
Beijing 140
Bari 88
New York 81
Lauterbourg 71
Los Angeles 71
Roxbury 68
Munich 65
Lawrence 63
Rome 63
Boardman 51
Nanjing 51
Helsinki 47
São Paulo 46
Dallas 45
Abidjan 44
Ho Chi Minh City 44
Des Moines 40
Council Bluffs 38
Inglewood 34
Princeton 34
London 30
Santa Clara 30
Columbus 28
Hanoi 27
Brooklyn 24
Montreal 22
Brussels 21
Jakarta 21
San Diego 21
Buffalo 19
Chennai 19
Tokyo 18
Orem 16
Atlanta 15
Moscow 15
Nanchang 15
Pune 15
Shenyang 15
Tashkent 15
Turku 15
Dhaka 14
Dong Ket 14
Falkenstein 14
Belo Horizonte 13
Figino 13
Frankfurt am Main 13
Jiaxing 13
Nuremberg 13
Paris 12
Toronto 12
Dearborn 11
Dublin 11
Hebei 11
Tianjin 11
Chicago 10
Curitiba 10
San Francisco 10
Baghdad 9
Guarulhos 9
Warsaw 9
Boston 8
Brasília 8
Brno 8
Changsha 8
Denver 8
Kingston 8
Kuala Lumpur 8
Mumbai 8
Nairobi 8
Osasco 8
Redwood City 8
Falls Church 7
Haiphong 7
Manchester 7
The Dalles 7
Waanrode 7
Foggia 6
Jeddah 6
Johannesburg 6
Mexico City 6
Naples 6
Poplar 6
Rio de Janeiro 6
Santo André 6
Tunis 6
Totale 6.144
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Nome #
Accurate classification of NF1 gene variants in 84 Italian patients with neurofibromatosis type 1 226
Deep Intronic ETFDH Variants Represent a Recurrent Pathogenic Event in Multiple Acyl-CoA Dehydrogenase Deficiency 225
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 183
Analysis of telomere dynamics in peripheral blood cells from patients with lynch syndrome 180
Beyond BRCA1/2: Homologous Recombination Repair Genetic Profile in a Large Cohort of Apulian Ovarian Cancers 177
Anticipation in Lynch Syndrome: Where We Are Where We Go 170
Gastric polyposis and desmoid tumours as a new familial adenomatous polyposis clinical variant associated with APC mutation at the extreme 3′-end 168
A long diagnostic delay in patients with Hereditary Haemorrhagic Telangiectasia: A questionnaire-based retrospective study 161
Blood-based test for diagnosis and functional subtyping of familial Mediterranean fever 161
Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: Results of an Italian multicenter study 160
An LKB1 AT-AC intron mutation causes Peutz-Jeghers syndrome via splicing at noncanonical cryptic splice sites 158
Clinical findings in a family with familial adenomatous polyposis and a missense mutation of the adenomatous polyposis coli gene 157
Breakpoint determination of 15 large deletions in Peutz-Jeghers subjects 153
Nine novel APC mutations in Italian FAP patients 144
Establishment and characterization of a highly immunogenic human renal carcinoma cell line 144
A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP family 139
Cancer family syndrome: cytogenetic investigations, in vitro tetraploidy, and biomarker studies in a large family 139
A homozygous frameshift mutation in the ESCO2 gene: evidence of intertissue and interindividual variation in NMD efficiency 138
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 134
Colorectal cancer and the Muir-Torre syndrome in a Gypsy family: a review 133
Novel Insights into Autophagy and Prostate Cancer: A Comprehensive Review 127
Familial Mediterranean Fever and COVID-19: Friends or Foes? 126
Functional analysis of LKB1/STK11 mutants and two aberrant isoforms found in Peutz-Jeghers Syndrome patients 124
Survey of KRAS, BRAF and PIK3CA mutational status in 209 consecutive Italian colorectal cancer patients 122
Population data for 17 Y-chromosome STRs in a sample from Apulia (Southern Italy) 122
In-silico analysis of NF1 missense variants in clinvar: Translating variant predictions into variant interpretation and classification 122
Alternative splicing in colorectal cancer 121
Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation 120
Germline novel MSH2 deletions and a founder MSH2 deletion associated with anticipation effects in HNPCC 118
DEPRESSED LEVEL OF NATURAL-KILLER CELLS IN CANCER FAMILY SYNDROME 118
CANCER FAMILY SYNDROME: REPORT ON A GENETIC STUDIES IN A FAMILY 116
Familial Mediterranean fever: Breaking all the (genetic) rules 116
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
The grandfather’s fever 116
Neurofibromatosis type 1 and melanoma of the iris arising from a dysplastic nevus: A rare yet casual association? 116
FAMILIAL ADENOMATOUS POLYPOSIS - IDENTIFICATION OF A NEW FRAMESHIFT MUTATION OF THE APC GENE IN AN ITALIAN FAMILY 114
Relief of transcriptional polarity by a mutation that creates a promoter in the hisG gene of Salmonella typhimurium LT2 113
The hUPF1-NMD factor controls the cellular transcript levels of different genes of complex I of the respiratory chain. 113
Infertility in carriers of two bisatellited marker chromosomes 112
Linkage studies in Italian families with familial adenomatous polyposis 111
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 111
Comparison of clinical and demographic features between affected pairs of italian Multiple Sclerosis multiplex families; relation to tumour necrosis factor genomic polymorphisms 110
Clinical presentation and genetic analyses of neurofibromatosis type 1 in independent patients with monoallelic double de novo closely spaced mutations in the NF1 gene 109
Mutations in the NDUFS4 gene of mitochondrial complex I alter stability of the splice variants 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 109
A Nonsense Mutation in MLH1 Causes Exon-Skipping in Three Unrelated HNPCC Families 108
Gut microbiota between environment and genetic background in familial mediterranean fever (Fmf) 108
EXCLUSION OF THE APC GENE AS THE CAUSE OF A VARIANT FORM OF FAMILIAL ADENOMATOUS POLYPOSIS (FAP) 107
Impact of High-to-Moderate Penetrance Genes on Genetic Testing: Looking over Breast Cancer 106
Renal Cell Carcinoma as a Metabolic Disease: An Update on Main Pathways, Potential Biomarkers, and Therapeutic Targets 104
APC is essential for targeting phosphorylated beta-catenin to the SCFbeta-TrCP ubiquitin ligase 103
Bioinformatica applicata alla consulenza genetica 103
Esiste un’influenza dei polimorfismi dell’enzima epossi-idrolasi microsomiale(mEH) sui marcatori citogenetici di danno genotossico? 103
Lateralized overgrowth with vascular malformation caused by a somatic PTPN11 pathogenic variant: another piece added to the puzzle of mosaic RASopathies 100
Four novel mutations of the APC (adenomatous polyposis coli) gene in FAP patients 100
Genetic and clinical features of Familial Mediterranean Fever (FMF) in a homogeneous cohort of patients from south-eastern Italy 99
Country-level factors dynamics and ABO/Rh blood groups contribution to COVID-19 mortality 98
A RARE MSH2 MUTATION CAUSING DEFECTIVE BINDING TO MSH6 NORMAL MSH2 STAINING AND LOSS OF MSH6 IN ADVANCED CANCER STAGE 94
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 92
Metabolomic Approaches for Detection and Identification of Biomarkers and Altered Pathways in Bladder Cancer 92
Clinical findings in a family with FAP and a missense mutation of APC gene 90
The familial adenomatous polyposis region exhibits many different haplotypes 89
Laminin alpha2 muscular dystrophy: genotype-phenotype studies of 22 patients 79
LOSS OF LKB1 EXPRESSION IS AN EARLY MOLECULAR EVENT IN PROSTATE CARCINOGENESIS 79
In silico and in vivo analysis of MLH1 and MSH2 missense mutations shows exon- and tissue-specific effects 73
Large expert-curated database for benchmarking document similarity detection in biomedical literature search 65
FAMILIAL ADENOMATOUS POLYPOSIS - HETEROGENEITY - REPLY 65
Comment on: Improvement of MEFV gene variants classification to aid treatment decision making in familial Mediterranean fever—reply 65
Histopathological characteristics of synovitis in Familial Mediterranean Fever (FMF) 64
Identification of a new frameshift mutation of the APC gene in an Italian family 64
Distinguishing between recent balancing selection and incomplete sweep using deep neural networks 63
Exclusion of the APC gene as a variant form of familial adenomatous polyposis 62
Oro-dental manifestations in a pediatric patient affected by helsmoortel-van der Aa syndrome 58
Clinical implications and molecular pathogenesis in colorectal tumors with microsatellite in stability. 55
Aftershock prediction for high-frequency financial markets' dynamics 53
Site directed mutagenesis of hMLH1 exonic splicing enhancer does not correlate with splicing disruption 52
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Metabolic dysfunction-associated gallstone disease: expecting more from critical care manifestations 48
Novel Splice Isoforms of STRADalpha Differentially Affect LKB1 Activity, Complex Assembly and Subcellular Localization 45
The unsolved mystery of MEFV variants variable expressivity in Familial Mediterranean Fever 44
L'impatto delle mutazioni del DNA sul processo di splicing: un'analisi statistica nel contesto del gene BRCA1 42
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Prognostic value of 18q allelic loss and microsatellite instability in colorectal cancer. 40
Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients 34
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Option pricing with non-Gaussian scaling and infinite-state switching volatility 26
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Totale 9.440
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Categoria #
all - tutte 40.588
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 40.588
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20263.252 461 146 211 313 371 171 343 116 326 335 119 340
2026/2027190 190 0 0 0 0 0 0 0 0 0 0 0
Totale 9.440