STELLA, Alessandro
 Distribuzione geografica
Continente #
NA - Nord America 3.380
EU - Europa 836
AS - Asia 247
OC - Oceania 2
SA - Sud America 2
AF - Africa 1
Totale 4.468
Nazione #
US - Stati Uniti d'America 3.377
SE - Svezia 269
CN - Cina 205
IT - Italia 159
UA - Ucraina 88
DE - Germania 74
GB - Regno Unito 73
FI - Finlandia 63
BE - Belgio 48
IN - India 23
NL - Olanda 14
VN - Vietnam 14
FR - Francia 12
IE - Irlanda 12
RU - Federazione Russa 10
CZ - Repubblica Ceca 6
AT - Austria 2
AU - Australia 2
BG - Bulgaria 2
CA - Canada 2
CL - Cile 2
HU - Ungheria 2
CR - Costa Rica 1
ES - Italia 1
IR - Iran 1
KE - Kenya 1
MY - Malesia 1
NP - Nepal 1
PH - Filippine 1
RO - Romania 1
TR - Turchia 1
Totale 4.468
Città #
Fairfield 531
Chandler 358
Woodbridge 326
Ashburn 273
Houston 238
Nyköping 212
Jacksonville 211
Cambridge 187
Seattle 185
Wilmington 167
Ann Arbor 144
Bari 74
Roxbury 68
Lawrence 67
Beijing 66
Nanjing 52
New York 48
Brussels 41
Des Moines 40
Princeton 35
Inglewood 34
Boardman 31
London 22
San Diego 21
Brooklyn 16
Nanchang 15
Pune 15
Dong Ket 14
Jiaxing 14
Shenyang 14
Dublin 12
Dearborn 11
Hebei 11
Helsinki 11
Tianjin 11
Paris 10
Redwood City 8
Falls Church 7
Waanrode 7
Washington 7
Brno 6
Foggia 6
Rome 6
Acton 5
Changsha 5
Auburn Hills 4
Guangzhou 4
Kilburn 4
Napoli 4
Norwalk 4
Mumbai 3
Prescot 3
San Francisco 3
Caerphilly 2
Capriati A Volturno 2
Grottaglie 2
Hangzhou 2
Hefei 2
Jinan 2
Melbourne 2
Modugno 2
San Mateo 2
Sofia 2
Valenzano 2
Vienna 2
Ahmedabad 1
Albenga 1
Augusta 1
Bergamo 1
Bucharest 1
Budapest 1
Chaoyang 1
Chicago 1
Chiswick 1
Costa Mesa 1
Darlington 1
Ercolano 1
Falkenstein 1
Florence 1
Genova 1
Haikou 1
Hounslow 1
Imbersago 1
Islington 1
Kathmandu 1
Kuala Lumpur 1
Kunming 1
Lanzhou 1
Las Vegas 1
Leawood 1
Linköping 1
Los Angeles 1
Manila 1
Markham 1
Martina Franca 1
Milan 1
Modena 1
Molfetta 1
Nairobi 1
Padova 1
Totale 3.730
Nome #
Loss of STK11 expression is an early event in prostate carcinogenesis and predicts therapeutic response to targeted therapy against MAPK/p38. 135
Accurate classification of NF1 gene variants in 84 Italian patients with neurofibromatosis type 1 116
Improvement of MEFV gene variants classification to aid treatment decision making in familial Mediterranean fever 103
Analysis of telomere dynamics in peripheral blood cells from patients with lynch syndrome 99
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 98
Clinical findings in a family with familial adenomatous polyposis and a missense mutation of the adenomatous polyposis coli gene 97
An LKB1 AT-AC intron mutation causes Peutz-Jeghers syndrome via splicing at noncanonical cryptic splice sites 94
Breakpoint determination of 15 large deletions in Peutz-Jeghers subjects 93
Colorectal cancer and the Muir-Torre syndrome in a Gypsy family: a review 92
Nine novel APC mutations in Italian FAP patients 90
Familial Mediterranean Fever and COVID-19: Friends or Foes? 88
Anticipation in Lynch Syndrome: Where We Are Where We Go 87
DEPRESSED LEVEL OF NATURAL-KILLER CELLS IN CANCER FAMILY SYNDROME 87
Population data for 17 Y-chromosome STRs in a sample from Apulia (Southern Italy) 86
Gastric polyposis and desmoid tumours as a new familial adenomatous polyposis clinical variant associated with APC mutation at the extreme 3′-end 85
Functional analysis of LKB1/STK11 mutants and two aberrant isoforms found in Peutz-Jeghers Syndrome patients 84
Survey of KRAS, BRAF and PIK3CA mutational status in 209 consecutive Italian colorectal cancer patients 83
Establishment and characterization of a highly immunogenic human renal carcinoma cell line 81
Cancer family syndrome: cytogenetic investigations, in vitro tetraploidy, and biomarker studies in a large family 80
Relief of transcriptional polarity by a mutation that creates a promoter in the hisG gene of Salmonella typhimurium LT2 79
FAMILIAL ADENOMATOUS POLYPOSIS - IDENTIFICATION OF A NEW FRAMESHIFT MUTATION OF THE APC GENE IN AN ITALIAN FAMILY 77
The mechanism of alternative splicing of the X-linked NDUFB11 gene of the respiratory chain complex I, impact of rotenone treatment in neuroblastoma cells 77
Infertility in carriers of two bisatellited marker chromosomes 76
A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP family 75
The mechanism of alternative splicing of the X-linked NDUFB11 gene of the respiratory chain complex I, impact of rotenone treatment in neuroblastoma cells 75
Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: Results of an Italian multicenter study 75
Linkage studies in Italian families with familial adenomatous polyposis 74
Comparison of clinical and demographic features between affected pairs of italian Multiple Sclerosis multiplex families; relation to tumour necrosis factor genomic polymorphisms 73
Germline novel MSH2 deletions and a founder MSH2 deletion associated with anticipation effects in HNPCC 72
Blood-based test for diagnosis and functional subtyping of familial Mediterranean fever 71
Four novel mutations of the APC (adenomatous polyposis coli) gene in FAP patients 70
Familial Mediterranean fever: Breaking all the (genetic) rules 70
A long diagnostic delay in patients with Hereditary Haemorrhagic Telangiectasia: A questionnaire-based retrospective study 68
EXCLUSION OF THE APC GENE AS THE CAUSE OF A VARIANT FORM OF FAMILIAL ADENOMATOUS POLYPOSIS (FAP) 66
The hUPF1-NMD factor controls the cellular transcript levels of different genes of complex I of the respiratory chain. 66
Alternative splicing in colorectal cancer 65
Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation 65
A homozygous frameshift mutation in the ESCO2 gene: evidence of intertissue and interindividual variation in NMD efficiency 61
Bioinformatica applicata alla consulenza genetica 54
Beyond BRCA1/2: Homologous Recombination Repair Genetic Profile in a Large Cohort of Apulian Ovarian Cancers 54
Clinical findings in a family with FAP and a missense mutation of APC gene 53
Mutations in the NDUFS4 gene of mitochondrial complex I alter stability of the splice variants 53
The familial adenomatous polyposis region exhibits many different haplotypes 53
CANCER FAMILY SYNDROME: REPORT ON A GENETIC STUDIES IN A FAMILY 51
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Esiste un’influenza dei polimorfismi dell’enzima epossi-idrolasi microsomiale(mEH) sui marcatori citogenetici di danno genotossico? 49
Laminin alpha2 muscular dystrophy: genotype-phenotype studies of 22 patients 48
Gut microbiota between environment and genetic background in familial mediterranean fever (Fmf) 48
A Nonsense Mutation in MLH1 Causes Exon-Skipping in Three Unrelated HNPCC Families 47
APC is essential for targeting phosphorylated beta-catenin to the SCFbeta-TrCP ubiquitin ligase 46
In silico and in vivo analysis of MLH1 and MSH2 missense mutations shows exon- and tissue-specific effects 45
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 45
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Identification of a new frameshift mutation of the APC gene in an Italian family 41
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Comment on: Improvement of MEFV gene variants classification to aid treatment decision making in familial Mediterranean fever—reply 39
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Exclusion of the APC gene as a variant form of familial adenomatous polyposis 34
FAMILIAL ADENOMATOUS POLYPOSIS - HETEROGENEITY - REPLY 30
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Clinical presentation and genetic analyses of neurofibromatosis type 1 in independent patients with monoallelic double de novo closely spaced mutations in the NF1 gene 26
Country-level factors dynamics and ABO/Rh blood groups contribution to COVID-19 mortality 26
Site directed mutagenesis of hMLH1 exonic splicing enhancer does not correlate with splicing disruption 25
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The grandfather’s fever 23
Large expert-curated database for benchmarking document similarity detection in biomedical literature search 22
In-silico analysis of NF1 missense variants in clinvar: Translating variant predictions into variant interpretation and classification 22
Clinical implications and molecular pathogenesis in colorectal tumors with microsatellite in stability. 20
Neurofibromatosis type 1 and melanoma of the iris arising from a dysplastic nevus: A rare yet casual association? 18
LOSS OF LKB1 EXPRESSION IS AN EARLY MOLECULAR EVENT IN PROSTATE CARCINOGENESIS 18
Metabolomic Approaches for Detection and Identification of Biomarkers and Altered Pathways in Bladder Cancer 18
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Novel Insights into Autophagy and Prostate Cancer: A Comprehensive Review 15
Distinguishing between recent balancing selection and incomplete sweep using deep neural networks 13
A RARE MSH2 MUTATION CAUSING DEFECTIVE BINDING TO MSH6 NORMAL MSH2 STAINING AND LOSS OF MSH6 IN ADVANCED CANCER STAGE 12
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 11
Renal Cell Carcinoma as a Metabolic Disease: An Update on Main Pathways, Potential Biomarkers, and Therapeutic Targets 10
Oro-dental manifestations in a pediatric patient affected by helsmoortel-van der aa syndrome 10
Novel Splice Isoforms of STRADalpha Differentially Affect LKB1 Activity, Complex Assembly and Subcellular Localization 9
Genetic and clinical features of Familial Mediterranean Fever (FMF) in a homogeneous cohort of patients from south-eastern Italy 7
Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients 6
Prognostic value of 18q allelic loss and microsatellite instability in colorectal cancer. 6
Aftershock prediction for high-frequency financial markets' dynamics 5
Lateralized overgrowth with vascular malformation caused by a somatic PTPN11 pathogenic variant: another piece added to the puzzle of mosaic RASopathies 5
Option pricing with non-Gaussian scaling and infinite-state switching volatility 2
Histopathological characteristics of synovitis in Familial Mediterranean Fever (FMF) 2
Papillary thyroid carcinoma in Peutz-Jeghers syndrome 2
Impact of High-to-Moderate Penetrance Genes on Genetic Testing: Looking over Breast Cancer 1
Totale 4.630
Categoria #
all - tutte 19.037
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 19.037


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019363 0 0 0 0 0 0 0 0 2 70 144 147
2019/20201.196 185 62 34 101 116 70 116 122 167 77 96 50
2020/2021782 59 53 59 129 102 26 52 52 55 104 39 52
2021/2022577 31 87 11 17 16 33 33 31 28 68 104 118
2022/2023985 129 109 77 90 102 138 16 128 149 9 19 19
2023/2024308 27 64 14 34 50 89 8 21 1 0 0 0
Totale 4.630