IRIS
SUSCA, Francesco Claudio
 Distribuzione geografica
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Continente #
NA - Nord America 4.176
AS - Asia 1.555
EU - Europa 1.549
SA - Sud America 382
AF - Africa 117
Continente sconosciuto - Info sul continente non disponibili 96
OC - Oceania 3
Totale 7.878
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Nazione #
US - Stati Uniti d'America 4.112
SG - Singapore 661
IT - Italia 435
CN - Cina 383
BR - Brasile 309
SE - Svezia 242
RU - Federazione Russa 188
HK - Hong Kong 164
DE - Germania 153
UA - Ucraina 123
FI - Finlandia 109
VN - Vietnam 95
GB - Regno Unito 81
FR - Francia 79
CI - Costa d'Avorio 69
BD - Bangladesh 61
BE - Belgio 51
IN - India 49
CA - Canada 28
ID - Indonesia 21
MX - Messico 21
AR - Argentina 19
ZA - Sudafrica 19
PL - Polonia 16
VE - Venezuela 16
IQ - Iraq 15
PK - Pakistan 15
CO - Colombia 14
IE - Irlanda 14
EC - Ecuador 13
TR - Turchia 13
JP - Giappone 12
NL - Olanda 11
CZ - Repubblica Ceca 10
PH - Filippine 10
ES - Italia 9
EG - Egitto 8
IR - Iran 7
SA - Arabia Saudita 7
TN - Tunisia 7
UZ - Uzbekistan 7
LT - Lituania 5
CL - Cile 4
HN - Honduras 4
MA - Marocco 4
MY - Malesia 4
OM - Oman 4
AE - Emirati Arabi Uniti 3
AL - Albania 3
AT - Austria 3
AU - Australia 3
ET - Etiopia 3
GT - Guatemala 3
HU - Ungheria 3
JM - Giamaica 3
JO - Giordania 3
CH - Svizzera 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
GE - Georgia 2
IL - Israele 2
KE - Kenya 2
KR - Corea 2
NP - Nepal 2
PE - Perù 2
PS - Palestinian Territory 2
PY - Paraguay 2
QA - Qatar 2
RS - Serbia 2
SI - Slovenia 2
UY - Uruguay 2
AM - Armenia 1
AO - Angola 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
CW - ???statistics.table.value.countryCode.CW??? 1
EE - Estonia 1
HR - Croazia 1
IS - Islanda 1
KH - Cambogia 1
KW - Kuwait 1
KZ - Kazakistan 1
LV - Lettonia 1
ME - Montenegro 1
MN - Mongolia 1
NI - Nicaragua 1
RO - Romania 1
SN - Senegal 1
SO - Somalia 1
SY - Repubblica araba siriana 1
TW - Taiwan 1
Totale 7.783
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Città #
Ashburn 407
Fairfield 391
Singapore 363
Chandler 312
Jacksonville 275
Woodbridge 261
San Jose 235
Houston 195
Nyköping 187
Seattle 166
Hong Kong 164
Cambridge 149
Ann Arbor 147
Milan 124
Beijing 119
Wilmington 115
Council Bluffs 81
New York 75
Abidjan 69
Nanjing 69
Los Angeles 64
Roxbury 61
Lawrence 59
Lauterbourg 57
Helsinki 43
Des Moines 41
Bari 40
Boardman 37
Inglewood 36
Rome 36
Princeton 33
Leuven 28
Munich 28
São Paulo 28
Brooklyn 25
Dallas 25
Santa Clara 25
Columbus 23
Hanoi 23
Ho Chi Minh City 23
San Diego 20
Buffalo 19
Brussels 18
Dearborn 18
Jiaxing 17
Nanchang 16
Chicago 14
San Francisco 14
Dublin 13
Falkenstein 13
London 12
Moscow 12
Tokyo 12
Figino 11
Shenyang 11
Turin 11
Chennai 10
Phoenix 10
Warsaw 10
Jakarta 9
Johannesburg 9
Mexico City 9
Montreal 9
Orem 9
Torino 9
Turku 9
Dong Ket 8
Guangzhou 8
Hebei 8
Pune 8
Tianjin 8
Toronto 8
Atlanta 7
Belo Horizonte 7
Boston 7
Caracas 7
Frankfurt am Main 7
Mumbai 7
Nuremberg 7
Poplar 7
Redwood City 7
Rio de Janeiro 7
Changsha 6
Dhaka 6
Guarulhos 6
Jinan 6
Manchester 6
Olomouc 6
Washington 6
Zhengzhou 6
Ardabil 5
Baghdad 5
Buenos Aires 5
Cairo 5
Chieti 5
Denver 5
Falls Church 5
Guayaquil 5
Medellín 5
Naples 5
Totale 5.179
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Nome #
The longevity SNP rs2802292 uncovered: HSF1 activates stress-dependent expression of FOXO3 through an intronic enhancer. 196
ANALISI MOLECOLARE E FUNZIONALE DEL RECETTORE MC1R NEL MELANOMA MALIGNO 180
Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants 177
Familly with two different cases of post- and pre-natal L1 syndrome; When hydrocephaly become "multidisciplinary headache" 176
In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS) 175
Effect of prostaglandin E2 on the proliferation, Ca2+ mobilization and cAMP in HT-29 human colon adenocarcinoma cells 173
An unusual dicentric Y chromosome with a functional centromere with no detectable alpha-satellite 166
Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: Results of an Italian multicenter study 164
Association of autoimmune thyroiditis and celiac disease with Juvenile Polyposis due to 10q23.1q23.31 deletion: Potential role of PI3K/Akt pathway dysregulation 159
Lack of effect by prostaglandin F2alpha on the proliferation of the HCT-8 and HT-29 human adenocarcinoma cell lines 158
Breakpoint determination of 15 large deletions in Peutz-Jeghers subjects 157
Translocation of the proto-oncogene Bcl-6 in human glioblastoma multiforme 156
Nine novel APC mutations in Italian FAP patients 151
Bradykinin stimulation does not induce intracellular Ca2+ elevation in cells from desmoid tumors 149
COACH syndrome: report of two brothers with congenital hepatic fibrosis, cerebellar vermis hypoplasia, oligophrenia, ataxia, and mental retardation 148
Cancer family syndrome: cytogenetic investigations, in vitro tetraploidy, and biomarker studies in a large family 144
17-alpha-ethinylestradiol and norgestrel in combination induce micronucleus increases and aneuploidy in human lymphocyte and fibroblast cultures 142
A novel genetic variant in the wfs1 gene in a patient with partial uniparental mero‐isodisomy of chromosome 4 142
A homozygous frameshift mutation in the ESCO2 gene: evidence of intertissue and interindividual variation in NMD efficiency 140
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 137
Sex chromosome loss, micronuclei, sister chromatid exchange and aging: a study including 16 centenarians 135
CORRELATION BETWEEN VASCULAR INFLAMMATION MARKERS, DIASTOLIC DYSFUNCTION AND CARDIOVASCULAR RISK IN PATIENTS WITH TAKAYASU ARTERITIS 132
Increment of sister chromatid exchange frequencies (SCE) due to epichlorohydrin (ECH) in vitro treatment in human lymphocytes 128
SCE frequency measurement could be useful in the prenatal diagnosis of Roberts syndrome 122
De novo unbalanced translocation leading to monosomy 9p24.3p24.1 and trisomy 19q13.42q13.43 characterized by microarray-based comparative genomic hybridization in a child with partial cortical dysplasia and craniofacial dysmorphisms without trigonocephaly. 122
A novel cell type-specific role of p38alpha in the control of autophagy and cell death in colorectal cancer cells 120
DEPRESSED LEVEL OF NATURAL-KILLER CELLS IN CANCER FAMILY SYNDROME 120
CANCER FAMILY SYNDROME: REPORT ON A GENETIC STUDIES IN A FAMILY 119
Trisomy 13 mosaicism in a phenotypically normal child: description of cytogenetic and clinical findings from early pregnancy beyond 2 years of age 119
FAMILIAL ADENOMATOUS POLYPOSIS - IDENTIFICATION OF A NEW FRAMESHIFT MUTATION OF THE APC GENE IN AN ITALIAN FAMILY 117
Benefit of serum screening, maternal age and ultrasound scans in amniocentesis-a six year survey 115
Infertility in carriers of two bisatellited marker chromosomes 115
A novel cell type-specific role of p38a in the control of autophagy and cell death in colorectal cancer cells. 115
Comparision of the cell growth of amniotic fluid samples in different culture media - how to obtain the best results at the lowest costs 114
Functional evidence of mTORβ splice variant involvement in the pathogenesis of congenital heart defects 114
Two B1 and B2 bradykinin receptor antagonists fail to inhibit the Ca2+ response elicited by bradykinin in human skin fibroblasts 113
Linkage studies in Italian families with familial adenomatous polyposis 113
ANALISI MOLECOLARE E FUNZIONALE DEL RECETTORE MC1R NEL MELANOMA MALIGNO 111
Caratterizzazione di geni coinvolti nei processi di trasformazione neoplastica. 111
EXCLUSION OF THE APC GENE AS THE CAUSE OF A VARIANT FORM OF FAMILIAL ADENOMATOUS POLYPOSIS (FAP) 109
Esiste un’influenza dei polimorfismi dell’enzima epossi-idrolasi microsomiale(mEH) sui marcatori citogenetici di danno genotossico? 108
Duplication of 9p11.2-p13.1:a benign cytogenetic variant 102
Age-associated increase of micronuclei, sister chromatid exchange and sex chromosomeaneuploidy in human lymphocytes with special look at 100 year old subjects 102
Four novel mutations of the APC (adenomatous polyposis coli) gene in FAP patients 100
Characterisation of chromosomal aberrations of amniotic fluid cells occurring in culture and its meaning 100
Ganglioma arising in a Peutz-Jeghers patient:a case report with molecular implications 97
Influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers between individuals exposed to very low doses of 1,3-butadiene 97
The influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers and its possible repercussion on gentoxic and cancerogenic process 95
Molecular characterization of novel melanoma cell lines 91
Relation between detoxification enzyme polymorphism and genotoxic cytogenetic biomarkers 91
The familial adenomatous polyposis region exhibits many different haplotypes 91
Cytogenetics and molecular studies in infertile males 90
Two B1 and B2 receptor antagonists fail to inhibit the Ca2+ response elicited by bradykinin in human skin fibroblasts 89
null 88
De novo balanced chromosome rearrangements in prenatal diagnosis 88
The Ultrasound Detection of Chromosomal Anomalies Vs Maternal Age and Serum Screening – six year survey 84
Sindrome di Holt-Oram: Valutazione cardiologica, Radiologica e Genetica 83
Xq deletion and premature ovarian failure 71
null 68
Identification of a new frameshift mutation of the APC gene in an Italian family 68
Mutazioni del gene STK11 nella sindrome di Peutz- Jeghers (PJS) e nel cancro colorettale sporadico. 68
Exclusion of the APC gene as a variant form of familial adenomatous polyposis 66
MOLECULAR AND FUNCTIONAL ANALYSIS OF MC1R RECEPTOR IN MALIGNANT MELANOMA 62
Influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers and its possible repercussion on genotoxic and cancerogeic process 57
The Italian external quality assessment scheme in classical cytogenetics: four years of activity 56
Pharmacological targeting of the novel β-catenin chromatin-associated kinase p38α in colorectal cancer stem cell tumorspheres and organoids 53
STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer 47
Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients 36
null 33
null 27
null 16
Totale 7.878
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Categoria #
all - tutte 32.877
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 32.877
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022394 0 0 6 22 12 27 30 27 25 46 93 106
2022/2023841 104 94 61 83 87 133 3 103 138 9 18 8
2023/2024306 19 62 14 28 44 70 5 24 1 11 0 28
2024/20251.069 34 11 85 34 37 84 134 93 41 47 163 306
2025/20262.351 304 141 159 234 310 118 245 61 210 234 82 253
2026/2027370 66 194 110 0 0 0 0 0 0 0 0 0
Totale 7.878