IRIS
SUSCA, Francesco Claudio
 Distribuzione geografica
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Continente #
NA - Nord America 4.566
EU - Europa 1.598
AS - Asia 1.560
SA - Sud America 388
AF - Africa 119
Continente sconosciuto - Info sul continente non disponibili 101
OC - Oceania 3
Totale 8.335
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Nazione #
US - Stati Uniti d'America 4.433
SG - Singapore 662
IT - Italia 469
CN - Cina 384
BR - Brasile 315
SE - Svezia 243
RU - Federazione Russa 191
HK - Hong Kong 164
DE - Germania 154
UA - Ucraina 124
FI - Finlandia 109
VN - Vietnam 96
GB - Regno Unito 83
FR - Francia 80
CI - Costa d'Avorio 69
BD - Bangladesh 61
BE - Belgio 51
CA - Canada 49
IN - India 49
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
CR - Costa Rica 12
JP - Giappone 12
NL - Olanda 12
CZ - Repubblica Ceca 10
NI - Nicaragua 10
PH - Filippine 10
ES - Italia 9
HN - Honduras 9
LT - Lituania 9
EG - Egitto 8
IR - Iran 7
SA - Arabia Saudita 7
SV - El Salvador 7
TN - Tunisia 7
UZ - Uzbekistan 7
CW - ???statistics.table.value.countryCode.CW??? 6
GT - Guatemala 6
PR - Porto Rico 6
CL - Cile 4
IL - Israele 4
MA - Marocco 4
MY - Malesia 4
OM - Oman 4
TT - Trinidad e Tobago 4
AE - Emirati Arabi Uniti 3
AL - Albania 3
AT - Austria 3
AU - Australia 3
ET - Etiopia 3
GP - Guadalupe 3
HU - Ungheria 3
JM - Giamaica 3
JO - Giordania 3
CH - Svizzera 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
GE - Georgia 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
SC - Seychelles 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
DK - Danimarca 1
EE - Estonia 1
HR - Croazia 1
HT - Haiti 1
IS - Islanda 1
KH - Cambogia 1
KW - Kuwait 1
KZ - Kazakistan 1
LV - Lettonia 1
ME - Montenegro 1
MN - Mongolia 1
RO - Romania 1
SN - Senegal 1
SO - Somalia 1
Totale 8.238
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Città #
Ashburn 496
Fairfield 391
Singapore 364
Chandler 312
San Jose 287
Jacksonville 276
Woodbridge 261
Houston 196
Nyköping 187
Seattle 167
Hong Kong 164
Cambridge 149
Ann Arbor 147
Milan 126
Beijing 119
Wilmington 115
Council Bluffs 84
New York 83
Los Angeles 70
Abidjan 69
Nanjing 69
Roxbury 61
Lawrence 59
Lauterbourg 57
Helsinki 43
Des Moines 41
Bari 40
Rome 38
Boardman 37
Inglewood 36
Princeton 33
São Paulo 33
Santa Clara 30
Leuven 28
Munich 28
Dallas 27
Brooklyn 26
Ho Chi Minh City 24
Columbus 23
Hanoi 23
San Diego 21
Buffalo 19
Brussels 18
Dearborn 18
Jiaxing 17
Nanchang 16
Toronto 16
Chicago 14
San Francisco 14
Dublin 13
Falkenstein 13
Figino 13
London 13
Moscow 12
Tokyo 12
Turin 12
Shenyang 11
Chennai 10
Managua 10
Montreal 10
Orem 10
Phoenix 10
Warsaw 10
Jakarta 9
Johannesburg 9
Mexico City 9
San José 9
Torino 9
Turku 9
Atlanta 8
Boston 8
Dong Ket 8
Guangzhou 8
Hebei 8
Naples 8
Pune 8
Tianjin 8
Washington 8
Belo Horizonte 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
Guatemala City 6
Jinan 6
Manchester 6
Olomouc 6
San Salvador 6
Willemstad 6
Zhengzhou 6
Ardabil 5
Baghdad 5
Brasília 5
Brescia 5
Totale 5.393
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Nome #
The longevity SNP rs2802292 uncovered: HSF1 activates stress-dependent expression of FOXO3 through an intronic enhancer. 214
ANALISI MOLECOLARE E FUNZIONALE DEL RECETTORE MC1R NEL MELANOMA MALIGNO 202
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 188
Familly with two different cases of post- and pre-natal L1 syndrome; When hydrocephaly become "multidisciplinary headache" 185
In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS) 181
An unusual dicentric Y chromosome with a functional centromere with no detectable alpha-satellite 176
Effect of prostaglandin E2 on the proliferation, Ca2+ mobilization and cAMP in HT-29 human colon adenocarcinoma cells 176
Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: Results of an Italian multicenter study 171
Breakpoint determination of 15 large deletions in Peutz-Jeghers subjects 167
Nine novel APC mutations in Italian FAP patients 164
Lack of effect by prostaglandin F2alpha on the proliferation of the HCT-8 and HT-29 human adenocarcinoma cell lines 163
Association of autoimmune thyroiditis and celiac disease with Juvenile Polyposis due to 10q23.1q23.31 deletion: Potential role of PI3K/Akt pathway dysregulation 163
Translocation of the proto-oncogene Bcl-6 in human glioblastoma multiforme 161
Bradykinin stimulation does not induce intracellular Ca2+ elevation in cells from desmoid tumors 157
COACH syndrome: report of two brothers with congenital hepatic fibrosis, cerebellar vermis hypoplasia, oligophrenia, ataxia, and mental retardation 154
17-alpha-ethinylestradiol and norgestrel in combination induce micronucleus increases and aneuploidy in human lymphocyte and fibroblast cultures 152
A novel genetic variant in the wfs1 gene in a patient with partial uniparental mero‐isodisomy of chromosome 4 150
Cancer family syndrome: cytogenetic investigations, in vitro tetraploidy, and biomarker studies in a large family 146
A homozygous frameshift mutation in the ESCO2 gene: evidence of intertissue and interindividual variation in NMD efficiency 145
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
Sex chromosome loss, micronuclei, sister chromatid exchange and aging: a study including 16 centenarians 140
CORRELATION BETWEEN VASCULAR INFLAMMATION MARKERS, DIASTOLIC DYSFUNCTION AND CARDIOVASCULAR RISK IN PATIENTS WITH TAKAYASU ARTERITIS 136
A novel cell type-specific role of p38alpha in the control of autophagy and cell death in colorectal cancer cells 134
Increment of sister chromatid exchange frequencies (SCE) due to epichlorohydrin (ECH) in vitro treatment in human lymphocytes 134
SCE frequency measurement could be useful in the prenatal diagnosis of Roberts syndrome 126
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. 126
Esiste un’influenza dei polimorfismi dell’enzima epossi-idrolasi microsomiale(mEH) sui marcatori citogenetici di danno genotossico? 126
Benefit of serum screening, maternal age and ultrasound scans in amniocentesis-a six year survey 124
CANCER FAMILY SYNDROME: REPORT ON A GENETIC STUDIES IN A FAMILY 124
Trisomy 13 mosaicism in a phenotypically normal child: description of cytogenetic and clinical findings from early pregnancy beyond 2 years of age 124
Comparision of the cell growth of amniotic fluid samples in different culture media - how to obtain the best results at the lowest costs 123
DEPRESSED LEVEL OF NATURAL-KILLER CELLS IN CANCER FAMILY SYNDROME 123
A novel cell type-specific role of p38a in the control of autophagy and cell death in colorectal cancer cells. 123
EXCLUSION OF THE APC GENE AS THE CAUSE OF A VARIANT FORM OF FAMILIAL ADENOMATOUS POLYPOSIS (FAP) 122
Functional evidence of mTORβ splice variant involvement in the pathogenesis of congenital heart defects 121
FAMILIAL ADENOMATOUS POLYPOSIS - IDENTIFICATION OF A NEW FRAMESHIFT MUTATION OF THE APC GENE IN AN ITALIAN FAMILY 120
Caratterizzazione di geni coinvolti nei processi di trasformazione neoplastica. 120
Infertility in carriers of two bisatellited marker chromosomes 119
Two B1 and B2 bradykinin receptor antagonists fail to inhibit the Ca2+ response elicited by bradykinin in human skin fibroblasts 117
Linkage studies in Italian families with familial adenomatous polyposis 117
ANALISI MOLECOLARE E FUNZIONALE DEL RECETTORE MC1R NEL MELANOMA MALIGNO 115
Characterisation of chromosomal aberrations of amniotic fluid cells occurring in culture and its meaning 109
Ganglioma arising in a Peutz-Jeghers patient:a case report with molecular implications 107
Age-associated increase of micronuclei, sister chromatid exchange and sex chromosomeaneuploidy in human lymphocytes with special look at 100 year old subjects 106
Four novel mutations of the APC (adenomatous polyposis coli) gene in FAP patients 105
Duplication of 9p11.2-p13.1:a benign cytogenetic variant 105
Influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers between individuals exposed to very low doses of 1,3-butadiene 102
Cytogenetics and molecular studies in infertile males 99
Two B1 and B2 receptor antagonists fail to inhibit the Ca2+ response elicited by bradykinin in human skin fibroblasts 99
Molecular characterization of novel melanoma cell lines 99
Relation between detoxification enzyme polymorphism and genotoxic cytogenetic biomarkers 99
The influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers and its possible repercussion on gentoxic and cancerogenic process 98
The familial adenomatous polyposis region exhibits many different haplotypes 96
De novo balanced chromosome rearrangements in prenatal diagnosis 94
null 88
Sindrome di Holt-Oram: Valutazione cardiologica, Radiologica e Genetica 87
The Ultrasound Detection of Chromosomal Anomalies Vs Maternal Age and Serum Screening – six year survey 86
Identification of a new frameshift mutation of the APC gene in an Italian family 80
Xq deletion and premature ovarian failure 74
Exclusion of the APC gene as a variant form of familial adenomatous polyposis 74
Mutazioni del gene STK11 nella sindrome di Peutz- Jeghers (PJS) e nel cancro colorettale sporadico. 71
null 68
MOLECULAR AND FUNCTIONAL ANALYSIS OF MC1R RECEPTOR IN MALIGNANT MELANOMA 66
Influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers and its possible repercussion on genotoxic and cancerogeic process 63
The Italian external quality assessment scheme in classical cytogenetics: four years of activity 62
Pharmacological targeting of the novel β-catenin chromatin-associated kinase p38α in colorectal cancer stem cell tumorspheres and organoids 58
STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer 51
Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients 42
null 33
null 27
null 16
Totale 8.335
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Categoria #
all - tutte 34.582
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 34.582
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022366 0 0 0 0 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
2026/2027827 66 194 224 310 33 0 0 0 0 0 0 0
Totale 8.335