PERCESEPE, Antonio
 Distribuzione geografica
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Continente #
NA - Nord America 12.374
AS - Asia 4.940
EU - Europa 4.318
SA - Sud America 685
AF - Africa 108
OC - Oceania 18
Continente sconosciuto - Info sul continente non disponibili 6
Totale 22.449
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Nazione #
US - Stati Uniti d'America 12.174
GB - Regno Unito 1.698
SG - Singapore 1.679
CN - Cina 1.331
VN - Vietnam 562
HK - Hong Kong 541
BR - Brasile 511
IT - Italia 482
SE - Svezia 474
DE - Germania 373
FI - Finlandia 309
UA - Ucraina 260
RU - Federazione Russa 222
TR - Turchia 201
FR - Francia 148
KR - Corea 117
CA - Canada 116
IN - India 111
BG - Bulgaria 92
BD - Bangladesh 74
AR - Argentina 62
NL - Olanda 54
ID - Indonesia 51
MX - Messico 47
IQ - Iraq 46
BE - Belgio 32
AE - Emirati Arabi Uniti 31
EC - Ecuador 31
JP - Giappone 28
IE - Irlanda 27
ES - Italia 26
ZA - Sudafrica 24
PK - Pakistan 22
CL - Cile 20
PL - Polonia 20
MY - Malesia 19
CO - Colombia 18
SA - Arabia Saudita 18
EG - Egitto 16
AU - Australia 15
LT - Lituania 15
UZ - Uzbekistan 15
KE - Kenya 13
PH - Filippine 13
TN - Tunisia 13
CH - Svizzera 12
CZ - Repubblica Ceca 12
PY - Paraguay 12
DZ - Algeria 11
JO - Giordania 11
MA - Marocco 11
PE - Perù 11
TW - Taiwan 11
DO - Repubblica Dominicana 9
IL - Israele 9
VE - Venezuela 9
DK - Danimarca 8
JM - Giamaica 8
AT - Austria 7
TH - Thailandia 7
NP - Nepal 6
UY - Uruguay 6
CR - Costa Rica 5
EE - Estonia 5
ET - Etiopia 5
IR - Iran 5
RO - Romania 5
SI - Slovenia 5
AZ - Azerbaigian 4
BH - Bahrain 4
BO - Bolivia 4
GR - Grecia 4
HU - Ungheria 4
MD - Moldavia 4
AL - Albania 3
AM - Armenia 3
CI - Costa d'Avorio 3
KG - Kirghizistan 3
KZ - Kazakistan 3
LK - Sri Lanka 3
NZ - Nuova Zelanda 3
RS - Serbia 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BA - Bosnia-Erzegovina 2
BS - Bahamas 2
BY - Bielorussia 2
CG - Congo 2
EU - Europa 2
GT - Guatemala 2
HN - Honduras 2
IS - Islanda 2
KH - Cambogia 2
LV - Lettonia 2
NI - Nicaragua 2
PA - Panama 2
PR - Porto Rico 2
PS - Palestinian Territory 2
SY - Repubblica araba siriana 2
Totale 22.427
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Città #
Fairfield 1.182
Southend 1.174
Singapore 1.133
Santa Clara 1.125
Ashburn 1.003
Woodbridge 773
Houston 609
Hong Kong 533
Chandler 508
Jacksonville 491
Seattle 462
Wilmington 449
Chicago 421
Cambridge 419
Hefei 402
Ann Arbor 377
Dearborn 354
San Jose 326
Nyköping 320
Los Angeles 262
Beijing 243
London 220
Helsinki 205
Salt Lake City 172
Ho Chi Minh City 169
The Dalles 161
Hanoi 135
Modena 133
New York 126
Izmir 122
Seoul 116
Council Bluffs 114
San Diego 113
Princeton 100
Elk Grove Village 91
Eugene 90
Sofia 90
Lauterbourg 82
Tampa 75
Des Moines 66
Shanghai 64
Moscow 62
Buffalo 56
Milan 55
Munich 51
Falls Church 50
Dallas 48
Lancaster 47
São Paulo 46
Columbus 45
Bologna 43
Frankfurt am Main 42
Cardiff 39
Sterling 39
Ottawa 37
Bremen 34
Orem 34
Jakarta 33
Vancouver 33
Rio de Janeiro 29
Dublin 27
Dulles 27
Brussels 26
Tokyo 26
Miami 25
Haiphong 24
Da Nang 21
Detroit 21
Guangzhou 21
Chennai 19
Mexico City 19
Phoenix 19
Toronto 19
Baghdad 18
Turku 18
Amsterdam 17
Dhaka 17
Fremont 17
Kent 16
Norwalk 16
Kunming 15
Nanjing 15
Warsaw 15
Belo Horizonte 14
Falkenstein 14
Kansas City 14
Pittsburgh 14
Rome 14
Tashkent 14
Atlanta 13
Boardman 13
Boston 13
Brasília 13
Denver 13
Hải Dương 13
Philadelphia 13
Redwood City 13
San Francisco 12
San Mateo 12
Changsha 11
Totale 16.514
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Nome #
A two-locus model for hereditary non-polyposis colorectal cancer in Modena, Italy 406
K-ras and p53 mutations in hereditary non-polyposis colorectal cancers 406
Unravelling the Complexity of Inherited Retinal Dystrophies Molecular Testing: Added Value of Targeted Next-Generation Sequencing 393
Microsatellite instability in multiple colorectal tumors 381
Molecular screening for Hereditary Non Polyposis Colorectal Cancer (HNPCC): a prospective, population-based study 365
Staging and survival of colorectal cancer: are we making progress? The 14-year experience of a Specialized cancer Registry 354
Biological parameters determining the clinical outcome of autologous cultures of limbal stem cells 349
Amplicon-based next-generation sequencing: an effective approach for the molecular diagnosis of epidermolysis bullosa 347
Frequency and clinical features of multiple tumors of the large bowel in the general population and in patients with hereditary colorectal carcinoma 337
Survival analysis in families affected by hereditary non-polyposis colorectal cancer 332
Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report 331
Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts 329
A 12.4 Mb direct duplication in 19q12-q13 in a boy with cardiac and CNS malformations and developmental delay 329
New and Rare GJB2 Alleles in Patients with Nonsyndromic Sensorineural Hearing Impairment: A Genotype/Auditory Phenotype Correlation 328
Pure segmental trisomy 1q42-qter in a boy with a severe phenotype 328
The homozygous deletion of the 3' enhancer of the SHOX gene causes Langer mesomelic dysplasia. 322
VACTERL (vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, cardiac defects, renal and limb anomalies) association: disease spectrum in 25 patients ascertained for their upper limb involvement 319
Small bowel carcinoma in hereditary nonpolyposis colorectal cancer 318
Problems in the identification of hereditary nonpolyposis colorectal cancer in two families with late development of full-blown clinical spectrum 314
Muir-Torre syndrome or phenocopy? The value of the immunohistochemical expression of mismatch repair proteins in sebaceous tumors of immunocompromised patients 314
Mismatch repair genes founder mutations and cancer susceptibility in Lynch syndrome 310
Genes and translocations involved in POF 308
A three-generation family with terminal microdeletion involving 5p15.33-32 due to a whole-arm 5;15 chromosomal translocation with a steady phenotype of atypical cri du chat syndrome 305
Methylation pattern of different regions of the MLH1 promoter and silencing of gene expression in hereditary and sporadic colorectal cancer. 297
Early diagnosis of branchio-oculo-facial syndrome in a patient with inner ear malformation and mild ocular involvement 296
Clinical features, frequency and prognosis of Dukes' a colorectal carcinoma: A population-based investigation 293
Predictive diagnostic value for the clinical features accompanying intellectual disability in children with pathogenic copy number variations: a multivariate analysis 290
Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis 288
Clinical and molecular diagnosis of hereditary non-polyposis colorectal cancer: problems and pitfalls in an extended pedigree 283
Age-specific risk of fetal loss post second trimester amniocentesis: analysis of 5043 cases 282
Familial Short Stature Associated to Terminal Microdeletion of 15q26.3: Variable Phenotype not Involving the IGF1 Receptor Gene 276
Colorectal carcinoma in different age groups: A population based investigation 269
Facioscapulohumeral muscular dystrophy: new insights from compound heterozygotes and implication for prenatal genetic counselling. 269
Genetic basis of congenital upper limb anomalies: analysis of 487 cases of a specialized clinic 268
Holoprosencephaly: report of four cases and genotype-phenotype correlations. 264
Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination 259
Circadian variations of epithelial cell proliferation in human rectal crypts. 253
Clinical and biologic heterogeneity of Hereditary NonPolyposis Colorectal Cancer. 252
Collection of Italian hereditary non-polyposis colorectal cancer (HNPCC) pedigrees 249
Pathogenesis of colorectal cancer 246
Second trimester amniocentesis is not a risk factor for very low birth weight and extremely low birth weight. 241
Clinical features and genotype-phenotype correlations in 41 Italian families with Adenomatosis Coli 240
Epidemiologic and genetic factor in colorectal cancer: development of cancer in dizygotic twins in a family with Lynch syndrome 239
A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAX 230
THE EFFECT OF FAMILY-SIZE ON ESTIMATES OF THE FREQUENCY OF HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER 229
First-trimester ultrasonographic diagnosis of Langer mesomelic dysplasia in a previously affected family. 229
The I1307K polymorphism of the APC gene in colorectal cancer 229
Cowden's disease with extensive gastrointestinal polyposis. 228
Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer. 227
Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele 226
SHOX point mutations and deletions in Leri-Weill dyschondrosteosis. 225
Pre- and post-natal growth in two sisters with 3-M syndrome 225
Non-invasive first trimester fetal gender assignment in pregnancies at risk for X-linked recessive diseases. 224
[Hereditary factors in tumors of the digestive system]. 223
Fenotipo lieve di sordità neurosensoriale e cheratoderma palmo-plantare causato da una nuova mutazione dominante di GJB2 222
Prenatal diagnosis and follow-up of a case of branchio-oto-renal syndrome displays renal growth impairment after the second trimester 218
The DNA repair gene MBD4 (MED1) is mutated in human carcinomas with microsatellite instability 217
First-trimester prenatal screening for the common 35delG GJB2 mutation causing prelingual deafness 216
Phenotype-genotype correlations in an extended family with adenomatosis coli and an unusual APC gene mutation 214
Mutations Affecting the BHLHA9 DNA-Binding Domain Cause MSSD, Mesoaxial Synostotic Syndactyly with Phalangeal Reduction, Malik-Percin Type 214
Il registro dei tumori colorettali 213
Prenatal diagnosis and postnatal follow-up of a child with mosaic trisomy 22 with several levels of mosaicism in different tissues 212
Structural chromosomal abnormalities detected during CVS analysis and their role in the prenatal ascertainment of cryptic subtelomeric rearrangements 212
Surface rendering of external genitalia of a fetus at the 32nd week of gestation affected by partial androgen insensitivity syndrome. 211
Frequency and type of colorectal tumors in asymptomatic high-risk individuals in families with hereditary nonpolyposis colorectal cancer 211
Molecular genetic analysis of the PLP1 gene in 38 families with PLP1-related disorders: identification and functional characterization of 11 novel PLP1 mutations. 207
Recurrent germline mutation in MSH2 arises frequently de novo 205
Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. 204
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses 203
DNA ploidy pattern in human chronic liver diseases and hepatic nodular lesions. Flow cytometric analysis on echo-guided needle liver biopsy. 202
Effects of different doses of fish oil on rectal cell proliferation in patients with sporadic colonic adenomas. 200
Epidemiology of cancer of the large bowel - The 12-year experience of a specialized registry in Northern Italy 197
Quantitation of fetal DNA in maternal serum during the first trimester of pregnancy by the use of a DAZ repetitive probe 194
Liquid biopsy with cell free DNA: new horizons for prostate cancer 192
Microsatellite instability and mismatch-repair protein expression in hereditary and sporadic colorectal carcinogenesis 187
Epidemiologia dei tumori del colon-retto. Incidenza, mortalità, familiarità e sopravvivenza nella ex USL di Modena, 1984-1998. 186
The role of hPMS1 and hPMS2 in predisposing to colorectal cancer 186
Mismatch repair genes and mononucleotide tracts as mutation targets in colorectal tumors with different degrees of microsatellite instability 184
Hereditary nonpolyposis colorectal cancer: an approach to the selection of candidates to genetic testing based on clinical and molecular characteristics 180
GENETIC EPIDEMIOLOGY OF HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER 179
MLH1 and MSH2 constitutional mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer. 175
Effect of omega-3 fatty acids on rectal mucosal cell proliferation in subjects at risk for colon cancer. 175
Multimodal molecular screening is required to improve the sensitivity of MLH1 and MSH2 mutation analysis - Reply 174
Role of clinical criteria in the diagnosis of HNPCC: results of a multivariate analysis 174
Rectal epithelial cell proliferation patterns as predictors of adenomatous colorectal polyp recurrence. 158
Reliability of rectal epithelial kinetic patterns as an intermediate biomarker of colon cancer. 156
Mutations of the minor mismatch repair gene MSH6 in typical and atypical HNPCC. 144
Modulating effect of omega-3 fatty acids on the proliferative pattern of human colorectal mucosa. 142
A large-scale genetic analysis reveals an autoimmune origin of idiopathic retroperitoneal fibrosis 131
A challenging case of melorheostosis involving the right upper limb 107
Diagnostic Yield and Clinical Impact of a Small Genetic Panel for Kidney Disease: A Multicenter, Retrospective European Study 90
Totale 22.566
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Categoria #
all - tutte 89.245
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 89.245
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021246 0 0 0 0 0 0 0 0 0 0 112 134
2021/20221.585 49 204 190 98 47 99 97 56 177 127 286 155
2022/20231.514 202 160 121 148 155 271 21 140 191 13 46 46
2023/2024931 50 58 43 69 240 77 91 110 21 10 56 106
2024/20253.469 126 30 43 244 792 535 215 200 354 189 327 414
2025/20267.489 466 331 520 1.106 1.860 469 852 424 679 622 160 0
Totale 22.566