PERCESEPE, Antonio
 Distribuzione geografica
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Continente #
NA - Nord America 13.692
AS - Asia 5.217
EU - Europa 4.478
SA - Sud America 695
Continente sconosciuto - Info sul continente non disponibili 123
AF - Africa 111
OC - Oceania 20
Totale 24.336
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Nazione #
US - Stati Uniti d'America 13.361
GB - Regno Unito 1.702
SG - Singapore 1.699
CN - Cina 1.361
IT - Italia 625
VN - Vietnam 571
HK - Hong Kong 549
BR - Brasile 514
SE - Svezia 474
DE - Germania 378
FI - Finlandia 309
BD - Bangladesh 271
UA - Ucraina 260
RU - Federazione Russa 222
CA - Canada 221
TR - Turchia 202
FR - Francia 149
KR - Corea 118
IN - India 113
BG - Bulgaria 93
AR - Argentina 63
NL - Olanda 55
ID - Indonesia 52
MX - Messico 50
IQ - Iraq 46
EC - Ecuador 33
JP - Giappone 33
BE - Belgio 32
AE - Emirati Arabi Uniti 31
IE - Irlanda 27
ES - Italia 26
ZA - Sudafrica 25
PK - Pakistan 23
CL - Cile 22
MY - Malesia 21
CO - Colombia 20
PL - Polonia 20
SA - Arabia Saudita 18
AU - Australia 16
EG - Egitto 16
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
CR - Costa Rica 11
DZ - Algeria 11
JM - Giamaica 11
JO - Giordania 11
MA - Marocco 11
PE - Perù 11
TW - Taiwan 11
DK - Danimarca 10
DO - Repubblica Dominicana 10
IL - Israele 9
VE - Venezuela 9
AT - Austria 7
TH - Thailandia 7
NP - Nepal 6
UY - Uruguay 6
EE - Estonia 5
ET - Etiopia 5
HU - Ungheria 5
IR - Iran 5
RO - Romania 5
SI - Slovenia 5
TT - Trinidad e Tobago 5
AZ - Azerbaigian 4
BH - Bahrain 4
BO - Bolivia 4
GR - Grecia 4
MD - Moldavia 4
NZ - Nuova Zelanda 4
PR - Porto Rico 4
AL - Albania 3
AM - Armenia 3
BS - Bahamas 3
CI - Costa d'Avorio 3
GT - Guatemala 3
KG - Kirghizistan 3
KZ - Kazakistan 3
LK - Sri Lanka 3
RS - Serbia 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
SV - El Salvador 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BA - Bosnia-Erzegovina 2
BY - Bielorussia 2
CG - Congo 2
EU - Europa 2
HN - Honduras 2
HR - Croazia 2
IS - Islanda 2
KH - Cambogia 2
LV - Lettonia 2
NI - Nicaragua 2
Totale 24.188
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Città #
Ashburn 1.237
Fairfield 1.182
Santa Clara 1.174
Southend 1.174
Singapore 1.139
Woodbridge 774
Houston 615
Hong Kong 539
Chandler 508
Jacksonville 491
San Jose 478
Seattle 464
Wilmington 454
Chicago 428
Cambridge 423
Hefei 402
Ann Arbor 377
Dearborn 354
Nyköping 320
Los Angeles 288
Council Bluffs 262
Beijing 249
London 221
Helsinki 205
Salt Lake City 172
Ho Chi Minh City 171
The Dalles 162
New York 155
Hanoi 139
Modena 135
Izmir 122
Seoul 117
San Diego 113
Princeton 100
Elk Grove Village 91
Eugene 90
Sofia 90
Lauterbourg 82
Milan 82
Tampa 77
Montreal 72
Columbus 69
Buffalo 68
Des Moines 67
Shanghai 66
Dallas 62
Moscow 62
Munich 51
Boardman 50
Falls Church 50
Lancaster 47
Bologna 46
São Paulo 46
Frankfurt am Main 43
Ottawa 40
Cardiff 39
Sterling 39
Bremen 34
Jakarta 34
Orem 34
Phoenix 34
Vancouver 34
Toronto 32
Rio de Janeiro 29
Dublin 27
Dulles 27
Tokyo 27
Brussels 26
Miami 26
Philadelphia 25
Haiphong 24
Detroit 23
Da Nang 21
Guangzhou 21
Mexico City 21
Rome 21
Chennai 19
Baghdad 18
Norwalk 18
Turku 18
Amsterdam 17
Atlanta 17
Dhaka 17
Fremont 17
Kent 16
Denver 15
Kunming 15
Nanjing 15
Pittsburgh 15
San Francisco 15
Warsaw 15
Belo Horizonte 14
Boston 14
Falkenstein 14
Kansas City 14
Tashkent 14
Washington 14
Brasília 13
Hải Dương 13
Miano 13
Totale 17.463
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Nome #
Mismatch repair genes founder mutations and cancer susceptibility in Lynch syndrome 435
K-ras and p53 mutations in hereditary non-polyposis colorectal cancers 430
A two-locus model for hereditary non-polyposis colorectal cancer in Modena, Italy 421
Unravelling the Complexity of Inherited Retinal Dystrophies Molecular Testing: Added Value of Targeted Next-Generation Sequencing 403
Microsatellite instability in multiple colorectal tumors 395
Molecular screening for Hereditary Non Polyposis Colorectal Cancer (HNPCC): a prospective, population-based study 392
Amplicon-based next-generation sequencing: an effective approach for the molecular diagnosis of epidermolysis bullosa 377
Biological parameters determining the clinical outcome of autologous cultures of limbal stem cells 376
Staging and survival of colorectal cancer: are we making progress? The 14-year experience of a Specialized cancer Registry 368
New and Rare GJB2 Alleles in Patients with Nonsyndromic Sensorineural Hearing Impairment: A Genotype/Auditory Phenotype Correlation 364
Frequency and clinical features of multiple tumors of the large bowel in the general population and in patients with hereditary colorectal carcinoma 358
Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report 352
A 12.4 Mb direct duplication in 19q12-q13 in a boy with cardiac and CNS malformations and developmental delay 345
Survival analysis in families affected by hereditary non-polyposis colorectal cancer 342
Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts 341
Pure segmental trisomy 1q42-qter in a boy with a severe phenotype 336
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 335
Muir-Torre syndrome or phenocopy? The value of the immunohistochemical expression of mismatch repair proteins in sebaceous tumors of immunocompromised patients 334
Problems in the identification of hereditary nonpolyposis colorectal cancer in two families with late development of full-blown clinical spectrum 330
The homozygous deletion of the 3' enhancer of the SHOX gene causes Langer mesomelic dysplasia. 327
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 326
Small bowel carcinoma in hereditary nonpolyposis colorectal cancer 326
Predictive diagnostic value for the clinical features accompanying intellectual disability in children with pathogenic copy number variations: a multivariate analysis 324
Genes and translocations involved in POF 321
Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis 319
Clinical features, frequency and prognosis of Dukes' a colorectal carcinoma: A population-based investigation 310
Facioscapulohumeral muscular dystrophy: new insights from compound heterozygotes and implication for prenatal genetic counselling. 310
Genetic basis of congenital upper limb anomalies: analysis of 487 cases of a specialized clinic 308
Methylation pattern of different regions of the MLH1 promoter and silencing of gene expression in hereditary and sporadic colorectal cancer. 307
Early diagnosis of branchio-oculo-facial syndrome in a patient with inner ear malformation and mild ocular involvement 304
Age-specific risk of fetal loss post second trimester amniocentesis: analysis of 5043 cases 301
Clinical and molecular diagnosis of hereditary non-polyposis colorectal cancer: problems and pitfalls in an extended pedigree 298
Familial Short Stature Associated to Terminal Microdeletion of 15q26.3: Variable Phenotype not Involving the IGF1 Receptor Gene 294
Colorectal carcinoma in different age groups: A population based investigation 284
Holoprosencephaly: report of four cases and genotype-phenotype correlations. 282
Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination 281
Pathogenesis of colorectal cancer 280
Circadian variations of epithelial cell proliferation in human rectal crypts. 271
The I1307K polymorphism of the APC gene in colorectal cancer 267
Clinical and biologic heterogeneity of Hereditary NonPolyposis Colorectal Cancer. 264
Collection of Italian hereditary non-polyposis colorectal cancer (HNPCC) pedigrees 263
Clinical features and genotype-phenotype correlations in 41 Italian families with Adenomatosis Coli 256
Cowden's disease with extensive gastrointestinal polyposis. 252
Second trimester amniocentesis is not a risk factor for very low birth weight and extremely low birth weight. 250
Epidemiologic and genetic factor in colorectal cancer: development of cancer in dizygotic twins in a family with Lynch syndrome 249
[Hereditary factors in tumors of the digestive system]. 249
Prenatal diagnosis and follow-up of a case of branchio-oto-renal syndrome displays renal growth impairment after the second trimester 247
A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAX 246
Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer. 245
Pre- and post-natal growth in two sisters with 3-M syndrome 245
Effects of different doses of fish oil on rectal cell proliferation in patients with sporadic colonic adenomas. 245
THE EFFECT OF FAMILY-SIZE ON ESTIMATES OF THE FREQUENCY OF HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER 243
Non-invasive first trimester fetal gender assignment in pregnancies at risk for X-linked recessive diseases. 243
SHOX point mutations and deletions in Leri-Weill dyschondrosteosis. 240
Phenotype-genotype correlations in an extended family with adenomatosis coli and an unusual APC gene mutation 237
First-trimester prenatal screening for the common 35delG GJB2 mutation causing prelingual deafness 237
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses 235
Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele 234
First-trimester ultrasonographic diagnosis of Langer mesomelic dysplasia in a previously affected family. 234
The DNA repair gene MBD4 (MED1) is mutated in human carcinomas with microsatellite instability 232
Fenotipo lieve di sordità neurosensoriale e cheratoderma palmo-plantare causato da una nuova mutazione dominante di GJB2 231
Structural chromosomal abnormalities detected during CVS analysis and their role in the prenatal ascertainment of cryptic subtelomeric rearrangements 230
Prenatal diagnosis and postnatal follow-up of a child with mosaic trisomy 22 with several levels of mosaicism in different tissues 228
Frequency and type of colorectal tumors in asymptomatic high-risk individuals in families with hereditary nonpolyposis colorectal cancer 228
Molecular genetic analysis of the PLP1 gene in 38 families with PLP1-related disorders: identification and functional characterization of 11 novel PLP1 mutations. 226
Mismatch repair genes and mononucleotide tracts as mutation targets in colorectal tumors with different degrees of microsatellite instability 224
Mutations Affecting the BHLHA9 DNA-Binding Domain Cause MSSD, Mesoaxial Synostotic Syndactyly with Phalangeal Reduction, Malik-Percin Type 223
Il registro dei tumori colorettali 222
Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. 222
Surface rendering of external genitalia of a fetus at the 32nd week of gestation affected by partial androgen insensitivity syndrome. 221
DNA ploidy pattern in human chronic liver diseases and hepatic nodular lesions. Flow cytometric analysis on echo-guided needle liver biopsy. 218
Recurrent germline mutation in MSH2 arises frequently de novo 217
Liquid biopsy with cell free DNA: new horizons for prostate cancer 210
Quantitation of fetal DNA in maternal serum during the first trimester of pregnancy by the use of a DAZ repetitive probe 206
Role of clinical criteria in the diagnosis of HNPCC: results of a multivariate analysis 205
Epidemiology of cancer of the large bowel - The 12-year experience of a specialized registry in Northern Italy 203
The role of hPMS1 and hPMS2 in predisposing to colorectal cancer 201
Epidemiologia dei tumori del colon-retto. Incidenza, mortalità, familiarità e sopravvivenza nella ex USL di Modena, 1984-1998. 199
Hereditary nonpolyposis colorectal cancer: an approach to the selection of candidates to genetic testing based on clinical and molecular characteristics 195
GENETIC EPIDEMIOLOGY OF HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER 194
Effect of omega-3 fatty acids on rectal mucosal cell proliferation in subjects at risk for colon cancer. 192
Microsatellite instability and mismatch-repair protein expression in hereditary and sporadic colorectal carcinogenesis 192
MLH1 and MSH2 constitutional mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer. 191
Multimodal molecular screening is required to improve the sensitivity of MLH1 and MSH2 mutation analysis - Reply 187
Rectal epithelial cell proliferation patterns as predictors of adenomatous colorectal polyp recurrence. 182
Reliability of rectal epithelial kinetic patterns as an intermediate biomarker of colon cancer. 174
Mutations of the minor mismatch repair gene MSH6 in typical and atypical HNPCC. 163
Modulating effect of omega-3 fatty acids on the proliferative pattern of human colorectal mucosa. 155
A large-scale genetic analysis reveals an autoimmune origin of idiopathic retroperitoneal fibrosis 140
A challenging case of melorheostosis involving the right upper limb 131
Diagnostic Yield and Clinical Impact of a Small Genetic Panel for Kidney Disease: A Multicenter, Retrospective European Study 106
Totale 24.336
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Categoria #
all - tutte 98.263
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 98.263
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.332 0 0 190 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
2025/20268.169 466 331 520 1.106 1.860 469 852 424 679 622 447 393
2026/20271.090 242 434 414 0 0 0 0 0 0 0 0 0
Totale 24.336