PERCESEPE, Antonio
 Distribuzione geografica
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Continente #
NA - Nord America 14.720
AS - Asia 5.236
EU - Europa 4.536
SA - Sud America 708
Continente sconosciuto - Info sul continente non disponibili 126
AF - Africa 111
OC - Oceania 20
Totale 25.457
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Nazione #
US - Stati Uniti d'America 14.314
GB - Regno Unito 1.716
SG - Singapore 1.702
CN - Cina 1.362
IT - Italia 649
VN - Vietnam 571
HK - Hong Kong 557
BR - Brasile 524
SE - Svezia 475
DE - Germania 383
FI - Finlandia 309
BD - Bangladesh 272
UA - Ucraina 262
CA - Canada 250
RU - Federazione Russa 223
TR - Turchia 202
FR - Francia 150
KR - Corea 118
IN - India 114
BG - Bulgaria 93
AR - Argentina 63
NL - Olanda 55
ID - Indonesia 52
MX - Messico 50
IQ - Iraq 46
EC - Ecuador 34
JP - Giappone 34
BE - Belgio 33
AE - Emirati Arabi Uniti 31
ES - Italia 28
IE - Irlanda 28
ZA - Sudafrica 25
MY - Malesia 23
PK - Pakistan 23
CL - Cile 22
CO - Colombia 22
CR - Costa Rica 22
PL - Polonia 21
SA - Arabia Saudita 18
AU - Australia 16
EG - Egitto 16
LT - Lituania 15
UZ - Uzbekistan 15
PH - Filippine 14
KE - Kenya 13
TN - Tunisia 13
CH - Svizzera 12
CZ - Repubblica Ceca 12
JM - Giamaica 12
PY - Paraguay 12
DK - Danimarca 11
DZ - Algeria 11
JO - Giordania 11
MA - Marocco 11
PE - Perù 11
TT - Trinidad e Tobago 11
TW - Taiwan 11
DO - Repubblica Dominicana 10
GT - Guatemala 10
IL - Israele 10
SV - El Salvador 10
VE - Venezuela 9
PR - Porto Rico 8
AT - Austria 7
EE - Estonia 7
NI - Nicaragua 7
TH - Thailandia 7
HU - Ungheria 6
NP - Nepal 6
UY - Uruguay 6
ET - Etiopia 5
IR - Iran 5
RO - Romania 5
SI - Slovenia 5
AL - Albania 4
AZ - Azerbaigian 4
BH - Bahrain 4
BO - Bolivia 4
GP - Guadalupe 4
GR - Grecia 4
MD - Moldavia 4
NZ - Nuova Zelanda 4
AM - Armenia 3
BS - Bahamas 3
CI - Costa d'Avorio 3
CW - ???statistics.table.value.countryCode.CW??? 3
HN - Honduras 3
KG - Kirghizistan 3
KZ - Kazakistan 3
LK - Sri Lanka 3
RS - Serbia 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BA - Bosnia-Erzegovina 2
BY - Bielorussia 2
CG - Congo 2
CU - Cuba 2
EU - Europa 2
HR - Croazia 2
Totale 25.305
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Città #
Ashburn 1.571
Santa Clara 1.186
Fairfield 1.182
Southend 1.174
Singapore 1.140
Woodbridge 775
Houston 619
San Jose 554
Hong Kong 539
Chandler 509
Jacksonville 492
Seattle 466
Wilmington 454
Chicago 438
Cambridge 423
Hefei 402
Ann Arbor 377
Council Bluffs 358
Dearborn 354
Nyköping 320
Los Angeles 296
Beijing 249
London 223
Helsinki 205
Salt Lake City 172
Ho Chi Minh City 171
The Dalles 170
New York 163
Hanoi 139
Modena 136
Izmir 122
Seoul 117
San Diego 114
Princeton 101
Elk Grove Village 91
Eugene 90
Sofia 90
Lauterbourg 82
Milan 82
Tampa 78
Montreal 75
Columbus 73
Buffalo 69
Des Moines 67
Dallas 66
Shanghai 66
Boardman 63
Moscow 62
Munich 51
São Paulo 51
Falls Church 50
Bologna 47
Lancaster 47
Frankfurt am Main 44
Phoenix 43
Ottawa 42
Toronto 41
Cardiff 39
Sterling 39
Vancouver 35
Bremen 34
Jakarta 34
Orem 34
Rio de Janeiro 29
Dublin 28
Philadelphia 28
Tokyo 28
Brussels 27
Dulles 27
Miami 27
Haiphong 24
Rome 24
Detroit 23
Newark 23
Washington 22
Atlanta 21
Da Nang 21
Guangzhou 21
Mexico City 21
North Bergen 21
Chennai 19
San Francisco 19
Baghdad 18
Norwalk 18
Turku 18
Amsterdam 17
Dhaka 17
Fremont 17
Denver 16
Kent 16
Warsaw 16
Kunming 15
Nanjing 15
Pittsburgh 15
Belo Horizonte 14
Boston 14
Brasília 14
Falkenstein 14
Kansas City 14
Naples 14
Totale 18.131
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Nome #
Mismatch repair genes founder mutations and cancer susceptibility in Lynch syndrome 457
K-ras and p53 mutations in hereditary non-polyposis colorectal cancers 439
A two-locus model for hereditary non-polyposis colorectal cancer in Modena, Italy 430
Molecular screening for Hereditary Non Polyposis Colorectal Cancer (HNPCC): a prospective, population-based study 418
Unravelling the Complexity of Inherited Retinal Dystrophies Molecular Testing: Added Value of Targeted Next-Generation Sequencing 412
Microsatellite instability in multiple colorectal tumors 404
Amplicon-based next-generation sequencing: an effective approach for the molecular diagnosis of epidermolysis bullosa 389
Biological parameters determining the clinical outcome of autologous cultures of limbal stem cells 388
New and Rare GJB2 Alleles in Patients with Nonsyndromic Sensorineural Hearing Impairment: A Genotype/Auditory Phenotype Correlation 386
Staging and survival of colorectal cancer: are we making progress? The 14-year experience of a Specialized cancer Registry 376
Frequency and clinical features of multiple tumors of the large bowel in the general population and in patients with hereditary colorectal carcinoma 375
Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report 362
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 355
A 12.4 Mb direct duplication in 19q12-q13 in a boy with cardiac and CNS malformations and developmental delay 353
Survival analysis in families affected by hereditary non-polyposis colorectal cancer 353
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 352
Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts 350
Genes and translocations involved in POF 343
Muir-Torre syndrome or phenocopy? The value of the immunohistochemical expression of mismatch repair proteins in sebaceous tumors of immunocompromised patients 343
Pure segmental trisomy 1q42-qter in a boy with a severe phenotype 342
Problems in the identification of hereditary nonpolyposis colorectal cancer in two families with late development of full-blown clinical spectrum 338
Genetic basis of congenital upper limb anomalies: analysis of 487 cases of a specialized clinic 335
The homozygous deletion of the 3' enhancer of the SHOX gene causes Langer mesomelic dysplasia. 334
Small bowel carcinoma in hereditary nonpolyposis colorectal cancer 334
Predictive diagnostic value for the clinical features accompanying intellectual disability in children with pathogenic copy number variations: a multivariate analysis 330
Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis 328
Facioscapulohumeral muscular dystrophy: new insights from compound heterozygotes and implication for prenatal genetic counselling. 322
Clinical features, frequency and prognosis of Dukes' a colorectal carcinoma: A population-based investigation 320
Methylation pattern of different regions of the MLH1 promoter and silencing of gene expression in hereditary and sporadic colorectal cancer. 317
Age-specific risk of fetal loss post second trimester amniocentesis: analysis of 5043 cases 316
Clinical and molecular diagnosis of hereditary non-polyposis colorectal cancer: problems and pitfalls in an extended pedigree 314
Early diagnosis of branchio-oculo-facial syndrome in a patient with inner ear malformation and mild ocular involvement 309
Familial Short Stature Associated to Terminal Microdeletion of 15q26.3: Variable Phenotype not Involving the IGF1 Receptor Gene 303
Colorectal carcinoma in different age groups: A population based investigation 300
Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination 293
Holoprosencephaly: report of four cases and genotype-phenotype correlations. 292
Pathogenesis of colorectal cancer 290
Circadian variations of epithelial cell proliferation in human rectal crypts. 288
The I1307K polymorphism of the APC gene in colorectal cancer 284
A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAX 277
Clinical and biologic heterogeneity of Hereditary NonPolyposis Colorectal Cancer. 273
Second trimester amniocentesis is not a risk factor for very low birth weight and extremely low birth weight. 269
Collection of Italian hereditary non-polyposis colorectal cancer (HNPCC) pedigrees 268
Clinical features and genotype-phenotype correlations in 41 Italian families with Adenomatosis Coli 266
Cowden's disease with extensive gastrointestinal polyposis. 264
Epidemiologic and genetic factor in colorectal cancer: development of cancer in dizygotic twins in a family with Lynch syndrome 258
[Hereditary factors in tumors of the digestive system]. 258
Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer. 257
Effects of different doses of fish oil on rectal cell proliferation in patients with sporadic colonic adenomas. 257
The DNA repair gene MBD4 (MED1) is mutated in human carcinomas with microsatellite instability 255
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses 255
Pre- and post-natal growth in two sisters with 3-M syndrome 254
Prenatal diagnosis and follow-up of a case of branchio-oto-renal syndrome displays renal growth impairment after the second trimester 253
Il registro dei tumori colorettali 249
First-trimester prenatal screening for the common 35delG GJB2 mutation causing prelingual deafness 249
Non-invasive first trimester fetal gender assignment in pregnancies at risk for X-linked recessive diseases. 248
THE EFFECT OF FAMILY-SIZE ON ESTIMATES OF THE FREQUENCY OF HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER 247
SHOX point mutations and deletions in Leri-Weill dyschondrosteosis. 246
Phenotype-genotype correlations in an extended family with adenomatosis coli and an unusual APC gene mutation 245
Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele 240
Structural chromosomal abnormalities detected during CVS analysis and their role in the prenatal ascertainment of cryptic subtelomeric rearrangements 239
First-trimester ultrasonographic diagnosis of Langer mesomelic dysplasia in a previously affected family. 238
Mismatch repair genes and mononucleotide tracts as mutation targets in colorectal tumors with different degrees of microsatellite instability 237
Molecular genetic analysis of the PLP1 gene in 38 families with PLP1-related disorders: identification and functional characterization of 11 novel PLP1 mutations. 236
Prenatal diagnosis and postnatal follow-up of a child with mosaic trisomy 22 with several levels of mosaicism in different tissues 236
Fenotipo lieve di sordità neurosensoriale e cheratoderma palmo-plantare causato da una nuova mutazione dominante di GJB2 234
Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. 234
Frequency and type of colorectal tumors in asymptomatic high-risk individuals in families with hereditary nonpolyposis colorectal cancer 234
Recurrent germline mutation in MSH2 arises frequently de novo 233
GENETIC EPIDEMIOLOGY OF HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER 232
Mutations Affecting the BHLHA9 DNA-Binding Domain Cause MSSD, Mesoaxial Synostotic Syndactyly with Phalangeal Reduction, Malik-Percin Type 231
Epidemiologia dei tumori del colon-retto. Incidenza, mortalità, familiarità e sopravvivenza nella ex USL di Modena, 1984-1998. 231
Effect of omega-3 fatty acids on rectal mucosal cell proliferation in subjects at risk for colon cancer. 229
Surface rendering of external genitalia of a fetus at the 32nd week of gestation affected by partial androgen insensitivity syndrome. 228
DNA ploidy pattern in human chronic liver diseases and hepatic nodular lesions. Flow cytometric analysis on echo-guided needle liver biopsy. 226
Liquid biopsy with cell free DNA: new horizons for prostate cancer 226
Role of clinical criteria in the diagnosis of HNPCC: results of a multivariate analysis 220
Quantitation of fetal DNA in maternal serum during the first trimester of pregnancy by the use of a DAZ repetitive probe 214
Epidemiology of cancer of the large bowel - The 12-year experience of a specialized registry in Northern Italy 214
The role of hPMS1 and hPMS2 in predisposing to colorectal cancer 210
Microsatellite instability and mismatch-repair protein expression in hereditary and sporadic colorectal carcinogenesis 206
Hereditary nonpolyposis colorectal cancer: an approach to the selection of candidates to genetic testing based on clinical and molecular characteristics 204
MLH1 and MSH2 constitutional mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer. 197
Multimodal molecular screening is required to improve the sensitivity of MLH1 and MSH2 mutation analysis - Reply 192
Rectal epithelial cell proliferation patterns as predictors of adenomatous colorectal polyp recurrence. 189
Reliability of rectal epithelial kinetic patterns as an intermediate biomarker of colon cancer. 183
Mutations of the minor mismatch repair gene MSH6 in typical and atypical HNPCC. 180
Modulating effect of omega-3 fatty acids on the proliferative pattern of human colorectal mucosa. 160
A large-scale genetic analysis reveals an autoimmune origin of idiopathic retroperitoneal fibrosis 149
A challenging case of melorheostosis involving the right upper limb 136
Diagnostic Yield and Clinical Impact of a Small Genetic Panel for Kidney Disease: A Multicenter, Retrospective European Study 117
Totale 25.457
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Categoria #
all - tutte 101.307
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 101.307
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.142 0 0 0 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
2026/20272.211 242 434 609 926 0 0 0 0 0 0 0 0
Totale 25.457