PERCESEPE, Antonio
 Distribuzione geografica
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Continente #
NA - Nord America 12.868
AS - Asia 5.170
EU - Europa 4.446
SA - Sud America 691
AF - Africa 108
OC - Oceania 19
Continente sconosciuto - Info sul continente non disponibili 6
Totale 23.308
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Nazione #
US - Stati Uniti d'America 12.629
GB - Regno Unito 1.698
SG - Singapore 1.692
CN - Cina 1.347
IT - Italia 601
VN - Vietnam 566
HK - Hong Kong 542
BR - Brasile 513
SE - Svezia 474
DE - Germania 377
FI - Finlandia 309
BD - Bangladesh 264
UA - Ucraina 260
RU - Federazione Russa 222
TR - Turchia 202
CA - Canada 149
FR - Francia 148
KR - Corea 117
IN - India 112
BG - Bulgaria 93
AR - Argentina 62
NL - Olanda 55
ID - Indonesia 51
MX - Messico 48
IQ - Iraq 46
BE - Belgio 32
EC - Ecuador 32
AE - Emirati Arabi Uniti 31
JP - Giappone 30
IE - Irlanda 27
ES - Italia 26
ZA - Sudafrica 24
PK - Pakistan 22
CL - Cile 21
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
DZ - Algeria 11
JO - Giordania 11
MA - Marocco 11
PE - Perù 11
TW - Taiwan 11
DO - Repubblica Dominicana 10
IL - Israele 9
VE - Venezuela 9
DK - Danimarca 8
JM - Giamaica 8
AT - Austria 7
TH - Thailandia 7
CR - Costa Rica 6
NP - Nepal 6
UY - Uruguay 6
EE - Estonia 5
ET - Etiopia 5
HU - Ungheria 5
IR - Iran 5
RO - Romania 5
SI - Slovenia 5
AZ - Azerbaigian 4
BH - Bahrain 4
BO - Bolivia 4
GR - Grecia 4
MD - Moldavia 4
AL - Albania 3
AM - Armenia 3
BS - Bahamas 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
BY - Bielorussia 2
CG - Congo 2
EU - Europa 2
GT - Guatemala 2
HN - Honduras 2
HR - Croazia 2
IS - Islanda 2
KH - Cambogia 2
LV - Lettonia 2
NI - Nicaragua 2
PA - Panama 2
PR - Porto Rico 2
PS - Palestinian Territory 2
Totale 23.282
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Città #
Fairfield 1.182
Southend 1.174
Santa Clara 1.161
Singapore 1.135
Ashburn 1.067
Woodbridge 774
Houston 612
Hong Kong 534
Chandler 508
Jacksonville 491
Seattle 462
Wilmington 449
Chicago 424
Cambridge 423
Hefei 402
San Jose 384
Ann Arbor 377
Dearborn 354
Nyköping 320
Los Angeles 277
Beijing 245
London 220
Helsinki 205
Salt Lake City 172
Ho Chi Minh City 170
The Dalles 162
Council Bluffs 156
New York 146
Hanoi 137
Modena 135
Izmir 122
Seoul 116
San Diego 113
Princeton 100
Elk Grove Village 91
Eugene 90
Sofia 90
Lauterbourg 82
Tampa 77
Milan 71
Des Moines 66
Shanghai 65
Buffalo 64
Moscow 62
Dallas 58
Munich 51
Falls Church 50
Columbus 47
Lancaster 47
Bologna 46
São Paulo 46
Frankfurt am Main 42
Cardiff 39
Ottawa 39
Sterling 39
Bremen 34
Orem 34
Vancouver 34
Jakarta 33
Rio de Janeiro 29
Dublin 27
Dulles 27
Tokyo 27
Toronto 27
Brussels 26
Miami 25
Haiphong 24
Detroit 23
Phoenix 23
Da Nang 21
Guangzhou 21
Mexico City 20
Rome 20
Boardman 19
Chennai 19
Baghdad 18
Turku 18
Amsterdam 17
Dhaka 17
Fremont 17
Norwalk 17
Kent 16
Philadelphia 16
Atlanta 15
Kunming 15
Nanjing 15
Pittsburgh 15
Warsaw 15
Belo Horizonte 14
Boston 14
Denver 14
Falkenstein 14
Kansas City 14
Tashkent 14
Brasília 13
Hải Dương 13
Miano 13
Naples 13
Redwood City 13
Montreal 12
Totale 16.856
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Nome #
K-ras and p53 mutations in hereditary non-polyposis colorectal cancers 421
A two-locus model for hereditary non-polyposis colorectal cancer in Modena, Italy 412
Unravelling the Complexity of Inherited Retinal Dystrophies Molecular Testing: Added Value of Targeted Next-Generation Sequencing 397
Microsatellite instability in multiple colorectal tumors 386
Molecular screening for Hereditary Non Polyposis Colorectal Cancer (HNPCC): a prospective, population-based study 380
Amplicon-based next-generation sequencing: an effective approach for the molecular diagnosis of epidermolysis bullosa 368
Biological parameters determining the clinical outcome of autologous cultures of limbal stem cells 361
Staging and survival of colorectal cancer: are we making progress? The 14-year experience of a Specialized cancer Registry 361
New and Rare GJB2 Alleles in Patients with Nonsyndromic Sensorineural Hearing Impairment: A Genotype/Auditory Phenotype Correlation 356
Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report 348
Frequency and clinical features of multiple tumors of the large bowel in the general population and in patients with hereditary colorectal carcinoma 345
Survival analysis in families affected by hereditary non-polyposis colorectal cancer 340
Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts 336
A 12.4 Mb direct duplication in 19q12-q13 in a boy with cardiac and CNS malformations and developmental delay 333
Pure segmental trisomy 1q42-qter in a boy with a severe phenotype 330
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 326
The homozygous deletion of the 3' enhancer of the SHOX gene causes Langer mesomelic dysplasia. 325
Muir-Torre syndrome or phenocopy? The value of the immunohistochemical expression of mismatch repair proteins in sebaceous tumors of immunocompromised patients 324
Small bowel carcinoma in hereditary nonpolyposis colorectal cancer 324
Problems in the identification of hereditary nonpolyposis colorectal cancer in two families with late development of full-blown clinical spectrum 321
Mismatch repair genes founder mutations and cancer susceptibility in Lynch syndrome 321
Predictive diagnostic value for the clinical features accompanying intellectual disability in children with pathogenic copy number variations: a multivariate analysis 320
Genes and translocations involved in POF 317
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 317
Genetic basis of congenital upper limb anomalies: analysis of 487 cases of a specialized clinic 303
Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis 303
Methylation pattern of different regions of the MLH1 promoter and silencing of gene expression in hereditary and sporadic colorectal cancer. 302
Clinical features, frequency and prognosis of Dukes' a colorectal carcinoma: A population-based investigation 300
Early diagnosis of branchio-oculo-facial syndrome in a patient with inner ear malformation and mild ocular involvement 299
Facioscapulohumeral muscular dystrophy: new insights from compound heterozygotes and implication for prenatal genetic counselling. 298
Clinical and molecular diagnosis of hereditary non-polyposis colorectal cancer: problems and pitfalls in an extended pedigree 290
Age-specific risk of fetal loss post second trimester amniocentesis: analysis of 5043 cases 290
Familial Short Stature Associated to Terminal Microdeletion of 15q26.3: Variable Phenotype not Involving the IGF1 Receptor Gene 287
Colorectal carcinoma in different age groups: A population based investigation 275
Holoprosencephaly: report of four cases and genotype-phenotype correlations. 275
Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination 273
Pathogenesis of colorectal cancer 260
Circadian variations of epithelial cell proliferation in human rectal crypts. 258
Clinical and biologic heterogeneity of Hereditary NonPolyposis Colorectal Cancer. 258
Collection of Italian hereditary non-polyposis colorectal cancer (HNPCC) pedigrees 253
The I1307K polymorphism of the APC gene in colorectal cancer 247
Second trimester amniocentesis is not a risk factor for very low birth weight and extremely low birth weight. 246
Epidemiologic and genetic factor in colorectal cancer: development of cancer in dizygotic twins in a family with Lynch syndrome 243
Prenatal diagnosis and follow-up of a case of branchio-oto-renal syndrome displays renal growth impairment after the second trimester 243
Clinical features and genotype-phenotype correlations in 41 Italian families with Adenomatosis Coli 242
A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAX 242
[Hereditary factors in tumors of the digestive system]. 240
Cowden's disease with extensive gastrointestinal polyposis. 240
Pre- and post-natal growth in two sisters with 3-M syndrome 239
THE EFFECT OF FAMILY-SIZE ON ESTIMATES OF THE FREQUENCY OF HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER 238
SHOX point mutations and deletions in Leri-Weill dyschondrosteosis. 236
First-trimester ultrasonographic diagnosis of Langer mesomelic dysplasia in a previously affected family. 230
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses 230
Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele 229
Non-invasive first trimester fetal gender assignment in pregnancies at risk for X-linked recessive diseases. 229
Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer. 229
Phenotype-genotype correlations in an extended family with adenomatosis coli and an unusual APC gene mutation 228
First-trimester prenatal screening for the common 35delG GJB2 mutation causing prelingual deafness 227
Effects of different doses of fish oil on rectal cell proliferation in patients with sporadic colonic adenomas. 226
Fenotipo lieve di sordità neurosensoriale e cheratoderma palmo-plantare causato da una nuova mutazione dominante di GJB2 223
The DNA repair gene MBD4 (MED1) is mutated in human carcinomas with microsatellite instability 221
Structural chromosomal abnormalities detected during CVS analysis and their role in the prenatal ascertainment of cryptic subtelomeric rearrangements 221
Prenatal diagnosis and postnatal follow-up of a child with mosaic trisomy 22 with several levels of mosaicism in different tissues 220
Surface rendering of external genitalia of a fetus at the 32nd week of gestation affected by partial androgen insensitivity syndrome. 220
Frequency and type of colorectal tumors in asymptomatic high-risk individuals in families with hereditary nonpolyposis colorectal cancer 220
Molecular genetic analysis of the PLP1 gene in 38 families with PLP1-related disorders: identification and functional characterization of 11 novel PLP1 mutations. 218
Mutations Affecting the BHLHA9 DNA-Binding Domain Cause MSSD, Mesoaxial Synostotic Syndactyly with Phalangeal Reduction, Malik-Percin Type 218
Mismatch repair genes and mononucleotide tracts as mutation targets in colorectal tumors with different degrees of microsatellite instability 217
Il registro dei tumori colorettali 215
Recurrent germline mutation in MSH2 arises frequently de novo 209
Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. 209
DNA ploidy pattern in human chronic liver diseases and hepatic nodular lesions. Flow cytometric analysis on echo-guided needle liver biopsy. 204
Quantitation of fetal DNA in maternal serum during the first trimester of pregnancy by the use of a DAZ repetitive probe 203
Liquid biopsy with cell free DNA: new horizons for prostate cancer 203
Epidemiology of cancer of the large bowel - The 12-year experience of a specialized registry in Northern Italy 199
Hereditary nonpolyposis colorectal cancer: an approach to the selection of candidates to genetic testing based on clinical and molecular characteristics 191
Microsatellite instability and mismatch-repair protein expression in hereditary and sporadic colorectal carcinogenesis 191
GENETIC EPIDEMIOLOGY OF HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER 188
The role of hPMS1 and hPMS2 in predisposing to colorectal cancer 188
Epidemiologia dei tumori del colon-retto. Incidenza, mortalità, familiarità e sopravvivenza nella ex USL di Modena, 1984-1998. 187
MLH1 and MSH2 constitutional mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer. 183
Effect of omega-3 fatty acids on rectal mucosal cell proliferation in subjects at risk for colon cancer. 181
Multimodal molecular screening is required to improve the sensitivity of MLH1 and MSH2 mutation analysis - Reply 180
Role of clinical criteria in the diagnosis of HNPCC: results of a multivariate analysis 176
Rectal epithelial cell proliferation patterns as predictors of adenomatous colorectal polyp recurrence. 165
Reliability of rectal epithelial kinetic patterns as an intermediate biomarker of colon cancer. 162
Mutations of the minor mismatch repair gene MSH6 in typical and atypical HNPCC. 146
Modulating effect of omega-3 fatty acids on the proliferative pattern of human colorectal mucosa. 145
A large-scale genetic analysis reveals an autoimmune origin of idiopathic retroperitoneal fibrosis 133
A challenging case of melorheostosis involving the right upper limb 113
Diagnostic Yield and Clinical Impact of a Small Genetic Panel for Kidney Disease: A Multicenter, Retrospective European Study 99
Totale 23.425
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Categoria #
all - tutte 93.894
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 93.894
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20268.169 466 331 520 1.106 1.860 469 852 424 679 622 447 393
2026/2027179 179 0 0 0 0 0 0 0 0 0 0 0
Totale 23.425