PERCESEPE, Antonio
 Distribuzione geografica
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Continente #
NA - Nord America 8.693
EU - Europa 3.155
AS - Asia 1.268
SA - Sud America 42
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 4
AF - Africa 3
Totale 13.177
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Nazione #
US - Stati Uniti d'America 8.634
GB - Regno Unito 1.426
SE - Svezia 444
CN - Cina 422
SG - Singapore 393
IT - Italia 344
DE - Germania 268
UA - Ucraina 238
HK - Hong Kong 175
TR - Turchia 174
FI - Finlandia 127
BG - Bulgaria 89
CA - Canada 53
FR - Francia 40
NL - Olanda 39
BR - Brasile 32
RU - Federazione Russa 32
IN - India 31
BE - Belgio 29
ID - Indonesia 22
IE - Irlanda 21
MY - Malesia 12
VN - Vietnam 12
LT - Lituania 10
AU - Australia 9
CZ - Repubblica Ceca 8
ES - Italia 8
CH - Svizzera 6
MX - Messico 6
PL - Polonia 5
CL - Cile 3
IL - Israele 3
IQ - Iraq 3
IR - Iran 3
JP - Giappone 3
NZ - Nuova Zelanda 3
RS - Serbia 3
SA - Arabia Saudita 3
SI - Slovenia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AM - Armenia 2
BD - Bangladesh 2
DK - Danimarca 2
EC - Ecuador 2
EG - Egitto 2
EU - Europa 2
GR - Grecia 2
KR - Corea 2
PE - Perù 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 2
AL - Albania 1
AR - Argentina 1
BA - Bosnia-Erzegovina 1
BO - Bolivia 1
CO - Colombia 1
EE - Estonia 1
HU - Ungheria 1
KH - Cambogia 1
KZ - Kazakistan 1
LK - Sri Lanka 1
LV - Lettonia 1
MA - Marocco 1
MD - Moldavia 1
NO - Norvegia 1
PK - Pakistan 1
TH - Thailandia 1
TW - Taiwan 1
Totale 13.177
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Città #
Fairfield 1.182
Southend 1.174
Santa Clara 1.077
Woodbridge 773
Houston 602
Ashburn 538
Chandler 508
Jacksonville 488
Seattle 455
Wilmington 422
Cambridge 419
Ann Arbor 377
Dearborn 354
Nyköping 320
Singapore 275
Hong Kong 172
Modena 130
Izmir 122
San Diego 113
Beijing 100
Princeton 99
Eugene 90
Sofia 89
Des Moines 66
New York 65
Falls Church 50
Shanghai 44
Helsinki 41
Ottawa 36
London 35
Bremen 34
Bologna 27
Brussels 24
Jakarta 22
Dublin 21
Frankfurt am Main 19
Milan 18
Fremont 17
Moscow 17
Norwalk 16
Chicago 14
Guangzhou 14
Nanjing 14
Boardman 13
Kunming 13
Redwood City 13
Toronto 13
San Mateo 11
Dong Ket 10
Hefei 10
Hounslow 10
Amsterdam 9
Kilburn 9
Munich 8
Parma 8
Philadelphia 8
Castelnuovo Rangone 7
Chiswick 7
Frechen 7
Jinan 7
San Jose 7
São Paulo 7
Washington 7
Brno 6
Nanchang 6
Prescot 6
Rio Saliceto 6
Rome 6
Chengdu 5
Grafing 5
Leawood 5
Los Angeles 5
Monmouth Junction 5
Phoenix 5
Saint Petersburg 5
Verona 5
Zhengzhou 5
Auburn Hills 4
Belo Horizonte 4
Florence 4
Mountain View 4
Porto Recanati 4
Saint Catharines 4
Southwark 4
Waanrode 4
Ardabil 3
Augusta 3
Belgrade 3
Busto Arsizio 3
Cary 3
Chongqing 3
Dallas 3
Fuzhou 3
Hebei 3
Hoogvliet 3
Indiana 3
Mumbai 3
New Bedfont 3
Norwich 3
San Francisco 3
Totale 10.809
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Nome #
Unravelling the Complexity of Inherited Retinal Dystrophies Molecular Testing: Added Value of Targeted Next-Generation Sequencing 244
Muir-Torre syndrome or phenocopy? The value of the immunohistochemical expression of mismatch repair proteins in sebaceous tumors of immunocompromised patients 232
Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report 231
Mismatch repair genes founder mutations and cancer susceptibility in Lynch syndrome 230
Amplicon-based next-generation sequencing: an effective approach for the molecular diagnosis of epidermolysis bullosa 227
Biological parameters determining the clinical outcome of autologous cultures of limbal stem cells 210
Early diagnosis of branchio-oculo-facial syndrome in a patient with inner ear malformation and mild ocular involvement 210
New and Rare GJB2 Alleles in Patients with Nonsyndromic Sensorineural Hearing Impairment: A Genotype/Auditory Phenotype Correlation 203
Predictive diagnostic value for the clinical features accompanying intellectual disability in children with pathogenic copy number variations: a multivariate analysis 196
K-ras and p53 mutations in hereditary non-polyposis colorectal cancers 194
Clinical features, frequency and prognosis of Dukes' a colorectal carcinoma: A population-based investigation 192
A 12.4 Mb direct duplication in 19q12-q13 in a boy with cardiac and CNS malformations and developmental delay 191
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 191
Genes and translocations involved in POF 186
Holoprosencephaly: report of four cases and genotype-phenotype correlations. 185
Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis 181
Facioscapulohumeral muscular dystrophy: new insights from compound heterozygotes and implication for prenatal genetic counselling. 181
Genetic basis of congenital upper limb anomalies: analysis of 487 cases of a specialized clinic 180
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 179
Age-specific risk of fetal loss post second trimester amniocentesis: analysis of 5043 cases 178
Pre- and post-natal growth in two sisters with 3-M syndrome 170
Second trimester amniocentesis is not a risk factor for very low birth weight and extremely low birth weight. 168
Mutations Affecting the BHLHA9 DNA-Binding Domain Cause MSSD, Mesoaxial Synostotic Syndactyly with Phalangeal Reduction, Malik-Percin Type 166
Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination 161
First-trimester ultrasonographic diagnosis of Langer mesomelic dysplasia in a previously affected family. 161
Molecular screening for Hereditary Non Polyposis Colorectal Cancer (HNPCC): a prospective, population-based study 161
Collection of Italian hereditary non-polyposis colorectal cancer (HNPCC) pedigrees 159
Structural chromosomal abnormalities detected during CVS analysis and their role in the prenatal ascertainment of cryptic subtelomeric rearrangements 159
Pure segmental trisomy 1q42-qter in a boy with a severe phenotype 159
Surface rendering of external genitalia of a fetus at the 32nd week of gestation affected by partial androgen insensitivity syndrome. 159
The I1307K polymorphism of the APC gene in colorectal cancer 158
Familial Short Stature Associated to Terminal Microdeletion of 15q26.3: Variable Phenotype not Involving the IGF1 Receptor Gene 157
A two-locus model for hereditary non-polyposis colorectal cancer in Modena, Italy 156
Frequency and clinical features of multiple tumors of the large bowel in the general population and in patients with hereditary colorectal carcinoma 156
Clinical and biologic heterogeneity of Hereditary NonPolyposis Colorectal Cancer. 156
Survival analysis in families affected by hereditary non-polyposis colorectal cancer 155
Prenatal diagnosis and postnatal follow-up of a child with mosaic trisomy 22 with several levels of mosaicism in different tissues 154
Microsatellite instability in multiple colorectal tumors 154
A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAX 154
Recurrent germline mutation in MSH2 arises frequently de novo 153
Staging and survival of colorectal cancer: are we making progress? The 14-year experience of a Specialized cancer Registry 153
SHOX point mutations and deletions in Leri-Weill dyschondrosteosis. 152
Cowden's disease with extensive gastrointestinal polyposis. 151
Molecular genetic analysis of the PLP1 gene in 38 families with PLP1-related disorders: identification and functional characterization of 11 novel PLP1 mutations. 148
The homozygous deletion of the 3' enhancer of the SHOX gene causes Langer mesomelic dysplasia. 148
Small bowel carcinoma in hereditary nonpolyposis colorectal cancer 148
THE EFFECT OF FAMILY-SIZE ON ESTIMATES OF THE FREQUENCY OF HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER 147
Circadian variations of epithelial cell proliferation in human rectal crypts. 147
First-trimester prenatal screening for the common 35delG GJB2 mutation causing prelingual deafness 147
Clinical and molecular diagnosis of hereditary non-polyposis colorectal cancer: problems and pitfalls in an extended pedigree 146
Quantitation of fetal DNA in maternal serum during the first trimester of pregnancy by the use of a DAZ repetitive probe 146
DNA ploidy pattern in human chronic liver diseases and hepatic nodular lesions. Flow cytometric analysis on echo-guided needle liver biopsy. 144
Colorectal carcinoma in different age groups: A population based investigation 143
Non-invasive first trimester fetal gender assignment in pregnancies at risk for X-linked recessive diseases. 143
Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer. 143
Effects of different doses of fish oil on rectal cell proliferation in patients with sporadic colonic adenomas. 141
Epidemiologic and genetic factor in colorectal cancer: development of cancer in dizygotic twins in a family with Lynch syndrome 140
Clinical features and genotype-phenotype correlations in 41 Italian families with Adenomatosis Coli 140
Mismatch repair genes and mononucleotide tracts as mutation targets in colorectal tumors with different degrees of microsatellite instability 140
Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts 139
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses 139
Fenotipo lieve di sordità neurosensoriale e cheratoderma palmo-plantare causato da una nuova mutazione dominante di GJB2 139
Pathogenesis of colorectal cancer 139
Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. 139
Hereditary nonpolyposis colorectal cancer: an approach to the selection of candidates to genetic testing based on clinical and molecular characteristics 138
Problems in the identification of hereditary nonpolyposis colorectal cancer in two families with late development of full-blown clinical spectrum 134
Prenatal diagnosis and follow-up of a case of branchio-oto-renal syndrome displays renal growth impairment after the second trimester 129
Methylation pattern of different regions of the MLH1 promoter and silencing of gene expression in hereditary and sporadic colorectal cancer. 124
Phenotype-genotype correlations in an extended family with adenomatosis coli and an unusual APC gene mutation 121
Effect of omega-3 fatty acids on rectal mucosal cell proliferation in subjects at risk for colon cancer. 120
The DNA repair gene MBD4 (MED1) is mutated in human carcinomas with microsatellite instability 119
Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele 118
Frequency and type of colorectal tumors in asymptomatic high-risk individuals in families with hereditary nonpolyposis colorectal cancer 116
Epidemiologia dei tumori del colon-retto. Incidenza, mortalità, familiarità e sopravvivenza nella ex USL di Modena, 1984-1998. 115
Il registro dei tumori colorettali 114
Rectal epithelial cell proliferation patterns as predictors of adenomatous colorectal polyp recurrence. 108
Epidemiology of cancer of the large bowel - The 12-year experience of a specialized registry in Northern Italy 106
Multimodal molecular screening is required to improve the sensitivity of MLH1 and MSH2 mutation analysis - Reply 103
Liquid biopsy with cell free DNA: new horizons for prostate cancer 103
Role of clinical criteria in the diagnosis of HNPCC: results of a multivariate analysis 101
Microsatellite instability and mismatch-repair protein expression in hereditary and sporadic colorectal carcinogenesis 101
The role of hPMS1 and hPMS2 in predisposing to colorectal cancer 101
GENETIC EPIDEMIOLOGY OF HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER 99
[Hereditary factors in tumors of the digestive system]. 98
MLH1 and MSH2 constitutional mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer. 92
Mutations of the minor mismatch repair gene MSH6 in typical and atypical HNPCC. 91
Modulating effect of omega-3 fatty acids on the proliferative pattern of human colorectal mucosa. 83
Reliability of rectal epithelial kinetic patterns as an intermediate biomarker of colon cancer. 79
A large-scale genetic analysis reveals an autoimmune origin of idiopathic retroperitoneal fibrosis 19
Totale 13.291
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Categoria #
all - tutte 61.594
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 61.594
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.807 0 0 0 0 0 436 426 273 336 87 135 114
2020/20211.913 187 92 148 169 220 106 170 252 78 245 112 134
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
2024/20251.683 126 30 43 244 792 448 0 0 0 0 0 0
Totale 13.291