TURCO, Alberto
 Distribuzione geografica
Continente #
NA - Nord America 3.577
EU - Europa 2.641
AS - Asia 1.991
SA - Sud America 199
AF - Africa 36
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 2
Totale 8.455
Nazione #
US - Stati Uniti d'America 3.530
RU - Federazione Russa 957
SG - Singapore 931
CN - Cina 527
GB - Regno Unito 495
SE - Svezia 221
DE - Germania 175
IE - Irlanda 175
IT - Italia 169
BR - Brasile 166
HK - Hong Kong 162
FI - Finlandia 154
VN - Vietnam 150
FR - Francia 129
KR - Corea 68
UA - Ucraina 56
BE - Belgio 34
IN - India 30
NL - Olanda 29
CA - Canada 26
JP - Giappone 20
TR - Turchia 19
BD - Bangladesh 18
MX - Messico 14
IQ - Iraq 13
AR - Argentina 12
ID - Indonesia 12
PL - Polonia 12
ZA - Sudafrica 11
NG - Nigeria 9
AU - Australia 8
ES - Italia 8
UZ - Uzbekistan 8
EC - Ecuador 6
SA - Arabia Saudita 6
MA - Marocco 5
PH - Filippine 5
PK - Pakistan 5
JO - Giordania 4
PE - Perù 4
PY - Paraguay 4
AT - Austria 3
BO - Bolivia 3
CL - Cile 3
ET - Etiopia 3
KZ - Kazakistan 3
LV - Lettonia 3
AE - Emirati Arabi Uniti 2
CR - Costa Rica 2
EG - Egitto 2
GR - Grecia 2
LI - Liechtenstein 2
LT - Lituania 2
MY - Malesia 2
PA - Panama 2
RO - Romania 2
RS - Serbia 2
TN - Tunisia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BS - Bahamas 1
BY - Bielorussia 1
CG - Congo 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
DZ - Algeria 1
HU - Ungheria 1
IL - Israele 1
IM - Isola di Man 1
IR - Iran 1
KE - Kenya 1
LU - Lussemburgo 1
LY - Libia 1
MS - Montserrat 1
MT - Malta 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
SI - Slovenia 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
VE - Venezuela 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 8.455
Città #
Singapore 523
Jacksonville 479
Southend 366
Ashburn 343
Chandler 342
Dallas 340
Moscow 327
Woodbridge 252
San Jose 234
Ann Arbor 182
Dublin 175
Hong Kong 160
Houston 129
Verona 104
The Dalles 98
New York 86
Wilmington 79
Los Angeles 58
Lawrence 57
Princeton 57
Beijing 56
Ho Chi Minh City 51
Nanjing 48
Hanoi 39
Kent 39
Munich 39
Jinan 34
Shenyang 33
Helsinki 32
Boardman 30
Tianjin 28
Buffalo 27
Columbus 27
Falls Church 26
Sindelfingen 26
Nanchang 22
Brussels 20
Hebei 20
Ningbo 20
Santa Clara 20
Tokyo 19
Turku 17
São Paulo 16
Changsha 15
Haikou 15
Waanrode 14
London 13
Philadelphia 13
San Francisco 13
Guangzhou 12
Hangzhou 12
Jiaxing 12
Norwalk 12
Orem 12
Zhengzhou 12
Amsterdam 11
Milan 11
Redmond 11
Seoul 11
Chennai 10
Frankfurt am Main 10
Redondo Beach 10
Seattle 10
Brooklyn 9
Chicago 9
Council Bluffs 9
Jakarta 9
Poplar 9
Rio de Janeiro 9
Da Nang 8
Johannesburg 8
Montreal 8
Mumbai 8
Stockholm 8
Taizhou 8
Tashkent 8
Toronto 8
Warsaw 8
Abuja 7
Denver 7
Lancaster 7
Melbourne 7
Taiyuan 7
Ansbach 6
Atlanta 6
Auburn Hills 6
Barnet 6
Belo Horizonte 6
Düsseldorf 6
Ankara 5
Dearborn 5
Erbil 5
Hải Dương 5
Mexico City 5
Phoenix 5
Baghdad 4
Boston 4
Fairfield 4
Haiphong 4
Porto Alegre 4
Totale 5.566
Nome #
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 256
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 246
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 227
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 224
Autosomal dominant polycystic kidney disease: clinical and genetic aspects 207
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 201
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 200
Association of promoter polymorphism -765G>C in the PTGS2 gene with malignant melanoma in Italian patients and its correlation to gene expression in dermal fibroblasts. 192
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 187
A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1) 182
A novel nonsense mutation in the PKD1 gene (C3817T) is associated with autosomal dominant polycystic kidney disease (ADPKD) in a large three-generation Italian family 178
Clinical applications of genetic linkage analysis for the molecular diagnostics of ADPKD, using DNA markers linked to the PKD1 and PKD2 genes 174
Autosomal dominant polycystic kidney disease (ADPKD) in an Italian family carrying a novel nonsense mutation and two missense changes in exons 44 and 45 of the PKD1 Gene 170
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 169
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 169
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene 167
Alport syndrome: the point of view of a pediatric nephrologist 165
Analysis of published PKD1 gene sequence variants. 164
Tracking disease genes by reverse genetics 162
Clinical value of PCR in diagnosis and follow-up of leukaemia and lymphoma: report of the Third Workshop of the Molecular Biology/BMT Study Group 160
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome 156
A mild phenotype of incontinentia pigmenti in a male child: DNA confirmation of a somatic mosaicism 156
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 156
Viral and cellular deoxyribonucleases are associated with herpes simplex virus replicative intermediates 155
A novel frameshift deletion in type IV collagen alpha 5 gene in a juvenile-type Alport syndrome patient: an adenine deletion (2940/2943 del A) in exon 34 of COL4A5 150
Capitolo 2: Le cellule e la divisione cellulare 150
Capitolo 1: Genetica umana: una prospettiva 150
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 148
Autosomal dominant polycystic kidney disease (ADPKD): screening for mutations and polymorphisms in the duplicated region of the PKD1 gene. 147
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 145
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene 144
Alport syndrome--is there a genotype-phenotype relationship? [editorial] 144
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers 144
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genes 143
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian families 142
Detection of two different nonsense mutations in exon 44 of the PKD1 gene in two unrelated Italian families with severe autosomal dominant polycystic kidney disease 130
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 130
Three novel mutations of the PKD1 gene in Italian families with autosomal dominant polycystic kidney disease 129
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reaction 126
Renin-angiotensin system (RAS) DNA polymorphisms and TGFbeta1-mediated fibrogenetic pathway gene expression studies in primary IgA naphropathy (Berger’s disease). 126
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) and familial adenomatous polyposis (FAP) 122
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresia 122
ERRONOUS GENETIC RISK ASSESMENT OF ALPORT SYNDROME 118
Evidence against the reported linkage of the cutaneous melanoma dysplastic nevus syndrome locus to chromosome 1p36. 116
Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's Syndrome 111
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers 110
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects 110
Molecular genetic investigations in autosomal dominant polycystic kidney disease. Gene Mutation detection, linkage analysis, and preliminary ACE gene I/D polymorphism association studies: an update 107
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome 107
Genetica e clinica della malattia policistica renale autosomica dominante (ADPKD): recenti acquisizioni su una malattia molto frequente e poco conosciuta 107
Recurrence of the PKD1 nonsense mutation Q4041X in Spanish, Italian, and British families 102
Rapid DNA-based prenatal diagnosis of autosomal dominant polycystic kidney disease 101
Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA) 100
Genetics and nephro-uropathies 99
Malformazioni renali non cistiche ad espressione fenotipica variabile : descrizione di una famiglia 90
Pregnancy, microchimerism and autoimmunity: An update 90
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndome 87
Totale 8.470
Categoria #
all - tutte 25.789
article - articoli 24.410
book - libri 0
conference - conferenze 551
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 828
Totale 51.578


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202195 0 0 0 0 0 0 0 0 0 2 76 17
2021/2022410 23 79 2 42 18 23 8 21 26 10 45 113
2022/20231.022 70 100 93 152 105 245 24 71 101 3 43 15
2023/2024444 13 51 38 46 57 78 15 29 4 14 78 21
2024/20251.144 88 77 23 183 63 10 46 60 198 64 116 216
2025/20263.246 264 183 279 493 845 264 380 162 185 191 0 0
Totale 8.470