IRIS Institutional Research Information System - OPENBS Open Archive UniBS

GARDELLA, Rita
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 3.626
EU - Europa 2.141
AS - Asia 1.754
SA - Sud America 267
AF - Africa 32
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 2
AN - Antartide 1
Totale 7.828
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 3.580
CN - Cina 747
PL - Polonia 637
SG - Singapore 508
UA - Ucraina 400
IT - Italia 344
BR - Brasile 229
DE - Germania 191
HK - Hong Kong 180
GB - Regno Unito 131
FI - Finlandia 123
FR - Francia 110
VN - Vietnam 87
TR - Turchia 62
IE - Irlanda 59
RU - Federazione Russa 59
IN - India 57
BD - Bangladesh 26
CA - Canada 25
BE - Belgio 20
KR - Corea 18
AR - Argentina 14
ID - Indonesia 14
ZA - Sudafrica 14
CZ - Repubblica Ceca 12
SE - Svezia 12
MX - Messico 11
NL - Olanda 11
ES - Italia 10
AT - Austria 9
IQ - Iraq 8
JP - Giappone 8
SA - Arabia Saudita 7
EC - Ecuador 6
IR - Iran 5
KE - Kenya 5
AU - Australia 4
LT - Lituania 4
MA - Marocco 4
PE - Perù 4
TW - Taiwan 4
UZ - Uzbekistan 4
AE - Emirati Arabi Uniti 3
CH - Svizzera 3
CO - Colombia 3
JM - Giamaica 3
MU - Mauritius 3
TT - Trinidad e Tobago 3
UY - Uruguay 3
VE - Venezuela 3
BO - Bolivia 2
EU - Europa 2
HN - Honduras 2
PA - Panama 2
PH - Filippine 2
PK - Pakistan 2
AL - Albania 1
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BH - Bahrain 1
CG - Congo 1
CL - Cile 1
CY - Cipro 1
EG - Egitto 1
ET - Etiopia 1
FK - Isole Falkland (Malvinas) 1
GE - Georgia 1
GS - Georgia del Sud e Isole Sandwich Australi 1
HU - Ungheria 1
IL - Israele 1
JO - Giordania 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LK - Sri Lanka 1
NZ - Nuova Zelanda 1
PS - Palestinian Territory 1
PY - Paraguay 1
RO - Romania 1
SC - Seychelles 1
SI - Slovenia 1
SN - Senegal 1
SY - Repubblica araba siriana 1
TN - Tunisia 1
Totale 7.828
Salva come PNG Salva come JPEG
Città #
Warsaw 636
Fairfield 435
Ashburn 324
Woodbridge 323
Jacksonville 286
Singapore 253
Houston 252
Seattle 188
Hong Kong 179
Ann Arbor 165
Cambridge 161
Beijing 156
Wilmington 152
Brescia 137
Chandler 132
Nanjing 112
Princeton 112
New York 102
Dearborn 88
Helsinki 62
Dublin 59
Los Angeles 55
Nanchang 55
Istanbul 46
Des Moines 42
Jinan 37
Shenyang 36
Hebei 32
Lancaster 31
Munich 30
Changsha 28
Milan 25
Moscow 25
Buffalo 23
San Diego 23
Dong Ket 22
The Dalles 20
Chicago 19
Ho Chi Minh City 19
Shanghai 19
Tianjin 19
Dallas 18
Redondo Beach 18
San Francisco 18
São Paulo 18
Hanoi 17
Kunming 17
Brussels 16
Jiaxing 16
London 16
Santa Clara 16
Hangzhou 15
Ningbo 14
San Mateo 14
Guangzhou 13
Zhengzhou 12
Rome 11
Seongnam 11
Boardman 10
Naples 10
Orem 10
Washington 10
Brooklyn 9
Jakarta 9
Turku 9
Brno 8
Hefei 8
Lanzhou 8
Leawood 8
Rio de Janeiro 8
Toronto 8
Verona 8
Atlanta 7
Boston 7
Fuzhou 7
Haikou 7
Manchester 7
Monmouth Junction 7
Mumbai 7
Norwalk 7
Tokyo 7
Bela-Bela 6
Charlotte 6
Frankfurt am Main 6
Johannesburg 6
Phoenix 6
Poplar 6
Riyadh 6
Stockholm 6
Belo Horizonte 5
Changchun 5
Chennai 5
Dhaka 5
Kilburn 5
Mantova 5
Nuremberg 5
Orange 5
Redwood City 5
Salt Lake City 5
Taizhou 5
Totale 5.469
Salva come PNG Salva come JPEG
Nome #
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome 344
Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways 309
New Copy Number Variations in Schizophrenia 302
Compound heterozygosity for a large CNV deletion and a rare missense mutation in the FSTL5 gene of a patient affected by schizophrenia. 269
Analysis of triplet repeats of the FRAXA locus using a novel sequencing procedure 225
Compound heterozygosity for a hemizygous rare missense variant (rs141999351) and a large CNV deletion affecting the FSTL5 gene in a patient with schizophrenia 212
Dystrophic epidermolysis bullosa pruriginosa in Italy: molecular characterization and pathogenesic aspects 193
Exclusion of stromelysin-1, stromelysin-2, interstitial collagenase and fibronectin genes as the mutant loci in a family with recessive epidermolysis bullosa dystrophica and a form of cerebellar ataxia 173
Gene per la neuregulina 1 e schizofrenia: ulteriori evidenze di associazione 169
Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia 168
Angiokeratoma Corporis Diffusum and arteriovenous fistulas with dominant transmission in the absence of metabolic disorders. 167
The type III-9 repeat of human fibronectin is encoded by a single exon which is not alternatively spliced. 166
Three homozygous PTC mutations in the collagen type VII gene of patients affected by recessive dystrophic epidermolysis bullosa: analysis of transcript levels in dermal fibroblasts 162
Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13 154
Analysis of Copy Number Variations in Schizophrenia Italian Patients 151
A frequent HaeIII RFLP of the human fibronectin gene 151
RT-PCR detection of fibronectin EDA+ and EDB+ mRNA isoforms: molecular markers for hepatocellular carcinoma 148
A common MspI RFLP of the human fibronectin gene (FN1) 147
Characterization of a 13 aminoacid human fibronectin peptide induce matrix assembly and inhibiting migration and invasion in tumor cells 131
Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient. 131
A -96C-T mutation in the promoter of the collagen type VII gene (COL7A1) abolishing transcription in a patient affected by recessive dystrophic epidermolys bullosa 130
Study on GRIA2, GRIA3 and GRIA4 genes highlights a positive association between schizophrenia and GRIA3 in female patients 128
Polymorphic CA repeat in IGF-I gene: lack of association with schizophrenia. 127
Reconstructing the genetic history of Italians: new insights from a male (Y-chromosome) perspective 126
Matrix assembly induction and cell migration and invasion inhibition by a 13-amino acid fibronectin peptide 123
A Taq RFLP for the human fibronectin (FN1) gene 123
Phenotypic correction of the defective fibronectin extracellular matrix of Ehlers-Danlos syndrome fibroblasts. 123
Genotype-phenotype correlation in Italian patients with epidermolysis bullosa dystrophica 122
Exclusion of candidate genes in a family with arterial tortuosity syndrome 122
RESEARCH OF THE DISEASE-GENE IN A FAMILY AFFECTED BY A TYPE OF CEREBELLAR ATAXIA WITH AN UNKNOWN MOLECULAR DEFECT 121
Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization 121
Association study between schizophrenia and the AMPA genes GRIA1, GRIA2 AND GRIA4 120
Angiocheratomas and arterovenous fistulas with dominant trasmission in the absence of metabolic disorders. 119
Glutamate AMPA receptor subunit 1 gene (GRIA1) and DSM-IV-TR schizophrenia: a pilot case-control association study in an Italian sample 117
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 117
Cerebellar ataxia in a family with recurrent epidermolysis bullosa dystrophica 116
A new Taq RFLP of the human fibronecin gene (FN1) 116
New Copy Number Variations in Schizophrenia Italian Patients 113
Effect of dexamethasone on the assembly of the matrix of fibronectin and its receptors organization in Ehlers-Danlos syndrome skin fibroblasts. 113
Detection of high level of autozygosity in a group of Italian schizophrenia patients 113
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 112
Human fibronectin gene (FN1) RFLPs: mapping and linkage disequilibrium analysis 108
Identification of two splicing mutations in the collagen type VII gene (COL7A1) of a patient affected by the localisata variant of recessive dystrophic epidermolysis bullosa 104
Genome wide study of Italian schizophrenia patients 103
Mitochondrial DNA haplogroups and age at onset of schizophrenia 101
A frequent Hind RFLP of the human fibronectin) gene (FN1) 98
Different phenotypes in recessive dystrophic epidermolysis bullosa patients sharing the same mutation in compound heterozygosity with two novel mutations in COL7A1. 98
The Italian Registry of Hereditary Epidermolysis Bullosa 97
Identificazione mediante exome sequencing di una variante del gene RBMXL1 in una famiglia affetta da atassia cerebellare pura 97
Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity sindrome 95
Ricerca del gene malattia in una famiglia affetta da una forma di atassia cerebellare a difetto molecolare sconosciuto 95
RT-PCR detection of EDA+ fibronectin mRNA isoforms as hepatocarcinoma markers. 92
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 91
Modulation of RNA editing by FMRP in mammals 90
In vitro Glutamate treatments modify AMPA RNA editing and ADARs activity 89
Analysis of the (TA) repeat polymorphism of the UGT1A1 (UDP-Glucuronosyltransferase) gene in schizophrenia 80
Genetic studies on the Tharu population of Nepal: restriction endonuclease polymorphisms of mithocondrial DNA 73
Human fibroblasts with mutations in COL5A1 and COL3A1 genes do not organize collagens and fibronectin in the extracellular matrix, down-regulate alpha2beta1 integrin and recruit alphavbeta3 instead of alpha5beta1 integrin 65
null 60
Totale 8.030
Salva come PNG Salva come JPEG
Categoria #
all - tutte 34.421
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 34.421
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021741 0 0 0 0 0 146 63 110 164 84 130 44
2021/2022543 30 137 9 9 9 18 33 20 21 65 70 122
2022/2023389 62 6 9 32 39 111 1 30 57 3 18 21
2023/2024505 29 11 37 41 30 112 23 19 111 17 3 72
2024/2025970 13 15 4 152 114 82 84 22 112 45 182 145
2025/20261.124 204 236 128 281 235 40 0 0 0 0 0 0
Totale 8.030