UNICA IRIS Institutional Research Information System

ORRU, SANDRO IGNAZIO GIOVANNI
 Distribuzione geografica
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Continente #
EU - Europa 162.303
NA - Nord America 8.519
AS - Asia 2.810
SA - Sud America 467
AF - Africa 37
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 2
Totale 174.145
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Nazione #
IT - Italia 159.993
US - Stati Uniti d'America 8.449
CN - Cina 1.297
SG - Singapore 1.033
UA - Ucraina 704
SE - Svezia 519
BR - Brasile 394
DE - Germania 339
FI - Finlandia 223
GB - Regno Unito 218
VN - Vietnam 170
FR - Francia 106
KR - Corea 86
RU - Federazione Russa 55
CA - Canada 49
IN - India 37
HK - Hong Kong 30
NL - Olanda 30
AR - Argentina 27
JP - Giappone 23
BE - Belgio 22
IQ - Iraq 19
BD - Bangladesh 18
AT - Austria 17
EC - Ecuador 13
ZA - Sudafrica 13
ID - Indonesia 12
MX - Messico 12
ES - Italia 11
MA - Marocco 11
IE - Irlanda 9
IR - Iran 9
LT - Lituania 9
PK - Pakistan 9
PL - Polonia 9
TR - Turchia 9
CZ - Repubblica Ceca 8
VE - Venezuela 8
AE - Emirati Arabi Uniti 7
CL - Cile 7
RO - Romania 7
CO - Colombia 6
AU - Australia 5
CH - Svizzera 5
KZ - Kazakistan 5
MY - Malesia 5
SA - Arabia Saudita 5
UY - Uruguay 5
GR - Grecia 4
IL - Israele 4
JO - Giordania 4
PE - Perù 4
TH - Thailandia 4
GE - Georgia 3
HN - Honduras 3
NP - Nepal 3
PH - Filippine 3
PY - Paraguay 3
TN - Tunisia 3
UZ - Uzbekistan 3
AZ - Azerbaigian 2
BY - Bielorussia 2
CR - Costa Rica 2
DK - Danimarca 2
EG - Egitto 2
EU - Europa 2
JM - Giamaica 2
KE - Kenya 2
KW - Kuwait 2
LV - Lettonia 2
MD - Moldavia 2
MK - Macedonia 2
NZ - Nuova Zelanda 2
TW - Taiwan 2
AL - Albania 1
AO - Angola 1
BG - Bulgaria 1
BH - Bahrain 1
DZ - Algeria 1
ET - Etiopia 1
HT - Haiti 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
ML - Mali 1
MN - Mongolia 1
MT - Malta 1
NG - Nigeria 1
PS - Palestinian Territory 1
QA - Qatar 1
RS - Serbia 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
TT - Trinidad e Tobago 1
Totale 174.145
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Città #
Cagliari 155.123
Uta 4.288
Fairfield 1.004
Woodbridge 770
Ashburn 709
Chandler 618
Singapore 512
Houston 451
Wilmington 444
Ann Arbor 434
Boardman 413
Seattle 392
Jacksonville 383
Dallas 364
Nyköping 348
Cambridge 327
Beijing 256
New York 158
Los Angeles 129
Nanjing 124
Hefei 113
Santa Clara 109
Boston 102
Dearborn 102
Helsinki 96
Shanghai 82
Milan 78
Seoul 75
Buffalo 60
San Diego 59
Dong Ket 56
Shenyang 47
Nanchang 46
Ho Chi Minh City 41
Hangzhou 40
Redwood City 38
Guangzhou 34
Changsha 33
Jiaxing 31
Tianjin 31
Hebei 30
Hong Kong 29
Munich 28
Verona 27
Hanoi 26
Rome 26
São Paulo 25
Norwalk 24
Redondo Beach 24
Toronto 24
Washington 24
London 23
Orange 23
The Dalles 23
Jinan 22
Atlanta 21
Mountain View 21
Chicago 20
Sassari 19
Dolianova 18
Nuremberg 16
Stockholm 15
Tokyo 15
Auburn Hills 14
Rio de Janeiro 14
Belo Horizonte 13
Brussels 13
Phoenix 13
Turku 13
Falls Church 12
Frankfurt am Main 12
Columbus 11
Council Bluffs 11
Haiphong 11
Kunming 10
Campinas 9
San Francisco 9
Waanrode 9
Warsaw 9
Casablanca 8
Denver 8
Dublin 8
Ningbo 8
San Mateo 8
Vienna 8
Baghdad 7
Florence 7
Gyeonggi-do 7
Pune 7
Redmond 7
Buenos Aires 6
Chennai 6
Düsseldorf 6
Elk Grove Village 6
Leawood 6
Montreal 6
Mumbai 6
Ribeirão Preto 6
Saint Petersburg 6
Salt Lake City 6
Totale 169.369
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Nome #
VGF protein and its C-terminal derived peptides in amyotrophic lateral sclerosis: Human and animal model studies 4.719
null 4.609
Exploring the Role of Killer Cell Immunoglobulin-Like Receptors and Their HLA Class I Ligands in Autoimmune Hepatitis 4.501
GUT MICROBIAL PROFILE IN WEIGHT CYCLING PATIENTS WITH OBESITY 4.497
Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients 3.887
Reduced stress granule formation and cell death in fibroblasts with the A382T mutation of TARDBP gene: evidence for loss of TDP-43 nuclear function. 3.570
Whole Genome Expression Analyses of miRNAs and mRNAs Suggest the Involvement of miR-320a and miR-155-3p and their Targeted Genes in Lithium Response in Bipolar Disorder 3.530
Comparison Between an Artificial Neural Network and Logistic Regression in Predicting Long Term Kidney Transplantation Outcome 3.399
Absence of activating killer immunoglobulin-like receptor genes combined with hepatitis C viral genotype is predictive of hepatocellular carcinoma 3.341
What unrelated hematopoietic stem cell transplantation in thalassemia taught us about transplant immunogenetics 3.282
Homozygosity for killer immunoglobin-like receptor haplotype A predicts complete molecular response to treatment with tyrosine kinase inhibitors in chronic myeloid leukemia patients 3.276
ALTERED STRESS GRANULE ASSEMBLY IN CULTURED FIBROBLASTS FROM ALS PATIENTS CARRYING A TARDBP MUTATION 3.262
Stress granules induced by oxidative stress in cultured fibroblast from TDP-43 mutant ALS patients 3.233
HLA-G molecules and clinical outcome in Chronic Myeloid Leukemia 3.185
Gene expression profiling of monozygotic twins affected by psoriatic arthritis 3.003
Stress granule assembly in cultured fibroblast from TDP-43 mutant ALS patients. 2.865
KIR and their HLA Class I ligands: Two more pieces towards completing the puzzle of chronic rejection and graft loss in kidney transplantation 2.865
Kir haplotype aa is a possible predictive marker of complete molecular response to tyrosine kinase inhibitors in patients with chronic myeloid leukemia 2.761
IMPACT OF KILLER-CELL IMMUNOGLOBULIN-LIKE RECEPTORS ON PROGRESSION OF HEPATOCELLULAR CARCINOMA 2.537
Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients 2.489
Maternal uniparental disomy of chromosome 4 and homozygous novel mutation in the WFS1 gene in a paediatric patient with Wolfram syndrome 2.188
Entropy of human leukocyte antigen and killer-cell immunoglobulin-like receptor systems in immune-mediated disorders: A pilot study on multiple sclerosis 2.159
Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia 2.155
High frequency of the TARDBP p.Ala382Thr mutation in Sardinian patients with amyotrophic lateral sclerosis 2.127
Role of human leukocyte antigen-G 14-base pair polymorphism in kidney transplantation outcomes 2.075
Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male 2.074
Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases 1.962
Human Leukocyte Antigen Complex and Other Immunogenetic and Clinical Factors Influence Susceptibility or Protection to SARS-CoV-2 Infection and Severity of the Disease Course. The Sardinian Experience 1.959
Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia 1.930
Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report 1.896
DNA alteration induced by ultraviolet light in human metaphase chromosomes substituted with 5′-bromodeoxy uridine: monitoring by monoclonal antibodies to double-stranded and single stranded DNA 1.880
null 1.879
A novel desmoplakin mutation associated with left dominant arrhythmogenic cardiomyopathy and cutaneous phenotype 1.871
Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature 1.868
A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristics 1.836
THE HLA-G 14-BP POLYMORPHISM IS AN INDEPENDENT GENETIC RISK MARKER OF LONG-TERM KIDNEY TRANSPLANTATION OUTCOME 1.783
The human leukocyte antigen-g 14-bp polymorphism is an independent genetic risk marker of long-term kidney transplantation outcome 1.733
Wilson's disease: A new perspective review on its genetics, diagnosis and treatment 1.729
De novo 15.5-Mb interstitial deletion in 5p in a male ascertained by oligospermia 1.698
Genetic Creutzfeldt-Jakob disease in Sardinia: a case series linked to the PRNP R208H mutation due to a single founder effect 1.636
A 9.1-kb gap in the genome reference map is shown to be a stable deletion/insertion polymorphism of ancestral origin 1.584
Star-related lipid transfer protein 10 (STARD10): a novel key player in alcohol-induced breast cancer progression 1.584
Distribution of HLA alleles and haplotypes in the Maldivian population 1.547
Nuclease activity in human metaphase chromosomes substituted with 5'-bromodeoxyuridine 1.531
Dilated lateral ventricles and micrognathia by ultrasound exsamination in fetus with mosaic trisomy 9 1.469
Cytogenetic and molecular characterization of a Small Supernumerary Marcker Chromosome (sSMC)found at prenatal diagnosis 1.354
Hodgkin's disease presenting in 1 of 4 siblings affected by hereditary spinocerebellar ataxia: clinical, immunological and genetic study 1.342
Expression of ATP7B in normal human liver 1.330
A 725 kb deletion at 22q13.1 chromosomal region including SOX10 gene in a boy with a neurologic variant of Waardenburg syndrome type 2 1.285
Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: A case report 1.284
Familial chronic B-cell malignancy. Hairy cell leukaemia in mother and daughter 1.281
A plea to search for deletion polymorphism through genome scans in populations 1.279
Tetrasomy 9p mosaicism associated with a normal phenotype in two cases 1.270
VAPB ER-Aggregates, A Possible New Biomarker in ALS Pathology 1.255
45, X karyotipe and abnormal ultrasound findings in early pregnancy loss 1.238
Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature 1.237
The role of inhibitory KIR 2DL5 in the outcome of autologous hematopoietic stem cell transplantation for multiple myeloma 1.169
Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature 1.160
Prenatal diagnosis of trisomy 18: time of evalutation, ultrasound markers and genetic counselling. A review 1.050
null 1.048
Nuchal translucency and other US markers in cases of trisomy 18 1.029
Diagnostic echographic diagnosis in sibs with the fetal hydrops, heart disease, cerebellar hypoplasia: Neu Laxsova Syndrome 981
The role of killer immunoglobulin-like receptor haplotypes on the outcome of unrelated donor haematopoietic SCT for thalassaemia 977
45, X karyotype and abnormal ultrasound findings in early pregnancy loss 967
SUMOylation Protects FASN Against Proteasomal Degradation in Breast Cancer Cells Treated with Grape Leaf Extract 935
Ultrasound findings in early pregnancy loss with 45, x karyotype 900
297. Abnormal ultrasound findings in 45,X early pregnancy loss 884
The use of array-CGH in a cohort of Greek children with developmental delay. 847
Recipient CTLA-4 genotype is a prognostic factor for acute GVHD in hematopoietic stem cell transplantation 839
Serological and molecular studies of HLA in Sardinian patients with Graves' disease 784
Prenatal diagnosis of a XX male in a fetus with increased nuchal translucency 763
Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization 745
The absence of 21-OH A and C4 B genes is a constant characteristic of the "Sardinian" HLA extended haplotype A30 Cw5 B18 BfF1 DR3 DRw52 DQw2 673
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis 673
Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: Molecular cytogenetic analysis and review of the literature 667
KIR2DS4*003 on donor natural killer cells increases the risk for acute GVHD following unrelated hematopoietic stem cell transplantation 661
Delezione distale del braccio corto del cromosoma 8:descrizione di un caso rilevato in diagnosi prenatale 648
Molecular analysis of HLA class II antigens in bone marrow transplanted thalassemic patients 640
BMT in thalassemia from unrelated donors: Role of KIR polymorphism 626
Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients 613
Case report: Prenatal diagnosis of mosaic trisomy 9 605
Cytogenetic and molecular characterization of a Small Supernumerary Marker Chromosome (sSMC) found at prenatal diagnosis 598
Defining the allelic variants of HLA-A30 in the Sardinian population using amplification refractory mutation system--polymerase chain reaction 587
Diagnosi Prenatale di maschio xx in un feto con translucenza nucale alterata 569
Serological and molecular studies of HLA in Insulin-Dependent Diabetes Mellitus in Sardinia 563
Case report: paracentric inversion of chromosome 1 in a man with azoospermia 554
Recipient CTLA-4 genotype is a prognostic factor for acute GvHD in hematopoietic stem cell transplantation for thalassemia 551
Recipient CTLA-4 genotype is a prognostic factor foe acute GvHD in hematopoietic stem cell transplantation. Haematologica/The Hematology Journal 550
Wilson's disease maps between the D13S169 and D13S173 loci 544
AML post BMT: donor or recipient? 537
MOLECULAR ANALYSIS OF HLA-DRB1-DR1 ASSOCIATED ALLELES IN LICHEN RUBER PLANUS 532
The human leucocyte antigen-G 14-basepair polymorphism correlates with graft-versus-host disease in unrelated bone marrow transplantation for thalassaemia 527
The combination of donor homozygosity for KIR-haplotype A and patient heterozygosity for HLA-C ligand groups 1 and 2 increases the risk of acute GvHD in unrelated hematopoietic stem cell transplantation 519
The EUROGEM map of human chromosome 2 511
Recipient CTLA-4 genotype is a prognostic factor foe acute GvHD in hematopoietic stem cell transplantation 508
Chromosomal gain: from MGUS to MULTIPLE MYELOMA 496
The HLA-DRB1*0101 allele is responsible for HLA susceptibility to lichen ruber planus 493
Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome) 487
Successful unrelated bone marrow transplantation in beta-thalassaemia 481
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH 478
Totale 160.088
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Categoria #
all - tutte 222.862
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 222.862
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202118.260 0 0 0 0 0 4.984 3.476 2.710 982 2.367 2.316 1.425
2021/20229.672 1.189 692 375 829 725 484 463 564 1.009 1.010 1.308 1.024
2022/202313.234 1.050 1.792 1.948 1.072 1.087 1.398 537 1.187 755 815 1.080 513
2023/202414.348 760 535 843 904 1.190 2.735 1.417 917 721 948 2.038 1.340
2024/202528.329 4.787 7.116 4.132 4.013 2.133 2.995 1.843 156 270 225 277 382
2025/20263.019 344 467 929 741 478 60 0 0 0 0 0 0
Totale 174.471