UNICA IRIS Institutional Research Information System

ORRU, SANDRO IGNAZIO GIOVANNI
 Distribuzione geografica
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Continente #
EU - Europa 162.405
NA - Nord America 8.564
AS - Asia 3.051
SA - Sud America 477
AF - Africa 37
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 2
Totale 174.543
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Nazione #
IT - Italia 160.088
US - Stati Uniti d'America 8.489
CN - Cina 1.305
SG - Singapore 1.232
UA - Ucraina 704
SE - Svezia 519
BR - Brasile 403
DE - Germania 340
FI - Finlandia 223
GB - Regno Unito 218
VN - Vietnam 186
FR - Francia 106
KR - Corea 86
RU - Federazione Russa 56
CA - Canada 51
IN - India 38
HK - Hong Kong 31
NL - Olanda 30
AR - Argentina 28
IQ - Iraq 23
JP - Giappone 23
BE - Belgio 22
AT - Austria 19
BD - Bangladesh 19
ID - Indonesia 14
EC - Ecuador 13
MX - Messico 13
ZA - Sudafrica 13
ES - Italia 11
MA - Marocco 11
PK - Pakistan 11
PL - Polonia 11
LT - Lituania 10
AE - Emirati Arabi Uniti 9
IE - Irlanda 9
IR - Iran 9
TR - Turchia 9
CZ - Repubblica Ceca 8
VE - Venezuela 8
CL - Cile 7
RO - Romania 7
CO - Colombia 6
MY - Malesia 6
AU - Australia 5
CH - Svizzera 5
KZ - Kazakistan 5
SA - Arabia Saudita 5
TH - Thailandia 5
UY - Uruguay 5
GR - Grecia 4
IL - Israele 4
JO - Giordania 4
PE - Perù 4
AZ - Azerbaigian 3
GE - Georgia 3
HN - Honduras 3
JM - Giamaica 3
NP - Nepal 3
PH - Filippine 3
PY - Paraguay 3
TN - Tunisia 3
UZ - Uzbekistan 3
BY - Bielorussia 2
CR - Costa Rica 2
DK - Danimarca 2
EG - Egitto 2
EU - Europa 2
KE - Kenya 2
KW - Kuwait 2
LV - Lettonia 2
MD - Moldavia 2
MK - Macedonia 2
NZ - Nuova Zelanda 2
PS - Palestinian Territory 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
OM - Oman 1
PA - Panama 1
QA - Qatar 1
RS - Serbia 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
TT - Trinidad e Tobago 1
Totale 174.543
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Città #
Cagliari 155.217
Uta 4.288
Fairfield 1.004
Woodbridge 770
Ashburn 715
Chandler 618
Singapore 572
Houston 451
Wilmington 444
Ann Arbor 434
Boardman 413
Seattle 392
Jacksonville 383
Dallas 364
Nyköping 348
Cambridge 327
Beijing 256
New York 161
Los Angeles 130
Nanjing 124
Hefei 113
Santa Clara 109
Boston 103
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 45
Hangzhou 41
Redwood City 38
The Dalles 38
Guangzhou 34
Changsha 33
Hanoi 32
Jiaxing 31
Tianjin 31
Hebei 30
Hong Kong 30
Munich 28
Verona 27
Rome 26
São Paulo 25
Toronto 25
Norwalk 24
Redondo Beach 24
Washington 24
London 23
Orange 23
Jinan 22
Atlanta 21
Mountain View 21
Chicago 20
Sassari 19
Dolianova 18
Nuremberg 16
Rio de Janeiro 16
Stockholm 15
Tokyo 15
Auburn Hills 14
Belo Horizonte 13
Brussels 13
Frankfurt am Main 13
Haiphong 13
Phoenix 13
Turku 13
Falls Church 12
Columbus 11
Council Bluffs 11
Warsaw 11
Kunming 10
Baghdad 9
Campinas 9
San Francisco 9
San Jose 9
Vienna 9
Waanrode 9
Casablanca 8
Denver 8
Dublin 8
Ningbo 8
San Mateo 8
Florence 7
Gyeonggi-do 7
Mumbai 7
Pune 7
Redmond 7
Brasília 6
Brooklyn 6
Buenos Aires 6
Chennai 6
Düsseldorf 6
Elk Grove Village 6
Jakarta 6
Leawood 6
Totale 169.576
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Nome #
VGF protein and its C-terminal derived peptides in amyotrophic lateral sclerosis: Human and animal model studies 4.723
null 4.609
Exploring the Role of Killer Cell Immunoglobulin-Like Receptors and Their HLA Class I Ligands in Autoimmune Hepatitis 4.510
GUT MICROBIAL PROFILE IN WEIGHT CYCLING PATIENTS WITH OBESITY 4.502
Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients 3.893
Reduced stress granule formation and cell death in fibroblasts with the A382T mutation of TARDBP gene: evidence for loss of TDP-43 nuclear function. 3.575
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 3.535
Comparison Between an Artificial Neural Network and Logistic Regression in Predicting Long Term Kidney Transplantation Outcome 3.404
Absence of activating killer immunoglobulin-like receptor genes combined with hepatitis C viral genotype is predictive of hepatocellular carcinoma 3.347
What unrelated hematopoietic stem cell transplantation in thalassemia taught us about transplant immunogenetics 3.285
Homozygosity for killer immunoglobin-like receptor haplotype A predicts complete molecular response to treatment with tyrosine kinase inhibitors in chronic myeloid leukemia patients 3.278
ALTERED STRESS GRANULE ASSEMBLY IN CULTURED FIBROBLASTS FROM ALS PATIENTS CARRYING A TARDBP MUTATION 3.267
Stress granules induced by oxidative stress in cultured fibroblast from TDP-43 mutant ALS patients 3.236
HLA-G molecules and clinical outcome in Chronic Myeloid Leukemia 3.190
Gene expression profiling of monozygotic twins affected by psoriatic arthritis 3.006
Stress granule assembly in cultured fibroblast from TDP-43 mutant ALS patients. 2.869
KIR and their HLA Class I ligands: Two more pieces towards completing the puzzle of chronic rejection and graft loss in kidney transplantation 2.869
Kir haplotype aa is a possible predictive marker of complete molecular response to tyrosine kinase inhibitors in patients with chronic myeloid leukemia 2.768
IMPACT OF KILLER-CELL IMMUNOGLOBULIN-LIKE RECEPTORS ON PROGRESSION OF HEPATOCELLULAR CARCINOMA 2.543
Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients 2.493
Maternal uniparental disomy of chromosome 4 and homozygous novel mutation in the WFS1 gene in a paediatric patient with Wolfram syndrome 2.193
Entropy of human leukocyte antigen and killer-cell immunoglobulin-like receptor systems in immune-mediated disorders: A pilot study on multiple sclerosis 2.163
Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia 2.157
High frequency of the TARDBP p.Ala382Thr mutation in Sardinian patients with amyotrophic lateral sclerosis 2.128
Role of human leukocyte antigen-G 14-base pair polymorphism in kidney transplantation outcomes 2.079
Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male 2.077
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 1.968
Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases 1.967
Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia 1.934
Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report 1.900
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 1.882
null 1.879
A novel desmoplakin mutation associated with left dominant arrhythmogenic cardiomyopathy and cutaneous phenotype 1.878
Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature 1.871
A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristics 1.839
THE HLA-G 14-BP POLYMORPHISM IS AN INDEPENDENT GENETIC RISK MARKER OF LONG-TERM KIDNEY TRANSPLANTATION OUTCOME 1.785
The human leukocyte antigen-g 14-bp polymorphism is an independent genetic risk marker of long-term kidney transplantation outcome 1.735
Wilson's disease: A new perspective review on its genetics, diagnosis and treatment 1.734
De novo 15.5-Mb interstitial deletion in 5p in a male ascertained by oligospermia 1.700
Genetic Creutzfeldt-Jakob disease in Sardinia: a case series linked to the PRNP R208H mutation due to a single founder effect 1.640
Star-related lipid transfer protein 10 (STARD10): a novel key player in alcohol-induced breast cancer progression 1.588
A 9.1-kb gap in the genome reference map is shown to be a stable deletion/insertion polymorphism of ancestral origin 1.585
Distribution of HLA alleles and haplotypes in the Maldivian population 1.549
Nuclease activity in human metaphase chromosomes substituted with 5'-bromodeoxyuridine 1.532
Dilated lateral ventricles and micrognathia by ultrasound exsamination in fetus with mosaic trisomy 9 1.475
Cytogenetic and molecular characterization of a Small Supernumerary Marcker Chromosome (sSMC)found at prenatal diagnosis 1.357
Hodgkin's disease presenting in 1 of 4 siblings affected by hereditary spinocerebellar ataxia: clinical, immunological and genetic study 1.343
Expression of ATP7B in normal human liver 1.332
Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: A case report 1.288
A 725 kb deletion at 22q13.1 chromosomal region including SOX10 gene in a boy with a neurologic variant of Waardenburg syndrome type 2 1.287
Familial chronic B-cell malignancy. Hairy cell leukaemia in mother and daughter 1.284
A plea to search for deletion polymorphism through genome scans in populations 1.280
Tetrasomy 9p mosaicism associated with a normal phenotype in two cases 1.272
VAPB ER-Aggregates, A Possible New Biomarker in ALS Pathology 1.261
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 1.241
45, X karyotipe and abnormal ultrasound findings in early pregnancy loss 1.241
The role of inhibitory KIR 2DL5 in the outcome of autologous hematopoietic stem cell transplantation for multiple myeloma 1.175
Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature 1.163
Prenatal diagnosis of trisomy 18: time of evalutation, ultrasound markers and genetic counselling. A review 1.054
null 1.048
Nuchal translucency and other US markers in cases of trisomy 18 1.030
Diagnostic echographic diagnosis in sibs with the fetal hydrops, heart disease, cerebellar hypoplasia: Neu Laxsova Syndrome 984
The role of killer immunoglobulin-like receptor haplotypes on the outcome of unrelated donor haematopoietic SCT for thalassaemia 980
45, X karyotype and abnormal ultrasound findings in early pregnancy loss 969
SUMOylation Protects FASN Against Proteasomal Degradation in Breast Cancer Cells Treated with Grape Leaf Extract 937
Ultrasound findings in early pregnancy loss with 45, x karyotype 906
297. Abnormal ultrasound findings in 45,X early pregnancy loss 886
The use of array-CGH in a cohort of Greek children with developmental delay. 849
Recipient CTLA-4 genotype is a prognostic factor for acute GVHD in hematopoietic stem cell transplantation 840
Serological and molecular studies of HLA in Sardinian patients with Graves' disease 787
Prenatal diagnosis of a XX male in a fetus with increased nuchal translucency 765
Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization 746
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis 677
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 674
Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: Molecular cytogenetic analysis and review of the literature 669
KIR2DS4*003 on donor natural killer cells increases the risk for acute GVHD following unrelated hematopoietic stem cell transplantation 662
Delezione distale del braccio corto del cromosoma 8:descrizione di un caso rilevato in diagnosi prenatale 650
Molecular analysis of HLA class II antigens in bone marrow transplanted thalassemic patients 643
BMT in thalassemia from unrelated donors: Role of KIR polymorphism 627
Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients 617
Case report: Prenatal diagnosis of mosaic trisomy 9 606
Cytogenetic and molecular characterization of a Small Supernumerary Marker Chromosome (sSMC) found at prenatal diagnosis 600
Defining the allelic variants of HLA-A30 in the Sardinian population using amplification refractory mutation system--polymerase chain reaction 589
Diagnosi Prenatale di maschio xx in un feto con translucenza nucale alterata 572
Serological and molecular studies of HLA in Insulin-Dependent Diabetes Mellitus in Sardinia 564
Case report: paracentric inversion of chromosome 1 in a man with azoospermia 558
Recipient CTLA-4 genotype is a prognostic factor for acute GvHD in hematopoietic stem cell transplantation for thalassemia 554
Recipient CTLA-4 genotype is a prognostic factor foe acute GvHD in hematopoietic stem cell transplantation. Haematologica/The Hematology Journal 551
Wilson's disease maps between the D13S169 and D13S173 loci 545
AML post BMT: donor or recipient? 539
MOLECULAR ANALYSIS OF HLA-DRB1-DR1 ASSOCIATED ALLELES IN LICHEN RUBER PLANUS 534
The human leucocyte antigen-G 14-basepair polymorphism correlates with graft-versus-host disease in unrelated bone marrow transplantation for thalassaemia 528
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 522
The EUROGEM map of human chromosome 2 512
Recipient CTLA-4 genotype is a prognostic factor foe acute GvHD in hematopoietic stem cell transplantation 511
Chromosomal gain: from MGUS to MULTIPLE MYELOMA 497
The HLA-DRB1*0101 allele is responsible for HLA susceptibility to lichen ruber planus 494
Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome) 489
Successful unrelated bone marrow transplantation in beta-thalassaemia 482
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH 480
Totale 160.391
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Categoria #
all - tutte 223.827
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 223.827
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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
2025/20263.417 344 467 929 741 478 458 0 0 0 0 0 0
Totale 174.869