UNICA IRIS Institutional Research Information System

ORRU, SANDRO IGNAZIO GIOVANNI
 Distribuzione geografica
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Continente #
EU - Europa 163.750
NA - Nord America 9.382
AS - Asia 3.988
SA - Sud America 573
AF - Africa 76
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 3
Totale 177.780
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Nazione #
IT - Italia 161.153
US - Stati Uniti d'America 9.295
CN - Cina 1.496
SG - Singapore 1.472
UA - Ucraina 708
SE - Svezia 520
BR - Brasile 449
VN - Vietnam 361
DE - Germania 354
FI - Finlandia 316
FR - Francia 238
GB - Regno Unito 236
HK - Hong Kong 156
IN - India 95
KR - Corea 87
RU - Federazione Russa 58
CA - Canada 54
AR - Argentina 48
BD - Bangladesh 44
IQ - Iraq 41
JP - Giappone 35
NL - Olanda 34
ZA - Sudafrica 27
ID - Indonesia 25
BE - Belgio 22
PK - Pakistan 22
EC - Ecuador 21
AT - Austria 19
MX - Messico 17
MY - Malesia 17
PH - Filippine 17
TR - Turchia 17
VE - Venezuela 17
MA - Marocco 15
SA - Arabia Saudita 14
CL - Cile 12
ES - Italia 12
PL - Polonia 12
IE - Irlanda 11
JO - Giordania 10
LT - Lituania 10
TN - Tunisia 10
AE - Emirati Arabi Uniti 9
AZ - Azerbaigian 9
CO - Colombia 9
IR - Iran 9
CZ - Repubblica Ceca 8
UZ - Uzbekistan 8
IL - Israele 7
KE - Kenya 7
KZ - Kazakistan 7
RO - Romania 7
AU - Australia 6
JM - Giamaica 6
UY - Uruguay 6
CH - Svizzera 5
GR - Grecia 5
PE - Perù 5
TH - Thailandia 5
EG - Egitto 4
ET - Etiopia 4
NP - Nepal 4
PY - Paraguay 4
CR - Costa Rica 3
DK - Danimarca 3
GE - Georgia 3
HN - Honduras 3
MD - Moldavia 3
OM - Oman 3
TW - Taiwan 3
AL - Albania 2
AO - Angola 2
BG - Bulgaria 2
BO - Bolivia 2
BY - Bielorussia 2
EU - Europa 2
KW - Kuwait 2
LV - Lettonia 2
MK - Macedonia 2
NZ - Nuova Zelanda 2
PS - Palestinian Territory 2
PT - Portogallo 2
TT - Trinidad e Tobago 2
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
CY - Cipro 1
DZ - Algeria 1
HT - Haiti 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LK - Sri Lanka 1
LY - Libia 1
ML - Mali 1
MN - Mongolia 1
MT - Malta 1
NG - Nigeria 1
PA - Panama 1
QA - Qatar 1
RS - Serbia 1
RW - Ruanda 1
Totale 177.775
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Città #
Cagliari 156.263
Uta 4.288
Fairfield 1.004
Ashburn 810
Woodbridge 770
Singapore 743
Chandler 618
San Jose 499
Houston 452
Wilmington 444
Ann Arbor 434
Boardman 413
Seattle 392
Jacksonville 383
Dallas 365
Nyköping 348
Cambridge 327
Beijing 258
Helsinki 186
Los Angeles 168
New York 164
Hong Kong 138
Nanjing 124
Lauterbourg 122
Hefei 113
Santa Clara 113
Ho Chi Minh City 106
Boston 104
Dearborn 102
The Dalles 89
Shanghai 86
Milan 79
Hanoi 75
Seoul 75
Buffalo 62
San Diego 59
Dong Ket 56
Council Bluffs 49
Shenyang 48
Nanchang 46
Hangzhou 45
Guangzhou 38
Redwood City 38
Tianjin 34
Changsha 33
Rome 33
Jiaxing 31
Hebei 30
Munich 28
São Paulo 27
Verona 27
Toronto 26
Orem 25
Frankfurt am Main 24
London 24
Norwalk 24
Redondo Beach 24
Tokyo 24
Washington 24
Jinan 23
Orange 23
Atlanta 21
Mountain View 21
Chicago 20
Sassari 19
Dolianova 18
Rio de Janeiro 18
Baghdad 17
Chennai 17
Belo Horizonte 16
Da Nang 16
Haiphong 16
Nuremberg 16
Stockholm 15
Auburn Hills 14
Brussels 13
Phoenix 13
Turku 13
Falls Church 12
Manchester 12
Mumbai 12
Columbus 11
Shenzhen 11
Warsaw 11
Wuhan 11
Casablanca 10
Dublin 10
Kunming 10
Pune 10
San Francisco 10
Campinas 9
Denver 9
Jakarta 9
Johannesburg 9
Quito 9
Vienna 9
Waanrode 9
Amman 8
Amsterdam 8
Biên Hòa 8
Totale 172.080
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Nome #
VGF protein and its C-terminal derived peptides in amyotrophic lateral sclerosis: Human and animal model studies 4.774
null 4.609
Exploring the Role of Killer Cell Immunoglobulin-Like Receptors and Their HLA Class I Ligands in Autoimmune Hepatitis 4.562
GUT MICROBIAL PROFILE IN WEIGHT CYCLING PATIENTS WITH OBESITY 4.541
Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients 3.943
Reduced stress granule formation and cell death in fibroblasts with the A382T mutation of TARDBP gene: evidence for loss of TDP-43 nuclear function. 3.616
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 3.566
Comparison Between an Artificial Neural Network and Logistic Regression in Predicting Long Term Kidney Transplantation Outcome 3.427
Absence of activating killer immunoglobulin-like receptor genes combined with hepatitis C viral genotype is predictive of hepatocellular carcinoma 3.363
What unrelated hematopoietic stem cell transplantation in thalassemia taught us about transplant immunogenetics 3.316
ALTERED STRESS GRANULE ASSEMBLY IN CULTURED FIBROBLASTS FROM ALS PATIENTS CARRYING A TARDBP MUTATION 3.315
Homozygosity for killer immunoglobin-like receptor haplotype A predicts complete molecular response to treatment with tyrosine kinase inhibitors in chronic myeloid leukemia patients 3.306
Stress granules induced by oxidative stress in cultured fibroblast from TDP-43 mutant ALS patients 3.268
HLA-G molecules and clinical outcome in Chronic Myeloid Leukemia 3.230
Gene expression profiling of monozygotic twins affected by psoriatic arthritis 3.058
KIR and their HLA Class I ligands: Two more pieces towards completing the puzzle of chronic rejection and graft loss in kidney transplantation 2.910
Stress granule assembly in cultured fibroblast from TDP-43 mutant ALS patients. 2.904
Kir haplotype aa is a possible predictive marker of complete molecular response to tyrosine kinase inhibitors in patients with chronic myeloid leukemia 2.824
IMPACT OF KILLER-CELL IMMUNOGLOBULIN-LIKE RECEPTORS ON PROGRESSION OF HEPATOCELLULAR CARCINOMA 2.595
Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients 2.521
Maternal uniparental disomy of chromosome 4 and homozygous novel mutation in the WFS1 gene in a paediatric patient with Wolfram syndrome 2.215
Entropy of human leukocyte antigen and killer-cell immunoglobulin-like receptor systems in immune-mediated disorders: A pilot study on multiple sclerosis 2.205
Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia 2.170
High frequency of the TARDBP p.Ala382Thr mutation in Sardinian patients with amyotrophic lateral sclerosis 2.144
Role of human leukocyte antigen-G 14-base pair polymorphism in kidney transplantation outcomes 2.108
Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male 2.098
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 2.017
Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases 1.978
Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia 1.959
Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report 1.919
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 1.911
Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature 1.906
A novel desmoplakin mutation associated with left dominant arrhythmogenic cardiomyopathy and cutaneous phenotype 1.905
null 1.879
A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristics 1.861
THE HLA-G 14-BP POLYMORPHISM IS AN INDEPENDENT GENETIC RISK MARKER OF LONG-TERM KIDNEY TRANSPLANTATION OUTCOME 1.806
The human leukocyte antigen-g 14-bp polymorphism is an independent genetic risk marker of long-term kidney transplantation outcome 1.754
Wilson's disease: A new perspective review on its genetics, diagnosis and treatment 1.754
De novo 15.5-Mb interstitial deletion in 5p in a male ascertained by oligospermia 1.711
Genetic Creutzfeldt-Jakob disease in Sardinia: a case series linked to the PRNP R208H mutation due to a single founder effect 1.661
A 9.1-kb gap in the genome reference map is shown to be a stable deletion/insertion polymorphism of ancestral origin 1.606
Star-related lipid transfer protein 10 (STARD10): a novel key player in alcohol-induced breast cancer progression 1.605
Distribution of HLA alleles and haplotypes in the Maldivian population 1.566
Nuclease activity in human metaphase chromosomes substituted with 5'-bromodeoxyuridine 1.546
Dilated lateral ventricles and micrognathia by ultrasound exsamination in fetus with mosaic trisomy 9 1.499
Cytogenetic and molecular characterization of a Small Supernumerary Marcker Chromosome (sSMC)found at prenatal diagnosis 1.374
Expression of ATP7B in normal human liver 1.366
Hodgkin's disease presenting in 1 of 4 siblings affected by hereditary spinocerebellar ataxia: clinical, immunological and genetic study 1.365
Familial chronic B-cell malignancy. Hairy cell leukaemia in mother and daughter 1.312
Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: A case report 1.312
A 725 kb deletion at 22q13.1 chromosomal region including SOX10 gene in a boy with a neurologic variant of Waardenburg syndrome type 2 1.304
Tetrasomy 9p mosaicism associated with a normal phenotype in two cases 1.295
A plea to search for deletion polymorphism through genome scans in populations 1.294
VAPB ER-Aggregates, A Possible New Biomarker in ALS Pathology 1.286
45, X karyotipe and abnormal ultrasound findings in early pregnancy loss 1.267
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 1.258
The role of inhibitory KIR 2DL5 in the outcome of autologous hematopoietic stem cell transplantation for multiple myeloma 1.214
Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature 1.179
Prenatal diagnosis of trisomy 18: time of evalutation, ultrasound markers and genetic counselling. A review 1.071
Nuchal translucency and other US markers in cases of trisomy 18 1.062
null 1.048
Diagnostic echographic diagnosis in sibs with the fetal hydrops, heart disease, cerebellar hypoplasia: Neu Laxsova Syndrome 1.007
The role of killer immunoglobulin-like receptor haplotypes on the outcome of unrelated donor haematopoietic SCT for thalassaemia 995
45, X karyotype and abnormal ultrasound findings in early pregnancy loss 985
SUMOylation Protects FASN Against Proteasomal Degradation in Breast Cancer Cells Treated with Grape Leaf Extract 958
Ultrasound findings in early pregnancy loss with 45, x karyotype 926
297. Abnormal ultrasound findings in 45,X early pregnancy loss 910
The use of array-CGH in a cohort of Greek children with developmental delay. 880
Recipient CTLA-4 genotype is a prognostic factor for acute GVHD in hematopoietic stem cell transplantation 861
Serological and molecular studies of HLA in Sardinian patients with Graves' disease 813
Prenatal diagnosis of a XX male in a fetus with increased nuchal translucency 781
Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization 764
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis 702
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 690
KIR2DS4*003 on donor natural killer cells increases the risk for acute GVHD following unrelated hematopoietic stem cell transplantation 686
Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: Molecular cytogenetic analysis and review of the literature 681
Delezione distale del braccio corto del cromosoma 8:descrizione di un caso rilevato in diagnosi prenatale 671
Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients 663
BMT in thalassemia from unrelated donors: Role of KIR polymorphism 656
Molecular analysis of HLA class II antigens in bone marrow transplanted thalassemic patients 656
Cytogenetic and molecular characterization of a Small Supernumerary Marker Chromosome (sSMC) found at prenatal diagnosis 621
Case report: Prenatal diagnosis of mosaic trisomy 9 621
Defining the allelic variants of HLA-A30 in the Sardinian population using amplification refractory mutation system--polymerase chain reaction 604
Diagnosi Prenatale di maschio xx in un feto con translucenza nucale alterata 596
Recipient CTLA-4 genotype is a prognostic factor foe acute GvHD in hematopoietic stem cell transplantation. Haematologica/The Hematology Journal 580
Case report: paracentric inversion of chromosome 1 in a man with azoospermia 578
Serological and molecular studies of HLA in Insulin-Dependent Diabetes Mellitus in Sardinia 578
Recipient CTLA-4 genotype is a prognostic factor for acute GvHD in hematopoietic stem cell transplantation for thalassemia 575
Wilson's disease maps between the D13S169 and D13S173 loci 558
The human leucocyte antigen-G 14-basepair polymorphism correlates with graft-versus-host disease in unrelated bone marrow transplantation for thalassaemia 557
AML post BMT: donor or recipient? 556
MOLECULAR ANALYSIS OF HLA-DRB1-DR1 ASSOCIATED ALLELES IN LICHEN RUBER PLANUS 548
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 542
Recipient CTLA-4 genotype is a prognostic factor foe acute GvHD in hematopoietic stem cell transplantation 537
The EUROGEM map of human chromosome 2 525
Chromosomal gain: from MGUS to MULTIPLE MYELOMA 516
Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome) 505
The HLA-DRB1*0101 allele is responsible for HLA susceptibility to lichen ruber planus 505
Successful unrelated bone marrow transplantation in beta-thalassaemia 502
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH 499
Totale 162.826
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Categoria #
all - tutte 228.457
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 228.457
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20216.108 0 0 0 0 0 0 0 0 0 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
2025/20266.654 344 467 929 741 478 481 1.401 573 496 744 0 0
Totale 178.106