UNICA IRIS Institutional Research Information System

ORRU, SANDRO IGNAZIO GIOVANNI
 Distribuzione geografica
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Continente #
EU - Europa 165.233
NA - Nord America 11.268
AS - Asia 4.058
SA - Sud America 619
Continente sconosciuto - Info sul continente non disponibili 335
AF - Africa 78
OC - Oceania 9
Totale 181.600
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Nazione #
IT - Italia 162.584
US - Stati Uniti d'America 11.088
CN - Cina 1.514
SG - Singapore 1.489
UA - Ucraina 712
SE - Svezia 526
BR - Brasile 491
VN - Vietnam 363
DE - Germania 356
FI - Finlandia 318
GB - Regno Unito 251
FR - Francia 242
HK - Hong Kong 164
CA - Canada 101
IN - India 96
KR - Corea 87
BD - Bangladesh 63
RU - Federazione Russa 60
AR - Argentina 48
IQ - Iraq 41
JP - Giappone 37
NL - Olanda 36
ZA - Sudafrica 27
ID - Indonesia 26
PK - Pakistan 23
BE - Belgio 22
EC - Ecuador 22
MX - Messico 22
AT - Austria 19
PH - Filippine 18
JM - Giamaica 17
MY - Malesia 17
TR - Turchia 17
VE - Venezuela 17
MA - Marocco 15
CR - Costa Rica 14
ES - Italia 14
LT - Lituania 14
SA - Arabia Saudita 14
CL - Cile 12
CO - Colombia 12
IE - Irlanda 12
PL - Polonia 12
HN - Honduras 10
JO - Giordania 10
TN - Tunisia 10
AE - Emirati Arabi Uniti 9
AZ - Azerbaigian 9
CZ - Repubblica Ceca 9
IR - Iran 9
UZ - Uzbekistan 8
CH - Svizzera 7
IL - Israele 7
KE - Kenya 7
KZ - Kazakistan 7
RO - Romania 7
AU - Australia 6
UY - Uruguay 6
CW - ???statistics.table.value.countryCode.CW??? 5
EG - Egitto 5
GR - Grecia 5
PE - Perù 5
TH - Thailandia 5
EE - Estonia 4
ET - Etiopia 4
NI - Nicaragua 4
NP - Nepal 4
PY - Paraguay 4
DK - Danimarca 3
GE - Georgia 3
MD - Moldavia 3
NZ - Nuova Zelanda 3
OM - Oman 3
PA - Panama 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
PS - Palestinian Territory 2
PT - Portogallo 2
SC - Seychelles 2
SV - El Salvador 2
TT - Trinidad e Tobago 2
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BZ - Belize 1
CY - Cipro 1
DZ - Algeria 1
GP - Guadalupe 1
HR - Croazia 1
HT - Haiti 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LC - Santa Lucia 1
Totale 181.259
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Città #
Cagliari 157.636
Uta 4.292
Ashburn 1.450
Fairfield 1.006
Woodbridge 771
Singapore 751
San Jose 746
Chandler 622
Houston 469
Wilmington 449
Boardman 438
Ann Arbor 435
Seattle 394
Jacksonville 385
Dallas 383
Nyköping 348
Cambridge 327
Beijing 266
Helsinki 187
New York 186
Los Angeles 182
Council Bluffs 158
Hong Kong 146
Santa Clara 143
Nanjing 125
Lauterbourg 123
Hefei 113
Boston 106
Ho Chi Minh City 106
Dearborn 102
The Dalles 90
Milan 89
Shanghai 87
Hanoi 76
Seoul 75
Buffalo 67
São Paulo 65
San Diego 59
Dong Ket 56
Shenyang 48
Nanchang 47
Hangzhou 45
Rome 41
Toronto 41
Guangzhou 38
Redwood City 38
Tianjin 34
Changsha 33
Columbus 33
Jiaxing 31
Hebei 30
Verona 29
Washington 29
Munich 28
Atlanta 27
Chicago 27
Phoenix 27
Frankfurt am Main 25
London 25
Orem 25
Tokyo 25
Norwalk 24
Redondo Beach 24
Jinan 23
Orange 23
Mountain View 21
Sassari 19
Dolianova 18
Rio de Janeiro 18
Baghdad 17
Chennai 17
Belo Horizonte 16
Da Nang 16
Haiphong 16
Nuremberg 16
San Francisco 15
Stockholm 15
Auburn Hills 14
Brooklyn 14
Brussels 13
Denver 13
Manchester 13
Turku 13
Falls Church 12
Mumbai 12
San José 12
Montreal 11
North Bergen 11
Pune 11
Shenzhen 11
Warsaw 11
Wuhan 11
Casablanca 10
Dublin 10
Kunming 10
Campinas 9
Jakarta 9
Johannesburg 9
Quito 9
Salt Lake City 9
Totale 174.790
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Nome #
VGF protein and its C-terminal derived peptides in amyotrophic lateral sclerosis: Human and animal model studies 4.804
null 4.609
Exploring the Role of Killer Cell Immunoglobulin-Like Receptors and Their HLA Class I Ligands in Autoimmune Hepatitis 4.592
GUT MICROBIAL PROFILE IN WEIGHT CYCLING PATIENTS WITH OBESITY 4.567
Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients 3.970
Reduced stress granule formation and cell death in fibroblasts with the A382T mutation of TARDBP gene: evidence for loss of TDP-43 nuclear function. 3.661
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 3.591
Comparison Between an Artificial Neural Network and Logistic Regression in Predicting Long Term Kidney Transplantation Outcome 3.451
Absence of activating killer immunoglobulin-like receptor genes combined with hepatitis C viral genotype is predictive of hepatocellular carcinoma 3.384
ALTERED STRESS GRANULE ASSEMBLY IN CULTURED FIBROBLASTS FROM ALS PATIENTS CARRYING A TARDBP MUTATION 3.339
Homozygosity for killer immunoglobin-like receptor haplotype A predicts complete molecular response to treatment with tyrosine kinase inhibitors in chronic myeloid leukemia patients 3.335
What unrelated hematopoietic stem cell transplantation in thalassemia taught us about transplant immunogenetics 3.334
Stress granules induced by oxidative stress in cultured fibroblast from TDP-43 mutant ALS patients 3.291
HLA-G molecules and clinical outcome in Chronic Myeloid Leukemia 3.254
Gene expression profiling of monozygotic twins affected by psoriatic arthritis 3.087
Stress granule assembly in cultured fibroblast from TDP-43 mutant ALS patients. 2.961
KIR and their HLA Class I ligands: Two more pieces towards completing the puzzle of chronic rejection and graft loss in kidney transplantation 2.933
Kir haplotype aa is a possible predictive marker of complete molecular response to tyrosine kinase inhibitors in patients with chronic myeloid leukemia 2.897
IMPACT OF KILLER-CELL IMMUNOGLOBULIN-LIKE RECEPTORS ON PROGRESSION OF HEPATOCELLULAR CARCINOMA 2.660
Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients 2.550
Entropy of human leukocyte antigen and killer-cell immunoglobulin-like receptor systems in immune-mediated disorders: A pilot study on multiple sclerosis 2.240
Maternal uniparental disomy of chromosome 4 and homozygous novel mutation in the WFS1 gene in a paediatric patient with Wolfram syndrome 2.236
Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia 2.189
High frequency of the TARDBP p.Ala382Thr mutation in Sardinian patients with amyotrophic lateral sclerosis 2.160
Role of human leukocyte antigen-G 14-base pair polymorphism in kidney transplantation outcomes 2.132
Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male 2.121
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 2.053
Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases 2.004
Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia 1.975
Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report 1.944
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 1.935
Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature 1.930
A novel desmoplakin mutation associated with left dominant arrhythmogenic cardiomyopathy and cutaneous phenotype 1.929
A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristics 1.885
null 1.879
THE HLA-G 14-BP POLYMORPHISM IS AN INDEPENDENT GENETIC RISK MARKER OF LONG-TERM KIDNEY TRANSPLANTATION OUTCOME 1.844
The human leukocyte antigen-g 14-bp polymorphism is an independent genetic risk marker of long-term kidney transplantation outcome 1.817
Wilson's disease: A new perspective review on its genetics, diagnosis and treatment 1.771
De novo 15.5-Mb interstitial deletion in 5p in a male ascertained by oligospermia 1.727
Genetic Creutzfeldt-Jakob disease in Sardinia: a case series linked to the PRNP R208H mutation due to a single founder effect 1.687
A 9.1-kb gap in the genome reference map is shown to be a stable deletion/insertion polymorphism of ancestral origin 1.628
Star-related lipid transfer protein 10 (STARD10): a novel key player in alcohol-induced breast cancer progression 1.627
Distribution of HLA alleles and haplotypes in the Maldivian population 1.586
Nuclease activity in human metaphase chromosomes substituted with 5'-bromodeoxyuridine 1.583
Dilated lateral ventricles and micrognathia by ultrasound exsamination in fetus with mosaic trisomy 9 1.521
Cytogenetic and molecular characterization of a Small Supernumerary Marcker Chromosome (sSMC)found at prenatal diagnosis 1.411
Expression of ATP7B in normal human liver 1.409
Hodgkin's disease presenting in 1 of 4 siblings affected by hereditary spinocerebellar ataxia: clinical, immunological and genetic study 1.382
Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: A case report 1.336
Familial chronic B-cell malignancy. Hairy cell leukaemia in mother and daughter 1.335
Tetrasomy 9p mosaicism associated with a normal phenotype in two cases 1.326
A 725 kb deletion at 22q13.1 chromosomal region including SOX10 gene in a boy with a neurologic variant of Waardenburg syndrome type 2 1.320
A plea to search for deletion polymorphism through genome scans in populations 1.312
VAPB ER-Aggregates, A Possible New Biomarker in ALS Pathology 1.308
45, X karyotipe and abnormal ultrasound findings in early pregnancy loss 1.288
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 1.278
The role of inhibitory KIR 2DL5 in the outcome of autologous hematopoietic stem cell transplantation for multiple myeloma 1.235
Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature 1.198
Prenatal diagnosis of trisomy 18: time of evalutation, ultrasound markers and genetic counselling. A review 1.099
Nuchal translucency and other US markers in cases of trisomy 18 1.077
Diagnostic echographic diagnosis in sibs with the fetal hydrops, heart disease, cerebellar hypoplasia: Neu Laxsova Syndrome 1.059
null 1.048
45, X karyotype and abnormal ultrasound findings in early pregnancy loss 1.010
The role of killer immunoglobulin-like receptor haplotypes on the outcome of unrelated donor haematopoietic SCT for thalassaemia 1.008
SUMOylation Protects FASN Against Proteasomal Degradation in Breast Cancer Cells Treated with Grape Leaf Extract 978
297. Abnormal ultrasound findings in 45,X early pregnancy loss 947
Ultrasound findings in early pregnancy loss with 45, x karyotype 944
The use of array-CGH in a cohort of Greek children with developmental delay. 899
Recipient CTLA-4 genotype is a prognostic factor for acute GVHD in hematopoietic stem cell transplantation 898
Serological and molecular studies of HLA in Sardinian patients with Graves' disease 833
Prenatal diagnosis of a XX male in a fetus with increased nuchal translucency 800
Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization 779
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis 732
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 705
KIR2DS4*003 on donor natural killer cells increases the risk for acute GVHD following unrelated hematopoietic stem cell transplantation 702
Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: Molecular cytogenetic analysis and review of the literature 697
Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients 694
Delezione distale del braccio corto del cromosoma 8:descrizione di un caso rilevato in diagnosi prenatale 689
Molecular analysis of HLA class II antigens in bone marrow transplanted thalassemic patients 673
BMT in thalassemia from unrelated donors: Role of KIR polymorphism 672
Cytogenetic and molecular characterization of a Small Supernumerary Marker Chromosome (sSMC) found at prenatal diagnosis 646
Case report: Prenatal diagnosis of mosaic trisomy 9 640
Defining the allelic variants of HLA-A30 in the Sardinian population using amplification refractory mutation system--polymerase chain reaction 620
Diagnosi Prenatale di maschio xx in un feto con translucenza nucale alterata 612
Wilson's disease maps between the D13S169 and D13S173 loci 598
Case report: paracentric inversion of chromosome 1 in a man with azoospermia 597
Recipient CTLA-4 genotype is a prognostic factor foe acute GvHD in hematopoietic stem cell transplantation. Haematologica/The Hematology Journal 594
Serological and molecular studies of HLA in Insulin-Dependent Diabetes Mellitus in Sardinia 593
Recipient CTLA-4 genotype is a prognostic factor for acute GvHD in hematopoietic stem cell transplantation for thalassemia 592
AML post BMT: donor or recipient? 576
The human leucocyte antigen-G 14-basepair polymorphism correlates with graft-versus-host disease in unrelated bone marrow transplantation for thalassaemia 569
MOLECULAR ANALYSIS OF HLA-DRB1-DR1 ASSOCIATED ALLELES IN LICHEN RUBER PLANUS 566
Recipient CTLA-4 genotype is a prognostic factor foe acute GvHD in hematopoietic stem cell transplantation 556
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 553
Chromosomal gain: from MGUS to MULTIPLE MYELOMA 540
The EUROGEM map of human chromosome 2 539
Molecular research on the HLA-DR2, DQw1 haplotypes in the Sardinian population: the DQw1.AZH allele characterizes the A2 Cw7 B17 3S31 DR2 DQw1 extended haplotype. 530
Successful unrelated bone marrow transplantation in beta-thalassaemia 529
Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome) 519
The HLA-DRB1*0101 allele is responsible for HLA susceptibility to lichen ruber planus 519
Totale 165.242
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Categoria #
all - tutte 240.447
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 240.447
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20226.592 0 0 0 0 725 484 463 566 1.010 1.010 1.308 1.026
2022/202313.267 1.052 1.793 1.951 1.075 1.088 1.403 538 1.197 758 816 1.081 515
2023/202414.379 760 537 844 907 1.196 2.738 1.419 918 723 950 2.045 1.342
2024/202528.359 4.790 7.118 4.141 4.014 2.135 3.002 1.844 157 272 225 277 384
2025/20267.638 344 467 933 742 479 483 1.414 576 497 845 515 343
2026/20272.342 188 300 743 1.094 17 0 0 0 0 0 0 0
Totale 181.600