UNICA IRIS Institutional Research Information System

ORRU, SANDRO IGNAZIO GIOVANNI
 Distribuzione geografica
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Continente #
EU - Europa 164.639
NA - Nord America 10.034
AS - Asia 4.050
SA - Sud America 580
Continente sconosciuto - Info sul continente non disponibili 330
AF - Africa 76
OC - Oceania 9
Totale 179.718
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Nazione #
IT - Italia 162.025
US - Stati Uniti d'America 9.908
CN - Cina 1.512
SG - Singapore 1.489
UA - Ucraina 710
SE - Svezia 520
BR - Brasile 453
VN - Vietnam 363
DE - Germania 355
FI - Finlandia 318
FR - Francia 241
GB - Regno Unito 239
HK - Hong Kong 164
IN - India 95
KR - Corea 87
CA - Canada 70
BD - Bangladesh 63
RU - Federazione Russa 58
AR - Argentina 48
IQ - Iraq 41
JP - Giappone 35
NL - Olanda 35
ZA - Sudafrica 27
ID - Indonesia 25
BE - Belgio 22
EC - Ecuador 22
PK - Pakistan 22
MX - Messico 20
AT - Austria 19
MY - Malesia 17
PH - Filippine 17
TR - Turchia 17
VE - Venezuela 17
JM - Giamaica 16
MA - Marocco 15
ES - Italia 14
SA - Arabia Saudita 14
CL - Cile 12
PL - Polonia 12
CO - Colombia 11
IE - Irlanda 11
JO - Giordania 10
LT - Lituania 10
TN - Tunisia 10
AE - Emirati Arabi Uniti 9
AZ - Azerbaigian 9
CZ - Repubblica Ceca 9
IR - Iran 9
CR - Costa Rica 8
UZ - Uzbekistan 8
CH - Svizzera 7
IL - Israele 7
KE - Kenya 7
KZ - Kazakistan 7
RO - Romania 7
AU - Australia 6
UY - Uruguay 6
GR - Grecia 5
PE - Perù 5
TH - Thailandia 5
EG - Egitto 4
ET - Etiopia 4
HN - Honduras 4
NP - Nepal 4
PY - Paraguay 4
DK - Danimarca 3
GE - Georgia 3
MD - Moldavia 3
NZ - Nuova Zelanda 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
PA - Panama 2
PS - Palestinian Territory 2
PT - Portogallo 2
TT - Trinidad e Tobago 2
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BZ - Belize 1
CY - Cipro 1
DZ - Algeria 1
HT - Haiti 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LC - Santa Lucia 1
LK - Sri Lanka 1
LY - Libia 1
ML - Mali 1
MN - Mongolia 1
MT - Malta 1
NG - Nigeria 1
NI - Nicaragua 1
Totale 179.383
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Città #
Cagliari 157.114
Uta 4.292
Fairfield 1.006
Ashburn 831
Woodbridge 771
Singapore 751
Chandler 622
San Jose 598
Houston 468
Wilmington 449
Boardman 438
Ann Arbor 435
Seattle 393
Jacksonville 385
Dallas 374
Nyköping 348
Cambridge 327
Beijing 266
Helsinki 187
Los Angeles 175
New York 175
Council Bluffs 158
Hong Kong 146
Santa Clara 128
Nanjing 125
Lauterbourg 123
Hefei 113
Ho Chi Minh City 106
Boston 105
Dearborn 102
The Dalles 89
Shanghai 87
Milan 80
Hanoi 76
Seoul 75
Buffalo 63
San Diego 59
Dong Ket 56
Shenyang 48
Nanchang 47
Hangzhou 45
Guangzhou 38
Redwood City 38
Rome 37
Tianjin 34
Changsha 33
Jiaxing 31
Hebei 30
Columbus 29
Munich 28
Verona 28
São Paulo 27
Washington 27
Toronto 26
Frankfurt am Main 25
London 25
Orem 25
Norwalk 24
Redondo Beach 24
Tokyo 24
Atlanta 23
Jinan 23
Orange 23
Chicago 22
Mountain View 21
Phoenix 21
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
Manchester 13
Turku 13
Falls Church 12
Mumbai 12
San Francisco 11
Shenzhen 11
Warsaw 11
Wuhan 11
Casablanca 10
Dublin 10
Kunming 10
Pune 10
Brooklyn 9
Campinas 9
Denver 9
Jakarta 9
Johannesburg 9
Quito 9
Vienna 9
Waanrode 9
Amman 8
Amsterdam 8
Totale 173.339
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Nome #
VGF protein and its C-terminal derived peptides in amyotrophic lateral sclerosis: Human and animal model studies 4.789
null 4.609
Exploring the Role of Killer Cell Immunoglobulin-Like Receptors and Their HLA Class I Ligands in Autoimmune Hepatitis 4.580
GUT MICROBIAL PROFILE IN WEIGHT CYCLING PATIENTS WITH OBESITY 4.553
Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients 3.955
Reduced stress granule formation and cell death in fibroblasts with the A382T mutation of TARDBP gene: evidence for loss of TDP-43 nuclear function. 3.638
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 3.581
Comparison Between an Artificial Neural Network and Logistic Regression in Predicting Long Term Kidney Transplantation Outcome 3.439
Absence of activating killer immunoglobulin-like receptor genes combined with hepatitis C viral genotype is predictive of hepatocellular carcinoma 3.372
ALTERED STRESS GRANULE ASSEMBLY IN CULTURED FIBROBLASTS FROM ALS PATIENTS CARRYING A TARDBP MUTATION 3.327
What unrelated hematopoietic stem cell transplantation in thalassemia taught us about transplant immunogenetics 3.321
Homozygosity for killer immunoglobin-like receptor haplotype A predicts complete molecular response to treatment with tyrosine kinase inhibitors in chronic myeloid leukemia patients 3.319
Stress granules induced by oxidative stress in cultured fibroblast from TDP-43 mutant ALS patients 3.280
HLA-G molecules and clinical outcome in Chronic Myeloid Leukemia 3.239
Gene expression profiling of monozygotic twins affected by psoriatic arthritis 3.075
Stress granule assembly in cultured fibroblast from TDP-43 mutant ALS patients. 2.922
KIR and their HLA Class I ligands: Two more pieces towards completing the puzzle of chronic rejection and graft loss in kidney transplantation 2.921
Kir haplotype aa is a possible predictive marker of complete molecular response to tyrosine kinase inhibitors in patients with chronic myeloid leukemia 2.834
IMPACT OF KILLER-CELL IMMUNOGLOBULIN-LIKE RECEPTORS ON PROGRESSION OF HEPATOCELLULAR CARCINOMA 2.605
Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients 2.534
Entropy of human leukocyte antigen and killer-cell immunoglobulin-like receptor systems in immune-mediated disorders: A pilot study on multiple sclerosis 2.230
Maternal uniparental disomy of chromosome 4 and homozygous novel mutation in the WFS1 gene in a paediatric patient with Wolfram syndrome 2.227
Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia 2.179
High frequency of the TARDBP p.Ala382Thr mutation in Sardinian patients with amyotrophic lateral sclerosis 2.151
Role of human leukocyte antigen-G 14-base pair polymorphism in kidney transplantation outcomes 2.118
Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male 2.112
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 2.030
Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases 1.991
Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia 1.963
Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report 1.936
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 1.925
Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature 1.919
A novel desmoplakin mutation associated with left dominant arrhythmogenic cardiomyopathy and cutaneous phenotype 1.919
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 1.874
THE HLA-G 14-BP POLYMORPHISM IS AN INDEPENDENT GENETIC RISK MARKER OF LONG-TERM KIDNEY TRANSPLANTATION OUTCOME 1.817
The human leukocyte antigen-g 14-bp polymorphism is an independent genetic risk marker of long-term kidney transplantation outcome 1.763
Wilson's disease: A new perspective review on its genetics, diagnosis and treatment 1.759
De novo 15.5-Mb interstitial deletion in 5p in a male ascertained by oligospermia 1.718
Genetic Creutzfeldt-Jakob disease in Sardinia: a case series linked to the PRNP R208H mutation due to a single founder effect 1.680
A 9.1-kb gap in the genome reference map is shown to be a stable deletion/insertion polymorphism of ancestral origin 1.616
Star-related lipid transfer protein 10 (STARD10): a novel key player in alcohol-induced breast cancer progression 1.615
Distribution of HLA alleles and haplotypes in the Maldivian population 1.576
Nuclease activity in human metaphase chromosomes substituted with 5'-bromodeoxyuridine 1.568
Dilated lateral ventricles and micrognathia by ultrasound exsamination in fetus with mosaic trisomy 9 1.512
Cytogenetic and molecular characterization of a Small Supernumerary Marcker Chromosome (sSMC)found at prenatal diagnosis 1.383
Expression of ATP7B in normal human liver 1.379
Hodgkin's disease presenting in 1 of 4 siblings affected by hereditary spinocerebellar ataxia: clinical, immunological and genetic study 1.375
Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: A case report 1.322
Familial chronic B-cell malignancy. Hairy cell leukaemia in mother and daughter 1.321
A 725 kb deletion at 22q13.1 chromosomal region including SOX10 gene in a boy with a neurologic variant of Waardenburg syndrome type 2 1.312
Tetrasomy 9p mosaicism associated with a normal phenotype in two cases 1.309
A plea to search for deletion polymorphism through genome scans in populations 1.302
VAPB ER-Aggregates, A Possible New Biomarker in ALS Pathology 1.299
45, X karyotipe and abnormal ultrasound findings in early pregnancy loss 1.276
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 1.268
The role of inhibitory KIR 2DL5 in the outcome of autologous hematopoietic stem cell transplantation for multiple myeloma 1.219
Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature 1.189
Prenatal diagnosis of trisomy 18: time of evalutation, ultrasound markers and genetic counselling. A review 1.077
Nuchal translucency and other US markers in cases of trisomy 18 1.071
null 1.048
Diagnostic echographic diagnosis in sibs with the fetal hydrops, heart disease, cerebellar hypoplasia: Neu Laxsova Syndrome 1.017
The role of killer immunoglobulin-like receptor haplotypes on the outcome of unrelated donor haematopoietic SCT for thalassaemia 1.000
45, X karyotype and abnormal ultrasound findings in early pregnancy loss 994
SUMOylation Protects FASN Against Proteasomal Degradation in Breast Cancer Cells Treated with Grape Leaf Extract 967
Ultrasound findings in early pregnancy loss with 45, x karyotype 933
297. Abnormal ultrasound findings in 45,X early pregnancy loss 922
The use of array-CGH in a cohort of Greek children with developmental delay. 887
Recipient CTLA-4 genotype is a prognostic factor for acute GVHD in hematopoietic stem cell transplantation 871
Serological and molecular studies of HLA in Sardinian patients with Graves' disease 821
Prenatal diagnosis of a XX male in a fetus with increased nuchal translucency 792
Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization 771
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis 717
KIR2DS4*003 on donor natural killer cells increases the risk for acute GVHD following unrelated hematopoietic stem cell transplantation 698
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 697
Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: Molecular cytogenetic analysis and review of the literature 689
Delezione distale del braccio corto del cromosoma 8:descrizione di un caso rilevato in diagnosi prenatale 682
Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients 679
BMT in thalassemia from unrelated donors: Role of KIR polymorphism 664
Molecular analysis of HLA class II antigens in bone marrow transplanted thalassemic patients 658
Cytogenetic and molecular characterization of a Small Supernumerary Marker Chromosome (sSMC) found at prenatal diagnosis 633
Case report: Prenatal diagnosis of mosaic trisomy 9 629
Defining the allelic variants of HLA-A30 in the Sardinian population using amplification refractory mutation system--polymerase chain reaction 614
Diagnosi Prenatale di maschio xx in un feto con translucenza nucale alterata 606
Recipient CTLA-4 genotype is a prognostic factor foe acute GvHD in hematopoietic stem cell transplantation. Haematologica/The Hematology Journal 587
Case report: paracentric inversion of chromosome 1 in a man with azoospermia 586
Serological and molecular studies of HLA in Insulin-Dependent Diabetes Mellitus in Sardinia 583
Recipient CTLA-4 genotype is a prognostic factor for acute GvHD in hematopoietic stem cell transplantation for thalassemia 579
Wilson's disease maps between the D13S169 and D13S173 loci 566
AML post BMT: donor or recipient? 565
The human leucocyte antigen-G 14-basepair polymorphism correlates with graft-versus-host disease in unrelated bone marrow transplantation for thalassaemia 561
MOLECULAR ANALYSIS OF HLA-DRB1-DR1 ASSOCIATED ALLELES IN LICHEN RUBER PLANUS 558
Recipient CTLA-4 genotype is a prognostic factor foe acute GvHD in hematopoietic stem cell transplantation 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 546
The EUROGEM map of human chromosome 2 529
Chromosomal gain: from MGUS to MULTIPLE MYELOMA 528
Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome) 515
Successful unrelated bone marrow transplantation in beta-thalassaemia 512
The HLA-DRB1*0101 allele is responsible for HLA susceptibility to lichen ruber planus 512
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH 506
Totale 163.842
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Categoria #
all - tutte 235.667
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 235.667
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20228.493 0 693 376 832 725 484 463 566 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
2026/2027460 188 272 0 0 0 0 0 0 0 0 0 0
Totale 179.718