UNICA IRIS Institutional Research Information System

ORRU, SANDRO IGNAZIO GIOVANNI
 Distribuzione geografica
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Continente #
EU - Europa 1.828
NA - Nord America 1.324
AS - Asia 167
AF - Africa 30
SA - Sud America 20
OC - Oceania 1
Totale 3.370
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Nazione #
IT - Italia 1.703
US - Stati Uniti d'America 1.305
CN - Cina 89
VN - Vietnam 29
DE - Germania 22
ZA - Sudafrica 19
CA - Canada 18
FI - Finlandia 16
GB - Regno Unito 15
UA - Ucraina 12
BR - Brasile 11
FR - Francia 11
RU - Federazione Russa 11
GR - Grecia 10
IN - India 9
AE - Emirati Arabi Uniti 7
JP - Giappone 7
IR - Iran 6
CL - Cile 5
CZ - Repubblica Ceca 5
IL - Israele 5
MW - Malawi 5
NL - Olanda 5
SG - Singapore 5
SE - Svezia 4
CO - Colombia 3
ES - Italia 3
CH - Svizzera 2
MY - Malesia 2
NG - Nigeria 2
PL - Polonia 2
RO - Romania 2
TZ - Tanzania 2
AT - Austria 1
AU - Australia 1
DZ - Algeria 1
EG - Egitto 1
HK - Hong Kong 1
HN - Honduras 1
ID - Indonesia 1
IE - Irlanda 1
IS - Islanda 1
KR - Corea 1
MK - Macedonia 1
PT - Portogallo 1
SA - Arabia Saudita 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
TR - Turchia 1
TW - Taiwan 1
UY - Uruguay 1
Totale 3.370
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Città #
Cagliari 1.612
Fairfield 196
Santa Cruz 116
Houston 108
Buffalo 93
Woodbridge 82
Ashburn 80
Seattle 76
Cambridge 66
Wilmington 59
Ann Arbor 32
Dong Ket 29
Mountain View 28
Hangzhou 22
Beijing 17
Chicago 17
Los Angeles 16
Helsinki 15
Muizenberg 15
Clearwater 13
Ottawa 13
San Diego 13
Las Vegas 11
Phoenix 11
University Park 11
Boardman 10
Shanghai 10
Wuhan 10
Odesa 9
Dallas 6
Athens 5
Easton 5
Lilongwe 5
Milan 5
Mumbai 5
Redmond 5
Riva 5
San Francisco 5
Boa Vista 4
Florence 4
Henderson 4
Manaus 4
Miami 4
Milpitas 4
Rome 4
Sassari 4
Singapore 4
Tianjin 4
Tokyo 4
Auburn 3
Casoria 3
Changsha 3
Chengdu 3
Olbia 3
Saint Louis 3
Saint Petersburg 3
Santiago de Cali 3
Silverton 3
Torino 3
Yellow Springs 3
Alghero 2
Austin 2
Birmingham 2
Bristol 2
Büdelsdorf 2
Council Bluffs 2
Dar es Salaam 2
Denver 2
Genoa 2
Guidonia 2
Hartford 2
Jersey City 2
Kenmore 2
Kunming 2
Lenoir 2
Marcallo Con Casone 2
Montreal 2
Moscow 2
New York 2
Nuoro 2
Parsippany 2
Pasadena 2
Portland 2
Poznan 2
Recife 2
Rochester 2
Salford 2
San Cipriano d'Aversa 2
San Jose 2
Scranton 2
Toronto 2
Ujjain 2
Zhengzhou 2
Amsterdam 1
Anguillara 1
Atlanta 1
Auxonne 1
Azzano Decimo 1
Bangkok 1
Bari 1
Totale 2.986
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Nome #
VGF protein and its C-terminal derived peptides in amyotrophic lateral sclerosis: Human and animal model studies, file e2f56ed5-80fc-3eaf-e053-3a05fe0a5d97 702
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, file e2f56ed9-3cdc-3eaf-e053-3a05fe0a5d97 420
A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristics, file e2f56ed6-accb-3eaf-e053-3a05fe0a5d97 303
Star-related lipid transfer protein 10 (STARD10): a novel key player in alcohol-induced breast cancer progression, file e2f56ed8-f14a-3eaf-e053-3a05fe0a5d97 244
Exploring the Role of Killer Cell Immunoglobulin-Like Receptors and Their HLA Class I Ligands in Autoimmune Hepatitis, file e2f56ed4-bff5-3eaf-e053-3a05fe0a5d97 214
null, file e2f56ed6-c0bc-3eaf-e053-3a05fe0a5d97 201
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, file e2f56ed9-5c39-3eaf-e053-3a05fe0a5d97 194
Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male, file e2f56ed4-9928-3eaf-e053-3a05fe0a5d97 173
What unrelated hematopoietic stem cell transplantation in thalassemia taught us about transplant immunogenetics, file e2f56ed5-ca06-3eaf-e053-3a05fe0a5d97 173
KIR and their HLA Class I ligands: Two more pieces towards completing the puzzle of chronic rejection and graft loss in kidney transplantation, file e2f56ed6-a2b9-3eaf-e053-3a05fe0a5d97 153
Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients, file e2f56ed7-4348-3eaf-e053-3a05fe0a5d97 133
Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature, file e2f56ed4-e69a-3eaf-e053-3a05fe0a5d97 127
Entropy of human leukocyte antigen and killer-cell immunoglobulin-like receptor systems in immune-mediated disorders: A pilot study on multiple sclerosis, file e2f56ed9-0821-3eaf-e053-3a05fe0a5d97 114
A novel desmoplakin mutation associated with left dominant arrhythmogenic cardiomyopathy and cutaneous phenotype, file e2f56ed9-446c-3eaf-e053-3a05fe0a5d97 62
The role of fetal programming in human carcinogenesis - May the Barker hypothesis explain interindividual variability in susceptibility to cancer insurgence and progression?, file 7ff92b55-0103-42d3-8d15-6ec203def5ec 45
Gene expression profiling of monozygotic twins affected by psoriatic arthritis, file e2f56eda-2127-3eaf-e053-3a05fe0a5d97 41
HLA-G molecules and clinical outcome in Chronic Myeloid Leukemia, file 7784ebad-6ea6-45cf-b7e9-e5956fdd35ae 32
Reduced stress granule formation and cell death in fibroblasts with the A382T mutation of TARDBP gene: evidence for loss of TDP-43 nuclear function., file e2f56ed5-75fc-3eaf-e053-3a05fe0a5d97 14
Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients, file d16a2089-c813-45fb-a0ff-1a036cb78509 8
GUT MICROBIAL PROFILE IN WEIGHT CYCLING PATIENTS WITH OBESITY, file e2f56ed5-6afa-3eaf-e053-3a05fe0a5d97 8
null, file e2f56ed6-adee-3eaf-e053-3a05fe0a5d97 8
Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia, file e2f56ed3-c5cc-3eaf-e053-3a05fe0a5d97 7
HLA-G molecules and clinical outcome in Chronic Myeloid Leukemia, file e2f56ed6-bf64-3eaf-e053-3a05fe0a5d97 7
Homozygosity for killer immunoglobin-like receptor haplotype A predicts complete molecular response to treatment with tyrosine kinase inhibitors in chronic myeloid leukemia patients, file e2f56ed3-c8e2-3eaf-e053-3a05fe0a5d97 6
Comparison Between an Artificial Neural Network and Logistic Regression in Predicting Long Term Kidney Transplantation Outcome, file e2f56ed3-a207-3eaf-e053-3a05fe0a5d97 5
Comparison Between an Artificial Neural Network and Logistic Regression in Predicting Long Term Kidney Transplantation Outcome, file e2f56ed3-a205-3eaf-e053-3a05fe0a5d97 4
The human leucocyte antigen-G 14-basepair polymorphism correlates with graft-versus-host disease in unrelated bone marrow transplantation for thalassaemia, file e2f56ed3-bdac-3eaf-e053-3a05fe0a5d97 4
HPRTSardinia: A new point mutation causing HPRT deficiency without Lesch-Nyhan disease, file e2f56ed6-0eaa-3eaf-e053-3a05fe0a5d97 4
Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases, file e2f56ed6-1ef9-3eaf-e053-3a05fe0a5d97 4
Status of donor-recipient HLA class I ligands and not the KIR genotype is predictive for the outcome of unrelated hematopoietic stem cell transplantation in beta-thalassemia patients, file e2f56ed3-83ca-3eaf-e053-3a05fe0a5d97 3
Comparison Between an Artificial Neural Network and Logistic Regression in Predicting Long Term Kidney Transplantation Outcome, file e2f56ed3-a206-3eaf-e053-3a05fe0a5d97 3
Absence of activating killer immunoglobulin-like receptor genes combined with hepatitis C viral genotype is predictive of hepatocellular carcinoma, file e2f56ed3-b230-3eaf-e053-3a05fe0a5d97 3
High frequency of the TARDBP p.Ala382Thr mutation in Sardinian patients with amyotrophic lateral sclerosis, file e2f56ed3-c040-3eaf-e053-3a05fe0a5d97 3
Genetic Creutzfeldt-Jakob disease in Sardinia: a case series linked to the PRNP R208H mutation due to a single founder effect, file e2f56ed9-1840-3eaf-e053-3a05fe0a5d97 3
Distribution of HLA alleles and haplotypes in the Maldivian population, file e2f56ed3-aeee-3eaf-e053-3a05fe0a5d97 2
The role of killer immunoglobulin-like receptor haplotypes on the outcome of unrelated donor haematopoietic SCT for thalassaemia, file e2f56ed3-b404-3eaf-e053-3a05fe0a5d97 2
Role of human leukocyte antigen-G 14-base pair polymorphism in kidney transplantation outcomes, file e2f56ed3-b5c4-3eaf-e053-3a05fe0a5d97 2
De novo 15.5-Mb interstitial deletion in 5p in a male ascertained by oligospermia, file e2f56ed6-b77d-3eaf-e053-3a05fe0a5d97 2
Expression of ATP7B in normal human liver, file e2f56ed3-84f4-3eaf-e053-3a05fe0a5d97 1
Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome), file e2f56ed3-87dd-3eaf-e053-3a05fe0a5d97 1
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH, file e2f56ed6-adef-3eaf-e053-3a05fe0a5d97 1
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, file e2f56ed6-ae9c-3eaf-e053-3a05fe0a5d97 1
Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization, file e2f56ed6-b31b-3eaf-e053-3a05fe0a5d97 1
Tetrasomy 9p mosaicism associated with a normal phenotype in two cases, file e2f56ed6-b4d4-3eaf-e053-3a05fe0a5d97 1
Maternal uniparental disomy of chromosome 4 and homozygous novel mutation in the WFS1 gene in a paediatric patient with Wolfram syndrome, file e2f56ed6-b65a-3eaf-e053-3a05fe0a5d97 1
Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: Molecular cytogenetic analysis and review of the literature, file e2f56ed6-b73c-3eaf-e053-3a05fe0a5d97 1
Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia, file e2f56ed6-b77b-3eaf-e053-3a05fe0a5d97 1
A 725 kb deletion at 22q13.1 chromosomal region including SOX10 gene in a boy with a neurologic variant of Waardenburg syndrome type 2, file e2f56ed6-b902-3eaf-e053-3a05fe0a5d97 1
Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report, file e2f56ed6-b9db-3eaf-e053-3a05fe0a5d97 1
Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature, file e2f56ed6-b9dd-3eaf-e053-3a05fe0a5d97 1
Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients, file e2f56ed6-d74b-3eaf-e053-3a05fe0a5d97 1
Wilson's disease: A new perspective review on its genetics, diagnosis and treatment, file e2f56ed9-508f-3eaf-e053-3a05fe0a5d97 1
Totale 3.447
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Categoria #
all - tutte 6.815
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 6.815
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019132 0 0 0 0 0 0 0 0 0 0 72 60
2019/2020772 44 35 24 42 159 155 90 55 78 27 19 44
2020/20211.182 42 55 21 303 214 102 76 52 37 55 104 121
2021/2022478 52 62 28 29 45 15 33 16 17 13 125 43
2022/2023290 21 14 96 44 14 13 4 14 35 11 16 8
2023/2024164 23 8 13 10 27 20 12 12 14 21 4 0
Totale 3.447