IRIS Institutional Research Information System - OPENBS Open Archive UniBS

MORATTO, Daniele
 Distribuzione geografica
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Continente #
NA - Nord America 2.558
EU - Europa 1.189
AS - Asia 317
OC - Oceania 6
SA - Sud America 3
AF - Africa 2
Continente sconosciuto - Info sul continente non disponibili 2
Totale 4.077
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Nazione #
US - Stati Uniti d'America 2.550
PL - Polonia 316
CN - Cina 275
UA - Ucraina 248
DE - Germania 152
IT - Italia 145
FI - Finlandia 106
GB - Regno Unito 81
IE - Irlanda 53
BE - Belgio 28
FR - Francia 20
VN - Vietnam 20
SE - Svezia 16
IN - India 10
CA - Canada 8
RU - Federazione Russa 8
AU - Australia 6
RO - Romania 5
NL - Olanda 4
JP - Giappone 3
TR - Turchia 3
BR - Brasile 2
EU - Europa 2
GR - Grecia 2
HK - Hong Kong 2
MU - Mauritius 2
PT - Portogallo 2
CL - Cile 1
ES - Italia 1
HU - Ungheria 1
ID - Indonesia 1
IL - Israele 1
IR - Iran 1
PS - Palestinian Territory 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 4.077
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Città #
Fairfield 385
Warsaw 313
Woodbridge 260
Houston 241
Chandler 198
Jacksonville 191
Ashburn 175
Cambridge 165
Seattle 154
Wilmington 151
Ann Arbor 146
Princeton 97
Helsinki 83
Beijing 67
Brescia 65
Dublin 53
Nanjing 51
Dearborn 30
Brussels 26
Changsha 23
Des Moines 22
Lancaster 22
Dong Ket 20
London 18
Hebei 17
Nanchang 16
Shenyang 16
Jinan 15
San Diego 14
Haikou 10
San Francisco 9
Hangzhou 8
Milan 8
Tianjin 8
Jiaxing 6
Ningbo 6
Redwood City 6
Taiyuan 6
Toronto 6
Lanzhou 5
Leawood 5
Verona 5
Barlassina 4
Casoria 4
Chicago 4
Chiswick 4
Norwalk 4
Rende 4
Rome 4
Sydney 4
Falkenstein 3
Hounslow 3
Kunming 3
New Bedfont 3
Phoenix 3
Zhengzhou 3
Athens 2
Central 2
Cluj-Napoca 2
Genoa 2
Guangzhou 2
Islington 2
Mantova 2
Melbourne 2
Monmouth Junction 2
Montichiari 2
Nürnberg 2
Orange 2
Palermo 2
Pavia 2
Prad am Stilfser Joch 2
Shanghai 2
Waanrode 2
Acton 1
Airdrie 1
Amsterdam 1
Augusta 1
Baotou 1
Boardman 1
Bratislava 1
Budapest 1
Castiglione Delle Stiviere 1
Changchun 1
Charlotte 1
Cisano Bergamasco 1
Cormeilles-en-Parisis 1
Dallas 1
Duncan 1
Eboli 1
Fano 1
Fuzhou 1
Gassino Torinese 1
Grafing 1
Groningen 1
Gunzenhausen 1
Haifa 1
Hefei 1
Iasi 1
Isfahan 1
Jakarta 1
Totale 3.233
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Nome #
Evaluation of a novel human IgG1 anti-claudin3 antibody that specifically recognizes its aberrantly localized antigen in ovarian cancer cells and that is suitable for selective drug delivery 211
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 183
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 176
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 173
Collapse of the Plasmacytoid Dendritic Cells compartment in advanced cutaneous melanomas by components of the tumor cell secretome 132
α- and β-Papillomavirus infection in a young patient with an unclassified primary T-cell immunodeficiency and multiple mucosal and cutaneous lesions 127
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 127
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 126
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 117
Functional defects of dendritic cells in patients with CD40 deficiency. 115
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 112
Stem cell transplantation for the Wiskott-Aldrich syndrome: a single-center experience confirms efficacy of matched unrelated donor transplantation 111
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 110
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 110
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 106
A novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency 104
Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia 101
Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content. 101
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 97
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation 97
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 94
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 91
The Wiskott-Aldrich syndrome: From genotype-phenotype correlation to treatment 90
Immune response in children with COVID-19 is characterized by lower levels of T-cell activation than infected adults 87
Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency. 83
Proteus syndrome: evaluation of the immunological profile 76
Low WASp expression in patients with no apparent mutation in the WASP gene 76
Plasmacytoid dendritic cell impairment in metastatic melanoma by lactic acidosis 74
Aicardi Goutieres Syndrome: New Insights on a Novel Set of Inborn Errors of Immunity 71
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 64
PROSPECTIVE STUDY OF 84 PATIENTS WITH WISKOTT-ALDRICH SYNDROME AND X-RECESSIVE PIASTRINOPENIA: RESULTS OF THE APPLICATION OF COMMON PROTOCOL FOR DIAGNOSIS AND TREATMENT OF WAS/XLT 63
Long-term outcome and lineage-specific chimerism in 194 Wiskott-Aldrich Syndrome patients treated by hematopoietic celltransplantation between 1980-2009: an international collaborative study. 61
WASP-WIP DEFICIENCIES: NEW INSIGHTS IN WASP-WIP INTERACTION 59
CASE REPORT: IDENTIFICATION OF A PATIENT WITH FAMILIAR MUTATIONS AFFECTING BOTH WASP AND FOXP3 GENES 59
Multi-lineage analysis of X-inactivation in female carriers of genetic alterations in the Wiskott-Aldrich syndrome protein (WASP) gene locus 57
Application of common recommendations for diagnosis and treatment of Wiskott-Aldrich syndrome and X-recessive piastrinopenia: clinical and immunological characteristics of 65 patients with WAS/XLT 55
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in three brothers with diarrhea, eczema and infections. 51
Flow Cytometry Identifies Risk Factors and Dynamic Changes in Patients with COVID-19 51
Transient Decrease of Circulating and Tissular Dendritic Cells in Patients With Mycobacterial Disease and With Partial Dominant IFNγR1 Deficiency 51
Long-Term Outcome of WHIM Syndrome in 18 Patients: High Risk of Lung Disease and HPV-Related Malignancies 38
Immunologic characterization of a immunosuppressed multiple sclerosis patient that recovered from SARS-CoV-2 infection 35
P1450: AUTOLOGOUS STEM CELL TRANSPLANTATION INDUCES HIGHER LEVEL OF EXHAUSTED T-CELLS IN DLBCL PATIENTS BEFORE LEUKAPHERESIS FOR CAR-T CELL THERAPY 34
Two X-linked agammaglobulinemia patients develop pneumonia as COVID-19 manifestation but recover 32
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in 3 brothers with diarrhea, eczema, and infections 31
Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency 31
Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing Cholangitis 28
Pseudomonas aeruginosa severe skin infection in a toddler with X-linked agammaglobulinemia due to a novel BTK mutation 26
Identical EP300 variant leading to Rubinstein–Taybi syndrome with different clinical and immunologic phenotype 19
Timely Leukapheresis May Interfere with the “Fitness” of Lymphocytes Collected for CAR-T Treatment in High Risk DLBCL Patients 18
Case Report: Analysis of Inflammatory Cytokines IL-6, CCL2/MCP1, CCL5/RANTES, CXCL9/MIG, and CXCL10/IP10 in a Cystic Fibrosis Patient Cohort During the First Wave of the COVID-19 Pandemic 18
Immunological Evaluation of Patients Affected with Jacobsen Syndrome Reveals Profound Not Age-Related Lymphocyte Alterations 16
Plasmacytoid Dendritic Cells Depletion and Elevation of IFN-γ Dependent Chemokines CXCL9 and CXCL10 in Children With Multisystem Inflammatory Syndrome 13
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis 10
Generation of induced Pluripotent Stem Cells (UNIBSi008-A, UNIBSi008-B, UNIBSi008-C) from an Ataxia-Telangiectasia (AT) patient carrying a novel homozygous deletion in ATM gene 10
Longitudinal Characterization of Immune Response in a Cohort of Children Hospitalized with Multisystem Inflammatory Syndrome 6
Inflammatory pathways signal transducers analysis in iPSC-derived neurons and 3D cerebral organoids 6
Reduced G protein signaling despite impaired internalization and β-arrestin recruitment in patients carrying a CXCR4Leu317fsX3 mutation causing WHIM syndrome 4
Abnormal B-Cell Maturation and Increased Transitional B Cells in CBL Syndrome 4
Totale 4.228
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Categoria #
all - tutte 15.560
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 15.560
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019422 0 0 0 0 40 7 33 39 15 68 113 107
2019/20201.191 150 55 54 129 80 132 105 128 90 148 59 61
2020/2021911 22 84 45 95 64 90 56 136 86 108 86 39
2021/2022479 43 50 5 29 10 25 14 31 30 70 58 114
2022/2023526 64 14 25 32 60 123 4 58 76 9 29 32
2023/2024220 37 14 78 54 37 0 0 0 0 0 0 0
Totale 4.228