IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

MASSA, VALENTINA
 Distribuzione geografica
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Continente #
EU - Europa 7.576
NA - Nord America 6.753
AS - Asia 6.098
SA - Sud America 522
AF - Africa 127
OC - Oceania 70
Continente sconosciuto - Info sul continente non disponibili 5
Totale 21.151
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Nazione #
US - Stati Uniti d'America 6.424
GB - Regno Unito 2.589
CN - Cina 1.909
IT - Italia 1.703
SG - Singapore 1.701
DE - Germania 1.020
HK - Hong Kong 532
BD - Bangladesh 523
VN - Vietnam 483
SE - Svezia 472
RU - Federazione Russa 402
BR - Brasile 387
FR - Francia 359
IN - India 312
CA - Canada 244
NL - Olanda 174
IE - Irlanda 163
FI - Finlandia 140
ID - Indonesia 125
DK - Danimarca 123
UA - Ucraina 101
KR - Corea 97
JP - Giappone 94
TR - Turchia 92
ES - Italia 63
AU - Australia 48
CH - Svizzera 46
MX - Messico 43
AR - Argentina 39
CI - Costa d'Avorio 35
IQ - Iraq 32
PL - Polonia 30
AT - Austria 29
BE - Belgio 28
CO - Colombia 26
NO - Norvegia 26
ZA - Sudafrica 25
EC - Ecuador 21
IL - Israele 21
PH - Filippine 21
NZ - Nuova Zelanda 20
PT - Portogallo 19
CL - Cile 18
PK - Pakistan 18
EU - Europa 17
GR - Grecia 16
SA - Arabia Saudita 16
CZ - Repubblica Ceca 14
MA - Marocco 14
MY - Malesia 12
TH - Thailandia 12
TW - Taiwan 12
JM - Giamaica 11
KE - Kenya 10
PE - Perù 10
NP - Nepal 9
UZ - Uzbekistan 9
AE - Emirati Arabi Uniti 8
JO - Giordania 8
RO - Romania 8
VE - Venezuela 8
KZ - Kazakistan 7
AZ - Azerbaigian 6
EG - Egitto 6
HU - Ungheria 6
LT - Lituania 6
LU - Lussemburgo 6
PY - Paraguay 6
SC - Seychelles 6
TN - Tunisia 6
DZ - Algeria 5
SI - Slovenia 5
AL - Albania 4
BG - Bulgaria 4
CR - Costa Rica 4
CY - Cipro 4
HR - Croazia 4
KW - Kuwait 4
LB - Libano 4
PA - Panama 4
QA - Qatar 4
SV - El Salvador 4
SY - Repubblica araba siriana 4
TT - Trinidad e Tobago 4
UY - Uruguay 4
BO - Bolivia 3
GT - Guatemala 3
KH - Cambogia 3
LA - Repubblica Popolare Democratica del Laos 3
MD - Moldavia 3
NG - Nigeria 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
AO - Angola 2
BA - Bosnia-Erzegovina 2
BB - Barbados 2
CU - Cuba 2
EE - Estonia 2
ET - Etiopia 2
HN - Honduras 2
Totale 21.126
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Città #
Southend 2.389
Singapore 1.013
Ashburn 983
Milan 680
Hanover 477
Hong Kong 469
Chandler 427
San Jose 358
Dallas 306
Beijing 278
Fairfield 256
Council Bluffs 253
Santa Clara 223
Seattle 209
Los Angeles 203
Wilmington 196
Frankfurt am Main 192
Dublin 163
Houston 156
Princeton 150
Ho Chi Minh City 139
New York 135
Hanoi 133
Ann Arbor 129
Woodbridge 128
Hefei 117
Buffalo 105
Toronto 105
Cambridge 96
Dearborn 95
Jakarta 94
Lauterbourg 94
Boardman 92
Shanghai 90
Bengaluru 87
Moscow 84
Guangzhou 80
Munich 73
Helsinki 69
Nanjing 69
Rome 64
Redwood City 62
Des Moines 59
Jinan 59
Columbus 51
São Paulo 47
The Dalles 46
Seoul 45
Tokyo 45
Redmond 43
Jacksonville 42
Naples 42
Shenyang 42
Istanbul 41
Berlin 40
Tianjin 37
London 36
Abidjan 35
Da Nang 35
Phoenix 35
Chicago 34
Cangzhou 33
Hangzhou 30
Changsha 29
Mountain View 29
Vancouver 29
Nuremberg 28
Amsterdam 27
Brooklyn 27
Atlanta 24
San Diego 24
Nanchang 23
Orem 23
Brussels 22
Lappeenranta 22
Bühl 21
Falls Church 21
Hebei 21
Warsaw 21
Bologna 20
Zhengzhou 20
Zurich 20
Haiphong 19
Montreal 19
Dong Ket 18
Florence 18
Fremont 18
Ningbo 18
Paris 18
Ankara 17
Baltimore 17
Sydney 17
Turin 17
Washington 17
Wayne 17
Boston 16
Jiaxing 16
Turku 16
Barcelona 15
Fuzhou 15
Totale 13.157
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Nome #
Modeling Cornelia de Lange Syndrome in vitro and in vivo reveals a role for cohesin complex in neuronal survival and differentiation 649
Lithium as a possible therapeutic strategy for Cornelia de Lange syndrome 547
Insights into the role of the microbiota and of short-chain fatty acids in Rubinstein–Taybi syndrome 541
Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes 460
Antenatal Microbial Colonization of Mammalian Gut 410
Vangl-dependent planar cell polarity signalling is not required for neural crest migration in mammals 406
Identical EP300 variant leading to Rubinstein–Taybi syndrome with different clinical and immunologic phenotype 367
Cell death and cell proliferation in human spina bifida 329
Lithium as a positive modulator of defective WNT pathway in Cornelia de Lange Syndrome models 328
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 322
Role of miRNAs in neural tube development 317
Identification of genetic factors associated with neural tube defects 317
Chromatinopathies: a focus on Cornelia de Lange Syndrome 315
Cornelia de Lange Syndrome : NIPBL haploinsufficiency downregulates canonical Wnt pathway in zebrafish embryos and patients fibroblasts 305
Chromatin Imbalance as the Vertex Between Fetal Valproate Syndrome and Chromatinopathies 298
Craniofacial and axial skeletal defects induced by the fungicide triadimefon in the mouse 296
Dynamic acetylation profile during mammalian neurulation 288
Inhibition of histone deacetylase activity on specific embryonic tissues as a new mechanism for teratogenicity 286
Microbial colonization during early phases of amphibian life 280
Krox20 is down-regulated following triazole in vitro embryonic exposure: a polycompetitor-based assay 269
Semaphorin Regulation by the Chromatin Remodeler CHD7 : An Emerging Genetic Interaction Shaping Neural Cells and Neural Crest in Development and Cancer 267
p300 inhibition delays premature cellular senescence 264
Genetic interaction of Pax3 mutation and canonical Wnt signaling modulates neural tube defects and neural crest abnormalities 264
Autism-linked NLGN3 is a key regulator of gonadotropin-releasing hormone deficiency 263
Rings and bricks : Expression of cohesin components is dynamic during development and adult life 262
Cornelia de Lange Syndrome: different models and strategies to study the disease 261
Gene-environment interactions in the causation of neural tube defects : folate deficiency increases susceptibility conferred by loss of Pax3 function 260
Convergent extension analysis in mouse whole embryo culture 256
Effects of excess and deprivation of serotonin on in vitro neuronal differentiation 252
Apoptosis is not required for mammalian neural tube closure 246
Study on the common teratogenic pathway elicited by the fungicides triazole-derivatives 245
Characterization of a novel HDAC2 pathogenetic variant: a missing puzzle piece for chromatinopathies 244
Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome 244
The Cornelia de Lange Syndrome-associated factor NIPBL interacts with BRD4 ET domain for transcription control of a common set of genes 244
Relationship between hindbrain segmentation, neural crest cell migration and branchial arch abnormalities in rat embryos exposed to fluconazole and retinoic acid in vitro 242
Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouse 239
Use of high-frequency ultrasound to study the prenatal development of cranial neural tube defects and hydrocephalus in Gldc-deficient mice 239
CyclinD1 down-regulation and increased apoptosis are common features of cohesinopathies 236
Saliva detection of SARS-CoV-2 for mitigating company outbreaks: A surveillance experience, Milan, Italy, March 2021 234
Interplay between Genetic Disorders and Gut Microbial Community: Rubinstein-Taybi Syndrome as a Model 228
KMT2A : umbrella gene for multiple diseases 227
Epigenetic disorders: Lessons from the animals-animal models in chromatinopathies 216
Maternal risk factors associated with antepartum stillbirth 215
Re: Clinical interventions to reduce stillbirths in sub-Saharan Africa: A mathematical model to estimate the potential reduction of stillbirths associated with specific obstetric conditions: Nuchal cord and stillbirths : True or false myth? 213
Saliva sampling for chasing SARS-CoV-2: A Game-changing strategy 212
Valproic acid-induced skeletal malformations : associated gene expression cascades 210
Drosophila melanogaster as a model to study WNT pathway alteration in Cornelia de Lange Syndrome 208
Long-Term Effects of SARS-CoV-2 Infection in Hospitalized Children: Findings from an Italian Single-Center Study 205
Customised next-generation sequencing multigene panel to screen a large cohort of individuals with chromatin-related disorder 205
Expanding the clinical spectrum of PPP3CA variants - alternative isoforms matter 203
Cohesins: Crossroad Between Cornelia de Lange Spectrum and Cancer Predisposition 202
Cornelia de Lange Syndrome: NIPBL haploinsufficiency downregulates canonical Wnt pathway in zebrafish embryos and patients fibroblasts 200
Cornelia de Lange syndrome : to diagnose or not to diagnose in utero? 199
Do cells become homeless during neural tube closure? 197
Does school reopening affect SARS-CoV-2 seroprevalence among school-age children in Milan? 195
Gestational diabetes affects fetal autophagy 193
LAM cells as potential drivers of senescence in lymphangioleiomyomatosis microenvironment 192
Cornelia de Lange Syndrome : from a disease to a broader spectrum 189
The differential roles for neurodevelopmental and neuroendocrine genes in shaping gnrh neuron physiology and deficiency 188
Modulating the WNT pathway in Drosophila models of Cornelia de Lange Syndrome 184
Feasibility and acceptability of saliva-based testing for the screening of SARS-CoV-2 infection in prison 183
SMC1A epilepsy syndrome: clinical data from a large international cohort 183
Myo-inositol enhances teratogenicity of valproic acid in the mouse 180
Inflammation modulates LC3 expression in human preterm delivery 180
Understanding the Causes and Prevention of Neural Tube Defects : Insights from the Splotch Mouse Model 179
Histopathology and molecular characterisation of intrauterine-diagnosed congenital craniopharyngioma 179
Interplay between genetic disorders and gut microbial community: Rubinstein-Taybi syndrome as a model 173
First evidence of a paediatric patient with Cornelia de Lange syndrome with acute lymphoblastic leukaemia 170
Cellular mechanisms underlying Pax3-related neural tube defects and their prevention by folic acid 170
Acetylation and neural tube defects 167
Long-term analysis of the effects of COVID-19 in people with epilepsy: Results from a multicenter on-line survey across the pandemic waves 157
Mechanisms underlying spina bifida in the Zic2 loss-of-function mutant, Kumba 148
In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear 148
Impairment of Retinoic Acid Signaling in Cornelia de Lange Syndrome Fibroblasts 146
Overview on neural tube defects : from development to physical characteristics 143
Risk of stillbirth in older mothers: a specific delivery plan might be considered for prevention 143
Fetal pancreatic Langerhans islets size in pregnancies with metabolic disorders 142
Intrauterine growth in chromatinopathies: A long road for better understanding and for improving clinical management 141
Cornelia de Lange syndrome, related disorders, and the Cohesin complex: Abstracts from the 8th biennial scientific and educational symposium 2018 138
Embedding public engagement in biomedical research : a pilot experience in the field of rare genetic disorders 138
Foregut separation and tracheo-oesophageal malformations : the role of tracheal outgrowth, dorso-ventral patterning and programmed cell death 134
Role of apoptosis in mammalian neurulation 129
Modulating the WNT pathway in Drosophila models of Cornelia de Lange Syndrome 127
Targeting senescence as a novel pharmacological approach in Lymphangioleiomyomatosis 125
Mechanisms of spina bifida in the Zic2-Kumba mouse 123
Targeting senescence in Lymphangioleyomyomatosis through senomorphic-like molecules as a paradigm to counteract senescence in lung tumor microenvironment 117
Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss 114
Cohesins involved in Cornelia de Lange syndrome aetiology are ubiquitously but differentially expressed in human tissues 113
Editorial: Impact on Embryonic Development of Chromatin Remodeling Alterations 113
Role of Zic2 in mammalian neural tube closure 112
Exploring the uncharted role of cell senescence in rare diseases 108
Potential role of STAG1 mutations in genetic predisposition to childhood hematological malignancies 108
Testing Saliva to Reveal the Submerged Cases of the COVID-19 Iceberg 98
Meconium-stained amniotic fluid and histologic signs of fetal distress in stillbirths 97
Extracellular vesicles from II trimester human amniotic fluid as paracrine conveyors counteracting oxidative stress 94
Exploring senescence-driven miscommunication in the lung microenvironment 92
Portrait of a spectrum: clinical and genetic characterization of a large cohort of chromatinopathies—30 years' experience from a third level center 81
Editorial: Maternal-foetal crosstalk impacts on offspring development 79
Tumor suppressive activities of the cohesin SA1/STAG2 and effects of PARP impairment during Drosophila brain development 52
MAU2 is required for zebrafish neurodevelopment 51
Totale 21.648
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Categoria #
all - tutte 58.981
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 58.981
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.013 104 115 205 178 194 111 128 297 202 119 90 270
2022/20231.692 176 171 160 183 192 298 46 134 148 42 82 60
2023/20241.547 45 113 107 104 321 80 64 268 44 84 150 167
2024/20252.974 117 252 105 266 195 162 164 312 157 279 316 649
2025/20267.562 641 565 749 548 584 437 954 351 747 558 731 697
2026/2027303 303 0 0 0 0 0 0 0 0 0 0 0
Totale 21.846