IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

FONTANA, LAURA
 Distribuzione geografica
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Continente #
EU - Europa 3.311
NA - Nord America 3.029
AS - Asia 1.523
SA - Sud America 145
AF - Africa 23
OC - Oceania 22
Continente sconosciuto - Info sul continente non disponibili 2
Totale 8.055
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Nazione #
US - Stati Uniti d'America 2.950
GB - Regno Unito 1.273
IT - Italia 808
CN - Cina 695
DE - Germania 354
SG - Singapore 311
SE - Svezia 285
IN - India 184
BR - Brasile 120
RU - Federazione Russa 114
IE - Irlanda 92
ID - Indonesia 76
CA - Canada 69
FR - Francia 69
DK - Danimarca 60
FI - Finlandia 59
HK - Hong Kong 56
TR - Turchia 42
BE - Belgio 37
UA - Ucraina 33
JP - Giappone 29
KR - Corea 27
PL - Polonia 20
AU - Australia 19
VN - Vietnam 19
AT - Austria 17
NL - Olanda 16
UZ - Uzbekistan 14
ES - Italia 12
CH - Svizzera 11
CZ - Repubblica Ceca 11
TW - Taiwan 11
IR - Iran 10
AR - Argentina 7
CL - Cile 7
MX - Messico 6
MY - Malesia 6
PT - Portogallo 6
RO - Romania 6
CO - Colombia 5
HU - Ungheria 5
LV - Lettonia 5
PH - Filippine 5
SA - Arabia Saudita 5
SC - Seychelles 5
GR - Grecia 4
KG - Kirghizistan 4
NG - Nigeria 4
ZA - Sudafrica 4
BD - Bangladesh 3
IL - Israele 3
KE - Kenya 3
NZ - Nuova Zelanda 3
AE - Emirati Arabi Uniti 2
BG - Bulgaria 2
BY - Bielorussia 2
EG - Egitto 2
EU - Europa 2
IQ - Iraq 2
KW - Kuwait 2
KZ - Kazakistan 2
LB - Libano 2
LU - Lussemburgo 2
MO - Macao, regione amministrativa speciale della Cina 2
MU - Mauritius 2
OM - Oman 2
PE - Perù 2
PK - Pakistan 2
RS - Serbia 2
SK - Slovacchia (Repubblica Slovacca) 2
VE - Venezuela 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AM - Armenia 1
AO - Angola 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BO - Bolivia 1
CR - Costa Rica 1
EC - Ecuador 1
GH - Ghana 1
IS - Islanda 1
JO - Giordania 1
LT - Lituania 1
MN - Mongolia 1
NI - Nicaragua 1
NP - Nepal 1
PA - Panama 1
PR - Porto Rico 1
PS - Palestinian Territory 1
TH - Thailandia 1
TN - Tunisia 1
Totale 8.056
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Città #
Southend 1.187
Ashburn 422
Milan 360
Chandler 286
Fairfield 265
Frankfurt am Main 211
Singapore 192
Wilmington 159
Ann Arbor 155
Seattle 155
Woodbridge 140
Houston 112
Beijing 105
Cambridge 98
Dublin 87
Princeton 80
Council Bluffs 77
Dearborn 75
Jakarta 66
Nanjing 62
Santa Clara 55
Verona 52
Redwood City 46
Hong Kong 45
Shanghai 45
Toronto 40
Helsinki 39
Boardman 36
Phoenix 35
Des Moines 32
New York 32
Bengaluru 31
Jinan 30
Mumbai 28
Guangzhou 27
Los Angeles 27
Shenyang 27
Rome 25
Brussels 22
Istanbul 21
Delhi 20
Falls Church 20
Nuremberg 20
San Diego 20
Tianjin 20
Hangzhou 19
Hebei 18
London 18
Berlin 15
Zhengzhou 15
Atlanta 14
Chicago 14
Turin 14
Wuhan 14
Mountain View 13
Nanchang 12
Changsha 11
Florence 11
Seoul 11
Silver Spring 11
Fuzhou 9
Ottawa 9
Warsaw 9
Lodz 8
Monza 8
Munich 8
Naples 8
Quanzhou 8
Rho 8
Taizhou 8
Tashkent 8
Manipal 7
São Paulo 7
Taipei 7
The Dalles 7
Tokyo 7
Vienna 7
Bologna 6
Brugherio 6
Cagliari 6
Fremont 6
Jiaxing 6
Nashua 6
Philadelphia 6
Piscataway 6
Rio de Janeiro 6
Shenzhen 6
Sydney 6
Xian 6
Bogotá 5
Brno 5
Gent 5
Kent 5
Kunming 5
Lanzhou 5
Mahé 5
Mannheim 5
Redmond 5
Riga 5
Roxbury 5
Totale 5.559
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Nome #
Mitochondrial DNA content and methylation in fetal cord blood of pregnancies with placental insufficiency 626
Differential signature of the centrosomal MARK4 isoforms in glioma 523
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer 310
The Genetic Landscape of Human Glioblastoma and Matched Primary Cancer Stem Cells Reveals Intratumour Similarity and Intertumour Heterogeneity 287
Molecular profiling of lung cancer specimens and liquid biopsies using MALDI-TOF mass spectrometry 267
Molecular Insights into the Classification of Luminal Breast Cancers : the Genomic Heterogeneity of Progesterone-Negative Tumors 259
A zebrafish model of Poikiloderma with Neutropenia recapitulates the human syndrome hallmarks and traces back neutropenia to the myeloid progenitor 241
Revertant mosaicism for family mutations is not observed in BRCA1/2 phenocopies 237
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins 236
SWITCH TO THE L ISOFORM OF THE MAP/MICROTUBULE AFFINITY-REGULATING KINASE 4 (MARK4) GENE, MAINLY EXPRESSED IN HUMAN GLIOMA, VIA PRE-MRNA ALTERNATIVE SPLICING MODULATED BY POLYPYRIMIDINE TRACT-BINDING PROTEIN (PTB) 233
MARK4 : a tricky balance of L and S isoforms rules glial differentiation and glioma progression 226
Angiogenesis in human brain tumors : screening of drug response through a patient-specific cell platform for personalized therapy 213
Mass spectrometry-based assay for the molecular diagnosis of glioma : Concomitant detection of chromosome 1p/19q codeletion, and IDH1, IDH2, and TERT mutation status 198
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi 194
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders 184
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome 178
A novel de novo DDX3X missense variant in a female with brachycephaly and intellectual disability : a case report 175
SINDROME DI ROTHMUND-THOMSON: CARATTERIZZAZIONE CLINICO-MOLECOLARE DI TRE NUOVI PAZIENTI 172
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients 172
Sequence variants identification at the KCNQ1OT1: TSS differentially Methylated region in isolated omphalocele cases 171
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome 167
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes 167
MGMT-Methylated Alleles Are Distributed Heterogeneously Within Glioma Samples Irrespective of IDH Status and Chromosome 10q Deletion 161
Extensive placental methylation profiling in normal pregnancies 159
Rothmund-Thomson syndrome: Insights from new patients on the genetic variability underpinning clinical presentation and cancer outcome 157
ANALISI SEMIQUANTITATIVA DELL’ESPRESSIONE DELLE ISOFORME DEL GENE C16orf57 IN UN PANNELLO DI LINEE CELLULARI E TESSUTI ED IN PAZIENTI CON POICHILODERMA CON NEUTROPENIA 156
Clinical and molecular diagnosis of beckwith-wiedemann syndrome with single-or multi-locus imprinting disturbance 151
Expanding the role of the splicing USB1 gene from Poikiloderma with Neutropenia to acquired myeloid neoplasms 142
Fragile X syndrome : A review of clinical and molecular diagnoses 142
Suggestive evidence on the involvement of polypyrimidine-tract binding protein in regulating alternative splicing of MAP/microtubule affinity-regulating kinase 4 in glioma 141
Analysis of BRCA1 and RAD51C promoter methylation in italian families at high-risk of breast and ovarian cancer 138
Microtubule-associated protein/microtubule affinity-regulating kinase 4 (MARK4) plays a role in cell cycle progression and cytoskeletal dynamics 135
Familial gastrointestinal stromal tumors, lentigines, and café-au-lait macules associated with germline c-kit mutation treated with imatinib 131
A miRNome analysis of drug-free manic psychotic bipolar patients versus healthy controls 127
Novel physiological RECQL4 alternative transcript disclosed by molecular characterisation of Rothmund-Thomson Syndrome sibs with mild phenotype 118
Cohesin mutations induce chromatin conformation perturbation of the H19/IGF2 imprinted region and gene expression dysregulation in Cornelia de Lange syndrome cell lines 118
Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome 114
Epigenetics of functional hypothalamic amenorrhea 103
Forecasting the burden of COVID-19 hospitalized patients during the SARS-CoV-2 second wave in Lombardy, Italy 99
Mental health and the effects on methylation of stress-related genes in front-line versus other health care professionals during the second wave of COVID-19 pandemic: an Italian pilot study 88
Novel pathogenetic variants in PTHLH and TRPS1 genes causing syndromic brachydactyly 76
The Genetic and Epigenetic Footprint in Idiopathic Pulmonary Fibrosis and Familial Pulmonary Fibrosis: A State-of-the-Art Review 68
Pitfalls of whole exome sequencing in undefined clinical conditions with a suspected genetic etiology 66
Decreased serum level of sphingosine-1-phosphate: a novel predictor of clinical severity in COVID-19 66
Hereditary Breast Cancer: BRCA and Other Susceptibility Genes 64
Unraveling the genetic causes of Moebius syndrome 47
Preferential X Chromosome Inactivation as a Mechanism to Explain Female Preponderance in Myasthenia Gravis 45
Case report: Chorea and cognitive decline in a young woman: instrumental and genetic assessment of a case originally diagnosed as multiple sclerosis 38
Exploring the Impact of Genetics in a Large Cohort of Moebius Patients by Trio Whole Exome Sequencing 34
Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith–Wiedemann Syndrome Cell Lines 34
Non-invasive biomarkers for sperm retrieval in non-obstructive patients: a comprehensive review 32
Totale 8.386
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Categoria #
all - tutte 26.651
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 26.651
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020434 0 0 0 0 0 0 0 0 161 172 47 54
2020/2021952 68 84 59 60 86 64 64 115 77 104 88 83
2021/20221.090 86 84 71 125 75 63 95 63 130 75 66 157
2022/20231.126 147 133 95 96 111 191 50 71 106 25 74 27
2023/20241.170 45 52 54 73 204 69 71 312 23 57 90 120
2024/20251.219 88 172 54 181 141 145 154 164 120 0 0 0
Totale 8.386