CRIS Current Research Information System

BONORA, ELENA
 Distribuzione geografica
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Continente #
NA - Nord America 7.965
AS - Asia 7.034
EU - Europa 5.397
SA - Sud America 425
AF - Africa 414
Continente sconosciuto - Info sul continente non disponibili 20
OC - Oceania 13
Totale 21.268
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Nazione #
US - Stati Uniti d'America 7.825
VN - Vietnam 1.935
SG - Singapore 1.757
CN - Cina 1.721
IT - Italia 1.540
GB - Regno Unito 929
DE - Germania 686
HK - Hong Kong 520
SE - Svezia 498
IN - India 310
BR - Brasile 287
FR - Francia 273
RU - Federazione Russa 233
NL - Olanda 205
FI - Finlandia 182
KR - Corea 175
IE - Irlanda 172
UA - Ucraina 159
JP - Giappone 127
CI - Costa d'Avorio 118
BD - Bangladesh 113
ZA - Sudafrica 94
BG - Bulgaria 89
CH - Svizzera 84
TG - Togo 84
CA - Canada 82
SC - Seychelles 66
EE - Estonia 64
ID - Indonesia 58
AR - Argentina 54
BE - Belgio 54
JO - Giordania 53
PH - Filippine 40
PL - Polonia 40
MX - Messico 38
AT - Austria 37
ES - Italia 37
TH - Thailandia 32
CZ - Repubblica Ceca 30
IQ - Iraq 30
TR - Turchia 29
CO - Colombia 22
SA - Arabia Saudita 21
EC - Ecuador 17
TW - Taiwan 17
EU - Europa 16
UZ - Uzbekistan 16
LT - Lituania 15
NG - Nigeria 15
PK - Pakistan 15
CL - Cile 14
GR - Grecia 14
HR - Croazia 13
IR - Iran 13
AE - Emirati Arabi Uniti 12
AU - Australia 11
PE - Perù 11
RO - Romania 9
MY - Malesia 8
DZ - Algeria 7
EG - Egitto 7
JM - Giamaica 7
MA - Marocco 7
VE - Venezuela 7
CR - Costa Rica 6
DK - Danimarca 6
BO - Bolivia 5
LB - Libano 5
UY - Uruguay 5
BA - Bosnia-Erzegovina 4
HU - Ungheria 4
KE - Kenya 4
MD - Moldavia 4
AZ - Azerbaigian 3
CY - Cipro 3
GH - Ghana 3
IL - Israele 3
KW - Kuwait 3
LV - Lettonia 3
RS - Serbia 3
SI - Slovenia 3
SK - Slovacchia (Repubblica Slovacca) 3
TN - Tunisia 3
XK - ???statistics.table.value.countryCode.XK??? 3
AL - Albania 2
BY - Bielorussia 2
DO - Repubblica Dominicana 2
GE - Georgia 2
KZ - Kazakistan 2
OM - Oman 2
SN - Senegal 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
BB - Barbados 1
BH - Bahrain 1
CD - Congo 1
DM - Dominica 1
ET - Etiopia 1
GY - Guiana 1
KG - Kirghizistan 1
Totale 21.253
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Città #
Singapore 1.184
Ashburn 877
Southend 784
Fairfield 625
Chandler 554
Ho Chi Minh City 526
Hong Kong 489
Hanoi 422
Bologna 421
Hefei 379
San Jose 374
Ann Arbor 362
Santa Clara 331
Seattle 302
Woodbridge 276
Houston 272
Wilmington 253
Cambridge 234
Princeton 184
Beijing 177
Dublin 167
Boardman 162
Seoul 156
Council Bluffs 149
Helsinki 142
Dallas 138
Munich 130
Los Angeles 128
Dong Ket 123
Redmond 121
Abidjan 118
New York 111
Lauterbourg 108
Tokyo 100
Milan 90
Sofia 89
Lomé 84
Jacksonville 83
Nanjing 83
Westminster 78
Padova 67
Bern 65
Haiphong 65
Rome 64
Berlin 62
Da Nang 59
São Paulo 59
Buffalo 56
Amman 52
Brussels 45
Turin 45
Jakarta 44
Redondo Beach 41
Bremen 40
San Diego 40
Bengaluru 38
Frankfurt am Main 38
Guangzhou 38
Saint Petersburg 38
Shanghai 38
Florence 36
Phoenix 36
Shenyang 36
Jinan 34
Changsha 33
Amsterdam 32
Toronto 32
Falls Church 31
Zhengzhou 30
Dearborn 28
London 28
Nuremberg 28
Tianjin 28
Warsaw 28
Chicago 27
Naples 27
Orem 26
Falkenstein 25
Hyderabad 25
Nanchang 25
The Dalles 25
Can Tho 23
Des Moines 23
Lappeenranta 23
Haikou 22
Hebei 22
Johannesburg 22
Medford 21
Yubileyny 21
Biên Hòa 20
Redwood City 20
Vienna 20
Modena 19
Mülheim 19
Rimini 19
Atlanta 18
Chennai 18
Parma 18
San Francisco 18
Thái Nguyên 18
Totale 13.384
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Nome #
Neuroactive Steroids in First-Episode Psychosis: A Role for Progesterone? 326
Glutamine Supplementation as a Novel Metabolic Therapeutic Strategy for LIG3-Dependent Chronic Intestinal Pseudo-obstruction 307
BRAF exon 15 mutations in papillary carcinoma and adjacent thyroid parenchyma: A search for the early molecular events associated with tumor development 294
Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy 278
Mutant MYO1F alters the mitochondrial network and induces tumor proliferation in thyroid cancer 277
Which elderly newly diagnosed glioblastoma patients can benefit from radiotherapy and temozolomide? A PERNO prospective study 275
Calcium and Reactive Oxygen Species Signaling Interplays in Cardiac Physiology and PathologiesCalcium and Reactive Oxygen Species Signaling Interplays in Cardiac Physiology and Pathologies 274
INPP4B overexpression and c-KIT downregulation in human achalasia. 262
Mast cell-nerve interactions correlate with bloating and abdominal pain severity in patients with non-celiac gluten / wheat sensitivity 262
Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant. 256
Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways 255
Expression of 19 microRNAs in glioblastoma and comparison with other brain neoplasia of grades I–III 254
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III 252
Novel Mutations in Neurogenic Chronic Intestinal Pseudo-Obstruction Identified by High-Throughput Sequencing 244
Analysis of a Sardinian Multiplex Family with Autism Spectrum Disorder Points to Post-Synaptic Density Gene Variants and Identifies CAPG as a Functionally Relevant Candidate Gene 243
Gut epithelial and vascular barrier abnormalities in patients with chronic intestinal pseudo-obstruction 243
A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism 242
Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next? 240
An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. 239
miRNA–221 and miRNA–483–3p Dysregulation in Esophageal Adenocarcinoma 238
Enteric neuron density correlates with clinical features of severe gut dysmotility 233
A Greek Family with a Follicular Variant of Familial Papillary Thyroid Carcinoma: TCO, MNG1, fPTC/PRN, and NMTC1 Excluded as Susceptibility Loci 232
A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder. 232
Definition of miRNAs expression profile in glioblastoma samples: the relevance of non-neoplastic brain reference. 223
Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients 223
L’encefalomiopatia Mitocondriale Neurogastrointestinale (MNGIE): Il Fegato Come Nuova Fonte Di Timidina Fosforilasi 221
The RET51/FKBP52 complex and its involvement in Parkinson disease. 219
Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients. 217
Genomic profiles of primary and metastatic esophageal adenocarcinoma identified via digital sorting of pure cell populations: Results from a case report 216
Enteric Neuromyopathies: Highlights on Genetic Mechanisms Underlying Chronic Intestinal Pseudo-Obstruction 210
Effectiveness and Impact of Transcript Analysis in Clinical Genetics Daily Practice 210
Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects. 206
The FAGenomicH project: Towards a whole candidate gene approach to identify markers associated with fatness and production traits in pigs and investigate the pig as a model for human obesity 206
Erratum to: Incidence of neuroepithelial primary brain tumors among adult population of Emilia-Romagna Region, Italy 206
HDAC8 Loss of Function and SHOX Haploinsufficiency: Two Independent Genetic Defects Responsible for a Complex Phenotype 206
Incidence of neuroepithelial primary brain tumors among adult population of Emilia-Romagna Region, Italy 205
Enteric neuropathies: Yesterday, Today and Tomorrow 205
Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction. 204
Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma 201
Expression of the Bitter taste receptor, T2R38, in enteroendocrine cells of the colonic mucosa of overweight/obese vs. Lean subjects 199
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours. 199
A New Homozygous CACNB2 Mutation has Functional Relevance and Supports a Role for Calcium Channels in Autism Spectrum Disorder 196
Oncocytic glioblastoma: a glioblastoma showing oncocytic changes and increased mitochondrial DNA copy number 192
Expression of RAD21 immunoreactivity in myenteric neurons of the human and mouse small intestine 188
miRNAs expression analysis in paired fresh/frozen and dissected formalin fixed and paraffin embedded glioblastoma using real-time pCR. 185
Mutant SPART causes defects in mitochondrial protein import and bioenergetics reversed by Coenzyme Q 184
Protective Actions of Epithelial 5-Hydroxytryptamine 4 Receptors in Normal and Inflamed Colon 184
Targeted Sequencing of Sorted Esophageal Adenocarcinoma Cells Unveils Known and Novel Mutations in the Separated Subpopulations 184
Evidence of RET/GDNF-related apolipoprotein B (APOB) activation and altered expression in patients with chronic intestinal pseudo-obstruction (CIPO) 183
Clinical Relevance of IFT140 Loss-of-Function Variants in Development of Renal Cysts 181
C620R mutation of the murine ret proto-oncogene: loss of function effect in homozygotes and possible gain of function effect in heterozygotes. 180
The tyrosine kinase receptor RET interacts in vivo with aryl hydrocarbon receptor-interacting protein to alter survivin availability. 178
A mutation screening of oncogenes, tumor suppressor gene TP53 and nuclear encoded mitochondrial complex I genes in oncocytic thyroid tumors 177
The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma 177
Dealing With BRCA1/2 unclassified variants in a cancer genetics clinic: Does cosegregation analysis help? 177
Identification of BRCA1/2 p.Ser1613Gly, p.Pro871Leu, p.Lys1183Arg, p.Glu1038Gly, p.Ser1140Gly, p.Ala2466Val, p.His2440Arg variants in women under 45 years old with breast nodules suspected of having breast cancer in Burkina Faso 177
PTEN Hamartoma Tumor Syndrome: Skin Manifestations and Insights Into Their Molecular Pathogenesis 175
Correlations between Molecular Alterations, Histopathological Characteristics, and Poor Prognosis in Esophageal Adenocarcinoma 172
Integrated web-based approach to multigenic diseases 171
HDAC9 structural variants disrupting TWIST1 transcriptional regulation lead to craniofacial and limb malformations 170
GSTT1 and M1 polymorphisms in Hurthle thyroid cancer patients 170
Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia 169
Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer 169
TOM: enhancement and extension of a tool suite for in silico approaches to multigenic complex disorders. 168
Distribution and Characterization of RAD21 Immunoreactivity in Mouse and Human Enteric Neurons 167
Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family 166
Mitochondrial Neurogastrointestinal Encephalomyopathy: The Liver As a Tissue Source to Restore Thymidine Phosphorylase Activity 165
Multi-disciplinary Insights from the First European Forum on Visceral Myopathy 2022 Meeting 163
Rasal1 and ros1 gene variants in hereditary breast cancer 163
Differences in Patterns of Stimulant Use and Their Impact on First-Episode Psychosis Incidence: An Analysis of the EUGEI Study 162
EXCAVATOR: detecting copy number variants from whole-exome sequencing data. 162
TOM: a web-based integrated approach for identification of candidate disease genes 162
The relationship between genetic liability, childhood maltreatment, and IQ: findings from the EU-GEI multicentric case–control study 161
Pattern of care and effectiveness of treatment for glioblastoma patients in the real world: Results from a prospective population-based registry. Could survival differ in a high-volume center? 159
The prognostic impact of histology in esophageal and esophago-gastric junction adenocarcinoma 158
Su1852 The 5-HT4 Selective Agonist Prucalopride Exerts Neural and Epithelial Protective Effects In Vitro 157
Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer. 156
DICER1 mutations in familial multinodular goiter with and without ovarian sertoli-leydig cell tumors 156
Clinical and Pathological Features of Severe Gut Dysmotility 154
The FAGenomicH project: a whole candidate gene approach to identify markers associated with fatness traits in pigs and investigate the pig as a model for human obesity 152
Omics Technologies Improving Breast Cancer Research and Diagnostics 151
Mutation screening and association analysis of six candidate genes for autism on chromosome 7q. 149
The impact of schizophrenia genetic load and heavy cannabis use on the risk of psychotic disorder in the EU-GEI case-control and UK Biobank studies 148
Association of the interleukin-4/interleukin-4 receptor genetic variants with hand osteoathrtitis. 147
Intestinal epithelial barrier disfunction in patients with chronic intestinal pseudo-obstruction 147
Genetic Predisposition to Familial Nonmedullary Thyroid Cancer: An Update of Molecular Findings and State-of-the-Art Studies 145
Su2019 Functional Characterization of a Novel RAD21 Mutation in Familial Chronic Intestinal Pseudo-Obstruction (CIPO) 144
Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma. 142
Novel understanding on genetic mechanisms of enteric neuropathies leading to severe gut dysmotility 141
Detection of a Novel MSI2-C17orf64 Transcript in a Patient with Aggressive Adenocarcinoma of the Gastroesophageal Junction: A Case Report 140
Use of multiple polygenic risk scores for distinguishing schizophrenia-spectrum disorder and affective psychosis categories in a first-episode sample; the EU-GEI study 140
Novel germline variants identified in the inner mitochondrial membrane transporter TIMM44 and their role in predisposition to oncocytic thyroid carcinomas. 140
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain 139
Molecular features of thyroid oncocytic tumors 138
Selective targeting BMP2 and 4 in SMAD4 negative esophageal adenocarcinoma inhibits tumor growth and aggressiveness in preclinical models 136
Liver tissue as new source to replace thymidine phosphorylase activity in mitochondrial neurogastrointestinal encephalomyopathy 136
Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): The liver as a new source of thymidine phosphorylase 133
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits 130
null 130
Interleukin-4/interleukin-4 receptor gene polymorphisms in hand osteoarthritis 129
Totale 19.209
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Categoria #
all - tutte 56.676
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 56.676
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021308 0 0 0 0 0 0 0 0 0 0 0 308
2021/20222.223 118 69 113 140 198 139 52 172 93 223 585 321
2022/20232.294 239 321 143 285 126 173 68 133 415 72 181 138
2023/2024981 94 117 58 94 68 180 62 67 31 77 47 86
2024/20253.256 149 369 271 290 456 174 257 180 110 228 196 576
2025/20268.104 704 884 718 623 728 363 926 234 1.674 609 320 321
Totale 21.715