CRIS Current Research Information System

BONORA, ELENA
 Distribuzione geografica
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Continente #
NA - Nord America 8.315
AS - Asia 7.087
EU - Europa 5.489
Continente sconosciuto - Info sul continente non disponibili 469
SA - Sud America 436
AF - Africa 417
OC - Oceania 13
Totale 22.226
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Nazione #
US - Stati Uniti d'America 8.125
VN - Vietnam 1.937
SG - Singapore 1.772
CN - Cina 1.727
IT - Italia 1.616
GB - Regno Unito 934
DE - Germania 686
HK - Hong Kong 534
SE - Svezia 505
IN - India 310
BR - Brasile 292
FR - Francia 274
RU - Federazione Russa 233
NL - Olanda 205
FI - Finlandia 182
KR - Corea 175
IE - Irlanda 172
UA - Ucraina 160
JP - Giappone 130
BD - Bangladesh 126
CI - Costa d'Avorio 118
CA - Canada 106
ZA - Sudafrica 94
BG - Bulgaria 89
CH - Svizzera 84
TG - Togo 84
SC - Seychelles 69
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 24
SA - Arabia Saudita 21
JM - Giamaica 19
EC - Ecuador 18
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
VE - Venezuela 9
CR - Costa Rica 8
DK - Danimarca 8
MY - Malesia 8
DZ - Algeria 7
EG - Egitto 7
MA - Marocco 7
UY - Uruguay 6
BO - Bolivia 5
LB - Libano 5
BA - Bosnia-Erzegovina 4
HU - Ungheria 4
KE - Kenya 4
MD - Moldavia 4
XK - ???statistics.table.value.countryCode.XK??? 4
AZ - Azerbaigian 3
BB - Barbados 3
CY - Cipro 3
GH - Ghana 3
GT - Guatemala 3
HN - Honduras 3
IL - Israele 3
KW - Kuwait 3
LV - Lettonia 3
RS - Serbia 3
SI - Slovenia 3
SK - Slovacchia (Repubblica Slovacca) 3
TN - Tunisia 3
AL - Albania 2
BY - Bielorussia 2
DO - Repubblica Dominicana 2
GE - Georgia 2
KZ - Kazakistan 2
NI - Nicaragua 2
OM - Oman 2
SN - Senegal 2
TT - Trinidad e Tobago 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
BH - Bahrain 1
CD - Congo 1
Totale 21.759
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Città #
Singapore 1.199
Ashburn 890
Southend 784
Fairfield 625
Chandler 554
Ho Chi Minh City 526
Hong Kong 501
Bologna 428
Hanoi 423
San Jose 395
Hefei 379
Ann Arbor 362
Santa Clara 339
Seattle 303
Houston 277
Woodbridge 276
Wilmington 254
Cambridge 235
Council Bluffs 227
Princeton 184
Beijing 178
Boardman 167
Dublin 167
Seoul 156
Dallas 143
Helsinki 142
Los Angeles 133
Munich 130
Dong Ket 123
Redmond 121
Abidjan 118
New York 118
Lauterbourg 108
Tokyo 103
Milan 99
Sofia 89
Jacksonville 85
Lomé 84
Nanjing 83
Westminster 78
Rome 73
Padova 67
Bern 65
Haiphong 65
Berlin 62
São Paulo 61
Da Nang 60
Buffalo 57
Amman 52
Brussels 45
Turin 45
Jakarta 44
Redondo Beach 41
Bremen 40
San Diego 40
Bengaluru 38
Florence 38
Frankfurt am Main 38
Guangzhou 38
Saint Petersburg 38
Shanghai 38
Phoenix 37
Shenyang 36
Jinan 34
Toronto 34
Changsha 33
Amsterdam 32
Falls Church 31
London 30
Zhengzhou 30
Chicago 28
Dearborn 28
Nuremberg 28
Tianjin 28
Warsaw 28
Naples 27
Orem 26
Atlanta 25
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
Chennai 18
Parma 18
San Francisco 18
Thái Nguyên 18
Totale 13.612
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Nome #
Neuroactive Steroids in First-Episode Psychosis: A Role for Progesterone? 327
Glutamine Supplementation as a Novel Metabolic Therapeutic Strategy for LIG3-Dependent Chronic Intestinal Pseudo-obstruction 317
BRAF exon 15 mutations in papillary carcinoma and adjacent thyroid parenchyma: A search for the early molecular events associated with tumor development 300
Calcium and Reactive Oxygen Species Signaling Interplays in Cardiac Physiology and PathologiesCalcium and Reactive Oxygen Species Signaling Interplays in Cardiac Physiology and Pathologies 284
Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy 282
Mutant MYO1F alters the mitochondrial network and induces tumor proliferation in thyroid cancer 279
Which elderly newly diagnosed glioblastoma patients can benefit from radiotherapy and temozolomide? A PERNO prospective study 278
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III 274
Mast cell-nerve interactions correlate with bloating and abdominal pain severity in patients with non-celiac gluten / wheat sensitivity 272
INPP4B overexpression and c-KIT downregulation in human achalasia. 267
Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant. 260
Expression of 19 microRNAs in glioblastoma and comparison with other brain neoplasia of grades I–III 260
Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways 258
Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next? 256
miRNA–221 and miRNA–483–3p Dysregulation in Esophageal Adenocarcinoma 251
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 247
A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism 247
Novel Mutations in Neurogenic Chronic Intestinal Pseudo-Obstruction Identified by High-Throughput Sequencing 246
Gut epithelial and vascular barrier abnormalities in patients with chronic intestinal pseudo-obstruction 246
An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. 241
A Greek Family with a Follicular Variant of Familial Papillary Thyroid Carcinoma: TCO, MNG1, fPTC/PRN, and NMTC1 Excluded as Susceptibility Loci 236
A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder. 236
Enteric neuron density correlates with clinical features of severe gut dysmotility 235
Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients 229
Definition of miRNAs expression profile in glioblastoma samples: the relevance of non-neoplastic brain reference. 226
L’encefalomiopatia Mitocondriale Neurogastrointestinale (MNGIE): Il Fegato Come Nuova Fonte Di Timidina Fosforilasi 224
The RET51/FKBP52 complex and its involvement in Parkinson disease. 222
Effectiveness and Impact of Transcript Analysis in Clinical Genetics Daily Practice 220
Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients. 219
Genomic profiles of primary and metastatic esophageal adenocarcinoma identified via digital sorting of pure cell populations: Results from a case report 218
Enteric Neuromyopathies: Highlights on Genetic Mechanisms Underlying Chronic Intestinal Pseudo-Obstruction 213
Erratum to: Incidence of neuroepithelial primary brain tumors among adult population of Emilia-Romagna Region, Italy 210
HDAC8 Loss of Function and SHOX Haploinsufficiency: Two Independent Genetic Defects Responsible for a Complex Phenotype 209
Enteric neuropathies: Yesterday, Today and Tomorrow 208
Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects. 207
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 207
Incidence of neuroepithelial primary brain tumors among adult population of Emilia-Romagna Region, Italy 207
Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction. 206
Clinical Relevance of IFT140 Loss-of-Function Variants in Development of Renal Cysts 201
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 200
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours. 200
A New Homozygous CACNB2 Mutation has Functional Relevance and Supports a Role for Calcium Channels in Autism Spectrum Disorder 200
Oncocytic glioblastoma: a glioblastoma showing oncocytic changes and increased mitochondrial DNA copy number 194
Expression of RAD21 immunoreactivity in myenteric neurons of the human and mouse small intestine 193
Protective Actions of Epithelial 5-Hydroxytryptamine 4 Receptors in Normal and Inflamed Colon 191
miRNAs expression analysis in paired fresh/frozen and dissected formalin fixed and paraffin embedded glioblastoma using real-time pCR. 186
Evidence of RET/GDNF-related apolipoprotein B (APOB) activation and altered expression in patients with chronic intestinal pseudo-obstruction (CIPO) 186
Targeted Sequencing of Sorted Esophageal Adenocarcinoma Cells Unveils Known and Novel Mutations in the Separated Subpopulations 186
PTEN Hamartoma Tumor Syndrome: Skin Manifestations and Insights Into Their Molecular Pathogenesis 186
Mutant SPART causes defects in mitochondrial protein import and bioenergetics reversed by Coenzyme Q 185
The tyrosine kinase receptor RET interacts in vivo with aryl hydrocarbon receptor-interacting protein to alter survivin availability. 182
C620R mutation of the murine ret proto-oncogene: loss of function effect in homozygotes and possible gain of function effect in heterozygotes. 182
A mutation screening of oncogenes, tumor suppressor gene TP53 and nuclear encoded mitochondrial complex I genes in oncocytic thyroid tumors 181
The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma 181
Dealing With BRCA1/2 unclassified variants in a cancer genetics clinic: Does cosegregation analysis help? 179
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 179
Correlations between Molecular Alterations, Histopathological Characteristics, and Poor Prognosis in Esophageal Adenocarcinoma 177
Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia 175
Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer 175
GSTT1 and M1 polymorphisms in Hurthle thyroid cancer patients 173
Integrated web-based approach to multigenic diseases 173
Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family 173
HDAC9 structural variants disrupting TWIST1 transcriptional regulation lead to craniofacial and limb malformations 171
TOM: enhancement and extension of a tool suite for in silico approaches to multigenic complex disorders. 170
Multi-disciplinary Insights from the First European Forum on Visceral Myopathy 2022 Meeting 169
Distribution and Characterization of RAD21 Immunoreactivity in Mouse and Human Enteric Neurons 169
Mitochondrial Neurogastrointestinal Encephalomyopathy: The Liver As a Tissue Source to Restore Thymidine Phosphorylase Activity 167
TOM: a web-based integrated approach for identification of candidate disease genes 166
Differences in Patterns of Stimulant Use and Their Impact on First-Episode Psychosis Incidence: An Analysis of the EUGEI Study 165
EXCAVATOR: detecting copy number variants from whole-exome sequencing data. 165
Rasal1 and ros1 gene variants in hereditary breast cancer 164
The prognostic impact of histology in esophageal and esophago-gastric junction adenocarcinoma 164
The relationship between genetic liability, childhood maltreatment, and IQ: findings from the EU-GEI multicentric case–control study 162
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? 161
Su1852 The 5-HT4 Selective Agonist Prucalopride Exerts Neural and Epithelial Protective Effects In Vitro 158
Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer. 157
DICER1 mutations in familial multinodular goiter with and without ovarian sertoli-leydig cell tumors 157
Clinical and Pathological Features of Severe Gut Dysmotility 155
Omics Technologies Improving Breast Cancer Research and Diagnostics 153
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 153
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 152
Mutation screening and association analysis of six candidate genes for autism on chromosome 7q. 151
Intestinal epithelial barrier disfunction in patients with chronic intestinal pseudo-obstruction 149
Association of the interleukin-4/interleukin-4 receptor genetic variants with hand osteoathrtitis. 147
Genetic Predisposition to Familial Nonmedullary Thyroid Cancer: An Update of Molecular Findings and State-of-the-Art Studies 146
Novel understanding on genetic mechanisms of enteric neuropathies leading to severe gut dysmotility 146
Use of multiple polygenic risk scores for distinguishing schizophrenia-spectrum disorder and affective psychosis categories in a first-episode sample; the EU-GEI study 145
Su2019 Functional Characterization of a Novel RAD21 Mutation in Familial Chronic Intestinal Pseudo-Obstruction (CIPO) 145
Detection of a Novel MSI2-C17orf64 Transcript in a Patient with Aggressive Adenocarcinoma of the Gastroesophageal Junction: A Case Report 143
Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma. 143
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain 142
Novel germline variants identified in the inner mitochondrial membrane transporter TIMM44 and their role in predisposition to oncocytic thyroid carcinomas. 142
Selective targeting BMP2 and 4 in SMAD4 negative esophageal adenocarcinoma inhibits tumor growth and aggressiveness in preclinical models 140
Molecular features of thyroid oncocytic tumors 140
Liver tissue as new source to replace thymidine phosphorylase activity in mitochondrial neurogastrointestinal encephalomyopathy 138
Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): The liver as a new source of thymidine phosphorylase 135
Prucalopride exerts neuroprotection in human enteric neurons 132
A germline mutation in the POT1 gene is a candidate for familial non-medullary thyroid cancer 132
Interleukin-4/interleukin-4 receptor gene polymorphisms in hand osteoarthritis 131
Totale 19.588
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Categoria #
all - tutte 59.339
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 59.339
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.105 0 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
2025/20268.143 704 884 718 623 728 363 926 234 1.674 609 320 360
2026/2027472 224 248 0 0 0 0 0 0 0 0 0 0
Totale 22.226