CRIS Current Research Information System

BONORA, ELENA
 Distribuzione geografica
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Continente #
NA - Nord America 6.730
EU - Europa 4.859
AS - Asia 4.814
AF - Africa 375
SA - Sud America 328
Continente sconosciuto - Info sul continente non disponibili 20
OC - Oceania 12
Totale 17.138
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Nazione #
US - Stati Uniti d'America 6.653
SG - Singapore 1.508
CN - Cina 1.471
IT - Italia 1.288
GB - Regno Unito 905
VN - Vietnam 694
DE - Germania 657
SE - Svezia 496
HK - Hong Kong 452
IN - India 264
RU - Federazione Russa 232
BR - Brasile 226
NL - Olanda 189
IE - Irlanda 167
FR - Francia 156
UA - Ucraina 155
KR - Corea 150
FI - Finlandia 146
CI - Costa d'Avorio 119
BG - Bulgaria 89
TG - Togo 83
ZA - Sudafrica 80
CH - Svizzera 76
JP - Giappone 68
EE - Estonia 64
SC - Seychelles 64
ID - Indonesia 52
BE - Belgio 51
CA - Canada 49
JO - Giordania 48
AR - Argentina 44
AT - Austria 37
ES - Italia 33
CZ - Repubblica Ceca 30
PL - Polonia 28
MX - Messico 23
EU - Europa 16
TR - Turchia 16
NG - Nigeria 15
EC - Ecuador 14
BD - Bangladesh 13
CO - Colombia 13
IR - Iran 13
HR - Croazia 12
IQ - Iraq 12
AE - Emirati Arabi Uniti 11
AU - Australia 10
PE - Perù 10
CL - Cile 9
GR - Grecia 9
LT - Lituania 9
RO - Romania 7
UZ - Uzbekistan 7
DK - Danimarca 6
SA - Arabia Saudita 5
DZ - Algeria 4
MY - Malesia 4
TH - Thailandia 4
UY - Uruguay 4
BA - Bosnia-Erzegovina 3
EG - Egitto 3
HU - Ungheria 3
KZ - Kazakistan 3
MA - Marocco 3
PH - Filippine 3
PK - Pakistan 3
SK - Slovacchia (Repubblica Slovacca) 3
VE - Venezuela 3
XK - ???statistics.table.value.countryCode.XK??? 3
BO - Bolivia 2
DO - Repubblica Dominicana 2
IL - Israele 2
LB - Libano 2
LV - Lettonia 2
MD - Moldavia 2
SI - Slovenia 2
TW - Taiwan 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
AZ - Azerbaigian 1
BY - Bielorussia 1
CD - Congo 1
CY - Cipro 1
DM - Dominica 1
GE - Georgia 1
GY - Guiana 1
JM - Giamaica 1
KG - Kirghizistan 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
MW - Malawi 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
PG - Papua Nuova Guinea 1
PY - Paraguay 1
RS - Serbia 1
SD - Sudan 1
SN - Senegal 1
SR - Suriname 1
Totale 17.138
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Città #
Singapore 968
Ashburn 784
Southend 784
Fairfield 625
Chandler 554
Hong Kong 449
Bologna 388
Hefei 365
Ann Arbor 362
Santa Clara 301
Seattle 300
Woodbridge 276
Houston 267
Wilmington 253
Cambridge 234
Ho Chi Minh City 190
Princeton 184
Beijing 163
Dublin 162
Seoul 150
Boardman 145
Dallas 134
Munich 130
Dong Ket 123
Redmond 121
Abidjan 119
Hanoi 119
Helsinki 109
Sofia 89
Los Angeles 85
Jacksonville 83
Lomé 83
Nanjing 83
Westminster 78
Milan 74
Padova 67
Bern 65
Berlin 61
Tokyo 60
Rome 56
New York 53
Amman 48
Brussels 42
Turin 42
Jakarta 41
Redondo Beach 41
Bremen 40
San Diego 40
Buffalo 38
Saint Petersburg 38
Shenyang 36
Florence 34
Jinan 34
Bengaluru 33
Changsha 33
Falls Church 31
Guangzhou 31
São Paulo 31
Dearborn 28
Tianjin 27
Zhengzhou 27
Nuremberg 26
Phoenix 26
Hyderabad 25
Nanchang 25
Shanghai 25
Chicago 23
Falkenstein 23
Toronto 23
Des Moines 22
Frankfurt am Main 22
Haikou 22
Hebei 22
Amsterdam 21
Lappeenranta 21
Medford 21
Yubileyny 21
Redwood City 20
Vienna 20
Warsaw 20
London 19
Mülheim 19
Parma 18
Abano Terme 17
Haiphong 17
Da Nang 16
Biên Hòa 15
Brno 15
Naples 14
Abeokuta 13
Chennai 13
Fuzhou 13
Jiaxing 13
Kuban 13
Washington 13
Hangzhou 12
Quận Bình Thạnh 12
Stockholm 12
Brooklyn 11
Can Tho 11
Totale 11.125
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Nome #
Neuroactive Steroids in First-Episode Psychosis: A Role for Progesterone? 306
BRAF exon 15 mutations in papillary carcinoma and adjacent thyroid parenchyma: A search for the early molecular events associated with tumor development 256
Which elderly newly diagnosed glioblastoma patients can benefit from radiotherapy and temozolomide? A PERNO prospective study 241
Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant. 235
Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy 234
Mutant MYO1F alters the mitochondrial network and induces tumor proliferation in thyroid cancer 230
Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways 228
INPP4B overexpression and c-KIT downregulation in human achalasia. 227
Calcium and Reactive Oxygen Species Signaling Interplays in Cardiac Physiology and PathologiesCalcium and Reactive Oxygen Species Signaling Interplays in Cardiac Physiology and Pathologies 225
A Greek Family with a Follicular Variant of Familial Papillary Thyroid Carcinoma: TCO, MNG1, fPTC/PRN, and NMTC1 Excluded as Susceptibility Loci 218
A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder. 216
A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism 215
An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. 214
Novel Mutations in Neurogenic Chronic Intestinal Pseudo-Obstruction Identified by High-Throughput Sequencing 214
Glutamine Supplementation as a Novel Metabolic Therapeutic Strategy for LIG3-Dependent Chronic Intestinal Pseudo-obstruction 213
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 213
Enteric neuron density correlates with clinical features of severe gut dysmotility 206
Gut epithelial and vascular barrier abnormalities in patients with chronic intestinal pseudo-obstruction 205
Mast cell-nerve interactions correlate with bloating and abdominal pain severity in patients with non-celiac gluten / wheat sensitivity 205
The RET51/FKBP52 complex and its involvement in Parkinson disease. 199
Definition of miRNAs expression profile in glioblastoma samples: the relevance of non-neoplastic brain reference. 197
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III 195
Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next? 191
Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma 190
Expression of 19 microRNAs in glioblastoma and comparison with other brain neoplasia of grades I–III 190
L’encefalomiopatia Mitocondriale Neurogastrointestinale (MNGIE): Il Fegato Come Nuova Fonte Di Timidina Fosforilasi 190
Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients 188
Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients. 187
Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects. 182
Enteric neuropathies: Yesterday, Today and Tomorrow 182
Genomic profiles of primary and metastatic esophageal adenocarcinoma identified via digital sorting of pure cell populations: Results from a case report 179
Erratum to: Incidence of neuroepithelial primary brain tumors among adult population of Emilia-Romagna Region, Italy 178
Expression of the Bitter taste receptor, T2R38, in enteroendocrine cells of the colonic mucosa of overweight/obese vs. Lean subjects 173
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 170
Enteric Neuromyopathies: Highlights on Genetic Mechanisms Underlying Chronic Intestinal Pseudo-Obstruction 168
Incidence of neuroepithelial primary brain tumors among adult population of Emilia-Romagna Region, Italy 168
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours. 168
miRNAs expression analysis in paired fresh/frozen and dissected formalin fixed and paraffin embedded glioblastoma using real-time pCR. 164
A new homozygous CACNB2 mutation has functional relevance and supports a role for calcium channels in autism spectrum disorder. 164
Oncocytic glioblastoma: a glioblastoma showing oncocytic changes and increased mitochondrial DNA copy number 163
Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction. 161
HDAC8 Loss of Function and SHOX Haploinsufficiency: Two Independent Genetic Defects Responsible for a Complex Phenotype 161
Expression of RAD21 immunoreactivity in myenteric neurons of the human and mouse small intestine 161
The tyrosine kinase receptor RET interacts in vivo with aryl hydrocarbon receptor-interacting protein to alter survivin availability. 159
C620R mutation of the murine ret proto-oncogene: loss of function effect in homozygotes and possible gain of function effect in heterozygotes. 158
A mutation screening of oncogenes, tumor suppressor gene TP53 and nuclear encoded mitochondrial complex I genes in oncocytic thyroid tumors 156
Integrated web-based approach to multigenic diseases 155
Dealing With BRCA1/2 unclassified variants in a cancer genetics clinic: Does cosegregation analysis help? 155
GSTT1 and M1 polymorphisms in Hurthle thyroid cancer patients 154
The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma 152
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 152
Evidence of RET/GDNF-related apolipoprotein B (APOB) activation and altered expression in patients with chronic intestinal pseudo-obstruction (CIPO) 151
Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer 151
Mutant SPART causes defects in mitochondrial protein import and bioenergetics reversed by Coenzyme Q 148
Distribution and Characterization of RAD21 Immunoreactivity in Mouse and Human Enteric Neurons 147
TOM: enhancement and extension of a tool suite for in silico approaches to multigenic complex disorders. 146
TOM: a web-based integrated approach for identification of candidate disease genes 145
Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family 144
HDAC9 structural variants disrupting TWIST1 transcriptional regulation lead to craniofacial and limb malformations 143
Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer. 143
Multi-disciplinary Insights from the First European Forum on Visceral Myopathy 2022 Meeting 139
EXCAVATOR: detecting copy number variants from whole-exome sequencing data. 139
Protective Actions of Epithelial 5-Hydroxytryptamine 4 Receptors in Normal and Inflamed Colon 139
PTEN Hamartoma Tumor Syndrome: Skin Manifestations and Insights Into Their Molecular Pathogenesis 139
Rasal1 and ros1 gene variants in hereditary breast cancer 138
Su1852 The 5-HT4 Selective Agonist Prucalopride Exerts Neural and Epithelial Protective Effects In Vitro 137
miRNA–221 and miRNA–483–3p Dysregulation in Esophageal Adenocarcinoma 136
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? 135
DICER1 mutations in familial multinodular goiter with and without ovarian sertoli-leydig cell tumors 133
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 131
Association of the interleukin-4/interleukin-4 receptor genetic variants with hand osteoathrtitis. 130
null 130
Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia 129
Mutation screening and association analysis of six candidate genes for autism on chromosome 7q. 129
Mitochondrial Neurogastrointestinal Encephalomyopathy: The Liver As a Tissue Source to Restore Thymidine Phosphorylase Activity 127
The relationship between genetic liability, childhood maltreatment, and IQ: findings from the EU-GEI multicentric case–control study 126
Genetic Predisposition to Familial Nonmedullary Thyroid Cancer: An Update of Molecular Findings and State-of-the-Art Studies 126
Molecular features of thyroid oncocytic tumors 124
Intestinal epithelial barrier disfunction in patients with chronic intestinal pseudo-obstruction 122
Omics Technologies Improving Breast Cancer Research and Diagnostics 121
Use of multiple polygenic risk scores for distinguishing schizophrenia-spectrum disorder and affective psychosis categories in a first-episode sample; the EU-GEI study 120
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain 120
Novel germline variants identified in the inner mitochondrial membrane transporter TIMM44 and their role in predisposition to oncocytic thyroid carcinomas. 120
Clinical and Pathological Features of Severe Gut Dysmotility 119
Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma. 118
Su2019 Functional Characterization of a Novel RAD21 Mutation in Familial Chronic Intestinal Pseudo-Obstruction (CIPO) 118
Interleukin-4/interleukin-4 receptor gene polymorphisms in hand osteoarthritis 117
Differences in Patterns of Stimulant Use and Their Impact on First-Episode Psychosis Incidence: An Analysis of the EUGEI Study 115
Detection of a Novel MSI2-C17orf64 Transcript in a Patient with Aggressive Adenocarcinoma of the Gastroesophageal Junction: A Case Report 114
Novel understanding on genetic mechanisms of enteric neuropathies leading to severe gut dysmotility 113
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 111
Selective targeting BMP2 and 4 in SMAD4 negative esophageal adenocarcinoma inhibits tumor growth and aggressiveness in preclinical models 110
Identifying Gene-Environment Interactions in Schizophrenia: Contemporary Challenges for Integrated, Large-scale Investigations 109
A germline mutation in the POT1 gene is a candidate for familial non-medullary thyroid cancer 108
Liver tissue as new source to replace thymidine phosphorylase activity in mitochondrial neurogastrointestinal encephalomyopathy 107
mtDNA inherited and somatic variability in Alzheimer’s disease 106
Targeted Sequencing of Sorted Esophageal Adenocarcinoma Cells Unveils Known and Novel Mutations in the Separated Subpopulations 105
Clinical Relevance of IFT140 Loss-of-Function Variants in Development of Renal Cysts 104
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits 104
Polynucleotide:adenosine glycosidase activity of ribosome-inactivating proteins: Effect on DNA, RNA and poly(A) 104
Totale 16.001
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Categoria #
all - tutte 48.171
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 48.171
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021923 0 0 0 0 0 78 100 92 165 99 81 308
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
2024/20253.254 149 369 271 290 456 174 257 180 105 234 197 572
2025/20263.935 697 868 712 625 728 305 0 0 0 0 0 0
Totale 17.544