BONORA, ELENA
 Distribuzione geografica
Continente #
NA - Nord America 5.144
EU - Europa 3.631
AS - Asia 855
AF - Africa 209
SA - Sud America 22
Continente sconosciuto - Info sul continente non disponibili 17
OC - Oceania 7
Totale 9.885
Nazione #
US - Stati Uniti d'America 5.130
GB - Regno Unito 866
IT - Italia 829
SE - Svezia 481
DE - Germania 452
CN - Cina 390
IN - India 183
IE - Irlanda 180
VN - Vietnam 179
UA - Ucraina 147
RU - Federazione Russa 124
FR - Francia 117
BE - Belgio 89
BG - Bulgaria 88
TG - Togo 83
CH - Svizzera 74
ZA - Sudafrica 66
EE - Estonia 64
JO - Giordania 46
FI - Finlandia 40
CI - Costa d'Avorio 38
EU - Europa 16
NL - Olanda 15
IR - Iran 13
NG - Nigeria 13
CA - Canada 12
AT - Austria 11
BR - Brasile 11
HR - Croazia 11
JP - Giappone 10
SC - Seychelles 9
TR - Turchia 9
ES - Italia 8
GR - Grecia 8
AU - Australia 7
CL - Cile 6
RO - Romania 6
DK - Danimarca 5
PL - Polonia 5
UZ - Uzbekistan 5
AE - Emirati Arabi Uniti 4
PE - Perù 4
HK - Hong Kong 3
HU - Ungheria 3
SK - Slovacchia (Repubblica Slovacca) 3
KZ - Kazakistan 2
LB - Libano 2
MX - Messico 2
SA - Arabia Saudita 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
AR - Argentina 1
BD - Bangladesh 1
CY - Cipro 1
CZ - Repubblica Ceca 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
LV - Lettonia 1
MD - Moldavia 1
PH - Filippine 1
PK - Pakistan 1
RS - Serbia 1
SI - Slovenia 1
Totale 9.885
Città #
Southend 784
Fairfield 625
Chandler 554
Ashburn 401
Ann Arbor 362
Seattle 292
Woodbridge 276
Houston 264
Wilmington 253
Bologna 236
Cambridge 234
Princeton 184
Dublin 179
Dong Ket 123
Redmond 121
Sofia 88
Brussels 86
Jacksonville 83
Lomé 83
Nanjing 78
Westminster 78
Padova 66
Bern 64
Berlin 61
Amman 46
New York 44
Turin 42
Bremen 40
San Diego 40
Abidjan 38
Saint Petersburg 38
Helsinki 37
Shenyang 35
Falls Church 31
Florence 31
Jinan 30
Milan 30
Boydton 29
Dearborn 28
Tianjin 26
Changsha 25
Nanchang 24
Des Moines 22
Hebei 22
Haikou 21
Medford 21
Redwood City 20
Mülheim 19
Beijing 18
Boardman 18
Abano Terme 17
Parma 16
Rome 14
Zhengzhou 14
Abeokuta 13
Kuban 13
Washington 13
Guangzhou 12
Jiaxing 12
Phoenix 12
Ravenna 11
São Paulo 11
Tappahannock 11
Amsterdam 10
Norwalk 10
Olalla 10
Paris 10
Vienna 10
Chicago 9
Costa Mesa 9
Fuzhou 9
Mahé 9
London 8
Taizhou 8
Toronto 8
Ferrara 7
Frankfurt Am Main 6
Hangzhou 6
Modena 6
Mountain View 6
Pune 6
Tokyo 6
Verona 6
Chengdu 5
Delhi 5
Imola 5
Istanbul 5
San Lazzaro di Savena 5
Bari 4
Castel Maggiore 4
Gallo 4
Lausanne 4
Leawood 4
Lima 4
Los Angeles 4
Naples 4
Portici 4
San Jose 4
Selargius 4
Shanghai 4
Totale 6.751
Nome #
BRAF exon 15 mutations in papillary carcinoma and adjacent thyroid parenchyma: A search for the early molecular events associated with tumor development 179
Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways 174
An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. 172
Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant. 170
A Greek Family with a Follicular Variant of Familial Papillary Thyroid Carcinoma: TCO, MNG1, fPTC/PRN, and NMTC1 Excluded as Susceptibility Loci 170
A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder. 170
A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism 162
INPP4B overexpression and c-KIT downregulation in human achalasia. 160
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 157
The RET51/FKBP52 complex and its involvement in Parkinson disease. 156
Mutant MYO1F alters the mitochondrial network and induces tumor proliferation in thyroid cancer 156
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III 153
Gut epithelial and vascular barrier abnormalities in patients with chronic intestinal pseudo-obstruction 149
Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma 144
Enteric neuron density correlates with clinical features of severe gut dysmotility 141
Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects. 137
Enteric neuropathies: Yesterday, Today and Tomorrow 137
Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients. 136
Definition of miRNAs expression profile in glioblastoma samples: the relevance of non-neoplastic brain reference. 136
Expression of 19 microRNAs in glioblastoma and comparison with other brain neoplasia of grades I–III 136
L’encefalomiopatia Mitocondriale Neurogastrointestinale (MNGIE): Il Fegato Come Nuova Fonte Di Timidina Fosforilasi 136
Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients 133
Neuroactive Steroids in First-Episode Psychosis: A Role for Progesterone? 132
Which elderly newly diagnosed glioblastoma patients can benefit from radiotherapy and temozolomide? A PERNO prospective study 131
null 130
miRNAs expression analysis in paired fresh/frozen and dissected formalin fixed and paraffin embedded glioblastoma using real-time pCR. 129
Expression of the Bitter taste receptor, T2R38, in enteroendocrine cells of the colonic mucosa of overweight/obese vs. Lean subjects 129
Erratum to: Incidence of neuroepithelial primary brain tumors among adult population of Emilia-Romagna Region, Italy 127
C620R mutation of the murine ret proto-oncogene: loss of function effect in homozygotes and possible gain of function effect in heterozygotes. 126
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 124
Oncocytic glioblastoma: a glioblastoma showing oncocytic changes and increased mitochondrial DNA copy number 124
Novel Mutations in Neurogenic Chronic Intestinal Pseudo-Obstruction Identified by High-Throughput Sequencing 123
Integrated web-based approach to multigenic diseases 121
Incidence of neuroepithelial primary brain tumors among adult population of Emilia-Romagna Region, Italy 121
TOM: enhancement and extension of a tool suite for in silico approaches to multigenic complex disorders. 118
A new homozygous CACNB2 mutation has functional relevance and supports a role for calcium channels in autism spectrum disorder. 117
Genomic profiles of primary and metastatic esophageal adenocarcinoma identified via digital sorting of pure cell populations: Results from a case report 116
Expression of RAD21 immunoreactivity in myenteric neurons of the human and mouse small intestine 116
TOM: a web-based integrated approach for identification of candidate disease genes 115
Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next? 114
The tyrosine kinase receptor RET interacts in vivo with aryl hydrocarbon receptor-interacting protein to alter survivin availability. 113
Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction. 113
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours. 113
Dealing With BRCA1/2 unclassified variants in a cancer genetics clinic: Does cosegregation analysis help? 113
Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy 112
A mutation screening of oncogenes, tumor suppressor gene TP53 and nuclear encoded mitochondrial complex I genes in oncocytic thyroid tumors 110
Distribution and Characterization of RAD21 Immunoreactivity in Mouse and Human Enteric Neurons 109
The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma 108
HDAC8 Loss of Function and SHOX Haploinsufficiency: Two Independent Genetic Defects Responsible for a Complex Phenotype 106
DICER1 mutations in familial multinodular goiter with and without ovarian sertoli-leydig cell tumors 105
Evidence of RET/GDNF-related apolipoprotein B (APOB) activation and altered expression in patients with chronic intestinal pseudo-obstruction (CIPO) 104
Association of the interleukin-4/interleukin-4 receptor genetic variants with hand osteoathrtitis. 103
Genetic Predisposition to Familial Nonmedullary Thyroid Cancer: An Update of Molecular Findings and State-of-the-Art Studies 103
Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family 102
Su1852 The 5-HT4 Selective Agonist Prucalopride Exerts Neural and Epithelial Protective Effects In Vitro 100
Molecular features of thyroid oncocytic tumors 99
Protective Actions of Epithelial 5-Hydroxytryptamine 4 Receptors in Normal and Inflamed Colon 99
EXCAVATOR: detecting copy number variants from whole-exome sequencing data. 98
GSTT1 and M1 polymorphisms in Hurthle thyroid cancer patients 96
Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer. 96
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 95
Mast cell-nerve interactions correlate with bloating and abdominal pain severity in patients with non-celiac gluten / wheat sensitivity 94
Interleukin-4/interleukin-4 receptor gene polymorphisms in hand osteoarthritis 92
Novel germline variants identified in the inner mitochondrial membrane transporter TIMM44 and their role in predisposition to oncocytic thyroid carcinomas. 90
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? 85
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain 85
Mutation screening and association analysis of six candidate genes for autism on chromosome 7q. 84
Erratum to: Survival prediction in high-grade gliomas using CT perfusion imaging [J Neurooncol (2015) 123, 93-102, DOI 10.1007/s11060-015-1766-5] 84
Mitochondrial Neurogastrointestinal Encephalomyopathy: The Liver As a Tissue Source to Restore Thymidine Phosphorylase Activity 83
PTEN Hamartoma Tumor Syndrome: Skin Manifestations and Insights Into Their Molecular Pathogenesis 83
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 82
Su2019 Functional Characterization of a Novel RAD21 Mutation in Familial Chronic Intestinal Pseudo-Obstruction (CIPO) 81
Rasal1 and ros1 gene variants in hereditary breast cancer 81
Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer 80
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits 79
Intestinal epithelial barrier disfunction in patients with chronic intestinal pseudo-obstruction 76
Liver tissue as new source to replace thymidine phosphorylase activity in mitochondrial neurogastrointestinal encephalomyopathy 73
Identifying Gene-Environment Interactions in Schizophrenia: Contemporary Challenges for Integrated, Large-scale Investigations 71
A germline mutation in the POT1 gene is a candidate for familial non-medullary thyroid cancer 67
Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma. 65
Targeted Sequencing of Sorted Esophageal Adenocarcinoma Cells Unveils Known and Novel Mutations in the Separated Subpopulations 65
Whole genome sequencing of familial non-medullary thyroid cancer identifies germline alterations in MAPK/ERK and PI3K/AKT signaling pathways 64
Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): The liver as a new source of thymidine phosphorylase 58
Novel understanding on genetic mechanisms of enteric neuropathies leading to severe gut dysmotility 56
The Liver as a New Tissue Source of Thymidine Phosphorylase for Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE) 53
Clinical and Pathological Features of Severe Gut Dysmotility 52
The Liver As a Tissue Source to Restore Thymidine Phosphorylase Activity 52
Prucalopride exerts neuroprotection in human enteric neurons 51
mtDNA inherited and somatic variability in Alzheimer Disease 50
The continuity of effect of schizophrenia polygenic risk score and patterns of cannabis use on transdiagnostic symptom dimensions at first-episode psychosis: findings from the EU-GEI study 49
mtDNA inherited and somatic variability in Alzheimer’s disease 48
Enteric Neuromyopathies: Highlights on Genetic Mechanisms Underlying Chronic Intestinal Pseudo-Obstruction 46
Genetics of familial non-medullary thyroid carcinoma (FNMTC) 44
Calcium and Reactive Oxygen Species Signaling Interplays in Cardiac Physiology and PathologiesCalcium and Reactive Oxygen Species Signaling Interplays in Cardiac Physiology and Pathologies 41
Correlations between Molecular Alterations, Histopathological Characteristics, and Poor Prognosis in Esophageal Adenocarcinoma 40
The prognostic impact of histology in esophageal and esophago-gastric junction adenocarcinoma 35
HDAC9 structural variants disrupting TWIST1 transcriptional regulation lead to craniofacial and limb malformations 28
Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia 21
Selective targeting BMP2 and 4 in SMAD4 negative esophageal adenocarcinoma inhibits tumor growth and aggressiveness in preclinical models 20
Use of multiple polygenic risk scores for distinguishing schizophrenia-spectrum disorder and affective psychosis categories in a first-episode sample; the EU-GEI study 14
Totale 10.196
Categoria #
all - tutte 22.818
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 22.818


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019307 0 0 0 0 0 0 0 45 44 93 47 78
2019/20202.480 323 59 27 136 265 243 311 346 386 160 104 120
2020/20211.527 273 98 51 91 91 78 100 92 165 99 81 308
2021/20222.223 118 69 113 140 198 139 52 172 93 223 585 321
2022/20232.398 239 321 143 285 126 173 78 151 442 86 205 149
2023/2024750 98 122 64 103 76 180 62 45 0 0 0 0
Totale 10.228