CRIS Current Research Information System

ROMEO, GIOVANNI
 Distribuzione geografica
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Continente #
NA - Nord America 5.557
EU - Europa 3.932
AS - Asia 3.255
AF - Africa 245
SA - Sud America 230
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 5
Totale 13.235
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Nazione #
US - Stati Uniti d'America 5.525
CN - Cina 1.040
SG - Singapore 1.011
GB - Regno Unito 955
IT - Italia 726
VN - Vietnam 532
DE - Germania 505
SE - Svezia 444
UA - Ucraina 356
HK - Hong Kong 246
RU - Federazione Russa 211
IN - India 197
BR - Brasile 168
FR - Francia 164
IE - Irlanda 131
NL - Olanda 88
JP - Giappone 76
ZA - Sudafrica 68
CI - Costa d'Avorio 65
EE - Estonia 60
TG - Togo 59
FI - Finlandia 58
KR - Corea 57
CH - Svizzera 53
SC - Seychelles 40
BE - Belgio 34
BG - Bulgaria 33
CZ - Repubblica Ceca 31
AR - Argentina 29
JO - Giordania 28
CA - Canada 23
ID - Indonesia 16
PL - Polonia 14
CL - Cile 12
ES - Italia 12
IR - Iran 11
AT - Austria 10
GR - Grecia 9
AU - Australia 8
MX - Messico 8
RO - Romania 8
EC - Ecuador 7
HR - Croazia 7
NG - Nigeria 7
LT - Lituania 6
TR - Turchia 6
BD - Bangladesh 5
IQ - Iraq 5
UZ - Uzbekistan 5
AE - Emirati Arabi Uniti 4
CO - Colombia 4
LB - Libano 4
SK - Slovacchia (Repubblica Slovacca) 4
MY - Malesia 3
PE - Perù 3
PT - Portogallo 3
VE - Venezuela 3
XK - ???statistics.table.value.countryCode.XK??? 3
BA - Bosnia-Erzegovina 2
DK - Danimarca 2
KZ - Kazakistan 2
MD - Moldavia 2
PK - Pakistan 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AZ - Azerbaigian 1
CG - Congo 1
CM - Camerun 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
ET - Etiopia 1
EU - Europa 1
GY - Guiana 1
IL - Israele 1
KG - Kirghizistan 1
LA - Repubblica Popolare Democratica del Laos 1
LU - Lussemburgo 1
MA - Marocco 1
NC - Nuova Caledonia 1
NZ - Nuova Zelanda 1
PG - Papua Nuova Guinea 1
PY - Paraguay 1
RS - Serbia 1
SI - Slovenia 1
SR - Suriname 1
TH - Thailandia 1
UY - Uruguay 1
ZW - Zimbabwe 1
Totale 13.235
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Città #
Southend 812
Singapore 636
Fairfield 598
Ashburn 493
Chandler 455
Ann Arbor 336
Wilmington 291
Santa Clara 286
Woodbridge 286
Houston 260
Jacksonville 254
Hong Kong 244
Seattle 231
Cambridge 229
Princeton 189
Hefei 179
Bologna 152
Dong Ket 147
Dublin 131
Boardman 123
Beijing 120
Padova 84
Westminster 84
Ho Chi Minh City 83
Nanjing 82
Tokyo 74
Los Angeles 71
Berlin 66
Abidjan 65
Lomé 59
Seoul 57
Milan 55
Helsinki 51
Dallas 49
New York 48
Bern 46
Mülheim 46
Buffalo 44
Shenyang 43
Changsha 40
Jinan 39
Saint Petersburg 38
San Diego 38
Hanoi 35
Turin 34
Brussels 33
Sofia 33
Hebei 29
Amman 28
Falls Church 28
Nanchang 26
Guangzhou 25
Mahé 25
Zhengzhou 25
Dearborn 24
Des Moines 24
Frankfurt am Main 22
Jiaxing 21
Tianjin 21
Florence 20
Medford 20
Verona 20
Bremen 19
Munich 19
Rome 19
Shanghai 19
Bengaluru 18
Brno 18
Redondo Beach 18
Yubileyny 18
São Paulo 16
Amsterdam 15
Chicago 15
Can Tho 12
Paris 12
Taizhou 12
Haikou 11
Hangzhou 11
Jakarta 11
London 11
Phoenix 11
The Dalles 11
Falkenstein 10
Fuzhou 10
Kuban 10
Norwalk 10
Nuremberg 10
Redwood City 10
Toronto 10
Warsaw 10
Brooklyn 9
Olalla 9
San Venanzo 9
Haiphong 8
Modena 8
Ningbo 8
Redmond 8
Shenzhen 8
Stockholm 8
Atlanta 7
Totale 8.665
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Nome #
Which elderly newly diagnosed glioblastoma patients can benefit from radiotherapy and temozolomide? A PERNO prospective study 239
Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant. 234
Association of hereditary thrombocythemia and distal limb defects with a thrombopoietin gene mutation. 231
Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways 226
Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells 222
A Greek Family with a Follicular Variant of Familial Papillary Thyroid Carcinoma: TCO, MNG1, fPTC/PRN, and NMTC1 Excluded as Susceptibility Loci 217
An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. 213
A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24. 213
Double-heterozygous mutations involving both HNF1A (MODY3) and HNF4A (MODY1) genes: a case report 206
The RET51/FKBP52 complex and its involvement in Parkinson disease. 198
The KIT Gene Is Associated with the English Spotting Coat Color Locus and Congenital Megacolon in Checkered Giant Rabbits (Oryctolagus cuniculus) 193
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III 192
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity. 191
Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma 190
An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene. 189
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines. 180
Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer. 175
Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration 174
Fluorescence quantitation of thyrocyte iodide accumulation with the yellow fluorescent protein variant YFP-H148Q/I152L 171
Mitochondrial DNA mutations in oncocytic adnexal lacrimal glands of the conjunctiva 169
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 169
Linkage disequilibrium patterns and tagSNP transferability among European populations. 168
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours. 168
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 166
Incidence of neuroepithelial primary brain tumors among adult population of Emilia-Romagna Region, Italy 166
Allelic loss on chromosomes 2q21 and 19p13.2 in Hürthle thyroid tumors. 163
A cellular model for cancer progression: Role of mitochondrial mutations and metabolism 161
A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function 160
Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction. 160
The tyrosine kinase receptor RET interacts in vivo with aryl hydrocarbon receptor-interacting protein to alter survivin availability. 158
A Yellow Fluorescent Protein variant as an intracellular iodide biosensor in thyroid cells 157
Polymorphic NumtS trace human population relationships 157
C620R mutation of the murine ret proto-oncogene: loss of function effect in homozygotes and possible gain of function effect in heterozygotes. 157
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 156
Discordant patterns of mtDNA and ethno-linguistic variation in 14 Iranian Ethnic groups. 156
GSTT1 and M1 polymorphisms in Hurthle thyroid cancer patients 153
The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma 152
Genetic Predisposition to Familial Neuroblastoma: Identification of Two Novel Genomic Regions at 2p and 12p. 149
EX-HOM (EXome-HOMozygosity): a proof of principle 148
Variabilità e funzione delle mutazioni mitocondriali in condizioni fisiologiche e patologiche 148
AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomics 148
First evidence of association between past environmental exposure to dioxin and DNA methylation of CYP1A1 and IGF2 genes in present day Vietnamese population 147
TOM: enhancement and extension of a tool suite for in silico approaches to multigenic complex disorders. 146
The Impairment of Cell Metabolism by Cardiovascular Toxicity of Doxorubicin Is Reversed by Bergamot Polyphenolic Fraction Treatment in Endothelial Cells 145
Simple Method for Haplotyping the Poly(TG) Repeat in Individuals Carrying the IVS8 5T Allele in the CFTR Gene. 145
The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q31.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomalies. 145
TOM: a web-based integrated approach for identification of candidate disease genes 145
Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genes. 144
An interdisciplinary approach to investigate the English spotting locus and its association with megacolon in the domestic rabbit: a new putative model of enteric neuronal dysfunction 144
The genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilization 143
Perchlorate transport and inhibition of the Sodium Iodide Symporter measured with the Yellow Fluorescent Protein variant YFP-H148Q/I152L. 142
Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer. 142
Molecular genetics of human enteric neuropathies. 141
EXCAVATOR: detecting copy number variants from whole-exome sequencing data. 139
Cell-based imaging of sodium iodide symporter activity with the yellow fluorescent protein variant YFP-H148Q/I152L. 139
Progetto Neurooncologia Emilia Romagna - PERNO 138
Mitochondrial Metabolism and Cancer 133
A de novo nonsense mutation of PAX6 gene in a patient with aniridia, ataxia, and mental retardation 132
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 130
Learning from oncocytic tumors: why choose inefficient mitochondria? 129
Endothelin receptor B (EDNRB) is not the causative gene of the English spotting locus in the domestic rabbit (Oryctolagus cuniculus) 126
Genetic Predisposition to Familial Nonmedullary Thyroid Cancer: An Update of Molecular Findings and State-of-the-Art Studies 125
Searching for a needle in the haystack: comparing six methods to evaluate heteroplasmy in difficult sequence context 125
Relevance of Mitochondrial Genetics and Metabolism in Cancer Development 125
Molecular features of thyroid oncocytic tumors 124
Psychological consequences of prenatal diagnosis in a case of familial Angelman syndrome 124
Thrombophilia and venous thromboembolism. International consensus statement. Guidelines according to scientific evidence. 123
PREVALENCE OF GJB2 , GJB6 AND A1555G MUTATIONS IN THE ITALIAN POPULATION 123
Novel germline variants identified in the inner mitochondrial membrane transporter TIMM44 and their role in predisposition to oncocytic thyroid carcinomas. 119
H+-slip correlated to rotor free-wheeling as cause of F1FO-ATPase dysfunction in primary mitochondrial disorders 118
Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma. 118
Plasma membrane oxidoreductase activity in cultured cells in relation to mitochondrial function and oxidative stress. 117
Interleukin-4/interleukin-4 receptor gene polymorphisms in hand osteoarthritis 116
Mitochondria Bioenergetic Functions and Cell Metabolism Are Modulated by the Bergamot Polyphenolic Fraction 115
Molecular mechanisms of naringenin modulation of mitochondrial permeability transition acting on F1FO-ATPase and counteracting saline load-induced injury in SHRSP cerebral endothelial cells 113
Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in renal oncocytoma 113
Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic Phenotype. 113
Ret, Abl1 (cAbl) and Trp53 gene fragmentations in comet-FISH assay act as in vivo biomarkers of radiation exposure in C57BL/6 and CBA/J mice 111
Mitochondrial activities of a cell line derived from thyroid Hurthle cell tumors 109
High variability of TLR4 gene in different ethnic groups in Iran 108
Functional genomics of thyroid oncocytoma 107
mtDNA inherited and somatic variability in Alzheimer’s disease 104
Synovitis, Acne, Pustulosis, Hyperostosis, Osteitis (SAPHO) syndrome: is PTPN22 involved? 103
H3M2: detection of runs of homozygosity from whole-exome sequencing data 102
TRANSMIT - Translational significance of mitochondrial mutations in tumors 97
RET Protooncogene 96
Bergamot derivative compounds affect on F1FO-ATPase and the mitochondrial permeability transition 88
null 82
NOVEL ANTICANCER THERAPEUTICS BASED ON MODULATION OF APOPTOSIS THROUGH DEPENDENCE RECEPTORS (HERMIONE) 80
Enjoy your journey: the bergamot polyphenols from the tree to the cell metabolism 74
Improving Diagnoses of Mental Retardation in Children in Central Eastern Europe and Central Asia through Genetic Characterisation and Bioinformatics/Statistics (CHERISH) 68
‘Rotor free-wheeling’ in impaired F1FO-ATPase induces congenital hypermetabolism 60
The RHNumtS compilation: features and bioinformatics approaches to locate and quantify Human NumtS 30
Totale 13.468
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Categoria #
all - tutte 36.017
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 36.017
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021838 0 0 0 0 0 67 17 107 107 94 84 362
2021/20221.936 160 50 117 144 156 125 47 104 68 211 487 267
2022/20231.843 203 251 109 240 117 133 70 111 302 47 167 93
2023/2024556 54 85 36 43 45 101 28 43 13 27 37 44
2024/20251.897 68 290 173 154 431 96 111 39 22 102 73 338
2025/20262.093 339 409 417 316 464 148 0 0 0 0 0 0
Totale 13.468