CRIS Current Research Information System

ROMEO, GIOVANNI
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 6.281
AS - Asia 4.297
EU - Europa 4.136
SA - Sud America 268
AF - Africa 266
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 5
Totale 15.264
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 6.225
CN - Cina 1.192
SG - Singapore 1.179
VN - Vietnam 1.023
GB - Regno Unito 967
IT - Italia 777
DE - Germania 512
SE - Svezia 446
UA - Ucraina 358
HK - Hong Kong 276
FR - Francia 252
IN - India 216
RU - Federazione Russa 212
BR - Brasile 189
IE - Irlanda 133
JP - Giappone 116
NL - Olanda 89
ZA - Sudafrica 78
FI - Finlandia 77
KR - Corea 67
CI - Costa d'Avorio 65
EE - Estonia 60
TG - Togo 59
CH - Svizzera 56
SC - Seychelles 40
CA - Canada 38
BD - Bangladesh 35
BE - Belgio 34
AR - Argentina 33
BG - Bulgaria 33
JO - Giordania 32
CZ - Repubblica Ceca 31
PL - Polonia 19
ID - Indonesia 18
TH - Thailandia 18
ES - Italia 16
IQ - Iraq 16
PH - Filippine 16
CL - Cile 15
TW - Taiwan 13
TR - Turchia 12
IR - Iran 11
MX - Messico 11
AT - Austria 10
GR - Grecia 9
SA - Arabia Saudita 9
AU - Australia 8
HR - Croazia 8
RO - Romania 8
CO - Colombia 7
EC - Ecuador 7
LT - Lituania 7
NG - Nigeria 7
UZ - Uzbekistan 7
PK - Pakistan 6
VE - Venezuela 6
AE - Emirati Arabi Uniti 5
LB - Libano 5
JM - Giamaica 4
KZ - Kazakistan 4
PY - Paraguay 4
SK - Slovacchia (Repubblica Slovacca) 4
DZ - Algeria 3
MA - Marocco 3
MY - Malesia 3
PE - Perù 3
PS - Palestinian Territory 3
PT - Portogallo 3
XK - ???statistics.table.value.countryCode.XK??? 3
AL - Albania 2
AM - Armenia 2
AZ - Azerbaigian 2
BA - Bosnia-Erzegovina 2
DK - Danimarca 2
ET - Etiopia 2
HN - Honduras 2
KG - Kirghizistan 2
MD - Moldavia 2
NP - Nepal 2
SI - Slovenia 2
SY - Repubblica araba siriana 2
TN - Tunisia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AO - Angola 1
BO - Bolivia 1
BW - Botswana 1
BY - Bielorussia 1
CG - Congo 1
CM - Camerun 1
DO - Repubblica Dominicana 1
EG - Egitto 1
EU - Europa 1
GE - Georgia 1
GH - Ghana 1
GY - Guiana 1
HU - Ungheria 1
IL - Israele 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LU - Lussemburgo 1
Totale 15.255
Salva come PNG Salva come JPEG
Città #
Southend 812
Singapore 791
Fairfield 598
Ashburn 545
Chandler 455
Ann Arbor 336
Santa Clara 299
Wilmington 291
San Jose 288
Woodbridge 286
Cambridge 264
Hong Kong 263
Houston 263
Jacksonville 254
Seattle 231
Ho Chi Minh City 216
Princeton 189
Hefei 179
Bologna 162
Hanoi 151
Dong Ket 147
Dublin 132
Boardman 126
Beijing 121
Council Bluffs 102
Tokyo 98
Lauterbourg 86
Padova 84
Westminster 84
Los Angeles 82
Nanjing 82
Helsinki 70
Berlin 66
Abidjan 65
New York 62
Lomé 59
Milan 59
Seoul 58
Buffalo 52
Dallas 50
Bern 46
Mülheim 46
Changsha 44
Shenyang 43
Jinan 39
San Diego 39
Saint Petersburg 38
Turin 34
Brussels 33
Guangzhou 33
Sofia 33
Amman 32
Haiphong 31
Hebei 29
Falls Church 28
Frankfurt am Main 27
Zhengzhou 27
Nanchang 26
Mahé 25
Dearborn 24
Des Moines 24
Rome 24
Shanghai 23
São Paulo 23
Tianjin 23
Da Nang 22
Jiaxing 21
Verona 21
Florence 20
Medford 20
Bremen 19
Munich 19
Bengaluru 18
Brno 18
Can Tho 18
Redondo Beach 18
Yubileyny 18
London 17
Orem 17
The Dalles 17
Amsterdam 16
Chicago 16
Hangzhou 16
Warsaw 15
Phoenix 14
Paris 13
Toronto 13
Jakarta 12
Johannesburg 12
Montreal 12
Taizhou 12
Biên Hòa 11
Brooklyn 11
Fuzhou 11
Haikou 11
Nuremberg 11
Atlanta 10
Falkenstein 10
Kuban 10
Norwalk 10
Totale 9.881
Salva come PNG Salva come JPEG
Nome #
Which elderly newly diagnosed glioblastoma patients can benefit from radiotherapy and temozolomide? A PERNO prospective study 275
Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells 260
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
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III 252
Association of hereditary thrombocythemia and distal limb defects with a thrombopoietin gene mutation. 251
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity. 243
An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. 239
Double-heterozygous mutations involving both HNF1A (MODY3) and HNF4A (MODY1) genes: a case report 235
A Greek Family with a Follicular Variant of Familial Papillary Thyroid Carcinoma: TCO, MNG1, fPTC/PRN, and NMTC1 Excluded as Susceptibility Loci 232
A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24. 231
The KIT Gene Is Associated with the English Spotting Coat Color Locus and Congenital Megacolon in Checkered Giant Rabbits (Oryctolagus cuniculus) 229
The RET51/FKBP52 complex and its involvement in Parkinson disease. 219
An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene. 216
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
Incidence of neuroepithelial primary brain tumors among adult population of Emilia-Romagna Region, Italy 205
Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration 204
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
Fluorescence quantitation of thyrocyte iodide accumulation with the yellow fluorescent protein variant YFP-H148Q/I152L 200
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours. 199
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines. 198
A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function 193
First evidence of association between past environmental exposure to dioxin and DNA methylation of CYP1A1 and IGF2 genes in present day Vietnamese population 189
The Impairment of Cell Metabolism by Cardiovascular Toxicity of Doxorubicin Is Reversed by Bergamot Polyphenolic Fraction Treatment in Endothelial Cells 188
Mitochondrial DNA mutations in oncocytic adnexal lacrimal glands of the conjunctiva 187
AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomics 187
Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer. 185
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 184
Polymorphic NumtS trace human population relationships 182
Linkage disequilibrium patterns and tagSNP transferability among European populations. 179
C620R mutation of the murine ret proto-oncogene: loss of function effect in homozygotes and possible gain of function effect in heterozygotes. 179
The tyrosine kinase receptor RET interacts in vivo with aryl hydrocarbon receptor-interacting protein to alter survivin availability. 178
The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma 177
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 176
Variabilità e funzione delle mutazioni mitocondriali in condizioni fisiologiche e patologiche 174
Discordant patterns of mtDNA and ethno-linguistic variation in 14 Iranian Ethnic groups. 173
Allelic loss on chromosomes 2q21 and 19p13.2 in Hürthle thyroid tumors. 171
A cellular model for cancer progression: Role of mitochondrial mutations and metabolism 171
GSTT1 and M1 polymorphisms in Hurthle thyroid cancer patients 170
A Yellow Fluorescent Protein variant as an intracellular iodide biosensor in thyroid cells 170
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 169
TOM: enhancement and extension of a tool suite for in silico approaches to multigenic complex disorders. 168
Genetic Predisposition to Familial Neuroblastoma: Identification of Two Novel Genomic Regions at 2p and 12p. 163
The genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilization 163
EXCAVATOR: detecting copy number variants from whole-exome sequencing data. 162
TOM: a web-based integrated approach for identification of candidate disease genes 162
Mitochondria Bioenergetic Functions and Cell Metabolism Are Modulated by the Bergamot Polyphenolic Fraction 162
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. 161
H+-slip correlated to rotor free-wheeling as cause of F1FO-ATPase dysfunction in primary mitochondrial disorders 160
Simple Method for Haplotyping the Poly(TG) Repeat in Individuals Carrying the IVS8 5T Allele in the CFTR Gene. 160
Perchlorate transport and inhibition of the Sodium Iodide Symporter measured with the Yellow Fluorescent Protein variant YFP-H148Q/I152L. 159
Molecular genetics of human enteric neuropathies. 158
Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genes. 158
EX-HOM (EXome-HOMozygosity): a proof of principle 158
Progetto Neurooncologia Emilia Romagna - PERNO 156
Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer. 156
Cell-based imaging of sodium iodide symporter activity with the yellow fluorescent protein variant YFP-H148Q/I152L. 154
Relevance of Mitochondrial Genetics and Metabolism in Cancer Development 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
A de novo nonsense mutation of PAX6 gene in a patient with aniridia, ataxia, and mental retardation 151
Mitochondrial Metabolism and Cancer 150
Searching for a needle in the haystack: comparing six methods to evaluate heteroplasmy in difficult sequence context 149
Learning from oncocytic tumors: why choose inefficient mitochondria? 148
Molecular mechanisms of naringenin modulation of mitochondrial permeability transition acting on F1FO-ATPase and counteracting saline load-induced injury in SHRSP cerebral endothelial cells 147
Endothelin receptor B (EDNRB) is not the causative gene of the English spotting locus in the domestic rabbit (Oryctolagus cuniculus) 147
Thrombophilia and venous thromboembolism. International consensus statement. Guidelines according to scientific evidence. 146
Genetic Predisposition to Familial Nonmedullary Thyroid Cancer: An Update of Molecular Findings and State-of-the-Art Studies 145
Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma. 142
Novel germline variants identified in the inner mitochondrial membrane transporter TIMM44 and their role in predisposition to oncocytic thyroid carcinomas. 140
Molecular features of thyroid oncocytic tumors 138
Psychological consequences of prenatal diagnosis in a case of familial Angelman syndrome 137
Plasma membrane oxidoreductase activity in cultured cells in relation to mitochondrial function and oxidative stress. 136
PREVALENCE OF GJB2 , GJB6 AND A1555G MUTATIONS IN THE ITALIAN POPULATION 134
Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in renal oncocytoma 131
Interleukin-4/interleukin-4 receptor gene polymorphisms in hand osteoarthritis 129
Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic Phenotype. 126
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 124
Functional genomics of thyroid oncocytoma 124
H3M2: detection of runs of homozygosity from whole-exome sequencing data 124
Mitochondrial activities of a cell line derived from thyroid Hurthle cell tumors 123
mtDNA inherited and somatic variability in Alzheimer’s disease 122
High variability of TLR4 gene in different ethnic groups in Iran 119
Synovitis, Acne, Pustulosis, Hyperostosis, Osteitis (SAPHO) syndrome: is PTPN22 involved? 115
TRANSMIT - Translational significance of mitochondrial mutations in tumors 113
Bergamot derivative compounds affect on F1FO-ATPase and the mitochondrial permeability transition 111
RET Protooncogene 110
‘Rotor free-wheeling’ in impaired F1FO-ATPase induces congenital hypermetabolism 93
NOVEL ANTICANCER THERAPEUTICS BASED ON MODULATION OF APOPTOSIS THROUGH DEPENDENCE RECEPTORS (HERMIONE) 92
Enjoy your journey: the bergamot polyphenols from the tree to the cell metabolism 90
null 82
Improving Diagnoses of Mental Retardation in Children in Central Eastern Europe and Central Asia through Genetic Characterisation and Bioinformatics/Statistics (CHERISH) 78
The RHNumtS compilation: features and bioinformatics approaches to locate and quantify Human NumtS 35
Totale 15.509
Salva come PNG Salva come JPEG
Categoria #
all - tutte 41.154
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 41.154
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021362 0 0 0 0 0 0 0 0 0 0 0 362
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
2025/20264.134 339 409 417 316 464 267 357 163 824 314 106 158
Totale 15.509