CRIS Current Research Information System

ROMEO, GIOVANNI
 Distribuzione geografica
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Continente #
NA - Nord America 6.030
AS - Asia 4.258
EU - Europa 4.110
AF - Africa 266
SA - Sud America 265
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 5
Totale 14.945
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Nazione #
US - Stati Uniti d'America 5.984
CN - Cina 1.189
SG - Singapore 1.171
VN - Vietnam 1.023
GB - Regno Unito 967
IT - Italia 751
DE - Germania 512
SE - Svezia 446
UA - Ucraina 358
HK - Hong Kong 272
FR - Francia 252
IN - India 216
RU - Federazione Russa 212
BR - Brasile 186
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
BE - Belgio 34
AR - Argentina 33
BG - Bulgaria 33
CA - Canada 32
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
BD - Bangladesh 12
TR - Turchia 12
IR - Iran 11
AT - Austria 10
MX - Messico 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
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
JM - Giamaica 2
KG - Kirghizistan 2
MD - Moldavia 2
NP - Nepal 2
SI - Slovenia 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
HN - Honduras 1
HU - Ungheria 1
IL - Israele 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LU - Lussemburgo 1
LV - Lettonia 1
Totale 14.936
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Città #
Southend 812
Singapore 785
Fairfield 598
Ashburn 533
Chandler 455
Ann Arbor 336
Santa Clara 291
Wilmington 291
Woodbridge 286
Cambridge 264
Houston 261
Hong Kong 259
Jacksonville 254
San Jose 248
Seattle 231
Ho Chi Minh City 216
Princeton 189
Hefei 179
Bologna 161
Hanoi 151
Dong Ket 147
Dublin 132
Boardman 123
Beijing 121
Tokyo 98
Lauterbourg 86
Padova 84
Westminster 84
Nanjing 82
Los Angeles 75
Helsinki 70
Berlin 66
Abidjan 65
Lomé 59
Seoul 58
Milan 57
New York 53
Dallas 50
Buffalo 47
Bern 46
Mülheim 46
Changsha 44
Shenyang 43
Jinan 39
Saint Petersburg 38
San Diego 38
Council Bluffs 37
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
Shanghai 23
Tianjin 23
Da Nang 22
Rome 22
Jiaxing 21
Verona 21
Florence 20
Medford 20
São Paulo 20
Bremen 19
Munich 19
Bengaluru 18
Brno 18
Can Tho 18
Redondo Beach 18
Yubileyny 18
London 17
Amsterdam 16
Chicago 16
Hangzhou 16
Warsaw 15
The Dalles 14
Orem 13
Paris 13
Jakarta 12
Johannesburg 12
Taizhou 12
Toronto 12
Biên Hòa 11
Fuzhou 11
Haikou 11
Nuremberg 11
Phoenix 11
Atlanta 10
Brooklyn 10
Falkenstein 10
Kuban 10
Montreal 10
Norwalk 10
Totale 9.697
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Nome #
Which elderly newly diagnosed glioblastoma patients can benefit from radiotherapy and temozolomide? A PERNO prospective study 272
Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells 257
Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant. 255
Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways 254
Association of hereditary thrombocythemia and distal limb defects with a thrombopoietin gene mutation. 249
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity. 238
An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. 238
Double-heterozygous mutations involving both HNF1A (MODY3) and HNF4A (MODY1) genes: a case report 231
A Greek Family with a Follicular Variant of Familial Papillary Thyroid Carcinoma: TCO, MNG1, fPTC/PRN, and NMTC1 Excluded as Susceptibility Loci 230
A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24. 229
The KIT Gene Is Associated with the English Spotting Coat Color Locus and Congenital Megacolon in Checkered Giant Rabbits (Oryctolagus cuniculus) 221
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III 216
The RET51/FKBP52 complex and its involvement in Parkinson disease. 215
An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene. 212
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 202
Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration 200
Fluorescence quantitation of thyrocyte iodide accumulation with the yellow fluorescent protein variant YFP-H148Q/I152L 198
Incidence of neuroepithelial primary brain tumors among adult population of Emilia-Romagna Region, Italy 198
Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma 196
Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction. 195
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours. 194
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines. 193
A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function 190
Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer. 185
Mitochondrial DNA mutations in oncocytic adnexal lacrimal glands of the conjunctiva 185
First evidence of association between past environmental exposure to dioxin and DNA methylation of CYP1A1 and IGF2 genes in present day Vietnamese population 185
The Impairment of Cell Metabolism by Cardiovascular Toxicity of Doxorubicin Is Reversed by Bergamot Polyphenolic Fraction Treatment in Endothelial Cells 184
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 182
AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomics 182
Polymorphic NumtS trace human population relationships 181
Linkage disequilibrium patterns and tagSNP transferability among European populations. 177
The tyrosine kinase receptor RET interacts in vivo with aryl hydrocarbon receptor-interacting protein to alter survivin availability. 175
C620R mutation of the murine ret proto-oncogene: loss of function effect in homozygotes and possible gain of function effect in heterozygotes. 175
Discordant patterns of mtDNA and ethno-linguistic variation in 14 Iranian Ethnic groups. 173
Variabilità e funzione delle mutazioni mitocondriali in condizioni fisiologiche e patologiche 173
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 171
A cellular model for cancer progression: Role of mitochondrial mutations and metabolism 171
The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma 171
Allelic loss on chromosomes 2q21 and 19p13.2 in Hürthle thyroid tumors. 170
GSTT1 and M1 polymorphisms in Hurthle thyroid cancer patients 168
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 168
A Yellow Fluorescent Protein variant as an intracellular iodide biosensor in thyroid cells 167
TOM: enhancement and extension of a tool suite for in silico approaches to multigenic complex disorders. 164
TOM: a web-based integrated approach for identification of candidate disease genes 161
Genetic Predisposition to Familial Neuroblastoma: Identification of Two Novel Genomic Regions at 2p and 12p. 160
Perchlorate transport and inhibition of the Sodium Iodide Symporter measured with the Yellow Fluorescent Protein variant YFP-H148Q/I152L. 158
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. 157
The genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilization 157
EXCAVATOR: detecting copy number variants from whole-exome sequencing data. 157
Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer. 156
Simple Method for Haplotyping the Poly(TG) Repeat in Individuals Carrying the IVS8 5T Allele in the CFTR Gene. 155
Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genes. 154
EX-HOM (EXome-HOMozygosity): a proof of principle 154
H+-slip correlated to rotor free-wheeling as cause of F1FO-ATPase dysfunction in primary mitochondrial disorders 153
Molecular genetics of human enteric neuropathies. 153
Progetto Neurooncologia Emilia Romagna - PERNO 152
Mitochondria Bioenergetic Functions and Cell Metabolism Are Modulated by the Bergamot Polyphenolic Fraction 152
Cell-based imaging of sodium iodide symporter activity with the yellow fluorescent protein variant YFP-H148Q/I152L. 151
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 148
Mitochondrial Metabolism and Cancer 148
Searching for a needle in the haystack: comparing six methods to evaluate heteroplasmy in difficult sequence context 148
A de novo nonsense mutation of PAX6 gene in a patient with aniridia, ataxia, and mental retardation 148
Endothelin receptor B (EDNRB) is not the causative gene of the English spotting locus in the domestic rabbit (Oryctolagus cuniculus) 146
Relevance of Mitochondrial Genetics and Metabolism in Cancer Development 146
Learning from oncocytic tumors: why choose inefficient mitochondria? 144
Molecular mechanisms of naringenin modulation of mitochondrial permeability transition acting on F1FO-ATPase and counteracting saline load-induced injury in SHRSP cerebral endothelial cells 142
Thrombophilia and venous thromboembolism. International consensus statement. Guidelines according to scientific evidence. 142
Genetic Predisposition to Familial Nonmedullary Thyroid Cancer: An Update of Molecular Findings and State-of-the-Art Studies 139
Novel germline variants identified in the inner mitochondrial membrane transporter TIMM44 and their role in predisposition to oncocytic thyroid carcinomas. 138
Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma. 137
Molecular features of thyroid oncocytic tumors 135
Plasma membrane oxidoreductase activity in cultured cells in relation to mitochondrial function and oxidative stress. 134
PREVALENCE OF GJB2 , GJB6 AND A1555G MUTATIONS IN THE ITALIAN POPULATION 134
Psychological consequences of prenatal diagnosis in a case of familial Angelman syndrome 133
Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in renal oncocytoma 130
Interleukin-4/interleukin-4 receptor gene polymorphisms in hand osteoarthritis 128
Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic Phenotype. 126
H3M2: detection of runs of homozygosity from whole-exome sequencing data 123
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 121
mtDNA inherited and somatic variability in Alzheimer’s disease 121
Mitochondrial activities of a cell line derived from thyroid Hurthle cell tumors 120
Functional genomics of thyroid oncocytoma 118
High variability of TLR4 gene in different ethnic groups in Iran 117
Synovitis, Acne, Pustulosis, Hyperostosis, Osteitis (SAPHO) syndrome: is PTPN22 involved? 114
TRANSMIT - Translational significance of mitochondrial mutations in tumors 111
Bergamot derivative compounds affect on F1FO-ATPase and the mitochondrial permeability transition 109
RET Protooncogene 108
NOVEL ANTICANCER THERAPEUTICS BASED ON MODULATION OF APOPTOSIS THROUGH DEPENDENCE RECEPTORS (HERMIONE) 90
Enjoy your journey: the bergamot polyphenols from the tree to the cell metabolism 89
‘Rotor free-wheeling’ in impaired F1FO-ATPase induces congenital hypermetabolism 89
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 34
Totale 15.190
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Categoria #
all - tutte 39.017
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 39.017
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021540 0 0 0 0 0 0 0 0 0 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
2025/20263.815 339 409 417 316 464 267 357 163 824 259 0 0
Totale 15.190