IRIS
COCOZZA, SERGIO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 5.843
AS - Asia 5.653
EU - Europa 4.325
SA - Sud America 712
AF - Africa 147
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 8
Totale 16.697
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 5.640
SG - Singapore 2.697
RU - Federazione Russa 1.792
VN - Vietnam 1.017
CN - Cina 961
IT - Italia 778
BR - Brasile 580
HK - Hong Kong 452
DE - Germania 427
FR - Francia 230
FI - Finlandia 218
UA - Ucraina 212
NL - Olanda 181
GB - Regno Unito 130
CA - Canada 124
IE - Irlanda 111
IN - India 96
SE - Svezia 85
JP - Giappone 80
BD - Bangladesh 70
AR - Argentina 45
ZA - Sudafrica 43
MX - Messico 42
PL - Polonia 42
IQ - Iraq 39
CI - Costa d'Avorio 36
PH - Filippine 33
ES - Italia 29
ID - Indonesia 27
EC - Ecuador 26
KR - Corea 25
AT - Austria 22
TH - Thailandia 22
PK - Pakistan 20
TR - Turchia 20
TW - Taiwan 15
VE - Venezuela 15
CO - Colombia 12
MT - Malta 12
TN - Tunisia 11
ET - Etiopia 10
PY - Paraguay 10
LT - Lituania 8
MA - Marocco 8
UY - Uruguay 8
BE - Belgio 7
IL - Israele 7
IR - Iran 7
JO - Giordania 7
SA - Arabia Saudita 7
UZ - Uzbekistan 7
AU - Australia 6
CL - Cile 6
CZ - Repubblica Ceca 6
JM - Giamaica 6
KZ - Kazakistan 6
PE - Perù 6
CR - Costa Rica 5
KE - Kenya 5
RO - Romania 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
EG - Egitto 4
LB - Libano 4
MY - Malesia 4
NI - Nicaragua 4
NP - Nepal 4
TT - Trinidad e Tobago 4
AL - Albania 3
BG - Bulgaria 3
BW - Botswana 3
DJ - Gibuti 3
DK - Danimarca 3
DZ - Algeria 3
EU - Europa 3
GA - Gabon 3
GD - Grenada 3
GR - Grecia 3
GT - Guatemala 3
KH - Cambogia 3
OM - Oman 3
PA - Panama 3
RS - Serbia 3
SN - Senegal 3
UG - Uganda 3
XK - ???statistics.table.value.countryCode.XK??? 3
BA - Bosnia-Erzegovina 2
BB - Barbados 2
BO - Bolivia 2
CG - Congo 2
CH - Svizzera 2
DO - Repubblica Dominicana 2
EE - Estonia 2
HN - Honduras 2
IS - Islanda 2
KG - Kirghizistan 2
LK - Sri Lanka 2
NC - Nuova Caledonia 2
PS - Palestinian Territory 2
SK - Slovacchia (Repubblica Slovacca) 2
Totale 16.668
Salva come PNG Salva come JPEG
Città #
Singapore 1.234
San Jose 841
Chandler 542
Ashburn 532
Moscow 483
Hong Kong 430
Beijing 288
Ho Chi Minh City 284
Jacksonville 254
Hanoi 238
Santa Clara 188
Millbury 172
The Dalles 172
Amsterdam 166
Los Angeles 157
Princeton 155
Dallas 150
Lauterbourg 149
Boston 123
Naples 119
Nanjing 115
Napoli 106
Wilmington 78
Tokyo 76
Buffalo 75
Munich 72
New York 68
São Paulo 55
Ottawa 54
Redondo Beach 43
Ann Arbor 42
Haiphong 42
Da Nang 40
Hefei 38
Frankfurt am Main 37
Helsinki 37
Chicago 33
Orem 33
Warsaw 33
Washington 33
Seattle 32
Rome 30
Chennai 29
Des Moines 29
Montreal 29
Nanchang 28
Council Bluffs 27
San Francisco 27
Shenyang 27
Brooklyn 26
Norwalk 25
Denver 24
Houston 24
Kronberg 22
Turku 22
Boardman 21
Changsha 21
Hebei 21
Mexico City 21
Dong Ket 20
Johannesburg 20
Jiaxing 19
Lawrence 19
Rio de Janeiro 19
Nuremberg 18
Poplar 17
Salerno 17
Toronto 17
Falls Church 16
Thái Bình 16
Woodbridge 16
Atlanta 15
Dearborn 15
London 15
Manchester 15
Tianjin 15
Biên Hòa 14
Stockholm 14
Baghdad 13
Kunming 13
Milan 13
Nocera Superiore 13
Cagliari 12
Melita 12
Phoenix 12
Shanghai 12
Belo Horizonte 11
Guayaquil 11
Mumbai 11
Porto Alegre 11
Campinas 10
Curitiba 10
Hải Dương 10
Manassas 10
Vienna 10
Bangkok 9
Falkenstein 9
Guangzhou 9
Guarulhos 9
Tân Tiến 9
Totale 8.828
Salva come PNG Salva come JPEG
Nome #
Tracking the evolution of epialleles during neural differentiation and brain development: D-Aspartate oxidase as a model gene 277
Association between DNA methylation profile and malignancy in follicular-patterned thyroid neoplasms 247
Sex-related alterations of gut microbiota composition in the BTBR mouse model of autism spectrum disorder. 216
DNA methylation landscape of the genes regulating D-serine and D-aspartate metabolism in post-mortem brain from controls and subjects with schizophrenia [*Keller S., Punzo D., Cuomo M co-primi autori] 194
Selective demethylation of two CpG sites causes postnatal activation of the Dao gene and consequent removal of D-serine within the mouse cerebellum 194
The genomic landscape of 8-oxodG reveals enrichment at specific inherently fragile promoters 193
Identification of candidate children for maturity-onset diabetes of the young type 2 (MODY2) gene testing: a seven-item clinical flowchart (7-iF). 189
Modelling DNA methylation by analyzing the individual configurations of single molecules 181
Epoetin alfa increases frataxin production in Friedreich's ataxia without affecting hematocrit. 176
ampliMethProfiler: a pipeline for the analysis of CpG methylation profiles of targeted deep bisulfite sequenced amplicons 164
Genome-wide mapping of 8-oxo-7,8-dihydro-2'-deoxyguanosine reveals accumulation of oxidatively-generated damage at DNA replication origins within transcribed long genes of mammalian cells 160
Adiponectin gene polymorphism and metabolic syndrome 158
A novel approach to simulate gene-environment interactions in complex diseases 157
Beta2-adrenergic receptor and UCP3 variants modulate the relationship between age and type 2 diabetes mellitus 152
Continuous and discontinuous phase transitions in the evolution of a polygenic trait under stabilizing selective pressure 152
Influence of GAA expansion size and disease duration on Central Nervous System impairment in Friedreich's Ataxia. Contribution to the understanding of the pathophysiology of the disease 151
Extra-mitochondrial localisation of frataxin and its association with IscU1 during enterocyte-like differentiation of the human colon adenocarcinoma cell line Caco-2. 151
The combination of UCP3-55CT and PPARγ2Pro12Ala polymorphisms affects BMI and substrate oxidation in two diabetic populations 150
Increased BDNF promoter methylation in the wernicke area of suicide subjects. 149
Dna methylation profiles of tph1a and bdnf in gut and brain of l. Rhamnosus-treated zebrafish 146
A novel workflow for the qualitative analysis of DNA methylation data 144
Autosomal dominant cerebellar ataxia type I: multimodal electrophysiological study and comparison between SCA1 and SCA2 patients 143
Improving the Estimation of Celiac Disease Sibling Risk by Non-HLA Genes. 142
Up-regulation of c-Jun N-terminal kinase pathway in Friedreich's ataxia cells. 139
Candidate genes and pathways downstream of PAX8 involved in ovarian high-grade serous carcinoma 139
Identification of C12orf4 as a gene for autosomal recessive intellectual disability 138
Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian families 137
A novel thyroid transcript negatively regulated by TSH. 137
Epigenetic remodelling of Fxyd1 promoters in developing heart and brain tissues [*Cuomo, M co-corresponding] 136
Recombinant human erythropoietin increasesfrataxin protein expression without increasing mRNA expression 135
Evidence for Evolutionary and Nonevolutionary Forces Shaping the Distribution of Human Genetic Variants near Transcription Start Sites 135
Pro12Ala polymorphism of the PPARgamma2 locus modulates the relationship between energy intake and body weight in type 2 diabetic patients 134
Uncoupling protein 2 G(-866)A polymorphism: a new gene polymorphism associated with C-reactive protein in type 2 diabetic patients. 134
PPAR-gamma Agonist Azelaoyl PAF Increases Frataxin Protein and mRNA Expression. New Implications for the Friedreich's Ataxia Therapy 133
Down-regulation of otospiralin mRNA in response to acoustic stress in guinea pig 132
MC profiling: a novel approach to analyze DNA methylation heterogeneity in genome-wide bisulfite sequencing data 131
Simulating gene-gene and gene-environment interactions in complex diseases: Gene-Environment iNteraction Simulator 2 131
Prevalence of GLA gene mutations and polymorphisms in patients with multiple sclerosis: A cross-sectional study 131
Subcellular localisation of frataxin in Human Colon Carcinoma Cell line 130
Granulocyte Macrophage-Colony Stimulating Factor receptor expression on human cardiomyocytes from end-stage heart failure patients 129
DNA Methylation variability among individuals is related to CpGs cluster density and evolutionary signatures 128
An Interactive Tool for Data Visualization and Clustering 126
Whole transcriptome targeted gene quantification provides new insights on pulmonary sarcomatoid carcinomas 125
A novel thyroid transcript negatively regulated by TSH. 124
Friedreich's disease. A linkage study in southern andcentral Italy. 123
The PPARγ2 Pro12Ala variant is protective against progression of nephropathy in people with type 2 diabetes 122
DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich's ataxia patients. 121
DNA methylation impact on Fabry disease 121
A distinct group of CpG islands shows differential DNA methylation between replicas of the same cell line in vitro 120
Clustering, Assessment and Validation: an application to gene expression data 116
INTERGENERATIONAL INSTABILITY AND MARKED ANTICIPATION IN SCA-17. 115
Ultra-deep dna methylation analysis of x-linked genes: Gla and ar as model genes [*De Riso G., Cuomo M co-primi autori] 115
Modeling DNA methylation profiles through a dynamic equilibrium between methylation and demethylation 114
Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPAR{gamma} pathway as a therapeutic target in Friedreich's ataxia. 113
Influence of GAA expansion size and disease duration on central nervous system impairment in Friedreich's ataxia: contribution to the understanding of the pathophysiology of the disease. 111
The energy intake modulates the association of the 55CT polymorphism of UCP3 with body weight in type 2 diabetic patients 111
An improved combinatorial biclustering algorithm 110
New clues on the origin of the Friedreich ataxia expanded alleles from the analysis of new polymorphisms closely linked to the mutation. 109
NIDDM Associated With Mutation In Tyrosine Kinase Domain of Insulin-receptor Gene 109
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease 108
Schizophrenia and Vitamin D Related Genes Could Have Been Subject to Latitude-driven Adaptation. 108
Triplet repeat instability correlates with dinucleotide instability in primary breast cancer. 107
Accuracy of clinical diagnostic criteria for Friedreich's ataxia. 107
Can telomere shortening in human peripheral blood leukocytes serve as a disease biomarker of Friedreich's ataxia? 107
3-Nitropropionic acid increases frataxin expression in human lymphoblasts and in transgenic rat PC12 cells. 106
Friedreich's disease. A linkage study in southern and central Italy. 105
CpG islands under selective pressure are enriched with H3K4me3, H3K27ac and H3K36me3 histone modifications. 105
Effect of human Granulocyte Macrophage Colony- Stimulating Factor on differentiation and apoptosis of human osteosarcoma cell line SaOS-2 104
Genome-wide scan for signatures of human population differentiation and their relationship with natural selection, functional pathways and diseases. 104
Progressive gaa expansions in dorsal root ganglia of Friedreich's ataxia patients. 103
Serum transferrin receptor levels in Friedreich's and other degenerative ataxias. 101
Oxidative DNA Damage and Activation of c-Jun N-Terminal Kinase Pathway in Fibroblasts from Patients with Hereditary Spastic Paraplegia. 101
Artificial intelligence for epigenetics: Towards personalized medicine 101
Early onset ataxia with cardiomyopathy and retained tendon reflexes maps to the Friedreich's ataxia locus on chromosome 9q. 100
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. 100
Participation to Leisure Activities and Well-Being in a Group of Residents of Naples-Italy: The Role of Resilience 100
Evidence of a genetic marker for early onset in Friedreich's ataxia. 99
Nucleotide distance influences co-methylation between nearby CpG sites 99
Quantitative evaluation of type I collagen in human cardiac tissue by real-time PCR: A possible usefulness in patients with a chronic cardiopathy 97
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease. 96
Interactive data analysis and clustering of genomic data. 95
GASTRIC CANCER BIOLOGICAL BEHAVIOUR: FROM BIOINFORMATIC HYPOTHESIS TO MOLECULAR ANALYSIS 95
Autosomal dominant cerebellar ataxia type I: multimodal electrophysiological study and comparison between SCA1 and SCA2 patients. 93
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. 92
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. 92
The Friedreich ataxia GAA triplet repeat: premutation and normal alleles. 91
Signs of selective pressure on genetic variants affecting human height 91
Methodological aspects of the assessment of gene-nutrient interactions at the population level 90
Ananlisi molecolari delle malattie genetiche ereditarie ad elevato impatto sociale. 90
3-Nitropropionic acid increases frataxin expression in humanlymphoblasts and in transgenic rat PC12 cells 88
Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian population. 85
Somatic instability of the expanded GAA triplet-repeat sequence in Friedreich ataxia progresses throughout life. 84
Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy. 84
Mitochondrial DNA haplogroups influence the Friedreich's ataxia phenotype. 82
Studio molecolare epidemiologico su alcune malattie ereditarie a maggiore impatto sociale e loro rapporto con il fenotipo. 81
Up-regulation of c-Jun N-terminal kinase pathway in Friedreich's ataxia cells. 80
A pathogenetic classification of hereditary ataxias: is the time ripe? 80
Spastic Paraplegia and OXOPHOS impairment caused by mutations in Paraplegin, a Nuclear-encoded mitochondrial metalloprotease 79
Friedreich's ataxia after gene cloning. The sensitivity and specificity of clinical diagnosis. 79
A combined nucleic acid and protein analysis in Friedreich ataxia: implications for diagnosis, pathogenesis and clinical trial design. 79
Totale 12.388
Salva come PNG Salva come JPEG
Categoria #
all - tutte 55.014
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 55.014
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202133 0 0 0 0 0 0 0 0 0 0 0 33
2021/2022921 22 0 13 11 3 16 5 27 128 60 209 427
2022/20231.275 196 110 23 122 134 143 26 99 179 172 61 10
2023/2024778 33 93 60 59 41 99 20 171 5 13 140 44
2024/20254.177 242 264 14 48 129 196 335 260 491 413 1.407 378
2025/20267.584 951 478 733 729 1.436 282 895 348 988 532 153 59
Totale 16.931