IRIS
COCOZZA, SERGIO
 Distribuzione geografica
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Continente #
NA - Nord America 6.861
AS - Asia 5.685
EU - Europa 4.404
SA - Sud America 729
Continente sconosciuto - Info sul continente non disponibili 243
AF - Africa 148
OC - Oceania 9
Totale 18.079
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Nazione #
US - Stati Uniti d'America 6.592
SG - Singapore 2.700
RU - Federazione Russa 1.793
VN - Vietnam 1.017
CN - Cina 972
IT - Italia 819
BR - Brasile 588
HK - Hong Kong 453
DE - Germania 427
FR - Francia 233
FI - Finlandia 218
UA - Ucraina 212
NL - Olanda 183
CA - Canada 151
GB - Regno Unito 149
IE - Irlanda 111
IN - India 96
SE - Svezia 85
BD - Bangladesh 81
JP - Giappone 80
AR - Argentina 46
MX - Messico 43
ZA - Sudafrica 43
PL - Polonia 42
IQ - Iraq 39
CI - Costa d'Avorio 36
PH - Filippine 33
ES - Italia 31
EC - Ecuador 28
ID - Indonesia 28
KR - Corea 25
TH - Thailandia 24
AT - Austria 22
PK - Pakistan 21
TR - Turchia 20
CO - Colombia 16
JM - Giamaica 16
TW - Taiwan 15
VE - Venezuela 15
MT - Malta 12
CR - Costa Rica 11
TN - Tunisia 11
ET - Etiopia 10
PY - Paraguay 10
BE - Belgio 8
EE - Estonia 8
LT - Lituania 8
MA - Marocco 8
NI - Nicaragua 8
UY - Uruguay 8
CL - Cile 7
IL - Israele 7
IR - Iran 7
JO - Giordania 7
PE - Perù 7
SA - Arabia Saudita 7
UZ - Uzbekistan 7
AU - Australia 6
CZ - Repubblica Ceca 6
HN - Honduras 6
KZ - Kazakistan 6
TT - Trinidad e Tobago 6
KE - Kenya 5
NP - Nepal 5
RO - Romania 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
BB - Barbados 4
DO - Repubblica Dominicana 4
EG - Egitto 4
GT - Guatemala 4
LB - Libano 4
MY - Malesia 4
PA - Panama 4
RS - Serbia 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
KH - Cambogia 3
OM - Oman 3
SN - Senegal 3
UG - Uganda 3
XK - ???statistics.table.value.countryCode.XK??? 3
AM - Armenia 2
BA - Bosnia-Erzegovina 2
BO - Bolivia 2
CG - Congo 2
CH - Svizzera 2
HU - Ungheria 2
IS - Islanda 2
KG - Kirghizistan 2
LK - Sri Lanka 2
NC - Nuova Caledonia 2
Totale 17.804
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Città #
Singapore 1.235
San Jose 1.021
Ashburn 657
Chandler 543
Moscow 483
Hong Kong 431
Council Bluffs 294
Beijing 289
Ho Chi Minh City 284
Jacksonville 255
Hanoi 238
Santa Clara 208
Millbury 172
The Dalles 172
Los Angeles 168
Amsterdam 166
Princeton 160
Dallas 157
Lauterbourg 149
Naples 127
Boston 123
Nanjing 115
Napoli 106
Wilmington 80
Buffalo 78
Tokyo 76
New York 75
Munich 72
São Paulo 58
Ottawa 54
Phoenix 49
Redondo Beach 43
Ann Arbor 42
Haiphong 42
Rome 41
Da Nang 40
Chicago 39
Hefei 38
Frankfurt am Main 37
Helsinki 37
Washington 36
Seattle 34
Orem 33
Warsaw 33
Montreal 32
Chennai 29
Des Moines 29
Brooklyn 28
Nanchang 28
San Francisco 28
Shenyang 27
Norwalk 26
Denver 25
Houston 25
Toronto 24
Kronberg 22
Mexico City 22
Turku 22
Boardman 21
Changsha 21
Hebei 21
Dong Ket 20
Johannesburg 20
Jiaxing 19
Lawrence 19
Rio de Janeiro 19
Atlanta 18
Nuremberg 18
Poplar 17
Salerno 17
Falls Church 16
Shanghai 16
Thái Bình 16
Woodbridge 16
Dearborn 15
London 15
Manchester 15
Tianjin 15
Biên Hòa 14
Milan 14
Stockholm 14
Baghdad 13
Kunming 13
Nocera Superiore 13
Cagliari 12
Melita 12
Bangkok 11
Belo Horizonte 11
Guayaquil 11
Mumbai 11
Porto Alegre 11
Campinas 10
Curitiba 10
Hải Dương 10
Kingston 10
Manassas 10
Philadelphia 10
Vienna 10
Columbus 9
Falkenstein 9
Totale 9.559
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Nome #
Tracking the evolution of epialleles during neural differentiation and brain development: D-Aspartate oxidase as a model gene 292
Association between DNA methylation profile and malignancy in follicular-patterned thyroid neoplasms 258
Sex-related alterations of gut microbiota composition in the BTBR mouse model of autism spectrum disorder. 226
Selective demethylation of two CpG sites causes postnatal activation of the Dao gene and consequent removal of D-serine within the mouse cerebellum 209
The genomic landscape of 8-oxodG reveals enrichment at specific inherently fragile promoters 205
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] 204
Identification of candidate children for maturity-onset diabetes of the young type 2 (MODY2) gene testing: a seven-item clinical flowchart (7-iF). 197
Modelling DNA methylation by analyzing the individual configurations of single molecules 191
Epoetin alfa increases frataxin production in Friedreich's ataxia without affecting hematocrit. 187
ampliMethProfiler: a pipeline for the analysis of CpG methylation profiles of targeted deep bisulfite sequenced amplicons 171
A novel approach to simulate gene-environment interactions in complex diseases 170
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 170
Adiponectin gene polymorphism and metabolic syndrome 162
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 161
Extra-mitochondrial localisation of frataxin and its association with IscU1 during enterocyte-like differentiation of the human colon adenocarcinoma cell line Caco-2. 160
The combination of UCP3-55CT and PPARγ2Pro12Ala polymorphisms affects BMI and substrate oxidation in two diabetic populations 160
Continuous and discontinuous phase transitions in the evolution of a polygenic trait under stabilizing selective pressure 160
Beta2-adrenergic receptor and UCP3 variants modulate the relationship between age and type 2 diabetes mellitus 158
Increased BDNF promoter methylation in the wernicke area of suicide subjects. 155
Identification of C12orf4 as a gene for autosomal recessive intellectual disability 154
Dna methylation profiles of tph1a and bdnf in gut and brain of l. Rhamnosus-treated zebrafish 154
A novel thyroid transcript negatively regulated by TSH. 153
A novel workflow for the qualitative analysis of DNA methylation data 150
Autosomal dominant cerebellar ataxia type I: multimodal electrophysiological study and comparison between SCA1 and SCA2 patients 150
Improving the Estimation of Celiac Disease Sibling Risk by Non-HLA Genes. 150
Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian families 148
Up-regulation of c-Jun N-terminal kinase pathway in Friedreich's ataxia cells. 147
Candidate genes and pathways downstream of PAX8 involved in ovarian high-grade serous carcinoma 147
Recombinant human erythropoietin increasesfrataxin protein expression without increasing mRNA expression 144
Pro12Ala polymorphism of the PPARgamma2 locus modulates the relationship between energy intake and body weight in type 2 diabetic patients 142
Uncoupling protein 2 G(-866)A polymorphism: a new gene polymorphism associated with C-reactive protein in type 2 diabetic patients. 142
Prevalence of GLA gene mutations and polymorphisms in patients with multiple sclerosis: A cross-sectional study 142
MC profiling: a novel approach to analyze DNA methylation heterogeneity in genome-wide bisulfite sequencing data 141
Down-regulation of otospiralin mRNA in response to acoustic stress in guinea pig 141
Evidence for Evolutionary and Nonevolutionary Forces Shaping the Distribution of Human Genetic Variants near Transcription Start Sites 141
Epigenetic remodelling of Fxyd1 promoters in developing heart and brain tissues [*Cuomo, M co-corresponding] 141
PPAR-gamma Agonist Azelaoyl PAF Increases Frataxin Protein and mRNA Expression. New Implications for the Friedreich's Ataxia Therapy 139
Simulating gene-gene and gene-environment interactions in complex diseases: Gene-Environment iNteraction Simulator 2 138
DNA Methylation variability among individuals is related to CpGs cluster density and evolutionary signatures 137
Granulocyte Macrophage-Colony Stimulating Factor receptor expression on human cardiomyocytes from end-stage heart failure patients 136
Subcellular localisation of frataxin in Human Colon Carcinoma Cell line 135
Whole transcriptome targeted gene quantification provides new insights on pulmonary sarcomatoid carcinomas 135
An Interactive Tool for Data Visualization and Clustering 133
A novel thyroid transcript negatively regulated by TSH. 131
The PPARγ2 Pro12Ala variant is protective against progression of nephropathy in people with type 2 diabetes 130
DNA methylation impact on Fabry disease 130
Ultra-deep dna methylation analysis of x-linked genes: Gla and ar as model genes [*De Riso G., Cuomo M co-primi autori] 130
Friedreich's disease. A linkage study in southern andcentral Italy. 127
DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich's ataxia patients. 127
Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPAR{gamma} pathway as a therapeutic target in Friedreich's ataxia. 124
INTERGENERATIONAL INSTABILITY AND MARKED ANTICIPATION IN SCA-17. 123
A distinct group of CpG islands shows differential DNA methylation between replicas of the same cell line in vitro 123
Clustering, Assessment and Validation: an application to gene expression data 119
Modeling DNA methylation profiles through a dynamic equilibrium between methylation and demethylation 119
New clues on the origin of the Friedreich ataxia expanded alleles from the analysis of new polymorphisms closely linked to the mutation. 118
The energy intake modulates the association of the 55CT polymorphism of UCP3 with body weight in type 2 diabetic patients 117
Triplet repeat instability correlates with dinucleotide instability in primary breast cancer. 116
Schizophrenia and Vitamin D Related Genes Could Have Been Subject to Latitude-driven Adaptation. 116
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. 116
NIDDM Associated With Mutation In Tyrosine Kinase Domain of Insulin-receptor Gene 115
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease 114
Artificial intelligence for epigenetics: Towards personalized medicine 114
Friedreich's disease. A linkage study in southern and central Italy. 113
Can telomere shortening in human peripheral blood leukocytes serve as a disease biomarker of Friedreich's ataxia? 113
An improved combinatorial biclustering algorithm 112
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. 112
CpG islands under selective pressure are enriched with H3K4me3, H3K27ac and H3K36me3 histone modifications. 111
Progressive gaa expansions in dorsal root ganglia of Friedreich's ataxia patients. 110
Effect of human Granulocyte Macrophage Colony- Stimulating Factor on differentiation and apoptosis of human osteosarcoma cell line SaOS-2 110
3-Nitropropionic acid increases frataxin expression in human lymphoblasts and in transgenic rat PC12 cells. 110
Accuracy of clinical diagnostic criteria for Friedreich's ataxia. 109
Genome-wide scan for signatures of human population differentiation and their relationship with natural selection, functional pathways and diseases. 109
Serum transferrin receptor levels in Friedreich's and other degenerative ataxias. 106
Participation to Leisure Activities and Well-Being in a Group of Residents of Naples-Italy: The Role of Resilience 106
Early onset ataxia with cardiomyopathy and retained tendon reflexes maps to the Friedreich's ataxia locus on chromosome 9q. 105
Oxidative DNA Damage and Activation of c-Jun N-Terminal Kinase Pathway in Fibroblasts from Patients with Hereditary Spastic Paraplegia. 105
Nucleotide distance influences co-methylation between nearby CpG sites 105
Evidence of a genetic marker for early onset in Friedreich's ataxia. 104
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease. 104
The Friedreich ataxia GAA triplet repeat: premutation and normal alleles. 103
Quantitative evaluation of type I collagen in human cardiac tissue by real-time PCR: A possible usefulness in patients with a chronic cardiopathy 103
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. 101
Interactive data analysis and clustering of genomic data. 100
Autosomal dominant cerebellar ataxia type I: multimodal electrophysiological study and comparison between SCA1 and SCA2 patients. 100
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. 99
GASTRIC CANCER BIOLOGICAL BEHAVIOUR: FROM BIOINFORMATIC HYPOTHESIS TO MOLECULAR ANALYSIS 98
Ananlisi molecolari delle malattie genetiche ereditarie ad elevato impatto sociale. 97
A genetic polymorphism of the apolipoprotein Al-CIII gene cluster is associated with coronary heart disease in non-insulin dependent diabetes mellitus 97
Methodological aspects of the assessment of gene-nutrient interactions at the population level 95
Signs of selective pressure on genetic variants affecting human height 95
Somatic instability of the expanded GAA triplet-repeat sequence in Friedreich ataxia progresses throughout life. 93
Mitochondrial DNA haplogroups influence the Friedreich's ataxia phenotype. 92
Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy. 91
3-Nitropropionic acid increases frataxin expression in humanlymphoblasts and in transgenic rat PC12 cells 91
Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian population. 88
THREE METHODS TO INCREASE THE LIKELY TO IDENTIFY GENE INVOLVED IN COMPLEX DISEASE 87
Up-regulation of c-Jun N-terminal kinase pathway in Friedreich's ataxia cells. 86
Studio molecolare epidemiologico su alcune malattie ereditarie a maggiore impatto sociale e loro rapporto con il fenotipo. 86
A combined nucleic acid and protein analysis in Friedreich ataxia: implications for diagnosis, pathogenesis and clinical trial design. 86
Friedreich's ataxia after gene cloning. The sensitivity and specificity of clinical diagnosis. 85
Totale 13.162
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Categoria #
all - tutte 62.822
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 62.822
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022886 0 0 0 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
2025/20267.677 951 478 733 729 1.436 282 895 348 988 532 153 152
2026/20271.055 136 250 297 372 0 0 0 0 0 0 0 0
Totale 18.079