Distribuzione geografica
Continente #
NA - Nord America 2.355
EU - Europa 1.622
AS - Asia 370
Continente sconosciuto - Info sul continente non disponibili 3
SA - Sud America 2
Totale 4.352
Nazione #
US - Stati Uniti d'America 2.301
IT - Italia 600
CN - Cina 329
DE - Germania 240
UA - Ucraina 186
NL - Olanda 165
FI - Finlandia 154
IE - Irlanda 109
SE - Svezia 73
CA - Canada 54
GB - Regno Unito 45
VN - Vietnam 20
FR - Francia 19
MT - Malta 12
IN - India 10
IR - Iran 6
PL - Polonia 4
RO - Romania 4
ES - Italia 3
EU - Europa 3
TR - Turchia 3
CH - Svizzera 2
RS - Serbia 2
SG - Singapore 2
BE - Belgio 1
BR - Brasile 1
DK - Danimarca 1
EE - Estonia 1
HU - Ungheria 1
PE - Perù 1
Totale 4.352
Città #
Chandler 542
Jacksonville 253
Millbury 172
Amsterdam 160
Princeton 155
Nanjing 114
Napoli 106
Boston 104
Wilmington 76
Beijing 62
Naples 59
Ottawa 51
Ann Arbor 42
Nanchang 28
Des Moines 27
Norwalk 25
Shenyang 25
Hebei 21
Dong Ket 20
Jiaxing 19
Lawrence 19
Falls Church 16
Woodbridge 16
Boardman 15
Dearborn 15
Changsha 14
Kunming 13
Nocera Superiore 13
Houston 12
Melita 12
Salerno 12
Tianjin 12
Rome 9
San Francisco 9
Brest 7
Lombard 7
Manassas 7
Orange 7
Pannarano 7
Ardabil 6
Ashburn 5
Bologna 5
Monmouth Junction 5
Noci 5
Pozzuoli 5
Redwood City 5
San Mateo 5
Tito 5
Vimercate 5
Augusta 4
Changchun 4
Fairfield 4
Milan 4
Paterno 4
Redmond 4
Scafati 4
Shanghai 4
Tappahannock 4
Washington 4
Berlin 3
Casoria 3
Dublin 3
Hangzhou 3
Lanzhou 3
Leawood 3
New York 3
Nola 3
Poli 3
Polska 3
Stockholm 3
Basel 2
Bisaccia 2
Caivano 2
Cambridge 2
Casale Cremasco 2
Caserta 2
Castiglione in Teverina 2
Formia 2
Guangzhou 2
Horia 2
Indiana 2
Marano 2
Melizzano 2
Mountain View 2
Mumbai 2
Oviedo 2
Paris 2
Quartu Sant'elena 2
Romainville 2
Sant'arpino 2
Somma Vesuviana 2
Toronto 2
Walnut 2
Acerra 1
Afragola 1
Altavilla Silentina 1
Arezzo 1
Barcelona 1
Bethesda 1
Brussels 1
Totale 2.460
Nome #
Association between DNA methylation profile and malignancy in follicular-patterned thyroid neoplasms 112
Tracking the evolution of epialleles during neural differentiation and brain development: D-Aspartate oxidase as a model gene 110
Sex-related alterations of gut microbiota composition in the BTBR mouse model of autism spectrum disorder. 83
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] 80
The genomic landscape of 8-oxodG reveals enrichment at specific inherently fragile promoters 75
Modelling DNA methylation by analyzing the individual configurations of single molecules 74
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 69
ampliMethProfiler: a pipeline for the analysis of CpG methylation profiles of targeted deep bisulfite sequenced amplicons 60
Triplet repeat instability correlates with dinucleotide instability in primary breast cancer. 56
Continuous and discontinuous phase transitions in the evolution of a polygenic trait under stabilizing selective pressure 55
Epoetin alfa increases frataxin production in Friedreich's ataxia without affecting hematocrit. 54
Extra-mitochondrial localisation of frataxin and its association with IscU1 during enterocyte-like differentiation of the human colon adenocarcinoma cell line Caco-2. 52
Identification of candidate children for maturity-onset diabetes of the young type 2 (MODY2) gene testing: a seven-item clinical flowchart (7-iF). 52
Dna methylation profiles of tph1a and bdnf in gut and brain of l. Rhamnosus-treated zebrafish 52
Effect of human Granulocyte Macrophage Colony- Stimulating Factor on differentiation and apoptosis of human osteosarcoma cell line SaOS-2 51
3-Nitropropionic acid increases frataxin expression in human lymphoblasts and in transgenic rat PC12 cells. 51
Adiponectin gene polymorphism and metabolic syndrome 49
Selective demethylation of two CpG sites causes postnatal activation of the Dao gene and consequent removal of D-serine within the mouse cerebellum 49
An Interactive Tool for Data Visualization and Clustering 48
Progressive gaa expansions in dorsal root ganglia of Friedreich's ataxia patients. 47
New clues on the origin of the Friedreich ataxia expanded alleles from the analysis of new polymorphisms closely linked to the mutation. 47
Recombinant human erythropoietin increasesfrataxin protein expression without increasing mRNA expression 43
Down-regulation of otospiralin mRNA in response to acoustic stress in guinea pig 42
PPAR-gamma Agonist Azelaoyl PAF Increases Frataxin Protein and mRNA Expression. New Implications for the Friedreich's Ataxia Therapy 42
Methodological aspects of the assessment of gene-nutrient interactions at the population level 41
Accuracy of clinical diagnostic criteria for Friedreich's ataxia. 41
Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian families 41
Evidence for Evolutionary and Nonevolutionary Forces Shaping the Distribution of Human Genetic Variants near Transcription Start Sites 41
Candidate genes and pathways downstream of PAX8 involved in ovarian high-grade serous carcinoma 40
Uncoupling protein 2 G(-866)A polymorphism: a new gene polymorphism associated with C-reactive protein in type 2 diabetic patients. 39
Improving the Estimation of Celiac Disease Sibling Risk by Non-HLA Genes. 39
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. 38
A novel thyroid transcript negatively regulated by TSH. 38
Beta2-adrenergic receptor and UCP3 variants modulate the relationship between age and type 2 diabetes mellitus 37
Oxidative DNA Damage and Activation of c-Jun N-Terminal Kinase Pathway in Fibroblasts from Patients with Hereditary Spastic Paraplegia. 37
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 36
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. 36
Pro12Ala polymorphism of the PPARgamma2 locus modulates the relationship between energy intake and body weight in type 2 diabetic patients 35
Granulocyte Macrophage-Colony Stimulating Factor receptor expression on human cardiomyocytes from end-stage heart failure patients 35
A novel thyroid transcript negatively regulated by TSH. 35
Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPAR{gamma} pathway as a therapeutic target in Friedreich's ataxia. 35
Somatic instability of the expanded GAA triplet-repeat sequence in Friedreich ataxia progresses throughout life. 34
Up-regulation of c-Jun N-terminal kinase pathway in Friedreich's ataxia cells. 34
An improved combinatorial biclustering algorithm 34
Evidence of a genetic marker for early onset in Friedreich's ataxia. 33
A distinct group of CpG islands shows differential DNA methylation between replicas of the same cell line in vitro 33
Whole transcriptome targeted gene quantification provides new insights on pulmonary sarcomatoid carcinomas 33
Autosomal dominant cerebellar ataxia type I: multimodal electrophysiological study and comparison between SCA1 and SCA2 patients 32
Ananlisi molecolari delle malattie genetiche ereditarie ad elevato impatto sociale. 32
A novel approach to simulate gene-environment interactions in complex diseases 32
3-Nitropropionic acid increases frataxin expression in humanlymphoblasts and in transgenic rat PC12 cells 32
The PPARγ2 Pro12Ala variant is protective against progression of nephropathy in people with type 2 diabetes 32
Friedreich's disease. A linkage study in southern andcentral Italy. 31
Mitochondrial DNA haplogroups influence the Friedreich's ataxia phenotype. 31
Subcellular localisation of frataxin in Human Colon Carcinoma Cell line 31
Mutations in the insulin receptor gene: Val996 allele in caucasian NIDDM patients. 31
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. . 30
A pathogenetic classification of hereditary ataxias: is the time ripe? 30
A combined nucleic acid and protein analysis in Friedreich ataxia: implications for diagnosis, pathogenesis and clinical trial design. 30
DNA Methylation variability among individuals is related to CpGs cluster density and evolutionary signatures 30
Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy. 29
Friedreich's disease. A linkage study in southern and central Italy. 29
Clustering, Assessment and Validation: an application to gene expression data 29
The Friedreich ataxia GAA triplet repeat: premutation and normal alleles. 28
Identification of C12orf4 as a gene for autosomal recessive intellectual disability 28
Increased BDNF promoter methylation in the wernicke area of suicide subjects. 27
Serum transferrin receptor levels in Friedreich's and other degenerative ataxias. 26
Real-time PCR quantification of frataxin mRNA in the peripheral blood leucocytes of Friedreich ataxia patients and carriers. 26
DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich's ataxia patients. 26
Simulating gene-gene and gene-environment interactions in complex diseases: Gene-Environment iNteraction Simulator 2 26
The combination of UCP3-55CT and PPARγ2Pro12Ala polymorphisms affects BMI and substrate oxidation in two diabetic populations 26
Prevalence of GLA gene mutations and polymorphisms in patients with multiple sclerosis: A cross-sectional study 26
DNA sequence context as a marker of CpG methylation instability in normal and cancer tissues 25
A genetic polymorphism of the apolipoprotein Al-CIII gene cluster is associated with coronary heart disease in non-insulin dependent diabetes mellitus 24
NIDDM Associated With Mutation In Tyrosine Kinase Domain of Insulin-receptor Gene 24
Nucleotide distance influences co-methylation between nearby CpG sites 24
Polymorphism at the 5' end flanking region of the insulin gene is associated with reduced insulin secretion in healthy individuals 23
A dinucleotide repeat polymorphism (D9S202) in the Friedreich's ataxia region on chromosome 9q13-q21.1 23
Antiaging effect of exercise training on the rat heart: Gene expression profile approach 23
CpG islands under selective pressure are enriched with H3K4me3, H3K27ac and H3K36me3 histone modifications. 23
The energy intake modulates the association of the 55CT polymorphism of UCP3 with body weight in type 2 diabetic patients 23
Participation to Leisure Activities and Well-Being in a Group of Residents of Naples-Italy: The Role of Resilience 23
Up-regulation of c-Jun N-terminal kinase pathway in Friedreich's ataxia cells. 22
Early onset ataxia with cardiomyopathy and retained tendon reflexes maps to the Friedreich's ataxia locus on chromosome 9q. 22
Identification of a novel transcript of X25, the human gene involved in Friedreich ataxia 22
Quantitative evaluation of type I collagen in human cardiac tissue by real-time PCR: A possible usefulness in patients with a chronic cardiopathy 22
Schizophrenia and Vitamin D Related Genes Could Have Been Subject to Latitude-driven Adaptation. 22
Accuracy of clinical diagnostic criteria for Friedreich's ataxia. 22
Signs of selective pressure on genetic variants affecting human height 22
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. 22
Spastic Paraplegia and OXOPHOS impairment caused by mutations in Paraplegin, a Nuclear-encoded mitochondrial metalloprotease 21
Serum transferrin receptor levels in Friedreich's and other degenerative ataxias. 21
Can telomere shortening in human peripheral blood leukocytes serve as a disease biomarker of Friedreich's ataxia? 21
Modeling DNA methylation profiles through a dynamic equilibrium between methylation and demethylation 21
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease 20
Intergenerational instability and marked anticipation in SCA-17 19
The Complete Structure of the Rat Thyroglobulin Gene 19
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 18
Totale 3.651
Categoria #
all - tutte 12.976
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 12.976

Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019341 0 0 8 11 7 134 103 14 30 6 8 20
2019/2020625 199 3 48 5 70 27 24 8 14 47 71 109
2020/2021689 27 47 67 52 54 125 56 25 67 38 98 33
2021/2022921 22 0 13 11 3 16 5 27 128 60 209 427
2022/20231.276 196 110 23 122 134 143 26 99 180 172 61 10
2023/2024186 33 93 60 0 0 0 0 0 0 0 0 0
Totale 4.579