CRIS Current Research Information System

MARESCA, ALESSANDRA
 Distribuzione geografica
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Continente #
NA - Nord America 3.152
EU - Europa 2.251
AS - Asia 993
AF - Africa 159
SA - Sud America 17
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 2
Totale 6.583
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Nazione #
US - Stati Uniti d'America 3.136
IT - Italia 779
GB - Regno Unito 432
CN - Cina 393
SE - Svezia 272
SG - Singapore 260
DE - Germania 250
IN - India 116
VN - Vietnam 108
IE - Irlanda 89
RU - Federazione Russa 74
FR - Francia 72
CI - Costa d'Avorio 64
TG - Togo 53
UA - Ucraina 49
CH - Svizzera 33
ZA - Sudafrica 33
NL - Olanda 32
EE - Estonia 30
FI - Finlandia 30
BG - Bulgaria 29
ID - Indonesia 28
JO - Giordania 26
HK - Hong Kong 25
BE - Belgio 17
CA - Canada 16
ES - Italia 11
CL - Cile 10
AU - Australia 8
HR - Croazia 8
JP - Giappone 8
PL - Polonia 8
SC - Seychelles 8
CZ - Repubblica Ceca 7
BR - Brasile 6
GR - Grecia 5
RO - Romania 5
TR - Turchia 5
DK - Danimarca 4
PK - Pakistan 4
AE - Emirati Arabi Uniti 3
AT - Austria 3
IR - Iran 3
KR - Corea 3
LT - Lituania 3
TW - Taiwan 3
A2 - ???statistics.table.value.countryCode.A2??? 2
MT - Malta 2
MY - Malesia 2
SK - Slovacchia (Repubblica Slovacca) 2
BD - Bangladesh 1
HU - Ungheria 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
LU - Lussemburgo 1
LV - Lettonia 1
MD - Moldavia 1
NG - Nigeria 1
NZ - Nuova Zelanda 1
PE - Perù 1
PH - Filippine 1
PT - Portogallo 1
TH - Thailandia 1
UZ - Uzbekistan 1
Totale 6.583
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Città #
Southend 400
Fairfield 362
Chandler 332
Bologna 239
Ashburn 234
Singapore 225
Woodbridge 154
Wilmington 136
Houston 133
Seattle 130
Santa Clara 128
Ann Arbor 124
Cambridge 116
Princeton 114
Redmond 107
Dublin 88
Abidjan 64
Boardman 61
Turin 61
Lomé 53
New York 45
Milan 41
Berlin 40
Westminster 39
Nanjing 37
Padova 36
Sofia 29
Bern 28
Dong Ket 28
Jakarta 28
Amman 26
Redwood City 26
Boydton 25
Helsinki 24
Hong Kong 23
Jinan 22
San Diego 22
Warrington 21
Doylestown 20
Florence 18
Brussels 17
Nijmegen 17
Shanghai 17
Beijing 16
Nanchang 16
Guangzhou 15
Jacksonville 15
Saint Petersburg 15
Shenyang 15
Los Angeles 14
Rome 14
Phoenix 13
Zhengzhou 13
Changsha 12
Falls Church 12
Hebei 12
Bari 11
Olalla 11
Ancona 10
Des Moines 10
Kuban 10
Medford 10
Tianjin 10
Dearborn 9
London 9
Modena 9
Pune 9
Paris 8
Parma 8
Sant Angelo 8
Taiyuan 8
Taizhou 8
Hangzhou 7
Mülheim 7
Ningbo 7
Amsterdam 6
Ferrara 6
Jiaxing 6
Toronto 6
Washington 6
Catania 5
Imola 5
Lappeenranta 5
Livorno 5
Lynchburg 5
Munich 5
Ponte San Pietro 5
Qingdao 5
Shenzhen 5
Aprilia 4
Botticino 4
Brno 4
Cesena 4
Dongguan 4
Frankfurt Am Main 4
Frankfurt am Main 4
Fremont 4
Latisana 4
Mahé 4
Marina Di Carrara 4
Totale 4.360
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Nome #
An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder. 244
Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy 213
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome 201
Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways 179
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy 164
Haplogroup J mitogenomes are the most sensitive to the pesticide rotenone: Relevance for human diseases 164
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism 164
Mitochondrial Mass Assessment in a Selected Cell Line under Different Metabolic Conditions 160
Mitochondrial abnormalities in fibroblasts carrying DNMT1 mutations 155
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models 154
Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations 150
Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy 150
Genetic Basis of Mitochondrial Optic Neuropathies. 146
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions. 141
Mitochondrial optic neuropathies: how two genomes may kill the same cell type? 139
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy. 137
OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions 136
Oncocytic glioblastoma: a glioblastoma showing oncocytic changes and increased mitochondrial DNA copy number 134
Mitochondrial DNA influences the susceptibility to Autism Spectrum Disorders and the severity of the clinical phenotype 126
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy 126
Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α. 125
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder 121
Syndromic parkinsonism and dementia associated with OPA1 missense mutations 120
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy 120
Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations 116
Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutation 116
Incomplete penetrance in mitochondrial optic neuropathies 114
DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions 114
Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease Models 112
OPA3, a new regulator of mitochondrial fission? 110
Idebenone treatment in patients with OPA1-mutant dominant optic atrophy. 110
Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations 108
Exploring metabolic adaptations to the acidic microenvironment of osteosarcoma cells unveils sphingosine 1-phosphate as a valuable therapeutic target 108
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance. 106
Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutations 105
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder 104
DNA methyltransferase 1 mutations and mitochondrial pathology: Is mtDNA methylated? 101
The optic nerve: a "mito-window" on mitochondrial neurodegeneration. 87
Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversion 84
null 83
Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies 82
Searching for genetic modifiers of Leber's hereditary optic neuropathy penetrance 82
Screening of candidate nuclear genes for modifying role in Leber's hereditary optic neuropathy penetrance: A signal from manganese superoxide dismutase 81
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy. 81
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder 80
OPA3 IS AN INNER MITOCHONDRIAL MEMBRANE PROTEIN INVOLVED IN MITOCHONDRIAL DYNAMICS REGULATION 79
The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs 79
null 78
Functional investigation of the mitochondrial protein OPA3 78
Expanding and validating the biomarkers for mitochondrial diseases 74
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates 72
Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON) 72
Retinal nerve fiber layer thickness in dominant optic atrophy: measurements by optical coherence tomography and correlation with age. 69
Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys 65
Author Correction: Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome (Scientific Reports, (2020), 10, 1, (4785), 10.1038/s41598-020-61735-3) 58
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy 54
Exploring metabolic reprogramming in melanoma via acquired resistance to the oxidative phosphorylation inhibitor phenformin 49
Mitochondrial diseases in adults 45
Impaired complex I repair causes recessive Leber's hereditary optic neuropathy 42
Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives 35
Glutamine Supplementation as a Novel Metabolic Therapeutic Strategy for LIG3-Dependent Chronic Intestinal Pseudo-obstruction 30
Molecular mechanisms behind inherited neurodegeneration of the optic nerve 28
Methyl carbamates of phosphatidylethanolamines and phosphatidylserines reveal bacterial contamination in mitochondrial lipid extracts of mouse embryonic fibroblasts 23
Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy 23
Totale 6.806
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Categoria #
all - tutte 18.787
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 18.787
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020858 0 0 0 0 0 114 141 178 222 65 75 63
2020/2021855 152 47 24 39 21 40 14 90 137 51 56 184
2021/20221.283 51 37 69 75 111 46 48 168 77 108 267 226
2022/20231.528 157 189 76 155 119 179 70 92 231 40 131 89
2023/2024562 27 71 28 40 38 110 49 44 18 46 58 33
2024/2025924 85 222 153 150 232 82 0 0 0 0 0 0
Totale 6.806