CRIS Current Research Information System

MARESCA, ALESSANDRA
 Distribuzione geografica
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Continente #
NA - Nord America 3.768
EU - Europa 2.765
AS - Asia 2.542
AF - Africa 231
SA - Sud America 158
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 4
Totale 9.480
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Nazione #
US - Stati Uniti d'America 3.717
IT - Italia 951
SG - Singapore 872
CN - Cina 828
GB - Regno Unito 456
DE - Germania 300
SE - Svezia 281
VN - Vietnam 243
HK - Hong Kong 184
IN - India 147
RU - Federazione Russa 135
NL - Olanda 114
FR - Francia 105
BR - Brasile 101
CI - Costa d'Avorio 101
KR - Corea 93
IE - Irlanda 92
FI - Finlandia 53
TG - Togo 53
UA - Ucraina 53
ZA - Sudafrica 46
JP - Giappone 39
ID - Indonesia 35
CA - Canada 34
CH - Svizzera 33
JO - Giordania 31
EE - Estonia 30
BG - Bulgaria 29
AR - Argentina 24
ES - Italia 23
AT - Austria 22
SC - Seychelles 22
BE - Belgio 20
PL - Polonia 20
PK - Pakistan 15
CL - Cile 13
MX - Messico 12
TR - Turchia 12
AU - Australia 11
BD - Bangladesh 9
EC - Ecuador 8
HR - Croazia 8
IR - Iran 8
CZ - Repubblica Ceca 7
LT - Lituania 7
CO - Colombia 5
GR - Grecia 5
RO - Romania 5
AE - Emirati Arabi Uniti 4
DK - Danimarca 4
PY - Paraguay 3
TW - Taiwan 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AZ - Azerbaigian 2
DZ - Algeria 2
KE - Kenya 2
LK - Sri Lanka 2
MT - Malta 2
MY - Malesia 2
NG - Nigeria 2
PA - Panama 2
PH - Filippine 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
UZ - Uzbekistan 2
VE - Venezuela 2
XK - ???statistics.table.value.countryCode.XK??? 2
AL - Albania 1
AM - Armenia 1
BB - Barbados 1
BO - Bolivia 1
BY - Bielorussia 1
DO - Repubblica Dominicana 1
GN - Guinea 1
GT - Guatemala 1
HU - Ungheria 1
IQ - Iraq 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
LI - Liechtenstein 1
LU - Lussemburgo 1
LV - Lettonia 1
MA - Marocco 1
MD - Moldavia 1
NZ - Nuova Zelanda 1
PE - Perù 1
PT - Portogallo 1
SN - Senegal 1
TL - Timor Orientale 1
Totale 9.480
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Città #
Singapore 585
Ashburn 431
Southend 400
Fairfield 362
Chandler 332
Bologna 284
Hefei 195
Hong Kong 180
Woodbridge 154
Houston 138
Seattle 138
Wilmington 136
Santa Clara 133
Ann Arbor 124
Cambridge 116
Princeton 114
Redmond 107
Beijing 102
Abidjan 101
Dallas 94
Dublin 91
Seoul 90
Boardman 71
Los Angeles 63
Turin 62
New York 61
Milan 56
Lomé 53
Ho Chi Minh City 47
Berlin 41
Westminster 39
Nanjing 37
Padova 36
Helsinki 34
Amman 31
Jakarta 31
Hanoi 30
Tokyo 30
Sofia 29
Bern 28
Dong Ket 28
Redondo Beach 28
Redwood City 26
São Paulo 26
Boydton 25
Doylestown 25
Jinan 22
Parma 22
San Diego 22
Warrington 21
Florence 20
Brussels 19
Rome 19
Bengaluru 18
Munich 18
Shanghai 18
Buffalo 17
Guangzhou 17
London 17
Nijmegen 17
Nanchang 16
Phoenix 16
Zhengzhou 16
Frankfurt am Main 15
Jacksonville 15
Saint Petersburg 15
Shenyang 15
Changsha 14
Lappeenranta 14
Vienna 14
Warsaw 14
Bari 13
Falls Church 12
Hebei 12
Nuremberg 12
Modena 11
Montreal 11
Olalla 11
Stockholm 11
Amsterdam 10
Ancona 10
Des Moines 10
Falkenstein 10
Kuban 10
Medford 10
Pune 10
Tianjin 10
Dearborn 9
Hangzhou 9
Paris 9
Brooklyn 8
Haiphong 8
Sant Angelo 8
Taiyuan 8
Taizhou 8
Tongling 8
Toronto 8
Boston 7
Chicago 7
Da Nang 7
Totale 6.052
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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. 312
Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy 254
Mitochondrial DNA influences the susceptibility to Autism Spectrum Disorders and the severity of the clinical phenotype 251
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates 242
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome 236
Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy 234
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism 224
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy 223
Glutamine Supplementation as a Novel Metabolic Therapeutic Strategy for LIG3-Dependent Chronic Intestinal Pseudo-obstruction 213
Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways 201
Mitochondrial Mass Assessment in a Selected Cell Line under Different Metabolic Conditions 199
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models 198
Haplogroup J mitogenomes are the most sensitive to the pesticide rotenone: Relevance for human diseases 194
Genetic Basis of Mitochondrial Optic Neuropathies. 191
Mitochondrial optic neuropathies: how two genomes may kill the same cell type? 179
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions. 179
Mitochondrial abnormalities in fibroblasts carrying DNMT1 mutations 179
Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations 170
Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys 168
OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions 167
Syndromic parkinsonism and dementia associated with OPA1 missense mutations 166
Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations 165
Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutation 164
Oncocytic glioblastoma: a glioblastoma showing oncocytic changes and increased mitochondrial DNA copy number 163
Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α. 162
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder 158
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy 157
Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutations 156
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder 155
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance. 152
Exploring metabolic adaptations to the acidic microenvironment of osteosarcoma cells unveils sphingosine 1-phosphate as a valuable therapeutic target 152
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy. 150
Idebenone treatment in patients with OPA1-mutant dominant optic atrophy. 149
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy 147
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) 146
Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease Models 139
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy. 138
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy 136
OPA3, a new regulator of mitochondrial fission? 136
DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions 136
Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations 133
Incomplete penetrance in mitochondrial optic neuropathies 133
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder 133
DNA methyltransferase 1 mutations and mitochondrial pathology: Is mtDNA methylated? 126
Genomic analysis of 116 families with Autism Spectrum Disorder: rare de novo and inherited variants further delineate the role of risk genes and highlight new candidates 116
Lipidomics reveals the reshaping of the mitochondrial phospholipid profile in cells lacking OPA1 and mitofusins 113
The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs 111
The optic nerve: a "mito-window" on mitochondrial neurodegeneration. 108
Screening of candidate nuclear genes for modifying role in Leber's hereditary optic neuropathy penetrance: A signal from manganese superoxide dismutase 108
OPA3 IS AN INNER MITOCHONDRIAL MEMBRANE PROTEIN INVOLVED IN MITOCHONDRIAL DYNAMICS REGULATION 105
Methyl carbamates of phosphatidylethanolamines and phosphatidylserines reveal bacterial contamination in mitochondrial lipid extracts of mouse embryonic fibroblasts 104
Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversion 104
Expanding and validating the biomarkers for mitochondrial diseases 103
Functional investigation of the mitochondrial protein OPA3 102
Searching for genetic modifiers of Leber's hereditary optic neuropathy penetrance 99
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) 97
Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies 96
Retinal nerve fiber layer thickness in dominant optic atrophy: measurements by optical coherence tomography and correlation with age. 88
null 83
Impaired complex I repair causes recessive Leber's hereditary optic neuropathy 79
null 78
Exploring metabolic reprogramming in melanoma via acquired resistance to the oxidative phosphorylation inhibitor phenformin 66
Mitochondrial diseases in adults 58
Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives 57
Molecular mechanisms behind inherited neurodegeneration of the optic nerve 57
Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy 40
Progressive encephalopathy in m.3243A > G/MT-TL1 mutation carriers: a quantitative EEG analysis 3
Totale 9.741
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Categoria #
all - tutte 27.445
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 27.445
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021572 0 0 0 0 0 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
2024/20251.703 85 222 153 150 232 104 159 78 40 117 109 254
2025/20262.156 358 394 382 393 443 186 0 0 0 0 0 0
Totale 9.741