CRIS Current Research Information System

MARESCA, ALESSANDRA
 Distribuzione geografica
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Continente #
NA - Nord America 4.234
AS - Asia 3.489
EU - Europa 3.022
AF - Africa 253
SA - Sud America 184
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 4
Totale 11.198
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Nazione #
US - Stati Uniti d'America 4.162
IT - Italia 1.015
SG - Singapore 985
CN - Cina 977
VN - Vietnam 734
GB - Regno Unito 471
DE - Germania 309
SE - Svezia 283
HK - Hong Kong 199
FR - Francia 175
IN - India 166
RU - Federazione Russa 135
NL - Olanda 119
BR - Brasile 116
KR - Corea 109
FI - Finlandia 102
CI - Costa d'Avorio 101
IE - Irlanda 96
JP - Giappone 63
ZA - Sudafrica 61
UA - Ucraina 56
TG - Togo 53
CA - Canada 45
ES - Italia 38
CH - Svizzera 36
ID - Indonesia 36
JO - Giordania 31
BG - Bulgaria 30
EE - Estonia 30
AR - Argentina 29
PH - Filippine 28
AT - Austria 24
PK - Pakistan 24
PL - Polonia 23
SC - Seychelles 22
TR - Turchia 22
BD - Bangladesh 21
TH - Thailandia 21
BE - Belgio 20
MX - Messico 17
CL - Cile 13
TW - Taiwan 12
AU - Australia 11
SA - Arabia Saudita 11
HR - Croazia 10
LT - Lituania 10
EC - Ecuador 8
IQ - Iraq 8
IR - Iran 8
CZ - Repubblica Ceca 7
CO - Colombia 6
GR - Grecia 6
MY - Malesia 6
RO - Romania 6
UZ - Uzbekistan 6
VE - Venezuela 5
AE - Emirati Arabi Uniti 4
AL - Albania 4
DK - Danimarca 4
PY - Paraguay 4
AZ - Azerbaigian 3
DZ - Algeria 3
KE - Kenya 3
KZ - Kazakistan 3
SK - Slovacchia (Repubblica Slovacca) 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BB - Barbados 2
ET - Etiopia 2
JM - Giamaica 2
LB - Libano 2
LK - Sri Lanka 2
MA - Marocco 2
MT - Malta 2
NG - Nigeria 2
PA - Panama 2
SN - Senegal 2
XK - ???statistics.table.value.countryCode.XK??? 2
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
CY - Cipro 1
DO - Repubblica Dominicana 1
GN - Guinea 1
GT - Guatemala 1
GY - Guiana 1
HU - Ungheria 1
KG - Kirghizistan 1
LA - Repubblica Popolare Democratica del Laos 1
LI - Liechtenstein 1
LU - Lussemburgo 1
LV - Lettonia 1
MD - Moldavia 1
MM - Myanmar 1
NI - Nicaragua 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PE - Perù 1
PT - Portogallo 1
Totale 11.195
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Città #
Singapore 688
Ashburn 466
Southend 400
Fairfield 362
Chandler 332
Bologna 300
San Jose 199
Hefei 196
Hong Kong 187
Ho Chi Minh City 176
Woodbridge 154
Hanoi 147
Santa Clara 141
Houston 138
Seattle 138
Wilmington 136
Ann Arbor 124
Cambridge 116
Princeton 114
Beijing 108
Redmond 107
Abidjan 101
Dallas 97
Dublin 91
Seoul 91
Helsinki 80
Boardman 72
Council Bluffs 72
Los Angeles 69
Lauterbourg 66
New York 65
Turin 64
Milan 58
Lomé 53
Tokyo 47
Berlin 41
Westminster 39
Nanjing 38
Padova 36
Jakarta 32
São Paulo 32
Amman 31
Sofia 29
Bern 28
Dong Ket 28
Haiphong 28
Redondo Beach 28
Da Nang 27
Redwood City 26
Shanghai 26
Boydton 25
Doylestown 25
Parma 24
Jinan 23
Frankfurt am Main 22
Guangzhou 22
Johannesburg 22
San Diego 22
Bengaluru 21
London 21
Warrington 21
Florence 20
Rome 20
Brussels 19
Buffalo 19
Nanchang 19
Phoenix 19
Munich 18
Nijmegen 18
Lappeenranta 17
Jacksonville 16
Warsaw 16
Zhengzhou 16
Changsha 15
Montreal 15
Saint Petersburg 15
Shenyang 15
Modena 14
Vienna 14
Bari 13
Falls Church 12
Hebei 12
Nuremberg 12
Orem 12
Stockholm 12
Valladolid 12
Olalla 11
Paris 11
Tianjin 11
Amsterdam 10
Ancona 10
Bangkok 10
Des Moines 10
Falkenstein 10
Hải Dương 10
Kuban 10
Medford 10
Pune 10
Can Tho 9
Chicago 9
Totale 7.003
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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. 348
Mitochondrial DNA influences the susceptibility to Autism Spectrum Disorders and the severity of the clinical phenotype 287
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates 287
Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy 285
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models 275
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome 269
Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy 269
Glutamine Supplementation as a Novel Metabolic Therapeutic Strategy for LIG3-Dependent Chronic Intestinal Pseudo-obstruction 268
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism 262
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy 247
Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways 224
Haplogroup J mitogenomes are the most sensitive to the pesticide rotenone: Relevance for human diseases 220
Mitochondrial Mass Assessment in a Selected Cell Line under Different Metabolic Conditions 220
Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations 214
Syndromic parkinsonism and dementia associated with OPA1 missense mutations 205
Mitochondrial optic neuropathies: how two genomes may kill the same cell type? 202
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions. 202
Genetic Basis of Mitochondrial Optic Neuropathies. 199
Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutation 199
Mitochondrial abnormalities in fibroblasts carrying DNMT1 mutations 198
OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions 198
Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutations 196
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder 195
Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys 193
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) 190
Oncocytic glioblastoma: a glioblastoma showing oncocytic changes and increased mitochondrial DNA copy number 187
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder 186
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy 186
Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations 185
Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease Models 183
Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α. 183
Exploring metabolic adaptations to the acidic microenvironment of osteosarcoma cells unveils sphingosine 1-phosphate as a valuable therapeutic target 180
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance. 179
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder 167
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy 166
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy. 166
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy 165
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy. 163
Idebenone treatment in patients with OPA1-mutant dominant optic atrophy. 162
Incomplete penetrance in mitochondrial optic neuropathies 153
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 152
OPA3, a new regulator of mitochondrial fission? 152
Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations 152
DNA methyltransferase 1 mutations and mitochondrial pathology: Is mtDNA methylated? 151
DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions 145
Lipidomics reveals the reshaping of the mitochondrial phospholipid profile in cells lacking OPA1 and mitofusins 141
The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs 141
Screening of candidate nuclear genes for modifying role in Leber's hereditary optic neuropathy penetrance: A signal from manganese superoxide dismutase 138
Methyl carbamates of phosphatidylethanolamines and phosphatidylserines reveal bacterial contamination in mitochondrial lipid extracts of mouse embryonic fibroblasts 127
The optic nerve: a "mito-window" on mitochondrial neurodegeneration. 126
OPA3 IS AN INNER MITOCHONDRIAL MEMBRANE PROTEIN INVOLVED IN MITOCHONDRIAL DYNAMICS REGULATION 124
Functional investigation of the mitochondrial protein OPA3 118
Expanding and validating the biomarkers for mitochondrial diseases 117
Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversion 113
Searching for genetic modifiers of Leber's hereditary optic neuropathy penetrance 111
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) 108
Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies 107
Impaired complex I repair causes recessive Leber's hereditary optic neuropathy 104
Retinal nerve fiber layer thickness in dominant optic atrophy: measurements by optical coherence tomography and correlation with age. 102
Exploring metabolic reprogramming in melanoma via acquired resistance to the oxidative phosphorylation inhibitor phenformin 84
null 83
Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives 82
null 78
Molecular mechanisms behind inherited neurodegeneration of the optic nerve 75
Mitochondrial diseases in adults 69
Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy 54
Progressive encephalopathy in m.3243A > G/MT-TL1 mutation carriers: a quantitative EEG analysis 48
Totale 11.465
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Categoria #
all - tutte 30.352
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 30.352
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021240 0 0 0 0 0 0 0 0 0 0 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
2025/20263.880 358 394 382 393 443 229 405 180 768 290 38 0
Totale 11.465