CRIS Current Research Information System

MARESCA, ALESSANDRA
 Distribuzione geografica
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Continente #
NA - Nord America 1.311
EU - Europa 597
AS - Asia 145
AF - Africa 14
SA - Sud America 8
OC - Oceania 7
Totale 2.082
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Nazione #
US - Stati Uniti d'America 1.293
IT - Italia 221
FR - Francia 94
IE - Irlanda 77
GB - Regno Unito 59
CN - Cina 41
DE - Germania 37
BG - Bulgaria 26
IN - India 24
CA - Canada 18
AE - Emirati Arabi Uniti 17
JP - Giappone 16
NL - Olanda 16
VN - Vietnam 15
HK - Hong Kong 13
UA - Ucraina 11
CZ - Repubblica Ceca 9
ZA - Sudafrica 8
AU - Australia 7
ES - Italia 7
SE - Svezia 7
CL - Cile 6
RU - Federazione Russa 6
FI - Finlandia 5
MA - Marocco 5
CH - Svizzera 4
BH - Bahrain 3
GR - Grecia 3
MK - Macedonia 3
PL - Polonia 3
SA - Arabia Saudita 3
SG - Singapore 3
AT - Austria 2
BR - Brasile 2
HU - Ungheria 2
PK - Pakistan 2
RS - Serbia 2
TR - Turchia 2
TW - Taiwan 2
IR - Iran 1
KR - Corea 1
LV - Lettonia 1
PH - Filippine 1
RO - Romania 1
SI - Slovenia 1
SY - Repubblica araba siriana 1
UG - Uganda 1
Totale 2.082
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Città #
Ashburn 185
Santa Cruz 88
Fairfield 86
Dublin 76
Bologna 72
Los Angeles 50
Seattle 50
Chicago 46
Houston 41
Buffalo 38
Woodbridge 36
Boardman 34
Cambridge 31
New York 30
Columbus 28
Sofia 26
Southend 20
Milan 19
Wilmington 19
Chandler 18
Las Vegas 13
Paris 11
Ann Arbor 10
San Diego 10
Central 9
Dong Ket 9
Mountain View 9
Rome 8
Council Bluffs 7
Dallas 7
Henderson 7
San Francisco 7
Bengaluru 6
Falls Church 6
Lake Forest 6
Naples 6
Stockholm 6
Amsterdam 5
Clearwater 5
Melbourne 5
Milpitas 5
Parma 5
Pune 5
Russi 5
Santa Clara 5
Tokyo 5
York 5
Arlington 4
Basking Ridge 4
Bern 4
Birmingham 4
Denver 4
El Jadida 4
Forlì 4
Groningen 4
Guangzhou 4
London 4
Ottawa 4
Phoenix 4
Riva 4
Shanghai 4
Waltham 4
Ancona 3
Atlanta 3
Cedar Knolls 3
Chengdu 3
Chennai 3
Comano 3
Encino 3
Fleming Island 3
Florence 3
Helsinki 3
Imola 3
Madison 3
Manama 3
Monzuno 3
Muizenberg 3
Oakville 3
Providence 3
Provo 3
San Jose 3
Sunnyvale 3
Verona 3
Waterford 3
Wembley 3
Abha 2
Beijing 2
Broomfield 2
Budrio 2
Calvizzano 2
Casarano 2
Chalcis 2
Cologne 2
Delhi 2
Dulles 2
Düsseldorf 2
Frankfurt am Main 2
Grenoble 2
Grodzisk Mazowiecki 2
Hangzhou 2
Totale 1.339
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Nome #
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models, file e1dcb331-3922-7715-e053-1705fe0a6cc9 255
An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder., file e1dcb337-6bb6-7715-e053-1705fe0a6cc9 153
Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy, file e1dcb339-ea5f-7715-e053-1705fe0a6cc9 136
Haplogroup J mitogenomes are the most sensitive to the pesticide rotenone: Relevance for human diseases, file e1dcb331-57ea-7715-e053-1705fe0a6cc9 131
OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions, file e1dcb331-5546-7715-e053-1705fe0a6cc9 125
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy., file e1dcb332-b5c6-7715-e053-1705fe0a6cc9 103
Mitochondrial Mass Assessment in a Selected Cell Line under Different Metabolic Conditions, file e1dcb333-67d3-7715-e053-1705fe0a6cc9 100
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy, file e1dcb337-6018-7715-e053-1705fe0a6cc9 97
Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α., file e1dcb334-b0bd-7715-e053-1705fe0a6cc9 82
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome, file e1dcb335-e990-7715-e053-1705fe0a6cc9 80
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy, file e1dcb335-6972-7715-e053-1705fe0a6cc9 76
Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways, file e1dcb335-7448-7715-e053-1705fe0a6cc9 74
DNA methyltransferase 1 mutations and mitochondrial pathology: Is mtDNA methylated?, file e1dcb335-6977-7715-e053-1705fe0a6cc9 66
Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease Models, file e1dcb335-7641-7715-e053-1705fe0a6cc9 64
Syndromic parkinsonism and dementia associated with OPA1 missense mutations, file e1dcb337-b68e-7715-e053-1705fe0a6cc9 56
Exploring metabolic adaptations to the acidic microenvironment of osteosarcoma cells unveils sphingosine 1-phosphate as a valuable therapeutic target, file e1dcb337-930b-7715-e053-1705fe0a6cc9 52
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder, file e1dcb338-854c-7715-e053-1705fe0a6cc9 46
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome, file e1dcb335-e991-7715-e053-1705fe0a6cc9 44
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism, file e1dcb339-8982-7715-e053-1705fe0a6cc9 36
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy, file 03603a86-29f8-406d-9e5e-af6dc2a898e6 33
Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys, file 4cd55add-9309-4689-90da-118e29f63896 33
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism, file e1dcb339-854a-7715-e053-1705fe0a6cc9 27
The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs, file dd9681d9-dec4-4639-a26d-ffa641ba9e82 24
Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations, file e1dcb337-3f6d-7715-e053-1705fe0a6cc9 23
Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutations, file 991e2af6-7b87-4ae2-b311-b4884368f3c0 20
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), file 04efa871-36ee-4e40-8dfc-0257db6b1794 18
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder, file 25c79b53-f2dd-4e15-818c-7c1235da3d2d 18
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy, file 668c9708-4cc7-4fa6-99b2-459818c1040d 17
Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease Models, file e1dcb335-76b2-7715-e053-1705fe0a6cc9 15
Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives, file e7407959-fd81-4edb-ad5b-4fdb3d55b7a9 15
Molecular mechanisms behind inherited neurodegeneration of the optic nerve, file 7ef38730-0ddb-4e9c-beb1-9dbad5ff0b51 14
Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutations, file c9cd2ce1-9426-43ef-8771-55c866e1f063 14
Impaired complex I repair causes recessive Leber's hereditary optic neuropathy, file 41414005-8459-4086-ba99-8618181bd26e 12
Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys, file 51cca6c1-8f49-4d07-9999-5186b9ccd89c 10
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), file e1888d3c-8e19-424a-b20a-526b407fefff 8
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder, file e1dcb338-854d-7715-e053-1705fe0a6cc9 8
Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations, file dc3ec34b-d906-4004-9782-e393b5290ca1 7
Expanding and validating the biomarkers for mitochondrial diseases, file cae163c1-9f41-430a-8077-623669104c81 6
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), file 6dfcc37b-47e7-4d0b-9028-d30a5e1b3d09 5
Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways, file e1dcb335-35a2-7715-e053-1705fe0a6cc9 5
Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy, file e1dcb338-a379-7715-e053-1705fe0a6cc9 5
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder, file 7e62d7bc-3575-4815-bcaa-aa5a011395b6 3
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder, file e1dcb338-4c25-7715-e053-1705fe0a6cc9 3
Expanding and validating the biomarkers for mitochondrial diseases, file 264a49ca-e5bb-4d4e-92c3-900ce1890aae 2
Methyl carbamates of phosphatidylethanolamines and phosphatidylserines reveal bacterial contamination in mitochondrial lipid extracts of mouse embryonic fibroblasts, file 572e7321-d273-41a6-8773-ad347f2b5da0 2
Impaired complex I repair causes recessive Leber's hereditary optic neuropathy, file 5b50056e-caa5-4a5c-9981-5f08ce7734da 2
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy, file e1dcb335-6974-7715-e053-1705fe0a6cc9 2
Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy, file e1dcb32f-a5eb-7715-e053-1705fe0a6cc9 1
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder, file e1dcb338-6427-7715-e053-1705fe0a6cc9 1
Totale 2.129
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Categoria #
all - tutte 7.066
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 7.066
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20191 0 0 0 0 0 0 0 0 0 0 0 1
2019/2020119 1 0 0 3 10 11 10 13 21 11 26 13
2020/2021257 15 20 5 20 16 17 14 15 39 38 31 27
2021/2022449 17 23 17 23 42 12 17 50 28 24 125 71
2022/2023730 28 27 110 73 38 34 38 55 138 58 81 50
2023/2024569 29 28 33 63 41 134 101 44 45 22 29 0
Totale 2.129