CNR Institutional Research Information System

ANNESI, FERDINANDA
 Distribuzione geografica
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Continente #
AS - Asia 3.847
NA - Nord America 1.721
EU - Europa 716
SA - Sud America 710
AF - Africa 62
Continente sconosciuto - Info sul continente non disponibili 52
OC - Oceania 5
Totale 7.113
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Nazione #
SG - Singapore 1.657
US - Stati Uniti d'America 1.631
CN - Cina 826
BR - Brasile 584
HK - Hong Kong 392
VN - Vietnam 365
FR - Francia 278
IT - Italia 172
JP - Giappone 164
KR - Corea 155
BD - Bangladesh 65
IN - India 62
NL - Olanda 62
DE - Germania 45
GB - Regno Unito 43
CA - Canada 38
AR - Argentina 35
EC - Ecuador 28
FI - Finlandia 26
ID - Indonesia 24
CO - Colombia 23
MX - Messico 23
IL - Israele 22
ZA - Sudafrica 20
PK - Pakistan 16
TR - Turchia 16
ES - Italia 15
RU - Federazione Russa 12
UA - Ucraina 11
IQ - Iraq 10
PY - Paraguay 10
UZ - Uzbekistan 10
VE - Venezuela 10
AT - Austria 9
EG - Egitto 9
AE - Emirati Arabi Uniti 7
MA - Marocco 7
MY - Malesia 7
PE - Perù 7
PL - Polonia 7
SA - Arabia Saudita 7
TN - Tunisia 7
CL - Cile 6
NI - Nicaragua 6
AZ - Azerbaigian 5
DZ - Algeria 5
KE - Kenya 5
TT - Trinidad e Tobago 5
GE - Georgia 4
HN - Honduras 4
KZ - Kazakistan 4
LV - Lettonia 4
NP - Nepal 4
PS - Palestinian Territory 4
UY - Uruguay 4
AL - Albania 3
CH - Svizzera 3
GT - Guatemala 3
JM - Giamaica 3
LB - Libano 3
NZ - Nuova Zelanda 3
SE - Svezia 3
SN - Senegal 3
TH - Thailandia 3
BG - Bulgaria 2
BO - Bolivia 2
BY - Bielorussia 2
DO - Repubblica Dominicana 2
GR - Grecia 2
IE - Irlanda 2
IR - Iran 2
KG - Kirghizistan 2
LK - Sri Lanka 2
PA - Panama 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 2
AU - Australia 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BW - Botswana 1
CR - Costa Rica 1
CY - Cipro 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
ET - Etiopia 1
GF - Guiana Francese 1
IS - Islanda 1
JO - Giordania 1
LA - Repubblica Popolare Democratica del Laos 1
LT - Lituania 1
LU - Lussemburgo 1
ME - Montenegro 1
MT - Malta 1
NC - Nuova Caledonia 1
NG - Nigeria 1
OM - Oman 1
PH - Filippine 1
PR - Porto Rico 1
Totale 7.052
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Città #
Singapore 957
Santa Clara 532
Hong Kong 385
Hefei 347
San Jose 259
Lauterbourg 197
Seoul 153
Beijing 144
Tokyo 143
Ho Chi Minh City 140
Ashburn 107
Hanoi 82
Los Angeles 63
Dallas 58
São Paulo 51
Buffalo 37
Rende 23
Rio de Janeiro 22
Helsinki 21
Minamishinagawa 18
Belo Horizonte 17
Frankfurt am Main 17
New York 17
Haiphong 16
Bengaluru 15
Brasília 15
Da Nang 15
Brooklyn 14
Guangzhou 13
Milan 13
Naples 13
Curitiba 11
Orem 11
Quito 11
Biên Hòa 10
Jakarta 9
Johannesburg 9
Mumbai 9
Shanghai 9
Tashkent 9
Chennai 8
Chicago 8
Cosenza 8
Madrid 8
Manchester 8
Montreal 8
Porto Alegre 8
Salvador 8
Taranto 8
Atlanta 7
Bogotá 7
Caltanissetta 7
Can Tho 7
Dhaka 7
Guarulhos 7
Ribeirão Preto 7
Rome 7
Boardman 6
Campinas 6
Council Bluffs 6
Goiânia 6
Houston 6
Joinville 6
London 6
Phoenix 6
Santo André 6
Turin 6
Ankara 5
Aparecida de Goiânia 5
Bologna 5
Cairo 5
Denver 5
Detroit 5
Hortolândia 5
Hải Dương 5
Lahore 5
Lappeenranta 5
Managua 5
Manaus 5
Mauá 5
Nairobi 5
Phủ Lý 5
Recife 5
Sorocaba 5
Tunis 5
Warsaw 5
Arlington 4
Asunción 4
Baghdad 4
Baku 4
Bari 4
Boston 4
Bình An 4
Bắc Giang 4
Bắc Ninh 4
Cerisano 4
Chengdu 4
Diadema 4
Feira de Santana 4
Fortaleza 4
Totale 4.331
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Nome #
Biocompatible and biomimetic keratin capped Au nanoparticles enable the inactivation of mesophilic bacteria via photo-thermal therapy 112
G-463A myeloperoxidase polymorphism and parkinson s disease 84
TARGETING CANCER CELLS WITH FLUORESCENTLY LABELED GNR S /DNA COMPLEXES 81
Ataxia with oculomotor apraxia in a family from southern italy : a clinical and genetic study 77
Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 76
Micro- and Nano-Structured Bacteria Growth Media for Planar Bio-Photonics 75
Clinic and genetic study in a family with a clinical picture of pantothenate kinase-associated neurodegeneration . 74
Identification of a novel mutation homozygous mutation in the SIL1 gene in Marinesco-Sjögren syndrome (MSS). 73
ASSOCIATION STUDY BETWEEN THE LINGO1 GENE AND PARKINSON S DISEASE IN THE ITALIAN POPULATION 71
Alpha synuclein in familial parkinson s disease and lewy body dementia. 67
Thermo-Plasmonic Killing of Escherichia coli TG1 Bacteria 65
Association study between the LINGO1 gene and Parkinson s disease in the Italian population 65
No evidence for association of high and low activity alleles of COMT with Parkinson's disease. 63
Thermal liquid biopsy (TLB) of blood plasma as a potential tool to help in the early diagnosis of multiple sclerosis 63
Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's disease 63
ATR-FTIR spectroscopy of plasma supported by multivariate analysis discriminates multiple sclerosis disease 63
Molecular studies of the PANK2 gene in patients with PKAN 62
DJ-1 is a Parkinson's disease susceptibility gene in southern Italy. 61
Tailoring Resonant Energy Transfer Processes for Sustainable and Bio-Inspired Sensing 61
Biological metasurfaces based on tailored Luria Bertani Agar growth medium formulations for photonic applications 60
Analisi mutazionale del gene SCN2A in famiglie italiane con Convulsioni Neonatali-Infantili Familiari Benigne (BFINS). 58
G-protein-coupled receptor kinase 5 and dementia in Parkinson s disease 58
Envisioning quantum electrodynamic frameworks based on bio-photonic cavities 57
Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease. 56
Myocardial 123metaiodobenzylguadine uptake in genetic Parkinson's disease 55
Genetic analysis of SCA2 and SCA17 in familial Parkinson s disease. 55
Plasmonics Meets Biology through Optics 55
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy. 54
Mutational Analysis of the CHRNA4 and CHRNB2 genes in a family with autosomal dominant nocturnal frontal lobe epilepsy 53
Liquid crystalline DNA: A smart polymer with a variety of applications ranging from photonics to plasmonics 53
DESCRIPTION OF A FOUR-GENERATION FAMILY WITH AUTOSOMAL DOMINANT CEREBELLAR ATAXIA: CLINICAL AND GENETIC ANALYSIS 52
DJ-1 gene confers susceptibility to Parkinson s disease. 52
A comprehensive mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 49
Author's reply to the comment of Sironi et al. on "Compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism" 47
Templating gold nanorods with liquid crystalline DNA 46
G-protein-coupled receptor kinase 5 and dementia in Parkinsons disease. 44
Genome wide linkage of a large serbian family with GEFS+. 43
Identification of the novel D297fsX318 PINK1 mutation and phenotype variation in a family with early-onset Parkinson's disease 43
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 43
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy. 42
Antimicrobial effects of chemically functionalized and/or photo-heated nanoparticles 42
DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex. 42
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism. 41
Association study of NACP-REP1 polymorphism and Parkinson's disease 41
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms. 41
Linkage analysis in three families from southern Italy with autosomal dominant nocturnal frontal lobe epilepsy . 39
Association study between G-protein-coupled receptor kinase 5 gene and Parkinson s disease 39
Biomedical application di "hot" gold nanorods/DNA complexes 38
null 37
Genetic study of SCN1A-related epilepsies in southern Italy. 36
A novel mutation in the sodium-channel gene SCN1A in a patient with severe myoclonic epilepsy (SMEI) 36
Increased Risk for Alzheimer disease with the interaction of MPO and A2M Polymorphisms 36
Mutational Analysis of the DCX, LIS1, FLNA genes in patients with neuronal migration disorders from Southern Italy 34
A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. 34
Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinson s disease 33
Fragile X premutation alleles in movement disorders. 33
Glucocerebrosidase gene mutations are associated with Parkinson s disease in a population from Souther Italy. 33
Analisi Genetica e Clinica in 5 famiglie con espansione nucleotidica CAG del gene SCA1 33
Early-onset Parkinson's disease associated with a new parkin mutation in an Italian patient 33
Analisi mutazionale del gene parkina in pazienti affetti da malattia a insorgenza giovanile: identificazione di nuove varianti. 32
A rapid non - isotopic method for sizing CTG repeat expansion in myotonic dystrophy 32
A rapid non-isotopic method for sizing CTG repeat expansion in myiotonic dystrophy. 32
MOLECULAR ANALYSIS OF THE SCN1A GENE IN SOUTHERN ITALIAN PATIENTS WITH SEVERE MYOCLONIC EPILEPSY OF INFANCY. 32
No evidence of association between Alpha 2 macroglobulin gene and Parkinson's disease in a case-control sample 32
Alpha-synuclein in familial Parkinson s disease and Lewy Body Dementia 32
Huntington disease like 2 in Southern Italy: screening of JPH3 and other genes involved in huntington like phenotypes. 32
Ceruloplasmin gene variations and Parkinson s disease: an association study in Southern Italian population. 32
Molecular analysis of the SCN1A gene in patients with Severe Myoclonic Epilepsy of Infancy 31
Parkinsonism and essential tremor in a family with pseudo-dominant inheritance of PARK2: an FP-CIT SPECT study. 31
The fragile X premutation presenting as postprandial hypotension. 31
Effetto del sesso su fattori di rischio clinico-genetici associati allo sviluppo delle discinesie di picco indotte dalla levodopa nella malattia di Parkinson. 31
Association of 5-HT6 receptor gene polymorphism C267T with Parkinson's disease 31
Association of tau polymorphism with Parkinson's disease 31
Association study of NACP-Rep1 polymorphism and Parkinson?s Disease 30
Studio clinico-genetico in una famiglia con quadro clinico di neurodegenerazione associata alla Pantotenato Chinasi. 30
Association study between HFE, TF, TFR1 genes and Parkinson disease. 30
CAG repeat lenght and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocity 30
Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease. 30
GIGYF2 (TRNC15) MUTATION ANALYSIS IN PATIENTS WITH FAMILIAL PARKINSON DISEASE WITH AUTOSOMAL-DOMINANT TRANSMISSION 30
Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy. 30
A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. 30
LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease 30
Correlazione Genotipo - fenotipo in alcune famiglie Italiane con Atassia Spinocerebellare tipo 2 (SCA2) 29
Mutational analysis of EFHC1 gene in Italy families with Juvenile Myoclonic Epilepsy 29
Association of the 5-HT6 receptor gene polymorphism C26TT with Parkinson's disease 29
Gene-dosage influences the age at onset of SCA2 in a family from southern Italy 29
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus. 29
Analisi di linkage in tre famiglie con Epilessia Frontale Notturna autosomica dominante. 29
The dopamine D2 receptor gene is a susceptibility locus for Parkinson's disease 29
Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy. 29
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 29
Mutational analysis of SCN2A gene in italian families with benign familial neonatal-infantile seizures (BFNIS) . 28
Parkin, Pink1 and DJ-1 heterozygous mutations in southern italian patients with early-onset parkinsonism. 27
No evidence of association between the alpha-2 macroglobulin gene and Parkinson's disease in a case-control study 27
Electroclinical features of a family with simple febrile seizures and temporal lobe epilepsy associated with SCN1A loss-of-function mutation. 27
Studio di linkage in tre famiglie calabresi con epilessia frontale notturna autosomica dominante 27
Genetic analysis of SCA2 and SCA17 in familial Parkinson s disease. 27
Description of a four-generation family with autosomal dominant cerebellar ataxia: clinical and genetic analysis. 26
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy. 26
IDENTIFICATION OF A NOVEL HOMOZYGOUS MUTATION IN THE SIL1 GENE IN MARINESCO-SJOGREN SYNDROME 26
Totale 4.346
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Categoria #
all - tutte 25.021
article - articoli 9.999
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 186
Totale 35.206
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202440 0 0 0 0 0 0 0 0 2 0 27 11
2024/20252.624 30 11 182 139 508 63 53 75 41 99 731 692
2025/20264.236 201 416 405 673 702 136 666 249 358 236 99 95
2026/2027213 205 8 0 0 0 0 0 0 0 0 0 0
Totale 7.113