CNR Institutional Research Information System

CITRIGNO, LUIGI
 Distribuzione geografica
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Continente #
AS - Asia 3.456
NA - Nord America 1.697
EU - Europa 1.201
SA - Sud America 661
AF - Africa 64
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 1
Totale 7.091
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Nazione #
US - Stati Uniti d'America 1.610
SG - Singapore 1.331
CN - Cina 861
IT - Italia 567
BR - Brasile 532
HK - Hong Kong 355
VN - Vietnam 329
FR - Francia 226
KR - Corea 171
JP - Giappone 149
NL - Olanda 95
IN - India 67
DE - Germania 66
GB - Regno Unito 53
FI - Finlandia 51
AR - Argentina 44
BD - Bangladesh 35
MX - Messico 31
CA - Canada 30
IL - Israele 28
EC - Ecuador 25
IE - Irlanda 23
AT - Austria 20
ZA - Sudafrica 18
ID - Indonesia 17
CO - Colombia 16
ES - Italia 15
PL - Polonia 14
VE - Venezuela 14
PK - Pakistan 12
PY - Paraguay 12
UA - Ucraina 12
IQ - Iraq 11
SA - Arabia Saudita 11
TR - Turchia 11
RU - Federazione Russa 9
IR - Iran 8
MA - Marocco 8
MY - Malesia 8
TN - Tunisia 8
CL - Cile 7
EG - Egitto 7
KE - Kenya 7
AU - Australia 6
DZ - Algeria 6
NO - Norvegia 6
OM - Oman 6
PE - Perù 6
SE - Svezia 6
TT - Trinidad e Tobago 6
HN - Honduras 5
KG - Kirghizistan 5
PH - Filippine 5
UZ - Uzbekistan 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
CZ - Repubblica Ceca 4
JM - Giamaica 4
KZ - Kazakistan 4
LT - Lituania 4
TH - Thailandia 4
BE - Belgio 3
BG - Bulgaria 3
BO - Bolivia 3
EE - Estonia 3
HU - Ungheria 3
JO - Giordania 3
MD - Moldavia 3
NG - Nigeria 3
NZ - Nuova Zelanda 3
AL - Albania 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
GR - Grecia 2
NP - Nepal 2
PA - Panama 2
PS - Palestinian Territory 2
RO - Romania 2
SI - Slovenia 2
UY - Uruguay 2
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BN - Brunei Darussalam 1
BS - Bahamas 1
BY - Bielorussia 1
CI - Costa d'Avorio 1
CM - Camerun 1
CY - Cipro 1
DK - Danimarca 1
ET - Etiopia 1
GP - Guadalupe 1
GT - Guatemala 1
KH - Cambogia 1
KI - Kiribati 1
LB - Libano 1
LC - Santa Lucia 1
LU - Lussemburgo 1
ML - Mali 1
MT - Malta 1
NI - Nicaragua 1
Totale 7.081
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Città #
Singapore 854
Santa Clara 563
Hefei 387
Hong Kong 352
San Jose 199
Seoul 170
Lauterbourg 147
Beijing 129
Tokyo 122
Ashburn 108
Ho Chi Minh City 98
Naples 85
Hanoi 84
Los Angeles 74
Dallas 68
New York 62
São Paulo 45
Milan 40
Catania 39
Bari 34
Taranto 28
Frankfurt am Main 27
Minamishinagawa 26
Rome 26
Helsinki 24
Dublin 23
Buffalo 22
Haiphong 22
Orem 19
Amsterdam 18
Lappeenranta 17
Vienna 17
Council Bluffs 14
Rio de Janeiro 14
Bengaluru 13
Da Nang 13
Belo Horizonte 12
Mexico City 12
Curitiba 11
Montreal 11
Guayaquil 10
Messina 10
Phoenix 10
Acri 9
Atlanta 9
London 9
Mumbai 9
Palermo 9
Porto Alegre 9
Quito 9
Turin 9
Warsaw 9
Brooklyn 8
Campinas 8
Dhaka 8
Düsseldorf 8
Fortaleza 8
Hải Dương 8
Johannesburg 8
New Delhi 8
Nuremberg 8
Quận Bình Thạnh 8
Asunción 7
Brasília 7
Can Tho 7
Chennai 7
Elk Grove Village 7
Guangzhou 7
Riyadh 7
Turku 7
Altamura 6
Biên Hòa 6
Charlotte 6
Las Vegas 6
Paris 6
Poplar 6
Portsmouth 6
Quận Một 6
Thái Bình 6
Bishkek 5
Cabo Frio 5
Chicago 5
Cosenza 5
Kyiv 5
Luzzi 5
Manchester 5
Nairobi 5
Osasco 5
Piracicaba 5
Salvador 5
San Francisco 5
Stockholm 5
Baghdad 4
Baku 4
Boardman 4
Bonn 4
Buenos Aires 4
Bắc Ninh 4
Denver 4
Dourados 4
Totale 4.427
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Nome #
Secondary metabolites of wild plants from Pollino National Park(CS), Gentiana lutea L. and Hypericum perforatum L. and their cytoprotective and anti-obesity activity 131
In vitro study of the cytoprotective effects of chitosan polymeric nanoparticles carrying active ingredients in response to exogenous stimuli of oxidative nature 129
The Role of Mitochondrial Copy Number in Neurodegenerative Diseases: Present Insights and Future Directions 123
MALDI-ISD mass spectrometry analysis as a simple and reliable tool to detect post-translational modifications of hemoglobin variants: the case of Hb Raleigh 122
Exploring the FKRP Gene in Calabrian Patients with Duchenne/Becker-like Phenotype 105
Genomics landscape of mitochondrial DNA variations in patients from South Italy affected by mitochondriopathies 95
LC-MALDI-TOF ISD MS analysis is an effective, simple and rapid method of investigation for histones characterization: Application to EBV lymphoblastoid cell lines 93
Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes 87
A novel homozygous variant in DYSF gene is associated with Autosomal Recessive Limb Girdle Muscular Dystrophy R2/2B 86
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis 84
Isolation and characterization of soil microorganisms from two National Parks located in the middle of the Mediterranean area as potential biocontrol agents 83
Identificato in un paziente del Sud Italia la variante Arg596Gly in omozigosi associata a Distrofia Muscolare dei Cingoli recessiva di tipo 8 82
Targeted next-generation sequencing revealed a new mutation in GLRA1 gene in a family with Hereditary Hyperekplexia 81
A new mutation detected by NGS in MT-ATP6 gene associated with MELAS and in silico 3D protein analysis 81
Exome sequencing reveals two FA2H mutations in a family with a complicated form of Hereditary Spastic Paraplegia and psychiatric impairments 80
Isolation and Characterization of Soil Degrading Matter Bacteria from Mediterranean Area as Potential Biocontrol and Bioindicator Agents 79
Mutational screening of the eIF2B5 gene in sib pairs affected by multiple sclerosis. 77
Sex and APOE genotype modulate neuropsychological profile and depression in temporal lobe epilepsy 77
Targeted NGS-panel can improve the simultaneous identification of CNVs and SNVs in Mendelian diseases 76
Molecular Study of the Fukutin-Related Protein (FKRP) Gene in Patients from Southern Italy with Duchenne/Becker-like Phenotype 75
RAPID IDENTIFICATION OF PATHOGENIC VARIANTS IN NEUROFIBROMATOSIS DISEASE BY GENE-PANEL SEQUENCING. 75
Potential cytoprotective effects of chitosan polymeric nanoparticles carrying active ingredients in response to external oxidative stimuli 73
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 72
HOMOZYGOUS R596G VARIANT IN TRIM32 GENE RELATED TO LGMD IN A NON-HUTTERITE PATIENT 72
Arg143Ser is the most frequent variant in Limb Girdle Muscular Dystrophy-R9 in southern Italy 71
EBV immortalized human lymphoblastoid cell lines as a source for iPSCs generation by nucleofection 71
A NEW CYS1678TYR MUTATION RESPONSIBLE OF LGMD2B IDENTIFIED IN A FAMILY FROM SOUTHERN ITALY 70
Gene Symbol: MECP2. Disease: Rett Syndrome. 69
Seizures and epilepsy in neurofibromatosis type 1 (NF1): a genotype-phenotype study. 68
Interruptions of the FXN GAA repeat tract delay the age at onset of Friedreich's ataxia in a location dependent manner. 67
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 66
A WHOLE mtDNA NGS APPROACH TO IDENTIFY NOVEL VARIANTS IN PATIENTS AFFECTED BY MITOCHONDRIAL DISEASES 66
Mutational Screening in Patient with Charcot-Marie-Tooth Disease Type 2A 65
A novel missense mutation (p.Arg309His) in the nuclear localization signal sequence of spastin protein causes a complicated form of Hereditary Spastic Paraplegia 63
Alzheimer's Disease as A Viral Infectious Disease: Revisiting the Infectious Hypothesis 63
Rare variants detected by Next Generation Sequencing in two siblings affected by late onset Parkinson's disease 62
Exome sequencing reveals two FA2H mutations in a non-consanguineous Italian family 61
A Blood-Based Molecular Clock for Biological Age Estimation 61
A novel mutation in the 3 UTR of SPG4 gene identified in an apparently sporadic patient affected by spastic paraplegia. 60
NOTCH3 gene mutations in twins with CADASIL 58
First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia. 58
Genomic analysis identifies a new EIF2B3 gene variant detected in an uncertain case of CADASIL disease 57
ISOLATION AND CHARACTERIZATION OF FOREST SOIL ORGANIC MATTER DEGRADATION BACTERIA IN CALABRIA REGION, SOUTHERN ITALY 57
Targeted Next Generation Sequencing is a valuable diagnostic tool for Inherited Peripheral Neuropathies 57
CHARGE syndrome and ALS: a clinical and genetic study of a family from Southern Italy. 56
ALS and CHARGE syndrome: a clinical and genetic study 56
A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness 55
Epigenetic Clocks and Their Prospective Application in the Complex Landscape of Aging and Alzheimer’s Disease 55
A novel locus for dHMN with pyramidal features maps to chromosome 4q34.3-q35.2. 54
Exploring Mitochondrial DNA Copy Number in Italian Children with ADHD: Implications for Neurobiological Mechanisms 53
VarHunter: a platform to process and analyze data from patients with neurological diseases 53
Discovery novel variations in Sleep-related Hypermotor Epilepsy (SHE) using Next Generation Sequencing approach 53
Clinical and genetic study of an Italian family linked to SPG26 locus 52
Fast and accurate SNVs and CNVs screening in Parkinson's Disease patients using Next-Generation approach 52
A 71-nucleotide Deletion in the Periaxin Gene in an Italian Patient With Late-Onset Slowly Progressive Demyelinating CMT 52
FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis. 51
NOTCH3 gene analysis in two couples of twins 50
Characterizing Fractal Genetic Variation in the Human Genome from the Hapmap Project 50
Kinesins in neurological inherited diseases: a novel motor-domain mutation in KIF5A gene in a patient from Southern Italy affected by hereditary spastic paraplegia. 50
Clinical features and genetic analysis of two siblings with Startle disease in a family of South Italy 49
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report 48
A large Italian family with R521C mutation in the FUS/TLS gene 47
The Mitochondrial Dysfunction Hypothesis in Autism Spectrum Disorders: Current Status and Future Perspectives 46
Next-generation sequencing: identificazione di varianti geniche con effetto additivo nell'espressione del fenotipo patologico LGMD e cardiomiopatia dilatativa. 46
Clinical and molecular investigation in an unusual Rett Syndrome case 45
Identification of a Transthyretin (TTR) Variant by MALDI-TOF Protein Profiling Analysis 44
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 43
A Novel Mutation In The X-Linked Cyclin-Dependent Kinase-Like 5 (CDKL5) Gene Associated With A Severe Rett Phenotype. 43
Spastin Gene Mutations In Italian Patients With Pure And Complicated Forms Of Spastic Paraplegia 42
A novel mutation in the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene associated with a severe Rett phenotype. 42
Exome sequencing reveals two compound heterozygous DDHD2 mutations in a non consanguineous family with ARHSP-TCC 42
Thymic function and survival at advance ages in nursing home residents from Southern Italy 40
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1 40
Autosomal dominant lateral temporal epilepsy (ADLTE): Absence of chromosomal rearrangements in LGI1 gene 40
High-resolution genomic analysis of an amyotrophic lateral sclerosis case in a large spinocerebellar ataxia type 1 family 38
Seizures and epilepsy in neurofibromatosis type 1 (NF1): a genotype-phenotype study. 38
Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia 38
Polymorphisms and mutational analysis of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy. 37
Genetic analysis of TARDBP gene in a color of South Italian ALS patients 37
An ELOVL2-Based Epigenetic Clock for Forensic Age Prediction: A Systematic Review 36
Charcot-Marie-Tooth disease tipe 2A associate with two novel MFN2 mutations 36
Nuove mutazioni identificate nel gene della spastina in soggetti affetti da Paraplegia Spastica Ereditaria 35
EXOME SEQUENCING REVEALS TWO COMPOUND HETEROZYGOUS DDHD2 MUTATIONS IN A NON CONSANGUINEOUS SICILIAN FAMILY WITH ARHSP-TCC 34
SPASTIN GENE MUTATIONS IN ITALIAN PATIENTS WITH A PURE AND COMPLICATED FORMS OF SPASTIC PARAPLEGIA. 34
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis. 34
Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene. 34
SUGGESTIVE EVIDENCE FOR LINKAGE TO CHROMOSOME 4qter FOR AUTOSOMAL DOMINANT DISTAL MOTOR NEURONOPATHY 33
Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum 33
Targeted Next-Generation Sequencing revealed rare variations in two siblings affected by late onset Parkinson's disease. 33
Clinical and genetic study of an Italian family with Autosomal Recessive Spastic Paraplegia associated with dysarthria and hearing loss. 33
The p.Arg416Cys mutation in SPG3a gene associated with a pure form of spastic paraplegia. 33
Charcot-Marie-Tooth X-linked: five novel mutations in Italian patients 32
CADASIL: extended polymorphisms and mutational analysis of the NOTCH3 gene. 32
A novel SPG3A mutation in an Italian patient with Hereditary Spastic Paraplegia 32
A novel locus for Autosomal Dominant Distal Motor Neuronopathy maps to chromosome 4q-ter 32
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 31
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy 31
CADASIL: molecular screening of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy. 31
Huntington disease like 2 in Southern Italy: screening of JPH3 and other genes involved in huntington like phenotypes. 31
Angiogenin Gene And Amyotrophic Lateral Sclerosis In Southern Italy 30
Totale 5.735
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Categoria #
all - tutte 20.988
article - articoli 10.046
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 31.034
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202428 0 0 0 0 0 0 0 0 6 0 20 2
2024/20252.821 86 23 223 120 639 125 57 69 137 146 657 539
2025/20264.378 305 520 397 606 832 191 581 236 309 280 121 0
Totale 7.227