CNR Institutional Research Information System

CITRIGNO, LUIGI
 Distribuzione geografica
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Continente #
AS - Asia 3.510
NA - Nord America 1.953
EU - Europa 1.281
SA - Sud America 665
AF - Africa 66
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 1
Totale 7.487
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Nazione #
US - Stati Uniti d'America 1.834
SG - Singapore 1.333
CN - Cina 862
IT - Italia 642
BR - Brasile 535
HK - Hong Kong 355
VN - Vietnam 330
FR - Francia 227
KR - Corea 171
JP - Giappone 149
NL - Olanda 95
BD - Bangladesh 83
IN - India 67
DE - Germania 66
GB - Regno Unito 53
FI - Finlandia 52
AR - Argentina 44
CA - Canada 44
MX - Messico 31
IL - Israele 28
EC - Ecuador 25
IE - Irlanda 23
AT - Austria 20
ZA - Sudafrica 18
ID - Indonesia 17
CO - Colombia 16
ES - Italia 16
PL - Polonia 16
VE - Venezuela 14
PK - Pakistan 12
PY - Paraguay 12
UA - Ucraina 12
IQ - Iraq 11
SA - Arabia Saudita 11
TR - Turchia 11
JM - Giamaica 10
IR - Iran 9
RU - Federazione Russa 9
TN - Tunisia 9
CL - Cile 8
EG - Egitto 8
MA - Marocco 8
MY - Malesia 8
KE - Kenya 7
AU - Australia 6
DZ - Algeria 6
NI - Nicaragua 6
NO - Norvegia 6
OM - Oman 6
PE - Perù 6
SE - Svezia 6
TT - Trinidad e Tobago 6
CR - Costa Rica 5
HN - Honduras 5
KG - Kirghizistan 5
PH - Filippine 5
TH - Thailandia 5
UZ - Uzbekistan 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
CZ - Repubblica Ceca 4
KZ - Kazakistan 4
LT - Lituania 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
SV - El Salvador 3
AL - Albania 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
KY - Cayman, isole 1
LB - Libano 1
LC - Santa Lucia 1
LU - Lussemburgo 1
Totale 7.475
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Città #
Singapore 856
Santa Clara 570
Hefei 387
Hong Kong 352
San Jose 201
Seoul 170
Lauterbourg 147
Beijing 129
Tokyo 122
Ashburn 120
Ho Chi Minh City 98
Naples 91
Hanoi 84
Los Angeles 79
Dallas 71
New York 70
Catania 45
São Paulo 45
Milan 42
Rome 38
Bari 34
Taranto 29
Buffalo 28
Frankfurt am Main 27
Minamishinagawa 26
Helsinki 24
Dublin 23
Haiphong 22
Orem 19
Amsterdam 18
Lappeenranta 17
Vienna 17
Council Bluffs 16
Brooklyn 14
Rio de Janeiro 14
Bengaluru 13
Da Nang 13
Belo Horizonte 12
Mexico City 12
Montreal 12
Atlanta 11
Curitiba 11
Phoenix 11
Guayaquil 10
Messina 10
Palermo 10
Warsaw 10
Acri 9
London 9
Mumbai 9
Porto Alegre 9
Quito 9
Turin 9
Campinas 8
Dhaka 8
Düsseldorf 8
Fortaleza 8
Hải Dương 8
Johannesburg 8
Kingston 8
Las Vegas 8
New Delhi 8
Nuremberg 8
Quận Bình Thạnh 8
Asunción 7
Boardman 7
Brasília 7
Can Tho 7
Charlotte 7
Chennai 7
Chicago 7
Elk Grove Village 7
Genoa 7
Guangzhou 7
Portsmouth 7
Riyadh 7
Turku 7
Altamura 6
Biên Hòa 6
Denver 6
Houston 6
Managua 6
Newark 6
Paris 6
Poplar 6
Quận Một 6
Salvador 6
Thái Bình 6
Bishkek 5
Cabo Frio 5
Cosenza 5
Florence 5
Kyiv 5
Luzzi 5
Manchester 5
Nairobi 5
Osasco 5
Piracicaba 5
San Francisco 5
Seattle 5
Totale 4.539
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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 138
In vitro study of the cytoprotective effects of chitosan polymeric nanoparticles carrying active ingredients in response to exogenous stimuli of oxidative nature 134
MALDI-ISD mass spectrometry analysis as a simple and reliable tool to detect post-translational modifications of hemoglobin variants: the case of Hb Raleigh 124
The Role of Mitochondrial Copy Number in Neurodegenerative Diseases: Present Insights and Future Directions 124
Exploring the FKRP Gene in Calabrian Patients with Duchenne/Becker-like Phenotype 112
Targeted next-generation sequencing revealed a new mutation in GLRA1 gene in a family with Hereditary Hyperekplexia 100
Genomics landscape of mitochondrial DNA variations in patients from South Italy affected by mitochondriopathies 97
Isolation and Characterization of Soil Degrading Matter Bacteria from Mediterranean Area as Potential Biocontrol and Bioindicator Agents 97
LC-MALDI-TOF ISD MS analysis is an effective, simple and rapid method of investigation for histones characterization: Application to EBV lymphoblastoid cell lines 94
A new mutation detected by NGS in MT-ATP6 gene associated with MELAS and in silico 3D protein analysis 94
RAPID IDENTIFICATION OF PATHOGENIC VARIANTS IN NEUROFIBROMATOSIS DISEASE BY GENE-PANEL SEQUENCING. 92
A novel homozygous variant in DYSF gene is associated with Autosomal Recessive Limb Girdle Muscular Dystrophy R2/2B 91
Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes 89
Identificato in un paziente del Sud Italia la variante Arg596Gly in omozigosi associata a Distrofia Muscolare dei Cingoli recessiva di tipo 8 88
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis 85
Isolation and characterization of soil microorganisms from two National Parks located in the middle of the Mediterranean area as potential biocontrol agents 84
Exome sequencing reveals two FA2H mutations in a family with a complicated form of Hereditary Spastic Paraplegia and psychiatric impairments 80
Sex and APOE genotype modulate neuropsychological profile and depression in temporal lobe epilepsy 80
Mutational screening of the eIF2B5 gene in sib pairs affected by multiple sclerosis. 79
Targeted NGS-panel can improve the simultaneous identification of CNVs and SNVs in Mendelian diseases 79
Potential cytoprotective effects of chitosan polymeric nanoparticles carrying active ingredients in response to external oxidative stimuli 79
Molecular Study of the Fukutin-Related Protein (FKRP) Gene in Patients from Southern Italy with Duchenne/Becker-like Phenotype 78
Rare variants detected by Next Generation Sequencing in two siblings affected by late onset Parkinson's disease 77
Arg143Ser is the most frequent variant in Limb Girdle Muscular Dystrophy-R9 in southern Italy 77
A NEW CYS1678TYR MUTATION RESPONSIBLE OF LGMD2B IDENTIFIED IN A FAMILY FROM SOUTHERN ITALY 77
HOMOZYGOUS R596G VARIANT IN TRIM32 GENE RELATED TO LGMD IN A NON-HUTTERITE PATIENT 74
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 73
A WHOLE mtDNA NGS APPROACH TO IDENTIFY NOVEL VARIANTS IN PATIENTS AFFECTED BY MITOCHONDRIAL DISEASES 73
EBV immortalized human lymphoblastoid cell lines as a source for iPSCs generation by nucleofection 72
Interruptions of the FXN GAA repeat tract delay the age at onset of Friedreich's ataxia in a location dependent manner. 70
Gene Symbol: MECP2. Disease: Rett Syndrome. 69
Seizures and epilepsy in neurofibromatosis type 1 (NF1): a genotype-phenotype study. 69
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 67
Alzheimer's Disease as A Viral Infectious Disease: Revisiting the Infectious Hypothesis 67
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 65
A Blood-Based Molecular Clock for Biological Age Estimation 64
Exome sequencing reveals two FA2H mutations in a non-consanguineous Italian family 63
Epigenetic Clocks and Their Prospective Application in the Complex Landscape of Aging and Alzheimer’s Disease 63
Genomic analysis identifies a new EIF2B3 gene variant detected in an uncertain case of CADASIL disease 61
A novel mutation in the 3 UTR of SPG4 gene identified in an apparently sporadic patient affected by spastic paraplegia. 60
ISOLATION AND CHARACTERIZATION OF FOREST SOIL ORGANIC MATTER DEGRADATION BACTERIA IN CALABRIA REGION, SOUTHERN ITALY 60
NOTCH3 gene mutations in twins with CADASIL 59
First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia. 59
Targeted Next Generation Sequencing is a valuable diagnostic tool for Inherited Peripheral Neuropathies 59
A 71-nucleotide Deletion in the Periaxin Gene in an Italian Patient With Late-Onset Slowly Progressive Demyelinating CMT 59
CHARGE syndrome and ALS: a clinical and genetic study of a family from Southern Italy. 58
Exploring Mitochondrial DNA Copy Number in Italian Children with ADHD: Implications for Neurobiological Mechanisms 57
VarHunter: a platform to process and analyze data from patients with neurological diseases 57
A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness 57
Fast and accurate SNVs and CNVs screening in Parkinson's Disease patients using Next-Generation approach 56
ALS and CHARGE syndrome: a clinical and genetic study 56
A novel locus for dHMN with pyramidal features maps to chromosome 4q34.3-q35.2. 55
Kinesins in neurological inherited diseases: a novel motor-domain mutation in KIF5A gene in a patient from Southern Italy affected by hereditary spastic paraplegia. 54
Discovery novel variations in Sleep-related Hypermotor Epilepsy (SHE) using Next Generation Sequencing approach 54
NOTCH3 gene analysis in two couples of twins 52
Clinical and genetic study of an Italian family linked to SPG26 locus 52
FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis. 52
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report 52
Characterizing Fractal Genetic Variation in the Human Genome from the Hapmap Project 50
Clinical features and genetic analysis of two siblings with Startle disease in a family of South Italy 50
Next-generation sequencing: identificazione di varianti geniche con effetto additivo nell'espressione del fenotipo patologico LGMD e cardiomiopatia dilatativa. 50
A large Italian family with R521C mutation in the FUS/TLS gene 47
Identification of a Transthyretin (TTR) Variant by MALDI-TOF Protein Profiling Analysis 47
The Mitochondrial Dysfunction Hypothesis in Autism Spectrum Disorders: Current Status and Future Perspectives 47
Clinical and molecular investigation in an unusual Rett Syndrome case 45
A Novel Mutation In The X-Linked Cyclin-Dependent Kinase-Like 5 (CDKL5) Gene Associated With A Severe Rett Phenotype. 45
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 44
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1 44
Spastin Gene Mutations In Italian Patients With Pure And Complicated Forms Of Spastic Paraplegia 43
Exome sequencing reveals two compound heterozygous DDHD2 mutations in a non consanguineous family with ARHSP-TCC 43
A novel mutation in the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene associated with a severe Rett phenotype. 42
Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia 42
Thymic function and survival at advance ages in nursing home residents from Southern Italy 42
Autosomal dominant lateral temporal epilepsy (ADLTE): Absence of chromosomal rearrangements in LGI1 gene 42
High-resolution genomic analysis of an amyotrophic lateral sclerosis case in a large spinocerebellar ataxia type 1 family 40
Genetic analysis of TARDBP gene in a color of South Italian ALS patients 40
Polymorphisms and mutational analysis of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy. 39
Seizures and epilepsy in neurofibromatosis type 1 (NF1): a genotype-phenotype study. 38
An ELOVL2-Based Epigenetic Clock for Forensic Age Prediction: A Systematic Review 38
Nuove mutazioni identificate nel gene della spastina in soggetti affetti da Paraplegia Spastica Ereditaria 37
Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum 37
Association between gut microbiota composition and physical functioning in patients with knee osteoarthritis: a machine learning study 37
Charcot-Marie-Tooth disease tipe 2A associate with two novel MFN2 mutations 37
EXOME SEQUENCING REVEALS TWO COMPOUND HETEROZYGOUS DDHD2 MUTATIONS IN A NON CONSANGUINEOUS SICILIAN FAMILY WITH ARHSP-TCC 36
CADASIL: extended polymorphisms and mutational analysis of the NOTCH3 gene. 35
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis. 35
Charcot-Marie-Tooth X-linked: five novel mutations in Italian patients 34
SUGGESTIVE EVIDENCE FOR LINKAGE TO CHROMOSOME 4qter FOR AUTOSOMAL DOMINANT DISTAL MOTOR NEURONOPATHY 34
Targeted Next-Generation Sequencing revealed rare variations in two siblings affected by late onset Parkinson's disease. 34
SPASTIN GENE MUTATIONS IN ITALIAN PATIENTS WITH A PURE AND COMPLICATED FORMS OF SPASTIC PARAPLEGIA. 34
The p.Arg416Cys mutation in SPG3a gene associated with a pure form of spastic paraplegia. 34
Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene. 34
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 33
CADASIL: molecular screening of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy. 33
Clinical and genetic study of an Italian family with Autosomal Recessive Spastic Paraplegia associated with dysarthria and hearing loss. 33
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy 32
A novel SPG3A mutation in an Italian patient with Hereditary Spastic Paraplegia 32
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy 32
Huntington disease like 2 in Southern Italy: screening of JPH3 and other genes involved in huntington like phenotypes. 32
Totale 6.035
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Categoria #
all - tutte 23.693
article - articoli 11.340
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 35.033
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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
2025/20264.578 305 520 397 606 832 191 581 236 309 280 178 143
2026/2027207 207 0 0 0 0 0 0 0 0 0 0 0
Totale 7.634