CNR Institutional Research Information System

CITRIGNO, LUIGI
 Distribuzione geografica
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Continente #
AS - Asia 3.570
NA - Nord America 2.471
EU - Europa 1.353
SA - Sud America 705
Continente sconosciuto - Info sul continente non disponibili 150
AF - Africa 68
OC - Oceania 11
Totale 8.328
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Nazione #
US - Stati Uniti d'America 2.312
SG - Singapore 1.334
CN - Cina 863
IT - Italia 694
BR - Brasile 555
HK - Hong Kong 357
VN - Vietnam 342
FR - Francia 232
KR - Corea 171
JP - Giappone 149
NL - Olanda 97
BD - Bangladesh 94
IN - India 69
DE - Germania 67
GB - Regno Unito 60
CA - Canada 58
FI - Finlandia 52
AR - Argentina 44
MX - Messico 33
EC - Ecuador 29
CO - Colombia 28
IL - Israele 28
ID - Indonesia 25
IE - Irlanda 23
AT - Austria 20
VE - Venezuela 18
ZA - Sudafrica 18
ES - Italia 16
PL - Polonia 16
UA - Ucraina 15
JM - Giamaica 14
MY - Malesia 13
SA - Arabia Saudita 13
TR - Turchia 13
PK - Pakistan 12
PY - Paraguay 12
TH - Thailandia 12
IQ - Iraq 11
NI - Nicaragua 10
PH - Filippine 10
CR - Costa Rica 9
IR - Iran 9
RU - Federazione Russa 9
TN - Tunisia 9
TT - Trinidad e Tobago 9
CL - Cile 8
EG - Egitto 8
MA - Marocco 8
HN - Honduras 7
KE - Kenya 7
AU - Australia 6
DZ - Algeria 6
NO - Norvegia 6
OM - Oman 6
PE - Perù 6
SE - Svezia 6
GT - Guatemala 5
KG - Kirghizistan 5
UZ - Uzbekistan 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
BG - Bulgaria 4
CZ - Repubblica Ceca 4
EE - Estonia 4
KZ - Kazakistan 4
LT - Lituania 4
BE - Belgio 3
BO - Bolivia 3
HU - Ungheria 3
JO - Giordania 3
MD - Moldavia 3
NG - Nigeria 3
NP - Nepal 3
NZ - Nuova Zelanda 3
PA - Panama 3
SV - El Salvador 3
AL - Albania 2
CW - ???statistics.table.value.countryCode.CW??? 2
DO - Repubblica Dominicana 2
GR - Grecia 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
BZ - Belize 1
CG - Congo 1
CI - Costa d'Avorio 1
CM - Camerun 1
CY - Cipro 1
DK - Danimarca 1
ET - Etiopia 1
GD - Grenada 1
GP - Guadalupe 1
KH - Cambogia 1
KI - Kiribati 1
Totale 8.163
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Città #
Singapore 857
Santa Clara 577
Hefei 387
Hong Kong 354
San Jose 246
Seoul 170
Lauterbourg 147
Ashburn 141
Beijing 129
Tokyo 122
Ho Chi Minh City 107
Naples 95
Los Angeles 87
Hanoi 86
Dallas 72
New York 72
Milan 47
Rome 47
São Paulo 47
Catania 45
Bari 35
Buffalo 31
Taranto 29
Frankfurt am Main 27
Minamishinagawa 26
Council Bluffs 25
Dublin 24
Helsinki 24
Haiphong 22
Brooklyn 19
Orem 19
Amsterdam 18
Lappeenranta 17
Vienna 17
Atlanta 16
Chicago 14
Da Nang 14
Montreal 14
Newark 14
Rio de Janeiro 14
Bengaluru 13
Guayaquil 13
Mexico City 13
Phoenix 13
Belo Horizonte 12
Philadelphia 12
Curitiba 11
Houston 11
Kingston 11
Las Vegas 11
Turin 11
Managua 10
Messina 10
Palermo 10
Quito 10
Warsaw 10
Acri 9
Brasília 9
Charlotte 9
Dhaka 9
London 9
Mumbai 9
New Delhi 9
Porto Alegre 9
Boardman 8
Campinas 8
Düsseldorf 8
Fortaleza 8
Hải Dương 8
Johannesburg 8
Kuala Lumpur 8
Nuremberg 8
Quận Bình Thạnh 8
The Bronx 8
Asunción 7
Baltimore 7
Bogotá 7
Can Tho 7
Chennai 7
Denver 7
Elk Grove Village 7
Genoa 7
Guangzhou 7
Memphis 7
Portsmouth 7
Princeton 7
Riyadh 7
San José 7
Toronto 7
Turku 7
Altamura 6
Birmingham 6
Biên Hòa 6
Cabo Frio 6
Kyiv 6
Osasco 6
Paris 6
Poplar 6
Queens 6
Quận Một 6
Totale 4.759
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Nome #
Targeted next-generation sequencing revealed a new mutation in GLRA1 gene in a family with Hereditary Hyperekplexia 149
Secondary metabolites of wild plants from Pollino National Park(CS), Gentiana lutea L. and Hypericum perforatum L. and their cytoprotective and anti-obesity activity 143
In vitro study of the cytoprotective effects of chitosan polymeric nanoparticles carrying active ingredients in response to exogenous stimuli of oxidative nature 139
MALDI-ISD mass spectrometry analysis as a simple and reliable tool to detect post-translational modifications of hemoglobin variants: the case of Hb Raleigh 130
The Role of Mitochondrial Copy Number in Neurodegenerative Diseases: Present Insights and Future Directions 128
Exploring the FKRP Gene in Calabrian Patients with Duchenne/Becker-like Phenotype 115
A new mutation detected by NGS in MT-ATP6 gene associated with MELAS and in silico 3D protein analysis 106
Genomics landscape of mitochondrial DNA variations in patients from South Italy affected by mitochondriopathies 102
Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes 101
Isolation and Characterization of Soil Degrading Matter Bacteria from Mediterranean Area as Potential Biocontrol and Bioindicator Agents 101
LC-MALDI-TOF ISD MS analysis is an effective, simple and rapid method of investigation for histones characterization: Application to EBV lymphoblastoid cell lines 100
RAPID IDENTIFICATION OF PATHOGENIC VARIANTS IN NEUROFIBROMATOSIS DISEASE BY GENE-PANEL SEQUENCING. 100
A novel homozygous variant in DYSF gene is associated with Autosomal Recessive Limb Girdle Muscular Dystrophy R2/2B 97
Identificato in un paziente del Sud Italia la variante Arg596Gly in omozigosi associata a Distrofia Muscolare dei Cingoli recessiva di tipo 8 94
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis 87
Targeted NGS-panel can improve the simultaneous identification of CNVs and SNVs in Mendelian diseases 87
Isolation and characterization of soil microorganisms from two National Parks located in the middle of the Mediterranean area as potential biocontrol agents 85
Rare variants detected by Next Generation Sequencing in two siblings affected by late onset Parkinson's disease 84
Potential cytoprotective effects of chitosan polymeric nanoparticles carrying active ingredients in response to external oxidative stimuli 84
Arg143Ser is the most frequent variant in Limb Girdle Muscular Dystrophy-R9 in southern Italy 84
EBV immortalized human lymphoblastoid cell lines as a source for iPSCs generation by nucleofection 84
Mutational screening of the eIF2B5 gene in sib pairs affected by multiple sclerosis. 83
Exome sequencing reveals two FA2H mutations in a family with a complicated form of Hereditary Spastic Paraplegia and psychiatric impairments 83
Sex and APOE genotype modulate neuropsychological profile and depression in temporal lobe epilepsy 83
A NEW CYS1678TYR MUTATION RESPONSIBLE OF LGMD2B IDENTIFIED IN A FAMILY FROM SOUTHERN ITALY 82
Molecular Study of the Fukutin-Related Protein (FKRP) Gene in Patients from Southern Italy with Duchenne/Becker-like Phenotype 81
Interruptions of the FXN GAA repeat tract delay the age at onset of Friedreich's ataxia in a location dependent manner. 81
HOMOZYGOUS R596G VARIANT IN TRIM32 GENE RELATED TO LGMD IN A NON-HUTTERITE PATIENT 79
A WHOLE mtDNA NGS APPROACH TO IDENTIFY NOVEL VARIANTS IN PATIENTS AFFECTED BY MITOCHONDRIAL DISEASES 79
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 74
Alzheimer's Disease as A Viral Infectious Disease: Revisiting the Infectious Hypothesis 72
Gene Symbol: MECP2. Disease: Rett Syndrome. 71
Seizures and epilepsy in neurofibromatosis type 1 (NF1): a genotype-phenotype study. 70
A Blood-Based Molecular Clock for Biological Age Estimation 70
Mutational Screening in Patient with Charcot-Marie-Tooth Disease Type 2A 69
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 69
Targeted Next Generation Sequencing is a valuable diagnostic tool for Inherited Peripheral Neuropathies 69
A novel missense mutation (p.Arg309His) in the nuclear localization signal sequence of spastin protein causes a complicated form of Hereditary Spastic Paraplegia 68
Genomic analysis identifies a new EIF2B3 gene variant detected in an uncertain case of CADASIL disease 67
ISOLATION AND CHARACTERIZATION OF FOREST SOIL ORGANIC MATTER DEGRADATION BACTERIA IN CALABRIA REGION, SOUTHERN ITALY 67
A novel mutation in the 3 UTR of SPG4 gene identified in an apparently sporadic patient affected by spastic paraplegia. 66
FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis. 66
Epigenetic Clocks and Their Prospective Application in the Complex Landscape of Aging and Alzheimer’s Disease 66
Exome sequencing reveals two FA2H mutations in a non-consanguineous Italian family 64
Exploring Mitochondrial DNA Copy Number in Italian Children with ADHD: Implications for Neurobiological Mechanisms 63
NOTCH3 gene mutations in twins with CADASIL 62
First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia. 62
CHARGE syndrome and ALS: a clinical and genetic study of a family from Southern Italy. 62
Fast and accurate SNVs and CNVs screening in Parkinson's Disease patients using Next-Generation approach 62
VarHunter: a platform to process and analyze data from patients with neurological diseases 62
ALS and CHARGE syndrome: a clinical and genetic study 61
A 71-nucleotide Deletion in the Periaxin Gene in an Italian Patient With Late-Onset Slowly Progressive Demyelinating CMT 61
A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness 60
Discovery novel variations in Sleep-related Hypermotor Epilepsy (SHE) using Next Generation Sequencing approach 59
A novel locus for dHMN with pyramidal features maps to chromosome 4q34.3-q35.2. 58
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report 58
Kinesins in neurological inherited diseases: a novel motor-domain mutation in KIF5A gene in a patient from Southern Italy affected by hereditary spastic paraplegia. 58
Clinical features and genetic analysis of two siblings with Startle disease in a family of South Italy 56
Clinical and genetic study of an Italian family linked to SPG26 locus 55
Characterizing Fractal Genetic Variation in the Human Genome from the Hapmap Project 55
Next-generation sequencing: identificazione di varianti geniche con effetto additivo nell'espressione del fenotipo patologico LGMD e cardiomiopatia dilatativa. 55
NOTCH3 gene analysis in two couples of twins 54
Identification of a Transthyretin (TTR) Variant by MALDI-TOF Protein Profiling Analysis 51
The Mitochondrial Dysfunction Hypothesis in Autism Spectrum Disorders: Current Status and Future Perspectives 51
A large Italian family with R521C mutation in the FUS/TLS gene 50
Spastin Gene Mutations In Italian Patients With Pure And Complicated Forms Of Spastic Paraplegia 48
Clinical and molecular investigation in an unusual Rett Syndrome case 48
Autosomal dominant lateral temporal epilepsy (ADLTE): Absence of chromosomal rearrangements in LGI1 gene 48
A Novel Mutation In The X-Linked Cyclin-Dependent Kinase-Like 5 (CDKL5) Gene Associated With A Severe Rett Phenotype. 47
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1 47
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 46
A novel mutation in the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene associated with a severe Rett phenotype. 46
Exome sequencing reveals two compound heterozygous DDHD2 mutations in a non consanguineous family with ARHSP-TCC 46
Thymic function and survival at advance ages in nursing home residents from Southern Italy 46
Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum 45
Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia 45
Genetic analysis of TARDBP gene in a color of South Italian ALS patients 44
High-resolution genomic analysis of an amyotrophic lateral sclerosis case in a large spinocerebellar ataxia type 1 family 43
Polymorphisms and mutational analysis of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy. 42
Seizures and epilepsy in neurofibromatosis type 1 (NF1): a genotype-phenotype study. 41
Nuove mutazioni identificate nel gene della spastina in soggetti affetti da Paraplegia Spastica Ereditaria 40
EXOME SEQUENCING REVEALS TWO COMPOUND HETEROZYGOUS DDHD2 MUTATIONS IN A NON CONSANGUINEOUS SICILIAN FAMILY WITH ARHSP-TCC 40
Association between gut microbiota composition and physical functioning in patients with knee osteoarthritis: a machine learning study 40
An ELOVL2-Based Epigenetic Clock for Forensic Age Prediction: A Systematic Review 40
Targeted Next-Generation Sequencing revealed rare variations in two siblings affected by late onset Parkinson's disease. 39
Charcot-Marie-Tooth disease tipe 2A associate with two novel MFN2 mutations 39
Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene. 39
CADASIL: molecular screening of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy. 38
The p.Arg416Cys mutation in SPG3a gene associated with a pure form of spastic paraplegia. 38
A Novel Notch3 Gene Mutation In A Patient With Cadasil From Southern Italy 37
SPASTIN GENE MUTATIONS IN ITALIAN PATIENTS WITH A PURE AND COMPLICATED FORMS OF SPASTIC PARAPLEGIA. 37
Charcot-Marie-Tooth X-linked: five novel mutations in Italian patients 36
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 36
CADASIL: extended polymorphisms and mutational analysis of the NOTCH3 gene. 36
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis. 36
Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Italian patients with hereditary spastic paraparesis 36
SUGGESTIVE EVIDENCE FOR LINKAGE TO CHROMOSOME 4qter FOR AUTOSOMAL DOMINANT DISTAL MOTOR NEURONOPATHY 35
A novel SPG3A mutation in an Italian patient with Hereditary Spastic Paraplegia 35
Clinical and genetic study of an Italian family with Autosomal Recessive Spastic Paraplegia associated with dysarthria and hearing loss. 35
Angiogenin Gene And Amyotrophic Lateral Sclerosis In Southern Italy 34
Totale 6.522
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Categoria #
all - tutte 26.278
article - articoli 12.656
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 38.934
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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
2026/2027901 294 238 369 0 0 0 0 0 0 0 0 0
Totale 8.328