Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

ROMANO, Valentino
 Distribuzione geografica
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Continente #
NA - Nord America 5.214
EU - Europa 2.666
AS - Asia 1.985
SA - Sud America 346
Continente sconosciuto - Info sul continente non disponibili 224
AF - Africa 59
OC - Oceania 7
Totale 10.501
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Nazione #
US - Stati Uniti d'America 5.110
IT - Italia 719
SG - Singapore 679
RU - Federazione Russa 601
CN - Cina 532
UA - Ucraina 253
BR - Brasile 229
FI - Finlandia 220
DE - Germania 205
HK - Hong Kong 199
VN - Vietnam 173
GB - Regno Unito 139
PL - Polonia 135
IE - Irlanda 93
FR - Francia 89
JP - Giappone 68
BD - Bangladesh 63
SE - Svezia 61
KR - Corea 57
IN - India 54
CA - Canada 44
NL - Olanda 33
BE - Belgio 32
EC - Ecuador 31
MX - Messico 28
TR - Turchia 28
AR - Argentina 25
CO - Colombia 23
IQ - Iraq 19
UZ - Uzbekistan 16
AT - Austria 15
CI - Costa d'Avorio 15
RO - Romania 14
ID - Indonesia 12
PK - Pakistan 12
SA - Arabia Saudita 12
VE - Venezuela 12
MA - Marocco 11
MY - Malesia 11
ES - Italia 8
JM - Giamaica 8
PH - Filippine 8
ZA - Sudafrica 8
AL - Albania 7
CL - Cile 7
PY - Paraguay 7
CZ - Repubblica Ceca 6
KE - Kenya 6
LB - Libano 6
AE - Emirati Arabi Uniti 5
AU - Australia 5
BO - Bolivia 5
GR - Grecia 5
LT - Lituania 5
UY - Uruguay 5
AZ - Azerbaigian 4
CH - Svizzera 4
CR - Costa Rica 4
GT - Guatemala 4
NG - Nigeria 4
PT - Portogallo 4
SN - Senegal 4
TT - Trinidad e Tobago 4
EE - Estonia 3
IR - Iran 3
JO - Giordania 3
KG - Kirghizistan 3
KZ - Kazakistan 3
MD - Moldavia 3
NI - Nicaragua 3
QA - Qatar 3
BG - Bulgaria 2
BH - Bahrain 2
DZ - Algeria 2
EU - Europa 2
HN - Honduras 2
MM - Myanmar 2
NP - Nepal 2
PA - Panama 2
PE - Perù 2
RS - Serbia 2
SV - El Salvador 2
TH - Thailandia 2
AD - Andorra 1
BA - Bosnia-Erzegovina 1
BW - Botswana 1
BY - Bielorussia 1
CG - Congo 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EG - Egitto 1
ET - Etiopia 1
GA - Gabon 1
GH - Ghana 1
IL - Israele 1
LC - Santa Lucia 1
LV - Lettonia 1
MC - Monaco 1
MF - Saint Martin 1
MK - Macedonia 1
Totale 10.270
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Città #
Ashburn 579
Fairfield 466
Singapore 463
San Jose 325
Woodbridge 283
Chandler 263
Houston 255
Ann Arbor 229
Hong Kong 192
Seattle 190
Wilmington 181
Jacksonville 143
Cambridge 138
Zgierz 110
Palermo 104
Council Bluffs 100
Moscow 94
Des Moines 91
Dublin 88
Beijing 86
Medford 84
New York 78
Santa Clara 77
Frankfurt am Main 75
Los Angeles 73
Tokyo 66
Dallas 65
Nanjing 55
Princeton 54
Ho Chi Minh City 53
Hanoi 50
Hefei 47
Lauterbourg 46
Altamura 42
Boardman 39
Milan 38
San Diego 36
Dearborn 34
Tulsa 33
Buffalo 32
Lawrence 29
Brussels 27
Helsinki 26
Seongnam 24
The Dalles 24
Nanchang 23
Rome 23
Shenyang 21
Chicago 19
São Paulo 19
Changsha 18
Kumar 18
Phoenix 18
Warsaw 18
Jiaxing 17
Ludwigshafen am Rhein 17
Abidjan 15
Hebei 14
Izmir 14
London 14
Montreal 14
Falls Church 13
Tianjin 13
Verona 13
Denver 12
Quito 12
San Francisco 12
Tashkent 12
Amsterdam 11
Da Nang 11
Orem 11
Cardiff 10
Chennai 10
Guangzhou 10
Jinan 10
Philadelphia 10
Rio de Janeiro 10
Seoul 10
Venice 10
Vienna 10
Baghdad 9
Catania 9
City of London 9
Guayaquil 9
Naples 9
Toronto 9
Auburn Hills 8
Bari 8
Bologna 8
Brooklyn 8
Haiphong 8
Hangzhou 8
Atlanta 7
Boston 7
Brasília 7
Casablanca 7
Columbus 7
Manchester 7
Mexico City 7
Ningbo 7
Totale 6.237
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Nome #
Ancient human genomes suggest three ancestral populations for present-day Europeans 356
Analysis of the gastrin-releasing peptide receptor gene in Italian patients with autism spectrum disorders 304
Are mutations in the dhrs9 gene causally linked to epilepsy? A case report 293
Suggestive evidence for association of D2S2188 marker (2q31.1) with autism in 143 Sicilian (Italian) TRIO families 277
mtDNA analysis of the human remains buried in the sarcophagus of Federico II 269
Screening of subtelomeric rearrangements in autistic disorder: identification of a partial trisomy of 13q34 in a patient bearing a 13q;21p translocation 257
Analisi molecolare di 3 geni (NLGN3, NLGN4, GRPR) localizzati sul cromosoma X in una popolazione autistica siciliana. 249
The Greeks in the West: genetic signatures of the Hellenic colonisation in southern Italy and Sicily. 247
Analisi molecolare del gene GRPR in una popolazione autistica siciliana 243
Y-chromosomal STR haplotypes in Sicily 243
Assessing the Impact of Copy Number Variants on miRNA Genes in Autism by Monte Carlo Simulation 236
Analisi delle mutazioni del gene Cx26 (GJB2) in famiglie siciliane con sordità neurosensoriale non sindromica 232
Association of a functional deficit of the BKCa channel, a synaptic regulator of neuronal excitability, with autism and mental retardation 227
Population Structure in the Mediterranean Basin: A Y Chromosome Perspective 224
Differential Greek and northern African migrations to Sicily are supported by genetic evidence from the Y chromosome 221
Autism Spectrum Disorders: From Candidate Genes to Candidate Ontology Terms 216
The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape. 216
Screening of subtelomeric rearrangements in autism spectrum disorder. Identification of a partial trisomy of 13q in a patient 212
ATTUALITÀ E PROSPETTIVE DELLA RICERCA GENOMICA SULL’AUTISMO 211
Functional Annotation of Genes Overlapping Copy Number Variants in Autistic Patients: Focus on Axon Pathfinding 209
Analisi MLPA del gene CREB-binding protein (CREBBP) in un paziente con la sindrome di Rubinstein Taybi 204
Dall’analisi del genoma al vocabolario biologico dell’autismo 201
mtDNA markers for Celtic and Germanic Language Areas in the British Isles 197
Modeling of Hardy-Weinberg Equilibrium Using Dynamic Random Networks in an ABM Framework 195
ABSENCE OF MUTATIONS R451C AND D396TER (1186 INST) IN THE NEUROLIGINS NOS. 3 AND 4,GENES, RESPECTIVELY, IN 140 ITALIAN PATIENTS WITH AUTISM SPECTRUM DISORDERS. 190
Novel deletion of the E3A ubiquitin protein ligase gene detected by multiplex ligation-dependent probe amplification in a patient with Angelman syndrome 183
Comparative multiplex dosage analysis in spinocerebellar ataxia type 2 patients 181
Analisi di delezioni esoniche del gene PAH in pazienti affetti da iperfenilalaninemia 179
Timing of a back-migration into Africa 173
Carrier screening for spinal muscular atrophy in Italian population 169
Boolean Networks: A Primer 168
Absence of mutations R451C and D396ter (1186 INST) in the neuroligins nos. 3 and 4, genes, respectively, in 140 italian patients with autism spectrum disorder 165
ARCHEOGENETICA DELLA POPOLAZIONE SICILIANA: CONTESTI E PROSPETTIVE 164
Multiplex ligation-dependent probe amplification detection of an unknown large deletion of the CREB-binding protein gene in a patient with Rubinstein-Taybi syndrome 164
A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encephalopathy 163
Molecular analyses of NLGN3, NLGN4, GRPR genes in a Sicilian autistic population 160
Exon deletions of the PAH gene in Italian hyperphenylalaninemics 152
The Arabs in Europe: Estimating medieval North Africa male legacy into Southern Europe 147
Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM™ platform 147
Analisi MLPA di delezioni/duplicazioni nel gene PAH in pazienti italiani con iperfenilalaninemia 144
Analisi MLPA della regione 15q11-q14 in pazienti affetti da Idic15 143
Archaeogenetics and landscape dynamics in sicily during the holocene: A review 139
Moors and Saracens in Europe: estimating the medieval North African male legacy in southern Europe 138
Neurobeachin (NBEA) is downregulated in blood cells from a patient with autism spectrum disorders (ASD) 137
Una nuova applicazione della Comparative Multiplex Dosage Analysis (CMDA) 124
Percolation model of axon guidance 121
Studio citogenetico e genetico-molecolare di una paziente con sindrome di Opitz e Iperfenilalaninemia 121
Epilessia e disturbi dello spettro autistico: c'è un rischio genetico condiviso ? 117
Exome sequencing in a child with neurodevelopmental disorder and epilepsy: Variant analysis of the AHNAK2 gene 114
Nuovi approcci diagnostici per le malattie rare: la fenilchetonuria quale esempio di correlazione genotipo-fenotipo 114
null 109
Letter to the Editor Regarding the Article Whole-Exome Sequencing in NF1-Related West's Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for Epilepsy 108
Copy Number Variants and microRNAs in Autism Spectrum Disorders: a whole-genome analysis 104
A novel splice acceptor site mutation in the ATP2A2 gene in a family with Darier disease. 101
Maternal phenylketonuria in two Sicilian families identified by maternal blood phenylalanine level screening and identification of a new phenylalanine hydroxylase gene mutation (P407L) 100
Il neurone autistico: analisi funzionale in silico dei geni coinvolti nelle Copy Number Variants 95
Neuronal Cytoskeleton in Intellectual Disability: From Systems Biology and Modeling to Therapeutic Opportunities 91
Multiplex PCR-Based Next-Generation Sequencing Approach Has Detected a Common Large Deletion in STS Gene in a Patient with X-Linked Ichthyosis 90
null 47
Totale 10.501
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Categoria #
all - tutte 34.878
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 34.878
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022483 0 0 32 19 28 19 35 42 83 69 43 113
2022/2023856 108 135 21 78 94 118 75 64 92 10 35 26
2023/2024372 17 67 22 26 36 90 36 26 4 7 3 38
2024/20251.007 44 59 49 91 34 59 50 53 80 124 144 220
2025/20263.460 255 86 177 244 308 509 472 352 246 571 156 84
2026/2027799 272 118 409 0 0 0 0 0 0 0 0 0
Totale 10.501