ArTS Archivio della ricerca di Trieste

SPEDICATI, BEATRICE
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
AS - Asia 1.744
NA - Nord America 1.577
EU - Europa 1.073
SA - Sud America 212
AF - Africa 70
OC - Oceania 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 4.679
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 1.504
SG - Singapore 616
CN - Cina 406
IT - Italia 348
VN - Vietnam 247
BR - Brasile 153
HK - Hong Kong 139
KR - Corea 138
DE - Germania 109
FR - Francia 103
NL - Olanda 87
GB - Regno Unito 82
FI - Finlandia 60
RU - Federazione Russa 60
PL - Polonia 54
IN - India 39
SE - Svezia 38
MA - Marocco 27
MX - Messico 27
CH - Svizzera 26
CA - Canada 25
IQ - Iraq 21
BD - Bangladesh 20
IE - Irlanda 17
AT - Austria 16
BG - Bulgaria 14
ES - Italia 14
ZA - Sudafrica 14
AR - Argentina 13
CO - Colombia 13
JP - Giappone 13
TR - Turchia 13
ID - Indonesia 12
SA - Arabia Saudita 11
SN - Senegal 10
VE - Venezuela 9
LT - Lituania 8
PK - Pakistan 8
UZ - Uzbekistan 8
PY - Paraguay 7
UA - Ucraina 7
AE - Emirati Arabi Uniti 6
CZ - Repubblica Ceca 6
EG - Egitto 6
PH - Filippine 6
CL - Cile 5
EC - Ecuador 5
JO - Giordania 5
DO - Repubblica Dominicana 4
IR - Iran 4
KE - Kenya 4
KZ - Kazakistan 4
AZ - Azerbaigian 3
BE - Belgio 3
BO - Bolivia 3
MY - Malesia 3
NO - Norvegia 3
PA - Panama 3
TH - Thailandia 3
TT - Trinidad e Tobago 3
AU - Australia 2
CR - Costa Rica 2
DK - Danimarca 2
ET - Etiopia 2
GT - Guatemala 2
HU - Ungheria 2
IM - Isola di Man 2
JM - Giamaica 2
LK - Sri Lanka 2
NI - Nicaragua 2
NP - Nepal 2
PE - Perù 2
RO - Romania 2
RS - Serbia 2
TN - Tunisia 2
AL - Albania 1
AM - Armenia 1
AO - Angola 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BW - Botswana 1
BY - Bielorussia 1
BZ - Belize 1
CG - Congo 1
CY - Cipro 1
DZ - Algeria 1
GE - Georgia 1
GR - Grecia 1
IL - Israele 1
KG - Kirghizistan 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LC - Santa Lucia 1
LV - Lettonia 1
MD - Moldavia 1
MM - Myanmar 1
MN - Mongolia 1
MU - Mauritius 1
MV - Maldive 1
OM - Oman 1
Totale 4.670
Salva come PNG Salva come JPEG
Città #
Singapore 374
Ashburn 248
San Jose 210
Hefei 176
Hong Kong 136
Seoul 135
Dallas 100
Trieste 91
Chicago 84
Ho Chi Minh City 71
Los Angeles 68
Beijing 66
Hanoi 63
Santa Clara 56
Boardman 46
Lauterbourg 41
London 41
Council Bluffs 38
Frankfurt am Main 38
Chandler 35
Zgierz 34
New York 29
The Dalles 28
Columbus 27
Lappeenranta 27
Casablanca 25
Milan 24
Moscow 24
Bern 23
Boydton 23
Helsinki 22
Buffalo 19
São Paulo 19
Munich 18
Warsaw 18
Dublin 17
Nuremberg 16
Redondo Beach 14
Salt Lake City 14
Atlanta 13
Haiphong 13
Sofia 13
Düsseldorf 12
Tokyo 12
Boston 11
Da Nang 11
Mexico City 11
Rome 11
Chennai 10
Dakar 10
Elk Grove Village 10
Montreal 10
Vienna 10
Bologna 9
Brooklyn 9
Denver 9
Johannesburg 8
Phoenix 8
Poplar 8
Shanghai 8
Stockholm 8
Tampa 8
Baghdad 7
City of London 7
Hải Dương 7
Mumbai 7
Orem 7
Triggiano 7
Turku 7
Amsterdam 6
Bari 6
Biên Hòa 6
Dong Ket 6
Guangzhou 6
Jeddah 6
Manchester 6
Princeton 6
Seattle 6
Sterling 6
Tashkent 6
Wilmington 6
Amman 5
San Francisco 5
Thái Bình 5
Toronto 5
Treviso 5
Venice 5
Xi'an 5
Asunción 4
Bremen 4
Brno 4
Bến Tre 4
Cairo 4
Can Tho 4
Cape Town 4
Colombo 4
Desio 4
Fortaleza 4
Guarulhos 4
Houston 4
Totale 2.974
Salva come PNG Salva come JPEG
Nome #
Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric Study 210
Lights and shadows in the genetics of syndromic and non-syndromic hearing loss in the Italian population 182
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures 170
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals 157
Proangiogenic properties of complement protein C1q can contribute to endometriosis 154
Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates 151
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature 143
Odontostomatological Traits in North-Eastern Italy's Isolated Populations: An Epidemiological Cross-Sectional Study 139
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits 135
A possible association between low MBL/lectin pathway functionality and microbiota dysbiosis in endometriosis patients 133
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population 131
Genome‐Wide Interaction Analyses of Serum Calcium on Ventricular Repolarization Time in 125 393 Participants 130
Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort 129
The role of knockout olfactory receptor genes in odor discrimination 129
Whole-exome sequencing: Clinical characterization of pediatric and adult Italian patients affected by different forms of hereditary cardiovascular diseases 128
Infant with a big head and 'crossed' polysyndactyly 125
The Bittersweet Symphony of COVID-19: Associations between TAS1Rs and TAS2R38 Genetic Variations and COVID-19 Symptoms 124
Exome sequencing efficacy and phenotypic expansions involving esophageal atresia/tracheoesophageal fistula plus 123
Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders 121
Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations 120
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications 117
Impact of cultural and genetic structure on food choices along the Silk Road 114
Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci 109
Understanding the genetic complexity of puberty timing across the allele frequency spectrum 109
Clenching the Strings of Bruxism Etiopathogenesis: Association Analyses on Genetics and Environmental Risk Factors in a Deeply Characterized Italian Cohort 102
TBC1D24 and non-syndromic autosomal dominant hearing loss: the identification of an additional Italo-American family carrying the p.(S178L) mutation 102
A genome‐wide association meta‐analysis of all‐cause and vascular dementia 101
Normal hearing function genetics: have you heard all about it? An integrated approach of genome-wide association studies and transcriptome-wide association studies in three Italian cohorts 101
Scent of COVID-19: Whole-Genome Sequencing Analysis Reveals the Role of ACE2, IFI44, and NDUFAF4 in Long-Lasting Olfactory Dysfunction 98
A Hitchhiker Guide to Structural Variant Calling: A Comprehensive Benchmark Through Different Sequencing Technologies 96
Polygenic prediction of body mass index and obesity through the life course and across ancestries 93
Expanding the Molecular Spectrum of MMP21 Missense Variants: Clinical Insights and Literature Review 93
Uncovering a Novel Pathogenic Mechanism of BCS1L in Mitochondrial Disorders: Insights from Functional Studies on the c.38A>G Variant 89
Prediction and prognostic role of left ventricular systolic dysfunction in family screening for dilated cardiomyopathy and non-dilated left ventricular cardiomyopathy 87
Unravelling the genetic bases of the sense of smell: clinical and molecular characterisation of a large cohort of COVID-19 patients with persistent olfactory dysfunction 78
Does It Run in Your Family? Inherited Truncating PSMD12 Variants Broaden the Phenotypic Spectrum of Stankiewicz-Isidor Syndrome 75
Hidden in the Genome: The First Italian Family with North Carolina Macular Dystrophy Carrying a Novel PRDM13 and CCNC Duplication 73
Prevalence of rare missense TTN variants in a cohort of patients with cardiomyopathy 73
Regulator of G-Protein Signalling 9: A New Candidate Gene for Sweet Food Liking? 65
Unveiling the spectrum of sudden cardiac death: a multidisciplinary analysis from the Friuli Venezia Giulia registry 50
Beyond the Curtains: Identification of the Genetic Cause of Foetal Developmental Abnormalities Through the Application of Molecular Autopsy 34
Unraveling the Functional Impact of Splicing Variants in Inherited Hearing Disorders Through Minigene Splicing Assays 34
The homoplasmic MT-TK m.8357T > C mtDNA variant as a cause of multiorgan mitochondrial disease 32
Variability of transposable elements in six genetic isolates from North-Eastern Italy and their relationship with alcohol consumption, tobacco use and BMI 32
Large-scale blood pressure GWAS accounting for gene-depression interactions in 564,680 individuals from diverse populations 23
Discovery of gene-alcohol interaction loci influencing blood pressure in 1.1 million individuals from multiple populations 9
Totale 4.823
Salva come PNG Salva come JPEG
Categoria #
all - tutte 14.308
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 14.308
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20214 0 0 0 0 0 0 0 0 0 3 0 1
2021/202233 5 1 11 0 1 2 0 1 3 3 0 6
2022/2023213 13 17 9 15 36 22 3 16 18 28 24 12
2023/2024329 30 16 20 31 21 24 60 80 2 10 22 13
2024/20251.042 51 57 111 52 74 128 51 41 83 159 92 143
2025/20263.176 280 289 397 374 263 271 455 154 321 372 0 0
Totale 4.823