ArTS Archivio della ricerca di Trieste

SPEDICATI, BEATRICE
 Distribuzione geografica
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Continente #
NA - Nord America 2.336
AS - Asia 1.952
EU - Europa 1.259
SA - Sud America 216
Continente sconosciuto - Info sul continente non disponibili 145
AF - Africa 75
OC - Oceania 5
Totale 5.988
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Nazione #
US - Stati Uniti d'America 2.218
SG - Singapore 623
IT - Italia 515
CN - Cina 415
VN - Vietnam 247
BD - Bangladesh 195
BR - Brasile 156
HK - Hong Kong 141
KR - Corea 138
DE - Germania 110
FR - Francia 103
NL - Olanda 94
GB - Regno Unito 83
FI - Finlandia 60
RU - Federazione Russa 60
PL - Polonia 55
CA - Canada 51
SE - Svezia 41
IN - India 40
MX - Messico 29
MA - Marocco 27
CH - Svizzera 26
IQ - Iraq 21
IE - Irlanda 18
AT - Austria 17
TR - Turchia 17
ZA - Sudafrica 15
BG - Bulgaria 14
CO - Colombia 14
ES - Italia 14
JP - Giappone 14
AR - Argentina 13
ID - Indonesia 13
PK - Pakistan 13
SA - Arabia Saudita 11
SN - Senegal 10
VE - Venezuela 9
LT - Lituania 8
UZ - Uzbekistan 8
AE - Emirati Arabi Uniti 7
PH - Filippine 7
PY - Paraguay 7
UA - Ucraina 7
CZ - Repubblica Ceca 6
EG - Egitto 6
TT - Trinidad e Tobago 6
CL - Cile 5
EC - Ecuador 5
JM - Giamaica 5
JO - Giordania 5
KE - Kenya 5
AU - Australia 4
CR - Costa Rica 4
DO - Repubblica Dominicana 4
IR - Iran 4
KZ - Kazakistan 4
AZ - Azerbaigian 3
BE - Belgio 3
BO - Bolivia 3
MY - Malesia 3
NI - Nicaragua 3
NO - Norvegia 3
NP - Nepal 3
PA - Panama 3
RS - Serbia 3
TH - Thailandia 3
BA - Bosnia-Erzegovina 2
BS - Bahamas 2
DK - Danimarca 2
ET - Etiopia 2
GT - Guatemala 2
HN - Honduras 2
HR - Croazia 2
HU - Ungheria 2
IM - Isola di Man 2
LK - Sri Lanka 2
PE - Perù 2
RO - Romania 2
TN - Tunisia 2
AG - Antigua e Barbuda 1
AL - Albania 1
AM - Armenia 1
AO - Angola 1
BB - Barbados 1
BW - Botswana 1
BY - Bielorussia 1
BZ - Belize 1
CG - Congo 1
CV - Capo Verde 1
CY - Cipro 1
DZ - Algeria 1
GE - Georgia 1
GM - Gambi 1
GP - Guadalupe 1
GR - Grecia 1
IL - Israele 1
KG - Kirghizistan 1
KN - Saint Kitts e Nevis 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
Totale 5.824
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Città #
Singapore 379
Ashburn 369
San Jose 248
Hefei 176
Council Bluffs 144
Hong Kong 138
Seoul 135
Dallas 107
Trieste 100
Chicago 87
Los Angeles 85
Ho Chi Minh City 71
Beijing 69
Santa Clara 69
Columbus 66
Hanoi 63
New York 61
Milan 55
Boardman 49
London 42
Lauterbourg 41
Frankfurt am Main 38
Chandler 35
Zgierz 34
Buffalo 29
Phoenix 29
Rome 28
The Dalles 28
Lappeenranta 27
Casablanca 25
Moscow 24
Bern 23
Boydton 23
Helsinki 22
Atlanta 19
São Paulo 19
Montreal 18
Munich 18
Warsaw 18
Dublin 17
Nuremberg 16
Salt Lake City 15
Boston 14
Brooklyn 14
Redondo Beach 14
Haiphong 13
Sofia 13
Tokyo 13
Düsseldorf 12
Mexico City 12
Da Nang 11
Elk Grove Village 11
Naples 11
Bari 10
Bologna 10
Chennai 10
Dakar 10
Denver 10
Shanghai 10
Stockholm 10
Toronto 10
Vienna 10
Seattle 9
Johannesburg 8
Mumbai 8
Orem 8
Poplar 8
Tampa 8
Baghdad 7
City of London 7
Houston 7
Hải Dương 7
Lahore 7
Princeton 7
San Francisco 7
Triggiano 7
Turku 7
Wilmington 7
Amsterdam 6
Biên Hòa 6
Charlotte 6
Dong Ket 6
Genoa 6
Guangzhou 6
Jeddah 6
Manchester 6
Sterling 6
Tashkent 6
Venice 6
Amman 5
Brasília 5
Cape Town 5
Istanbul 5
Lakewood 5
Miami 5
Querétaro 5
Thái Bình 5
Treviso 5
Turin 5
Udine 5
Totale 3.527
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Nome #
Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric Study 235
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals 220
Odontostomatological Traits in North-Eastern Italy's Isolated Populations: An Epidemiological Cross-Sectional Study 218
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures 209
Lights and shadows in the genetics of syndromic and non-syndromic hearing loss in the Italian population 197
Proangiogenic properties of complement protein C1q can contribute to endometriosis 178
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits 178
Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort 172
Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates 163
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population 159
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature 158
Uncovering a Novel Pathogenic Mechanism of BCS1L in Mitochondrial Disorders: Insights from Functional Studies on the c.38A>G Variant 154
A possible association between low MBL/lectin pathway functionality and microbiota dysbiosis in endometriosis patients 154
Hidden in the Genome: The First Italian Family with North Carolina Macular Dystrophy Carrying a Novel PRDM13 and CCNC Duplication 153
The role of knockout olfactory receptor genes in odor discrimination 149
The Bittersweet Symphony of COVID-19: Associations between TAS1Rs and TAS2R38 Genetic Variations and COVID-19 Symptoms 146
Whole-exome sequencing: Clinical characterization of pediatric and adult Italian patients affected by different forms of hereditary cardiovascular diseases 139
Exome sequencing efficacy and phenotypic expansions involving esophageal atresia/tracheoesophageal fistula plus 139
Genome‐Wide Interaction Analyses of Serum Calcium on Ventricular Repolarization Time in 125 393 Participants 139
Infant with a big head and 'crossed' polysyndactyly 137
Prevalence of rare missense TTN variants in a cohort of patients with cardiomyopathy 137
A Hitchhiker Guide to Structural Variant Calling: A Comprehensive Benchmark Through Different Sequencing Technologies 134
Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations 134
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications 131
Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders 128
Understanding the genetic complexity of puberty timing across the allele frequency spectrum 127
Impact of cultural and genetic structure on food choices along the Silk Road 123
Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci 122
A genome‐wide association meta‐analysis of all‐cause and vascular dementia 119
Clenching the Strings of Bruxism Etiopathogenesis: Association Analyses on Genetics and Environmental Risk Factors in a Deeply Characterized Italian Cohort 115
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 114
Polygenic prediction of body mass index and obesity through the life course and across ancestries 113
Scent of COVID-19: Whole-Genome Sequencing Analysis Reveals the Role of ACE2, IFI44, and NDUFAF4 in Long-Lasting Olfactory Dysfunction 113
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 112
TBC1D24 and non-syndromic autosomal dominant hearing loss: the identification of an additional Italo-American family carrying the p.(S178L) mutation 110
Expanding the Molecular Spectrum of MMP21 Missense Variants: Clinical Insights and Literature Review 105
Does It Run in Your Family? Inherited Truncating PSMD12 Variants Broaden the Phenotypic Spectrum of Stankiewicz-Isidor Syndrome 104
Prediction and prognostic role of left ventricular systolic dysfunction in family screening for dilated cardiomyopathy and non-dilated left ventricular cardiomyopathy 99
Variability of transposable elements in six genetic isolates from North-Eastern Italy and their relationship with alcohol consumption, tobacco use and BMI 77
Unveiling the spectrum of sudden cardiac death: a multidisciplinary analysis from the Friuli Venezia Giulia registry 74
Regulator of G-Protein Signalling 9: A New Candidate Gene for Sweet Food Liking? 69
Unraveling the Functional Impact of Splicing Variants in Inherited Hearing Disorders Through Minigene Splicing Assays 64
The homoplasmic MT-TK m.8357T > C mtDNA variant as a cause of multiorgan mitochondrial disease 54
Beyond the Curtains: Identification of the Genetic Cause of Foetal Developmental Abnormalities Through the Application of Molecular Autopsy 49
Large-scale blood pressure GWAS accounting for gene-depression interactions in 564,680 individuals from diverse populations 41
Discovery of gene-alcohol interaction loci influencing blood pressure in 1.1 million individuals from multiple populations 23
Totale 5.988
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Categoria #
all - tutte 18.287
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 18.287
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/202227 0 0 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
2025/20263.736 280 289 397 374 263 271 455 154 321 409 292 231
2026/2027605 187 248 170 0 0 0 0 0 0 0 0 0
Totale 5.988