ArTS Archivio della ricerca di Trieste

SPEDICATI, BEATRICE
 Distribuzione geografica
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Continente #
AS - Asia 1.922
NA - Nord America 1.848
EU - Europa 1.174
SA - Sud America 212
AF - Africa 70
OC - Oceania 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 5.229
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Nazione #
US - Stati Uniti d'America 1.758
SG - Singapore 619
IT - Italia 440
CN - Cina 409
VN - Vietnam 247
BD - Bangladesh 185
BR - Brasile 153
HK - Hong Kong 141
KR - Corea 138
DE - Germania 109
FR - Francia 103
NL - Olanda 89
GB - Regno Unito 83
FI - Finlandia 60
RU - Federazione Russa 60
PL - Polonia 54
IN - India 39
SE - Svezia 39
CA - Canada 35
MX - Messico 28
MA - Marocco 27
CH - Svizzera 26
IQ - Iraq 21
IE - Irlanda 18
AT - Austria 17
BG - Bulgaria 14
ES - Italia 14
ZA - Sudafrica 14
AR - Argentina 13
CO - Colombia 13
JP - Giappone 13
PK - Pakistan 13
TR - Turchia 13
ID - Indonesia 12
SA - Arabia Saudita 11
SN - Senegal 10
VE - Venezuela 9
LT - Lituania 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
TT - Trinidad e Tobago 4
AZ - Azerbaigian 3
BE - Belgio 3
BO - Bolivia 3
CR - Costa Rica 3
JM - Giamaica 3
MY - Malesia 3
NO - Norvegia 3
PA - Panama 3
TH - Thailandia 3
AU - Australia 2
BA - Bosnia-Erzegovina 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
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
BB - Barbados 1
BS - Bahamas 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
Totale 5.217
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Città #
Singapore 375
Ashburn 299
San Jose 240
Hefei 176
Hong Kong 138
Seoul 135
Dallas 103
Trieste 96
Chicago 85
Los Angeles 81
Ho Chi Minh City 71
Beijing 68
Hanoi 63
Santa Clara 62
Council Bluffs 57
New York 57
Boardman 46
Lauterbourg 41
London 41
Frankfurt am Main 38
Chandler 35
Zgierz 34
Milan 33
Buffalo 28
Columbus 28
The Dalles 28
Lappeenranta 27
Casablanca 25
Moscow 24
Bern 23
Boydton 23
Helsinki 22
São Paulo 19
Munich 18
Rome 18
Warsaw 18
Atlanta 17
Dublin 17
Nuremberg 16
Redondo Beach 14
Salt Lake City 14
Haiphong 13
Montreal 13
Sofia 13
Düsseldorf 12
Mexico City 12
Tokyo 12
Boston 11
Da Nang 11
Bologna 10
Chennai 10
Dakar 10
Elk Grove Village 10
Vienna 10
Brooklyn 9
Denver 9
Shanghai 9
Toronto 9
Johannesburg 8
Naples 8
Orem 8
Phoenix 8
Poplar 8
Stockholm 8
Tampa 8
Baghdad 7
Bari 7
City of London 7
Hải Dương 7
Lahore 7
Mumbai 7
Seattle 7
Triggiano 7
Turku 7
Amsterdam 6
Biên Hòa 6
Dong Ket 6
Guangzhou 6
Jeddah 6
Manchester 6
Princeton 6
Sterling 6
Tashkent 6
Venice 6
Wilmington 6
Amman 5
Charlotte 5
Houston 5
San Francisco 5
Thái Bình 5
Treviso 5
Turin 5
Udine 5
Xi'an 5
Asunción 4
Bremen 4
Brescia 4
Brno 4
Bến Tre 4
Cairo 4
Totale 3.190
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Nome #
Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric Study 219
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures 197
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals 194
Lights and shadows in the genetics of syndromic and non-syndromic hearing loss in the Italian population 188
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits 168
Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort 163
Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates 158
Proangiogenic properties of complement protein C1q can contribute to endometriosis 156
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature 148
A possible association between low MBL/lectin pathway functionality and microbiota dysbiosis in endometriosis patients 148
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population 145
Odontostomatological Traits in North-Eastern Italy's Isolated Populations: An Epidemiological Cross-Sectional Study 144
The role of knockout olfactory receptor genes in odor discrimination 141
Whole-exome sequencing: Clinical characterization of pediatric and adult Italian patients affected by different forms of hereditary cardiovascular diseases 135
Exome sequencing efficacy and phenotypic expansions involving esophageal atresia/tracheoesophageal fistula plus 132
The Bittersweet Symphony of COVID-19: Associations between TAS1Rs and TAS2R38 Genetic Variations and COVID-19 Symptoms 132
Genome‐Wide Interaction Analyses of Serum Calcium on Ventricular Repolarization Time in 125 393 Participants 132
Hidden in the Genome: The First Italian Family with North Carolina Macular Dystrophy Carrying a Novel PRDM13 and CCNC Duplication 131
Infant with a big head and 'crossed' polysyndactyly 131
Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations 125
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications 123
Uncovering a Novel Pathogenic Mechanism of BCS1L in Mitochondrial Disorders: Insights from Functional Studies on the c.38A>G Variant 122
Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders 121
Understanding the genetic complexity of puberty timing across the allele frequency spectrum 119
Impact of cultural and genetic structure on food choices along the Silk Road 117
A Hitchhiker Guide to Structural Variant Calling: A Comprehensive Benchmark Through Different Sequencing Technologies 115
Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci 111
A genome‐wide association meta‐analysis of all‐cause and vascular dementia 111
TBC1D24 and non-syndromic autosomal dominant hearing loss: the identification of an additional Italo-American family carrying the p.(S178L) mutation 106
Clenching the Strings of Bruxism Etiopathogenesis: Association Analyses on Genetics and Environmental Risk Factors in a Deeply Characterized Italian Cohort 103
Scent of COVID-19: Whole-Genome Sequencing Analysis Reveals the Role of ACE2, IFI44, and NDUFAF4 in Long-Lasting Olfactory Dysfunction 103
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 102
Expanding the Molecular Spectrum of MMP21 Missense Variants: Clinical Insights and Literature Review 101
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 100
Polygenic prediction of body mass index and obesity through the life course and across ancestries 99
Prevalence of rare missense TTN variants in a cohort of patients with cardiomyopathy 96
Prediction and prognostic role of left ventricular systolic dysfunction in family screening for dilated cardiomyopathy and non-dilated left ventricular cardiomyopathy 92
Does It Run in Your Family? Inherited Truncating PSMD12 Variants Broaden the Phenotypic Spectrum of Stankiewicz-Isidor Syndrome 92
Regulator of G-Protein Signalling 9: A New Candidate Gene for Sweet Food Liking? 66
Variability of transposable elements in six genetic isolates from North-Eastern Italy and their relationship with alcohol consumption, tobacco use and BMI 62
Unveiling the spectrum of sudden cardiac death: a multidisciplinary analysis from the Friuli Venezia Giulia registry 56
Unraveling the Functional Impact of Splicing Variants in Inherited Hearing Disorders Through Minigene Splicing Assays 51
The homoplasmic MT-TK m.8357T > C mtDNA variant as a cause of multiorgan mitochondrial disease 40
Beyond the Curtains: Identification of the Genetic Cause of Foetal Developmental Abnormalities Through the Application of Molecular Autopsy 37
Large-scale blood pressure GWAS accounting for gene-depression interactions in 564,680 individuals from diverse populations 27
Discovery of gene-alcohol interaction loci influencing blood pressure in 1.1 million individuals from multiple populations 14
Totale 5.373
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Categoria #
all - tutte 16.043
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 16.043
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211 0 0 0 0 0 0 0 0 0 0 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
2025/20263.726 280 289 397 374 263 271 455 154 321 409 292 221
Totale 5.373