ArTS Archivio della ricerca di Trieste

MORGAN, ANNA
 Distribuzione geografica
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Continente #
NA - Nord America 4.687
EU - Europa 3.768
AS - Asia 3.269
SA - Sud America 436
AF - Africa 168
OC - Oceania 25
Continente sconosciuto - Info sul continente non disponibili 5
Totale 12.358
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Nazione #
US - Stati Uniti d'America 4.569
PL - Polonia 1.382
SG - Singapore 1.060
CN - Cina 797
IT - Italia 694
VN - Vietnam 381
HK - Hong Kong 353
BR - Brasile 321
SE - Svezia 250
DE - Germania 246
FR - Francia 177
KR - Corea 156
RU - Federazione Russa 152
GB - Regno Unito 144
FI - Finlandia 140
NL - Olanda 120
IN - India 103
UA - Ucraina 98
BG - Bulgaria 87
IE - Irlanda 64
TR - Turchia 63
CA - Canada 58
JP - Giappone 48
MA - Marocco 47
IR - Iran 43
ES - Italia 42
MX - Messico 38
AR - Argentina 36
CH - Svizzera 33
BD - Bangladesh 32
ZA - Sudafrica 32
IQ - Iraq 31
AT - Austria 30
SN - Senegal 30
PK - Pakistan 29
BE - Belgio 26
AU - Australia 21
IL - Israele 21
SA - Arabia Saudita 20
CZ - Repubblica Ceca 19
EG - Egitto 18
EC - Ecuador 17
UZ - Uzbekistan 17
CO - Colombia 16
NO - Norvegia 16
VE - Venezuela 16
ID - Indonesia 14
JO - Giordania 12
PH - Filippine 11
CL - Cile 10
LT - Lituania 10
PS - Palestinian Territory 9
PY - Paraguay 9
AE - Emirati Arabi Uniti 8
RO - Romania 8
TW - Taiwan 8
AZ - Azerbaigian 7
DZ - Algeria 7
KE - Kenya 7
KZ - Kazakistan 6
PE - Perù 6
DK - Danimarca 5
LB - Libano 5
DO - Repubblica Dominicana 4
EE - Estonia 4
ET - Etiopia 4
EU - Europa 4
MY - Malesia 4
TN - Tunisia 4
TT - Trinidad e Tobago 4
BO - Bolivia 3
CI - Costa d'Avorio 3
CR - Costa Rica 3
CY - Cipro 3
GT - Guatemala 3
HR - Croazia 3
LK - Sri Lanka 3
LU - Lussemburgo 3
NP - Nepal 3
NZ - Nuova Zelanda 3
TH - Thailandia 3
TZ - Tanzania 3
AL - Albania 2
AM - Armenia 2
BA - Bosnia-Erzegovina 2
BN - Brunei Darussalam 2
BW - Botswana 2
CG - Congo 2
GE - Georgia 2
IM - Isola di Man 2
IS - Islanda 2
MN - Mongolia 2
NG - Nigeria 2
OM - Oman 2
PR - Porto Rico 2
QA - Qatar 2
AO - Angola 1
BH - Bahrain 1
BS - Bahamas 1
BY - Bielorussia 1
Totale 12.331
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Città #
Warsaw 1.317
Singapore 634
Ashburn 577
Fairfield 330
Hong Kong 328
Chandler 303
San Jose 302
Woodbridge 245
Houston 214
Trieste 203
Ann Arbor 201
Wilmington 160
Seoul 147
Hefei 144
Beijing 141
Seattle 133
Cambridge 111
Ho Chi Minh City 105
Jacksonville 100
Boardman 99
Los Angeles 96
Chicago 86
Princeton 84
Sofia 84
Hanoi 83
Council Bluffs 73
Santa Clara 73
Helsinki 70
Dallas 65
Dublin 63
Columbus 62
Lauterbourg 60
Zgierz 54
Frankfurt am Main 50
Munich 48
Dearborn 46
New York 44
Moscow 41
London 39
Casablanca 38
The Dalles 37
Izmir 35
Nuremberg 33
Dong Ket 32
Düsseldorf 32
Guangzhou 32
Milan 32
São Paulo 31
Dakar 30
Buffalo 29
Nanjing 28
Saint Petersburg 28
Bern 24
Lappeenranta 24
Orem 23
Redwood City 23
Shanghai 23
Tokyo 23
Bremen 22
Brussels 22
Tehran 22
San Diego 21
Montreal 19
Amsterdam 18
Da Nang 18
Johannesburg 18
Atlanta 17
Madrid 17
Phoenix 17
Tashkent 17
Haiphong 16
Mumbai 15
Vienna 15
Belo Horizonte 14
Bologna 14
Denver 14
Tianjin 14
Changsha 13
Redondo Beach 13
Rome 13
Stockholm 13
Amman 12
Boston 12
Brno 12
Brooklyn 12
Chennai 12
Shenyang 12
Toronto 12
Wuhan 12
Boydton 11
Chengdu 11
Kunming 11
Mexico City 11
Trondheim 11
Turku 11
Bari 10
Absecon 9
Ankara 9
Des Moines 9
Florence 9
Totale 8.162
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Nome #
Identification of New Hereditary Hearing Loss Genes Using High-Throughput Sequencing Technologies. 527
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus 520
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 448
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 442
Assessment of the olfactory function in Italian patients with type 3 von Willebrand disease caused by a homozygous 253 Kb deletion involving VWF and TMEM16B/ANO2 398
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 367
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis 366
Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number Variations 351
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 326
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 308
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss 298
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk 268
TBL1Y: a new gene involved in syndromic hearing loss 257
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 251
A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways 244
Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability 243
Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort. 241
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney 240
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta 236
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 220
New age-related hearing loss candidate genes in humans: an ongoing challenge 205
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients 203
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families 193
Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection 187
Lights and shadows in the genetics of syndromic and non-syndromic hearing loss in the Italian population 182
Two Novel COH1 Mutations in an Italian Patient with Cohen Syndrome. 173
Rare and low-frequency coding variants alter human adult height 172
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures 170
A saturated map of common genetic variants associated with human height 166
Genetics, odor perception and food liking: The intriguing role of cinnamon 161
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals 157
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity 155
Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates 151
Pendred syndrome, or not pendred syndrome? That is the question 151
There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss 140
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour 138
Genetic dissection of temperament personality traits in Italian isolates 137
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids 135
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population 131
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders 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
Cardiovascular Risk Factors and MRI Markers of Cerebral Small Vessel Disease 125
A new case of TAR syndrome confirms the importance of noncoding variants in the etiopathogenesis of the disease 124
Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability 124
Hearing loss and brain abnormalities due to pathogenic mutations in ADGRV1 gene: a case report 122
Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders 121
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution 121
Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations 120
Sensory Capacities and Eating Behavior: Intriguing Results from a Large Cohort of Italian Individuals 117
Non-syndromic autosomal dominant hearing loss: The first italian family carrying a mutation in the NCOA3 gene 117
Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance 114
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss 110
High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis 107
Non-syndromic sensorineural prelingual and postlingual hearing loss due to col11a1 gene mutation 102
TBC1D24 and non-syndromic autosomal dominant hearing loss: the identification of an additional Italo-American family carrying the p.(S178L) mutation 102
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
A Hitchhiker Guide to Structural Variant Calling: A Comprehensive Benchmark Through Different Sequencing Technologies 96
Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure 96
In-Depth Phenotyping of PIGW-Related Disease and Its Role in 17q12 Genomic Disorder 90
Uncovering a Novel Pathogenic Mechanism of BCS1L in Mitochondrial Disorders: Insights from Functional Studies on the c.38A>G Variant 89
SLC12A2: a new gene associated with autosomal dominant Non-Syndromic hearing loss in humans 89
Molecular testing for the study of non-syndromic hearing loss 87
Novel genetic determinants contribute to hearing loss in a central European cohort with enlarged vestibular aqueduct 76
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
Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction 70
Unraveling the Functional Impact of Splicing Variants in Inherited Hearing Disorders Through Minigene Splicing Assays 34
Totale 12.648
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Categoria #
all - tutte 34.746
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 34.746
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021180 0 0 0 0 0 0 0 0 0 100 27 53
2021/2022554 37 25 52 23 39 37 39 15 70 49 37 131
2022/2023991 93 117 65 134 101 146 22 121 97 15 57 23
2023/2024907 56 47 29 74 65 99 182 159 10 34 83 69
2024/20252.086 89 128 221 176 172 233 131 144 206 247 190 149
2025/20264.313 428 245 368 446 413 416 676 178 591 552 0 0
Totale 12.648