ArTS Archivio della ricerca di Trieste

MORGAN, ANNA
 Distribuzione geografica
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Continente #
NA - Nord America 3.796
EU - Europa 3.348
AS - Asia 2.153
SA - Sud America 313
AF - Africa 115
OC - Oceania 17
Continente sconosciuto - Info sul continente non disponibili 4
Totale 9.746
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Nazione #
US - Stati Uniti d'America 3.717
PL - Polonia 1.314
CN - Cina 699
SG - Singapore 630
IT - Italia 586
HK - Hong Kong 326
BR - Brasile 244
SE - Svezia 244
DE - Germania 215
RU - Federazione Russa 143
VN - Vietnam 139
GB - Regno Unito 116
FR - Francia 110
NL - Olanda 109
FI - Finlandia 100
UA - Ucraina 88
BG - Bulgaria 84
IE - Irlanda 62
KR - Corea 60
TR - Turchia 52
IN - India 46
IR - Iran 43
MA - Marocco 43
CA - Canada 42
JP - Giappone 35
CH - Svizzera 31
ES - Italia 31
AT - Austria 28
SN - Senegal 28
BE - Belgio 25
AR - Argentina 23
MX - Messico 23
PK - Pakistan 21
ZA - Sudafrica 20
CZ - Repubblica Ceca 17
AU - Australia 14
IL - Israele 14
NO - Norvegia 14
BD - Bangladesh 13
EC - Ecuador 13
EG - Egitto 11
IQ - Iraq 8
LT - Lituania 8
PS - Palestinian Territory 8
VE - Venezuela 8
CL - Cile 7
CO - Colombia 7
ID - Indonesia 6
SA - Arabia Saudita 6
UZ - Uzbekistan 6
DK - Danimarca 5
PY - Paraguay 5
RO - Romania 5
TW - Taiwan 5
EU - Europa 4
JO - Giordania 4
LB - Libano 4
TT - Trinidad e Tobago 4
AE - Emirati Arabi Uniti 3
AZ - Azerbaigian 3
DO - Repubblica Dominicana 3
LU - Lussemburgo 3
NP - Nepal 3
NZ - Nuova Zelanda 3
PE - Perù 3
AM - Armenia 2
BA - Bosnia-Erzegovina 2
BO - Bolivia 2
CR - Costa Rica 2
CY - Cipro 2
ET - Etiopia 2
IM - Isola di Man 2
IS - Islanda 2
KE - Kenya 2
KZ - Kazakistan 2
LK - Sri Lanka 2
MY - Malesia 2
OM - Oman 2
PR - Porto Rico 2
QA - Qatar 2
TN - Tunisia 2
BN - Brunei Darussalam 1
BW - Botswana 1
CG - Congo 1
CI - Costa d'Avorio 1
DZ - Algeria 1
GE - Georgia 1
GR - Grecia 1
GT - Guatemala 1
GY - Guiana 1
HR - Croazia 1
HU - Ungheria 1
LA - Repubblica Popolare Democratica del Laos 1
LV - Lettonia 1
MO - Macao, regione amministrativa speciale della Cina 1
MW - Malawi 1
NG - Nigeria 1
PA - Panama 1
PH - Filippine 1
UG - Uganda 1
Totale 9.745
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Città #
Warsaw 1.306
Ashburn 467
Fairfield 330
Singapore 321
Hong Kong 307
Chandler 303
Woodbridge 245
Houston 214
Ann Arbor 201
Trieste 199
Wilmington 160
Hefei 144
Beijing 137
Seattle 133
Cambridge 110
Jacksonville 100
Boardman 96
Princeton 84
Sofia 83
Los Angeles 70
Dallas 64
Columbus 62
Dublin 61
Santa Clara 59
Seoul 55
Dearborn 46
Munich 46
Moscow 40
Casablanca 38
Frankfurt am Main 38
Helsinki 38
London 37
Ho Chi Minh City 35
Izmir 35
Dong Ket 32
Düsseldorf 32
Nuremberg 30
Dakar 28
Guangzhou 28
Saint Petersburg 28
Buffalo 26
Nanjing 26
Hanoi 24
Milan 24
São Paulo 24
Bern 23
New York 23
Redwood City 23
Shanghai 23
Bremen 22
Tehran 22
Brussels 21
Lappeenranta 20
San Diego 20
Chicago 16
Tokyo 16
Amsterdam 15
Vienna 14
Phoenix 13
Redondo Beach 13
Belo Horizonte 12
Brno 12
Changsha 12
San Jose 12
Shenyang 12
Boston 11
Boydton 11
Johannesburg 11
Kunming 11
Madrid 11
Mexico City 11
Montreal 11
Trondheim 11
Turku 11
Wuhan 11
Atlanta 10
Council Bluffs 10
Absecon 9
Brooklyn 9
Florence 9
Toronto 9
Ankara 8
Bologna 8
Chengdu 8
Des Moines 8
Fuzhou 8
San Francisco 8
San Nicola Manfredi 8
Stockholm 8
Tianjin 8
Campinas 7
Denver 7
Jinan 7
Lauterbourg 7
Mashhad 7
Mumbai 7
Nanchang 7
Padova 7
Barletta 6
Coimbatore 6
Totale 6.616
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Nome #
Identification of New Hereditary Hearing Loss Genes Using High-Throughput Sequencing Technologies. 483
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 412
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus 395
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 391
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 358
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 332
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 311
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis 297
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 292
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 284
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss 274
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk 218
TBL1Y: a new gene involved in syndromic hearing loss 217
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 214
A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways 213
Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort. 203
Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability 194
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney 194
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta 192
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families 180
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 177
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients 169
Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection 163
New age-related hearing loss candidate genes in humans: an ongoing challenge 155
Rare and low-frequency coding variants alter human adult height 148
Lights and shadows in the genetics of syndromic and non-syndromic hearing loss in the Italian population 147
Two Novel COH1 Mutations in an Italian Patient with Cohen Syndrome. 138
A saturated map of common genetic variants associated with human height 125
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals 120
Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates 116
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour 116
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity 115
Genetics, odor perception and food liking: The intriguing role of cinnamon 110
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders 105
Pendred syndrome, or not pendred syndrome? That is the question 104
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures 102
Genetic dissection of temperament personality traits in Italian isolates 102
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution 100
There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss 100
Hearing loss and brain abnormalities due to pathogenic mutations in ADGRV1 gene: a case report 96
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population 92
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids 92
A new case of TAR syndrome confirms the importance of noncoding variants in the etiopathogenesis of the disease 91
Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort 88
Sensory Capacities and Eating Behavior: Intriguing Results from a Large Cohort of Italian Individuals 87
Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability 87
Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations 83
The role of knockout olfactory receptor genes in odor discrimination 83
Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders 79
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss 79
Non-syndromic sensorineural prelingual and postlingual hearing loss due to col11a1 gene mutation 76
High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis 75
Molecular testing for the study of non-syndromic hearing loss 75
TBC1D24 and non-syndromic autosomal dominant hearing loss: the identification of an additional Italo-American family carrying the p.(S178L) mutation 74
Non-syndromic autosomal dominant hearing loss: The first italian family carrying a mutation in the NCOA3 gene 71
Cardiovascular Risk Factors and MRI Markers of Cerebral Small Vessel Disease 70
Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance 69
SLC12A2: a new gene associated with autosomal dominant Non-Syndromic hearing loss in humans 69
Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure 68
In-Depth Phenotyping of PIGW-Related Disease and Its Role in 17q12 Genomic Disorder 57
A Hitchhiker Guide to Structural Variant Calling: A Comprehensive Benchmark Through Different Sequencing Technologies 55
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 54
Uncovering a Novel Pathogenic Mechanism of BCS1L in Mitochondrial Disorders: Insights from Functional Studies on the c.38A>G Variant 51
Does It Run in Your Family? Inherited Truncating PSMD12 Variants Broaden the Phenotypic Spectrum of Stankiewicz-Isidor Syndrome 42
Novel genetic determinants contribute to hearing loss in a central European cohort with enlarged vestibular aqueduct 39
Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction 38
Hidden in the Genome: The First Italian Family with North Carolina Macular Dystrophy Carrying a Novel PRDM13 and CCNC Duplication 27
Totale 10.033
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Categoria #
all - tutte 30.269
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 30.269
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021579 0 0 0 0 93 87 80 66 73 100 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
2025/20261.698 428 245 368 446 211 0 0 0 0 0 0 0
Totale 10.033