ArTS Archivio della ricerca di Trieste

MORGAN, ANNA
 Distribuzione geografica
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Continente #
NA - Nord America 5.065
EU - Europa 3.954
AS - Asia 3.573
SA - Sud America 436
AF - Africa 168
OC - Oceania 27
Continente sconosciuto - Info sul continente non disponibili 5
Totale 13.228
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Nazione #
US - Stati Uniti d'America 4.928
PL - Polonia 1.382
SG - Singapore 1.063
IT - Italia 854
CN - Cina 813
VN - Vietnam 381
HK - Hong Kong 356
BR - Brasile 321
BD - Bangladesh 311
SE - Svezia 250
DE - Germania 249
FR - Francia 180
KR - Corea 156
RU - Federazione Russa 152
GB - Regno Unito 150
FI - Finlandia 140
NL - Olanda 121
IN - India 103
UA - Ucraina 98
BG - Bulgaria 87
CA - Canada 72
IE - Irlanda 65
TR - Turchia 63
JP - Giappone 49
MA - Marocco 47
IR - Iran 43
ES - Italia 42
MX - Messico 39
AR - Argentina 36
CH - Svizzera 36
AT - Austria 34
ZA - Sudafrica 32
IQ - Iraq 31
PK - Pakistan 31
SN - Senegal 30
BE - Belgio 26
AU - Australia 23
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
DK - Danimarca 7
DZ - Algeria 7
KE - Kenya 7
KZ - Kazakistan 6
PE - Perù 6
HR - Croazia 5
LB - Libano 5
CR - Costa Rica 4
DO - Repubblica Dominicana 4
EE - Estonia 4
ET - Etiopia 4
EU - Europa 4
GT - Guatemala 4
MY - Malesia 4
TN - Tunisia 4
TT - Trinidad e Tobago 4
BA - Bosnia-Erzegovina 3
BO - Bolivia 3
CI - Costa d'Avorio 3
CY - Cipro 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
BN - Brunei Darussalam 2
BS - Bahamas 2
BW - Botswana 2
CG - Congo 2
GE - Georgia 2
IM - Isola di Man 2
IS - Islanda 2
JM - Giamaica 2
MN - Mongolia 2
NG - Nigeria 2
OM - Oman 2
PR - Porto Rico 2
QA - Qatar 2
AO - Angola 1
BH - Bahrain 1
Totale 13.201
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Città #
Warsaw 1.317
Ashburn 648
Singapore 634
Hong Kong 331
San Jose 331
Fairfield 330
Chandler 303
Woodbridge 245
Houston 216
Trieste 208
Ann Arbor 201
Wilmington 162
Seoul 147
Beijing 146
Hefei 144
Seattle 133
Los Angeles 123
Cambridge 113
Ho Chi Minh City 105
Jacksonville 100
Boardman 99
Council Bluffs 93
Chicago 87
Princeton 84
Sofia 84
Hanoi 83
Santa Clara 80
New York 74
Dallas 72
Helsinki 70
Columbus 63
Dublin 63
Lauterbourg 60
Milan 57
Zgierz 54
Frankfurt am Main 50
Munich 48
Dearborn 46
Buffalo 41
Moscow 41
London 40
Casablanca 38
The Dalles 37
Izmir 35
Nuremberg 33
Dong Ket 32
Düsseldorf 32
Guangzhou 32
São Paulo 31
Dakar 30
Nanjing 29
Saint Petersburg 28
Shanghai 26
Orem 25
Bern 24
Lappeenranta 24
Montreal 24
Tokyo 24
Redwood City 23
Rome 23
Bremen 22
Brussels 22
San Diego 22
Tehran 22
Atlanta 19
Amsterdam 18
Da Nang 18
Johannesburg 18
Phoenix 18
Madrid 17
Tashkent 17
Bologna 16
Haiphong 16
Toronto 16
Denver 15
Mumbai 15
Vienna 15
Belo Horizonte 14
Brooklyn 14
Tianjin 14
Boston 13
Changsha 13
Redondo Beach 13
Stockholm 13
Amman 12
Bari 12
Brno 12
Chennai 12
Mexico City 12
Shenyang 12
Wuhan 12
Boydton 11
Chengdu 11
Kunming 11
Trondheim 11
Turku 11
Florence 10
Naples 10
Absecon 9
Ankara 9
Totale 8.453
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Nome #
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus 554
Identification of New Hereditary Hearing Loss Genes Using High-Throughput Sequencing Technologies. 536
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 453
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 452
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 405
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis 390
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 374
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 358
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 331
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 310
TBL1Y: a new gene involved in syndromic hearing loss 305
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss 300
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk 293
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 256
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney 253
A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways 249
Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability 246
Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort. 245
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 244
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta 237
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families 221
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients 220
New age-related hearing loss candidate genes in humans: an ongoing challenge 213
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures 198
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals 194
Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection 194
Lights and shadows in the genetics of syndromic and non-syndromic hearing loss in the Italian population 188
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity 176
Two Novel COH1 Mutations in an Italian Patient with Cohen Syndrome. 176
Rare and low-frequency coding variants alter human adult height 175
A saturated map of common genetic variants associated with human height 169
Genetics, odor perception and food liking: The intriguing role of cinnamon 169
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
Pendred syndrome, or not pendred syndrome? That is the question 158
Cardiovascular Risk Factors and MRI Markers of Cerebral Small Vessel Disease 157
There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss 151
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population 145
Genetic dissection of temperament personality traits in Italian isolates 144
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders 141
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution 141
The role of knockout olfactory receptor genes in odor discrimination 141
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour 138
Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance 137
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids 137
Sensory Capacities and Eating Behavior: Intriguing Results from a Large Cohort of Italian Individuals 134
Hidden in the Genome: The First Italian Family with North Carolina Macular Dystrophy Carrying a Novel PRDM13 and CCNC Duplication 131
Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability 130
A new case of TAR syndrome confirms the importance of noncoding variants in the etiopathogenesis of the disease 129
Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations 125
Hearing loss and brain abnormalities due to pathogenic mutations in ADGRV1 gene: a case report 124
Uncovering a Novel Pathogenic Mechanism of BCS1L in Mitochondrial Disorders: Insights from Functional Studies on the c.38A>G Variant 122
Non-syndromic autosomal dominant hearing loss: The first italian family carrying a mutation in the NCOA3 gene 122
Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders 121
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss 118
A Hitchhiker Guide to Structural Variant Calling: A Comprehensive Benchmark Through Different Sequencing Technologies 115
Novel genetic determinants contribute to hearing loss in a central European cohort with enlarged vestibular aqueduct 114
High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis 112
In-Depth Phenotyping of PIGW-Related Disease and Its Role in 17q12 Genomic Disorder 108
Non-syndromic sensorineural prelingual and postlingual hearing loss due to col11a1 gene mutation 108
TBC1D24 and non-syndromic autosomal dominant hearing loss: the identification of an additional Italo-American family carrying the p.(S178L) mutation 107
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
Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure 101
SLC12A2: a new gene associated with autosomal dominant Non-Syndromic hearing loss in humans 93
Does It Run in Your Family? Inherited Truncating PSMD12 Variants Broaden the Phenotypic Spectrum of Stankiewicz-Isidor Syndrome 92
Molecular testing for the study of non-syndromic hearing loss 91
Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction 73
Unraveling the Functional Impact of Splicing Variants in Inherited Hearing Disorders Through Minigene Splicing Assays 51
Totale 13.518
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Categoria #
all - tutte 37.312
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 37.312
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202153 0 0 0 0 0 0 0 0 0 0 0 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
2025/20265.183 428 245 368 446 413 416 676 178 591 651 501 270
Totale 13.518