ArTS Archivio della ricerca di Trieste

MORGAN, ANNA
 Distribuzione geografica
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Continente #
NA - Nord America 5.574
EU - Europa 4.034
AS - Asia 3.620
SA - Sud America 444
Continente sconosciuto - Info sul continente non disponibili 295
AF - Africa 168
OC - Oceania 28
Totale 14.163
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Nazione #
US - Stati Uniti d'America 5.401
PL - Polonia 1.382
SG - Singapore 1.066
IT - Italia 907
CN - Cina 821
VN - Vietnam 381
HK - Hong Kong 362
BR - Brasile 328
BD - Bangladesh 324
DE - Germania 253
SE - Svezia 251
FR - Francia 182
KR - Corea 158
GB - Regno Unito 156
RU - Federazione Russa 152
FI - Finlandia 142
NL - Olanda 126
IN - India 107
UA - Ucraina 98
CA - Canada 91
BG - Bulgaria 87
IE - Irlanda 65
TR - Turchia 63
JP - Giappone 57
MA - Marocco 47
ES - Italia 44
IR - Iran 43
MX - Messico 41
AR - Argentina 37
CH - Svizzera 37
AT - Austria 34
ZA - Sudafrica 32
IQ - Iraq 31
PK - Pakistan 31
SN - Senegal 30
BE - Belgio 26
AU - Australia 24
SA - Arabia Saudita 22
CZ - Repubblica Ceca 21
IL - Israele 21
EG - Egitto 18
EC - Ecuador 17
UZ - Uzbekistan 17
CO - Colombia 16
NO - Norvegia 16
VE - Venezuela 16
ID - Indonesia 15
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
GT - Guatemala 7
HR - Croazia 7
KE - Kenya 7
TT - Trinidad e Tobago 7
KZ - Kazakistan 6
PE - Perù 6
LB - Libano 5
CR - Costa Rica 4
DO - Repubblica Dominicana 4
EE - Estonia 4
ET - Etiopia 4
EU - Europa 4
MY - Malesia 4
TN - Tunisia 4
BA - Bosnia-Erzegovina 3
BO - Bolivia 3
BS - Bahamas 3
CI - Costa d'Avorio 3
CY - Cipro 3
HN - Honduras 3
JM - Giamaica 3
LK - Sri Lanka 3
LU - Lussemburgo 3
NP - Nepal 3
NZ - Nuova Zelanda 3
PR - Porto Rico 3
TH - Thailandia 3
TZ - Tanzania 3
AL - Albania 2
AM - Armenia 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
QA - Qatar 2
AO - Angola 1
Totale 13.842
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Città #
Warsaw 1.317
Ashburn 712
Singapore 636
San Jose 349
Hong Kong 335
Fairfield 330
Chandler 303
Woodbridge 245
Houston 218
Trieste 208
Ann Arbor 201
Council Bluffs 194
Wilmington 163
Beijing 150
Seoul 147
Hefei 144
Seattle 137
Los Angeles 134
Cambridge 114
Ho Chi Minh City 105
Boardman 100
Jacksonville 100
Chicago 92
Santa Clara 88
Columbus 87
Princeton 85
Sofia 84
Hanoi 83
New York 81
Dallas 73
Helsinki 70
Milan 69
Dublin 63
Lauterbourg 60
Zgierz 54
Frankfurt am Main 50
Munich 48
Dearborn 47
Buffalo 41
London 41
Moscow 41
Casablanca 38
The Dalles 37
Phoenix 36
Izmir 35
Nuremberg 33
Dong Ket 32
Düsseldorf 32
Guangzhou 32
São Paulo 31
Dakar 30
Nanjing 30
Rome 29
Saint Petersburg 28
Montreal 27
Shanghai 27
Tokyo 26
Orem 25
Bern 24
Lappeenranta 24
Redwood City 23
Bremen 22
Brussels 22
San Diego 22
Tehran 22
Atlanta 21
Amsterdam 18
Brooklyn 18
Da Nang 18
Johannesburg 18
Madrid 18
Toronto 18
Bologna 17
Mumbai 17
Tashkent 17
Denver 16
Haiphong 16
Bari 15
Boston 15
Vienna 15
Belo Horizonte 14
Stockholm 14
Tianjin 14
Changsha 13
Chennai 13
Mexico City 13
Redondo Beach 13
Amman 12
Brno 12
Florence 12
Shenyang 12
Wuhan 12
Boydton 11
Charlotte 11
Chengdu 11
Kunming 11
Naples 11
Trondheim 11
Turku 11
Rio de Janeiro 10
Totale 8.784
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Nome #
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus 579
Identification of New Hereditary Hearing Loss Genes Using High-Throughput Sequencing Technologies. 548
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 459
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 455
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis 416
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 411
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 395
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 362
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 335
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 314
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk 312
TBL1Y: a new gene involved in syndromic hearing loss 309
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss 306
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 262
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 259
Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability 256
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney 255
Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort. 252
A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways 252
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta 240
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families 229
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients 225
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals 220
New age-related hearing loss candidate genes in humans: an ongoing challenge 218
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures 208
Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection 201
Lights and shadows in the genetics of syndromic and non-syndromic hearing loss in the Italian population 197
Genetics, odor perception and food liking: The intriguing role of cinnamon 191
A saturated map of common genetic variants associated with human height 187
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity 184
Two Novel COH1 Mutations in an Italian Patient with Cohen Syndrome. 182
Rare and low-frequency coding variants alter human adult height 178
Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort 172
Pendred syndrome, or not pendred syndrome? That is the question 171
Cardiovascular Risk Factors and MRI Markers of Cerebral Small Vessel Disease 169
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
There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss 155
Uncovering a Novel Pathogenic Mechanism of BCS1L in Mitochondrial Disorders: Insights from Functional Studies on the c.38A>G Variant 154
Genetic dissection of temperament personality traits in Italian isolates 154
Hidden in the Genome: The First Italian Family with North Carolina Macular Dystrophy Carrying a Novel PRDM13 and CCNC Duplication 153
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders 150
The role of knockout olfactory receptor genes in odor discrimination 149
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution 148
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour 148
Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance 146
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids 142
Sensory Capacities and Eating Behavior: Intriguing Results from a Large Cohort of Italian Individuals 140
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
Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability 133
Hearing loss and brain abnormalities due to pathogenic mutations in ADGRV1 gene: a case report 132
A new case of TAR syndrome confirms the importance of noncoding variants in the etiopathogenesis of the disease 130
Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders 128
Non-syndromic autosomal dominant hearing loss: The first italian family carrying a mutation in the NCOA3 gene 126
Novel genetic determinants contribute to hearing loss in a central European cohort with enlarged vestibular aqueduct 125
High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis 124
In-Depth Phenotyping of PIGW-Related Disease and Its Role in 17q12 Genomic Disorder 121
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss 119
Non-syndromic sensorineural prelingual and postlingual hearing loss due to col11a1 gene mutation 114
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
Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure 109
Does It Run in Your Family? Inherited Truncating PSMD12 Variants Broaden the Phenotypic Spectrum of Stankiewicz-Isidor Syndrome 101
SLC12A2: a new gene associated with autosomal dominant Non-Syndromic hearing loss in humans 100
Molecular testing for the study of non-syndromic hearing loss 98
Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction 79
Unraveling the Functional Impact of Splicing Variants in Inherited Hearing Disorders Through Minigene Splicing Assays 64
Totale 14.163
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Categoria #
all - tutte 40.171
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 40.171
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022492 0 0 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
2025/20265.209 428 245 368 446 413 416 676 178 591 651 501 296
2026/2027619 193 266 160 0 0 0 0 0 0 0 0 0
Totale 14.163