ArTS Archivio della ricerca di Trieste

MORGAN, ANNA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 3.120
EU - Europa 2.903
AS - Asia 1.279
SA - Sud America 56
AF - Africa 48
OC - Oceania 15
Continente sconosciuto - Info sul continente non disponibili 4
Totale 7.425
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 3.087
PL - Polonia 1.294
IT - Italia 549
CN - Cina 426
SG - Singapore 344
HK - Hong Kong 266
SE - Svezia 238
RU - Federazione Russa 135
DE - Germania 115
UA - Ucraina 86
BG - Bulgaria 82
FI - Finlandia 81
GB - Regno Unito 61
IE - Irlanda 55
BR - Brasile 46
TR - Turchia 44
IR - Iran 39
VN - Vietnam 36
NL - Olanda 35
FR - Francia 33
CH - Svizzera 28
SN - Senegal 28
BE - Belgio 25
CA - Canada 24
JP - Giappone 24
IN - India 22
AT - Austria 19
PK - Pakistan 18
ES - Italia 16
CZ - Repubblica Ceca 15
KR - Corea 14
IL - Israele 13
NO - Norvegia 13
AU - Australia 12
EG - Egitto 8
MX - Messico 6
PS - Palestinian Territory 6
DK - Danimarca 5
RO - Romania 5
ZA - Sudafrica 5
EU - Europa 4
LB - Libano 4
CO - Colombia 3
LU - Lussemburgo 3
NZ - Nuova Zelanda 3
TW - Taiwan 3
AM - Armenia 2
CY - Cipro 2
EC - Ecuador 2
ET - Etiopia 2
IM - Isola di Man 2
IS - Islanda 2
LK - Sri Lanka 2
LT - Lituania 2
MA - Marocco 2
PE - Perù 2
PR - Porto Rico 2
QA - Qatar 2
SA - Arabia Saudita 2
TN - Tunisia 2
AE - Emirati Arabi Uniti 1
AR - Argentina 1
BA - Bosnia-Erzegovina 1
BD - Bangladesh 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CG - Congo 1
CL - Cile 1
CR - Costa Rica 1
GE - Georgia 1
GR - Grecia 1
HR - Croazia 1
ID - Indonesia 1
LA - Repubblica Popolare Democratica del Laos 1
LV - Lettonia 1
MO - Macao, regione amministrativa speciale della Cina 1
MY - Malesia 1
OM - Oman 1
PH - Filippine 1
Totale 7.425
Salva come PNG Salva come JPEG
Città #
Warsaw 1.290
Fairfield 330
Chandler 303
Hong Kong 248
Woodbridge 245
Singapore 214
Houston 211
Ashburn 204
Ann Arbor 201
Trieste 188
Wilmington 159
Seattle 129
Cambridge 110
Jacksonville 100
Boardman 95
Princeton 84
Sofia 82
Beijing 67
Columbus 61
Dublin 55
Santa Clara 50
Dearborn 46
Helsinki 37
Moscow 37
Izmir 35
Dong Ket 32
Dakar 28
Saint Petersburg 28
Guangzhou 26
Los Angeles 25
Nuremberg 24
Bern 23
Nanjing 23
Redwood City 23
Shanghai 23
Bremen 22
Brussels 21
Milan 21
San Diego 20
Tehran 19
Munich 17
Amsterdam 13
Hefei 13
Lappeenranta 13
Brno 12
Changsha 12
Shenyang 12
Chicago 11
Kunming 11
New York 11
San Jose 11
Wuhan 11
Boydton 10
London 10
Phoenix 10
Trondheim 10
Vienna 10
Absecon 9
Florence 9
Seoul 9
Bologna 8
Dallas 8
Des Moines 8
Fuzhou 8
San Nicola Manfredi 8
Chengdu 7
Düsseldorf 7
Jinan 7
Mashhad 7
Nanchang 7
Padova 7
Atlanta 6
Barletta 6
Campinas 6
Dongguan 6
Fremont 6
Madrid 6
Montreal 6
Tianjin 6
Triggiano 6
Washington 6
Bahawalpur 5
Cagliari 5
Coimbatore 5
Erechim 5
Frankfurt am Main 5
Heidelberg 5
Melbourne 5
Omaha 5
Ottawa 5
Ramallah 5
Scuola 5
Southwark 5
Tanta 5
Tel Aviv 5
Tokyo 5
Turi 5
Beirut 4
Bochum 4
Council Bluffs 4
Totale 5.397
Salva come PNG Salva come JPEG
Nome #
Identification of New Hereditary Hearing Loss Genes Using High-Throughput Sequencing Technologies. 469
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 376
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 344
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus 332
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 325
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 320
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 274
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 264
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 255
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis 241
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss 235
A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways 196
TBL1Y: a new gene involved in syndromic hearing loss 190
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 181
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta 173
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk 172
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families 170
Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort. 169
Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability 168
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney 167
Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection 150
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients 144
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 144
Two Novel COH1 Mutations in an Italian Patient with Cohen Syndrome. 125
New age-related hearing loss candidate genes in humans: an ongoing challenge 116
Rare and low-frequency coding variants alter human adult height 112
Lights and shadows in the genetics of syndromic and non-syndromic hearing loss in the Italian population 108
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour 99
Hearing loss and brain abnormalities due to pathogenic mutations in ADGRV1 gene: a case report 83
Genetics, odor perception and food liking: The intriguing role of cinnamon 80
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals 75
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution 74
Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates 74
There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss 69
Genetic dissection of temperament personality traits in Italian isolates 67
A saturated map of common genetic variants associated with human height 65
Pendred syndrome, or not pendred syndrome? That is the question 63
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss 63
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity 61
A new case of TAR syndrome confirms the importance of noncoding variants in the etiopathogenesis of the disease 60
The role of knockout olfactory receptor genes in odor discrimination 57
Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability 55
TBC1D24 and non-syndromic autosomal dominant hearing loss: the identification of an additional Italo-American family carrying the p.(S178L) mutation 55
Sensory Capacities and Eating Behavior: Intriguing Results from a Large Cohort of Italian Individuals 52
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures 51
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders 51
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids 50
Non-syndromic autosomal dominant hearing loss: The first italian family carrying a mutation in the NCOA3 gene 50
Non-syndromic sensorineural prelingual and postlingual hearing loss due to col11a1 gene mutation 49
Molecular testing for the study of non-syndromic hearing loss 46
Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations 44
SLC12A2: a new gene associated with autosomal dominant Non-Syndromic hearing loss in humans 44
High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis 39
Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort 37
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population 35
Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders 34
Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure 31
Cardiovascular Risk Factors and MRI Markers of Cerebral Small Vessel Disease 24
Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance 20
Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction 14
Totale 7.691
Salva come PNG Salva come JPEG
Categoria #
all - tutte 23.666
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 23.666
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020334 0 0 0 0 0 0 0 0 115 72 83 64
2020/2021927 84 78 80 106 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
2024/20251.442 89 128 221 176 172 233 131 144 148 0 0 0
Totale 7.691