IRIS
FRANZE', Annamaria
 Distribuzione geografica
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Continente #
AS - Asia 2.468
NA - Nord America 2.340
EU - Europa 1.929
SA - Sud America 315
AF - Africa 76
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 1
Totale 7.133
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Nazione #
US - Stati Uniti d'America 2.244
SG - Singapore 1.173
RU - Federazione Russa 856
VN - Vietnam 511
CN - Cina 402
IT - Italia 327
BR - Brasile 248
HK - Hong Kong 169
DE - Germania 152
NL - Olanda 111
FR - Francia 101
UA - Ucraina 90
FI - Finlandia 75
CA - Canada 57
GB - Regno Unito 54
JP - Giappone 42
IE - Irlanda 41
IN - India 34
AR - Argentina 32
SE - Svezia 29
CI - Costa d'Avorio 26
IQ - Iraq 22
PL - Polonia 21
MX - Messico 20
ZA - Sudafrica 19
BD - Bangladesh 17
ES - Italia 16
TH - Thailandia 14
PK - Pakistan 13
BE - Belgio 12
ID - Indonesia 12
LT - Lituania 12
KR - Corea 11
PH - Filippine 11
EC - Ecuador 10
RO - Romania 9
IR - Iran 8
PY - Paraguay 8
AT - Austria 6
BG - Bulgaria 6
EG - Egitto 6
TW - Taiwan 6
CL - Cile 5
KE - Kenya 5
AE - Emirati Arabi Uniti 4
AU - Australia 4
CO - Colombia 4
DO - Repubblica Dominicana 4
VE - Venezuela 4
IL - Israele 3
LB - Libano 3
MA - Marocco 3
PA - Panama 3
SA - Arabia Saudita 3
BA - Bosnia-Erzegovina 2
BH - Bahrain 2
BZ - Belize 2
DZ - Algeria 2
GP - Guadalupe 2
MW - Malawi 2
TN - Tunisia 2
TR - Turchia 2
TT - Trinidad e Tobago 2
TZ - Tanzania 2
UY - Uruguay 2
UZ - Uzbekistan 2
ZM - Zambia 2
AD - Andorra 1
BB - Barbados 1
BJ - Benin 1
BO - Bolivia 1
CD - Congo 1
CG - Congo 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
ET - Etiopia 1
GD - Grenada 1
GH - Ghana 1
GR - Grecia 1
GT - Guatemala 1
HU - Ungheria 1
IM - Isola di Man 1
JO - Giordania 1
KH - Cambogia 1
KZ - Kazakistan 1
LC - Santa Lucia 1
LV - Lettonia 1
MK - Macedonia 1
NI - Nicaragua 1
PE - Perù 1
PR - Porto Rico 1
PT - Portogallo 1
RE - Reunion 1
SN - Senegal 1
SY - Repubblica araba siriana 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 7.133
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Città #
Singapore 529
San Jose 365
Chandler 256
Moscow 218
Ashburn 194
Hong Kong 160
Beijing 157
Ho Chi Minh City 140
Hanoi 122
Santa Clara 119
Amsterdam 94
Millbury 64
Lauterbourg 58
Dallas 55
Naples 55
Los Angeles 52
Munich 52
Jacksonville 51
The Dalles 50
Princeton 38
Des Moines 36
São Paulo 36
Tokyo 36
Boston 32
Napoli 31
Frankfurt am Main 29
Redondo Beach 29
Lawrence 28
Milan 28
Council Bluffs 26
New York 26
Ottawa 26
Dong Ket 24
Hefei 24
Turku 24
Nanjing 23
Da Nang 20
Buffalo 19
Wilmington 19
Atlanta 16
Haiphong 16
Orem 15
Falkenstein 13
Helsinki 13
London 13
Rome 12
Brooklyn 11
Kronberg 11
Toronto 11
Chicago 10
Seattle 10
Fairfield 9
Mexico City 9
Montreal 9
Rio de Janeiro 9
Timisoara 9
Trieste 9
Biên Hòa 8
Chennai 8
Dearborn 8
Denver 8
Houston 8
Nanchang 8
Nuremberg 8
Poplar 8
Shenyang 8
Brasília 7
Guangzhou 7
Hải Dương 7
Johannesburg 7
Sanremo 7
Thái Nguyên 7
Warsaw 7
Woodbridge 7
Boardman 6
Brussels 6
Nijmegen 6
Ninh Bình 6
Perugia 6
Phoenix 6
Stockholm 6
Waanrode 6
Baghdad 5
Bangkok 5
Cassolnovo 5
Changsha 5
Dublin 5
Hebei 5
Jiaxing 5
Lappeenranta 5
Pune 5
Saludecio 5
San Francisco 5
Seoul 5
Sofia 5
Tianjin 5
Turin 5
Wroclaw 5
Asunción 4
Bến Tre 4
Totale 3.814
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Nome #
”Sviluppo comunicativo linguistico nel bambino ipoacusico” 167
Novel compound heterozygous mutations in BCS1L gene causing Bjornstad syndrome in two siblings 163
NeonaTal Assisted TelerehAbilitation (T.A.T.A. Web App) for Hearing-Impaired Children: A Family-Centered Care Model for Early Intervention in Congenital Hearing Loss 162
Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss 158
Integrated Bimodal Fitting for Unilateral CI Users with Residual Contralateral Hearing 158
Otosclerosi:analisi di associazione cromosomica e identificazione di geni candidati 151
Hearing impairment: new frontiers of regenerative medicine 144
Genetica della funzione uditiva normale e patologica 144
Vascular Factors in Patients with Midlife Sensorineural Hearing Loss and the Progression to Mild Cognitive Impairment 142
Analisi di associazione cromosomica in famiglie con ricorrenza di otosclerosi 139
Screening uditivo neonatale: implementazione del processo ed esperienza della Regione Campania 137
Forme ereditarie di ipoacusie neurosensoriali isolate e sindromiche nel bambino 135
Current research trends in clinical audiology 135
SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing loss 132
Down-regulation of otospiralin mRNA in response to acoustic stress in guinea pig 129
Mutational analysis for GJB2, GJB6, and GJB3 genes in Campania within a universal neonatal hearing screening programme 129
Audio-Vestibular Alterations During the Phases of the Menstrual Cycle in Patients with Cochlear Implant 125
Ipoacusie Di Tipo Genetico: Identificazione Di Geni-Malattia 124
Targeted Audiological Surveillance Program in Campania, Italy 123
Methodological approach to select patients with genetic ipoacusia and otosclerosis: identification and characterization of putative involved genes 122
Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing loss 122
Exclusion of TNFRS11B as a candidate gene for otosclerosis in Campania population 122
Intragenic deletion in macrod2: A family with complex phenotypes including microcephaly, intellectual disability, polydactyly, renal and pancreatic malformations 122
New evidence for the correlation of the p.G130V mutation in the GJB2 gene and syndromic hearing loss with palmoplantar keratoderma 121
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 121
Screening del gene connessina 26 e connessina 30 (DELB6-D1351830) in soggetti della regione Campania affetti da ipoacusia non sindromica 120
Correlazione genetica nei DSA 118
Age-related hearing loss in four Italian genetic isolates: An epidemiological study 118
Statistical evaluation of the coding capacity of complementary DNA strands. 118
X-Linked Sensorineural Hearing Loss: A Literature Review 118
R75Q dominant mutation in GJB2 gene silenced by the in Cis recessive mutation c.35delG 115
The Absence of Permanent Sensorineural Hearing Loss in a Cohort of Children with SARS-CoV-2 Infection and the Importance of Performing the Audiological “Work-Up" 114
Functional characterization of a novel Cx26 (T55N) mutation associated to non-syndromic hearing loss. 109
Bimodal strategy for excellent audiological rehabilitation in a subject with a novel nonsense mutation of the SLC26A4 gene: A case report 108
A novel X-linked member of the human zinc finger protein gene family: isolation, mapping, and expression. 107
Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian families 107
Computer programs for the characterization of protein coding genes 104
Audiometric evaluation of carriers of the connexin 26 mutation 35delG 103
Effect over time of allopurinol on noise-induced hearing loss in guinea pigs. 103
Analysis of otospiralin down-regulation and acoustic damage to organ of Corti in guinea pig. 103
Effetto protettivo dell’ allopurinolo nel danno uditivo da rumore in relazione a piu’ fattori 102
Coding region intron/exon organization, alternative splicing, and X-chromosome inactivation of the KRAB/FPB-domain-containing human zinc finger gene ZNF41 102
Genetica della funzione uditiva normale e patologica 100
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 100
Assembly of the Auditory Circuitry by a Hox Genetic Network in the Mouse Brainstem 99
GJB2 Gene Mutations in Syndromic Skin Diseases with Sensorineural Hearing Loss. 94
Genetics Aspects in Non-Syndromic Forms of Sensorineural Hearing Loss 90
Newborn hearing screening in the Campania region (Italy): early language and perceptual outcomes of infants with permanent hearing los 88
Members of the zinc finger protein gene family sharing a conserved N-terminal module 88
Semeiotica Clinica 87
Feasibility and effectiveness of a population-based newborn hearing screening in an economically deprived region of Italy 86
Very good performance with bimodal stimulation in a like-hybrid modality in a patient with profound bilateral sensorineural hearing loss with low-frequencies preservation. 85
Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11). 83
Genetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic sequence variants 83
Human Synaptobrevin-like 1 Gene Basal Transcription Is Regulated through the Interaction of Selenocysteine tRNA Gene Transcription Activating Factor-Zinc Finger 143 Factors with Evolutionary Conserved Cis-elements 81
Performance and characteristics of the Newborn Hearing Screening Program in Campania region (Italy) between 2013 and 2019 75
Enhanced glutathione levels and oxidoresistance mediated by increased glucose-6-phosphate dehydrogenase expression 74
Symmetric transcription of bacteriophage T4 base plate genes 67
GJB2 gene mutations in syndromic skin diseases with sensorineural hearing loss 66
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss. 65
Connexin 26 variant carriers have a better gastrointestinal health: Is this the heterozygote advantage? 62
Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11). 61
Statistical analysis of the coding capacity of complementary DNA strands 61
Molecular anatomy of the human glucose 6-phosphate dehydrogenase core promoter 54
Isolation and expression analysis of a human zinc finger gene (ZNF41) located on the short arm of the X chromosome 54
An upsteam enhancer and a negative element in the 5' flanking region of the human urokinase plasminogen activator gene 54
Molecular biology of plasminogen activator and its role in the invasiveness of malignant cells 52
The rs39335 polymorphism of the RELN gene is not associated with otosclerosis in a southern Italian population. 47
Isolation and analysis of genomic sequences from mycorrhizal fung 39
Totale 7.291
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Categoria #
all - tutte 22.251
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 22.251
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202165 0 0 0 0 0 0 0 0 0 25 13 27
2021/2022395 9 2 14 13 1 8 5 6 39 52 97 149
2022/2023596 75 64 16 29 73 63 14 57 76 83 30 16
2023/2024346 21 51 27 35 23 45 18 41 6 9 48 22
2024/20251.934 97 130 4 10 71 115 195 134 127 142 712 197
2025/20263.454 387 280 342 297 751 113 403 203 419 259 0 0
Totale 7.291