IRIS
FRANZE', Annamaria
 Distribuzione geografica
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Continente #
NA - Nord America 1.124
EU - Europa 574
AS - Asia 344
AF - Africa 25
OC - Oceania 2
SA - Sud America 1
Totale 2.070
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Nazione #
US - Stati Uniti d'America 1.102
SG - Singapore 215
IT - Italia 211
CN - Cina 92
NL - Olanda 89
UA - Ucraina 76
DE - Germania 42
IE - Irlanda 39
FI - Finlandia 36
CI - Costa d'Avorio 25
VN - Vietnam 25
SE - Svezia 24
CA - Canada 21
GB - Regno Unito 16
RO - Romania 9
IN - India 8
PL - Polonia 8
BE - Belgio 6
FR - Francia 6
BG - Bulgaria 5
ES - Italia 5
AU - Australia 2
TH - Thailandia 2
CL - Cile 1
HK - Hong Kong 1
IL - Israele 1
IM - Isola di Man 1
LV - Lettonia 1
MX - Messico 1
Totale 2.070
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Città #
Chandler 256
Singapore 179
Amsterdam 83
Ashburn 66
Millbury 64
Santa Clara 57
Jacksonville 50
Princeton 38
Des Moines 36
Napoli 31
Boston 28
Lawrence 28
Dong Ket 24
Nanjing 23
Naples 21
Milan 20
Ottawa 20
Wilmington 19
Beijing 14
Kronberg 11
Fairfield 9
Timisoara 9
Nanchang 8
Shenyang 8
Dearborn 7
Rome 7
Sanremo 7
Boardman 6
Waanrode 6
Woodbridge 6
Hebei 5
Jiaxing 5
Pune 5
Saludecio 5
Sofia 5
Tianjin 5
Changsha 4
Dallas 4
Munich 4
Padova 4
Salerno 4
Bari 3
Bologna 3
Delhi 3
Dublin 3
Falls Church 3
Frankfurt am Main 3
Guangzhou 3
Indiana 3
Lappeenranta 3
Montecorvino Rovella 3
Perugia 3
Saint-Paul-Trois-Châteaux 3
San Mateo 3
Aachen 2
Amorosi 2
Ann Arbor 2
Bergamo 2
Casalecchio di Reno 2
Ferrara di Monte Baldo 2
Florence 2
Gerace 2
Lanzhou 2
Madrid 2
Marano Di Napoli 2
Marigliano 2
Medicina 2
Norwalk 2
Roccaraso 2
Sabadell 2
Spin 2
Torre Del Greco 2
Torrebelvicino 2
Washington 2
Abbiategrasso 1
Alvignano 1
Baotou 1
Barano D'ischia 1
Bath 1
Birmingham 1
Cagliari 1
Cambridge 1
Casalnuovo di Napoli 1
Castel Morrone 1
Douglas 1
Edinburgh 1
Erlangen 1
Esslingen am Neckar 1
Falconara Marittima 1
Formia 1
Genova 1
Guiyang 1
Hangzhou 1
Hefei 1
Houston 1
Kunming 1
Las Vegas 1
London 1
Mainz 1
Melito di Napoli 1
Totale 1.296
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Nome #
Novel compound heterozygous mutations in BCS1L gene causing Bjornstad syndrome in two siblings 77
”Sviluppo comunicativo linguistico nel bambino ipoacusico” 71
Otosclerosi:analisi di associazione cromosomica e identificazione di geni candidati 66
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 54
Down-regulation of otospiralin mRNA in response to acoustic stress in guinea pig 51
SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing loss 51
Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11). 49
Analisi di associazione cromosomica in famiglie con ricorrenza di otosclerosi 49
Genetica della funzione uditiva normale e patologica 49
Performance and characteristics of the Newborn Hearing Screening Program in Campania region (Italy) between 2013 and 2019 46
Methodological approach to select patients with genetic ipoacusia and otosclerosis: identification and characterization of putative involved genes 45
New evidence for the correlation of the p.G130V mutation in the GJB2 gene and syndromic hearing loss with palmoplantar keratoderma 44
Integrated Bimodal Fitting for Unilateral CI Users with Residual Contralateral Hearing 42
A novel X-linked member of the human zinc finger protein gene family: isolation, mapping, and expression. 41
Age-related hearing loss in four Italian genetic isolates: An epidemiological study 41
Exclusion of TNFRS11B as a candidate gene for otosclerosis in Campania population 41
Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss 40
Correlazione genetica nei DSA 39
Audio-Vestibular Alterations During the Phases of the Menstrual Cycle in Patients with Cochlear Implant 39
Ipoacusie Di Tipo Genetico: Identificazione Di Geni-Malattia 38
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 38
Forme ereditarie di ipoacusie neurosensoriali isolate e sindromiche nel bambino 38
Audiometric evaluation of carriers of the connexin 26 mutation 35delG 36
Functional characterization of a novel Cx26 (T55N) mutation associated to non-syndromic hearing loss. 36
Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing loss 36
Computer programs for the characterization of protein coding genes 36
Screening uditivo neonatale: implementazione del processo ed esperienza della Regione Campania 36
Statistical evaluation of the coding capacity of complementary DNA strands. 35
Feasibility and effectiveness of a population-based newborn hearing screening in an economically deprived region of Italy 35
Targeted Audiological Surveillance Program in Campania, Italy 34
R75Q dominant mutation in GJB2 gene silenced by the in Cis recessive mutation c.35delG 33
Mutational analysis for GJB2, GJB6, and GJB3 genes in Campania within a universal neonatal hearing screening programme 33
Assembly of the Auditory Circuitry by a Hox Genetic Network in the Mouse Brainstem 33
Effetto protettivo dell’ allopurinolo nel danno uditivo da rumore in relazione a piu’ fattori 32
Effect over time of allopurinol on noise-induced hearing loss in guinea pigs. 32
Bimodal strategy for excellent audiological rehabilitation in a subject with a novel nonsense mutation of the SLC26A4 gene: A case report 32
Current research trends in clinical audiology 32
Genetica della funzione uditiva normale e patologica 31
Screening del gene connessina 26 e connessina 30 (DELB6-D1351830) in soggetti della regione Campania affetti da ipoacusia non sindromica 31
Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian families 29
Analysis of otospiralin down-regulation and acoustic damage to organ of Corti in guinea pig. 28
Newborn hearing screening in the Campania region (Italy): early language and perceptual outcomes of infants with permanent hearing los 28
GJB2 gene mutations in syndromic skin diseases with sensorineural hearing loss 27
Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11). 26
Intragenic deletion in macrod2: A family with complex phenotypes including microcephaly, intellectual disability, polydactyly, renal and pancreatic malformations 26
Very good performance with bimodal stimulation in a like-hybrid modality in a patient with profound bilateral sensorineural hearing loss with low-frequencies preservation. 25
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 25
X-Linked Sensorineural Hearing Loss: A Literature Review 24
GJB2 Gene Mutations in Syndromic Skin Diseases with Sensorineural Hearing Loss. 23
Coding region intron/exon organization, alternative splicing, and X-chromosome inactivation of the KRAB/FPB-domain-containing human zinc finger gene ZNF41 23
Hearing impairment: new frontiers of regenerative medicine 22
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 22
Connexin 26 variant carriers have a better gastrointestinal health: Is this the heterozygote advantage? 21
Members of the zinc finger protein gene family sharing a conserved N-terminal module 21
Genetics Aspects in Non-Syndromic Forms of Sensorineural Hearing Loss 20
Enhanced glutathione levels and oxidoresistance mediated by increased glucose-6-phosphate dehydrogenase expression 19
Semeiotica Clinica 19
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 18
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss. 18
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" 17
The rs39335 polymorphism of the RELN gene is not associated with otosclerosis in a southern Italian population. 16
Molecular anatomy of the human glucose 6-phosphate dehydrogenase core promoter 15
Vascular Factors in Patients with Midlife Sensorineural Hearing Loss and the Progression to Mild Cognitive Impairment 14
Symmetric transcription of bacteriophage T4 base plate genes 14
Molecular biology of plasminogen activator and its role in the invasiveness of malignant cells 13
Isolation and expression analysis of a human zinc finger gene (ZNF41) located on the short arm of the X chromosome 12
An upsteam enhancer and a negative element in the 5' flanking region of the human urokinase plasminogen activator gene 11
Statistical analysis of the coding capacity of complementary DNA strands 9
Isolation and analysis of genomic sequences from mycorrhizal fung 7
Totale 2.214
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Categoria #
all - tutte 10.401
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 10.401
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202086 0 0 0 0 18 1 17 6 2 5 12 25
2020/2021247 13 12 11 16 15 28 25 41 21 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
2024/2025311 97 130 4 10 70 0 0 0 0 0 0 0
Totale 2.214