CINECA IRIS Institutional Research Information System

TRAVERSA, ALICE
 Distribuzione geografica
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Continente #
AS - Asia 92
NA - Nord America 42
EU - Europa 16
AF - Africa 3
SA - Sud America 1
Totale 154
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Nazione #
HK - Hong Kong 54
US - Stati Uniti d'America 39
SG - Singapore 27
IT - Italia 4
EG - Egitto 3
AZ - Azerbaigian 2
IL - Israele 2
AE - Emirati Arabi Uniti 1
AM - Armenia 1
BE - Belgio 1
BO - Bolivia 1
CH - Svizzera 1
DO - Repubblica Dominicana 1
ES - Italia 1
GR - Grecia 1
IE - Irlanda 1
KG - Kirghizistan 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
LT - Lituania 1
LU - Lussemburgo 1
MX - Messico 1
NL - Olanda 1
NO - Norvegia 1
PA - Panama 1
PH - Filippine 1
PT - Portogallo 1
RU - Federazione Russa 1
SK - Slovacchia (Repubblica Slovacca) 1
VN - Vietnam 1
Totale 154
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Città #
Hong Kong 54
Singapore 6
Los Angeles 5
Rome 4
Cairo 3
Baku 2
Seattle 2
Ashburn 1
Athens 1
Bishkek 1
Boston 1
Bratislava 1
Brussels 1
Council Bluffs 1
Dubai 1
Dublin 1
Jerusalem 1
La Paz 1
Luxembourg 1
Manila 1
Mexico City 1
Oslo 1
Phnom Penh 1
Tel Aviv 1
Vientiane 1
Yerevan 1
Zurich 1
Totale 96
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Nome #
GDF5 mutation case report and a systematic review of molecular and clinical spectrum: Expanding current knowledge on genotype-phenotype correlations 14
Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges—Systematic Review of the Literature and Meta-Analysis 12
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration 10
Sialylated human milk oligosaccharides program cognitive development through a non-genomic transmission mode 10
Small RNAs and tooth development: The role of microRNAs in tooth agenesis and impaction 9
Polyethylene Micro/Nanoplastics Exposure Induces Epithelial-Mesenchymal Transition in Human Bronchial and Alveolar Epithelial Cells 9
Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co-inheritance 8
Additional lesions identified by genomic microarrays are associated with an inferior outcome in low-risk chronic lymphocytic leukaemia patients 8
Exposure to 3′sialyllactose‐poor milk during lactation impairs cognitive capabilities in adulthood 8
Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy-Walker malformation 8
Small 7p22.3 microdeletion: case report of Snx8 haploinsufficiency and neurological findings 8
Exploring non-coding genetic variability in ACE2: Functional annotation and in vitro validation of regulatory variants 8
Deciphering the Transcriptional Metabolic Profile of Adipose-Derived Stem Cells During Osteogenic Differentiation and Epigenetic Drug Treatment 8
Genomic and physiological resilience in extreme environments are associated with a secure attachment style 8
Novel SMAD4 mutation causing Myhre syndrome 7
Potassium Channel {KCNH}1 Activating Variants Cause Altered Functional and Morphological Ciliogenesis 7
Mutations impairing GSK3-mediated MAF phosphorylation cause cataract, deafness, intellectual disability, seizures, and a down syndrome-like facies 7
Long-term consequences of reduced availability and compensatory supplementation of sialylated HMOs on cognitive capabilities 7
SMAD4 mutations causing Myhre syndrome are under positive selection in the male germline 7
MiRLog and dbmiR: Prioritization and functional annotation tools to study human microRNA sequence variants 7
Unusual Segregation of APP Mutations in Monogenic Alzheimer Disease 5
Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomalies 3
Totale 178
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Categoria #
all - tutte 1.289
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 1.289
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/20241 0 0 0 0 0 0 0 0 1 0 0 0
2024/2025177 0 0 0 0 0 79 37 20 21 20 0 0
Totale 178