TRAVERSA, ALICE
 Distribuzione geografica
Continente #
NA - Nord America 659
EU - Europa 520
AS - Asia 173
AF - Africa 10
SA - Sud America 4
OC - Oceania 2
Totale 1.368
Nazione #
US - Stati Uniti d'America 646
IT - Italia 362
SG - Singapore 88
SE - Svezia 34
IN - India 29
CN - Cina 28
DE - Germania 27
FI - Finlandia 23
FR - Francia 14
IE - Irlanda 12
CA - Canada 11
ID - Indonesia 10
BG - Bulgaria 8
GB - Regno Unito 8
KR - Corea 6
TG - Togo 6
BE - Belgio 5
NL - Olanda 5
RO - Romania 5
UA - Ucraina 5
CL - Cile 4
IR - Iran 4
ZA - Sudafrica 3
AM - Armenia 2
CH - Svizzera 2
ES - Italia 2
MX - Messico 2
RU - Federazione Russa 2
VN - Vietnam 2
AL - Albania 1
AU - Australia 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
GR - Grecia 1
IL - Israele 1
JP - Giappone 1
KG - Kirghizistan 1
LT - Lituania 1
MA - Marocco 1
NZ - Nuova Zelanda 1
RS - Serbia 1
TW - Taiwan 1
Totale 1.368
Città #
Fairfield 92
Rome 89
Singapore 72
Chandler 52
Ashburn 48
Woodbridge 35
Houston 33
Seattle 32
Santa Clara 31
Cambridge 30
Wilmington 29
Princeton 21
Helsinki 18
Boston 11
Dublin 11
New York 11
San Diego 11
San Paolo di Civitate 11
Ann Arbor 10
Lawrence 10
Jakarta 9
Milan 9
Bremen 8
Sofia 8
Beijing 7
Dearborn 7
Toronto 7
Andover 6
Cagliari 6
Lomé 6
Millbury 6
Alba 5
Hamburg 5
Norwalk 5
Plano 5
Redwood City 5
Assebroek 4
Des Moines 4
London 4
Palermo 4
Santiago 4
Boardman 3
Capannelle 3
Falkenstein 3
Florence 3
Frankfurt am Main 3
Munich 3
Ottawa 3
Parma 3
Salerno 3
Turin 3
Berlin 2
Bronx 2
Buffalo 2
Bühl 2
Caserta 2
Changsha 2
Chicago 2
Ciudad Nezahualcoyotl 2
Fiumicino 2
Fonte Nuova 2
Fremont 2
Giugliano In Campania 2
Guidonia Montecelio 2
Jacksonville 2
Johannesburg 2
Lappeenranta 2
Latina 2
Laurel 2
Los Angeles 2
Macerata 2
Napoli 2
Paliano 2
Paris 2
Perris 2
Phoenix 2
Piedimonte San Germano 2
Redmond 2
Reggio Emilia 2
San Mateo 2
Seongnam 2
Seoul 2
Tehran 2
Tumba 2
Verona 2
Yerevan 2
Absecon 1
Andrano 1
Arenys De Munt 1
Athens 1
Auckland 1
Bari 1
Belfast 1
Bilbao 1
Bishkek 1
Bologna 1
Brno 1
Bromma 1
Brookings 1
Cachan 1
Totale 895
Nome #
Mutations impairing GSK3-mediated MAF phosphorylation cause cataract, deafness, intellectual disability, seizures, and a down syndrome-like facies 143
Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomalies 118
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration 100
Characterization of molecular bases of Myhre syndrome 92
Small 7p22.3 microdeletion: case report of Snx8 haploinsufficiency and neurological findings 90
GDF5 mutation case report and a systematic review of molecular and clinical spectrum: Expanding current knowledge on genotype-phenotype correlations 81
Co-occurring WARS2 and CHRNA6 mutations in a child with a severe form of infantile parkinsonism 80
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 78
Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy-Walker malformation. 75
Genomic and physiological resilience in extreme environments are associated with a secure attachment style 72
Absence of 6’Sialyllactose during lactation impairs cognitive capabilities and modulates gene expression 65
Sialylated human milk oligosaccharides program cognitive development through a non-genomic transmission mode 60
Reduced availability of a selective human milk oligosaccharide during lactation impairs post-weaning executive functions 46
Increased availability of the human milk oligosaccharide sialyl(alpha2,3)lactose during lactation promotes the development of executive functions 45
MiRLog and dbmiR: Prioritization and functional annotation tools to study human microRNA sequence variants 44
Potassium Channel {KCNH}1 Activating Variants Cause Altered Functional and Morphological Ciliogenesis 42
Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges—Systematic Review of the Literature and Meta-Analysis 41
Novel SMAD4 mutation causing Myhre syndrome 39
null 25
Unusual Segregation of APP Mutations in Monogenic Alzheimer Disease 23
null 20
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Exposure to 3′sialyllactose‐poor milk during lactation impairs cognitive capabilities in adulthood 13
Additional lesions identified by genomic microarrays are associated with an inferior outcome in low-risk chronic lymphocytic leukaemia patients 13
Exploring non-coding genetic variability in ACE2: Functional annotation and in vitro validation of regulatory variants 10
SMAD4 mutations causing Myhre syndrome are under positive selection in the male germline 9
Long-term consequences of reduced availability and compensatory supplementation of sialylated HMOs on cognitive capabilities 8
Totale 1.452
Categoria #
all - tutte 4.831
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 4.831


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020171 0 0 0 0 0 15 35 19 36 17 7 42
2020/2021244 22 21 15 6 20 10 12 31 24 34 45 4
2021/2022245 7 8 24 8 23 14 21 21 14 10 52 43
2022/2023252 43 42 19 21 34 23 8 26 22 3 7 4
2023/2024198 8 23 11 14 16 23 11 23 18 15 18 18
2024/2025203 10 62 18 18 66 29 0 0 0 0 0 0
Totale 1.452