POLLI, ROBERTA
 Distribuzione geografica
Continente #
EU - Europa 54
NA - Nord America 35
AS - Asia 20
SA - Sud America 1
Totale 110
Nazione #
US - Stati Uniti d'America 35
IT - Italia 20
FR - Francia 17
CN - Cina 9
DE - Germania 8
DK - Danimarca 2
HK - Hong Kong 2
TR - Turchia 2
UA - Ucraina 2
AE - Emirati Arabi Uniti 1
AT - Austria 1
BR - Brasile 1
CH - Svizzera 1
FI - Finlandia 1
IR - Iran 1
JP - Giappone 1
KW - Kuwait 1
NL - Olanda 1
PL - Polonia 1
QA - Qatar 1
SG - Singapore 1
TW - Taiwan 1
Totale 110
Città #
Boulogne-sur-Mer 12
Beijing 8
Ashburn 6
Padova 6
Boardman 4
Chicago 3
Phoenix 3
Buffalo 2
Central 2
Fontanelle 2
Frederiksberg 2
Freiburg im Breisgau 2
Houston 2
Milan 2
Rome 2
Ankara 1
Austin 1
Brendola 1
Chapel Hill 1
Chiari 1
Cinisello Balsamo 1
Cirò Marina 1
Evanston 1
Gelsenkirchen 1
Helsinki 1
Istanbul 1
Kornwestheim 1
Koszalin 1
Las Vegas 1
Lausanne 1
Lille 1
Mishrif 1
New York 1
Ooltewah 1
Palermo 1
Paris 1
Parlin 1
Sant'elena 1
Santa Clara 1
Seattle 1
Secaucus 1
São Paulo 1
Taipei 1
Tampa 1
Trieste 1
Tübingen 1
Vienna 1
Woodbridge 1
Totale 91
Nome #
Genetics and Mathematics: FMR1 premutation female carriers, file e14fb267-a307-3de1-e053-1705fe0ac030 28
Identification of SETBP1 Mutations by Gene Panel Sequencing in Individuals With Intellectual Disability or With “Developmental and Epileptic Encephalopathy”, file e14fb26f-6ce7-3de1-e053-1705fe0ac030 19
PPP2R5D variants in patients with variable neurodevelopmental phenotype, file e14fb26d-8eae-3de1-e053-1705fe0ac030 18
Clinical and molecular description of 19 patients with GATAD2B-Associated Neurodevelopmental Disorder (GAND), file e14fb26e-4243-3de1-e053-1705fe0ac030 16
A Novel WAC Loss of Function Mutation in an Individual Presenting with Encephalopathy Related to Status Epilepticus during Sleep (ESES), file e14fb270-3941-3de1-e053-1705fe0ac030 13
Characterization of intellectual disability and autism comorbidity through gene panel sequencing, file e14fb26f-12ee-3de1-e053-1705fe0ac030 10
Molecular analysis of two uncharacterized sequence variants of the VHL gene., file e14fb267-8a80-3de1-e053-1705fe0ac030 4
Angelman Syndrome due to a novel splicing mutation of the UBE3A gene., file e14fb267-92e8-3de1-e053-1705fe0ac030 1
TARGETED GENE PANEL FOR COMORBID NEUROLOGICAL DISORDERS, file e14fb26d-6a64-3de1-e053-1705fe0ac030 1
Totale 110
Categoria #
all - tutte 570
article - articoli 523
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 1.093


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212 0 0 0 0 0 0 1 0 0 0 0 1
2021/20225 0 0 0 0 0 1 0 0 2 0 0 2
2022/202363 9 9 15 5 9 1 0 2 0 6 7 0
2023/202438 1 0 6 4 4 2 4 6 7 4 0 0
Totale 110