BIANCIARDI, LAURA
 Distribuzione geografica
Continente #
NA - Nord America 772
EU - Europa 721
AS - Asia 77
OC - Oceania 1
Totale 1.571
Nazione #
US - Stati Uniti d'America 768
GB - Regno Unito 292
IT - Italia 121
IE - Irlanda 93
CN - Cina 60
SE - Svezia 53
UA - Ucraina 48
DE - Germania 41
FR - Francia 28
BE - Belgio 14
FI - Finlandia 12
NL - Olanda 5
RU - Federazione Russa 5
TR - Turchia 5
ES - Italia 4
IR - Iran 4
CA - Canada 3
CZ - Repubblica Ceca 3
IL - Israele 2
IN - India 2
SG - Singapore 2
AU - Australia 1
ID - Indonesia 1
KR - Corea 1
MS - Montserrat 1
PT - Portogallo 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 1.571
Città #
Southend 273
Fairfield 108
Dublin 89
Ashburn 81
Ann Arbor 69
Chandler 62
Woodbridge 61
Houston 54
Cambridge 48
Siena 45
Wilmington 41
Seattle 40
Jacksonville 37
Princeton 18
Menlo Park 16
Nanjing 16
Beijing 13
San Diego 13
Brussels 12
Dearborn 11
Boardman 9
San Mateo 9
Shanghai 7
Falls Church 6
Rome 6
Milan 5
Norwalk 5
Venezia 5
Hebei 4
Helsinki 4
Izmir 4
Nanchang 4
San Giuliano Milanese 4
Florence 3
Genova 3
Jinan 3
Kunming 3
Moscow 3
Zanjan 3
Caserta 2
Certaldo 2
Changsha 2
Empoli 2
Lancaster 2
Los Angeles 2
Monteriggioni 2
Málaga 2
Petah Tikva 2
Rignano Sull'arno 2
Sesto Fiorentino 2
Shenyang 2
Simi Valley 2
Toronto 2
Waanrode 2
Zhengzhou 2
Auburn Hills 1
Balıkesir 1
Bergamo 1
Bratislava 1
Brindisi 1
Brno 1
Costa Mesa 1
Düsseldorf 1
Fremont 1
Groningen 1
Hefei 1
Hounslow 1
Jakarta 1
Jiaxing 1
Lappeenranta 1
Leawood 1
Licodia Eubea 1
Madrid 1
Markham 1
Munich 1
Narni 1
Nürnberg 1
Olomouc 1
Phoenix 1
Prague 1
Prato 1
Sacramento 1
Salerno 1
San Francisco 1
Santa Fiora 1
Singapore 1
Statte 1
Surfers Paradise 1
Tappahannock 1
Temecula 1
Tianjin 1
Trento 1
Wandsworth 1
Washington 1
Totale 1.268
Nome #
iPSC-derived neurons profiling reveals GABAergic circuit disruption and acetylated α-tubulin defect which improves after iHDAC6 treatment in Rett syndrome 236
Revealing the complexity of a monogenic disease: rett syndrome exome sequencing 218
Potentially treatable disorder diagnosed post Mortem by exome analysis in a boy with respiratory distress 201
Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene 192
Combined ultrasound and exome sequencing approach recognizes Opitz G/BBB syndrome in two malformed fetuses 188
Exome sequencing analysis in a pair of monozygotic twins re-evaluates the genetics behind their intellectual disability and reveals a CHD2 mutation 180
Exploiting the potential of next-generation sequencing in genomic medicine 166
null 123
The seroprevalence of the hepatitis B virus in Italian medical students after 3 decades since the introduction of universal vaccination 54
MECP2 missense mutations outside the canonical MBD and TRD domains in males with intellectual disability 38
Totale 1.596
Categoria #
all - tutte 4.406
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 4.406


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020357 41 15 22 45 29 24 33 40 47 32 12 17
2020/2021298 10 30 10 31 20 20 13 31 21 79 20 13
2021/2022171 11 16 9 13 7 7 8 4 10 25 24 37
2022/2023206 13 26 29 32 25 34 5 16 14 4 6 2
2023/2024147 9 4 14 17 5 34 46 1 0 3 7 7
Totale 1.596