SEVERI, GIULIA
 Distribuzione geografica
Continente #
NA - Nord America 312
EU - Europa 245
AS - Asia 84
AF - Africa 15
SA - Sud America 2
Totale 658
Nazione #
US - Stati Uniti d'America 312
IT - Italia 88
SE - Svezia 39
CN - Cina 38
GB - Regno Unito 36
VN - Vietnam 28
DE - Germania 26
IE - Irlanda 14
IN - India 10
FR - Francia 7
CH - Svizzera 6
FI - Finlandia 5
NG - Nigeria 5
RU - Federazione Russa 5
BG - Bulgaria 4
CI - Costa d'Avorio 4
BE - Belgio 3
JO - Giordania 3
TG - Togo 3
ZA - Sudafrica 3
CL - Cile 2
EE - Estonia 2
HK - Hong Kong 2
HR - Croazia 2
NL - Olanda 2
PL - Polonia 2
UA - Ucraina 2
AT - Austria 1
CZ - Repubblica Ceca 1
IR - Iran 1
PH - Filippine 1
SA - Arabia Saudita 1
Totale 658
Città #
Chandler 50
Fairfield 34
Southend 27
Ashburn 26
Bologna 21
Woodbridge 19
Ann Arbor 14
Dublin 14
Wilmington 14
Seattle 13
Princeton 12
Redmond 11
Houston 9
Cambridge 8
Jinan 8
Turin 8
Florence 7
Milan 6
Abeokuta 5
Abidjan 4
Bern 4
Brescia 4
Helsinki 4
Nanjing 4
New York 4
Sofia 4
Amman 3
Haikou 3
Hangzhou 3
Lomé 3
Mountain View 3
Nanchang 3
San Diego 3
Westminster 3
Zhengzhou 3
Amsterdam 2
Bastogne 2
Beijing 2
Berlin 2
Des Moines 2
Frankfurt Am Main 2
Hong Kong 2
Jiaxing 2
Kingston upon Thames 2
Köln 2
London 2
Motta Sant'Anastasia 2
Saint Petersburg 2
Sassari 2
Sasso Marconi 2
Sorrento 2
Vicenza 2
Warsaw 2
Ardabil 1
Boardman 1
Bremen 1
Brno 1
Brussels 1
Changsha 1
Comacchio 1
Como 1
Core 1
Davao City 1
Falls Church 1
Ferrara 1
Forlì 1
Guangzhou 1
Hebei 1
Imola 1
Lappeenranta 1
Lausanne 1
Loreto Aprutino 1
Los Angeles 1
Morges 1
Padova 1
Palermo 1
Paris 1
Parma 1
Peymeinade 1
Pinerolo 1
Prescot 1
Pune 1
Redwood City 1
Savignano sul Rubicone 1
Shenyang 1
Shijiazhuang 1
Silver Spring 1
Silverton 1
Taizhou 1
Tianjin 1
Toulouse 1
Trana 1
Vienna 1
Washington 1
Windesheim 1
Totale 439
Nome #
A de novo PUF60 mutation in a child with a syndromic form of coloboma and persistent fetal vasculature 130
Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East 117
A new homozygous CACNB2 mutation has functional relevance and supports a role for calcium channels in autism spectrum disorder. 115
New patients with Temple syndrome caused by 14q32 deletion: Genotype-phenotype correlations and risk of thyroid cancer 109
HDAC8 Loss of Function and SHOX Haploinsufficiency: Two Independent Genetic Defects Responsible for a Complex Phenotype 106
Whole-exome sequencing in adult patients with developmental and epileptic encephalopathy: It is never too late 69
HDAC9 structural variants disrupting TWIST1 transcriptional regulation lead to craniofacial and limb malformations 28
Mutant SPART causes defects in mitochondrial protein import and bioenergetics reversed by Coenzyme Q 13
Clinical interpretation of aCGH results in patients with neurodevelopmental disorders by geneticists: impact on diagnostic yield 5
Totale 692
Categoria #
all - tutte 2.079
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 2.079


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020109 9 2 4 5 8 6 17 12 12 28 3 3
2020/2021120 10 6 2 6 17 0 2 17 8 9 6 37
2021/2022138 4 6 6 12 14 4 2 12 4 11 50 13
2022/2023199 15 16 9 19 20 15 3 16 44 11 18 13
2023/202497 10 15 12 3 6 21 8 4 5 2 4 7
Totale 692