SEVERI, GIULIA
 Distribuzione geografica
Continente #
NA - Nord America 328
EU - Europa 254
AS - Asia 114
AF - Africa 16
SA - Sud America 2
Totale 714
Nazione #
US - Stati Uniti d'America 328
IT - Italia 95
CN - Cina 46
SE - Svezia 39
GB - Regno Unito 36
DE - Germania 28
VN - Vietnam 28
SG - Singapore 21
IE - Irlanda 14
IN - India 11
FR - Francia 7
CH - Svizzera 6
CI - Costa d'Avorio 5
FI - Finlandia 5
NG - Nigeria 5
RU - Federazione Russa 5
BG - Bulgaria 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 714
Città #
Chandler 50
Fairfield 34
Ashburn 30
Southend 27
Bologna 24
Singapore 20
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 5
Bern 4
Brescia 4
Helsinki 4
Nanjing 4
New York 4
Sofia 4
Amman 3
Berlin 3
Desenzano del Garda 3
Haikou 3
Hangzhou 3
Lomé 3
Los Angeles 3
Mountain View 3
Nanchang 3
San Diego 3
Santa Clara 3
Westminster 3
Zhengzhou 3
Amsterdam 2
Bastogne 2
Beijing 2
Des Moines 2
Fort Worth 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
Shijiazhuang 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
Foshan 1
Frankfurt am Main 1
Guangzhou 1
Hebei 1
Hyderabad 1
Imola 1
Lappeenranta 1
Lausanne 1
Loreto Aprutino 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
Shenzhen 1
Silver Spring 1
Silverton 1
Taizhou 1
Tianjin 1
Toulouse 1
Trana 1
Totale 480
Nome #
A de novo PUF60 mutation in a child with a syndromic form of coloboma and persistent fetal vasculature 138
Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East 124
A new homozygous CACNB2 mutation has functional relevance and supports a role for calcium channels in autism spectrum disorder. 119
New patients with Temple syndrome caused by 14q32 deletion: Genotype-phenotype correlations and risk of thyroid cancer 112
HDAC8 Loss of Function and SHOX Haploinsufficiency: Two Independent Genetic Defects Responsible for a Complex Phenotype 109
Whole-exome sequencing in adult patients with developmental and epileptic encephalopathy: It is never too late 73
HDAC9 structural variants disrupting TWIST1 transcriptional regulation lead to craniofacial and limb malformations 35
Mutant SPART causes defects in mitochondrial protein import and bioenergetics reversed by Coenzyme Q 27
Clinical interpretation of aCGH results in patients with neurodevelopmental disorders by geneticists: impact on diagnostic yield 9
Familial DMRT1-related non-obstructive azoospermia: a case report 3
Totale 749
Categoria #
all - tutte 2.303
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 2.303


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202098 0 0 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
2024/202557 10 22 25 0 0 0 0 0 0 0 0 0
Totale 749