SEVERI, GIULIA
 Distribuzione geografica
Continente #
NA - Nord America 360
EU - Europa 271
AS - Asia 158
AF - Africa 16
SA - Sud America 2
Totale 807
Nazione #
US - Stati Uniti d'America 359
IT - Italia 101
CN - Cina 74
SE - Svezia 39
GB - Regno Unito 38
SG - Singapore 32
DE - Germania 30
VN - Vietnam 28
IE - Irlanda 14
IN - India 11
FI - Finlandia 9
RU - Federazione Russa 8
FR - Francia 7
CH - Svizzera 6
CI - Costa d'Avorio 5
NG - Nigeria 5
BG - Bulgaria 4
ID - Indonesia 4
BE - Belgio 3
HK - Hong Kong 3
JO - Giordania 3
TG - Togo 3
ZA - Sudafrica 3
CL - Cile 2
EE - Estonia 2
HR - Croazia 2
NL - Olanda 2
PL - Polonia 2
UA - Ucraina 2
AT - Austria 1
CA - Canada 1
CZ - Repubblica Ceca 1
IR - Iran 1
PH - Filippine 1
SA - Arabia Saudita 1
Totale 807
Città #
Chandler 50
Fairfield 34
Singapore 31
Ashburn 30
Southend 27
Bologna 24
Santa Clara 20
Woodbridge 19
Ann Arbor 14
Dublin 14
Wilmington 14
Seattle 13
Princeton 12
Redmond 11
Boardman 10
Houston 9
Cambridge 8
Helsinki 8
Jinan 8
Turin 8
Florence 7
Milan 6
Abeokuta 5
Abidjan 5
Bern 4
Brescia 4
Guangzhou 4
Jakarta 4
Nanchang 4
Nanjing 4
New York 4
Sofia 4
Amman 3
Berlin 3
Desenzano del Garda 3
Haikou 3
Hangzhou 3
Hong Kong 3
Lomé 3
London 3
Los Angeles 3
Mountain View 3
Rome 3
San Diego 3
Westminster 3
Zhengzhou 3
Amsterdam 2
Bastogne 2
Beijing 2
Changsha 2
Des Moines 2
Fort Worth 2
Frankfurt Am Main 2
Jiaxing 2
Kingston upon Thames 2
Köln 2
Motta Sant'Anastasia 2
Nuremberg 2
Saint Petersburg 2
Sassari 2
Sasso Marconi 2
Shijiazhuang 2
Sorrento 2
Taizhou 2
Tianjin 2
Vicenza 2
Warsaw 2
Ardabil 1
Bremen 1
Brno 1
Brussels 1
Changchun 1
Chengdu 1
Comacchio 1
Como 1
Core 1
Davao City 1
Falls Church 1
Ferrara 1
Forlì 1
Foshan 1
Frankfurt am Main 1
Hebei 1
Hyderabad 1
Imola 1
Kunming 1
Lappeenranta 1
Lausanne 1
Loreto Aprutino 1
Miami 1
Morges 1
Novosibirsk 1
Padova 1
Palermo 1
Paris 1
Parma 1
Peymeinade 1
Phoenix 1
Pinerolo 1
Prescot 1
Totale 536
Nome #
A de novo PUF60 mutation in a child with a syndromic form of coloboma and persistent fetal vasculature 151
Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East 133
A new homozygous CACNB2 mutation has functional relevance and supports a role for calcium channels in autism spectrum disorder. 126
New patients with Temple syndrome caused by 14q32 deletion: Genotype-phenotype correlations and risk of thyroid cancer 117
HDAC8 Loss of Function and SHOX Haploinsufficiency: Two Independent Genetic Defects Responsible for a Complex Phenotype 116
Whole-exome sequencing in adult patients with developmental and epileptic encephalopathy: It is never too late 79
HDAC9 structural variants disrupting TWIST1 transcriptional regulation lead to craniofacial and limb malformations 50
Mutant SPART causes defects in mitochondrial protein import and bioenergetics reversed by Coenzyme Q 39
Clinical interpretation of aCGH results in patients with neurodevelopmental disorders by geneticists: impact on diagnostic yield 17
Familial DMRT1-related non-obstructive azoospermia: a case report 15
Totale 843
Categoria #
all - tutte 2.654
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 2.654


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202075 0 0 0 0 0 0 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
2024/2025151 10 22 39 29 31 19 1 0 0 0 0 0
Totale 843