Frangella, Silvia
 Distribuzione geografica
Continente #
NA - Nord America 217
EU - Europa 191
AS - Asia 97
Continente sconosciuto - Info sul continente non disponibili 2
AF - Africa 1
OC - Oceania 1
SA - Sud America 1
Totale 510
Nazione #
US - Stati Uniti d'America 215
IT - Italia 63
CN - Cina 56
SE - Svezia 52
SG - Singapore 21
DE - Germania 15
FR - Francia 15
IE - Irlanda 11
NL - Olanda 9
ID - Indonesia 7
BE - Belgio 5
IN - India 5
RU - Federazione Russa 5
GB - Regno Unito 4
PT - Portogallo 4
TR - Turchia 3
CA - Canada 2
FI - Finlandia 2
HK - Hong Kong 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AT - Austria 1
AU - Australia 1
CH - Svizzera 1
CI - Costa d'Avorio 1
CL - Cile 1
CZ - Repubblica Ceca 1
EU - Europa 1
IL - Israele 1
IR - Iran 1
JP - Giappone 1
NO - Norvegia 1
PL - Polonia 1
RO - Romania 1
Totale 510
Città #
Chandler 67
Ashburn 32
Milan 20
Singapore 17
Hangzhou 14
Dublin 11
New York 10
Beijing 8
Jakarta 7
Trieste 7
Marseille 6
Princeton 6
Dearborn 5
Los Angeles 5
Rome 5
Wilmington 5
Funchal 4
Morlupo 4
Naaldwijk 4
Salt Lake City 4
San Diego 4
San Mateo 4
Boston 3
Bremen 3
Brussels 3
Cattolica 3
Changsha 3
Hyderabad 3
Lamézia 3
Redwood City 3
Shenyang 3
Busto Arsizio 2
Central 2
Chengdu 2
Ferrara 2
Helsinki 2
Izmir 2
Moscow 2
Oshkosh 2
Ottawa 2
Redmond 2
Tianjin 2
Waanrode 2
Washington 2
Abidjan 1
Alexandria 1
Andover 1
Ann Arbor 1
Augusta 1
Botzingen 1
Brno 1
Camden 1
Chicago 1
Chongqing 1
Clearwater 1
Dalian 1
Desio 1
Falls Church 1
Frankfurt am Main 1
Fuzhou 1
Guidonia 1
Handan 1
Harbin 1
Houston 1
Huizhou 1
Hunedoara 1
Kemerovo 1
London 1
Melbourne 1
Mumbai 1
Nanjing 1
Norwalk 1
Phoenix 1
Riano 1
San Francisco 1
Seattle 1
Tokyo 1
Vienna 1
Zurich 1
Totale 337
Nome #
Complex Muco-cutaneous Manifestations of CARMIL2-associated Combined Immunodeficiency: A Novel Presentation of Dysfunctional Epithelial Barriers 112
A novel truncating variant within exon 7 of KAT6B associated with features of both Say–Barber–Bieseker–Young–Simpson syndrome and genitopatellar syndrome: Further evidence of a continuum in the clinical spectrum of KAT6B-related disorders 91
Adult phenotype in Koolen-de Vries/KANSL1 haploinsufficiency syndrome 91
Impairment of different protein domains causes variable clinical presentation within Pitt-Hopkins syndrome and suggests intragenic molecular syndromology of TCF4 73
Clinical genetics can solve the pitfalls of genome-wide investigations: Lesson from mismapping a loss-of-function variant in KANSL1 67
Syndromic craniosynostosis can define new candidate genes for suture development or result from the non-specifc effects of pleiotropic genes: Rasopathies and chromatinopathies as examples 48
CHAMP1-related disorders: pathomechanisms triggered by different genomic alterations define distinct nosological categories 43
Totale 525
Categoria #
all - tutte 2.634
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 2.634


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202018 0 0 0 0 0 0 5 1 2 3 7 0
2020/202132 1 1 0 0 0 1 9 0 5 5 9 1
2021/202283 13 0 1 11 1 1 0 9 9 4 15 19
2022/2023185 26 26 14 30 2 22 7 12 11 16 14 5
2023/2024103 3 17 4 8 3 17 9 6 2 3 12 19
2024/202562 2 4 8 8 31 9 0 0 0 0 0 0
Totale 525