DE LUCA, CHIARA
 Distribuzione geografica
Continente #
NA - Nord America 110
EU - Europa 84
AS - Asia 12
Continente sconosciuto - Info sul continente non disponibili 1
Totale 207
Nazione #
US - Stati Uniti d'America 109
IE - Irlanda 43
DE - Germania 14
IT - Italia 14
CN - Cina 9
GB - Regno Unito 4
FR - Francia 3
TR - Turchia 2
UA - Ucraina 2
CA - Canada 1
CZ - Repubblica Ceca 1
EU - Europa 1
FI - Finlandia 1
KZ - Kazakistan 1
NL - Olanda 1
PT - Portogallo 1
Totale 207
Città #
Dublin 40
Chandler 21
L’Aquila 13
Ashburn 10
New York 10
Jacksonville 8
Boardman 6
Lawrence 5
Princeton 5
Bremen 3
Seattle 3
Wilmington 3
Ann Arbor 2
Cedar Knolls 2
Edinburgh 2
Nuremberg 2
Pawtucket 2
Philadelphia 2
San Mateo 2
Amsterdam 1
Beijing 1
Berlin 1
Brno 1
Chicago 1
Guangzhou 1
Hamburg 1
Itri 1
Izmir 1
Jiaxing 1
Kitzingen 1
Kunming 1
Lisbon 1
Los Angeles 1
Nanjing 1
Oral 1
San Francisco 1
Shanghai 1
Tianjin 1
Woodbridge 1
Totale 161
Nome #
Bilateral internal mammary artery for multi-territory myocardial revascularization: long-term follow-up of pedicled versus skeletonized conduits† 56
RIPK4 regulates cell-cell adhesion in epidermal development and homeostasis 40
A recurrent, de novo pathogenic variant in ARPC4 disrupts actin filament formation and causes microcephaly and speech delay 25
Truncating variants in the penultimate exon of TGFBR1 escaping nonsense-mediated mRNA decay cause Loeys-Dietz syndrome 23
Clinical and Genetic Features in Patients With Reflex Bathing Epilepsy 20
Craniosynostosis is a feature of CHD7-related CHARGE syndrome 18
De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway 14
The spectrum of heart defects in the TRAF7-related multiple congenital anomalies-intellectual disability syndrome 6
Loss-of-function variants in exon 4 of TAB2 cause a recognizable multisystem disorder with cardiovascular, facial, cutaneous, and musculoskeletal involvement 4
MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia 4
First and second branchial arch involvement in mandibulofacial dysostosis Guion-Almeida type 4
Agnathia otocephaly: A case from the Katanga Copperbelt 3
Expanding the clinical spectrum of Fowler syndrome: Three siblings with survival into adulthood and systematic review of the literature 3
Challenges in molecular diagnosis of X-linked Intellectual disability 3
Totale 223
Categoria #
all - tutte 1.349
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 1.349


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20209 2 0 1 0 0 1 1 0 2 0 1 1
2020/20217 0 1 0 1 1 0 1 0 1 0 2 0
2021/202217 0 1 0 0 0 0 0 4 5 0 1 6
2022/2023100 5 4 2 7 5 8 1 10 45 3 5 5
2023/202451 12 1 2 4 6 13 1 3 1 1 1 6
2024/202523 23 0 0 0 0 0 0 0 0 0 0 0
Totale 223