DE LUCA, CHIARA
 Distribuzione geografica
Continente #
NA - Nord America 153
EU - Europa 113
AS - Asia 69
Continente sconosciuto - Info sul continente non disponibili 1
Totale 336
Nazione #
US - Stati Uniti d'America 150
SG - Singapore 49
IE - Irlanda 43
IT - Italia 27
DE - Germania 22
CN - Cina 15
GB - Regno Unito 7
FR - Francia 5
BE - Belgio 2
CA - Canada 2
IN - India 2
TR - Turchia 2
UA - Ucraina 2
BZ - Belize 1
CZ - Repubblica Ceca 1
EU - Europa 1
FI - Finlandia 1
KZ - Kazakistan 1
NL - Olanda 1
PL - Polonia 1
PT - Portogallo 1
Totale 336
Città #
Singapore 46
Dublin 40
L’Aquila 22
Boardman 21
Chandler 21
Santa Clara 15
Ashburn 10
New York 10
Jacksonville 8
Munich 6
Lawrence 5
Princeton 5
Beijing 4
Bremen 3
London 3
Pescara 3
Seattle 3
Wilmington 3
Ann Arbor 2
Brussels 2
Cedar Knolls 2
Edinburgh 2
Hamburg 2
Los Angeles 2
Mumbai 2
Nuremberg 2
Pawtucket 2
Philadelphia 2
San Mateo 2
Shanghai 2
Amsterdam 1
Berlin 1
Brno 1
Chicago 1
Guangzhou 1
Itri 1
Izmir 1
Jiaxing 1
Kitzingen 1
Kunming 1
Lisbon 1
Nanjing 1
Oral 1
Potomac 1
Saint-Martin-Bellevue 1
San Francisco 1
Tianjin 1
Toronto 1
Woodbridge 1
Xi'an 1
Totale 272
Nome #
Bilateral internal mammary artery for multi-territory myocardial revascularization: long-term follow-up of pedicled versus skeletonized conduits† 62
RIPK4 regulates cell-cell adhesion in epidermal development and homeostasis 49
Truncating variants in the penultimate exon of TGFBR1 escaping nonsense-mediated mRNA decay cause Loeys-Dietz syndrome 35
A recurrent, de novo pathogenic variant in ARPC4 disrupts actin filament formation and causes microcephaly and speech delay 34
Clinical and Genetic Features in Patients With Reflex Bathing Epilepsy 32
De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway 25
Craniosynostosis is a feature of CHD7-related CHARGE syndrome 24
The spectrum of heart defects in the TRAF7-related multiple congenital anomalies-intellectual disability syndrome 18
APPLICATION OF ADVANCED DNA ANALYSIS TECHNOLOGIES FOR THE IDENTIFICATION OF NEW ETIOPATHOGENETIC MECHANISMS AND MOLECULAR PROFILING IN GENOMIC MEDICINE 15
Expanding the clinical spectrum of Fowler syndrome: Three siblings with survival into adulthood and systematic review of the literature 11
MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia 11
Loss-of-function variants in exon 4 of TAB2 cause a recognizable multisystem disorder with cardiovascular, facial, cutaneous, and musculoskeletal involvement 10
First and second branchial arch involvement in mandibulofacial dysostosis Guion-Almeida type 10
Challenges in molecular diagnosis of X-linked Intellectual disability 9
Agnathia otocephaly: A case from the Katanga Copperbelt 8
Totale 353
Categoria #
all - tutte 2.320
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 2.320


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20206 0 0 0 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
2024/2025153 37 4 35 17 58 2 0 0 0 0 0 0
Totale 353