IRIS
DE LUCA, CHIARA
 Distribuzione geografica
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Continente #
NA - Nord America 168
EU - Europa 114
AS - Asia 75
Continente sconosciuto - Info sul continente non disponibili 1
Totale 358
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Nazione #
US - Stati Uniti d'America 165
SG - Singapore 49
IE - Irlanda 43
IT - Italia 28
DE - Germania 22
CN - Cina 20
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
JP - Giappone 1
KZ - Kazakistan 1
NL - Olanda 1
PL - Polonia 1
PT - Portogallo 1
Totale 358
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Città #
Singapore 46
Dublin 40
Santa Clara 30
L’Aquila 22
Boardman 21
Chandler 21
Ashburn 10
New York 10
Jacksonville 8
Munich 6
Lawrence 5
Princeton 5
Beijing 4
Pescara 4
Bremen 3
London 3
Seattle 3
Shanghai 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
Amsterdam 1
Berlin 1
Brno 1
Chengdu 1
Chicago 1
Dongguan 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 291
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Nome #
Bilateral internal mammary artery for multi-territory myocardial revascularization: long-term follow-up of pedicled versus skeletonized conduits† 63
RIPK4 regulates cell-cell adhesion in epidermal development and homeostasis 50
Truncating variants in the penultimate exon of TGFBR1 escaping nonsense-mediated mRNA decay cause Loeys-Dietz syndrome 38
Clinical and Genetic Features in Patients With Reflex Bathing Epilepsy 36
A recurrent, de novo pathogenic variant in ARPC4 disrupts actin filament formation and causes microcephaly and speech delay 35
De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway 27
Craniosynostosis is a feature of CHD7-related CHARGE syndrome 25
The spectrum of heart defects in the TRAF7-related multiple congenital anomalies-intellectual disability syndrome 19
APPLICATION OF ADVANCED DNA ANALYSIS TECHNOLOGIES FOR THE IDENTIFICATION OF NEW ETIOPATHOGENETIC MECHANISMS AND MOLECULAR PROFILING IN GENOMIC MEDICINE 17
Expanding the clinical spectrum of Fowler syndrome: Three siblings with survival into adulthood and systematic review of the literature 12
MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia 12
Loss-of-function variants in exon 4 of TAB2 cause a recognizable multisystem disorder with cardiovascular, facial, cutaneous, and musculoskeletal involvement 11
First and second branchial arch involvement in mandibulofacial dysostosis Guion-Almeida type 11
Challenges in molecular diagnosis of X-linked Intellectual disability 10
Agnathia otocephaly: A case from the Katanga Copperbelt 9
Totale 375
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Categoria #
all - tutte 2.452
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 2.452
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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
2024/2025175 37 4 35 17 58 24 0 0 0 0 0 0
Totale 375