Catalogo dei prodotti della ricerca

PICECI SPARASCIO, FRANCESCA
 Distribuzione geografica
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Continente #
NA - Nord America 450
EU - Europa 172
AS - Asia 100
AF - Africa 6
SA - Sud America 1
Totale 729
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Nazione #
US - Stati Uniti d'America 435
IT - Italia 104
SG - Singapore 39
IN - India 33
CN - Cina 20
DE - Germania 19
SE - Svezia 14
CA - Canada 13
RO - Romania 6
FI - Finlandia 4
FR - Francia 4
ID - Indonesia 4
UA - Ucraina 4
IE - Irlanda 3
PT - Portogallo 3
RU - Federazione Russa 3
SC - Seychelles 3
CH - Svizzera 2
MX - Messico 2
PK - Pakistan 2
TG - Togo 2
AT - Austria 1
BE - Belgio 1
BG - Bulgaria 1
CL - Cile 1
GB - Regno Unito 1
IL - Israele 1
IR - Iran 1
LT - Lituania 1
NL - Olanda 1
ZA - Sudafrica 1
Totale 729
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Città #
Fairfield 79
Chandler 47
Ashburn 38
Woodbridge 31
Rome 29
Singapore 29
Cambridge 26
Seattle 24
Wilmington 21
Houston 19
San Paolo di Civitate 16
Santa Clara 14
San Diego 13
Princeton 12
Bremen 11
Millbury 11
Ann Arbor 10
Beijing 8
Mumbai 8
Lawrence 7
Ottawa 7
Toronto 6
Norwalk 5
Plano 5
Helsinki 4
Jakarta 4
New York 4
Andover 3
Bologna 3
Boston 3
Council Bluffs 3
Dublin 3
Hebei 3
Bühl 2
Guangzhou 2
Hyderabad 2
Lomé 2
Los Angeles 2
Mahé 2
Mexico City 2
Moscow 2
Naples 2
Porto 2
Reggio Emilia 2
Sannois 2
Bern 1
Braga 1
Bucharest 1
Caserta 1
Chieti 1
Chongqing 1
Dearborn 1
Falkenstein 1
Frankfurt am Main 1
Fucecchio 1
Kunming 1
Laojunmiao 1
Latina 1
London 1
Mannheim 1
Milan 1
Nanjing 1
Nuremberg 1
Oisquercq 1
Silverton 1
Sofia 1
Terracina 1
Torino 1
Vienna 1
Viterbo 1
Totale 555
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Nome #
The global emergency of novel coronavirus (SARS-CoV-2). An update of the current status and forecasting 101
Common atrium/atrioventricular canal defect and postaxial polydactyly: a mild clinical subtype of Ellis-van Creveld syndrome caused by hypomorphic mutations in the EVC gene 79
Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co-inheritance 78
Genome-wide DNA methylation analysis of a cohort of 41 patients affected by oculo-auriculo-vertebral spectrum (OAVS) 74
Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect 71
GLI1 inactivation is associated with developmental phenotypes overlapping with Ellis-van Creveld syndrome 63
Identification of a second HOXA2 nonsense mutation in a family with autosomal dominant non-syndromic microtia and distinctive ear morphology 59
Identification of a Second HOXA2 Nonsense Mutation in a Family with Autosomal Dominant Non-Syndromic Microtia and distinctive ear morphology 53
Germline and mosaic variants in PRKACA and PRKACB cause a multiple congenital malformation syndrome 49
null 38
Clinical variability in DYNC2H1-related skeletal ciliopathies includes Ellis-van Creveld syndrome 30
Weyers acrofacial dysostosis (WAD) 27
null 27
Copy number variation analysis implicates novel pathways in patients with oculo-auriculo-vertebral-spectrum and congenital heart defects 25
Heterozygosity for loss-of-function variants in LZTR1 is associated with isolated multiple café-au-lait macules 6
null 3
Totale 783
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Categoria #
all - tutte 2.463
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 2.463
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202060 0 0 0 0 0 0 13 10 10 8 6 13
2020/2021152 5 6 5 45 2 3 0 7 12 7 13 47
2021/2022202 32 4 8 15 25 14 4 26 13 10 25 26
2022/2023144 25 32 6 25 14 15 3 6 10 3 2 3
2023/202471 3 12 1 9 15 8 4 2 0 7 6 4
2024/202598 8 12 20 10 23 21 4 0 0 0 0 0
Totale 783