Catalogo dei prodotti della ricerca

PIZZI, SIMONE
 Distribuzione geografica
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Continente #
NA - Nord America 319
EU - Europa 239
AS - Asia 97
AF - Africa 1
Totale 656
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Nazione #
US - Stati Uniti d'America 317
IT - Italia 158
SG - Singapore 56
CN - Cina 17
SE - Svezia 16
DE - Germania 10
IN - India 10
NL - Olanda 9
FI - Finlandia 8
ID - Indonesia 8
BG - Bulgaria 7
FR - Francia 7
RU - Federazione Russa 5
CZ - Repubblica Ceca 4
IE - Irlanda 4
GB - Regno Unito 3
BE - Belgio 2
CA - Canada 2
IR - Iran 2
TR - Turchia 2
UA - Ucraina 2
DK - Danimarca 1
LT - Lituania 1
MY - Malesia 1
PL - Polonia 1
PT - Portogallo 1
QA - Qatar 1
TG - Togo 1
Totale 656
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Città #
Fairfield 58
Rome 52
Singapore 45
Ashburn 32
Chandler 22
Woodbridge 20
Houston 16
Cambridge 15
Seattle 15
Wilmington 15
Milan 11
Princeton 11
Santa Clara 10
Dearborn 8
Jakarta 8
New York 8
Beijing 7
Boardman 7
Sofia 7
Plano 6
Boston 5
Ann Arbor 4
Dublin 4
Helsinki 4
Romainville 4
Lappeenranta 3
Moscow 3
Munich 3
Naples 3
Prague 3
Bremen 2
Brussels 2
Cormano 2
Florence 2
Istanbul 2
Lawrence 2
Marseille 2
Phoenix 2
San Diego 2
San Paolo di Civitate 2
Siena 2
Toronto 2
Viterbo 2
Absecon 1
Amsterdam 1
Bühl 1
Caserta 1
Chaoyang 1
Ciciliano 1
Delft 1
Des Moines 1
Doha 1
Falkenstein 1
Galdo 1
Genoa 1
Groningen 1
Hamburg 1
Hefei 1
Latina 1
Lomé 1
London 1
Mannheim 1
Marino 1
Millbury 1
Nanchang 1
Nanjing 1
Norwalk 1
Palermo 1
Paris 1
Pavia 1
Perugia 1
Ramacca 1
Redmond 1
Redwood City 1
Roskilde 1
San Mateo 1
Vestec 1
Warsaw 1
Washington 1
Xi'an 1
Totale 472
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Nome #
Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomalies 121
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome 85
Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypes 76
Dominant {ARF}3 variants disrupt Golgi integrity and cause a neurodevelopmental disorder recapitulated in zebrafish 59
null 50
Genome-Wide DNA Methylation Profiling Solves Uncertainty in Classifying NSD1 Variants 44
null 40
Reversing vemurafenib-resistance in primary melanoma cells by combined romidepsin and type I IFN treatment through blocking of tumorigenic signals and induction of immunogenic effects 36
Identification of a robust DNA methylation signature for Fanconi anemia 34
Posterior fossa ependymoma in neurodevelopmental syndrome caused by a de novo germline pathogenic Polr2a variant 31
Expanding the molecular spectrum of pathogenic SHOC2 variants underlying Mazzanti syndrome 30
Evaluating cell culture reliability in pediatric brain tumor primary cells through DNA methylation profiling 20
null 18
Virtual screening for the development of dual-inhibitors targeting topoisomerase IB and tyrosyl-DNA phosphodiesterase 1 17
Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A 12
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis 12
Biallelic variants of MRPS36 cause a new form of Leigh syndrome 11
Clinical spectrum of Kabuki-like syndrome caused by HNRNPK haploinsufficiency 11
Upfront treatment with mTOR inhibitor everolimus in pediatric low-grade gliomas: A single-center experience 9
Totale 716
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Categoria #
all - tutte 2.766
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 2.766
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202058 0 0 0 0 0 0 16 13 13 7 6 3
2020/202135 4 4 1 0 3 2 1 1 5 8 4 2
2021/202261 2 2 9 2 6 2 0 6 7 4 2 19
2022/2023124 15 16 9 7 10 19 5 14 13 5 11 0
2023/2024144 9 5 7 11 10 27 12 11 5 16 17 14
2024/2025145 6 21 17 28 35 36 2 0 0 0 0 0
Totale 716