Catalogo dei prodotti della ricerca

PIZZI, SIMONE
 Distribuzione geografica
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Continente #
NA - Nord America 289
EU - Europa 173
AS - Asia 40
AF - Africa 1
Totale 503
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Nazione #
US - Stati Uniti d'America 288
IT - Italia 120
SE - Svezia 16
SG - Singapore 16
CN - Cina 11
IN - India 10
BG - Bulgaria 7
FR - Francia 6
DE - Germania 5
CZ - Repubblica Ceca 4
FI - Finlandia 3
IE - Irlanda 3
NL - Olanda 3
IR - Iran 2
UA - Ucraina 2
BE - Belgio 1
CA - Canada 1
DK - Danimarca 1
GB - Regno Unito 1
PT - Portogallo 1
QA - Qatar 1
TG - Togo 1
Totale 503
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Città #
Fairfield 58
Rome 41
Ashburn 29
Chandler 22
Woodbridge 20
Houston 16
Cambridge 15
Wilmington 15
Seattle 14
Princeton 11
Singapore 9
Dearborn 8
Milan 8
New York 8
Sofia 7
Beijing 6
Plano 6
Boston 5
Ann Arbor 4
Romainville 4
Dublin 3
Prague 3
Boardman 2
Bremen 2
Florence 2
Lawrence 2
Marseille 2
Phoenix 2
San Diego 2
San Paolo di Civitate 2
Siena 2
Viterbo 2
Absecon 1
Brussels 1
Bühl 1
Chaoyang 1
Ciciliano 1
Delft 1
Des Moines 1
Doha 1
Galdo 1
Genoa 1
Groningen 1
Hamburg 1
Hefei 1
Helsinki 1
Lappeenranta 1
Latina 1
Lomé 1
Millbury 1
Nanchang 1
Nanjing 1
Naples 1
Norwalk 1
Palermo 1
Pavia 1
Perugia 1
Ramacca 1
Redmond 1
Redwood City 1
Roskilde 1
San Mateo 1
Toronto 1
Vestec 1
Washington 1
Totale 365
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Nome #
Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomalies 114
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome 81
Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypes 71
null 50
Dominant {ARF}3 variants disrupt Golgi integrity and cause a neurodevelopmental disorder recapitulated in zebrafish 40
null 40
Genome-Wide DNA Methylation Profiling Solves Uncertainty in Classifying NSD1 Variants 29
Posterior fossa ependymoma in neurodevelopmental syndrome caused by a de novo germline pathogenic Polr2a variant 26
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 19
null 18
Identification of a robust DNA methylation signature for Fanconi anemia 17
Expanding the molecular spectrum of pathogenic SHOC2 variants underlying Mazzanti syndrome 17
Virtual screening for the development of dual-inhibitors targeting topoisomerase IB and tyrosyl-DNA phosphodiesterase 1 13
Clinical spectrum of Kabuki-like syndrome caused by HNRNPK haploinsufficiency 9
Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A 7
Evaluating cell culture reliability in pediatric brain tumor primary cells through DNA methylation profiling 4
Upfront treatment with mTOR inhibitor everolimus in pediatric low-grade gliomas: A single-center experience 2
Totale 557
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Categoria #
all - tutte 1.726
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 1.726
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201914 0 0 0 0 0 0 0 0 0 0 0 14
2019/2020109 12 2 0 4 14 19 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
2023/2024130 9 5 7 11 10 27 12 11 5 16 17 0
Totale 557