PANNONE, LUCA
 Distribuzione geografica
Continente #
NA - Nord America 231
EU - Europa 133
AS - Asia 62
OC - Oceania 3
SA - Sud America 3
AF - Africa 2
Totale 434
Nazione #
US - Stati Uniti d'America 228
IT - Italia 78
SG - Singapore 23
IN - India 21
GB - Regno Unito 12
SE - Svezia 12
DE - Germania 5
JP - Giappone 5
CN - Cina 4
IE - Irlanda 4
KR - Corea 4
UA - Ucraina 4
AU - Australia 3
BG - Bulgaria 3
CA - Canada 3
FI - Finlandia 3
BO - Bolivia 2
CH - Svizzera 2
FR - Francia 2
GR - Grecia 2
HK - Hong Kong 2
LT - Lituania 2
NL - Olanda 2
TG - Togo 2
AR - Argentina 1
ES - Italia 1
IQ - Iraq 1
RO - Romania 1
TH - Thailandia 1
VN - Vietnam 1
Totale 434
Città #
Rome 35
Fairfield 24
Ashburn 19
Houston 15
Chandler 14
Leeds 11
Singapore 11
Seattle 10
Woodbridge 10
Bethesda 9
Princeton 9
Mumbai 8
San Paolo di Civitate 8
Wilmington 8
Cambridge 7
Cagliari 6
Wakefield 6
Lawrence 5
Millbury 5
Ann Arbor 4
Boston 4
Dearborn 4
Dublin 4
Jinju 4
New York 4
Beijing 3
Milan 3
Plano 3
Sofia 3
Tokyo 3
Toronto 3
Anacapri 2
Andover 2
Bari 2
Boardman 2
Bordeaux 2
Bremen 2
Geneva 2
Karystos 2
Lomé 2
Los Angeles 2
Norwalk 2
Philadelphia 2
San Diego 2
Santa Cruz 2
Vilnius 2
Viterbo 2
Zurich 2
Augusta 1
Bangkok 1
Biella 1
Buffalo 1
Bühl 1
Central 1
Cesena 1
Chicago 1
Chieti 1
Cori 1
Des Moines 1
Düsseldorf 1
Federal 1
Florence 1
Genzano di Roma 1
Hanoi 1
Jacksonville 1
Jinan 1
Kingston 1
Lappeenranta 1
Melbourne 1
Nuremberg 1
Redwood City 1
Rochester 1
Salamanca 1
Sandston 1
Sydney 1
Utrecht 1
Vigonza 1
Totale 325
Nome #
C. elegans as a model to identify and functionally characterize novel genes causing RASopathies and other developmental diseases 73
Molecular Diversity and Associated Phenotypic Spectrum of Germline CBL Mutations 68
Structural, functional, and clinical characterization of a novel PTPN11 mutation cluster underlying noonan syndrome 58
Functional characterization of novel germline mutations affecting CDC42 highlighted their differential impact on multiple signaling pathways. 44
Gain of function mutations in Malate Dehydrogenase 2 (MDH2) cause familial diabetes of the adulthood 36
Malate Dehydrogenase 2 (MDH2) as a New Diabetogene Causing Hyperglycemia in Families with Multigenerational Diabetes 34
Mutations at the C-terminus of CDC42 cause distinct post-translational modifications and hematopoietic and autoinflammatory disorders 28
null 27
Mutations at the C-terminus of CDC42 cause distinct hematopoietic and autoinflammatory disorders 21
The recurrent pathogenic Pro890Leu substitution in CLTC causes a generalized defect in synaptic transmission in Caenorhabditis elegans 20
C. elegans-based chemosensation strategy for the early detection of cancer metabolites in urine samples 18
De novo mutations involving the C-terminal tail of CDC42 cause distinct dyshematopoietic and autoinflammatory disorders 16
Functional variability of novel CDC42 pathogenic variants is associated with phenotypic heterogeneity of neurodevelopmental and immune-hematologic related disorders 15
Enhanced MAPK1 Function Causes a Neurodevelopmental Disorder within the RASopathy Clinical Spectrum 13
SHP2's gain-of-function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction 10
Totale 481
Categoria #
all - tutte 1.717
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 1.717


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20196 0 0 0 0 0 0 0 0 0 0 0 6
2019/202061 5 1 5 1 4 8 14 5 6 5 1 6
2020/202126 2 5 0 2 1 2 0 4 3 0 2 5
2021/202291 2 2 7 2 7 3 2 8 14 5 15 24
2022/202390 13 16 2 5 6 16 3 11 11 2 2 3
2023/2024172 5 17 12 29 26 26 3 18 4 12 12 8
Totale 481