PANNONE, LUCA
 Distribuzione geografica
Continente #
NA - Nord America 236
EU - Europa 147
AS - Asia 81
OC - Oceania 3
SA - Sud America 3
AF - Africa 2
Totale 472
Nazione #
US - Stati Uniti d'America 233
IT - Italia 80
SG - Singapore 30
IN - India 22
GB - Regno Unito 16
CN - Cina 12
SE - Svezia 12
DE - Germania 6
JP - Giappone 5
KR - Corea 5
GR - Grecia 4
IE - Irlanda 4
NO - Norvegia 4
UA - Ucraina 4
AU - Australia 3
BG - Bulgaria 3
CA - Canada 3
FI - Finlandia 3
TH - Thailandia 3
BO - Bolivia 2
CH - Svizzera 2
FR - Francia 2
HK - Hong Kong 2
LT - Lituania 2
NL - Olanda 2
TG - Togo 2
AR - Argentina 1
CZ - Repubblica Ceca 1
ES - Italia 1
IQ - Iraq 1
RO - Romania 1
VN - Vietnam 1
Totale 472
Città #
Rome 36
Fairfield 24
Ashburn 19
Houston 15
Singapore 15
Chandler 14
Leeds 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
Guangzhou 4
Jinju 4
New York 4
Oslo 4
Bangkok 3
Beijing 3
Milan 3
Plano 3
Sofia 3
Tokyo 3
Toronto 3
Anacapri 2
Andover 2
Bari 2
Boardman 2
Bordeaux 2
Bremen 2
Chongqing 2
Ealing 2
Geneva 2
Karystos 2
Lomé 2
Los Angeles 2
Norwalk 2
Oxford 2
Philadelphia 2
San Diego 2
Santa Cruz 2
St Louis 2
Vilnius 2
Viterbo 2
Zurich 2
Augusta 1
Biella 1
Brno 1
Buffalo 1
Bühl 1
Central 1
Cesena 1
Chicago 1
Chieti 1
Cori 1
Des Moines 1
Düsseldorf 1
Federal 1
Florence 1
Freiburg im Breisgau 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
Santa Clara 1
Sydney 1
Utrecht 1
Vigonza 1
Totale 351
Nome #
C. elegans as a model to identify and functionally characterize novel genes causing RASopathies and other developmental diseases 80
Molecular Diversity and Associated Phenotypic Spectrum of Germline CBL Mutations 69
Structural, functional, and clinical characterization of a novel PTPN11 mutation cluster underlying noonan syndrome 58
Gain of function mutations in Malate Dehydrogenase 2 (MDH2) cause familial diabetes of the adulthood 51
Functional characterization of novel germline mutations affecting CDC42 highlighted their differential impact on multiple signaling pathways. 45
Malate Dehydrogenase 2 (MDH2) as a New Diabetogene Causing Hyperglycemia in Families with Multigenerational Diabetes 37
Mutations at the C-terminus of CDC42 cause distinct post-translational modifications and hematopoietic and autoinflammatory disorders 28
null 27
The recurrent pathogenic Pro890Leu substitution in CLTC causes a generalized defect in synaptic transmission in Caenorhabditis elegans 23
Mutations at the C-terminus of CDC42 cause distinct hematopoietic and autoinflammatory disorders 21
C. elegans-based chemosensation strategy for the early detection of cancer metabolites in urine samples 19
Functional variability of novel CDC42 pathogenic variants is associated with phenotypic heterogeneity of neurodevelopmental and immune-hematologic related disorders 18
De novo mutations involving the C-terminal tail of CDC42 cause distinct dyshematopoietic and autoinflammatory disorders 17
Enhanced MAPK1 Function Causes a Neurodevelopmental Disorder within the RASopathy Clinical Spectrum 14
SHP2's gain-of-function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction 12
Totale 519
Categoria #
all - tutte 1.944
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 1.944


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202055 0 0 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
2023/2024185 5 17 12 29 26 26 3 18 4 12 12 21
2024/202525 10 15 0 0 0 0 0 0 0 0 0 0
Totale 519