MARCONI, CATERINA
 Distribuzione geografica
Continente #
NA - Nord America 964
EU - Europa 593
AS - Asia 333
AF - Africa 46
SA - Sud America 3
OC - Oceania 1
Totale 1940
Nazione #
US - Stati Uniti d'America 961
VN - Vietnam 192
GB - Regno Unito 176
SE - Svezia 149
CN - Cina 77
IT - Italia 63
DE - Germania 53
IE - Irlanda 43
IN - India 34
RU - Federazione Russa 30
FR - Francia 27
JO - Giordania 22
TG - Togo 22
ZA - Sudafrica 16
EE - Estonia 15
UA - Ucraina 15
BE - Belgio 6
CI - Costa d'Avorio 4
BR - Brasile 3
CH - Svizzera 3
GR - Grecia 3
LB - Libano 3
NL - Olanda 3
CA - Canada 2
EG - Egitto 2
FI - Finlandia 2
NG - Nigeria 2
AE - Emirati Arabi Uniti 1
AU - Australia 1
BG - Bulgaria 1
ES - Italia 1
HR - Croazia 1
ID - Indonesia 1
IR - Iran 1
MY - Malesia 1
PA - Panama 1
RO - Romania 1
SK - Slovacchia (Repubblica Slovacca) 1
UZ - Uzbekistan 1
Totale 1940
Città #
Southend 160
Fairfield 159
Chandler 110
Dong Ket 100
Woodbridge 79
Ashburn 75
Wilmington 66
Houston 65
Seattle 60
Cambridge 48
Dublin 43
Ann Arbor 42
Princeton 42
Amman 22
Lomé 22
Bologna 20
Nanjing 20
Westminster 17
Redmond 16
Padova 14
Jinan 10
Beijing 9
Saint Petersburg 9
San Diego 9
Berlin 8
Hebei 8
Boydton 7
Brussels 6
Nanchang 6
Boardman 5
Jacksonville 5
Abidjan 4
Milan 4
Haikou 3
New York 3
São Paulo 3
Abeokuta 2
Amsterdam 2
Bremen 2
Cairo 2
Changsha 2
Dearborn 2
Des Moines 2
Falls Church 2
Helsinki 2
Kuban 2
London 2
Marzabotto 2
Moscow 2
Ningbo 2
Paris 2
San Venanzo 2
Shenyang 2
Taizhou 2
Tappahannock 2
Tianjin 2
Zhengzhou 2
Andover 1
Aquila 1
Barletta 1
Blitar 1
Boston 1
Bratislava 1
Castel Volturno 1
Chicago 1
Dubai 1
Geneva 1
Groningen 1
Guangzhou 1
Hangzhou 1
Hefei 1
Jiaxing 1
Kiev 1
Kuala Lumpur 1
Lanzhou 1
Lausanne 1
Lviv 1
Madrid 1
Marburg 1
Medford 1
Morges 1
Muizenberg 1
Nuremberg 1
Odesa 1
Olalla 1
Orange 1
Panama City 1
Pisa 1
Plauen 1
Racconigi 1
Redwood City 1
Silverton 1
Sydney 1
Taiyuan 1
Toronto 1
Totale 1359
Nome #
5′UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia 152
A novel missense mutation in ANO5/TMEM16E is causative for gnathodiaphyseal dyplasia in a large Italian pedigree. 149
Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies 144
ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia 122
A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene 114
FA2H-related disorders: a novel c.270+3A>T splice-site mutation leads to a complex neurodegenerative phenotype. 111
Clinical and pathogenetic features of ETV6 related thrombocytopenia with predisposition to acute lymphoblastic leukemia 111
ANKRD26-related thrombocytopenia and myeloid malignancies. 104
Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia. 102
null 102
Mutations of RUNX1 in families with inherited thrombocytopenia 99
Search for genetic factors in bicuspid aortic valve disease: ACTA2 mutations do not play a major role 96
Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East 96
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families. 91
SLFN14-related thrombocytopenia: Identification within a large series of patients with inherited thrombocytopenia 90
Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2 88
Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia 87
Synovitis, Acne, Pustulosis, Hyperostosis, Osteitis (SAPHO) syndrome: is PTPN22 involved? 55
Pathogenetic and clinical study of a patient with thrombocytopenia due to the p.E527K gain-of-function variant of SRC 39
ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization. 21
Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy 16
Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup 16
Dysregulation of oncogenic factors by GFI1B p32: investigation of a novel GFI1B germline mutation 5
Totale 2010
Categoria #
all - tutte 2979
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 2979


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/201827 0000 00 00 00270
2018/2019108 01503 211 310 10171522
2019/2020585 7716437 6860 8172 81362924
2020/2021333 5417126 66 614 29169158
2021/2022456 90172126 3021 1025 122911956
2022/2023479 44804052 3638 2940 120000
Totale 2010