CRIS Current Research Information System

MARCONI, CATERINA
 Distribuzione geografica
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Continente #
NA - Nord America 1.173
EU - Europa 769
AS - Asia 509
AF - Africa 48
SA - Sud America 6
OC - Oceania 1
Totale 2.506
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Nazione #
US - Stati Uniti d'America 1.165
VN - Vietnam 192
GB - Regno Unito 185
SE - Svezia 151
IT - Italia 146
CN - Cina 142
SG - Singapore 97
DE - Germania 75
RU - Federazione Russa 52
IE - Irlanda 38
IN - India 35
FR - Francia 28
JO - Giordania 22
TG - Togo 22
ZA - Sudafrica 16
EE - Estonia 15
UA - Ucraina 15
FI - Finlandia 12
BG - Bulgaria 10
CH - Svizzera 10
ID - Indonesia 8
CA - Canada 7
NL - Olanda 7
BE - Belgio 6
BR - Brasile 6
CI - Costa d'Avorio 6
AT - Austria 5
HK - Hong Kong 4
PL - Polonia 4
ES - Italia 3
GR - Grecia 3
LB - Libano 3
EG - Egitto 2
NG - Nigeria 2
AE - Emirati Arabi Uniti 1
AU - Australia 1
BT - Bhutan 1
CZ - Repubblica Ceca 1
HR - Croazia 1
IR - Iran 1
MY - Malesia 1
PA - Panama 1
PH - Filippine 1
RO - Romania 1
SK - Slovacchia (Repubblica Slovacca) 1
UZ - Uzbekistan 1
Totale 2.506
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Città #
Southend 160
Fairfield 159
Chandler 110
Dong Ket 100
Ashburn 96
Woodbridge 79
Singapore 74
Wilmington 66
Houston 65
Seattle 62
Cambridge 48
Ann Arbor 42
Princeton 42
Dublin 38
Santa Clara 37
Bologna 32
Boardman 27
Amman 22
Lomé 22
Nanjing 20
Padova 17
Westminster 17
Redmond 16
Florence 15
New York 13
Helsinki 12
Los Angeles 12
Jinan 11
Beijing 10
Milan 9
Saint Petersburg 9
San Diego 9
Berlin 8
Hebei 8
Bern 7
Jakarta 7
Sofia 7
Abidjan 6
Fornovo di Taro 6
Nanchang 6
Turin 6
Boydton 5
Brussels 5
Jacksonville 5
London 5
Shanghai 5
Brescia 4
Edinburgh 4
Hong Kong 4
Moscow 4
Mülheim 4
Sant'Elpidio a Mare 4
São Paulo 4
Warsaw 4
Yubileyny 4
Zhengzhou 4
Amsterdam 3
Changsha 3
Desenzano del Garda 3
Haikou 3
Ningbo 3
Parma 3
Tianjin 3
Abeokuta 2
Bremen 2
Cairo 2
Chicago 2
Dearborn 2
Des Moines 2
Falkenstein 2
Falls Church 2
Gravina in Puglia 2
Guangzhou 2
Hangzhou 2
Harbin 2
Hefei 2
Henstedt-Ulzburg Municipality 2
Kingston 2
Kuban 2
Lanzhou 2
Marzabotto 2
Modena 2
Murcia 2
Paris 2
Perugia 2
Rostock 2
San Venanzo 2
Sasso Marconi 2
Shenyang 2
Suzhou 2
Taizhou 2
Tappahannock 2
Toronto 2
Vienna 2
Wenzhou 2
Andover 1
Aquila 1
Barletta 1
Belo Horizonte 1
Blitar 1
Totale 1.667
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Nome #
5′UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia 216
Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies 182
A novel missense mutation in ANO5/TMEM16E is causative for gnathodiaphyseal dyplasia in a large Italian pedigree. 173
FA2H-related disorders: a novel c.270+3A>T splice-site mutation leads to a complex neurodegenerative phenotype. 150
A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene 140
ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia 138
Clinical and pathogenetic features of ETV6 related thrombocytopenia with predisposition to acute lymphoblastic leukemia 136
Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East 134
SLFN14-related thrombocytopenia: Identification within a large series of patients with inherited thrombocytopenia 124
Mutations of RUNX1 in families with inherited thrombocytopenia 121
Search for genetic factors in bicuspid aortic valve disease: ACTA2 mutations do not play a major role 115
ANKRD26-related thrombocytopenia and myeloid malignancies. 114
Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia 111
Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia. 108
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families. 107
Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2 106
null 102
Synovitis, Acne, Pustulosis, Hyperostosis, Osteitis (SAPHO) syndrome: is PTPN22 involved? 74
Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup 59
Pathogenetic and clinical study of a patient with thrombocytopenia due to the p.E527K gain-of-function variant of SRC 55
Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy 47
Dysregulation of oncogenic factors by GFI1B p32: investigation of a novel GFI1B germline mutation 42
ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization. 32
Totale 2.586
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Categoria #
all - tutte 6.795
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 6.795
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020323 0 0 0 0 0 0 81 72 81 36 29 24
2020/2021333 54 17 12 6 6 6 6 14 29 16 9 158
2021/2022456 90 17 21 26 30 21 10 25 12 29 119 56
2022/2023552 44 80 40 52 36 38 28 39 100 15 60 20
2023/2024158 6 30 15 16 11 26 10 14 9 9 8 4
2024/2025345 16 95 57 39 60 36 42 0 0 0 0 0
Totale 2.586