IRIS
CASELLI, ROSSELLA
 Distribuzione geografica
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Continente #
NA - Nord America 764
EU - Europa 461
AS - Asia 76
OC - Oceania 2
SA - Sud America 1
Totale 1.304
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Nazione #
US - Stati Uniti d'America 762
GB - Regno Unito 118
IE - Irlanda 113
CN - Cina 61
SE - Svezia 58
UA - Ucraina 44
IT - Italia 32
FR - Francia 27
DE - Germania 20
FI - Finlandia 18
BE - Belgio 11
TR - Turchia 7
ES - Italia 6
SG - Singapore 6
NL - Olanda 5
CZ - Repubblica Ceca 4
RU - Federazione Russa 3
AU - Australia 2
CA - Canada 2
IN - India 2
AL - Albania 1
BR - Brasile 1
RO - Romania 1
Totale 1.304
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Città #
Dublin 112
Fairfield 107
Southend 104
Ann Arbor 72
Chandler 72
Ashburn 68
Woodbridge 66
Seattle 55
Houston 52
Wilmington 50
Cambridge 39
Jacksonville 38
Beijing 19
New York 18
Princeton 18
Siena 18
Helsinki 11
Nanjing 11
Boardman 9
Brussels 7
Tianjin 7
Izmir 6
Nanchang 6
Shanghai 6
Menlo Park 5
Málaga 5
Brno 4
San Diego 4
Waanrode 4
Dearborn 3
Moscow 3
San Mateo 3
Shenyang 3
Trieste 3
Hebei 2
Mestre 2
Milan 2
Nagpur 2
Norwalk 2
Toronto 2
Canberra 1
Changchun 1
Changsha 1
Chiswick 1
Falkenstein 1
Groningen 1
Guangzhou 1
Jiaxing 1
Jinan 1
Kilburn 1
Kocaeli 1
Kunming 1
Lanzhou 1
Leawood 1
Los Angeles 1
Melbourne 1
Palermo 1
Philadelphia 1
Phoenix 1
San Francisco 1
Singapore 1
Southwark 1
Trento 1
Villa Guardia 1
Washington 1
Totale 1.045
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Nome #
Low-level TP53 mutational load antecedes clonal expansion in chronic lymphocytic leukaemia 193
Germline mosaicism in Rett syndrome identified by prenatal diagnosis 168
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome 165
A 2.6 Mb deletion of 6q24.3-25.1 in a patient with growth failure, cardiac septal defect, thin upperlip and asymmetric dysmorphic ears 163
Private inherited microdeletion/microduplications: implications in clinical practice 160
A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett-like features 147
2q24-q31 deletion: report of a case and review of the literature 140
Expanding the phenotype of 22q11 deletion syndrome: the MURCS association 138
Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array-based detection rate 56
Totale 1.330
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Categoria #
all - tutte 4.101
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 4.101
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020286 38 10 16 39 23 26 31 33 22 24 8 16
2020/2021229 6 42 23 21 11 24 2 34 10 25 20 11
2021/2022137 8 25 4 13 0 3 10 10 2 12 11 39
2022/2023205 11 32 23 31 19 39 3 11 16 10 7 3
2023/2024182 3 4 28 16 1 51 64 3 0 1 0 11
2024/20255 5 0 0 0 0 0 0 0 0 0 0 0
Totale 1.330