PRAMPARO, TIZIANO
 Distribuzione geografica
Continente #
NA - Nord America 610
EU - Europa 557
AS - Asia 293
SA - Sud America 8
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 1.472
Nazione #
US - Stati Uniti d'America 600
CN - Cina 232
IE - Irlanda 142
UA - Ucraina 84
RU - Federazione Russa 76
DE - Germania 66
FI - Finlandia 57
SG - Singapore 42
GB - Regno Unito 40
SE - Svezia 36
IT - Italia 18
BE - Belgio 17
CA - Canada 9
FR - Francia 9
BR - Brasile 8
HK - Hong Kong 6
JP - Giappone 6
AT - Austria 4
LT - Lituania 3
AU - Australia 2
TR - Turchia 2
AZ - Azerbaigian 1
BD - Bangladesh 1
CH - Svizzera 1
EU - Europa 1
IN - India 1
KZ - Kazakistan 1
MK - Macedonia 1
MX - Messico 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PL - Polonia 1
PT - Portogallo 1
UZ - Uzbekistan 1
Totale 1.472
Città #
Dublin 140
Chandler 128
Jacksonville 90
Nanjing 59
Ann Arbor 55
Beijing 47
Boardman 42
Nanchang 26
Helsinki 23
Ashburn 20
Princeton 19
Lawrence 18
Brussels 17
Shenyang 17
Singapore 16
Hebei 14
Changsha 13
Wilmington 13
Jiaxing 12
Woodbridge 12
Los Angeles 11
Hangzhou 10
Milan 10
New York 10
Dallas 9
Medford 9
Shanghai 7
Tianjin 7
Toronto 7
Falkenstein 6
Tokyo 6
Des Moines 5
Hong Kong 5
London 5
Moscow 5
Verona 4
Jinan 3
Kunming 3
Piscataway 3
San Francisco 3
Vienna 3
Canberra 2
Chicago 2
Lanzhou 2
Nuremberg 2
Ottawa 2
Phoenix 2
Portland 2
Redwood City 2
Zhengzhou 2
Almaty 1
Auburn Hills 1
Baku 1
Brasília 1
Campo Grande 1
Campos dos Goytacazes 1
Central 1
Chengdu 1
Council Bluffs 1
Dearborn 1
Dhaka 1
El Lobo 1
Erechim 1
Fairfield 1
Frankfurt am Main 1
Geislingen an der Steige 1
Guangzhou 1
Ibirité 1
Irecê 1
Jacutinga 1
Las Vegas 1
Lisbon 1
Ningbo 1
Norwalk 1
Prineville 1
Pune 1
Seattle 1
Secaucus 1
Skopje 1
Taicang 1
Tashkent 1
Valparaíso de Goiás 1
Volgograd 1
Warsaw 1
Washington 1
Zurich 1
Totale 966
Nome #
A 2.3 Mb duplication of chromosome 8q24.3 associated with severe mental retardation and epilepsy detected standard karyotype. 111
Direct duplication 12p11.21-p13.31 mediated by segmental duplications: a new recurrent rearrangements? 101
Chromosomal rearrangements in Xq and premature ovarian failure: mapping of 25 new cases and review of the literature. 99
Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome 93
Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy 93
The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype. 89
Inversion polymorphisms and non-contiguous terminal deletions: the cause and the (unpredicted) effect of our genome architecture. 85
Reciprocal translocations: how many are complex rearrangements? 83
5p13 microduplication syndrome: a new case and better clinical definition of the syndrome. 81
SPAN-CGH (Simple Plot Analysis & Normalization for array-CGH): un software user-friendly per la visualizzazione e l'analisi statistica dei dati di array-CGH 79
Periventricular heterotopia in fragile X syndrome. 74
A patient with duplication (7)(p22.1pter) characterized by array-CGH 66
Identification of a recurrent brerakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome. 65
Epigenetic analysis of the Critical Region I for Premature Ovarian Failure (POF): demonstration of a highly heterochromatic domain on the long arm of the mammalian X chromosome. 64
SPAN-CGH: a tool for array CGH data analysis and visualization 58
Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization of 11 cases. 52
Reciprocal translocations: a trap for cytogenetists? 49
Is Brain-Derived Neurotropic Factor Methylation Involved in the Association Between Prenatal Stress and Maternal Postnatal Anxiety During the COVID-19 Pandemic? 41
De novo unbalanced translocations have a complex history/aetiology 41
GRIN2B predicts attention problems among disadvantaged children 24
Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samples 18
An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia 16
Totale 1.482
Categoria #
all - tutte 5.809
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 5.809


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202070 0 0 0 0 0 0 0 0 1 40 27 2
2020/2021156 20 14 6 18 0 21 2 18 7 23 21 6
2021/2022110 3 8 5 6 1 6 4 6 2 3 14 52
2022/2023388 37 38 2 25 50 34 0 20 167 2 12 1
2023/2024142 34 22 6 8 14 26 1 2 1 8 3 17
2024/2025229 4 35 6 10 4 24 10 29 107 0 0 0
Totale 1.482