IRIS
PRAMPARO, TIZIANO
 Distribuzione geografica
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Continente #
NA - Nord America 546
EU - Europa 451
AS - Asia 246
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 1.247
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Nazione #
US - Stati Uniti d'America 539
CN - Cina 230
IE - Irlanda 141
UA - Ucraina 84
DE - Germania 58
FI - Finlandia 57
SE - Svezia 36
GB - Regno Unito 34
IT - Italia 17
BE - Belgio 14
FR - Francia 9
CA - Canada 7
JP - Giappone 6
SG - Singapore 4
AU - Australia 2
HK - Hong Kong 2
TR - Turchia 2
BD - Bangladesh 1
EU - Europa 1
IN - India 1
MK - Macedonia 1
NZ - Nuova Zelanda 1
Totale 1.247
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Città #
Dublin 139
Chandler 128
Jacksonville 90
Nanjing 59
Ann Arbor 55
Beijing 47
Nanchang 26
Helsinki 23
Ashburn 20
Boardman 20
Princeton 19
Lawrence 18
Shenyang 17
Brussels 14
Hebei 14
Changsha 13
Wilmington 13
Jiaxing 12
Woodbridge 12
Hangzhou 10
Milan 10
New York 10
Medford 9
Shanghai 7
Tianjin 7
Tokyo 6
Toronto 6
Des Moines 5
Los Angeles 5
Verona 4
Falkenstein 3
Jinan 3
Kunming 3
Piscataway 3
San Francisco 3
Canberra 2
Chicago 2
Lanzhou 2
Phoenix 2
Portland 2
Redwood City 2
Singapore 2
Zhengzhou 2
Auburn Hills 1
Central 1
Dearborn 1
Dhaka 1
Fairfield 1
Geislingen an der Steige 1
Guangzhou 1
Hong Kong 1
Las Vegas 1
London 1
Ningbo 1
Norwalk 1
Ottawa 1
Prineville 1
Pune 1
Seattle 1
Secaucus 1
Skopje 1
Washington 1
Totale 868
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Nome #
A 2.3 Mb duplication of chromosome 8q24.3 associated with severe mental retardation and epilepsy detected standard karyotype. 100
Direct duplication 12p11.21-p13.31 mediated by segmental duplications: a new recurrent rearrangements? 89
Chromosomal rearrangements in Xq and premature ovarian failure: mapping of 25 new cases and review of the literature. 88
Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome 84
Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy 84
The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype. 77
Inversion polymorphisms and non-contiguous terminal deletions: the cause and the (unpredicted) effect of our genome architecture. 75
Reciprocal translocations: how many are complex rearrangements? 72
5p13 microduplication syndrome: a new case and better clinical definition of the syndrome. 70
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 67
Periventricular heterotopia in fragile X syndrome. 62
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. 57
A patient with duplication (7)(p22.1pter) characterized by array-CGH 55
Identification of a recurrent brerakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome. 55
SPAN-CGH: a tool for array CGH data analysis and visualization 53
Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization of 11 cases. 44
Reciprocal translocations: a trap for cytogenetists? 39
De novo unbalanced translocations have a complex history/aetiology 31
Is Brain-Derived Neurotropic Factor Methylation Involved in the Association Between Prenatal Stress and Maternal Postnatal Anxiety During the COVID-19 Pandemic? 28
GRIN2B predicts attention problems among disadvantaged children 12
Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samples 8
An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia 7
Totale 1.257
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Categoria #
all - tutte 4.169
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 4.169
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020291 66 96 2 17 1 16 6 17 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
2024/20254 4 0 0 0 0 0 0 0 0 0 0 0
Totale 1.257