IRIS
GIMELLI, STEFANIA
 Distribuzione geografica
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Continente #
NA - Nord America 258
EU - Europa 227
AS - Asia 127
OC - Oceania 2
SA - Sud America 1
Totale 615
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Nazione #
US - Stati Uniti d'America 256
CN - Cina 125
IE - Irlanda 73
UA - Ucraina 52
FI - Finlandia 32
DE - Germania 26
GB - Regno Unito 12
IT - Italia 11
SE - Svezia 11
FR - Francia 9
AU - Australia 2
CA - Canada 2
IN - India 1
NL - Olanda 1
PE - Perù 1
SG - Singapore 1
Totale 615
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Città #
Chandler 73
Dublin 73
Jacksonville 55
Nanjing 47
Ashburn 17
Nanchang 16
Princeton 12
Boardman 11
Hebei 11
Lawrence 11
Changsha 10
Helsinki 10
Milan 9
Beijing 8
Jiaxing 7
Medford 7
Shenyang 7
Wilmington 7
Hangzhou 6
Tianjin 6
San Francisco 3
Fairfield 2
Lanzhou 2
Los Angeles 2
Norwalk 2
Sydney 2
Toronto 2
Verona 2
Auburn Hills 1
Borås 1
Dearborn 1
Des Moines 1
Hyderabad 1
Lima 1
Ningbo 1
Oklahoma City 1
Salt Lake City 1
Shanghai 1
Singapore 1
Walnut 1
Zhengzhou 1
Totale 433
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Nome #
A 46,X,inv(Y) young woman with gonadal dysgenesis and gonadoblastoma: cytogenetics, molecular, and methylation studies. 70
2q24-q31 deletion: report of a case and review of the literature. 69
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 65
The tumor suppressor gene TRC8/RNF139 is disrupted by a constitutional balanced translocation t(8;22)(q24;q11.21) in a young girl with dysgerminoma. 60
Characterization of a recurrent 15q24 microdeletion syndrome. 59
Identification and molecular modelling of a novel familial mutation in the SRY gene implicated in the pure gonadal dysgenesis. 57
A large analphoid invdup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko's lines. 51
Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomics hybridization. 50
Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation. 48
Mutationss in SOX17 are associated with congenital anomalies of the kidney and the urinary tract. 47
The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q131.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomalies. 39
Totale 615
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Categoria #
all - tutte 1.762
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 1.762
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20191 0 0 0 0 0 0 0 0 0 0 0 1
2019/2020152 41 66 0 9 0 9 0 10 0 10 7 0
2020/202172 9 9 1 8 0 10 0 12 1 10 10 2
2021/202250 0 0 2 0 0 4 0 3 3 0 5 33
2022/2023203 21 20 0 17 23 17 0 10 87 1 6 1
2023/202443 2 15 0 1 12 11 0 0 0 2 0 0
Totale 615