IRIS
GIMELLI, STEFANIA
 Distribuzione geografica
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Continente #
NA - Nord America 271
EU - Europa 228
AS - Asia 147
OC - Oceania 2
AF - Africa 1
SA - Sud America 1
Totale 650
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Nazione #
US - Stati Uniti d'America 268
CN - Cina 132
IE - Irlanda 73
UA - Ucraina 52
FI - Finlandia 32
DE - Germania 27
GB - Regno Unito 12
IT - Italia 11
SE - Svezia 11
SG - Singapore 11
FR - Francia 9
CA - Canada 3
AU - Australia 2
IN - India 1
JP - Giappone 1
KG - Kirghizistan 1
NL - Olanda 1
PE - Perù 1
PH - Filippine 1
ZA - Sudafrica 1
Totale 650
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Città #
Chandler 73
Dublin 73
Jacksonville 55
Nanjing 47
Boardman 22
Ashburn 17
Nanchang 16
Princeton 12
Hebei 11
Lawrence 11
Changsha 10
Helsinki 10
Milan 9
Beijing 8
Shanghai 8
Singapore 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
Bishkek 1
Borås 1
Dallas 1
Dearborn 1
Des Moines 1
Frankfurt am Main 1
Hyderabad 1
Lima 1
Manila 1
Ningbo 1
Oklahoma City 1
Ottawa 1
Salt Lake City 1
Tokyo 1
Walnut 1
Zhengzhou 1
Totale 464
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Nome #
A 46,X,inv(Y) young woman with gonadal dysgenesis and gonadoblastoma: cytogenetics, molecular, and methylation studies. 74
2q24-q31 deletion: report of a case and review of the literature. 73
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 70
Characterization of a recurrent 15q24 microdeletion syndrome. 62
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. 62
Identification and molecular modelling of a novel familial mutation in the SRY gene implicated in the pure gonadal dysgenesis. 58
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. 55
Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomics hybridization. 53
Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation. 51
Mutationss in SOX17 are associated with congenital anomalies of the kidney and the urinary tract. 50
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. 42
Totale 650
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Categoria #
all - tutte 2.388
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 2.388
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202036 0 0 0 0 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
2023/202452 2 15 0 1 12 11 0 0 0 2 4 5
2024/202526 1 14 4 5 0 2 0 0 0 0 0 0
Totale 650