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Genome-wide CNV analysis replicates the association between GSTM1 deletion and bladder cancer: a support for using continuous measurement from SNP-array data

Overview of attention for article published in BMC Genomics, July 2012
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  • Above-average Attention Score compared to outputs of the same age and source (55th percentile)

Mentioned by

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3 X users

Citations

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14 Dimensions

Readers on

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39 Mendeley
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1 CiteULike
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Title
Genome-wide CNV analysis replicates the association between GSTM1 deletion and bladder cancer: a support for using continuous measurement from SNP-array data
Published in
BMC Genomics, July 2012
DOI 10.1186/1471-2164-13-326
Pubmed ID
Authors

Gaëlle Marenne, Francisco X Real, Nathaniel Rothman, Benjamin Rodríguez-Santiago, Luis Pérez-Jurado, Manolis Kogevinas, Montse García-Closas, Debra T Silverman, Stephen J Chanock, Emmanuelle Génin, Núria Malats

Abstract

Structural variations such as copy number variants (CNV) influence the expression of different phenotypic traits. Algorithms to identify CNVs through SNP-array platforms are available. The ability to evaluate well-characterized CNVs such as GSTM1 (1p13.3) deletion provides an important opportunity to assess their performance.

X Demographics

X Demographics

The data shown below were collected from the profiles of 3 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 39 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Korea, Republic of 1 3%
Ireland 1 3%
Sweden 1 3%
Israel 1 3%
Spain 1 3%
Unknown 34 87%

Demographic breakdown

Readers by professional status Count As %
Researcher 13 33%
Student > Ph. D. Student 7 18%
Student > Bachelor 4 10%
Student > Master 3 8%
Student > Doctoral Student 2 5%
Other 7 18%
Unknown 3 8%
Readers by discipline Count As %
Agricultural and Biological Sciences 16 41%
Medicine and Dentistry 10 26%
Biochemistry, Genetics and Molecular Biology 4 10%
Pharmacology, Toxicology and Pharmaceutical Science 1 3%
Unspecified 1 3%
Other 4 10%
Unknown 3 8%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 26 July 2012.
All research outputs
#13,364,385
of 22,671,366 outputs
Outputs from BMC Genomics
#4,973
of 10,614 outputs
Outputs of similar age
#90,401
of 163,875 outputs
Outputs of similar age from BMC Genomics
#51
of 118 outputs
Altmetric has tracked 22,671,366 research outputs across all sources so far. This one is in the 39th percentile – i.e., 39% of other outputs scored the same or lower than it.
So far Altmetric has tracked 10,614 research outputs from this source. They receive a mean Attention Score of 4.7. This one has gotten more attention than average, scoring higher than 50% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 163,875 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 43rd percentile – i.e., 43% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 118 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 55% of its contemporaries.