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X Demographics
Mendeley readers
Attention Score in Context
Title |
Identification of candidate intergenic risk loci in autism spectrum disorder
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---|---|
Published in |
BMC Genomics, July 2013
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DOI | 10.1186/1471-2164-14-499 |
Pubmed ID | |
Authors |
Susan Walker, Stephen W Scherer |
Abstract |
Copy number variations (CNVs) and DNA sequence alterations affecting specific neuronal genes are established risk factors for Autism Spectrum Disorder (ASD). In what is largely considered a genetic condition, so far, these mutations account for ~20% of individuals having an ASD diagnosis. However, non-coding genomic sequence also contains functional elements introducing additional disease risk loci for investigation. |
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.
Geographical breakdown
Country | Count | As % |
---|---|---|
Brazil | 1 | 33% |
Unknown | 2 | 67% |
Demographic breakdown
Type | Count | As % |
---|---|---|
Practitioners (doctors, other healthcare professionals) | 1 | 33% |
Members of the public | 1 | 33% |
Scientists | 1 | 33% |
Mendeley readers
The data shown below were compiled from readership statistics for 74 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
Country | Count | As % |
---|---|---|
United States | 1 | 1% |
Iceland | 1 | 1% |
Portugal | 1 | 1% |
Unknown | 71 | 96% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Ph. D. Student | 20 | 27% |
Researcher | 9 | 12% |
Student > Master | 8 | 11% |
Student > Bachelor | 8 | 11% |
Professor | 4 | 5% |
Other | 11 | 15% |
Unknown | 14 | 19% |
Readers by discipline | Count | As % |
---|---|---|
Agricultural and Biological Sciences | 23 | 31% |
Biochemistry, Genetics and Molecular Biology | 10 | 14% |
Medicine and Dentistry | 10 | 14% |
Neuroscience | 7 | 9% |
Psychology | 3 | 4% |
Other | 5 | 7% |
Unknown | 16 | 22% |
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 27 July 2013.
All research outputs
#15,512,216
of 25,373,627 outputs
Outputs from BMC Genomics
#5,701
of 11,244 outputs
Outputs of similar age
#117,026
of 209,580 outputs
Outputs of similar age from BMC Genomics
#87
of 179 outputs
Altmetric has tracked 25,373,627 research outputs across all sources so far. This one is in the 38th percentile – i.e., 38% of other outputs scored the same or lower than it.
So far Altmetric has tracked 11,244 research outputs from this source. They receive a mean Attention Score of 4.8. This one is in the 49th percentile – i.e., 49% of its peers scored the same or lower than it.
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 209,580 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 44th percentile – i.e., 44% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 179 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 51% of its contemporaries.