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X Demographics
Mendeley readers
Attention Score in Context
| Title |
X-exome sequencing in Finnish families with Intellectual Disability - four novel mutations and two novel syndromic phenotypes
|
|---|---|
| Published in |
Orphanet Journal of Rare Diseases, April 2014
|
| DOI | 10.1186/1750-1172-9-49 |
| Pubmed ID | |
| Authors |
Anju K Philips, Auli Sirén, Kristiina Avela, Mirja Somer, Maarit Peippo, Minna Ahvenainen, Fatma Doagu, Maria Arvio, Helena Kääriäinen, Hilde Van Esch, Guy Froyen, Stefan A Haas, Hao Hu, Vera M Kalscheuer, Irma Järvelä |
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 % |
|---|---|---|
| India | 1 | 33% |
| Unknown | 2 | 67% |
Demographic breakdown
| Type | Count | As % |
|---|---|---|
| Members of the public | 2 | 67% |
| Scientists | 1 | 33% |
Mendeley readers
The data shown below were compiled from readership statistics for 78 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Finland | 1 | 1% |
| United Kingdom | 1 | 1% |
| Unknown | 76 | 97% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Student > Bachelor | 12 | 15% |
| Researcher | 11 | 14% |
| Student > Master | 9 | 12% |
| Student > Ph. D. Student | 7 | 9% |
| Unspecified | 5 | 6% |
| Other | 18 | 23% |
| Unknown | 16 | 21% |
| Readers by discipline | Count | As % |
|---|---|---|
| Biochemistry, Genetics and Molecular Biology | 17 | 22% |
| Agricultural and Biological Sciences | 16 | 21% |
| Medicine and Dentistry | 14 | 18% |
| Unspecified | 5 | 6% |
| Nursing and Health Professions | 3 | 4% |
| Other | 8 | 10% |
| Unknown | 15 | 19% |
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 14 April 2014.
All research outputs
#16,681,672
of 26,017,215 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,813
of 3,175 outputs
Outputs of similar age
#134,033
of 243,250 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#30
of 47 outputs
Altmetric has tracked 26,017,215 research outputs across all sources so far. This one is in the 33rd percentile – i.e., 33% of other outputs scored the same or lower than it.
So far Altmetric has tracked 3,175 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 8.2. This one is in the 38th percentile – i.e., 38% 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 243,250 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 41st percentile – i.e., 41% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 47 others from the same source and published within six weeks on either side of this one. This one is in the 25th percentile – i.e., 25% of its contemporaries scored the same or lower than it.