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X Demographics
Mendeley readers
Attention Score in Context
Title |
CNS involvement in OFD1 syndrome: a clinical, molecular, and neuroimaging study
|
---|---|
Published in |
Orphanet Journal of Rare Diseases, May 2014
|
DOI | 10.1186/1750-1172-9-74 |
Pubmed ID | |
Authors |
Ennio Del Giudice, Marina Macca, Floriana Imperati, Alessandra D’Amico, Philippe Parent, Laurent Pasquier, Valerie Layet, Stanislas Lyonnet, Veronique Stamboul-Darmency, Christel Thauvin-Robinet, Brunella Franco, Oral-Facial-Digital Type I (OFD1) Collaborative Group |
Abstract |
Oral-facial-digital type 1 syndrome (OFD1; OMIM 311200) belongs to the expanding group of disorders ascribed to ciliary dysfunction. With the aim of contributing to the understanding of the role of primary cilia in the central nervous system (CNS), we performed a thorough characterization of CNS involvement observed in this disorder. |
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 % |
---|---|---|
Unknown | 3 | 100% |
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 41 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 41 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Other | 6 | 15% |
Student > Ph. D. Student | 5 | 12% |
Researcher | 3 | 7% |
Student > Bachelor | 3 | 7% |
Student > Postgraduate | 3 | 7% |
Other | 8 | 20% |
Unknown | 13 | 32% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 8 | 20% |
Psychology | 5 | 12% |
Biochemistry, Genetics and Molecular Biology | 4 | 10% |
Agricultural and Biological Sciences | 3 | 7% |
Nursing and Health Professions | 2 | 5% |
Other | 6 | 15% |
Unknown | 13 | 32% |
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 19 June 2019.
All research outputs
#13,713,271
of 22,755,127 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,466
of 2,610 outputs
Outputs of similar age
#115,208
of 227,074 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#14
of 32 outputs
Altmetric has tracked 22,755,127 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 2,610 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.5. This one is in the 42nd percentile – i.e., 42% 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 227,074 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 48th percentile – i.e., 48% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 32 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 56% of its contemporaries.