Mutations in the forkhead transcription factor gene (FOXC1) have been recently shown to cause some cases of juvenile glaucoma associated with a variety of anterior-segment anomalies. The purpose of this study was to investigate the clinical features of Axenfeld-Rieger syndrome caused by FOXC1 mutations in Japanese patients.
Pharmacology, Toxicology and Pharmaceutical Science
1
13%
Biochemistry, Genetics and Molecular Biology
1
13%
Sports and Recreations
1
13%
Medicine and Dentistry
1
13%
Other
0
0%
Unknown
2
25%
Attention Score in Context
Attention Score in Context
This research output has an Altmetric Attention Score of 6. 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 11 May 2021.
All research outputs
#6,087,168
of 27,781,301 outputs
Outputs from Journal of Glaucoma
#250
of 2,926 outputs
Outputs of similar age
#17,470
of 143,354 outputs
Outputs of similar age from Journal of Glaucoma
#1
of 3 outputs
Altmetric has tracked 27,781,301 research outputs across all sources so far. This one has received more attention than most of these and is in the 74th percentile.
So far Altmetric has tracked 2,926 research outputs from this source. They receive a mean Attention Score of 2.7. This one has done particularly well, scoring higher than 90% 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 143,354 tracked outputs that were published within six weeks on either side of this one in any source. This one has done well, scoring higher than 80% of its contemporaries.
We're also able to compare this research output to 3 others from the same source and published within six weeks on either side of this one. This one has scored higher than all of them
