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Phenylketonuria screening in the Republic of Macedonia

Overview of attention for article published in Orphanet Journal of Rare Diseases, August 2016
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1 tweeter

Citations

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Readers on

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Title
Phenylketonuria screening in the Republic of Macedonia
Published in
Orphanet Journal of Rare Diseases, August 2016
DOI 10.1186/s13023-016-0483-2
Pubmed ID
Authors

Mirjana Kocova, Violeta Anastasovska

Abstract

Phenylketonuria is an autosomal recessive inborn error of metabolism which can be prevented by early and continuous treatment. Therefore newborn screening for phenylketonuria has been introduced in many countries. We present here the results of the selective newborn screening for inborn errors of metabolism, including PKU, performed by tandem mass spectrometry which has been introduced in Macedonia since 2011.

Twitter Demographics

The data shown below were collected from the profile of 1 tweeter who shared this research output. Click here to find out more about how the information was compiled.

Mendeley readers

The data shown below were compiled from readership statistics for 11 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 11 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 3 27%
Professor 1 9%
Student > Bachelor 1 9%
Student > Doctoral Student 1 9%
Researcher 1 9%
Other 1 9%
Unknown 3 27%
Readers by discipline Count As %
Medicine and Dentistry 5 45%
Agricultural and Biological Sciences 1 9%
Neuroscience 1 9%
Pharmacology, Toxicology and Pharmaceutical Science 1 9%
Unknown 3 27%

Attention Score in Context

This research output has an Altmetric Attention Score of 1. 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 06 August 2016.
All research outputs
#7,072,689
of 8,172,683 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,030
of 1,122 outputs
Outputs of similar age
#217,350
of 257,394 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#45
of 46 outputs
Altmetric has tracked 8,172,683 research outputs across all sources so far. This one is in the 1st percentile – i.e., 1% of other outputs scored the same or lower than it.
So far Altmetric has tracked 1,122 research outputs from this source. They receive a mean Attention Score of 4.9. This one is in the 1st percentile – i.e., 1% 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 257,394 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 46 others from the same source and published within six weeks on either side of this one. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.