↓ Skip to main content

Diagnosis of Niemann-Pick disease type C with 7-ketocholesterol screening followed by NPC1/NPC2 gene mutation confirmation in Chinese patients

Overview of attention for article published in Orphanet Journal of Rare Diseases, June 2014
Altmetric Badge

Mentioned by

twitter
1 X user

Readers on

mendeley
56 Mendeley
citeulike
1 CiteULike
You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output. Click here to find out more.
Title
Diagnosis of Niemann-Pick disease type C with 7-ketocholesterol screening followed by NPC1/NPC2 gene mutation confirmation in Chinese patients
Published in
Orphanet Journal of Rare Diseases, June 2014
DOI 10.1186/1750-1172-9-82
Pubmed ID
Authors

Huiwen Zhang, Yu Wang, Na Lin, Rui Yang, Wenjuan Qiu, Lianshu Han, Jun Ye, Xuefan Gu

Abstract

It has been reported that oxidation product of cholesterol, 7-ketocholesterol, increases in plasma of patients with NP-C. Previously, we established a rapid test to determine the plasma 7-ketocholesterol level and found it elevated significantly in patients with acid sphingomyelinase deficient NPD and NP-C disease.

X Demographics

X Demographics

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

Mendeley readers

The data shown below were compiled from readership statistics for 56 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 56 100%

Demographic breakdown

Readers by professional status Count As %
Other 10 18%
Researcher 9 16%
Student > Ph. D. Student 9 16%
Student > Postgraduate 7 13%
Student > Bachelor 4 7%
Other 6 11%
Unknown 11 20%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 13 23%
Agricultural and Biological Sciences 12 21%
Medicine and Dentistry 9 16%
Nursing and Health Professions 1 2%
Linguistics 1 2%
Other 5 9%
Unknown 15 27%
Attention Score in Context

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 10 June 2014.
All research outputs
#18,373,576
of 22,757,090 outputs
Outputs from Orphanet Journal of Rare Diseases
#2,129
of 2,611 outputs
Outputs of similar age
#164,495
of 229,145 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#31
of 39 outputs
Altmetric has tracked 22,757,090 research outputs across all sources so far. This one is in the 11th percentile – i.e., 11% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,611 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 6th percentile – i.e., 6% 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 229,145 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 15th percentile – i.e., 15% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 39 others from the same source and published within six weeks on either side of this one. This one is in the 10th percentile – i.e., 10% of its contemporaries scored the same or lower than it.