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Genotype-phenotype correlation in 22q11.2 deletion syndrome

Overview of attention for article published in BMC Medical Genomics, December 2012
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125 Mendeley
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Title
Genotype-phenotype correlation in 22q11.2 deletion syndrome
Published in
BMC Medical Genomics, December 2012
DOI 10.1186/1471-2350-13-122
Pubmed ID
Authors

Elena Michaelovsky, Amos Frisch, Miri Carmel, Miriam Patya, Omer Zarchi, Tamar Green, Lina Basel-Vanagaite, Abraham Weizman, Doron Gothelf

Abstract

The 22q11.2 deletion syndrome (22q11.2DS) is caused by hemizygous microdeletions on chromosome 22q11.2 with highly variable physical and neuropsychiatric manifestations. We explored the genotype-phenotype relationship in a relatively large 22q11.2DS cohort treated and monitored in our clinic using comprehensive clinical evaluation and detailed molecular characterization of the deletion.

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 125 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Japan 1 <1%
United Kingdom 1 <1%
United States 1 <1%
Unknown 122 98%

Demographic breakdown

Readers by professional status Count As %
Researcher 22 18%
Student > Bachelor 22 18%
Student > Master 21 17%
Student > Ph. D. Student 9 7%
Student > Doctoral Student 7 6%
Other 21 17%
Unknown 23 18%
Readers by discipline Count As %
Medicine and Dentistry 28 22%
Agricultural and Biological Sciences 26 21%
Biochemistry, Genetics and Molecular Biology 22 18%
Psychology 7 6%
Neuroscience 5 4%
Other 7 6%
Unknown 30 24%
Attention Score in Context

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 05 June 2015.
All research outputs
#16,048,009
of 25,374,647 outputs
Outputs from BMC Medical Genomics
#1,102
of 2,444 outputs
Outputs of similar age
#172,602
of 275,903 outputs
Outputs of similar age from BMC Medical Genomics
#20
of 46 outputs
Altmetric has tracked 25,374,647 research outputs across all sources so far. This one is in the 34th percentile – i.e., 34% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,444 research outputs from this source. They receive a mean Attention Score of 4.4. This one has gotten more attention than average, scoring higher than 51% 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 275,903 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 35th percentile – i.e., 35% 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 has gotten more attention than average, scoring higher than 50% of its contemporaries.