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The Evidence for Association of ATP2B2 Polymorphisms with Autism in Chinese Han Population

Overview of attention for article published in PLOS ONE, April 2013
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Title
The Evidence for Association of ATP2B2 Polymorphisms with Autism in Chinese Han Population
Published in
PLOS ONE, April 2013
DOI 10.1371/journal.pone.0061021
Pubmed ID
Authors

Wen Yang, Jing Liu, Fanfan Zheng, Meixiang Jia, Linnan Zhao, Tianlan Lu, Yanyan Ruan, Jishui Zhang, Weihua Yue, Dai Zhang, Lifang Wang

Abstract

Autism is a neurodevelopmental disorder with a high estimated heritability. ATP2B2, located on human chromosome 3p25.3, encodes the plasma membrane calcium-transporting ATPase 2 which extrudes Ca(2+) from cytosol into extracellular space. Recent studies reported association between ATP2B2 and autism in samples from Autism Genetic Resource Exchange (AGRE) and Italy. In this study, we investigated whether ATP2B2 polymorphisms were associated with autism in Chinese Han population.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 57 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 2%
Portugal 1 2%
Germany 1 2%
Unknown 54 95%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 16 28%
Student > Master 10 18%
Researcher 5 9%
Student > Bachelor 4 7%
Student > Doctoral Student 4 7%
Other 5 9%
Unknown 13 23%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 8 14%
Nursing and Health Professions 8 14%
Agricultural and Biological Sciences 8 14%
Psychology 6 11%
Medicine and Dentistry 5 9%
Other 9 16%
Unknown 13 23%