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Replication of the Association of a MET Variant with Autism in a Chinese Han Population

Overview of attention for article published in PLOS ONE, November 2011
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Title
Replication of the Association of a MET Variant with Autism in a Chinese Han Population
Published in
PLOS ONE, November 2011
DOI 10.1371/journal.pone.0027428
Pubmed ID
Authors

Xue Zhou, Yang Xu, Jia Wang, Hongbo Zhou, Xian Liu, Qasim Ayub, Xuelai Wang, Chris Tyler-Smith, Lijie Wu, Yali Xue

Abstract

Autism is a common, severe and highly heritable neurodevelopmental disorder in children, affecting up to 100 children per 10,000. The MET gene has been regarded as a promising candidate gene for this disorder because it is located within a replicated linkage interval, is involved in pathways affecting the development of the cerebral cortex and cerebellum in ways relevant to autism patients, and has shown significant association signals in previous studies.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 31 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 3%
Unknown 30 97%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 5 16%
Student > Bachelor 5 16%
Other 3 10%
Researcher 3 10%
Student > Doctoral Student 2 6%
Other 7 23%
Unknown 6 19%
Readers by discipline Count As %
Medicine and Dentistry 6 19%
Agricultural and Biological Sciences 4 13%
Neuroscience 3 10%
Psychology 3 10%
Biochemistry, Genetics and Molecular Biology 2 6%
Other 6 19%
Unknown 7 23%