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Ontogenetic De Novo Copy Number Variations (CNVs) as a Source of Genetic Individuality: Studies on Two Families with MZD Twins for Schizophrenia

Overview of attention for article published in PLOS ONE, March 2011
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100 Mendeley
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3 CiteULike
Title
Ontogenetic De Novo Copy Number Variations (CNVs) as a Source of Genetic Individuality: Studies on Two Families with MZD Twins for Schizophrenia
Published in
PLOS ONE, March 2011
DOI 10.1371/journal.pone.0017125
Pubmed ID
Authors

Sujit Maiti, Kiran Halagur Bhoge Gowda Kumar, Christina A. Castellani, Richard O'Reilly, Shiva M. Singh

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X Demographics

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 100 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 4 4%
Germany 1 1%
India 1 1%
Sweden 1 1%
Japan 1 1%
Canada 1 1%
Unknown 91 91%

Demographic breakdown

Readers by professional status Count As %
Researcher 20 20%
Student > Ph. D. Student 18 18%
Student > Master 11 11%
Student > Bachelor 11 11%
Student > Doctoral Student 8 8%
Other 29 29%
Unknown 3 3%
Readers by discipline Count As %
Agricultural and Biological Sciences 46 46%
Medicine and Dentistry 19 19%
Biochemistry, Genetics and Molecular Biology 13 13%
Psychology 9 9%
Neuroscience 4 4%
Other 5 5%
Unknown 4 4%