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Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization

Overview of attention for article published in BMC Genomics, November 2009
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Citations

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Title
Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization
Published in
BMC Genomics, November 2009
DOI 10.1186/1471-2164-10-526
Pubmed ID
Authors

JM Friedman, Shelin Adam, Laura Arbour, Linlea Armstrong, Agnes Baross, Patricia Birch, Cornelius Boerkoel, Susanna Chan, David Chai, Allen D Delaney, Stephane Flibotte, William T Gibson, Sylvie Langlois, Emmanuelle Lemyre, H Irene Li, Patrick MacLeod, Joan Mathers, Jacques L Michaud, Barbara C McGillivray, Millan S Patel, Hong Qian, Guy A Rouleau, Margot I Van Allen, Siu-Li Yong, Farah R Zahir, Patrice Eydoux, Marco A Marra

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 49 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 3 6%
Colombia 1 2%
Belgium 1 2%
Unknown 44 90%

Demographic breakdown

Readers by professional status Count As %
Researcher 8 16%
Student > Ph. D. Student 7 14%
Professor > Associate Professor 5 10%
Student > Master 5 10%
Professor 4 8%
Other 11 22%
Unknown 9 18%
Readers by discipline Count As %
Agricultural and Biological Sciences 13 27%
Medicine and Dentistry 12 24%
Biochemistry, Genetics and Molecular Biology 5 10%
Engineering 2 4%
Psychology 1 2%
Other 3 6%
Unknown 13 27%