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Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype

Overview of attention for article published in Orphanet Journal of Rare Diseases, December 2011
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Title
Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype
Published in
Orphanet Journal of Rare Diseases, December 2011
DOI 10.1186/1750-1172-6-88
Pubmed ID
Authors

Freya KR Swinnen, Paul J Coucke, Anne M De Paepe, Sofie Symoens, Fransiska Malfait, Filomena V Gentile, Luca Sangiorgi, Patrizia D'Eufemia, Mauro Celli, Ton JTM Garretsen, Cor WRJ Cremers, Ingeborg JM Dhooge, Els MR De Leenheer

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 51 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Turkey 1 2%
Unknown 50 98%

Demographic breakdown

Readers by professional status Count As %
Other 7 14%
Researcher 7 14%
Student > Master 5 10%
Student > Doctoral Student 5 10%
Student > Bachelor 5 10%
Other 14 27%
Unknown 8 16%
Readers by discipline Count As %
Medicine and Dentistry 18 35%
Biochemistry, Genetics and Molecular Biology 6 12%
Agricultural and Biological Sciences 5 10%
Nursing and Health Professions 3 6%
Neuroscience 2 4%
Other 9 18%
Unknown 8 16%