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Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness

Overview of attention for article published in PLOS ONE, June 2014
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Title
Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness
Published in
PLOS ONE, June 2014
DOI 10.1371/journal.pone.0099797
Pubmed ID
Authors

Zied Riahi, Crystel Bonnet, Rim Zainine, Malek Louha, Yosra Bouyacoub, Nadia Laroussi, Mariem Chargui, Rym Kefi, Laurence Jonard, Imen Dorboz, Jean-Pierre Hardelin, Sihem Belhaj Salah, Jacqueline Levilliers, Dominique Weil, Kenneth McElreavey, Odile Tanguy Boespflug, Ghazi Besbes, Sonia Abdelhak, Christine Petit

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X Demographics

The data shown below were collected from the profiles of 3 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 40 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Iran, Islamic Republic of 1 3%
Lithuania 1 3%
Unknown 38 95%

Demographic breakdown

Readers by professional status Count As %
Student > Master 6 15%
Unspecified 4 10%
Other 4 10%
Researcher 4 10%
Student > Ph. D. Student 4 10%
Other 8 20%
Unknown 10 25%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 13 33%
Agricultural and Biological Sciences 8 20%
Unspecified 4 10%
Medicine and Dentistry 3 8%
Nursing and Health Professions 1 3%
Other 1 3%
Unknown 10 25%