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Mendeley readers
| Title |
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis
|
|---|---|
| Published in |
Orphanet Journal of Rare Diseases, May 2011
|
| DOI | 10.1186/1750-1172-6-21 |
| Pubmed ID | |
| Authors |
Crystel Bonnet, M'hamed Grati, Sandrine Marlin, Jacqueline Levilliers, Jean-Pierre Hardelin, Marine Parodi, Magali Niasme-Grare, Diana Zelenika, Marc Délépine, Delphine Feldmann, Laurence Jonard, Aziz El-Amraoui, Dominique Weil, Bruno Delobel, Christophe Vincent, Hélène Dollfus, Marie-Madeleine Eliot, Albert David, Catherine Calais, Jacqueline Vigneron, Bettina Montaut-Verient, Dominique Bonneau, Jacques Dubin, Christel Thauvin, Alain Duvillard, Christine Francannet, Thierry Mom, Didier Lacombe, Françoise Duriez, Valérie Drouin-Garraud, Marie-Françoise Thuillier-Obstoy, Sabine Sigaudy, Anne-Marie Frances, Patrick Collignon, Georges Challe, Rémy Couderc, Mark Lathrop, José-Alain Sahel, Jean Weissenbach, Christine Petit, Françoise Denoyelle |
Mendeley readers
The data shown below were compiled from readership statistics for 109 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Portugal | 1 | <1% |
| Brazil | 1 | <1% |
| Unknown | 107 | 98% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Researcher | 18 | 17% |
| Student > Ph. D. Student | 16 | 15% |
| Student > Master | 13 | 12% |
| Other | 9 | 8% |
| Student > Bachelor | 8 | 7% |
| Other | 21 | 19% |
| Unknown | 24 | 22% |
| Readers by discipline | Count | As % |
|---|---|---|
| Agricultural and Biological Sciences | 37 | 34% |
| Biochemistry, Genetics and Molecular Biology | 23 | 21% |
| Medicine and Dentistry | 18 | 17% |
| Veterinary Science and Veterinary Medicine | 2 | 2% |
| Neuroscience | 2 | 2% |
| Other | 3 | 3% |
| Unknown | 24 | 22% |