The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound

Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

[search][options]

Editor

Personal info

View

About

Terms

Javascript disabled

Please enable Javascript support in your browser to use this application.

Instructions on how to enable JavaScript on different browsers can be found here: http://www.google.com/support/bin/answer.py?answer=23852.

Joachim Pohlenz

Children's Hospital

Johannes Gutenberg University Mainz

Langenbeckstrasse 1

Building 109

Germany

[email]@*.*.uni-mainz.de

Name/email consistency: high

[Claim this account]

Affiliation

Children's Hospital, Johannes Gutenberg University Mainz, Langenbeckstrasse 1, Building 109, Germany. 2006

References

Goitrous congenital hypothyroidism and hearing impairment associated with mutations in the TPO and SLC26A4/PDS genes. Pfarr, N., Borck, G., Turk, A., Napiontek, U., Keilmann, A., Müller-Forell, W., Kopp, P., Pohlenz, J. J. Clin. Endocrinol. Metab. (2006) [Pubmed]
Subclinical hyperthyroidism due to a thyrotropin receptor (TSHR) gene mutation (S505R). Pohlenz, J., Pfarr, N., Krüger, S., Hesse, V. Acta Paediatr. (2006) [Pubmed]