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

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M.M. Nöthen

Institute of Human Genetics

University of Bonn

Germany

[email]@*.uni-bonn.de

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Affiliation

Institute of Human Genetics, University of Bonn, Germany. 1998 - 1999

References

Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families. Nöthen, M.M., Cichon, S., Rohleder, H., Hemmer, S., Franzek, E., Fritze, J., Albus, M., Borrmann-Hassenbach, M., Kreiner, R., Weigelt, B., Minges, J., Lichtermann, D., Maier, W., Craddock, N., Fimmers, R., Höller, T., Baur, M.P., Rietschel, M., Propping, P. Mol. Psychiatry (1999) [Pubmed]
Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15. Nöthen, M.M., Schulte-Körne, G., Grimm, T., Cichon, S., Vogt, I.R., Müller-Myhsok, B., Propping, P., Remschmidt, H. Eur. Child. Adolesc. Psychiatry (1999) [Pubmed]
A gene for universal congenital alopecia maps to chromosome 8p21-22. Nöthen, M.M., Cichon, S., Vogt, I.R., Hemmer, S., Kruse, R., Knapp, M., Höller, T., Faiyaz ul Haque, M., Haque, S., Propping, P., Ahmad, M., Rietschel, M. Am. J. Hum. Genet. (1998) [Pubmed]