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

Tero Ylisaukko-Oja

Department of Molecular Medicine

National Public Health Institute




Name/email consistency: high



  • Department of Molecular Medicine, National Public Health Institute, Helsinki, Finland. 2005


  1. Family-based association study of DYX1C1 variants in autism. Ylisaukko-Oja, T., Peyrard-Janvid, M., Lindgren, C.M., Rehnström, K., Vanhala, R., Peltonen, L., Järvelä, I., Kere, J. Eur. J. Hum. Genet. (2005) [Pubmed]
  2. MECP2 mutation analysis in patients with mental retardation. Ylisaukko-Oja, T., Rehnström, K., Vanhala, R., Kempas, E., von Koskull, H., Tengström, C., Mustonen, A., Ounap, K., Lähdetie, J., Järvelä, I. Am. J. Med. Genet. A (2005) [Pubmed]
  3. Analysis of four neuroligin genes as candidates for autism. Ylisaukko-oja, T., Rehnström, K., Auranen, M., Vanhala, R., Alen, R., Kempas, E., Ellonen, P., Turunen, J.A., Makkonen, I., Riikonen, R., Nieminen-von Wendt, T., von Wendt, L., Peltonen, L., Järvelä, I. Eur. J. Hum. Genet. (2005) [Pubmed]
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