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  • Finland

20042017
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International and National Collaboration Publications and projects within past five years.

Publications 2004 2017

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

The Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium, 22 May 2017, In : Molecular Autism. 8, 17 p., 21.

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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Weiner, D. J., Wigdor, E. M., Ripke, S., Walters, R. K., Kosmicki, J. A., Grove, J., Samocha, K. E., Goldstein, J. I., Okbay, A., Bybjerg-Grauholm, J., Werge, T., Hougaard, D. M., Taylor, J., Skuse, D., Devlin, B., Anney, R., Sanders, S. J., Bishop, S., Mortensen, P. B., Borglum, A. D. & 32 others, Smith, G. D., Daly, M. J., Robinson, E. B., Baekvad-Hansen, M., Dumont, A., Hansen, C., Hansen, T. F., Howrigan, D., Mattheisen, M., Moran, J., Mors, O., Nordentoft, M., Norgaard-Pedersen, B., Poterba, T., Poulsen, J., Stevens, C., Anttila, V., Holmans, P., Huang, H., Klei, L., Lee, P. H., Medland, S. E., Neale, B., Weiss, L. A., Zwaigenbaum, L., Yu, T. W., Wittemeyer, K., Willsey, A. J., Rehnström, K., iPSYCH-Broad Autism Grp, Psychiat Genomics Consortium & Palotie, A., Jul 2017, In : Nature Genetics. 49, 7, p. 978-985 11 p.

Research output: Contribution to journalArticleScientificpeer-review

A framework for the interpretation of de novo mutation in human disease

Samocha, K. E., Robinson, E. B., Sanders, S. J., Stevens, C., Sabo, A., McGrath, L. M., Kosmicki, J. A., Rehnstrom, K., Mallick, S., Kirby, A., Wall, D. P., MacArthur, D. G., Gabriel, S. B., DePristo, M., Purcell, S. M., Palotie, A., Boerwinkle, E., Buxbaum, J. D., Cook, Jr., E. H., Gibbs, R. A. & 6 others, Schellenberg, G. D., Sutcliffe, J. S., Devlin, B., Roeder, K., Neale, B. M. & Daly, M. J., 1 Sep 2014, In : Nature Genetics. 46, 9, p. 944+

Research output: Contribution to journalArticleScientificpeer-review

Common variant at 16p11.2 conferring risk of psychosis

Steinberg, S., de Jong, S., Mattheisen, M., Costas, J., Demontis, D., Jamain, S., Pietiläinen, O. P. H., Lin, K., Papiol, S., Huttenlocher, J., Sigurdsson, E., Vassos, E., Giegling, I., Breuer, R., Fraser, G., Walker, N., Melle, I., Djurovic, S., Agartz, I., Tuulio-Henriksson, A. & 32 others, Suvisaari, J., Lönnqvist, J., Paunio, T., Olsen, L., Hansen, T., Ingason, A., Pirinen, M., Strengman, E., Hougaard, D. M., Orntoft, T., Didriksen, M., Hollegaard, M. V., Nordentoft, M., Abramova, L., Kaleda, V., Arrojo, M., Sanjuan, J., Arango, C., Etain, B., Bellivier, F., Meary, A., Schuerhoff, F., Szoke, A., Ribolsi, M., Magni, V., Siracusano, A., Sperling, S., Rehnstrom, K., Kilpinen, L. H., Palotie, A., GROUP & Wellcome Trust Case Control Consor, Jan 2014, In : Molecular Psychiatry. 19, 1, p. 108-114 7 p.

Research output: Contribution to journalArticleScientificpeer-review

A Genome-Wide Analysis of Populations from European Russia Reveals a New Pole of Genetic Diversity in Northern Europe

Khrunin, A. V., Khokhrin, D. V., Filippova, I. N., Esko, T., Nelis, M., Bebyakova, N. A., Bolotova, N. L., Klovins, J., Nikitina-Zake, L., Rehnström, K. H., Ripatti, S., Schreiber, S., Franke, A., Macek, M., Krulisova, V., Lubinski, J., Metspalu, A. & Limborska, S. A., 7 Mar 2013, In : PLoS One. 8, 3, p. Article Number: e58552 9 p.

Research output: Contribution to journalArticleScientificpeer-review

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