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  1. Rayner, Christopher [Author]; Domschke, Katharina [Author]; Breen, Gerome [Author]; Eley, Thalia C. [Author]

    A genome-wide association meta-analysisof prognostic outcomes following cognitive behavioural therapy in individuals with anxiety and depressive disorders

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    London: Nature Publishing Group, 2019

    Published in: Translational psychiatry ; 9 (2019), 150

  2. Van Rheenen, Wouter [Author]; van der Spek, Rick A. A. [Author]; Bakker, Mark K. [Author]; van Vugt, Joke J. F. A. [Author]; Hop, Paul J. [Author]; Zwamborn, Ramona A. J. [Author]; de Klein, Niek [Author]; Westra, Harm-Jan [Author]; Bakker, Olivier B. [Author]; Deelen, Patrick [Author]; Shireby, Gemma [Author]; Hannon, Eilis [Author]; Moisse, Matthieu [Author]; Baird, Denis [Author]; Restuadi, Restuadi [Author]; Dolzhenko, Egor [Author]; Dekker, Annelot M. [Author]; Gawor, Klara [Author]; Westeneng, Henk-Jan [Author]; Tazelaar, Gijs H. P. [Author]; van Eijk, Kristel R. [Author]; Kooyman, Maarten [Author]; Byrne, Ross P. [Author]; Doherty, Mark [Author]; [...]

    Author correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology : amendments

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    31 January 2022

    Published in: Nature genetics ; 54(2022), 3, Seite 361-361

  3. Huckins, Laura M [Author]; Boraska, Vesna [Author]; Southam, L [Author]; Karhunen, L [Author]; Meulenbelt, I [Author]; Slagboom, P E [Author]; Tortorella, A [Author]; Maj, M [Author]; Dedoussis, G [Author]; Dikeos, D [Author]; Gonidakis, F [Author]; Tziouvas, K [Author]; Tsitsika, A [Author]; Rayner, N William [Author]; Papezova, H [Author]; Slachtova, L [Author]; Martaskova, D [Author]; Kennedy, J L [Author]; Levitan, R D [Author]; Yilmaz, Z [Author]; Huemer, J [Author]; Koubek, D [Author]; Merl, E [Author]; Wagner, G [Author]; [...]

    Using ancestry-informative markers to identify fine structure across 15 populations of European origin

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    Stockton Press, 2014

    Published in: European journal of human genetics 22, 1190–1200 (2014). doi:10.1038/ejhg.2014.1