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Barbu, MC, Zeng, Y, Shen, X, Cox, SR, Clarke, TK, Gibson, J, Adams, MJ, Johnstone, M, Haley, CS, Lawrie, SM
et al (show 90 more authors) (2019) Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging, 4 (1). 91 - 100.


Gormley, Padhraig, Kurki, Mitja I, Hiekkala, Marjo Eveliina, Veerapen, Kumar, Häppölä, Paavo, Mitchell, Adele A, Lal, Dennis, Palta, Priit, Surakka, Ida, Kaunisto, Mari Anneli
et al (show 124 more authors) (2018) Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families. Neuron, 98 (4). 743 - 753.e4.


Grove, Jakob, Ripke, Stephan, Als, Thomas D, Mattheisen, Manuel, Walters, Raymond K, Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A, Anney, Richard
et al (show 269 more authors) (2019) Identification of common genetic risk variants for autism spectrum disorder. NATURE GENETICS, 51 (3). 431 - +.

This list was generated on Fri Nov 15 20:56:26 2019 GMT.