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Barbu, Miruna C, Zeng, Yanni, Shen, Xueyi, Cox, Simon R, Clarke, Toni-Kim, Gibson, Jude, Adams, Mark J, Johnstone, Mandy, Haley, Chris S, Lawrie, Stephen M
et al (show 224 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.


Polimanti, Renato, Peterson, Roseann E, Ong, Jue-Sheng, MacGregor, Stuart, Edwards, Alexis C, Clarke, Toni-Kim, Frank, Josef, Gerring, Zachary, Gillespie, Nathan A, Lind, Penelope A
et al (show 364 more authors) (2019) Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium. PSYCHOLOGICAL MEDICINE, 49 (7). 1218 - 1226.


Gallagher, CS, Makinen, N, Harris, HR, Rahmioglu, N, Uimari, O, Cook, JP, Shigesi, N, Ferreira, T, Velez-Edwards, DR, Edwards, TL
et al (show 50 more authors) (2019) Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. NATURE COMMUNICATIONS, 10.


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 Sun Mar 8 07:40:28 2020 GMT.