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Haas, Shalaila S; Ge, Ruiyang; Agartz, Ingrid; Amminger, G Paul; Andreassen, Ole A; Bachman, Peter; Baeza, Inmaculada; Choi, Sunah; Colibazzi, Tiziano; Cropley, Vanessa L; de la Fuente-Sandoval, Camilo; Ebdrup, Bjørn H; Fortea, Adriana; Fusar-Poli, Paolo; Glenthøj, Birte Yding; Glenthøj, Louise Birkedal; Haut, Kristen M; Hayes, Rebecca A; Heekeren, Karsten; Hooker, Christine I; ... (2024). Normative Modeling of Brain Morphometry in Clinical High Risk for Psychosis. JAMA psychiatry, 81(1), pp. 77-88. American Medical Association 10.1001/jamapsychiatry.2023.3850
Baldwin, Helen; Radua, Joaquim; Antoniades, Mathilde; Haas, Shalaila S; Frangou, Sophia; Agartz, Ingrid; Allen, Paul; Andreassen, Ole A; Atkinson, Kimberley; Bachman, Peter; Baeza, Inmaculada; Bartholomeusz, Cali F; Chee, Michael W L; Colibazzi, Tiziano; Cooper, Rebecca E; Corcoran, Cheryl M; Cropley, Vanessa L; Ebdrup, Bjørn H; Fortea, Adriana; Glenthøj, Louise Birkedal; ... (2022). Neuroanatomical heterogeneity and homogeneity in individuals at clinical high risk for psychosis. Translational Psychiatry, 12(1), p. 297. Springer Nature 10.1038/s41398-022-02057-y
Anttila, Verneri; Bulik-Sullivan, Brendan; Finucane, Hilary K; Walters, Raymond K; Bras, Jose; Duncan, Laramie; Escott-Price, Valentina; Falcone, Guido J; Gormley, Padhraig; Malik, Rainer; Patsopoulos, Nikolaos A; Ripke, Stephan; Wei, Zhi; Yu, Dongmei; Lee, Phil H; Turley, Patrick; Grenier-Boley, Benjamin; Chouraki, Vincent; Kamatani, Yoichiro; Berr, Claudine; ... (2018). Analysis of shared heritability in common disorders of the brain. Science, 360(6395) American Association for the Advancement of Science 10.1126/science.aap8757
Adams, Hieab H H; Hibar, Derrek P; Chouraki, Vincent; Stein, Jason L; Nyquist, Paul A; Rentería, Miguel E; Trompet, Stella; Arias-Vasquez, Alejandro; Seshadri, Sudha; Desrivières, Sylvane; Beecham, Ashley H; Jahanshad, Neda; Wittfeld, Katharina; Van der Lee, Sven J; Abramovic, Lucija; Alhusaini, Saud; Amin, Najaf; Andersson, Micael; Arfanakis, Konstantinos; Aribisala, Benjamin S; ... (2016). Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature neuroscience, 19(12), pp. 1569-1582. Nature America 10.1038/nn.4398
Håvik, Bjarte; Degenhardt, Franziska A; Johansson, Stefan; Fernandes, Carla P D; Hinney, Anke; Scherag, André; Lybæk, Helle; Djurovic, Srdjan; Christoforou, Andrea; Ersland, Kari M; Giddaluru, Sudheer; O'Donovan, Michael C; Owen, Michael J; Craddock, Nick; Mühleisen, Thomas W; Mattheisen, Manuel; Schimmelmann, Benno G; Renner, Tobias; Warnke, Andreas; Herpertz-Dahlmann, Beate; ... (2012). DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. PLoS ONE, 7(4), e35424. Lawrence, Kans.: Public Library of Science 10.1371/journal.pone.0035424
