Showing items 1 - 2 of 2

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

- Marshall, Christian R., Howrigan, Daniel P., Gujral, Madhusudan, Brandler, William M., Malhotra, Dheeraj, Wang, Zhouzhi, Fuentes Fajarado, Karin V., Maile, Michelle S., Ripke, Stephan, Agartz, Ingrud, Albus, Margot, Alexander, Madeline, Merico, Daniele, Atkins, Joshua, Cairns, Murray J., Carr, Vaughan J., Henskens, Frans A., Kelly, Brian J., Loughland, Carmel L., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Thiruvahindrapuram, Bhooma, Wu, Jing Qin, Wu, Wenting, Greer, Douglas S., Antaki, Douglas, Shetty, Aniket, Holmans, Peter A., Pinto, Dalila

Rare genome-wide copy number variation and expression of schizophrenia in 22q11.2 deletion syndrome

- Bassett, Anne S., Lowther, Chelsea, Murphy, Kieran, Gothelf, Doron, Bearden, Carrie E., Eliez, Stephan, Kates, Wendy, Philip, Nicole, Sashi, Vandana, Campbell, Linda, Vorstman, Jacob, Cubells, Joseph, Merico, Daniele, Costain, Gregory, Chow, Eva W. C., van Amelsvoort, Therese, McDonald-McGinn, Donna, Gur, Raquel E., Swillen, Ann, Van den Bree, Marianne

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