NCA Publications

New NCA Publications

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Sullivan, P. F., Agrawal, A., Bulik, C. M., Andreassen, O. A., Børglum, A. D., Breen, G., Cichon, S., Edenberg, H. J., Faraone, S. V., Gelernter, J., Mathews, C. A., Nievergelt, C. M., Smoller, J. W., O'Donovan, M. C. & Psychiatric Genomics Consortium (2018). Psychiatric Genomics: An Update and an Agenda. The American Journal of Psychiatry (Spanish Edition), 175(1), 15-27. https://doi.org/10.1176/appi.ajp.2017.17030283
GoT2D/T2D-GENES Consortium (2018). Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum. American Journal of Human Genetics, 102(6), 1204-1211. https://doi.org/10.1016/j.ajhg.2018.05.002
Walsh, R. R., Krismer, F., Galpern, W. R., Wenning, G. K., Low, P. A., Halliday, G., Koroshetz, W. J., Holton, J., Quinn, N. P., Rascol, O., Shaw, L. M., Eidelberg, D., Bower, P., Cummings, J. L., Abler, V., Biedenharn, J., Brooks, D. J., Brundin, P., Fernandez, H. ... Wenning Gregor (2018). Recommendations of the Global Multiple System Atrophy Research Roadmap Meeting. Neurology, 90(2), 74-82. https://doi.org/10.1212/WNL.0000000000004798
Ryyppö, E., Glerean, E., Brattico, E., Saramäki, J. & Korhonen, O. (2018). Regions of Interest as nodes of dynamic functional brain networks. Network Neuroscience, 2(4), 513-535. https://doi.org/10.1162/netn_a_00047
Smith, A. H., Ovesen, P. L., Skeldal, S., Yeo, S., Jensen, K. P., Olsen, D., Diazgranados, N., Zhao, H., Farrer, L. A., Goldman, D., Glerup, S., Kranzler, H. R., Nykjaer, A. & Gelernter, J. (2018). Risk Locus Identification Ties Alcohol Withdrawal Symptoms to SORCS2. Alcoholism: Clinical and Experimental Research, 42(12), 2337-2348. https://doi.org/10.1111/acer.13890