Polygenic risk score for bipolar disorder associates with divergent thinking and brain structures in the prefrontal cortex

by Araki, T., dos S. Kawata, K.H, Hanawa, S., Iizuka, K., Ikeda, S., Imanishi, T., Kawashima, R., Kikuchi, Y., Kimura, R., Kotozaki, Y., Magistro, D., Matsudaira, I., Miyauchi, C.M, Nakagawa, S., Nouchi, R., Nozawa, T., Ono, C., Sakaki, K., Sekiguchi, A., Takeuchi, H., Taki, Y., Tomita, H., Yokota, S., Yokoyama, R., Yu, Z.
Published 2021

Cross-sex shifts in two brain imaging phenotypes and their relation to polygenic scores for same-sex sexual behavior: A study of 18,645 individuals from the UK Biobank

by Abé, C., Bergen, S.E, Ingvar, M., Jonsson, L., Landén, M., Lebedev, A., Rahman, Q., Zhang, R.
Published 2021

Genetic scores for adult subcortical volumes associate with subcortical volumes during infancy and childhood

by Ikram, M.A, Jansen, P.R, Labrecque, J.A, Lamballais, S., White, T.
Published 2021

A mutation-based gene set predicts survival benefit after immunotherapy across multiple cancers and reveals the immune response landscape

by Bian, J., Chen, P., Lin, Y., Long, J., Sang, X., Wang, A., Wang, D., Yang, X., Zhang, H., Zhao, H., Zheng, M., Zheng, Y.
Published 2022

Somatic mutational profiles and germline polygenic risk scores in human cancer

by Alexandrov, L.B, Gusev, A., Heng, Y.J, Kraft, P., Liu, Y.
Published 2022

What can genetics tell us about the schizophrenia construct?

by Smoller, J.W
Published 2022

Genetic risk score for ovarian cancer based on chromosomal-scale length variation

by Brody, J.P, Toh, C.
Published 2021

GenRisk: A tool for comprehensive genetic risk modeling

by Aldisi, R., Buness, A., Fröhlich, H., Hassanin, E., Klinkhammer, H., Krawitz, P., Maj, C., Mayr, A., Sivalingam, S.
Published 2022

Sensitive period-regulating genetic pathways and exposure to adversity shape risk for depression

by Crawford, K.M, Davis, K.A, de Leeuw, C., Dunn, E.C, Hensch, T.K, Lussier, A.A, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Ramírez-Tapia, J.C, Smoller, J.W, Takesian, A.E, Wang, M.-J, Zhu, Y.
Published 2022

Association of clonal hematopoiesis with chronic obstructive pulmonary disease

by Barr, R.G, Bick, A.G, Cade, B.E, Cho, M.H, Correa, A., Cupples, L.A, Ebert, B.L, for the COPDGene Study Investigators, National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine Consortium, Gharib, S.A, Gibson, C.J, Gogarten, S.M, Honigberg, M.C, Jain, D., Jaiswal, S., Lange, L.A, Leventhal, M., Levy, B.D, London, S.J, Manichaikul, A., McConkey, M.E, Miller, B.C, Miller, P.G, Moll, M., Natarajan, P., Neuberg, D., Niroula, A., O'Connor, G.T, Oelsner, E.C, Owen, C.A, Qiao, D., Ramachandran, V., Redline, S., Rich, S.S, Rojas-Quintero, J., Rotter, J.I, Sandoval, B., Shi, W., Sholl, L., Silverman, E.K, Sperling, A.S, Tesfaigzi, Y., van Galen, P., Viswanathan, K., Werner, L., Yu, B.
Published 2022

Biomedical Data Commons (BMDC) prioritizes B-lymphocyte non-coding genetic variants in Type 1 Diabetes

by Bhardwaj, P., Gaddam, S., Guha, R.V, Oro, A.E, Piekos, S.N, Radhakrishnan, P.
Published 2021

Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass Disorders

by Barvencik, F., Beller, G., Delsmann, A., Ehmke, N., Genest, F., Hofbauer, L.C, Jakob, F., Kornak, U., Krüger, U., Mundlos, S., Oheim, R., Rolvien, T., Schinke, T., Schubach, M., Seefried, L., Stürznickel, J., Tsourdi, E., Vettorazzi, E., Zemojtel, T.
Published 2022