What can genetics tell us about the schizophrenia construct?

by Smoller, J.W
Published 2022

Indian genetic heritage in Southeast Asian populations

by Altınışık, N.E, Boonthai, W., Changmai, P., Flegontov, P., Flegontova, O., Inta, A., Jaisamut, K., Kampuansai, J., Kutanan, W., Pamjav, H., Reich, D., Yüncü, E.
Published 2022

Sparse deep neural networks on imaging genetics for schizophrenia case–control classification

by Agartz, I., Andreassen, O.A, Calhoun, V.D, Chen, J., Ford, J.M, Ji, S., Jönsson, E., Li, X., Liu, J., Macciardi, F., Mathalon, D.H, O'Leary, D.S, Turner, J.A, van Erp, T.G.M, Wang, L., Westlye, L.T
Published 2021

Genetic researches among Malaysian familial hypercholesterolaemic population

by Al-Khateeb, A.R, Al-Talib, H.
Published 2016

Gene Set Enrichment Analsyes Identiify Pathways Involved in Genetic Risk for Diabetic Retinopathy: GSEA Identify Pathways Involved in Genetic Risk for DR

by Adler, S.G, Bowden, D.W, Burdon, K.P, Chen, C.J, Chew, E.Y, Cotch, M.F, Craig, J.E, Freedman, B.I, Igo Jr, R.P, Iyengar, S.K, Jensen, R.A, Klein, B.E.K, Kuo, J.Z, Li, A., Li, X., Mitchell, P., Ng, M.C.Y, Penman, A., Pollack, S., Rotter, J.I, Rouhana, J.M, Segrè, A.V, Smith, A.V, Sobrin, L., Stanwyck, L., Susarla, G., Taylor, K.D, Wang, J.J, Wong, T.Y, Yaspan, B.
Published 2022

The morphometry of left cuneus mediating the genetic regulation on working memory

by Fu, J., He, X., Li, W., Li, X., Liu, H., Qin, W., Xu, J., Ye, Z., Yu, C., Zhang, P.
Published 2021

Unravelling the genetic history of Negritos and Indigenous populations of Southeast Asia

by Aghakhanian, F., Hoh, B.P, Jinam, T., Manica, A., Naidu, R., Phipps, M.E, Yunus, Y.
Published 2015

Genetic dissection of complex traits using hierarchical biological knowledge

by Ideker, T., Kreisberg, J.F, Tanaka, H.
Published 2021

Exploration of the Genetic Diversity of Solina Wheat and Its Implication for Grain Quality

by De Flaviis, R., Mastrocola, D., Morcia, C., Sacchetti, G., Santarelli, V., Terzi, V., Tumino, G.
Published 2022

VEGF-A-related genetic variants protect against Alzheimer's disease

by Dedoussis, G., Fitzgerald, P., Kafyra, M., Lamont, J., Masson, C., Murray, H., Petrelis, A.M, Stathopoulou, M.G, Visvikis-Siest, S., Yen, F.T
Published 2022

Genome-wide variant-based study of genetic effects with the largest neuroanatomic coverage

by Bao, P., Chen, F., Fang, S., Gao, Y., Jiang, H., Li, H., Li, J., Li, Y., Liang, H., Liu, W., Luo, H.
Published 2021

Inferred expression regulator activities suggest genes mediating cardiometabolic genetic signals

by Amundadottir, L.T, Chung, C.C, Collins, I., Connelly, K., Hoskins, J.W, O'Brien, A., Shi, J., Zhong, J.
Published 2021

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

Subtype-specific and co-occurring genetic alterations in B-cell non-Hodgkin lymphoma

by Akhter, A., Bhalla, K., Bouska, A., Buckley, S., Carey, C., Chen, B.J, Davidson, M., Davis, R.E, Deng, Q., Fowler, N.H, Gandhi, M., Ghosh, S., Green, M.R, Greiner, T., Hartert, K., Heavican, T., Iqbal, J., Jain, N., Lunning, M.A, Ma, M.C.J, Mansoor, A., Moore, D., Nastoupil, L.J, Neelapu, S., Parekh, S., Perumal, D., Rodig, S.J, Showell, J., Sohani, A.R, Stewart, D., Street, L., Tadros, S., Tobin, J., Vose, J.M, Westin, J.R, Yang, H.
Published 2022

Estimation of regional polygenicity from GWAS provides insights into the genetic architecture of complex traits

by Burch, K.S, Hou, K., Johnson, R., Paciuc, M., Pasaniuc, B., Sankararaman, S.
Published 2021

Genome-wide association studies dissect the genetic architecture of seed shape and size in common bean

by Chiorato, A.F, Gama, H.C, Garcia, A.A.F, Giordani, W., Vieira, M.L.C
Published 2022

Transcript annotation tool (TransAT): an R package for retrieving annotations for transcript-specific genetic variants

by Chattopadhyay, A., Lu, T.-P, Shih, C.-Y, Tien, Y.-W, Wu, C.-H
Published 2021

Genetic analysis of 39 erythrocytosis and hereditary hemochromatosis-associated genes in the Slovenian family with idiopathic erythrocytosis

by Anžej Doma, S., Debeljak, N., Fink, M., Gašperšič, J., Količ, R., Kristan, A., Kunej, T., Pajič, T., Podgornik, H., Preložnik Zupan, I., Režen, T., Vuga, A., Žula, Š
Published 2021

Genetic analysis of over half a million people characterises C-reactive protein loci

by Alizadeh, B.Z, Bodinier, B., Chadeau-Hyam, M., Chasman, D.I, Dehghan, A., Elliott, P., Evangelou, E., Jarvelin, M.-R, Karhunen, V., Koskeridis, F., Ligthart, S., Pazoki, R., Said, S., Sattar, N., Tzoulaki, I., Võsa, U., Welsh, P.
Published 2022

Meta-Analysis of the Genetic Association between PTPN22 and CTLA-4 Variants and Risk of Uveitis

by Hu, S., Qi, J., Zhang, J., Zhou, P.
Published 2022