What can genetics tell us about the schizophrenia construct?

by Smoller, J.W
Published 2022

Genetic dissection of complex traits using hierarchical biological knowledge

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

Genetic analysis and prenatal diagnosis of 20 Chinese families with oculocutaneous albinism

by Li, H., Mao, Y., Tang, S., Xiang, Y., Xu, C., Xu, X., Xu, Y., Zhou, L.
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

CYP2D6 Genetic Polymorphisms and Phenotypes in Different Ethnicities of Malaysian Breast Cancer Patients

by Abdul Rahman, S., Chan, S.C, Chin, F.W, Noor Akmal, S., Rosli, R.
Published 2016

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

Gene-Environment Interaction Analysis Incorporating Sex, Cardiometabolic Diseases, and Multiple Deprivation Index Reveals Novel Genetic Associations With COVID-19 Severity

by Lin, J., Manning, A.K, Marchek, C., Sevilla-Gonzalez, M.D.R, Tadess, B., Westerman, K.E
Published 2022

PharmGKB, an Integrated Resource of Pharmacogenomic Knowledge

by Gong, L., Klein, T.E, Whirl-Carrillo, M.
Published 2021

Genetic differences in the behavioral organization of binge eating, conditioned food reward, and compulsive-like eating in C57BL/6J and DBA/2J strains

by Babbs, R.K, Bryant, C.D, Kelliher, J.C, Luttik, K.P, Mulligan, M.K, Scotellaro, J.L
Published 2018

Reward Deficiency Syndrome (RDS) Surprisingly Is Evolutionary and Found Everywhere: Is It “Blowin’ in the Wind”?

by Badgaiyan, R.D, Baron, D., Blum, K., Bowirrat, A., Braverman, E.R, Cadet, J.L, Ceccanti, M., Elman, I., Gold, M.S, Gomez, L.L, Green, R., Gupta, A., Jalali, R., McLaughlin, T., Modestino, E.J, Simpatico, T.A, Thanos, P.K
Published 2022

CADA: Phenotype-driven gene prioritization based on a case-enriched knowledge graph

by Ahmad, A., Brunet, T., Danyel, M., Dieck, S., Ehmke, N., Fleischer, N., Fröhlich, H., Haack, T., Kamphans, T., Knaus, A., Krawitz, P., Mehnert, L., Nadav, G., Ossowski, S., Peng, C., Rosnev, S., Schmid, A., Wagner, M., Wenzel, M., Zirn, B.
Published 2021

Molecular cytogenetic studies of a male carrier with a unique (Y;14) translocation: Case report

by Chen, S., Jiang, Y., Li, L., Liu, R., Xi, Q., Zhang, H., Zhang, X.
Published 2021

Using the PhenX Toolkit to Select Standard Measurement Protocols for Your Research Study

by Cox, L.A, Engle, M.L, Haines, J., Hamilton, C.M, Hendershot, T., Hwang, S., Marazita, M.L, McCarty, C.A, Pan, H., Ramos, E.M
Published 2021

Redundancy-selection trade-off in phenotype-structured populations

by Azaele, S., Evans, R.M.L, Miele, L.
Published 2021

Genome-wide identification of tomato xylem sap fitness factors for three plant-pathogenic ralstonia species

by Carlson, H.K, Deutschbauer, A.M, Georgoulis, S.J, Hamilton, C.D, Helmann, T.C, Lowe-Power, T.M, Shalvarjian, K.E
Published 2021

Novel GREM1 variations in Sub-Saharan African patients with cleft lip and/or cleft palate

by Abdur-Rahman, L.O, Adeyemo, A.A, Adeyemo, W.L, Agbenorku, P., Aregbesola, B.S, Audu, R., Bello, S.A, Busch, T.D, Butali, A., Donkor, P., Eshete, M.A, Gowans, L.J.J, Marazita, M.L, Mossey, P.A, Murray, J.C, Obiri-Yeboah, S., Oginni, F.O, Ogunlewe, M.O, Olaitan, P.B, Onwuamah, C., Oseni, G., Oti, A.A, Owais, A., Plange-Rhule, G.
Published 2018

Learning, visualizing and exploring 16S rRNA structure using an attention-based deep neural network

by Agbavor, F., Mell, J.C, Rosen, G.L, Sokhansanj, B.A, Woloszynek, S., Zhao, Z.
Published 2021

Application of high-throughput sequencing for hereditary thrombocytopenia in southwestern China

by Dou, Y., Guan, X., Guo, Y., Luo, M., Wen, X., Xian, Y., Yu, J., Zhang, L.
Published 2021

Investigation of SOSTDC1 gene in non-syndromic patients with supernumerary teeth

by Arikan, V., Cumaogullari, O., Oz, F.-T, Ozgul, B.-M
Published 2018