Silviu-Alin Bacanu
Affiliations: | Virginia Commonwealth University School of Medicine, Richmond, VA |
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Publications
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Dahl A, Thompson M, An U, et al. (2023) Phenotype integration improves power and preserves specificity in biobank-based genetic studies of major depressive disorder. Nature Genetics |
Ahangari M, Gentry AE, Hassan MF, et al. (2023) Improving the discovery of rare variants associated with alcohol problems by leveraging machine learning phenotype prediction and functional information. Biorxiv : the Preprint Server For Biology |
Nievergelt CM, Maihofer AX, Atkinson EG, et al. (2023) Discovery of 95 PTSD loci provides insight into genetic architecture and neurobiology of trauma and stress-related disorders. Medrxiv : the Preprint Server For Health Sciences |
Gedik H, Peterson RE, Riley BP, et al. (2023) Integrative Post-Genome-Wide Association Study Analyses Relevant to Psychiatric Disorders: Imputing Transcriptome and Proteome Signals. Complex Psychiatry. 9: 130-144 |
Gedik H, Nguyen TH, Peterson RE, et al. (2023) Identifying potential risk genes and pathways for neuropsychiatric and substance use disorders using intermediate molecular mediator information. Frontiers in Genetics. 14: 1191264 |
Denham AN, Drake J, Gavrilov M, et al. (2022) Long Non-Coding RNAs: The New Frontier into Understanding the Etiology of Alcohol Use Disorder. Non-Coding Rna. 8 |
Ahangari M, Everest E, Nguyen TH, et al. (2022) Genome-wide analysis of schizophrenia and multiple sclerosis identifies shared genomic loci with mixed direction of effects. Brain, Behavior, and Immunity. 104: 183-190 |
Sahajpal NS, Jill Lai CY, Hastie A, et al. (2022) Optical genome mapping identifies rare structural variations as predisposition factors associated with severe COVID-19. Iscience. 103760 |
Nguyen TH, He X, Brown RC, et al. (2021) DECO: a framework for jointly analyzing de novo and rare case/control variants, and biological pathways. Briefings in Bioinformatics |
Chatzinakos C, Lee D, Cai N, et al. (2021) Increasing the resolution and precision of psychiatric genome-wide association studies by re-imputing summary statistics using a large, diverse reference panel. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics |