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MH077139

Funded outputs count: 101
Funder award ID: MH077139
OpenAlex ID: G8163728846
Analysis of Rare Coding Variation Identifies New Genetic Contributors to Schizophrenia
2026 · Julia M. Sealock, Connor Dowd, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 1
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Classification of schizophrenia, bipolar disorder and major depressive disorder with comorbid traits and deep learning algorithms
2025 · Xiangning Chen, Yimei Lu, et al. · Schizophrenia · 9
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Meta-analysis of epigenetic aging in schizophrenia reveals multifaceted relationships with age, sex, illness duration, and polygenic risk
2024 · Ori, Anil P. S., Mill, Jonathan, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
2024 · Foster, Alison, Curtis, David, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
Technological readiness and implementation of genomic-driven precision medicine for complex diseases
2024 · Melin B, Hagström H, et al. · UTUPub (University of Turku)
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The impact of educational attainment, intelligence and intellectual disability on schizophrenia: a Swedish population-based register and genetic study
2024 · Song J, Larsson H, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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The state of the science in psychiatric genomics
2024 · Kendler K.S, Sullivan P.F · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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The association between family history and genomic burden with schizophrenia mortality: a Swedish population-based register and genetic sample study
2024 · Lichtenstein P, Kowalec K, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
Methylation age acceleration does not predict mortality in schizophrenia
2024 · Ophoff R.A, Hannon E, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
Increasing the clinical psychiatric knowledge base about pathogenic copy number variation
2024 · Sullivan P.F, Owen M.J · Carolina Digital Repository (University of North Carolina at Chapel Hill)
Increased schizophrenia family history burden and reduced premorbid IQ in treatment-resistant schizophrenia: a Swedish National Register and Genomic Study
2024 · Kowalec K, Dalman C, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill) · 1
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Familial risk and heritability of intellectual disability: a population-based cohort study in Sweden
2024 · Butwicka A, Serlachius E, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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Genetic heterogeneity and subtypes of major depression
2024 · Hägg S, Nguyen T.-D, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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Genome-wide association study of patients with a severe major depressive episode treated with electroconvulsive therapy
2024 · Rück C, Landén M, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders
2024 · Geschwind D.H, Sullivan P.F · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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Editorial overview: Rare CNV disorders and neuropsychiatric phenotypes: opportunities, challenges, solutions
2024 · Mulle J.G, Hjerling-Leffler J, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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Characterization of Single Gene Copy Number Variants in Schizophrenia
2024 · Ancalade N, Holmans P, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia
2024 · Pallotto L.M, Farrell M, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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Meta-analysis of epigenetic aging in schizophrenia reveals multifaceted relationships with age, sex, illness duration, and polygenic risk
2024 · Anil P. S. Ori, Loes M. Olde Loohuis, et al. · Clinical Epigenetics · 19
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Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia
2022 · Jia Wen, Brett Trost, et al. · Molecular Psychiatry · 33
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The impact of educational attainment, intelligence and intellectual disability on schizophrenia: a Swedish population-based register and genetic study
2022 · Jie Song, Shuyang Yao, et al. · Molecular Psychiatry · 23
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Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia
2022 · Antonio F. Pardiñas, Sophie E. Smart, et al. · JAMA Psychiatry · 110
Genetic heterogeneity and subtypes of major depression
2022 · Thuy-Dung Nguyen, Arvid Harder, et al. · Molecular Psychiatry · 129
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Familial risk and heritability of intellectual disability: a population‐based cohort study in Sweden
2021 · Paul Lichtenstein, Magnus Tideman, et al. · Journal of Child Psychology and Psychiatry · 33
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Technological readiness and implementation of genomic‐driven precision medicine for complex diseases
2021 · P. W. Franks, E. Melén, et al. · Journal of Internal Medicine · 32
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