Search Results - "Dahl, Andy"
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A robust model for cell type-specific interindividual variation in single-cell RNA sequencing data
Published in Nature communications (19-06-2024)“…Single-cell RNA sequencing (scRNA-seq) has been widely used to characterize cell types based on their average gene expression profiles. However, most studies…”
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Cross-trait assortative mating is widespread and inflates genetic correlation estimates
Published in Science (American Association for the Advancement of Science) (18-11-2022)“…The observation of genetic correlations between disparate human traits has been interpreted as evidence of widespread pleiotropy. Here, we introduce…”
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A Robust Method Uncovers Significant Context-Specific Heritability in Diverse Complex Traits
Published in American journal of human genetics (02-01-2020)“…Gene-environment interactions (GxE) can be fundamental in applications ranging from functional genomics to precision medicine and is a conjectured source of…”
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Molecular Genetic Analysis Subdivided by Adversity Exposure Suggests Etiologic Heterogeneity in Major Depression
Published in The American journal of psychiatry (01-06-2018)“…Objective:The extent to which major depression is the outcome of a single biological mechanism or represents a final common pathway of multiple disease…”
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Reverse GWAS: Using genetics to identify and model phenotypic subtypes
Published in PLoS genetics (05-04-2019)“…Recent and classical work has revealed biologically and medically significant subtypes in complex diseases and traits. However, relevant subtypes are often…”
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Genetic Influences on Disease Subtypes
Published in Annual review of genomics and human genetics (31-08-2020)“…Disease classification, or nosology, was historically driven by careful examination of clinical features of patients. As technologies to measure and understand…”
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Factorizing polygenic epistasis improves prediction and uncovers biological pathways in complex traits
Published in American journal of human genetics (02-11-2023)“…Epistasis is central in many domains of biology, but it has not yet been proven useful for understanding the etiology of complex traits. This is partly because…”
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On Negative Heritability and Negative Estimates of Heritability
Published in Genetics (Austin) (01-06-2020)“…Abstract We consider the problem of interpreting negative maximum likelihood estimates of heritability that sometimes arise from popular statistical models of…”
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Adjusting for Principal Components of Molecular Phenotypes Induces Replicating False Positives
Published in Genetics (Austin) (01-04-2019)“…High-throughput measurements of molecular phenotypes provide an unprecedented opportunity to model cellular processes and their impact on disease. These highly…”
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46. DISENTANGLE THE GENETIC HETEROGENEITY OF MAJOR DEPRESSIVE DISORDER (MDD)
Published in European neuropsychopharmacology (01-10-2024)“…Major Depressive Disorder (MDD) is a highly prevalent and heterogeneous disease. MDD patients diagnosed with the diagnostic and statistical manual of mental…”
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COORDINATED EPISTASIS DETECTS HETEROGENOUS PATHWAYS ACROSS PSYCHIATRIC DISORDERS AND COMORBIDITIES
Published in European neuropsychopharmacology (01-10-2024)“…Cross-disorder analyses in psychiatry often center around genetic correlation, which quantifies the average similarity of genetic effects across two disorders…”
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A model and test for coordinated polygenic epistasis in complex traits
Published in Proceedings of the National Academy of Sciences - PNAS (13-04-2021)“…Interactions between genetic variants—epistasis—is pervasive in model systems and can profoundly impact evolutionary adaption, population disease dynamics,…”
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Deep learning-based phenotype imputation on population-scale biobank data increases genetic discoveries
Published in Nature genetics (01-12-2023)“…Biobanks that collect deep phenotypic and genomic data across many individuals have emerged as a key resource in human genetics. However, phenotypes in…”
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On Negative Heritability and Negative Estimates of Heritability
Published in Genetics (Austin) (01-06-2020)“…We consider the problem of interpreting negative maximum likelihood estimates of heritability that sometimes arise from popular statistical models of additive…”
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14. COORDINATED EPISTASIS REVEALS SYMPTOM-SPECIFIC POLYGENIC PATHWAY INTERACTIONS IN MAJOR DEPRESSIVE DISORDER
Published in European neuropsychopharmacology (01-10-2023)“…Patients diagnosed with Major Depressive Disorder (MDD) often exhibit very diverse symptom profiles, some of which have no symptoms in common. As a result, MDD…”
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83. FAMILY HISTORY SCORES COMPLEMENT POLYGENIC SCORE DESCRIPTIONS OF PSYCHIATRIC GENETIC ARCHITECTURE: THEORY AND PRACTICE
Published in European neuropsychopharmacology (01-10-2022)Get full text
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22 - MOLECULAR GENETIC ANALYSIS SUBDIVIDED BY ADVERSITY EXPOSURE SUGGESTS ETIOLOGIC HETEROGENEITY IN MAJOR DEPRESSION
Published in European neuropsychopharmacology (2019)“…The extent to which Major Depression (MD) is the outcome of a single biological mechanism or represents a final common pathway of multiple disease processes…”
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Network inference in matrix-variate Gaussian models with non-independent noise
Published 05-12-2013“…Inferring a graphical model or network from observational data from a large number of variables is a well studied problem in machine learning and computational…”
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