Are your covariates under control? How normalization can re-introduce covariate effects

por Pain, Oliver, Dudbridge, Frank, Ronald, Angelica
Publicado 2018

Genetic overlap between psychotic experiences in the community across age and with psychiatric disorders

por Barkhuizen, Wikus, Pain, Oliver, Dudbridge, Frank, Ronald, Angelica
Publicado 2020

Delineating the Genetic Component of Gene Expression in Major Depression

por Dall’Aglio, Lorenza, Lewis, Cathryn M., Pain, Oliver
Publicado 2021

Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence

por Donati, Georgina, Dumontheil, Iroise, Pain, Oliver, Asbury, Kathryn, Meaburn, Emma L.
Publicado 2021

Clinicians’ Perceptions towards Precision Medicine Tools for Cardiovascular Disease Risk Stratification in South Africa

por Kamp, Michelle, Pain, Oliver, May, Andrew, Lewis, Cathryn M., Ramsay, Michèle
Publicado 2022

Transcriptome-wide association study of treatment-resistant depression and depression subtypes for drug repurposing

por Fabbri, Chiara, Pain, Oliver, Hagenaars, Saskia P., Lewis, Cathryn M., Serretti, Alessandro
Publicado 2021

Impute.me: An Open-Source, Non-profit Tool for Using Data From Direct-to-Consumer Genetic Testing to Calculate and Interpret Polygenic Risk Scores

por Folkersen, Lasse, Pain, Oliver, Ingason, Andrés, Werge, Thomas, Lewis, Cathryn M., Austin, Jehannine
Publicado 2020

A tool for translating polygenic scores onto the absolute scale using summary statistics

por Pain, Oliver, Gillett, Alexandra C., Austin, Jehannine C., Folkersen, Lasse, Lewis, Cathryn M.
Publicado 2022

Stratified genome-wide association analysis of type 2 diabetes reveals subgroups with genetic and environmental heterogeneity

por Christiansen, Colette E, Arathimos, Ryan, Pain, Oliver, Molokhia, Mariam, Bell, Jordana T, Lewis, Cathryn M
Publicado 2023

Could interventions on physical activity mitigate genomic liability for obesity? Applying the health disparity framework in genetically informed studies

por Herle, Moritz, Pickles, Andrew, Pain, Oliver, Viner, Russell, Pingault, Jean-Baptiste, De Stavola, Bianca L.
Publicado 2023

Transcriptome-wide association study of HIV-1 acquisition identifies HERC1 as a susceptibility gene

por Duarte, Rodrigo R.R., Pain, Oliver, Furler, Robert L., Nixon, Douglas F., Powell, Timothy R.
Publicado 2022

Genome‐wide analysis of adolescent psychotic‐like experiences shows genetic overlap with psychiatric disorders

por Pain, Oliver, Dudbridge, Frank, Cardno, Alastair G., Freeman, Daniel, Lu, Yi, Lundstrom, Sebastian, Lichtenstein, Paul, Ronald, Angelica
Publicado 2018

Cis-effects on gene expression in the human prenatal brain associated with genetic risk for neuropsychiatric disorders

por Hall, Lynsey S., Pain, Oliver, O’Brien, Heath E., Anney, Richard, Walters, James T. R., Owen, Michael J., O’Donovan, Michael C., Bray, Nicholas J.
Publicado 2021

Imputed gene expression risk scores: a functionally informed component of polygenic risk

por Pain, Oliver, Glanville, Kylie P, Hagenaars, Saskia, Selzam, Saskia, Fürtjes, Anna, Coleman, Jonathan R I, Rimfeld, Kaili, Breen, Gerome, Folkersen, Lasse, Lewis, Cathryn M
Publicado 2021

Exploring polygenic‐environment and residual‐environment interactions for depressive symptoms within the UK Biobank

por Gillett, Alexandra C., Jermy, Bradley S., Lee, Sang Hong, Pain, Oliver, Howard, David M., Hagenaars, Saskia P., Hanscombe, Ken B., Coleman, Jonathan R. I., Lewis, Cathryn M.
Publicado 2022

Harnessing Transcriptomic Signals for Amyotrophic Lateral Sclerosis to Identify Novel Drugs and Enhance Risk Prediction

por Pain, Oliver, Jones, Ashley, Al Khleifat, Ahmad, Agarwal, Devika, Hramyka, Dzmitry, Karoui, Hajer, Kubica, Jędrzej, Llewellyn, David J., Ranson, Janice M., Yao, Zhi, Iacoangeli, Alfredo, Al-Chalabi, Ammar
Publicado 2023

Novel Insight Into the Etiology of Autism Spectrum Disorder Gained by Integrating Expression Data With Genome-wide Association Statistics

por Pain, Oliver, Pocklington, Andrew J., Holmans, Peter A., Bray, Nicholas J., O’Brien, Heath E., Hall, Lynsey S., Pardiñas, Antonio F., O’Donovan, Michael C., Owen, Michael J., Anney, Richard
Publicado 2019

Multiple measures of depression to enhance validity of major depressive disorder in the UK Biobank

por Glanville, Kylie P., Coleman, Jonathan R. I., Howard, David M., Pain, Oliver, Hanscombe, Ken B., Jermy, Bradley, Arathimos, Ryan, Hübel, Christopher, Breen, Gerome, O'Reilly, Paul F., Lewis, Cathryn M.
Publicado 2021

Evaluation of polygenic prediction methodology within a reference-standardized framework

por Pain, Oliver, Glanville, Kylie P., Hagenaars, Saskia P., Selzam, Saskia, Fürtjes, Anna E., Gaspar, Héléna A., Coleman, Jonathan R. I., Rimfeld, Kaili, Breen, Gerome, Plomin, Robert, Folkersen, Lasse, Lewis, Cathryn M.
Publicado 2021

A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia

por Hall, Lynsey S, Medway, Christopher W, Pain, Oliver, Pardiñas, Antonio F, Rees, Elliott G, Escott-Price, Valentina, Pocklington, Andrew, Bray, Nicholas J, Holmans, Peter A, Walters, James T R, Owen, Michael J, O’Donovan, Michael C
Publicado 2020