Publications by authors named "David Porteous"

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Methylome-wide association studies and epigenetic biomarker development for 133 mass spectrometry-assessed circulating proteins in 14,671 Generation Scotland participants.
Josephine A Robertson, Jakub Bajzik, Spyros Vernardis, Aleksandra D Chybowska, Daniel L McCartney, David J Porteous

Genome Biol· December 2025

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Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortex.
Kuldeep Kumar, Sayeh Kazem, Guillaume Huguet, Worrawat Engchuan, Jakub Kopal, David Porteous

bioRxiv· November 2025

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Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortex.
Kuldeep Kumar, Sayeh Kazem, Guillaume Huguet, Worrawat Engchuan, Jakub Kopal, David Porteous

Res Sq· November 2025

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Effectiveness and Costs of Participant Recruitment Strategies to a Web-Based Population Cohort: Observational Study.
Hannah Milbourn, Archie Campbell, Fiona Clark, Elly Darrah, Robin Flaig, David J Porteous

J Med Internet Res· October 2025

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Polygenic prediction of body mass index and obesity through the life course and across ancestries.
Roelof A J Smit, Kaitlin H Wade, Qin Hui, Joshua D Arias, Xianyong Yin, David J Porteous

Nat Med· September 2025

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Data Resource Profile: Whole-Blood DNA Methylation Resource in Generation Scotland (MeGS).
Rosie M Walker, Daniel L McCartney, Kevin Carr, Michael Barber, Xueyi Shen, David J Porteous

Int J Epidemiol· June 2025

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UK Longitudinal Linkage Collaboration (UK LLC): The National Trusted Research Environment for Longitudinal Research.
Andy Boyd, Katharine M Evans, Emma L Turner, Robin Flaig, Jacqui Oakley, David Porteous

Int J Popul Data Sci· May 2025

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Genome-wide characterization of 54 urinary metabolites reveals molecular impact of kidney function.
Erkka Valo, Anne Richmond, Stefan Mutter, Emma H Dahlström, Archie Campbell, David J Porteous

Nat Commun· January 2025

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Methods applied to neonatal dried blood spot samples for secondary research purposes: a scoping review.
Jordan Canning, Rona J Strawbridge, Zosia Miedzybrodzka, Riccardo E Marioni, Mads Melbye, David J Porteous

Crit Rev Clin Lab Sci· December 2024

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Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes.
Guillaume Huguet, Thomas Renne, Cécile Poulain, Alma Dubuc, Kuldeep Kumar, David Porteous

Cell Genom· December 2024

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Genetic architecture reconciles linkage and association studies of complex traits.
Julia Sidorenko, Baptiste Couvy-Duchesne, Kathryn E Kemper, Gunn-Helen Moen, Laxmi Bhatta, David Porteous

Nat Genet· November 2024

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Generation Scotland: an update on Scotland's longitudinal family health study.
Hannah Milbourn, Daniel McCartney, Anne Richmond, Archie Campbell, Robin Flaig, David J Porteous

BMJ Open· June 2024

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Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
Nick Shrine, Anna L Guyatt, A Mesut Erzurumluoglu, Victoria E Jackson, Brian D Hobbs, David J Porteous

Nat Genet· May 2024

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Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability.
Zoe Schmilovich, Vincent-Raphaël Bourque, Elise Douard, Guillaume Huguet, Cécile Poulain, David Porteous

Front Psychiatry· May 2024

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X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements.
Markus Scholz, Katrin Horn, Janne Pott, Matthias Wuttke, Andreas Kühnapfel, David J Porteous

Nat Commun· January 2024

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Correction: Epigenetic scores for the circulating proteome as tools for disease prediction.
Danni A Gadd, Robert F Hillary, Daniel L McCartney, Shaza B Zaghlool, Anna J Stevenson, David J Porteous

Elife· November 2023

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Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability.
Zoe Schmilovich, Vincent-Raphaël Bourque, Elise Douard, Guillaume Huguet, Cécile Poulain, David Porteous

medRxiv· November 2023

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Genome-wide association study of susceptibility to hospitalised respiratory infections.
Alexander T Williams, Nick Shrine, Hardeep Naghra-van Gijzel, Joanna C Betts, Jing Chen, David J Porteous

Wellcome Open Res· November 2023

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Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.
Nick Shrine, Abril G Izquierdo, Jing Chen, Richard Packer, Robert J Hall, David Porteous

Nat Genet· October 2023

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Elevated symptoms of depression and anxiety among family members and friends of critically ill COVID-19 patients - an observational study of five cohorts across four countries.
Anikó Lovik, Juan González-Hijón, Asle Hoffart, Chloe Fawns-Ritchie, Ingibjörg Magnúsdóttir, David J Porteous

Lancet Reg Health Eur· October 2023

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Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization.
Sara M Willems, Natasha H J Ng, Juan Fernandez, Rebecca S Fine, Eleanor Wheeler, David Porteous

Wellcome Open Res· October 2023

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Genetic insights into resting heart rate and its role in cardiovascular disease.
Yordi J van de Vegte, Ruben N Eppinga, M Yldau van der Ende, Yanick P Hagemeijer, Yuvaraj Mahendran, David J Porteous

Nat Commun· August 2023

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Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans.
Chenhao Gao, Carmen Amador, Rosie M Walker, Archie Campbell, Rebecca A Madden, David J Porteous

Genome Biol· May 2023

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Development and validation of DNA methylation scores in two European cohorts augment 10-year risk prediction of type 2 diabetes.
Yipeng Cheng, Danni A Gadd, Christian Gieger, Karla Monterrubio-Gómez, Yufei Zhang, David J Porteous

Nat Aging· April 2023

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