Linking the Twins Early Development Study (TEDS) With NHS Electronic Health Records

The Twins Early Development Study (TEDS) is a longitudinal population study of over 10,000 twin pairs born in England and Wales between 1994 and 1996. As the twins enter their thirties, a primary focus of TEDS is to better understand the development of common physical and mental health problems and the relationship with the different social milestones of adulthood (e.g., employment, partnerships, and/or parenthood). With over 30 years of prospectively collected questionnaire and genetic data, the study is uniquely placed to answer questions about the health challenges facing young adults today. Incorporating linked medical records with the existing research data will provide a different data perspective on our twin's health status and outcomes and support more equitable research by helping to address both response and attrition bias. This article provides an overview of the protocol to link TEDS participants to electronic health records collected by the UK National Health Service (NHS). It will outline the linkage process, characterize the available linked study sample and NHS datasets, and describe the legal basis for this work.

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Publication Details

Journal
Twin Research and Human Genetics
Published
2026-05-21
DOI
https://doi.org/10.1017/thg.2026.10066
Primary Topic
Cognitive Abilities and Testing
Type
article
Field-Weighted Citation Impact
0.00

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article

Linking the Twins Early Development Study (TEDS) With NHS Electronic Health Records

Shannon Bristow, T. C. Eley, Ray Leal, Megan Skelton et al.
Twin Research and Human Genetics
Cognitive Abilities and Testing
article

Linking the Twins Early Development Study (TEDS) With NHS Electronic Health Records

Shannon Bristow, T. C. Eley, Ray Leal, Megan Skelton, Rachel Ogden, Andy Boyd, Andrew McMillan, Alex Dregan, Johnny Downs, Robert Plomin, Celestine Lockhart, Louise Webster, Helen L. Fisher
article en

Abstract

The Twins Early Development Study (TEDS) is a longitudinal population study of over 10,000 twin pairs born in England and Wales between 1994 and 1996. As the twins enter their thirties, a primary focus of TEDS is to better understand the development of common physical and mental health problems and the relationship with the different social milestones of adulthood (e.g., employment, partnerships, and/or parenthood). With over 30 years of prospectively collected questionnaire and genetic data, the study is uniquely placed to answer questions about the health challenges facing young adults today. Incorporating linked medical records with the existing research data will provide a different data perspective on our twin's health status and outcomes and support more equitable research by helping to address both response and attrition bias. This article provides an overview of the protocol to link TEDS participants to electronic health records collected by the UK National Health Service (NHS). It will outline the linkage process, characterize the available linked study sample and NHS datasets, and describe the legal basis for this work.

Twin Research and Human Genetics
King's College London (GB), South London and Maudsley NHS Foundation Trust (GB), University of Bristol (GB), NIHR Maudsley Dementia Biomedical Research Unit (GB), Hologic (Germany) (DE)
Government of the United Kingdom, National Institute for Health and Care Research, King's College London, Swansea University, NIHR Maudsley Biomedical Research Centre, Medical Research Council, Economic and Social Research Council
Partnerships for the goals
Openalex Percentile: Top 5%
Cognitive Abilities and Testing
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