Diversity and Inclusion

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The NIHR BioResource Centre Maudsley Team's Commitment to responsible and ethical science

The NIHR BioResource department strives to be a diverse and supportive research environment that is open and welcoming to all. We recognise that certain groups have a more difficult journey into academia, so we would especially like to hear from you and recruit more individuals from diverse minority and marginalised backgrounds into our teams. We are committed to contributing to the Open Science Movement, to make scientific research and data accessible to all.

Our efforts and general principles in these domains are listed below.

Commitment to participants

We recognise that our research involves sensitive research topics, thus we have set out our commitments to our participants below:

  • The NIHR BioResource Centre Maudsley, and its studies included in the NIHR Mental Health BioResource such as GLAD and EDGI, recognises that research involving genetics is especially sensitive and as such, we have a responsibility to be transparent about how we collect, analyse and store your data, as well as who has access to this.
  • All of the data we gather is stored securely in accordance with the necessary legislation. We take the protection and privacy of your data very seriously, and you can find out how we do this here.
  • New collaborators' requests to use the research data we collect will be closely examined by a multidisciplinary data access panel, and will be assessed for research justification and potential, and ethicality. Where appropriate, public representatives from the groups involved in research will sit on this panel.
  • Any data that is shared with researchers or companies for ethically approved projects will be securely transferred with your personal details (such as name) removed prior to sharing it, so that it is anonymous to anyone outside NIHR Mental Health BioResource or NIHR BioResource Centre Maudsley teams. If for some reason we need to pass on your contact details, for example so a clinical trial team can contact, we will ensure you are contacted by us to specifically consent to this.
  • Specifically, we commit that NIHR Mental Health BioResource or NIHR BioResource Centre Maudsley will never knowingly share data with projects that intend to link genetics to race. Researchers within the NIHR Mental Health BioResource or NIHR BioResource Centre Maudsley at King's College London firmly state that the social construct of race is not based on science and that this idea has no place in our research.
  • We are committed to building relationships with underrepresented communities, to achieve better diversity within our research studies and research staff.

Research methods

Our team will conduct research using up-to-date guidance and best practice within the field. These are likely to change over time according to changes in society or new findings in science.

How will we use information about self-reported ancestry?

Analyses that stratify by self-reported ethnicity will only be done to compare social risk factors and specific symptoms or disorders rates between groups. The way we ask people about their ethnicity follows NHS guidance and practise, and allows us to compare the cohorts we recruit with NHS baseline data. These analyses will be undertaken in collaboration with individuals from representative communities to ensure fair and balanced assessment of results.

How do we use population genetics in our studies?

Population genetics is the study of genetic variation within populations, and involves the examination and modelling of changes in the frequencies of genetic variants in populations over space (distance) and time (measured in thousands of years). Specifically, it examines genetic variations that differ in their frequency between (1) European ancestral populations, (2) diverse South Asian ancestral populations, and (3) highly diverse African ancestral populations as well as other populations.

[You'll find we use the term “ancestry” over “race” or “ethnicity” when discussing genetics research. Race and ethnicity are not valid indicators for any underlying biological differences between individuals (e.g., genetics). For these reasons, racial categories and ethnic groups should only be used when discussing social constructs such as racial or cultural experiences.]

Research has shown that the vast majority of genetic variations that differ between ancestries have no association with either diseases or traits. So, if a disease occurs more frequently in a certain group, it is not definitively because this group has a genetic predisposition that makes them more vulnerable to this disease, but rather it would be important and helpful to examine both genetic and social/environmental potential risk factors. To prevent false positive and false negative findings that mistake genetic differences for social differences, or the reverse, we use the methods of population genetics to adjust for population ancestry in our analyses.

Most frequently, we use population genetic methods to prevent us reaching false conclusions due to slightly different ancestry between the groups we wish to compare in a study, such as when we compare cases of depression to an unaffected control group. Another benefit is that, by allowing us to find true associations in different ancestry groups, they allow the discovery of new biological causes of the disorders we look at. We know if we look at just one population we will not be able to find all of the biological mechanisms relevant to a disorder, including mechanisms that may suggest new treatments or interventions.

Diversity

The NIHR Mental Health BioResource and NIHR BioResource Centre Maudsley team commits to:

  • Staying up to date with guidance and best practice in this area.
  • Designing research that is thoughtful and proactive regarding diverse recruitment.
  • Actively pursuing diversity within the team.
  • Acknowledging and supporting all forms of diversity, including within race, gender, sexuality, socio-economic status, and the intersectionality of diversity.
  • Supporting the LGBTQIA+ community and acknowledging the difference between sex and gender.
  • Influencing local research practice via participation in local Anti-Racism Groups.
  • Constantly learning more about issues of diversity, cultural sensitivity, and regularly discussing these within team meetings.
  • Ensuring our staff group include those with lived experience of these issues, working with external highly experienced consultants on sensitive issues when necessary.
  • Sharing and learning from best practice on all matters of inclusivity within our department and across wider KCL faculties.
  • Supporting individuals from groups that are under-represented in academia, and to offer mentoring on a case by case basis (please email gursharan.kalsi@kcl.ac.uk if interested).
  • We will publish a yearly report detailing our efforts and work within diversity and inclusion.

Open Science

  • We particularly focus on collaborative approaches, across populations and cultures, and inclusive, replicable science. We encourage open science strategies including preprints, the Open Science Framework, open access publication and publishing of analysis scripts regularly in the group, with more established team members providing support and examples to newer members of the lab.
  • We pre-register new analysis plans, wherever possible, on the Open Science Framework and support local open, reproducible science networks.
  • Lab members are actively facilitating collaborative research practices to improve peer based review and sharing of code.
  • We support sharing of code and data (where possible) on publication of our papers.
  • We archive our papers at the point of submission whenever possible.
  • We view mistakes made by those at all levels as opportunities for shared learning.
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Am I Eligible?

To take part in the GLAD Study you must either:

  • Have ever experienced anxiety or depressive disorders (with or without a medical diagnosis)
  • Have never experienced any mental health disorder.

AND you must:

  • Be aged 16 or over
  • Live in the United Kingdom

Sign up to the GLAD Study

The Genetic Links to Anxiety and Depression (GLAD) Study is currently only recruiting individuals over the age of 16. If you are younger than 16, unfortunately you are not eligible for the GLAD Study.

You can withdraw from the study at any time.

Already have an account? Login or Recover Password

After completing the sign-up form, the study enrollment process consists of the following four steps:

  • Reading the Information Sheet
  • Providing consent
  • Completing our questionnaire
  • Providing a saliva sample
Talk to us

Our Office hours are:
Monday to Friday 9:00am to 5:00pm

Please note that we will not be able to call you back if the number provided is not a UK based telephone number

Need any help?