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Tag: Legal

New Public Dialogue Highlights Hopes and Concerns for Genomic Medicine in the UK

A major new report based on a public dialogue around genomic medicine was launched last week. A Public Dialogue on … More

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Anna Middleton, Data, DNA, Genomics, Legal, NHS, Research, Research participant, Society and Ethics Research, Survey
Articulating the contract between science and people: DNA data sharing

Articulating the contract between science and people: DNA data sharing

A new deal on data: are you with us? For most of us it is hard to unpick the various … More

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Anna Middleton, Consent, Data, Data - Big, DNA, Genome Research, Genomethics, Legal, Research, Research participant, Scientists, Society and Ethics Research
editing-embryos-could-you-would-you-should-you

Editing embryos – Could you? Would you? Should you? Views from Genetic Counsellors

Genetic counsellors sit on the front line of genomics – translating (literally) the science for people who are trying to … More

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Embryo Editing, Genetic Counselling, Genetic Testing, Legal, Research
Legal duty to share genetic information goes to trial

Legal duty to share genetic information goes to trial

By Vicky Chico and Anna Middleton Following on from our previous blog on the legal duty to share genetic information, … More

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Data, Doctor, Duty of Care, Ethics posts, Family Communication about Genetics, Genetic Testing, Genomethics, Guest Authors, Legal, Society and Ethics Research
Legal duty to share genetic information? ABC v St George’s Healthcare NHS Trust

Legal duty to share genetic information? ABC v St George’s Healthcare NHS Trust

Guest blog by Dr Vicky Chico, Legal Consultant, Society and Ethics Research Group, Wellcome Genome Campus, Cambridge Yesterday myself and … More

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Data, Doctor, Duty of Care, Family Communication about Genetics, Genetic Testing, Guest Authors, Healthcare, Legal
DNA and Big Data

DNA and Big Data: be part of the conversation

The Global Alliance for Genomics and Health (GA4GH) and the Wellcome Genome Campus have launched a new project to explore … More

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Anna Middleton, Attitudes, Consent, Data, Data - Big, DNA, Genomic Research, Healthcare, Legal, Questionnaire, Research, Research participant, Society and Ethics Research, Survey

Recent Posts

  • I:DNA – an immersive exploration into the view of people living with genetic conditions
  • So Much More Than Just a Test, the introductory film to the Voices of Genetic Counsellors short documentary series, is an official selection for the 2020 Imagine Science Film Festival
  • Wellcome Genome Campus Society and Ethics Research Lead on a UK Citizens Assembly.
  • Future of Genomic Research at Risk Without Greater Public Trust in How Genetic Data is Shared, Survey Finds.
  • Genetic Counsellors: Walking on the genetics journey

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Anna Middleton PhD


Head of Society and Ethics Research, Connecting Science at Wellcome Genome Campus, Cambridge, UK. Chair of Association of Genetic Nurses and Counsellors. Continually asking 'how are people making sense of genomics?'


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