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List of works by Gill Haddow

"Because you're worth it?" The taking and selling of transplantable organs

scientific article

'Nothing is really safe': a focus group study on the processes of anonymizing and sharing of health data for research purposes

scientific article

Banking (on) the Brain

Biomedicine, self and society: An agenda for collaboration and engagement

scholarly article by Martyn Pickersgill published in January 2019

Can the governance of a population genetic data bank effect recruitment? Evidence from the public consultation of Generation Scotland

article

Cyborgs in the Everyday: Masculinity and Biosensing Prostate Cancer

scientific article published on 03 September 2015

Generation Scotland: consulting publics and specialists at an early stage in a genetic database's development

article

Generation Scotland: the Scottish Family Health Study; a new resource for researching genes and heritability

scientific article

Governing risk, engaging publics and engendering trust: New horizons for law and social science?

article by S. H. E. Harmon et al published 15 January 2013 in Science and Public Policy

Heredity and Hope: The Case for Genetic Screening (review)

Implantable Smart Technologies (IST): Defining the 'Sting' in Data and Device

scientific article

Not “human” enough to be human but not “animal” enough to be animal – the case of the HFEA, cybrids and xenotransplantation in the UK

Placing evidence in context: A response to Fry's commentary

article

Promoting research participation: why not advertise altruism?

scientific article published on 28 January 2008

Stakeholder perspectives on new ways of delivering unscheduled health care: the role of ownership and organizational identity

scientific article published on April 2007

Tackling community concerns about commercialisation and genetic research: A modest interdisciplinary proposal

scientific article (publication date: 2007)

The phenomenology of death, embodiment and organ transplantation

scientific article published in January 2005

The social sciences, humanities, and health

article

The “Life Costs” of Living with Rare Genetic Diseases