1. "I didn't take it too seriously because I'd just never heard of it": Experiential knowledge and genetic screening for thalassaemia in the UK. Issue 1 (24th December 2018) Authors: Boardman, Felicity K.; Hale, Rachel Journal: Journal of genetic counseling Issue: Volume 28:Issue 1(2019) Page Start: 141 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Attitudes toward population screening among people living with fragile X syndrome in the UK: 'I wouldn't wish him away, I'd just wish his fragile X syndrome away'. Issue 1 (12th November 2020) Authors: Boardman, Felicity K. Journal: Journal of genetic counseling Issue: Volume 30:Issue 1(2021) Page Start: 85 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Expanding the notion of "benefit": comparing public, parent, and professional attitudes towards whole genome sequencing in newborns. Issue 2 (3rd April 2022) Authors: Clark, Corinna C.A.; Boardman, Felicity K. Journal: New genetics and society Issue: Volume 41:Issue 2(2022) Page Start: 96 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Experience as knowledge: Disability, distillation and (reprogenetic) decision-making. (October 2017) Authors: Boardman, Felicity K. Journal: Social science & medicine Issue: Volume 191(2017) Page Start: 186 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Impairment Experiences, Identity and Attitudes Towards Genetic Screening: the Views of People with Spinal Muscular Atrophy. Issue 1 (30th June 2017) Authors: Boardman, Felicity K.; Young, Philip J.; Griffiths, Frances E. Journal: Journal of genetic counseling Issue: Volume 27:Issue 1(2018) Page Start: 69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Knowledge is power? The role of experiential knowledge in genetically 'risky' reproductive decisions. Issue 1 (23rd September 2013) Authors: Boardman, Felicity K. Journal: Sociology of health & illness Issue: Volume 36:Issue 1(2014) Page Start: 137 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Newborn genetic screening for spinal muscular atrophy in the UK: The views of the general population. Issue 1 (23rd November 2017) Authors: Boardman, Felicity K.; Sadler, Chloe; Young, Philip J. Journal: Molecular genetics & genomic medicine Issue: Volume 6:Issue 1(2018) Page Start: 99 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Newborn screening for haemophilia: The views of families and adults living with haemophilia in the UK. Issue 2 (28th February 2019) Authors: Boardman, Felicity K.; Hale, Rachel; Young, Philip J. Journal: Haemophilia Issue: Volume 25:Issue 2(2019) Page Start: 276 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Newborn screening for spinal muscular atrophy: The views of affected families and adults. Issue 6 (4th April 2017) Authors: Boardman, Felicity K.; Young, Philip J.; Griffiths, Frances E. Journal: American journal of medical genetics Issue: Volume 173:Issue 6(2017) Page Start: 1546 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Population screening for spinal muscular atrophy: A mixed methods study of the views of affected families. Issue 2 (28th October 2016) Authors: Boardman, Felicity K.; Young, Philip J.; Griffiths, Frances E. Journal: American journal of medical genetics Issue: Volume 173:Issue 2(2017) Page Start: 421 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗