Picture of WWI infirmary patient surrounded by wellwishers

Understanding our future through Open Access research about our past...

Strathprints makes available scholarly Open Access content by researchers in History, based within the School of Humanities. This include the Centre for the Social History of Health & Healthcare (CSHHH), considered Scotland's leading centre for the history of health and medicine.

Research at CSHHH explores the modern world since 1800 in locations as diverse as the UK, Asia, Africa, North America, and Europe. Areas of specialism include contraception and sexuality; family health and medical services; occupational health and medicine; disability; the history of psychiatry; conflict and warfare; and, drugs, pharmaceuticals and intoxicants.

Explore the Open Access research of the Centre for the Social History of Health and Healthcare. Or explore all of Strathclyde's Open Access research...

Image: Louis Théophile Binot entouré de patients et infirmières - 1915 | CC BY-SA.

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Jump to: 2021 | 2019 | 2015 | 2008
Number of items: 4.

2021

Martin, Antony P. and Downing, Jennifer and Collins, Brendan and Godman, Brian and Alfirevic, Ana and Greenhalgh, Karen Lynn and Pirmohamed, Munir (2021) Examining the uptake of predictive BRCA testing in the UK; findings and implications. European Journal of Human Genetics, 29 (4). pp. 699-708. ISSN 1018-4813

2019

Martin, Antony P. and Pedra, Gabriel and Downing, Jennifer and Collins, Brendan and Godman, Brian and Alfirevic, Ana and Pirmohamed, Munir and Greenhalgh, Kathryn (2019) Trends in BRCA testing and socioeconomic deprivation. European Journal of Human Genetics, 27 (9). pp. 1351-1360. ISSN 1018-4813

2015

Simpson, Nuala H and Ceroni, Fabiola and Reader, Rose H and Covill, Laura E and Knight, Julian C and Hennessy, Elizabeth R and Bolton, Patrick F and Conti-Ramsden, Gina and O'Hare, Anne and Baird, Gillian and Fisher, Simon E and Newbury, Dianne F and Nudel, R and Monaco, AP and Simonoff, E and Bolton, PF and Pickles, A and Slonims, V and Dworzynski, K and Everitt, A and Clark, A and Watson, J and Seckl, J and Cowie, H and Cohen, W and Nasir, J. and Bishop, DVM and Simkin, Z (2015) Genome-wide analysis identifies a role for common copy number variants in specific language impairment. European Journal of Human Genetics, 23 (10). pp. 1370-1377. ISSN 1018-4813

2008

Knight, Helen M. and Maclean, Alan and Irfan, Muhammad and Naeem, Farooq and Cass, Stephen and Pickard, B.S. and Muir, Walter J. and Blackwood, D.H.R. (2008) Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment. European Journal of Human Genetics, 16 (6). pp. 750-758. ISSN 1018-4813

This list was generated on Sat Sep 24 22:05:05 2022 BST.