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Open Access research that explores socio-technical phenomena & evolving information systems & behaviours...

Strathprints makes available scholarly Open Access content by researchers within the Department of Computer & Information Sciences working as part of the Strathclyde iSchool Research Group (SiRG). The SiRG specialises in understanding how people search for information and explores interactive search tools that support their information seeking and retrieval tasks. This research work also includes investigations into information behaviour, how users engage with information and the legal and ethical issues arising from information use.

Explore the Open Access research by the SiRG, or theDepartment of Computer & Information Sciences more generally. Or explore all of Strathclyde's Open Access research...

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Group by: Publication Date | Item type | No Grouping
Jump to: 2019 | 2015 | 2008
Number of items: 3.

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 Tue Feb 18 07:01:09 2020 GMT.