Research Output per year
Research Output per year
Personal profile
Research Interests
My main research interests lie in Cancer Genomics and Biology. Both my PhD and postdoctoral research have involved rare genetic diseases associated with cancer development. I am interested in applying Omics techniques to better understand the genetic variations and changes in gene expression underlying development and progression of complex diseases. My recent work at the University of Warwick involved translational research that focused on development of novel diagnostic next generation sequencing (NGS) methods for cancer and inherited diseases.
Another area of research interest is identification of biomarkers for the non-invasive detection of early cancer and I am currently a member of the Early Cancer Detection Consortium, a pan-UK initiative with an aim to develop a blood- based screening method for early cancer detection.
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Research Output
- 757 Citations
- 12 h-Index
- 18 Article
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Simultaneous detection of lung fusions using a multiplex RT-PCR next generation sequencing-based approach: A multi-institutional research study
Vaughn, C. P., Costa, J. L., Feilotter, H. E., Petraroli, R., Bagai, V., Rachiglio, A. M., Marino, F. Z., Tops, B., Kurth, H. M., Sakai, K., Mafficini, A., Bastien, R. R. L., Reiman, A., Le Corre, D., Boag, A., Crocker, S., Bihl, M., Hirschmann, A., Scarpa, A., Machado, J. C. & 8 others, , 16 Aug 2018, In : BMC Cancer. 18, 1, 8 p., 828.Research output: Contribution to journal › Article
Open AccessFile6 Citations (Scopus)20 Downloads (Pure) -
The evidence base for circulating tumour DNA blood-based biomarkers for the early detection of cancer: a systematic mapping review
Cree, I., Uttley, L., Buckley Woods, H., Kikuchi, H., Harnan, S., Whiteman, B. L., Taylor Phillips, S., Messenger, M., Cox, A., Teare, D., Sheils, O., Shaw, J. & UK Early Cancer Detection Consortium, 23 Oct 2017, In : BMC Cancer. 17, 697.Research output: Contribution to journal › Article
Open AccessFile48 Citations (Scopus)23 Downloads (Pure) -
Validation of an NGS mutation detection panel for melanoma
Reiman, A., Kikuchi, H., Scocchia, D., Smith, P., Tsang, Y. W., Snead, D. & Cree, I. A., 22 Feb 2017, In : BMC Cancer. 17, 1, 8 p., 150.Research output: Contribution to journal › Article
Open AccessFile20 Citations (Scopus)94 Downloads (Pure) -
Development and validation of a TaqMan Array for cancer mutation analysis
Kikuchi, H., Reiman, A., Nyoni, J., Lloyd, K., Savage, R., Wotherspoon, T., Berry, L., Snead, D. & Cree, I. A., Feb 2016, In : Pathogenesis. 3, 1, p. 1-8Research output: Contribution to journal › Article
Open AccessFile3 Citations (Scopus)26 Downloads (Pure) -
Molecular testing for familial hypercholesterolaemia-associated mutations in a UK-based cohort: Development of an NGS-based method and comparison with multiplex polymerase chain reaction and oligonucleotide arrays
Reiman, A., Pandey, S., Lloyd, K. L., Dyer, N., Khan, M., Crockard, M., Latten, M. J., Watson, T. L., Cree, I. A. & Grammatopoulos, D. K., 1 Nov 2016, In : Annals of Clinical Biochemistry. 53, 6, p. 654-662 9 p.Research output: Contribution to journal › Article
3 Citations (Scopus)