Research output per year
Research output per year
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Dive into the research topics where David Parry is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Signatures of TOP1 transcription-associated mutagenesis in cancer and germline
Reijns, M. A. M., Parry, D. A., Williams, T. C., Nicholson, M. D., Carroll, P., Ridout, K., The Genomics England Research Consortium, Colorectal Cancer Domain UK 100,000 Genomes Project, Schuh, A., Aden, K., Palles, C., Campo, E., Stankovic, T., Taylor, M. S. & Jackson, A. P., 9 Feb 2022, In: Nature.Research output: Contribution to journal › Article › peer-review
Open AccessFile -
Loss of Integrin-linked kinase sensitizes breast cancer to SRC inhibitors
Beetham, H., Griffith, B., Murina, O., Loftus, A., Parry, D. A., Temps, C., Culley, J., Muir, M., Unciti-Broceta, A., Sims, A. H., Byron, A. & Brunton, V. G., 17 Dec 2021, (E-pub ahead of print) In: Cancer Research.Research output: Contribution to journal › Article › peer-review
Open AccessFile -
A sensitive and affordable multiplex RT-qPCR assay for SARS-CoV-2 detection
Reijns, M. A. M., Thompson, L., Acosta, J. C., Black, H. A., Sanchez-Luque, F. J., Diamond, A., Parry, D. A., Daniels, A., O'Shea, M., Uggenti, C., Sanchez, M. C., O'Callaghan, A., McNab, M. L. L., Adamowicz, M., Friman, E. T., Hurd, T., Jarman, E. J., Chee, F. L. M., Rainger, J. K., Walker, M. & 18 others, , 15 Dec 2020, (E-pub ahead of print) In: PLoS Biology. 18, 12, p. e3001030Research output: Contribution to journal › Article › peer-review
Open Access -
PRIM1 Deficiency Causes a Distinctive Primordial Dwarfism Syndrome
The Scottish Genomes Partnership, Káposzta, R., Merő, G., Nagy, A., Orlik, B., Kovács-Pászthy, B., Quigley, A. J., Riszter, M., Rankin, J., Reijns, M. A. M., Szakszon, K. & Jackson, A. P., 1 Nov 2020, In: Genes & Development.Research output: Contribution to journal › Article › peer-review
Open AccessFile -
Heterozygous Lamin B1 and Lamin B2 Variants cause Primary Microcephaly and Define a Novel Laminopathy
Genomics England Research Consortium, Blyth, M., Cox, H., Donnelly, D. E., Greenhalgh, L., Greville-Heygate, S., Harrison, V., Lachlan, K., McKenna, C., Quigley, A., Rea, G., Robertson, L., Suri, M. & Jackson, A. P., 9 Oct 2020, (E-pub ahead of print) In: Genetics in Medicine. 23, 2, p. 408–414Research output: Contribution to journal › Article › peer-review
Open AccessFile
Projects
- 1 Active
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Prototype development for real-time diagnostic analysis of genome-wide sequence data
Parry, D., Canela Xandri, O. & FitzPatrick, D.
3/01/22 → 31/07/22
Project: Research