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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Research output
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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 -
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 -
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 -
Biallelic variants in DNA2 cause microcephalic primordial dwarfism
Tarnauskaitė, Ž., Bicknell, L. S., Marsh, J. A., Murray, J. E., Parry, D. A., Logan, C. V., Bober, M. B., de Silva, D. C., Duker, A. L., Sillence, D., Wise, C., Jackson, A. P., Murina, O. & Reijns, M. A. M., Aug 2019, In: Human Mutation. 40, 8, p. 1063-1070Research output: Contribution to journal › Article › peer-review
Open AccessFile -
Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes
University of Washington Center for Mendelian Genomics, 7 Mar 2019, In: American Journal of Human Genetics.Research output: Contribution to journal › Article › peer-review
Open AccessFile