Research output per year
Research output per year
Personal profile
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
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Dive into the research topics where Glenda Beaman is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Hereditary renal cancer patient and public involvement group: a collaborative, consensus decision process to develop a communication tool for patient use
Colvin, E., Ng, S., Hepworth, J., Hepworth, J., Hartley, T., Godfrey, N., Tricker, K., Rothwell, J., Beaman, G. & Woodward, E., 27 Mar 2023, In: Journal of Cardiovascular Translational Research.Research output: Contribution to journal › Article › peer-review
Open Access -
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
Beaman, G., Newman, W., Woolf, A. S. & et al., 11 Oct 2022, (Accepted/In press) In: Communications Biology.Research output: Contribution to journal › Article › peer-review
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Diverse ancestry whole-genome sequencing association study identifies TBX5 and PTK7 as susceptibility genes for posterior urethral valves
Genomics England Research Consortium, Chan, M. M. Y., Sadeghi-Alavijeh, O., Lopes, F. M., Hilger, A. C., Stanescu, H. C., Voinescu, C. D., Beaman, G., Newman, W. G., Zaniew, M., Weber, S., Ho, Y. M., Connolly, J. O., Wood, D., Maj, C., Stuckey, A., Kousathanas, A., Kleta, R., Woolf, A. S., Bockenhauer, D., & 2 others, 15 Aug 2022, (Accepted/In press) In: eLife.Research output: Contribution to journal › Article › peer-review
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Expanding the genotypic spectrum of TXNL4A variants in Burn-McKeown syndrome
Newman, W., Wood, K., O'Keefe, R., Ellingford, J., Thomas, H., Douzgou, S., Beaman, G., Hobson, E. & Prescott, K., 1 Feb 2022, In: Clinical Genetics. 101, 2, p. 255-259Research output: Contribution to journal › Article › peer-review
Open Access -
Expanding the HPSE2 genotypic spectrum in urofacial syndrome, a disease featuring a peripheral neuropathy of the urinary bladder
Beaman, G., Lopes, F., Hofmann, A., Roesch, W., Promm, M., Bijlsma, E. K., Patel, C., Akinci, A., Burgu, B., Knijnenburg, J., Ho, G., Aufschlaeger, C., Dathe, S., Voelckel, M. A., Cohen, M., Yue, W. W., Stuart, H., Mckenzie, E., Elvin, M., Roberts, N., & 2 others, 23 May 2022, (Accepted/In press) In: Frontiers in Genetics.Research output: Contribution to journal › Article › peer-review
Impacts
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World-first bedside genetic test to prevent babies going deaf
William Newman (Participant), John Mcdermott (Participant), Rick Body (Participant), Fiona Ulph (Participant), Paul Wilson (Participant), Iain Bruce (Participant) & Glenda Beaman (Participant)
Impact: Health and wellbeing, Economic, Technological, Policy
Press/Media
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The simple genetic test for newborns that can prevent profound deafness and save the NHS millions every year
William Newman, John Mcdermott, Rick Body, Ajit Mahaveer, Paul Wilson, Iain Bruce, Nicola Booth, Rachel James, Glenda Beaman, Karen Tricker, Mark Turner, Karen Harvey, Fiona Ulph & Rhona Macleod
29/03/22
1 item of Media coverage
Press/Media: Research