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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SDG 3 Good Health and Well-being
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SDG 16 Peace, Justice and Strong Institutions
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Collaborations and top research areas from the last five years
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CYP2C19 genotyping and mavacamten: predicting outcomes in normal, intermediate and rapid metabolisers in obstructive hypertrophic cardiomyopathy
Kasolo, Y., Burford, E., Obeidat, M., Beaman, G. M., Monk, T., Bastiaenen, R., Newman, W. G. & Cooper, R. M., 6 Feb 2026, In: European journal of clinical pharmacology. 82, 3, 67.Research output: Contribution to journal › Article › peer-review
Open Access -
Acute-onset axonal neuropathy following infection in children with biallelic RCC1 variants: a case series
Harkness, J. R., Mcdermott, J. H., Marsden, S., Jamieson, P., Metcalfe, K. A., Khan, N., Macken, W. L., Pitceathly, R. D. S., Record, C. J., Maroofian, R., Kleopa, K., Christodoulou, K., Sabir, A., Islam, L., Santra, S., Durmusalioglu, E. A., Atik, T., Isik, E., Cogulu, O. & Urquhart, J. E. & 43 others, , 1 Aug 2025, In: The Lancet Neurology. 24, 8, p. 667-680 14 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Case Report: Prolonged survival in Schinzel–Giedion syndrome featuring megaureter and de novo SETBP1 mutation
Newman, W., Beaman, G., Woolf, A. S., Jarvis, B., Metcalfe, K., Keene, D., Goyal, A., Cervellione, R. & Lopes, F., 7 Mar 2025, In: Frontiers in pediatrics. 13, 1534192.Research output: Contribution to journal › Article › peer-review
Open Access -
Deletion of CH25H and LIPA Genes in Human Abolishes Biosynthesis of 25-Hydroxycholesterol but not of 7α,25-Dihydroxysterols and Enhances Non-enzymatic Cholesterol Oxidation: Metabolic Changes are Partially Reversed by Hematopoietic Stem Cell Transplant‡
Yutuc, E., Ghosh, A., Abdel-Khalik, J., Goenka, A., Asgari, M. A., Lopez-Castejon, G., Beaman, G. M., Wynn, R. F., Newman, W. G., Jones, S. A., Griffiths, W. J. & Wang, Y., 30 Jul 2025, medRxiv.Research output: Preprint/Working paper › Preprint
Open Access -
Genetic Risk of Axonal Neuropathy Following Infection
Harkness, J. R., McDermott, J. H., Marsden, S., Jamieson, P., Metcalfe, K. A., Khan, N., Macken, W. L., Pitceathly, R. D. S., Record, C. J., Maroofian, R., Kloepas, K., Sabir, A., Islam, L., Santra, S., Durmusalioglu, E. A., Atik, T., Isik, E., Cogulu, O., Urquhart, J. E. & Beaman, G. M. & 43 others, , 6 Oct 2024, medRxiv, 21 p.Research output: Preprint/Working paper › Preprint
Open Access
Impacts
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World-first bedside genetic test to prevent babies going deaf
Newman, W. (Corresponding participant), Mcdermott, J. (Participant), Body, R. (Participant), Ulph, F. (Participant), Wilson, P. (Participant), Bruce, I. (Participant) & Beaman, G. (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
Newman, W., Mcdermott, J., Body, R., Mahaveer, A., Wilson, P., Bruce, I., Booth, N., James, R., Beaman, G., Tricker, K., Turner, M., Harvey, K., Ulph, F. & Macleod, R.
29/03/22
1 item of Media coverage
Press/Media: Research