Research output per year
Research output per year
Personal profile
Overview
- Clinical Lecturer
- Trainee in Clinical Genetics
Memberships of committees and professional bodies
- British Society for Genetic Medicine
- UK Clinical Genetics Society
- Royal College of Paediatrics and Child Health
- General Medical Council
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):
Research Beacons, Institutes and Platforms
- Manchester Regenerative Medicine Network
- Christabel Pankhurst Institute
Fingerprint
Dive into the research topics where Helen Stuart is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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Detection of Alport gene variants in children and young people with persistent haematuria
Ng, N. S. L., Yamamura, T., Shenoy, M., Stuart, H. M. & Lennon, R., 1 Oct 2024, (E-pub ahead of print) In: Pediatric Nephrology.Research output: Contribution to journal › Article › peer-review
Open Access -
Predicting congenital renal tract malformation genes using machine learning
Kabir, M., Stuart, H., Lopes, F., Fotiou, E., Keavney, B., Doig, A., Woolf, A. S. & Hentges, K., 14 Aug 2023, In: Scientific Reports. 13, 13204.Research output: Contribution to journal › Article › peer-review
Open Access -
A basement membrane discovery pipeline uncovers network complexity, new regulators, and human disease associations
Genomics England Research Consortium, 20 May 2022, In: Science Advances. 8, 20, 19 p., eabn2265.Research output: Contribution to journal › Article › peer-review
Open Access -
De novo mutations in the BMP signaling pathway in lambdoid craniosynostosis
Yale Center for Genome Analysis, 2022, In: Human Genetics.Research output: Contribution to journal › Article › peer-review
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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
Thesis
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Urofacial Syndrome: A genetic model to understand human urinary tract abnormalities.
Stuart, H. (Author), Woolf, A. S. (Supervisor) & Newman, W. (Supervisor), 1 Aug 2015Student thesis: Unknown
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