Research output per year
Research output per year
Personal profile
Education/Academic qualification
Microbiology, MSc, Northumbria University
Award Date: 31 Aug 2018
Biomedical Science, BSc (Hons), Royal Holloway University of London
Award Date: 30 Jun 2015
PhD, Development and Remodelling of the Human Embryonic Arterial Valves , Newcastle University
1 Sept 2021 → …
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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Spatial transcriptomics reveals novel genes during the remodelling of the embryonic human arterial valves
Queen, R., Crosier, M., Eley, L., Kerwin, J., Turner, J. E., Yu, J., Alqahtani, A., Dhanaseelan, T., Overman, L., Soetjoadi, H., Baldock, R., Coxhead, J., Boczonadi, V., Laude, A., Cockell, S. J., Kane, M. A., Lisgo, S. & Henderson, D. J., 27 Nov 2023, In: PLoS Genetics. 19, 11, 30 p., e1010777.Research output: Contribution to journal › Article › peer-review
Open AccessFile6 Citations (Scopus) -
Validation of RNA Extraction Methods and Suitable Reference Genes for Gene Expression Studies in Developing Fetal Human Inner Ear Tissue
Steinacher, C., Rieder, D., Turner, J. E., Solanky, N., Nishio, S.-Y., Usami, S.-I., Hausott, B., Schrott-Fischer, A. & Dudas, J., 2 Mar 2024, In: International Journal of Molecular Sciences. 25, 5, 15 p., 2907.Research output: Contribution to journal › Article › peer-review
Open AccessFile1 Citation (Scopus) -
The morphogenesis of abnormal coronary arteries in the congenitally malformed heart
Anderson, R. H., Turner, J. E. & Henderson, D. J., 1 Aug 2022, In: Journal of Thoracic and Cardiovascular Surgery. 164, 2, p. 344-349 6 p.Research output: Contribution to journal › Editorial › peer-review
Open Access5 Citations (Scopus) -
Development of the Human Arterial Valves: Understanding Bicuspid Aortic Valve
Henderson, D. J., Eley, L., Turner, J. E. & Chaudhry, B., 27 Jan 2022, In: Frontiers in Cardiovascular Medicine. 8, p. 1-11 11 p., 802930.Research output: Contribution to journal › Review article › peer-review
Open AccessFile10 Citations (Scopus)4 Downloads (Pure) -
SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile
Al-Jawahiri, R., Foroutan, A., Kerkhof, J., McConkey, H., Levy, M., Haghshenas, S., Rooney, K., Turner, J., Shears, D., Holder, M., Lefroy, H., Castle, B., Reis, L. M., Semina, E. V., University of Washington Centre for Mendelian Genomics (UW-CMG), Nickerson, D., Bamshad, M., Leal, S., Lachlan, K. & Chandler, K. & 39 others, , 1 Jun 2022, In: Genetics in Medicine. 24, 6, p. 1261-1273 13 p.Research output: Contribution to journal › Article › peer-review
Open AccessFile19 Citations (Scopus)1 Downloads (Pure)