Research output per year
Research output per year
Personal profile
Research interests
Molecular basis of inherited skin disorders: discovering genes for specific diseases, understanding disease mechanisms and determining relevance to diseased and healthy skin; translational research therapies - developing new gene, protein, cell and drug therapies for patients with inherited skin diseases such as epidermolysis bullosa (inherited skin fragility); prenatal diagnosis - development of preimplantation genetic haplotyping for severe inherited skin diseases
Research interests (short)
Molecular basis of inherited skin disorders; translational research therapies; prenatal diagnosis
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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Collaborations and top research areas from the last five years
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P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
Stefanski, H. E., Xing, Y., Nicholls, J., Jonart, L., Goren, E., Taylor, P. A., Mills, A. A., Riddle, M., McGrath, J., Tolar, J., Hollander, G. A. & Blazar, B. R., Jan 2022, In: PLoS ONE. 17, 1 1, e0261770.Research output: Contribution to journal › Article › peer-review
Open Access7 Citations (Scopus) -
Single-cell transcriptomics in human skin research: available technologies, technical considerations and disease applications
Theocharidis, G., Tekkela, S., Veves, A., McGrath, J. A. & Onoufriadis, A., May 2022, In: Experimental Dermatology. 31, 5, p. 655-673 19 p.Research output: Contribution to journal › Review article › peer-review
Open AccessFile20 Citations (Scopus)175 Downloads (Pure) -
The epidemiology of epidermolysis bullosa in England and Wales: data from the national epidermolysis bullosa database
Petrof, G., Papanikolaou, M., Martinez, A. E., Mellerio, J. E., McGrath, J. A., Bardhan, A., Harper, N., Heagerty, A., Ogboli, M., Chiswell, C. & Moss, C., May 2022, In: British Journal of Dermatology. 186, 5, p. 843-848 6 p.Research output: Contribution to journal › Article › peer-review
22 Citations (Scopus) -
Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility
Has, C., Bauer, J. W., Bodemer, C., Bolling, M. C., Bruckner-Tuderman, L., Diem, A., Fine, J. D., Heagerty, A., Hovnanian, A., Marinkovich, M. P., Martinez, A. E., McGrath, J. A., Moss, C., Murrell, D. F., Palisson, F., Schwieger-Briel, A., Sprecher, E., Tamai, K., Uitto, J. & Woodley, D. T. & 2 others, , 1 Oct 2020, In: British Journal of Dermatology. 183, 4, p. 614-627 14 p.Research output: Contribution to journal › Review article › peer-review
Open Access451 Citations (Scopus) -
Genomics-based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathica
Vahidnezhad, H., Youssefian, L., Sotoudeh, S., Liu, L., Guy, A., Lovell, P. A., Kariminejad, A., Zeinali, S., McGrath, J. A. & Uitto, J., 1 May 2020, In: Human Mutation. 41, 5, p. 906-912 7 p.Research output: Contribution to journal › Article › peer-review
12 Citations (Scopus)