Laffan, Michael
University Hospitals Birmingham NHS Foundation Trust · Queen Mary University of London · Guy's and St Thomas' NHS Foundation Trust · Cambridge University Hospitals NHS Foundation Trust · University College London · Imperial College London
5 papers on CoChatORCID 0000-0002-8268-3268
Most cited papers
- Verified
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity
Wahl, S., Drong, A., Lehne, B., Loh, M., Scott, W. R., Kunze, S., Tsai, P.-C., Ried, J. S., Zhang, W., Yang, Y., et al. (2017) · Nature
Epigenetics and DNA MethylationGenetic Associations and Epidemiology
Cited by 945
- Verified
AAV5–Factor VIII Gene Transfer in Severe Hemophilia A
Rangarajan, S., Walsh, L., Lester, W., Perry, D., Madan, B., Laffan, M., Yu, H., Vettermann, C., Pierce, G. F., Wong, W. Y., et al. (2017) · New England Journal of Medicine
Hemophilia Treatment and ResearchVirus-based gene therapy research
Cited by 694
- Verified
Multiyear Follow-up of AAV5-hFVIII-SQ Gene Therapy for Hemophilia A
Pasi, K. J., Rangarajan, S., Mitchell, N., Lester, W., Symington, E., Madan, B., Laffan, M., Russell, C. B., Li, M., Pierce, G. F., et al. (2020) · New England Journal of Medicine
Hemophilia Treatment and ResearchVirus-based gene therapy research
Cited by 448
- Verified
The Effect of Iron Status on Risk of Coronary Artery Disease: A Mendelian Randomization Study—Brief Report
Gill, D., Del Greco M., F., Walker, A. P., Srai, S. K. S., Laffan, M. A., & Minelli, C. (2017) · Arteriosclerosis Thrombosis and Vascular Biology
Iron Metabolism and DisordersGenetic Associations and Epidemiology
Cited by 95
- Verified
De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures
Ito, Y., Carss, K. J., Duarte, S. T., Hartley, T., Keren, B., Kurian, M. A., Marey, I., Charles, P., Mendonça, C., Nava, C., et al. (2018) · The American Journal of Human Genetics
Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases
Cited by 41
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