Crooks, Lucy - Sheffield Hallam University - Department of Biosciences and Chemistry

个人简介

I studied Natural Sciences at the University of Cambridge and gained a PhD at the University of Edinburgh. I have applied bioinformatics to research in diverse fields for eight years, including at the Sanger Institute. I also worked in diagnostic genetics in the NHS for two years. It is increasingly valuable to have bioinformatic skills as a biologist and genomics can make a huge impact on our understanding. The University recognises this, and my appointment is an investment into these areas. My research focus is analysing next generation sequencing data to identify genetic causes of disease.

研究领域

I am just starting up my research program. I am interested in projects with next generation sequencing data. I am especially interested in understanding the genetic basis of disease.

近期论文

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BALASUBRAMANIAN, M., HURST, J., BROWN, S., BISHOP, N. J., ARUNDEL, P., DEVILE, C., POLLITT, R. C., CROOKS, L., LONGMAN, D., CACERES, J. F., SHACKLEY, F., CONNOLLY, S., PAYNE, J. H., OFFIAH, A. C., HUGHES, D., STUDY, D. D. D., PARKER, M. J., HIDE, W. and SKERRY, T. M. (2017). Compound heterozygous variants in NBAS as a cause of atypical osteogenesis imperfecta. Bone, 94, 65-74. CROOKS, Lucy and BARRETT, Jeffrey C (2016). Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. Nature Neuroscience, 19, 571-577. WALTER, Klaudi, MIN, Josine L., HUANG, Jie and CROOKS, Lucy (2015). The UK10K project identifies rare variants in health and disease. Nature, 526 (7571), 82-90.