Wood, William G
University of Oxford · MRC Weatherall Institute of Molecular Medicine · MRC Molecular Haematology Unit
7 papers on CoChat
Most cited papers
- Verified
Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease
Tufarelli, C., Stanley, J. A. S., Garrick, D., Sharpe, J. A., Ayyub, H., Wood, W. G., & Higgs, D. R. (2003) · Nature Genetics
Epigenetics and DNA MethylationCancer-related molecular mechanisms research
Cited by 547
- Verified
Intragenic Enhancers Act as Alternative Promoters
Kowalczyk, M. S., Hughes, J. R., Garrick, D., Lynch, M. D., Sharpe, J. A., Sloane-Stanley, J. A., McGowan, S. J., De Gobbi, M., Hosseini, M., Vernimmen, D., et al. (2012) · Molecular Cell
RNA Research and SplicingGenomics and Chromatin Dynamics
Cited by 267
- Verified
Long-range chromosomal interactions regulate the timing of the transition between poised and active gene expression
Vernimmen, D., Gobbi, M. D., Sloane‐Stanley, J. A., Wood, W. G., & Higgs, D. R. (2007) · The EMBO Journal
Genomics and Chromatin DynamicsChromatin Remodeling and Cancer
Cited by 244
- Verified
Globin gene activation during haemopoiesis is driven by protein complexes nucleated by GATA‐1 and GATA‐2
Anguita, E., Hughes, J., Heyworth, C., Blobel, G. A., Wood, W. G., & Higgs, D. R. (2004) · The EMBO Journal
Genomics and Chromatin DynamicsHemoglobinopathies and Related Disorders
Cited by 207
- Verified
Identification of a conserved erythroid specific domain of histone acetylation across the α-globin gene cluster
Anguita, E., Johnson, C. A., Wood, W. G., Turner, B. M., & Higgs, D. R. (2001) · Proceedings of the National Academy of Sciences
Genomics and Chromatin DynamicsEpigenetics and DNA Methylation
Cited by 70
- Verified
Deletion of the mouse α-globin regulatory element (HS −26) has an unexpectedly mild phenotype
Anguita, E., Sharpe, J. A., Sloane-Stanley, J. A., Tufarelli, C., Higgs, D. R., & Wood, W. G. (2002) · Blood
Hemoglobinopathies and Related DisordersHemoglobin structure and function
Cited by 58
- Verified
Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1α localization in erythroblasts
Renella, R., Roberts, N. A., Brown, J. M., De Gobbi, M., Bird, L. E., Hassanali, T., Sharpe, J. A., Sloane-Stanley, J., Ferguson, D. J. P., Cordell, J., et al. (2011) · Blood
Genomics and Chromatin DynamicsHemoglobinopathies and Related Disorders
Cited by 54
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