A Menin-MLL inhibitor induces specific chromatin changes and eradicates disease in models of MLL-rearranged leukemia

- Krivtsov, Andrei V., Evans, Kathryn, McDermott, Lisa, Jones, Connor D., Jing, Duohui, Braytee, Ali, Chacon, Diego, Earley, Eric, McKeever, Brian M., Claremon, David, Gifford, Andrew J., Lee, Heather J., Gadrey, Jayant Y., Teicher, Beverley A., Pimanda, John E., Beck, Dominik, Perry, Jennifer A., Smith, Malcolm A., McGeehan, Gerard M., Lock, Richard B., Armstrong, Scott A., Eschle, Benjamin K., Hatton, Charlie, Uckelmann, Hannah J., Ross, Kenneth N., Perner, Florian, Olsen, Sarah N., Pritchard, Tara

Crosstalk between DNA methylation and hypoxia in acute myeloid leukaemia

- Humphries, Sam, Bond, Danielle R., Germon, Zacary P., Keely, Simon, Enjeti, Anoop K., Dun, Matthew D., Lee, Heather J.

Genome-scale oscillations in DNA methylation during exit from pluripotency

- Rulands, Steffen, Lee, Heather J., Kelsey, Gavin, Stegle, Oliver, Simons, Benjamin D., Reik, Wolf, Clark, Stephen J., Angermueller, Christof, Smallwood, Sébastien A., Krueger, Felix, Mohammed, Hisham, Dean, Wendy, Nichols, Jennifer, Rugg-Gunn, Peter

Genome-wide analysis of DNA methylation in single cells using a post-bisulfite adapter tagging approach

- Lee, Heather J., Smallwood, Sébastien A.

Genome-wide base-resolution mapping of DNA methylation in single cells using single-cell bisulfite sequencing (scBS-seq)

- Clark, Stephen J., Smallwood, Sébastien A., Lee, Heather J., Krueger, Felix, Reik, Wolf, Kelsey, Gavin

Maternal SMCHD1 controls both imprinted Xist expression and imprinted X chromosome inactivation

- Wanigasuriya, Iromi, Kinkel, Sarah A., Beck, Tamara, Roper, Ellise A., Breslin, Kelsey, Lee, Heather J., Keniry, Andrew, Ritchie, Matthew E., Blewitt, Marnie E., Gouil, Quentin

ScNMT-seq enables joint profiling of chromatin accessibility DNA methylation and transcription in single cells

- Clark, Stephen J., Argelaguet, Ricard, Stegle, Oliver, Reik, Wolf, Kapourani, Chantriolnt-Andreas, Stubbs, Thomas M., Lee, Heather J., Alda-Catalinas, Celia, Krueger, Felix, Sanguinetti, Guido, Kelsey, Gavin, Marioni, John C.

scTEM-seq: Single-cell analysis of transposable element methylation to link global epigenetic heterogeneity with transcriptional programs

- Hunt, Kooper V., Burnard, Sean M., Roper, Ellise A., Bond, Danielle R., Dun, Matthew D., Verrills, Nicole M., Enjeti, Anoop K., Lee, Heather J.

Single-cell epigenomics in cancer: Charting a course to clinical impact

- Bond, Danielle R., Uddipto, Kumar, Enjeti, Anoop K., Lee, Heather J.

Smchd1 is a maternal effect gene required for genomic imprinting

- Wanigasuriya, Iromi, Gouil, Quentin, Keniry, Andrew, Ritchie, Matthew E., Blewitt, Marnie E., Kinkel, Sarah A., del Fierro, Andres Tapia, Beck, Tamara, Roper, Ellise A., Breslin, Kelsey, Stringer, Jessica, Hutt, Karla, Lee, Heather J.

The Promise of Single-cell Technology in Providing New Insights into the Molecular Heterogeneity and Management of Acute Lymphoblastic Leukemia

- Pearson, Holly C. L., Hunt, Kooper V., Trahair, Toby N., Lock, Richard B., Lee, Heather J., de Bock, Charles E.

Unravelling the epigenome of myelodysplastic syndrome: diagnosis, prognosis, and response to therapy

- Bond, Danielle R., Lee, Heather J., Enjeti, Anoop K.