Golledge, Jonathan, Thanigaimani, Shivshankar, Barratt, Kristen S., and Fadini, Gian Paolo (2024) Recent developments in targets for ischemic foot disease. Diabetes/Metabolism Research and Reviews. (In Press)

Barratt, Kristen S., Drover, Kyle A., Thomas, Zoë M., and Arkell, Ruth M. (2022) Patterning of the antero‐ventral mammalian brain: Lessons from holoprosencephaly comparative biology in man and mouse. WIREs Mechanisms of Disease, 14 (4). e1552.

Bellchambers, Helen M., Barratt, Kristen S., Diamand, Koula E.M., and Arkell, Ruth M. (2021) SUMOylation Potentiates ZIC Protein Activity to Influence Murine Neural Crest Cell Specification. International Journal of Molecular Sciences, 22. 10437.

Ali, Radiya G., Bellchambers, Helen M., Warr, Nicholas, Ahmed, Jehangir N., Barratt, Kristen S., Neill, Kieran, Diamand, Koula E.M., and Arkell, Ruth M. (2021) WNT-responsive SUMOylation of ZIC5 promotes murine neural crest cell development, having multiple effects on transcription. Journal of Cell Science, 134 (9). jcs256792.

Barratt, Kristen S., Diamand, Koula E.M., and Arkell, Ruth M. (2018) Identification of reference genes suitable for RT-qPCR studies of murine gastrulation and patterning. Mammalian Genome, 29. pp. 656-662.

Barratt, Kristen S., and Arkell, Ruth M. (2018) ZIC2 in Holoprosencephaly. In: UNSPECIFIED, (ed.) Zic family: Evolution, Development and Disease. Advances in Experimental Medicine and Biology, 1046 . Springer, Singapore, pp. 269-299.

Houtmeyers, Rob, Tchouate Gainkam, Olive, Glanville-Jones, Hannah A., Van den Bosch, Ben, Chappell, Anna, Barratt, Kristen S., Souopgui, Jacob, Tejpar, Sabine, and Arkell, Ruth M. (2016) Zic2mutation causes holoprosencephaly via disruption of NODAL signalling. Human Molecular Genetics, 25 (18). pp. 3946-3959.