ZFIN ID: ZDB-LAB-140717-1
Bhatia Lab
PI/Director: Bhatia, Shipra
Contact Person: Bhatia, Shipra
Email: shipra.bhatia@igmm.ed.ac.uk
URL: http://www.hgu.mrc.ac.uk/index.html
Address: MRC Human Genetics Unit The MRC Institute of Genetics and Molecular Medicine The University of Edinburgh Western General Hospital Crewe Road Edinburgh EH4 2XU Scotland United Kingdom
Country: United Kingdom
Phone: +44 (0)131 332 2471
Fax: +44 (0)131 467 8456
Line Designation: ue


GENOMIC FEATURES ORIGINATING FROM THIS LAB
Show all 8 genomic features


STATEMENT OF RESEARCH INTERESTS


LAB MEMBERS


ZEBRAFISH PUBLICATIONS OF LAB MEMBERS
Ravi, V., Bhatia, S., Shingate, P., Tay, B.H., Venkatesh, B., Kleinjan, D.A. (2019) Lampreys, the jawless vertebrates, contain three Pax6 genes with distinct expression in eye, brain and pancreas. Scientific Reports. 9:19559
Bhatia, S., Gordon, C.T., Foster, R.G., Melin, L., Abadie, V., Baujat, G., Vazquez, M.P., Amiel, J., Lyonnet, S., Heyningen, V.V., Kleinjan, D.A. (2015) Functional Assessment of Disease-Associated Regulatory Variants In Vivo Using a Versatile Dual Colour Transgenesis Strategy in Zebrafish. PLoS Genetics. 11:e1005193
Gordon, C.T., Attanasio, C., Bhatia, S., Benko, S., Ansari, M., Tan, T.Y., Munnich, A., Pennacchio, L.A., Abadie, V., Temple, I.K., Goldenberg, A., van Heyningen, V., Amiel, J., FitzPatrick, D., Kleinjan, D.A., Visel, A., Lyonnet, S. (2014) Identification of novel craniofacial regulatory domains located far upstream of SOX9 and disrupted in Pierre Robin sequence. Human Mutation. 35(8):1011-20
Rainger, J.K., Bhatia, S., Bengani, H., Gautier, P., Rainger, J., Pearson, M., Ansari, M., Crow, J., Mehendale, F., Palinkasova, B., Dixon, M.J., Thompson, P.J., Matarin, M., Sisodiya, S.M., Kleinjan, D.A., and Fitzpatrick, D.R. (2014) Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequence. Human molecular genetics. 23(10):2569-79
Bhatia, S., Bengani, H., Fish, M., Brown, A., Divizia, M.T., de Marco, R., Damante, G., Grainger, R., van Heyningen, V., Kleinjan, D.A. (2013) Disruption of autoregulatory feedback by a mutation in a remote, ultraconserved PAX6 enhancer causes aniridia. American journal of human genetics. 93:1126-34