Dr Elise Glen
Research Associate
- Tan HL, Glen E, Topf A, Hall D, O'Sullivan JJ, Sneddon L, Avery P, Lewis RJ, ten Dijke P, Arthur HM, Goodship JA, Keavney BD. Non-synonymous variants in the SMAD6 gene exhibit impaired inhibition of BMP signalling and predispose to congenital cardiovascular malformation.
Human Mutation 2012, (epub ahead of print).
- Soemedi R, Topf A, Wilson IJ, Darlay R, Rahman T, Glen E, Hall D, Huang N, Bentham J, Bhattacharya S, Cosgrove C, Brook JD, Granados-Riveron J, Setchfield K, Bu'lock F, Thornborough C, Devreindt K, Breckpot J, Hofbeck M, Lathrop M, Rauch A, Blue G, Winlaw D, Hurles M, Santibanez-Koref M, Cordell H, Goodship J, Keavney B. Phenotype-Specific Effect of Chromosome 1q21.1Rearrangements and GJA5 Duplications in 2437 CongenitalHeart Disease Patients and 6760 Controls.
Human Molecular Genetics 2012, (epub ahead of print).
- Tan HL, Glen EA, Topf AL, Hall DH, O'Sullivan JJ, Sneddon L, Wren C, Avery P, Lewis RJ, ten Dijke P, Arthur HM, Goodship JA, Keavney BD. Non-synonymous SMAD6 mutations impaired inhibition of BMP signalling in patients with congenital cardiovascular malformation.
In: Heart: Annual Conference of the British Cardiovascular Society (BCS). 2011, Manchester, UK: BMJ Group.
