Authors: Whibley, Annabel C Plagnol, Vincent Tarpey, Patrick S. Abidi, Fatima Raymond, F. Lucy

Citation: C. Whibley, Annabel et al., Fine-Scale Survey of X Chromosome Copy Number Variants and Indels Underlying Intellectual Disability, American journal of human genetics (Online) AJHG , 87(2), 2010, pp. 173-188

Authors: Plagnol, Vincent Smyth, Deborah J. Todd, John A. Clayton, David G.

Citation: Plagnol, Vincent et al., Statistical independence of the colocalized association signals for type 1 diabetes and RPS26 gene expression on chromosome 12q13, Biostatistics (Oxford. Print) , 10(2), 2009, pp. 327-334

Authors: Blaydon, Diana C. Lind,Lisbet K. Plagnol, Vincent

Citation: C. Blaydon, Diana et al., Mutations in AQP5, Encoding a Water-Channel Protein, Cause Autosomal-Dominant Diffuse Nonepidermolytic Palmoplantar Keratoderma, American journal of human genetics (Online) AJHG , 93(2), 2013, pp. 330-335

Authors: Kirwan, Michael Walne, Amanda J. Plagnol, Vincent

Citation: Kirwan, Michael et al., Exome Sequencing Identifies Autosomal-Dominant SRP72 Mutations Associated with Familial Aplasia and Myelodysplasia, American journal of human genetics (Online) AJHG , 90(5), 2012, pp. 888-892

Authors: Charlesworth, Gavin Plagnol, Vincent Holmström, Kira M.

Citation: Charlesworth, Gavin et al., Mutations in ANO3 Cause Dominant Craniocervical Dystonia: Ion Channel Implicated in Pathogenesis, American journal of human genetics (Online) AJHG , 91(6), 2012, pp. 1041-1050