Functional enrichment analysis with structural variants: pitfalls and strategies. by Webber, C

The roles of FMRP-regulated genes in autism spectrum disorder: single- and multiple-hit genetic etiologies. by Steinberg, J, Webber, C

Large-scale objective association of mouse phenotypes with human symptoms through structural variation identified in patients with developmental disorders by Boulding, H, Webber, C

Hotspots of mutation and breakage in dog and human chromosomes. by Webber, C, Ponting, C

The roles of FMRP-Regulated genes in autism spectrum disorder: Single- and multiple-hit genetic etiologies by Steinberg, J, Webber, C

Large-scale objective association of mouse phenotypes with human symptoms through structural variation identified in patients with developmental disorders. by Boulding, H, Webber, C

Genes and homology. by Webber, C, Ponting, C

Bias of selection on human copy-number variants by Nguyen, D, Webber, C, Ponting, C

Bias of selection on human copy-number variants. by Nguyen, D, Webber, C, Ponting, C

Bias of selection on human copy-number variants by Nguyen, D, Webber, C, Ponting, C

SCANPS: a web server for iterative protein sequence database searching by dynamic programing, with display in a hierarchical SCOP browser. by Walsh, T, Webber, C, Searle, S, Sturrock, S, Barton, G

An analysis of the gene complement of a marsupial, Monodelphis domestica: evolution of lineage-specific genes and giant chromosomes. by Goodstadt, L, Heger, A, Webber, C, Ponting, C

46% of individuals with ASD that harbour de novo CNVs have at least one de novo CNV that overlaps a gene associated with synaptic signalling by Webber, C, Marshall, C, Pinto, D, Scherer, S, Ponting, C

GAT: a simulation framework for testing the association of genomic intervals by Heger, A, Webber, C, Goodson, M, Ponting, C, Lunter, G

Genes and biological processes commonly disrupted in rare and heterogeneous developmental delay syndromes. by Shaikh, T, Haldeman-Englert, C, Geiger, E, Ponting, C, Webber, C

GAT: a simulation framework for testing the association of genomic intervals. by Heger, A, Webber, C, Goodson, M, Ponting, C, Lunter, G

Candidate genes and biological processes in de novo CNVs from autistic individuals by Noh, H, Marshall, C, Pinto, D, Scherer, S, Ponting, C, Webber, C

Birth, death or fixation of human segmental duplications by Nguyen, D, Webber, C, Hehir-Kwa, J, Pfundt, R, Veltman, J, Ponting, C

Human-specific transcriptome of ventral and dorsal midbrain dopamine neurons by Monzón-Sandoval, J, Poggiolini, I, Ilmer, T, Wade-Martins, R, Webber, C, Parkkinen, L

Reduced purifying selection prevails over positive selection in human copy number variant evolution. by Nguyen, D, Webber, C, Hehir-Kwa, J, Pfundt, R, Veltman, J, Ponting, C