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Publications

Reproducibility of Molecular Phenotypes after Long-Term Differentiation to Human iPSC-Derived Neurons: A Multi-Site Omics Study.

Volpato V. et al, (2018), Stem Cell Reports, 11, 897 - 911

Epistasis in Neuropsychiatric Disorders.

Webber C., (2017), Trends Genet, 33, 256 - 265

Transcriptomic profiling of purified patient-derived dopamine neurons identifies convergent perturbations and therapeutics for Parkinson's disease.

Sandor C. et al, (2017), Hum Mol Genet, 26, 552 - 566

Whole-exome sequencing of 228 patients with sporadic Parkinson's disease.

Sandor C. et al, (2017), Sci Rep, 7

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.

Gormley P. et al, (2016), Nat Genet, 48, 856 - 866

Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules.

Kochinke K. et al, (2016), Am J Hum Genet, 98, 149 - 164

Haploinsufficiency predictions without study bias.

Steinberg J. et al, (2015), Nucleic Acids Res, 43

GeneNet Toolbox for MATLAB: A flexible platform for the analysis of gene connectivity in biological networks

Taylor A. et al, (2015), Bioinformatics, 31, 442 - 444

The clustering of functionally related genes contributes to CNV-mediated disease.

Andrews T. et al, (2015), Genome Res, 25, 802 - 813

Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cells.

Tan JY. et al, (2015), Genome Res, 25, 655 - 666

Duplications in ADHD patients harbour neurobehavioural genes that are co-expressed with genes associated with hyperactivity in the mouse.

Taylor A. et al, (2015), Am J Med Genet B Neuropsychiatr Genet, 168B, 97 - 107

Gene networks underlying convergent and pleiotropic phenotypes in a large and systematically-phenotyped cohort with heterogeneous developmental disorders.

Andrews T. et al, (2015), PLoS Genet, 11

Synergistic interactions between Drosophila orthologues of genes spanned by de novo human CNVs support multiple-hit models of autism.

Grice SJ. et al, (2015), PLoS Genet, 11

GeneNet Toolbox for MATLAB: a flexible platform for the analysis of gene connectivity in biological networks.

Taylor A. et al, (2015), Bioinformatics, 31, 442 - 444

Unbiased functional clustering of gene variants with a phenotypic-linkage network.

Honti F. et al, (2014), PLoS Comput Biol, 10

Diagnostically relevant facial gestalt information from ordinary photos.

Ferry Q. et al, (2014), Elife, 3

Phenotype ontologies and cross-species analysis for translational research.

Robinson PN. and Webber C., (2014), PLoS Genet, 10

Clinical Significance of De Novo and Inherited Copy-Number Variation

Vulto-van Silfhout AT. et al, (2013), Human Mutation, 34, 1679 - 1687

Clinical significance of de novo and inherited copy-number variation.

Vulto-van Silfhout AT. et al, (2013), Hum Mutat, 34, 1679 - 1687

The roles of FMRP-Regulated genes in autism spectrum disorder: Single- and multiple-hit genetic etiologies

Steinberg J. and Webber C., (2013), American Journal of Human Genetics, 93, 825 - 839

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