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Epistasis in Neuropsychiatric Disorders.

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

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

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

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

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

Haploinsufficiency predictions without study bias.

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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

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

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

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

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

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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.

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

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

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

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

Diagnostically relevant facial gestalt information from ordinary photos.

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

Phenotype ontologies and cross-species analysis for translational research.

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

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

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

Clinical Significance of De Novo and Inherited Copy-Number Variation

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

The roles of FMRP-regulated genes in autism spectrum disorder: single- and multiple-hit genetic etiologies.

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Steinberg J. and Webber C., (2013), Am J Hum Genet, 93, 825 - 839

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