Publications

Complete list

For a complete list please click here.

Selected works and pre-prints

The PREGCARE study: Personalized recurrence risk assessment following the birth of a child with a pathogenic de novo mutation Bernkopf M, Abdullah UB, Bush SJ, Wood K, Ghaffari S, Giannoulatou E, ..., Davies RW, Wilkie AOM, Goriely A. bioRxiv, 2022 [pre-print]

Rapid genotype imputation from sequence with reference panels Davies RW, Kucka M, Su D, Shi S, Flanagan M, Cunnif CM, Chan YF, Myers S. Nature Genetics, 2021 [paper]

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome. Davies RW*, Fiksinski AM*, Breetvelt EJ, Williams NM, Hooper SR, Monfeuga T, ..., Scherer SW, International 22q11.2 Brain and Behavior Consortium, Bearden CE, Vorstman JAS. Nature Medicine, 2020 [paper]

Sequencing of human genomes with nanopore technology. Bowden R*, Davies RW*, Heger A*, Pagnamenta AT, de Cesare M, Oikkonen LE, ..., Buck D, Simpson MA, Donnelly P. Nature Communications, 2019 [paper]

Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders D'Abate L, Walker S, Yuen RKC, Tammimies K, Buchanan JA, Davies RW, ..., Young G, Zwaigenbaum L, Scherer SW. Nature communications, 2019 [paper]

A high-resolution map of non-crossover events reveals impacts of genetic diversity on mammalian meiotic recombination. Li R, Bitoun E, Altemose N, Davies RW, Davies B, Myers SR. Nature Communications, 2019 [paper]

Genomic Analyses from Non-invasive Prenatal Testing Reveal Genetic Associations, Patterns of Viral Infections, and Chinese Population History. Liu S, Huang S, Chen F, Zhao L, Yuan Y, Francis SS, ..., Jin X, Nielsen R, Xu X. Cell, 2018 [paper]

Rapid genotype imputation from sequence without reference panels. Davies RW, Flint J, Myers S, Mott R. Nature Genetics, 2016 [paper]

Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing. Nicod J, Davies RW, Cai N, Hassett C, Goodstadt L, Cosgrove C, …, Lionikas A, Mott R, Flint J. Nature Genetics, 2016 [paper]