Publications by Statistical Genetics and Epidemiology

Our research spans areas of statistical genetics, in particular the development of powerful statistical approaches to analyse genetic data, as well as studying infectious diseases.

Salih, A. et al. (2011) “Applications of Fluorescence Spectroscopy and Confocal Microscopy”, in Metallointercalators. Springer Nature, pp. 235–272.

Timbs, A. et al. (2010) “Quantitative Whole Genome Analysis of Sequential Samples From Patients with B CLL Identifies Novel Recurrent Copy Number Alterations Involving Critical B Cell Transcription Factors”, in BLOOD, pp. 1478–1478.

Heid, I. et al. (2010) “Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution”, Nature Genetics, 42(11), pp. 949–960.

McVean, G. and Myers, S. (2010) “PRDM9 marks the spot.”, Nature genetics, 42(10), pp. 821–822.

Durbin, R. et al. (2010) “A map of human genome variation from population-scale sequencing”, Nature, 467(7319), pp. 1061–1073.

Agam, A. et al. (2010) “Elusive copy number variation in the mouse genome.”, PloS one, 5(9).

Clark, T. et al. (2010) “A Bayesian approach using covariance of single nucleotide polymorphism data to detect differences in linkage disequilibrium patterns between groups of individuals”, Bioinformatics, 26(16), pp. 1999–2003.

Davies, J., Hein, J. and Holmes, C. (2010) “Detecting interacting genetic loci with effects on quantitative traits where the nature and order of the interaction are unknown”, Genetic Epidemiology, 34(4), pp. 299–308.

Craddock, N. et al. (2010) “Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls”, Nature, 464(7289), pp. 713–720.