Please see my google scholar profile for a comprehensive list of publications.
2016
Sharp K, Kretzschmar WW, Delaneau O, Marchini JPhasing for medical sequencing using rare variants and large haplotype reference panels. Bioinformatics
2015
McCarthy S*, Das S*, Kretzschmar WW*, Durbin R†, Abecasis G†, Marchini J†A reference panel of 64,976 haplotypes for genotype imputation. Nature Genetics
2015
Cai N*, Bigdeli TB*, Kretzschmar WW*, Li Y*, et al. Sparse whole-genome sequencing identifies two loci for major depressive disorder. Nature