Cherry ABC, Daley GQ. Reprogramming cellular identity for regenerative medicine. Cell. 2012;148(6):1110-22. doi:10.1016/j.cell.2012.02.031
Palotie A, Widén E, Ripatti S. From genetic discovery to future personalized health research. N Biotechnol. 2013;30(3):291-5. doi:10.1016/j.nbt.2012.11.013
Börnigen D, Pers TH, Thorrez L, Huttenhower C, Moreau Y, Brunak S. Concordance of gene expression in human protein complexes reveals tissue specificity and pathology. Nucleic Acids Res. 2013;41(18):e171. doi:10.1093/nar/gkt661
Agarwala V, Flannick J, Sunyaev S, GoT2D Consortium, Altshuler D. Evaluating empirical bounds on complex disease genetic architecture. Nat Genet. 2013;45(12):1418-27. doi:10.1038/ng.2804
Macarthur DG, Manolio TA, Dimmock DP, et al. Guidelines for investigating causality of sequence variants in human disease. Nature. 2014;508(7497):469-76. doi:10.1038/nature13127
Hutchinson JN, Raj T, Fagerness J, et al. Allele-specific methylation occurs at genetic variants associated with complex disease. PLoS One. 2014;9(6):e98464. doi:10.1371/journal.pone.0098464
Sahni N, Yi S, Taipale M, et al. Widespread macromolecular interaction perturbations in human genetic disorders. Cell. 2015;161(3):647-60. doi:10.1016/j.cell.2015.04.013
Roqueiro D, Witteveen MJ, Anttila V, Terwindt GM, van den Maagdenberg AMJM, Borgwardt K. In silico phenotyping via co-training for improved phenotype prediction from genotype. Bioinformatics. 2015;31(12):i303-10. doi:10.1093/bioinformatics/btv254