Leoni V, Strittmatter L, Zorzi G, et al. Metabolic consequences of mitochondrial coenzyme A deficiency in patients with PANK2 mutations. Mol Genet Metab. 2012;105(3):463-71. doi:10.1016/j.ymgme.2011.12.005
Zhu Z, Bakshi A, Vinkhuyzen AAE, et al. Dominance genetic variation contributes little to the missing heritability for human complex traits. Am J Hum Genet. 2015;96(3):377-85. doi:10.1016/j.ajhg.2015.01.001
Lubitz SA, Ellinor PT. Somatic mutations and atrial fibrillation: the end or just the beginning? Circ Cardiovasc Genet. 2015;8(1):2-3. doi:10.1161/CIRCGENETICS.115.000963
Gjoneska E, Pfenning AR, Mathys H, et al. Conserved epigenomic signals in mice and humans reveal immune basis of Alzheimer’s disease. Nature. 2015;518(7539):365-9. doi:10.1038/nature14252
Kosmicki JA, Sochat V, Duda M, Wall DP. Searching for a minimal set of behaviors for autism detection through feature selection-based machine learning. Transl Psychiatry. 2015;5:e514. doi:10.1038/tp.2015.7
Doyle AE. Commentary: Insights from across diagnostic boundaries: ADHD in the RDoC era--a commentary on Scerif and Baker (2015). J Child Psychol Psychiatry. 2015;56(3):274-7. doi:10.1111/jcpp.12401
Fall T, Hägg S, Ploner A, et al. Age- and sex-specific causal effects of adiposity on cardiovascular risk factors. Diabetes. 2015;64(5):1841-52. doi:10.2337/db14-0988
Mitchell SN, Kakani EG, South A, Howell PI, Waterhouse RM, Catteruccia F. Mosquito biology. Evolution of sexual traits influencing vectorial capacity in anopheline mosquitoes. Science. 2015;347(6225):985-8. doi:10.1126/science.1259435
Madison JM, Zhou F, Nigam A, et al. Characterization of bipolar disorder patient-specific induced pluripotent stem cells from a family reveals neurodevelopmental and mRNA expression abnormalities. Mol Psychiatry. 2015;20(6):703-17. doi:10.1038/mp.2015.7
Ramkissoon SH, Bi WL, Schumacher SE, et al. Clinical implementation of integrated whole-genome copy number and mutation profiling for glioblastoma. Neuro Oncol. 2015;17(10):1344-55. doi:10.1093/neuonc/nov015