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
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
Machiela MJ, Zhou W, Sampson JN, et al. Characterization of large structural genetic mosaicism in human autosomes. Am J Hum Genet. 2015;96(3):487-97. doi:10.1016/j.ajhg.2015.01.011
Huan T, Esko T, Peters MJ, et al. A meta-analysis of gene expression signatures of blood pressure and hypertension. PLoS Genet. 2015;11(3):e1005035. doi:10.1371/journal.pgen.1005035
Magnusson M, Wang TJ, Clish C, et al. Dimethylglycine Deficiency and the Development of Diabetes. Diabetes. 2015;64(8):3010-6. doi:10.2337/db14-1863
Huffman JE, Albrecht E, Teumer A, et al. Modulation of genetic associations with serum urate levels by body-mass-index in humans. PLoS One. 2015;10(3):e0119752. doi:10.1371/journal.pone.0119752
Palta P, Kaplinski L, Nagirnaja L, et al. Haplotype phasing and inheritance of copy number variants in nuclear families. PLoS One. 2015;10(4):e0122713. doi:10.1371/journal.pone.0122713
Nakayama T, Al-Maawali A, El-Quessny M, et al. Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination. Am J Hum Genet. 2015;96(5):709-19. doi:10.1016/j.ajhg.2015.03.003
Viatte S, Plant D, Han B, et al. Association of HLA-DRB1 haplotypes with rheumatoid arthritis severity, mortality, and treatment response. JAMA. 2015;313(16):1645-56. doi:10.1001/jama.2015.3435
Peyrot WJ, Lee SH, Milaneschi Y, et al. The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjects. Mol Psychiatry. 2015;20(6):735-43. doi:10.1038/mp.2015.50