Van Rheenen W, Shatunov A, Dekker AM, et al. Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nat Genet. 2016;48(9):1043-8. doi:10.1038/ng.3622
Publications
Shaikh AY, Wang N, Yin X, et al. Relations of Arterial Stiffness and Brachial Flow-Mediated Dilation With New-Onset Atrial Fibrillation: The Framingham Heart Study. Hypertension. 2016;68(3):590-6. doi:10.1161/HYPERTENSIONAHA.116.07650
Conde J, Shomron N, Artzi N. Biomaterials for Abrogating Metastasis: Bridging the Gap between Basic and Translational Research. Adv Healthc Mater. 2016;5(18):2312-9. doi:10.1002/adhm.201600414
Li Z, Xia Y, Feng LN, et al. Genetic risk of extranodal natural killer T-cell lymphoma: a genome-wide association study. Lancet Oncol. 2016;17(9):1240-7. doi:10.1016/S1470-2045(16)30148-6
Uren C, Kim M, Martin AR, et al. Fine-Scale Human Population Structure in Southern Africa Reflects Ecogeographic Boundaries. Genetics. 2016;204(1):303-14. doi:10.1534/genetics.116.187369
Pirhaji L, Milani P, Leidl M, et al. Revealing disease-associated pathways by network integration of untargeted metabolomics. Nat Methods. 2016;13(9):770-6. doi:10.1038/nmeth.3940
Xu L, Brito IL, Alm EJ, Blainey PC. Virtual microfluidics for digital quantification and single-cell sequencing. Nat Methods. 2016;13(9):759-62. doi:10.1038/nmeth.3955
Klein M, Berger S, Hoogman M, et al. Meta-analysis of the DRD5 VNTR in persistent ADHD. Eur Neuropsychopharmacol. 2016;26(9):1527-32. doi:10.1016/j.euroneuro.2016.06.012
Zhou K, Yee SW, Seiser EL, et al. Variation in the glucose transporter gene SLC2A2 is associated with glycemic response to metformin. Nat Genet. 2016;48(9):1055-9. doi:10.1038/ng.3632
Doench JG. CRISPR/Cas9 gene editing special issue. FEBS J. 2016;283(17):3160-1. doi:10.1111/febs.13823