Ovseiko PV, Greenhalgh T, Adam P, et al. A global call for action to include gender in research impact assessment. Health Res Policy Syst. 2016;14(1):50. doi:10.1186/s12961-016-0126-z
Publications
Rhee EP, Yang Q, Yu B, et al. An exome array study of the plasma metabolome. Nat Commun. 2016;7:12360. doi:10.1038/ncomms12360
Valenca GT, Srivastava GP, Oliveira-Filho J, et al. The Role of MAPT Haplotype H2 and Isoform 1N/4R in Parkinsonism of Older Adults. PLoS One. 2016;11(7):e0157452. doi:10.1371/journal.pone.0157452
Garofalo A, Sholl L, Reardon B, et al. The impact of tumor profiling approaches and genomic data strategies for cancer precision medicine. Genome Med. 2016;8(1):79. doi:10.1186/s13073-016-0333-9
Struzhkin VV, Kim DY, Stavrou E, et al. Synthesis of sodium polyhydrides at high pressures. Nat Commun. 2016;7:12267. doi:10.1038/ncomms12267
Brady CA, Rennekamp AJ, Peterson RT. Chemical Screening in Zebrafish. Methods Mol Biol. 2016;1451:3-16. doi:10.1007/978-1-4939-3771-4_1
Visschedijk MC, Alberts R, Mucha S, et al. Pooled Resequencing of 122 Ulcerative Colitis Genes in a Large Dutch Cohort Suggests Population-Specific Associations of Rare Variants in MUC2. PLoS One. 2016;11(8):e0159609. doi:10.1371/journal.pone.0159609
Mancuso N, Rohland N, Rand KA, et al. The contribution of rare variation to prostate cancer heritability. Nat Genet. 2016;48(1):30-5. doi:10.1038/ng.3446
Wolfson RL, Chantranupong L, Saxton RA, et al. Sestrin2 is a leucine sensor for the mTORC1 pathway. Science. 2016;351(6268):43-8. doi:10.1126/science.aab2674
Chen GB, Lee SH, Robinson MR, et al. Across-cohort QC analyses of GWAS summary statistics from complex traits. Eur J Hum Genet. 2016;25(1):137-146. doi:10.1038/ejhg.2016.106