Chibnik LB, Wolters FJ, Bäckman K, et al. Trends in the incidence of dementia: design and methods in the Alzheimer Cohorts Consortium. Eur J Epidemiol. 2017;32(10):931-938. doi:10.1007/s10654-017-0320-5
Publications
Meadows JRS, Lindblad-Toh K. Dissecting evolution and disease using comparative vertebrate genomics. Nat Rev Genet. 2017;18(10):624-636. doi:10.1038/nrg.2017.51
Leonenko G, Richards AL, Walters JT, et al. Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia. Am J Med Genet B Neuropsychiatr Genet. 2017;174(7):724-731. doi:10.1002/ajmg.b.32560
Rehm HL. A new era in the interpretation of human genomic variation. Genet Med. 2017;19(10):1092-1095. doi:10.1038/gim.2017.90
Dyke SOM, Knoppers BM, Hamosh A, et al. "Matching" consent to purpose: The example of the Matchmaker Exchange. Hum Mutat. 2017;38(10):1281-1285. doi:10.1002/humu.23278
Ladas I, Fitarelli-Kiehl M, Song C, et al. Multiplexed Elimination of Wild-Type DNA and High-Resolution Melting Prior to Targeted Resequencing of Liquid Biopsies. Clin Chem. 2017;63(10):1605-1613. doi:10.1373/clinchem.2017.272849
Felsky D, Xu J, Chibnik LB, et al. Genetic epistasis regulates amyloid deposition in resilient aging. Alzheimers Dement. 2017;13(10):1107-1116. doi:10.1016/j.jalz.2017.01.027
Lucas D, O’Leary HA, Ebert BL, Cowan CA, Tremblay CS. Utility of CRISPR/Cas9 systems in hematology research. Exp Hematol. 2017;54:1-3. doi:10.1016/j.exphem.2017.06.006
Johannessen L iv, Sundberg TB, O’Connell DJ, et al. Small-molecule studies identify CDK8 as a regulator of IL-10 in myeloid cells. Nat Chem Biol. 2017;13(10):1102-1108. doi:10.1038/nchembio.2458
Lee JM, Chao MJ, Harold D, et al. A modifier of Huntington’s disease onset at the MLH1 locus. Hum Mol Genet. 2017;26(19):3859-3867. doi:10.1093/hmg/ddx286