Factors influencing genetic variation in wild mice by Davies, RW

Private genomes and public SNPs: homomorphic encryption of genotypes and phenotypes for shared quantitative genetics by Mott, R, Fischer, C, Prins, P, Davies, RW

Inferring population histories for ancient genomes using genome-wide genealogies by Speidel, L, Cassidy, L, Davies, RW, Hellenthal, G, Skoglund, P, Myers, SR

Rapid genotype imputation from sequence with reference panels by Davies, RW, Kucka, M, Su, D, Shi, S, Flanaghan, M, Cunniff, CM, Chan, YF, Myers, S

Analysis of independent cohorts of outbred CFW mice reveals novel loci for behavioral and physiological traits and identifies factors determining reproducibility by Zou, J, Gopalakrishnan, S, Parker, CC, Nicod, J, Mott, R, Cai, N, Lionikas, A, Davies, RW, Palmer, AA, Flint, J

Differences in 5'untranslated regions highlight the importance of translational regulation of dosage sensitive genes by Wieder, N, D’Souza, EN, Martin-Geary, AC, Lassen, FH, Talbot-Martin, J, Fernandes, M, Chothani, SP, Rackham, OJL, Schafer, S, Aspden, JL, MacArthur, DG, Davies, RW, Whiffin, N

Personalized recurrence risk assessment following the birth of a child with a pathogenic de novo mutation by Bernkopf, M, Abdullah, UB, Bush, SJ, Wood, KA, Ghaffari, S, Koelling, N, Maher, GJ, Williams, J, Blair, EM, Kelly, FB, Bloss, A, Kini, U, Németh, AH, Saunders, K, Shears, DJ, Stewart, H, Clouston, P, Davies, RW, Wilkie, AOM, Goriely, A

Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders by D'Abate, L, Walker, S, Yuen, RKC, Tammimies, K, Buchanan, JA, Davies, RW, Thiruvahindrapuram, B, Wei, J, Brian, J, Bryson, SE, Dobkins, K, Howe, J, Landa, R, Leef, J, Messinger, D, Ozonoff, S, Smith, IM, Stone, WL, Warren, ZE, Young, G, Zwaigenbaum, L, Scherer, SW

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome by Davies, RW, Fiksinski, AM, Breetvelt, EJ, Williams, NM, Hooper, SR, Monfeuga, T, Bassett, AS, Owen, MJ, Gur, RE, Morrow, BE, McDonald-McGinn, DM, Swillen, A, Chow, EWC, van den Bree, M, Emanuel, BS, Vermeesch, JR, van Amelsvoort, T, Arango, C, Armando, M, Campbell, LE, Cubells, JF, Eliez, S, Garcia-Minaur, S, Gothelf, D, Kates, WR, Murphy, KC, Murphy, CM, Murphy, DG, Philip, N, Repetto, GM, Shashi, V, Simon, TJ, Suñer, DH, Vicari, S, Scherer, SW, Bearden, CE, Vorstman, JAS, International 22q11.2 Brain and Behavior Consortium

Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy by Roberts, JD, Murphy, NP, Hamilton, RM, Lubbers, ER, James, CA, Kline, CF, Gollob, MH, Krahn, AD, Sturm, AC, Musa, H, El-Refaey, M, Koenig, S, Aneq, MÅ, Hoorntje, ET, Graw, SL, Davies, RW, Rafiq, MA, Koopmann, TT, Aafaqi, S, Fatah, M, Chiasson, DA, Taylor, MRG, Simmons, SL, Han, M, Van Opbergen, CJM, Wold, LE, Sinagra, G, Mittal, K, Tichnell, C, Murray, B, Codima, A, Nazer, B, Nguyen, DT, Marcus, FI, Sobriera, N, Lodder, EM, Van Den Berg, MP, Spears, DA, Robinson, JF, Ursell, PC, Green, AK, Skanes, AC, Tang, AS, Gardner, MJ, Hegele, RA, Van Veen, TAB, Wilde, AAM, Healey, JS, Janssen, PML, Mestroni, L, Van Tintelen, JP, Calkins, H, Judge, DP, Hund, TJ, Scheinman, MM, Mohler, PJ