Schiff ER, Frampton M, Ben-Yosef N, et al. Rare coding variant analysis in a large cohort of Ashkenazi Jewish families with inflammatory bowel disease. Hum Genet. 2018;137(9):723-734. doi:10.1007/s00439-018-1927-7.

Ruderfer DM, Roberts DC, Schreiber SL, Perlstein EO, Kruglyak L. Using expression and genotype to predict drug response in yeast. PLoS One. 2009;4(9):e6907. doi:10.1371/journal.pone.0006907.

Perlstein EO, Ruderfer DM, Roberts DC, Schreiber SL, Kruglyak L. Genetic basis of individual differences in the response to small-molecule drugs in yeast. Nat Genet. 2007;39(4):496-502. doi:10.1038/ng1991.

Chen Z, Martinez DA, Gujja S, et al. Comparative genomic and transcriptomic analysis of wangiella dermatitidis, a major cause of phaeohyphomycosis and a model black yeast human pathogen. G3 (Bethesda). 2014;4(4):561-78. doi:10.1534/g3.113.009241.

Robertson HR, Feng G. Annual Research Review: Transgenic mouse models of childhood-onset psychiatric disorders. J Child Psychol Psychiatry. 2011;52(4):442-75. doi:10.1111/j.1469-7610.2011.02380.x.

Evrony GD, Cordero DR, Shen J, et al. Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor as the cause of microcephaly-micromelia syndrome. Genome Res. 2017;27(8):1323-1335. doi:10.1101/gr.219899.116.

Yu L, Lutz MW, Wilson RS, et al. APOE ε4-TOMM40 ’523 haplotypes and the risk of Alzheimer’s disease in older Caucasian and African Americans. PLoS One. 2017;12(7):e0180356. doi:10.1371/journal.pone.0180356.

Sun S, Yadav V, Billmyre B, et al. Fungal genome and mating system transitions facilitated by chromosomal translocations involving intercentromeric recombination. PLoS Biol. 2017;15(8):e2002527. doi:10.1371/journal.pbio.2002527.

Gupta R, Qaiser B, He L, et al. Neuregulin signaling pathway in smoking behavior. Transl Psychiatry. 2017;7(8):e1212. doi:10.1038/tp.2017.183.

Reich DE, Lander ES. On the allelic spectrum of human disease. Trends Genet. 2001;17(9):502-10.