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| Paine I, Posey JE, Grochowski CM, et al. (2019) Paralog Studies Augment Gene Discovery: DDX and DHX Genes. American Journal of Human Genetics |
| Cheng H, Dharmadhikari AV, Varland S, et al. (2018) Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies. American Journal of Human Genetics |
| Fang H, Wu Y, Yang H, et al. (2017) Whole genome sequencing of one complex pedigree illustrates challenges with genomic medicine. Bmc Medical Genomics. 10: 10 |
| Jiménez-Barrón LT, O'Rawe JA, Wu Y, et al. (2015) Genome-wide variant analysis of simplex autism families with an integrative clinical-bioinformatics pipeline. Cold Spring Harbor Molecular Case Studies. 1: a000422 |