1.
Khalil R, Kenny C, Hill S, et al. PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features. Am J Med Genet B Neuropsychiatr Genet. 2018;177(8):736-745. doi:10.1002/ajmg.b.32688.
1.
Guan Y, Roter DL, Erby LH, et al. Communication Predictors of Patient and Companion Satisfaction with Alzheimer’s Genetic Risk Disclosure. J Health Commun. 2018;23(8):807-814. doi:10.1080/10810730.2018.1528319.
1.
Wang S-H, Hsiao P-C, Yeh L-L, et al. Polygenic risk for schizophrenia and neurocognitive performance in patients with schizophrenia. Genes Brain Behav. 2018;17(1):49-55. doi:10.1111/gbb.12401.
1.
Huckins LM, Hatzikotoulas K, Southam L, et al. Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa. Mol Psychiatry. 2018;23(5):1169-1180. doi:10.1038/mp.2017.88.
1.
Holm IA, Agrawal PB, Ceyhan-Birsoy O, et al. The BabySeq project: implementing genomic sequencing in newborns. BMC Pediatr. 2018;18(1):225. doi:10.1186/s12887-018-1200-1.
1.
Tucker NR, McLellan MA, Hu D, et al. Novel Mutation in (Filamin C) Causes Familial Restrictive Cardiomyopathy. Circ Cardiovasc Genet. 2017;10(6). doi:10.1161/CIRCGENETICS.117.001780.
1.
Guan Y, Roter DL, Wolff JL, et al. The impact of genetic counselors’ use of facilitative strategies on cognitive and emotional processing of genetic risk disclosure for Alzheimer’s disease. Patient Educ Couns. 2018;101(5):817-823. doi:10.1016/j.pec.2017.11.019.
1.
Aneichyk T, Hendriks WT, Yadav R, et al. Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly. Cell. 2018;172(5):897-909.e21. doi:10.1016/j.cell.2018.02.011.
1.
Kaplanis J, Gordon A, Shor T, et al. Quantitative analysis of population-scale family trees with millions of relatives. Science. 2018;360(6385):171-175. doi:10.1126/science.aam9309.
1.
Dunn EC, Crawford KM, Soare TW, et al. Exposure to childhood adversity and deficits in emotion recognition: results from a large, population-based sample. J Child Psychol Psychiatry. 2018;59(8):845-854. doi:10.1111/jcpp.12881.