| Preview | Issue Date | Title | Author(s) |
| 2023 | Aicardi Syndrome Is a Genetically Heterogeneous Disorder | Ha, T.T.; Burgess, R.; Newman, M.; Moey, C.; Mandelstam, S.A.; Gardner, A.E.; Ivancevic, A.M.; Pham, D.; Kumar, R.; Smith, N.; Patel, C.; Malone, S.; Ryan, M.M.; Calvert, S.; van Eyk, C.L.; Lardelli, M.; Berkovic, S.F.; Leventer, R.J.; Richards, L.J.; Scheffer, I.E.; et al. |
| 2021 | Different types of disease-causing non-coding variants revealed by genomic and gene expression analyses in families with X-linked intellectual disability | Field, M.J.; Sharma, R.; Hackett, A.; Kayumi, S.; Shoubridge, C.; Ewans, L.J.; Ivancevic, A.M.; Dudding-Byth, T.; Carroll, R.; Kroes, T.; Gardner, A.E.; Sullivan, P.; Ha, T.T.; Schwartz, C.E.; Cowley, M.J.; Dinger, M.E.; Palmer, E.E.; Christie, L.; Shaw, M.; Roscioli, T.; et al. |
| 2023 | Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis | Ghaoui, R.; Ha, T.T.; Kerkhof, J.; McConkey, H.; Gao, S.; Babic, M.; King, R.; Ravenscroft, G.; Kocyzek, B.; Otto, S.; Laing, N.G.; Scott, H.; Sadikovic, B.; Kassahn, K.S. |
| 2023 | Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death | Byrne, A.B.; Arts, P.; Ha, T.T.; Kassahn, K.S.; Pais, L.S.; O'Donnell-Luria, A.; Broad Institute Center for Mendelian Genomics,; Babic, M.; Frank, M.S.B.; Feng, J.; Wang, P.; Lawrence, D.M.; Eshraghi, L.; Arriola, L.; Toubia, J.; Nguyen, H.; Genomic Autopsy Study Research Network,; McGillivray, G.; Pinner, J.; McKenzie, F.; et al. |
| 2023 | Somatic mutational landscape of hereditary hematopoietic malignancies caused by germ line RUNX1, GATA2, and DDX41 variants | Homan, C.C.; Drazer, M.W.; Yu, K.; Lawrence, D.M.; Feng, J.; Arriola-Martinez, L.A.; Pozsgai, M.J.; McNeely, K.E.; Ha, T.T.; Venugopal, P.; Arts, P.; King-Smith, S.; Cheah, J.J.; Armstrong, M.; Wang, P.; Bödör, C.; Cantor, A.B.; Cazzola, M.; Degelman, E.S.; DiNardo, C.D.; et al. |
