| Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease S Branford, P Wang, DT Yeung, D Thomson, A Purins, C Wadham, ... Blood, The Journal of the American Society of Hematology 132 (9), 948-961, 2018 | 182 | 2018 |
| Ectrodactyly and Lethal Pulmonary Acinar Dysplasia Associated with Homozygous FGFR2 Mutations Identified by Exome Sequencing CP Barnett, NJ Nataren, M Klingler‐Hoffmann, Q Schwarz, CE Chong, ... Human mutation 37 (9), 955-963, 2016 | 31 | 2016 |
| Allan–Herndon–Dudley syndrome with unusual profound sensorineural hearing loss L Gagliardi, N Nataren, J Feng, AW Schreiber, CN Hahn, LS Conwell, ... American Journal of Medical Genetics Part A 167 (8), 1872-1876, 2015 | 11 | 2015 |
| High incidence of mutated cancer-associated genes at diagnosis in CML patients with early transformation to blast crisis S Branford, PPS Wang, WT Parker, D Yeung, JE Marum, D Stangl, ... Blood 126 (23), 600, 2015 | 5 | 2015 |
| Molecular skin cancer diagnosis: Promise and limitations N Nataren, M Yamada, T Prow The Journal of Molecular Diagnostics 25 (1), 17-35, 2023 | 3 | 2023 |
| Novel fusion genes at CML diagnosis reveal a complex pattern of genomic rearrangements and sequence inversions associated with the Philadelphia chromosome in patients with … JE Marum, PPS Wang, D Stangl, DT Yeung, MC Mueller, CT Dietz, ... Blood 128 (22), 1219, 2016 | 3 | 2016 |
| Integrative genomics reveals cancer associated mutations are common at diagnosis of CML in patients with poor response to TKI therapy S Branford, P Wang, D Yeung, A Purins, JE Marum, N Nataren, H Shahrin, ... Blood 130, 251, 2017 | 1 | 2017 |
| Cover Image, Volume 37, Issue 9 CP Barnett, NJ Nataren, M Klingler‐Hoffmann, Q Schwarz, CE Chong, ... Human mutation 37 (9), i-i, 2016 | | 2016 |
