| Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia CN Hahn, CE Chong, CL Carmichael, EJ Wilkins, PJ Brautigan, XC Li, ... Nature genetics 43 (10), 1012-1017, 2011 | 711 | 2011 |
| A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia S Shah, KA Schrader, E Waanders, AE Timms, J Vijai, C Miething, ... Nature genetics 45 (10), 1226-1231, 2013 | 368 | 2013 |
| Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the … J Kazenwadel, GA Secker, YJ Liu, JA Rosenfeld, RS Wildin, ... Blood, The Journal of the American Society of Hematology 119 (5), 1283-1291, 2012 | 308 | 2012 |
| Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies M Lewinsohn, AL Brown, LM Weinel, C Phung, G Rafidi, MK Lee, ... Blood, The Journal of the American Society of Hematology 127 (8), 1017-1023, 2016 | 237 | 2016 |
| GATA2 is required for lymphatic vessel valve development and maintenance J Kazenwadel, KL Betterman, CE Chong, PH Stokes, YK Lee, GA Secker, ... The Journal of clinical investigation 125 (8), 2979-2994, 2015 | 232 | 2015 |
| Sphingosine kinase-1 enhances endothelial cell survival through a PECAM-1–dependent activation of PI-3K/Akt and regulation of Bcl-2 family members V Limaye, X Li, C Hahn, P Xia, MC Berndt, MA Vadas, JR Gamble Blood 105 (8), 3169-3177, 2005 | 218 | 2005 |
| 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 | 208 | 2018 |
| Generalized CNS disease and massive GM1-ganglioside accumulation in mice defective in lysosomal acid β-galactosidase CN Hahn, M del Pilar Martin, M Schröder, MT Vanier, K Suzuki, Y Hara, ... Human molecular genetics 6 (2), 205-211, 1997 | 186 | 1997 |
| PPARγ agonists ameliorate endothelial cell activation via inhibition of diacylglycerol–protein kinase C signaling pathway: role of diacylglycerol kinase E Verrier, L Wang, C Wadham, N Albanese, C Hahn, JR Gamble, ... Circulation research 94 (11), 1515-1522, 2004 | 147 | 2004 |
| Genomic subtyping and therapeutic targeting of acute erythroleukemia I Iacobucci, J Wen, M Meggendorfer, JK Choi, L Shi, SB Pounds, ... Nature genetics 51 (4), 694-704, 2019 | 146 | 2019 |
| RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML AL Brown, P Arts, CL Carmichael, M Babic, J Dobbins, CE Chong, ... Blood advances 4 (6), 1131-1144, 2020 | 143 | 2020 |
| Transcriptional synergism between vitamin D-responsive elements in the rat 25-hydroxyvitamin D3 24-hydroxylase (CYP24) promoter DM Kerry, PP Dwivedi, CN Hahn, HA Morris, JL Omdahl, BK May Journal of Biological Chemistry 271 (47), 29715-29721, 1996 | 142 | 1996 |
| Systemic and neurologic abnormalities distinguish the lysosomal disorders sialidosis and galactosialidosis in mice N de Geest, E Bonten, L Mann, J de Sousa-Hitzler, C Hahn, A d'Azzo Human molecular genetics 11 (12), 1455-1464, 2002 | 136 | 2002 |
| Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability LS Nguyen, L Jolly, C Shoubridge, WK Chan, L Huang, F Laumonnier, ... Molecular psychiatry 17 (11), 1103-1115, 2012 | 129 | 2012 |
| ARMC5 mutations are common in familial bilateral macronodular adrenal hyperplasia L Gagliardi, AW Schreiber, CN Hahn, J Feng, T Cranston, H Boon, C Hotu, ... The Journal of Clinical Endocrinology & Metabolism 99 (9), E1784-E1792, 2014 | 118 | 2014 |
| Effect of disrupted SOX18 transcription factor function on tumor growth, vascularization, and endothelial development N Young, CN Hahn, A Poh, C Dong, D Wilhelm, J Olsson, GEO Muscat, ... Journal of the National Cancer Institute 98 (15), 1060-1067, 2006 | 107 | 2006 |
| Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome MCJ Jongmans, RP Kuiper, CL Carmichael, EJ Wilkins, N Dors, ... Leukemia 24 (1), 242-246, 2010 | 105 | 2010 |
| Basal and angiopoietin-1–mediated endothelial permeability is regulated by sphingosine kinase-1 X Li, M Stankovic, CS Bonder, CN Hahn, M Parsons, SM Pitson, P Xia, ... Blood, The Journal of the American Society of Hematology 111 (7), 3489-3497, 2008 | 105 | 2008 |
| Ozz-E3, a muscle-specific ubiquitin ligase, regulates β-catenin degradation during myogenesis T Nastasi, A Bongiovanni, Y Campos, L Mann, JN Toy, J Bostrom, ... Developmental cell 6 (2), 269-282, 2004 | 104 | 2004 |
| Phenoxodiol, an experimental anticancer drug, shows potent antiangiogenic properties in addition to its antitumour effects JR Gamble, P Xia, CN Hahn, JJ Drew, CJ Drogemuller, D Brown, ... International journal of cancer 118 (10), 2412-2420, 2006 | 102 | 2006 |
Hamish S ScottCenter of Cancer BiologyПідтверджена електронна адреса в sa.gov.au
