Christopher Norman Hahn
Christopher Norman Hahn
Other namesChristopher Hahn
Genetics and Molecular Biology, Adelaide
Verified email at
Cited by
Cited by
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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