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David Lawrence
David Lawrence
Bioinformatics Research Fellow, ACRF Cancer Genomics Facility
Verified email at health.sa.gov.au
Title
Cited by
Cited by
Year
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
2112015
Genome‐wide identification of miR‐200 targets reveals a regulatory network controlling cell invasion
CP Bracken, X Li, JA Wright, DM Lawrence, KA Pillman, M Salmanidis, ...
The EMBO journal 33 (18), 2040-2056, 2014
1512014
HENMT1 and piRNA stability are required for adult male germ cell transposon repression and to define the spermatogenic program in the mouse
SL Lim, ZP Qu, RD Kortschak, DM Lawrence, J Geoghegan, ...
PLoS genetics 11 (10), e1005620, 2015
1132015
miR‐200/375 control epithelial plasticity‐associated alternative splicing by repressing the RNA‐binding protein Quaking
KA Pillman, CA Phillips, S Roslan, J Toubia, BK Dredge, AG Bert, R Lumb, ...
The EMBO journal 37 (13), e99016, 2018
872018
Naturally existing isoforms of miR-222 have distinct functions
F Yu, KA Pillman, CT Neilsen, J Toubia, DM Lawrence, A Tsykin, ...
Nucleic acids research 45 (19), 11371-11385, 2017
692017
p53 represses the oncogenic Sno-MiR-28 derived from a SnoRNA
F Yu, CP Bracken, KA Pillman, DM Lawrence, GJ Goodall, DF Callen, ...
PloS one 10 (6), e0129190, 2015
612015
Assessing the gene regulatory properties of Argonaute-bound small RNAs of diverse genomic origin
DW Thomson, KA Pillman, ML Anderson, DM Lawrence, J Toubia, ...
Nucleic acids research 43 (1), 470-481, 2015
472015
GATA2 deficiency syndrome: a decade of discovery
CC Homan, P Venugopal, P Arts, NH Shahrin, S Feurstein, L Rawlings, ...
Human Mutation 42 (11), 1399-1421, 2021
322021
Identification of an enhancer that increases miR-200b~ 200a~ 429 gene expression in breast cancer cells
JL Attema, AG Bert, YY Lim, N Kolesnikoff, DM Lawrence, KA Pillman, ...
PloS one 8 (9), e75517, 2013
322013
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy
CC Homan, SL King-Smith, DM Lawrence, P Arts, J Feng, J Andrews, ...
Haematologica 106 (11), 3004, 2021
312021
Transcriptome profiling reveals expression signatures of cranial neural crest cells arising from different axial levels
R Lumb, S Buckberry, G Secker, D Lawrence, Q Schwarz
BMC Developmental Biology 17, 1-12, 2017
302017
Self-reverting mutations partially correct the blood phenotype in a Diamond Blackfan anemia patient
P Venugopal, S Moore, DM Lawrence, AJ George, RD Hannan, SCE Bray, ...
Haematologica 102 (12), e506, 2017
292017
Nutlin-3a efficacy in sarcoma predicted by transcriptomic and epigenetic profiling
KI Pishas, SJ Neuhaus, MT Clayer, AW Schreiber, DM Lawrence, ...
Cancer research 74 (3), 921-931, 2014
282014
DNA barcoding reveals habitual clonal dominance of myeloma plasma cells in the bone marrow microenvironment
DR Hewett, K Vandyke, DM Lawrence, N Friend, JE Noll, JM Geoghegan, ...
Neoplasia 19 (12), 972-981, 2017
242017
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death
AB Byrne, P Arts, TT Ha, KS Kassahn, LS Pais, A O’Donnell-Luria, ...
Nature Medicine 29 (1), 180-189, 2023
172023
Clonal hematopoiesis in patients with ANKRD26 or ETV6 germline mutations
MW Drazer, CC Homan, K Yu, M Cavalcante de Andrade Silva, ...
Blood advances 6 (15), 4357-4359, 2022
142022
Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation
E Tudini, J Andrews, DM Lawrence, SL King-Smith, N Baker, L Baxter, ...
The American Journal of Human Genetics 109 (11), 1960-1973, 2022
82022
Detection of BCR-ABL1 compound and polyclonal mutants in chronic myeloid leukemia patients using a novel next generation sequencing approach that minimises PCR and sequencing …
WT Parker, SR Phillis, DT Yeung, D Lawrence, A Schreiber, P Wang, ...
Blood 124 (21), 399, 2014
62014
Implications of revertant somatic mosaicism in bone marrow failure syndromes
P Venugopal, M Babic, C Barnett, S Bray, A Brown, J Cheah, R D'Andrea, ...
Experimental Hematology 76, S90, 2019
12019
Development of a Data Portal for Aggregation and Analysis of Genomics Data in Familial Platelet Disorder with Predisposition to Myeloid Malignancy-the RUNX1. DB
AL Brown, M Armstrong, D Lawrence, P Wang, P Arts, N Duployez, ...
Blood, The Journal of the American Society of Hematology 132 (Supplement 1 …, 2018
2018
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Articles 1–20