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 | 211 | 2015 |
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 | 150 | 2014 |
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 | 113 | 2015 |
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 | 87 | 2018 |
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 | 69 | 2017 |
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 | 61 | 2015 |
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 | 47 | 2015 |
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 | 32 | 2021 |
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 | 32 | 2013 |
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 | 31 | 2021 |
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 | 30 | 2017 |
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 | 30 | 2017 |
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 | 28 | 2014 |
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 | 24 | 2017 |
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 | 18 | 2023 |
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 | 15 | 2022 |
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 | 8 | 2022 |
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 | 6 | 2014 |
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 | 1 | 2019 |
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 |