| An atlas of human long non-coding RNAs with accurate 5′ ends CC Hon, JA Ramilowski, J Harshbarger, N Bertin, OJL Rackham, J Gough, ... Nature 543 (7644), 199-204, 2017 | 1016 | 2017 |
| Site-specific DICER and DROSHA RNA products control the DNA-damage response S Francia, F Michelini, A Saxena, D Tang, M De Hoon, V Anelli, M Mione, ... Nature 488 (7410), 231-235, 2012 | 594 | 2012 |
| A genome wide survey of SNP variation reveals the genetic structure of sheep breeds JW Kijas, D Townley, BP Dalrymple, MP Heaton, JF Maddox, A McGrath, ... PloS one 4 (3), e4668, 2009 | 428 | 2009 |
| Analysis of early nephron patterning reveals a role for distal RV proliferation in fusion to the ureteric tip via a cap mesenchyme-derived connecting segment K Georgas, B Rumballe, MT Valerius, HS Chiu, RD Thiagarajan, ... Developmental biology 332 (2), 273-286, 2009 | 272 | 2009 |
| Identification of anchor genes during kidney development defines ontological relationships, molecular subcompartments and regulatory pathways RD Thiagarajan, KM Georgas, BA Rumballe, E Lesieur, HS Chiu, ... PloS one 6 (2), e17286, 2011 | 90 | 2011 |
| Suppression of artifacts and barcode bias in high-throughput transcriptome analyses utilizing template switching DTP Tang, C Plessy, M Salimullah, AM Suzuki, R Calligaris, S Gustincich, ... Nucleic acids research 41 (3), e44-e44, 2013 | 80 | 2013 |
| RNA-MATE: a recursive mapping strategy for high-throughput RNA-sequencing data N Cloonan, Q Xu, GJ Faulkner, DF Taylor, DTP Tang, G Kolle, ... Bioinformatics 25 (19), 2615-2616, 2009 | 63 | 2009 |
| The rare and undiagnosed diseases diagnostic service–application of massively parallel sequencing in a state-wide clinical service G Baynam, N Pachter, F McKenzie, S Townshend, J Slee, C Kiraly-Borri, ... Orphanet Journal of Rare Diseases 11, 1-7, 2016 | 62 | 2016 |
| High expression of insulin receptor on tumour‐associated blood vessels in invasive bladder cancer predicts poor overall and progression‐free survival F Roudnicky, LC Dieterich, C Poyet, L Buser, P Wild, D Tang, ... The Journal of pathology 242 (2), 193-205, 2017 | 34 | 2017 |
| CCL2 enhances pluripotency of human induced pluripotent stem cells by activating hypoxia related genes Y Hasegawa, D Tang, N Takahashi, Y Hayashizaki, ARR Forrest, ... Scientific reports 4 (1), 5228, 2014 | 34 | 2014 |
| Refining transcriptional programs in kidney development by integration of deep RNA-sequencing and array-based spatial profiling RD Thiagarajan, N Cloonan, BB Gardiner, TR Mercer, G Kolle, ... BMC genomics 12, 1-16, 2011 | 32 | 2011 |
| Comparative gene expression analysis of genital tubercle development reveals a putative appendicular Wnt7 network for the epidermal differentiation HS Chiu, JC Szucsik, KM Georgas, JL Jones, BA Rumballe, D Tang, ... Developmental biology 344 (2), 1071-1087, 2010 | 30 | 2010 |
| Analysis of the complement and molecular evolution of tRNA genes in cow DTP Tang, EA Glazov, SM McWilliam, WC Barris, BP Dalrymple BMC genomics 10, 1-13, 2009 | 30 | 2009 |
| Short stature and hypoparathyroidism in a child with Kenny-Caffey syndrome type 2 due to a novel mutation in FAM111A gene MB Abraham, D Li, D Tang, SM O’Connell, F McKenzie, EM Lim, ... International Journal of Pediatric Endocrinology 2017, 1-9, 2017 | 29 | 2017 |
| piRNAs warrant investigation in Rett Syndrome: an omics perspective A Saxena, D Tang, P Carninci Disease markers 33 (5), 261-275, 2012 | 28 | 2012 |
| Reference genotype and exome data from an Australian Aboriginal population for health-based research D Tang, D Anderson, RW Francis, G Syn, SE Jamieson, T Lassmann, ... Scientific data 3 (1), 1-7, 2016 | 22 | 2016 |
| The bone marrow microenvironment of pre-B acute lymphoblastic leukemia at single-cell resolution D Anderson, P Skut, AM Hughes, E Ferrari, J Tickner, J Xu, BH Mullin, ... Scientific Reports 10 (1), 19173, 2020 | 18 | 2020 |
| A novel, homozygous mutation in desert hedgehog (DHH) in a 46, XY patient with dysgenetic testes presenting with primary amenorrhoea: a case report KM Rothacker, KL Ayers, D Tang, K Joshi, JA Van Den Bergen, ... International journal of pediatric endocrinology 2018, 1-9, 2018 | 16 | 2018 |
| A flexible computational pipeline for research analyses of unsolved clinical exome cases T Lassmann, RW Francis, A Weeks, D Tang, SE Jamieson, S Broley, ... NPJ genomic medicine 5 (1), 54, 2020 | 8 | 2020 |
| International Sheep Genomics, C., 2009. A genome wide survey of SNP variation reveals the genetic structure of sheep breeds JW Kijas, D Townley, BP Dalrymple, MP Heaton, JF Maddox, A McGrath, ... PloS one 4, e4668, 0 | 8 | |
