Dave Tang
TitleCited byYear
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, 2012
2812012
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
2282009
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, 2017
2042017
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
1642009
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
602009
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
582011
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, 2012
352012
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), 441, 2011
252011
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), 77, 2016
222016
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
222010
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, 5228, 2014
182014
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), 188, 2009
152009
piRNAs warrant investigation in Rett Syndrome: an omics perspective
A Saxena, D Tang, P Carninci
Disease markers 33 (5), 261-275, 2012
142012
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, 160023, 2016
102016
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
10
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
32017
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), 2, 2018
2018
Arylsulphatase A Pseudodeficiency (ARSA-PD), hypertension and chronic renal disease in Aboriginal Australians
D Tang, M Fakiola, G Syn, D Anderson, HJ Cordell, ESH Scaman, E Davis, ...
Scientific reports 8 (1), 10912, 2018
2018
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), 1, 2017
2017
High-throughout transcriptome sequencing: data analysis and methods development of large expression data sets
DTP Tang
Amsterdam: Vrije Universiteit, 2015
2015
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Articles 1–20