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Brooke Gardiner
Brooke Gardiner
Genomic Service Coordinator, University of Queensland
Verified email at uq.edu.au
Title
Cited by
Cited by
Year
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes
AV Biankin, N Waddell, KS Kassahn, MC Gingras, LB Muthuswamy, ...
Nature 491 (7424), 399-405, 2012
21712012
Stem cell transcriptome profiling via massive-scale mRNA sequencing
N Cloonan, ARR Forrest, G Kolle, BBA Gardiner, GJ Faulkner, MK Brown, ...
Nature methods 5 (7), 613-619, 2008
13672008
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation
ME Dinger, PP Amaral, TR Mercer, KC Pang, SJ Bruce, BB Gardiner, ...
Genome research 18 (9), 1433-1445, 2008
9012008
Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture
HF Zheng, V Forgetta, YH Hsu, K Estrada, A Rosello‐Diez, PJ Leo, ...
Nature 526 (7571), 112-117, 2015
5262015
Brief report: intestinal dysbiosis in ankylosing spondylitis
ME Costello, F Ciccia, D Willner, N Warrington, PC Robinson, B Gardiner, ...
Arthritis & rheumatology 67 (3), 686-691, 2015
4412015
MicroRNAs and their isomiRs function cooperatively to target common biological pathways
N Cloonan, S Wani, Q Xu, J Gu, K Lea, S Heater, C Barbacioru, ...
Genome biology 12, 1-20, 2011
4082011
A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells
MR Tallack, T Whitington, WS Yuen, EN Wainwright, JR Keys, ...
Genome research 20 (8), 1052-1063, 2010
2482010
Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans
J Halbritter, AA Bizet, M Schmidts, JD Porath, DA Braun, HY Gee, ...
The American Journal of Human Genetics 93 (5), 915-925, 2013
2342013
Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy
M Schmidts, J Vodopiutz, S Christou-Savina, CR Cortés, ...
The American Journal of Human Genetics 93 (5), 932-944, 2013
1322013
Short-rib polydactyly and Jeune syndromes are caused by mutations in WDR60
AM McInerney-Leo, M Schmidts, CR Cortés, PJ Leo, B Gener, ...
The American Journal of Human Genetics 93 (3), 515-523, 2013
1302013
Reduced mucin sulfonation and impaired intestinal barrier function in the hyposulfataemic NaS1 null mouse
PA Dawson, S Huxley, B Gardiner, T Tran, JL McAuley, S Grimmond, ...
Gut 58 (7), 910-919, 2009
1192009
Regulated post-transcriptional RNA cleavage diversifies the eukaryotic transcriptome
TR Mercer, ME Dinger, CP Bracken, G Kolle, JM Szubert, DJ Korbie, ...
Genome research 20 (12), 1639-1650, 2010
1032010
Transcriptional analysis of early lineage commitment in human embryonic stem cells
AL Laslett, S Grimmond, B Gardiner, L Stamp, A Lin, SM Hawes, ...
BMC developmental biology 7, 1-18, 2007
1032007
Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6
DB Sparrow, A McInerney-Leo, ZS Gucev, B Gardiner, M Marshall, PJ Leo, ...
Human molecular genetics 22 (8), 1625-1631, 2013
962013
Dynamic transcription programs during ES cell differentiation towards mesoderm in serum versus serum-freeBMP4 culture
SJ Bruce, BB Gardiner, LJ Burke, MM Gongora, SM Grimmond, ...
BMC genomics 8, 1-26, 2007
812007
Temporal and spatial transcriptional programs in murine kidney development
G Challen, B Gardiner, G Caruana, X Kostoulias, G Martinez, M Crowe, ...
Physiological genomics 23 (2), 159-171, 2005
742005
Osteonectin/SPARC induction by ectopic β3 integrin in human radial growth phase primary melanoma cells
RA Sturm, K Satyamoorthy, F Meier, BB Gardiner, DJ Smit, B Vaidya, ...
Cancer research 62 (1), 226-232, 2002
682002
Inhibition of melanin synthesis by cystamine in human melanoma cells
L Qiu, M Zhang, I Tonks, G Kay, PG Parsons, RA Sturm, B Gardiner
Journal of investigative dermatology 114 (1), 21-27, 2000
682000
Profiling gene expression induced by protease-activated receptor 2 (PAR2) activation in human kidney cells
JY Suen, B Gardiner, S Grimmond, DP Fairlie
PLoS One 5 (11), e13809, 2010
622010
Whole exome sequencing is an efficient, sensitive and specific method for determining the genetic cause of short‐rib thoracic dystrophies
AM McInerney‐Leo, JE Harris, PJ Leo, MS Marshall, B Gardiner, ...
Clinical genetics 88 (6), 550-557, 2015
572015
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