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 | 2229 | 2012 |
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 | 1384 | 2008 |
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 | 908 | 2008 |
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 | 554 | 2015 |
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 | 456 | 2015 |
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 | 412 | 2011 |
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 | 257 | 2010 |
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 | 241 | 2013 |
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 | 137 | 2013 |
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 | 132 | 2013 |
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 | 125 | 2009 |
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 | 105 | 2007 |
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 | 102 | 2010 |
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 | 97 | 2013 |
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 | 82 | 2007 |
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 | 75 | 2005 |
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 | 74 | 2000 |
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 | 71 | 2002 |
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 | 65 | 2010 |
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 | 58 | 2015 |