Brooke Gardiner - Concepedia

Author

Brooke Gardiner

Also Known As

B Gardiner, B. Gardiner, Brooke B A Gardiner, Brooke B Gardiner, Brooke B. Gardiner, Brooke Gardiner, Gardiner, Brooke, Mark J. Cowley

Publications

Citations

H-Index

Concepts

All Affiliations

The University of Queensland Translational Research Institute Princess Alexandra Hospital Royal Brisbane and Women's Hospital The University of Sydney

About

Brooke Gardiner is an author at The University of Queensland specializing in medicine, cell biology, and gene expression.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	2.4K
2	Cell Biology	7	7	1.5K
3	Engineering	1	1	84
4	Natural Sciences	1	1	26
5	Biochemistry	1	1	26

Brooke Gardiner

Publications

4.9K

Citations

H-Index

Page 1

	Year	Citations
Stem cell transcriptome profiling via massive-scale mRNA sequencing Nicole Cloonan, Alistair R. R. Forrest, Gabriel Kolle, Nature Methods Functional GenomicsSingle Cell SequencingTranscriptome ProfilingTranscriptomics TechnologyCell Biology	2008	1K
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation Marcel E. Dinger, Paulo Amaral, Tim R. Mercer, Genome Research	2008	742
Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture Hou‐Feng Zheng, Vincenzo Forgetta, Yi‐Hsiang Hsu, Nature Bone DiseaseBone HealthFracture DiagnosticsGeneticsBone Remodeling	2015	616
Brief Report: Intestinal Dysbiosis in Ankylosing Spondylitis Mary‐Ellen Costello, Francesco Ciccia, Dana Willner, Arthritis & Rheumatology	2014	407
MicroRNAs and their isomiRs function cooperatively to target common biological pathways Nicole Cloonan, Shivangi Wani, Qinying Xu, Genome biology	2011	338
A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells Michael R. Tallack, Tom Whitington, Wai Shan Yuen, Genome Research Molecular RegulationBlood CellCellular PhysiologyTranscriptional RegulationCell Regulation	2010	225
Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans Jan Halbritter, Albane A. Bizet, Miriam Schmidts, The American Journal of Human Genetics	2013	225
Reduced mucin sulfonation and impaired intestinal barrier function in the hyposulfataemic NaS1 null mouse Paul A. Dawson, S Huxley, Brooke Gardiner, Gut	2009	140
Short-Rib Polydactyly and Jeune Syndromes Are Caused by Mutations in WDR60 Aideen McInerney‐Leo, Miriam Schmidts, Claudio R. Cortés, The American Journal of Human Genetics	2013	131
Mutations in the Gene Encoding IFT Dynein Complex Component WDR34 Cause Jeune Asphyxiating Thoracic Dystrophy Miriam Schmidts, Julia Vodopiutz, Sonia Christou-Savina, The American Journal of Human Genetics Genetic DisorderGeneticsDegenerative DiseaseMolecular GeneticsDisease Gene Identification	2013	122

Page 1