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Plos One|August 6, 2011
Expression of transposable elements in neural tissues during Xenopus developmentFernando Faunes, Natalia Sanchez, Mauricio Moreno, et al.European Journal of Endocrinology|February 22, 2017
Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumoursSunita M C De Sousa, Mark J McCabe, Kathy Wu, et al.Peerj|August 31, 2017
RNA-seq reveals more consistent reference genes for gene expression studies in human non-melanoma skin cancersVan L T Hoang, Lisa N Tom, Xiu-Cheng Quek, et al.Cell Cycle (Georgetown, Tex.)|August 23, 2011
RNA processing in human mitochondriaMaria I G Lopez Sanchez, Tim R Mercer, Stefan M K Davies, et al.Human Mutation|December 18, 2018
Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detectionMark J Cowley, Yu-Chi Liu, Karen L Oliver, et al.Non-Coding RNA|June 5, 2018
The Non-Coding RNA Journal Club: Highlights on Recent PapersManuela Ferracin, Daniel Gautheret, Florent Hubé, et al.Orphanet Journal of Rare Diseases|May 5, 2017
Initiating an undiagnosed diseases program in the Western Australian public health systemGareth Baynam, Stephanie Broley, Alicia Bauskis, et al.Neurology|May 31, 2022
Use of Whole-Genome Sequencing for Mitochondrial Disease DiagnosisRyan L Davis, Kishore R Kumar, Clare Puttick, et al.Oncotarget|November 5, 2017
Somatic mutations in salivary duct carcinoma and potential therapeutic targetsTimothy K Khoo, Bing Yu, Joel A Smith, et al.International Journal of Molecular Sciences|April 12, 2022
Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal DystrophiesBenjamin M Nash, Alan Ma, Gladys Ho, et al.Pageof 32