Browsing by Author Xu, Xun

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Issue DateTitleAuthor(s)Citation
2017Dual-stage deep learning framework for pigment epithelium detachment segmentation in polypoidal choroidal vasculopathyFeng, Dagan 'David'; Kim, Jinman; Li, Changyang; Wang, Xiu Ying; Yan, Ke; Su, Li; Xu, Xun; Xu, Yupeng; Yu, Suqin; Information Technologies; Information Technologies; Information Technologies; Information Technologies; Information TechnologiesDual-stage deep learning framework for pigment epithelium detachment segmentation in polypoidal choroidal vasculopathy, Biomedical Optics Express, vol.8, 9, 2017,pp 4061-4076
2011Evaluation of carbon incorporation and strain of doped MgB2 superconductor by Raman spectroscopyRinger, Simon; Yeoh, Wai; Zheng, Rongkun; Chen, S.; Dou, Shi; Li, W. X.; MacManus-Driscoll, J.L; Xu, Xun; Australian Centre for Microscopy and Microanalysis (ACMM); Australian Centre for Microscopy and Microanalysis (ACMM); Australian Centre for Microscopy and Microanalysis (ACMM)Evaluation of carbon incorporation and strain of doped MgB2 superconductor by Raman spectroscopy, Scripta Materialia, vol.64, 4, 2011,pp 323-326
2010Graphene doping to enhance the flux pinning and supercurrent carrying ability of a magnesium diboride superconductorRinger, Simon; Yeoh, Waikong; Zheng, Rongkun; Choucair, Mohammad; Dou, Shi Xue; Kim, J. H.; Stride, John Arron; Wang, Xiaolin; Xu, Xun; Aerospace Mech & Mtronic Eng; Aerospace Mech & Mtronic Eng; PhysicsGraphene doping to enhance the flux pinning and supercurrent carrying ability of a magnesium diboride superconductor, Superconductor Science and Technology, vol.23, 8, 2010,pp 1-5
2014Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1Al-Odaib, Ahmad; Barbaro, Pasquale; Bryan, Tracy; Christodoulou, John; Kartawinata, Melissa; Pickett, Hilda; Reddel, Roger; Chen, Yulan; Guo, Yiran; Hakonarson, Haron; Keating, Brendan; Kilo, Tatjana; Li, Jiankang; Teo, Juliana; Tian, Lifeng; Xu, Xun; Childrens Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research Ins; Childrens Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research InsInherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1, Blood, vol.124, 18, 2014,pp 2767-2774
2015Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemiaAlexander, Stephen; Christodoulou, John; Cooper, Sandra; Davis, Ryan; Menezes, Minal; Riley, Lisa; Sue, Carolyn; Arbuckle, Susan; Dong, Daoyuan; Glessner, Joseph; Guo, Yiran; Hakonarson, Haron; Keating, Brendan; Kirwan, Paul; Li, Jiankang; Li, Zhijun; Thorburn, David; Xu, Xun; Zhang, Jianguo; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Northern Clinical School: Kolling Institute; Childrens Hospital Westmead: Paediatrics & Child Health; Vet Science Faculty; Northern Clinical School: MedicineMutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia, Human Molecular Genetics, vol.24, 8, 2015,pp 2297-2307
2014Unabridged phase diagram for single-phased FeSexTe1-x thin filmsCui, Xiangyuan (Carl); Ringer, Simon; Yeoh, Waikong; Dou, Shixue; Du, Yi; Shi, Zhixiang; Wang, X; Xu, Xun; Zhuang, J; Aerospace Mech & M'tronic Eng; Aerospace Mech & M'tronic Eng; Aerospace Mech & M'tronic EngUnabridged phase diagram for single-phased FeSexTe1-x thin films, Scientific Reports, vol.4, 2014, 2014,pp 1-6
2016Utility of next-generation sequencing technologies for the efficient genetic resolution of haematological disordersAdes, Lesley; Alodaib, Ahmed; Christodoulou, John; Gold, Wendy; Barbaro, P.; Guo, Yiran; Hakonarson, Hákon H.; Keating, Brendan; Li, Jiankang; Teo, Juliana; Xu, Xun; Zhang, Jianguo; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child HealthUtility of next-generation sequencing technologies for the efficient genetic resolution of haematological disorders, Clinical Genetics, vol.89, 2, 2016,pp 163-172
2015Value of whole exome sequencing for syndromic retinal dystrophy diagnosis in young patientsJamieson, Robyn; Wilson, Meredith; Chen, Yulan; Goodwin, Linda; Guo, Yiran; Hakonarson, Hákon H.; He, Sijie; Keating, Brendan; Li, Dong; Liang, Jinlong; Prokudin, I; Rose, Loreto; Tian, Lifeng; Xu, Xun; Childrens Medical Research Institute (CMRI); Childrens Hospital Westmead: Paediatrics & Child HealthValue of whole exome sequencing for syndromic retinal dystrophy diagnosis in young patients, Clinical and Experimental Ophthalmology, vol.43, 2, 2015,pp 132-138
2017Whole Exome Sequencing Identifies the Genetic Basis of Late-Onset Leigh Syndrome in a Patient with MRI but Little Biochemical Evidence of a Mitochondrial DisorderChristodoulou, John; Gold, Wendy; Nafisinia, Michael; Riley, Lisa; Chen, Yulan; Dang, Xiao; Guo, Yiran; Hakonarson, Hakon; Keating, Brendan; Lake, Nicole; Li, Jiankang; Thornburn, David; Xu, Xun; Zhang, Jianguo; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child HealthWhole Exome Sequencing Identifies the Genetic Basis of Late-Onset Leigh Syndrome in a Patient with MRI but Little Biochemical Evidence of a Mitochondrial Disorder, JIMD Reports, vol.32, N/A, 2017,pp 117-124