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Author Details

Caroline E Walker
University of London
1998
20
16
PMIDPaper TitleJournal TitlePublished Year
28065523A Web-Based Registry for Familial Hypercholesterolaemia.Heart Lung Circ2017
28468665Initiating an undiagnosed diseases program in the Western Australian public health system.Orphanet J Rare Dis2017
284432723-Dimensional Facial Analysis-Facing Precision Public Health.Front Public Health2017
28344196Design of the Familial Hypercholesterolaemia Australasia Network Registry: Creating Opportunities for Greater International Collaboration.J Atheroscler Thromb2017
29214566Improved Diagnosis and Care for Rare Diseases through Implementation of Precision Public Health Framework.Adv Exp Med Biol2017
27657686The collective impact of rare diseases in Western Australia: an estimate using a population-based cohort.Genet Med2017
27287197The rare and undiagnosed diseases diagnostic service - application of massively parallel sequencing in a state-wide clinical service.Orphanet J Rare Dis2016
25943355Use of mechanical airway clearance devices in the home by people with neuromuscular disorders: effects on health service use and lifestyle benefits.Orphanet J Rare Dis2015
16354724Long-term effect of therapeutic laser photocoagulation on gene expression in the eye.FASEB J2006
17249575Laser photocoagulation: ocular research and therapy in diabetic retinopathy.Adv Exp Med Biol2006
16752188Long-term global retinal microvascular changes in a transgenic vascular endothelial growth factor mouse model.Diabetologia2006
16241904Characterization of retinaldehyde dehydrogenase 3.Biochem J2006
15965177Generation of transgenic mice with mild and severe retinal neovascularisation.Br J Ophthalmol2005
11136713The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophy.Hum Mol Genet2001
11238942Identification of a novel AU-Rich element in the 3' untranslated region of epidermal growth factor receptor mRNA that is the target for regulated RNA-binding proteins.Mol Cell Biol2001
11115851Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophy.Hum Mol Genet2000
10508919A novel ADP-ribosylation like factor (ARL-6), interacts with the protein-conducting channel SEC61beta subunit.FEBS Lett1999
10468971Mutation screening and isoform prevalence of the follicle stimulating hormone receptor gene in women with premature ovarian failure, resistant ovary syndrome and polycystic ovary syndrome.Clin Endocrinol (Oxf)1999
10572651Optimized RNA gel-shift and UV cross-linking assays for characterization of cytoplasmic RNA-protein interactions.Biotechniques1999
9839451Regulation of EGF-receptor expression by EGF and TGF alpha in epidermoid cancer cells is cell type-specific.Int J Biochem Cell Biol1998
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Collaborators

The University of Notre Dame Australia
Co-authored papers 8
Public Health and Clinical Services Division
Co-authored papers 6
King Edward Memorial Hospital
Co-authored papers 5
University of Western Australia
Co-authored papers 5
King Edward Memorial Hospital for Women Perth
Co-authored papers 4
King Edward Memorial Hospital
Co-authored papers 4
Stanford University School of Medicine
Co-authored papers 4
King Edward Memorial Hospital for Women
Co-authored papers 4
Co-authored papers 3
Cooperative Research Centre for Spatial Information
Co-authored papers 3
QEII Medical Centre
Co-authored papers 3
Royal Women's Hospital
Co-authored papers 3
King Edward Memorial Hospital
Co-authored papers 3
Princess Margaret Hospital
Co-authored papers 3
King Edward Memorial Hospital
Co-authored papers 3
University of Western Australia
Co-authored papers 3
King Edward Memorial Hospital
Co-authored papers 3
King Edward Memorial Hospital
Co-authored papers 3
National Center for Rare Diseases, Istituto Superiore di Sanita
Co-authored papers 2
QEII Medical Centre, Hospital Avenue
Co-authored papers 2
National Human Genome Research Institute
Co-authored papers 2
The University of Sydney
Co-authored papers 2
Center for Medical Genetics, Keio University School of Medicine
Co-authored papers 2
Perth Children's Hospital
Co-authored papers 2
The University of Sydney
Co-authored papers 2
Harry Perkins Institute of Medical Research, University of Western Australia
Co-authored papers 2
McGill University. Montreal
Co-authored papers 2
INSERM
Co-authored papers 2
Curtin University
Co-authored papers 2
Australia UNSW RNA Institute
Co-authored papers 2