Serological screening of farm dogs for Echinococcus granulosus infection in an endemic region

Autor: R. A. Lyford, Dawkins Hj, Marshall W. Lightowlers, Robin B. Gasser, Rickard

Publikováno v: Australian veterinary journal. 67(4)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aa9e57463af2a3edcba9e473f955699
https://pubmed.ncbi.nlm.nih.gov/2375726

Incidental inequity.

Autor: Nowak KJ; Department of Health, Office of Population Health Genomics, Public and Aboriginal Health Division, Government of Western Australia, East Perth, WA, Australia.; School of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Western Australia, Crawley, WA, Australia.; Harry Perkins Institute of Medical Research, QEII Medical Centre, Nedlands; Centre for Medical Research, University of Western Australia, Crawley, WA, Australia., Bauskis A; Department of Health, Office of Population Health Genomics, Public and Aboriginal Health Division, Government of Western Australia, East Perth, WA, Australia., Dawkins HJ; Department of Health, Office of Population Health Genomics, Public and Aboriginal Health Division, Government of Western Australia, East Perth, WA, Australia.; School of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Western Australia, Crawley, WA, Australia.; Centre for Population Health Research, Curtin Health Innovation Research Institute, Curtin University of Technology, Bentley, WA, Australia.; Centre for Comparative Genomics, Murdoch University, Murdoch, WA, Australia., Baynam G; Department of Health, Office of Population Health Genomics, Public and Aboriginal Health Division, Government of Western Australia, East Perth, WA, Australia. gareth.baynam@health.wa.gov.au.; Department of Health, Genetic Services of Western Australia, Government of Western Australia, Subiaco, WA, Australia. gareth.baynam@health.wa.gov.au.; School of Paediatrics and Child Health, University of Western Australia, Crawley, WA, Australia. gareth.baynam@health.wa.gov.au.; Institute for Immunology and Infectious Diseases, Murdoch University, Murdoch, WA, Australia. gareth.baynam@health.wa.gov.au.; Telethon Kids Institute, University of Western Australia, Subiaco, WA, Australia. gareth.baynam@health.wa.gov.au.; Western Australian Register of Developmental Anomalies, King Edward Memorial Hospital, Subiaco, WA, Australia. gareth.baynam@health.wa.gov.au.; School of Spatial Sciences, Curtin University, Bentley, WA, Australia. gareth.baynam@health.wa.gov.au.

Publikováno v: European journal of human genetics : EJHG [Eur J Hum Genet] 2018 May; Vol. 26 (5), pp. 616-617. Date of Electronic Publication: 2018 Feb 15.

Design of the Familial Hypercholesterolaemia Australasia Network Registry: Creating Opportunities for Greater International Collaboration.

Autor: Bellgard MI; Centre for Comparative Genomics, Murdoch University, Murdoch., Walker CE; Office of Population Health Genomics, Public Health Division, Department of Health, Government of Western Australia., Napier KR; Centre for Comparative Genomics, Murdoch University, Murdoch., Lamont L; Office of Population Health Genomics, Public Health Division, Department of Health, Government of Western Australia., Hunter AA; Centre for Comparative Genomics, Murdoch University, Murdoch., Render L; Centre for Comparative Genomics, Murdoch University, Murdoch., Radochonski M; Centre for Comparative Genomics, Murdoch University, Murdoch., Pang J; School of Medicine, Faculty of Health and Medical Sciences, University of Western Australia., Pedrotti A; Familial Hypercholesterolaemia Family Support Group of Western Australia., Sullivan DR; Sydney Medical School, University of Sydney., Kostner K; School of Medicine, University of Queensland., Bishop W; Menzies Institute for Medical Research, University of Tasmania., George PM; Canterbury Health Laboratories, University of Otago., O'Brien RC; Austin Clinical School, University of Melbourne., Clifton PM; School of Pharmacy and Medical Sciences, University of South Australia., Bockxmeer FMV; Department of Clinical Biochemistry, PathWest Laboratory Medicine WA, Royal Perth Hospital.; School of Surgery, University of Western Australia., Nicholls SJ; South Australian Health and Medical Research Institute, University of Adelaide., Hamilton-Craig I; School of Medicine, Flinders University., Dawkins HJ; Centre for Comparative Genomics, Murdoch University, Murdoch.; Office of Population Health Genomics, Public Health Division, Department of Health, Government of Western Australia.; Centre for Population Health Research, Curtin University of Technology.; School of Pathology and Laboratory Medicine, University of Western Australia., Watts GF; School of Medicine, Faculty of Health and Medical Sciences, University of Western Australia.; Lipid Disorders Clinic, Cardiometabolic Service, Royal Perth Hospital.

Publikováno v: Journal of atherosclerosis and thrombosis [J Atheroscler Thromb] 2017 Oct 01; Vol. 24 (10), pp. 1075-1084. Date of Electronic Publication: 2017 Mar 24.

Outcomes of an International Workshop on Preconception Expanded Carrier Screening: Some Considerations for Governments.

Autor: Molster CM; Office of Population Health Genomics, Public Health Division, Department of Health Western Australia , Perth, WA , Australia., Lister K; Office of Population Health Genomics, Public Health Division, Department of Health Western Australia , Perth, WA , Australia., Metternick-Jones S; Sir Charles Gairdner Hospital , Perth, WA , Australia., Baynam G; Office of Population Health Genomics, Public Health Division, Department of Health Western Australia, Perth, WA, Australia; Genetic Services WA, Perth, WA, Australia; School of Paediatrics and Child Health, University of Western Australia, Perth, WA, Australia; Institute for Immunology and Infectious Diseases, Murdoch University, Perth, WA, Australia; Telethon Kids Institute, University of Western Australia, Perth, WA, Australia; Western Australian Register of Developmental Anomalies, Perth, WA, Australia; Spatial Sciences, Department of Science and Engineering, Curtin University, Perth, WA, Australia., Clarke AJ; Division of Cancer and Genetics, School of Medicine, Cardiff University , Cardiff , UK., Straub V; Institute of Human Genetics, University of Newcastle upon Tyne , Newcastle upon Tyne , UK., Dawkins HJ; Office of Population Health Genomics, Public Health Division, Department of Health Western Australia, Perth, WA, Australia; Centre for Comparative Genomics, Murdoch University, Perth, WA, Australia; Centre for Population Health Research, Curtin University, Perth, WA, Australia; School of Pathology and Laboratory Medicine, University of Western Australia, Perth, WA, Australia., Laing N; Centre for Medical Research, Harry Perkins Institute of Medical Research, University of Western Australia, Perth, WA, Australia; Neurogenetics Unit, Department of Diagnostic Genomics, PathWest Laboratory Medicine, Department of Health Western Australia, Perth, WA, Australia.

Publikováno v: Frontiers in public health [Front Public Health] 2017 Feb 24; Vol. 5, pp. 25. Date of Electronic Publication: 2017 Feb 24 (Print Publication: 2017).

The Human Phenotype Ontology in 2017.

Autor: Köhler S; Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany dr.sebastian.koehler@gmail.com., Vasilevsky NA; Library and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University, Portland, OR 97239, USA., Engelstad M; Library and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University, Portland, OR 97239, USA., Foster E; Library and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University, Portland, OR 97239, USA., McMurry J; Library and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University, Portland, OR 97239, USA., Aymé S; Institut du Cerveau et de la Moelle épinière-ICM, CNRS UMR 7225-Inserm U 1127-UPMC-P6 UMR S 1127, Hôpital Pitié-Salpêtrière, 47, bd de l'Hôpital, 75013 Paris, France., Baynam G; Western Australian Register of Developmental Anomalies and Genetic Services of Western Australia, King Edward Memorial Hospital Department of Health, Government of Western Australia, Perth, WA 6008, Australia.; School of Paediatrics and Child Health, University of Western Australia, Perth, WA 6008, Australia., Bello SM; The Jackson Laboratory, 600 Main St, Bar Harbor, ME 04609, USA., Boerkoel CF; Imagenetics Research, Sanford Health, PO Box 5039, Route 5001, Sioux Falls, SD 57117-5039, USA., Boycott KM; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada., Brudno M; Department of Computer Science, University of Toronto, Toronto, ON M5S 2E4, Canada Centre for Computational Medicine, Hospital for Sick Children, Toronto, ON M5G 1L7, Canada., Buske OJ; Department of Computer Science, University of Toronto, Toronto, ON M5S 2E4, Canada Centre for Computational Medicine, Hospital for Sick Children, Toronto, ON M5G 1L7, Canada., Chinnery PF; Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge CB2 0QQ, UK.; NIHR Rare Diseases Translational Research Collaboration, Cambridge Biomedical Campus, Cambridge CB2 0QQ, UK., Cipriani V; UCL Institute of Ophthalmology, Department of Ocular Biology and Therapeutics, 11-43 Bath Street, London EC1V 9EL, UK.; UCL Genetics Institute, University College London, London WC1E 6BT, UK., Connell LE; Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, USA., Dawkins HJ; Office of Population Health Genomics, Public Health Division, Health Department of Western Australia, 189 Royal Street, Perth, WA, 6004 Australia., DeMare LE; Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, USA., Devereau AD; Genomics England, Queen Mary University of London, Dawson Hall, Charterhouse Square, London EC1M 6BQ, UK., de Vries BB; Department of Human Genetics, Radboud University, University Medical Centre, Nijmegen, The Netherlands., Firth HV; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SA, UK., Freson K; Department of Cardiovascular Sciences, Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium., Greene D; Department of Haematology, University of Cambridge, NHS Blood and Transplant Centre, Long Road, Cambridge CB2 0PT, UK.; Medical Research Council Biostatistics Unit, Cambridge Institute of Public Health, Cambridge Biomedical Campus, Cambridge, UK., Hamosh A; McKusick-Nathans Institute of Genetic Medicine, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA., Helbig I; Division of Neurology, The Children's Hospital of Philadelphia, 3501 Civic Center Blvd, Philadelphia, PA 19104, USA.; Department of Neuropediatrics, University Medical Center Schleswig-Holstein (UKSH), Kiel, Germany., Hum C; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, ON M5G 1H3, Canada., Jähn JA; Department of Neuropediatrics, University Medical Center Schleswig-Holstein (UKSH), Kiel, Germany., James R; NIHR Rare Diseases Translational Research Collaboration, Cambridge Biomedical Campus, Cambridge CB2 0QQ, UK.; Medical Research Council Biostatistics Unit, Cambridge Institute of Public Health, Cambridge Biomedical Campus, Cambridge, UK., Krause R; LuxembourgCentre for Systems Biomedicine, University of Luxembourg, 7, avenue des Hauts-Fourneaux, L-4362 Esch-sur-Alzette, Luxembourg., F Laulederkind SJ; Human and Molecular Genetics Center, Medical College of Wisconsin, USA., Lochmüller H; John Walton Muscular Dystrophy Research Centre, MRC Centre for Neuromuscular Diseases, Institute of Genetic Medicine, University of Newcastle, Newcastle upon Tyne, UK., Lyon GJ; Stanley Institute for Cognitive Genomics, Cold Spring Harbor Laboratory, New York, NY 11797, USA., Ogishima S; Dept of Bioclinical Informatics, Tohoku Medical Megabank Organization, Tohoku University, Tohoku Medical Megabank Organization Bldg 7F room #741,736, Seiryo 2-1, Aoba-ku, Sendai Miyagi 980-8573 Japan., Olry A; Orphanet-INSERM, US14, Plateforme Maladies Rares, 96 rue Didot, 75014 Paris, France., Ouwehand WH; Medical Research Council Biostatistics Unit, Cambridge Institute of Public Health, Cambridge Biomedical Campus, Cambridge, UK., Pontikos N; UCL Institute of Ophthalmology, Department of Ocular Biology and Therapeutics, 11-43 Bath Street, London EC1V 9EL, UK.; UCL Genetics Institute, University College London, London WC1E 6BT, UK., Rath A; Orphanet-INSERM, US14, Plateforme Maladies Rares, 96 rue Didot, 75014 Paris, France., Schaefer F; Division of Pediatric Nephrology and KFH Children's Kidney Center, Center for Pediatrics and Adolescent Medicine, 69120 Heidelberg, Germany., Scott RH; Genomics England, Queen Mary University of London, Dawson Hall, Charterhouse Square, London EC1M 6BQ, UK., Segal M; SimulConsult Inc., 27 Crafts Road, Chestnut Hill, MA 02467, USA., Sergouniotis PI; Manchester Royal Eye Hospital & University of Manchester, Manchester M13 9WL, UK., Sever R; Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, USA., Smith CL; The Jackson Laboratory, 600 Main St, Bar Harbor, ME 04609, USA., Straub V; John Walton Muscular Dystrophy Research Centre, MRC Centre for Neuromuscular Diseases, Institute of Genetic Medicine, University of Newcastle, Newcastle upon Tyne, UK., Thompson R; John Walton Muscular Dystrophy Research Centre, MRC Centre for Neuromuscular Diseases, Institute of Genetic Medicine, University of Newcastle, Newcastle upon Tyne, UK., Turner C; John Walton Muscular Dystrophy Research Centre, MRC Centre for Neuromuscular Diseases, Institute of Genetic Medicine, University of Newcastle, Newcastle upon Tyne, UK., Turro E; Department of Haematology, University of Cambridge, NHS Blood and Transplant Centre, Long Road, Cambridge CB2 0PT, UK.; Medical Research Council Biostatistics Unit, Cambridge Institute of Public Health, Cambridge Biomedical Campus, Cambridge, UK., Veltman MW; NIHR Rare Diseases Translational Research Collaboration, Cambridge Biomedical Campus, Cambridge CB2 0QQ, UK., Vulliamy T; Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, UK., Yu J; Nuffield Department of Clinical Neurosciences, University of Oxford, Level 6, West Wing, John Radcliffe Hospital, Oxford OX3 9DU, UK., von Ziegenweidt J; Department of Haematology, University of Cambridge, NHS Blood and Transplant Centre, Long Road, Cambridge CB2 0PT, UK., Zankl A; Discipline of Genetic Medicine, Sydney Medical School, The University of Sydney, Australia.; Academic Department of Medical Genetics, Sydney Childrens Hospitals Network (Westmead), Australia., Züchner S; JD McDonald Department of Human Genetics and Hussman Institute for Human Genomics, University of Miami, Miami, FL, USA., Zemojtel T; Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany., Jacobsen JO; Genomics England, Queen Mary University of London, Dawson Hall, Charterhouse Square, London EC1M 6BQ, UK., Groza T; Garvan Institute of Medical Research, Darlinghurst, Sydney, NSW 2010, Australia.; St Vincent's Clinical School, Faculty of Medicine, UNSW Australia., Smedley D; Genomics England, Queen Mary University of London, Dawson Hall, Charterhouse Square, London EC1M 6BQ, UK., Mungall CJ; Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 94720, USA., Haendel M; Library and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University, Portland, OR 97239, USA., Robinson PN; The Jackson Laboratory for Genomic Medicine, 10 Discovery Drive, Farmington, CT 06032, USA peter.robinson@jax.org.; Institute for Systems Genomics, University of Connecticut, Farmington, CT 06032, USA.

Publikováno v: Nucleic acids research [Nucleic Acids Res] 2017 Jan 04; Vol. 45 (D1), pp. D865-D876. Date of Electronic Publication: 2016 Nov 28.