Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities: Background Document to the ESHG recommendations on genetic testing and common disorders
- Author
- BECKER, Frauke1 ; VAN EL, Carla G2 ; JANSSENS, A. Cecile Jw11 ; KAARIAINEN, Helena12 ; KRAWCZAK, Michael13 ; KRISTOFFERSSON, Ulf14 ; LUBINSKI, Jan15 ; PATCH, Christine16 ; PENCHASZADEH, Victor B17 ; READ, Andrew18 ; ROGOWSKI, Wolf19 20 ; SEQUEIROS, Jorge21 ; IBARRETA, Dolores3 ; TRANEBJAERG, Lisbeth22 ; VAN LANGEN, Irene M23 ; WALLACE, Helen24 ; ZIMMERN, Ron25 ; SCHMIDTKE, Jörg1 ; CORNEL, Martina C2 ; ZIKA, Eleni3 ; HOGARTH, Stuart4 ; BORRY, Pascal2 5 6 ; CAMBON-THOMSEN, Anne7 ; CASSIMAN, Jean Jacques8 ; EVERS-KIEBOOMS, Gerry9 ; HODGSON, Shirley10
[1] Hannover Medical School, Department of Human Genetics, Hannover, Germany
[2] Department of Clinical Genetics and EMGO Institute for Health and Care Research, VU University Medical Center, Amsterdam, Netherlands
[3] IPTS Institute for Prospective Technological Studies, Joint Research Centre, European Commission, Seville, Spain
[4] Department of Social Sciences, Loughborough University, Loughborough, United Kingdom
[5] Centre for Biomedical Ethics and Law, Katholieke Universiteit Leuven, Leuven, Belgium
[6] Department of Medical Humanities and EMGO Institute for Health and Care Research, VU University Medical Center, Amsterdam, Netherlands
[7] Inserm, U 558, Department of Epidemiology, Health Economics and Public Health, University Paul Sabatier, Toulouse, France
[8] Center for Human Genetics, University of Leuven, Leuven, Belgium
[9] Psychosocial Genetics Unit University Hospitals, Katholieke Universiteit Leuven, Leuven, Belgium
[10] Department of Clinical Genetics, St George's University of London, London, United Kingdom
[11] Department of Epidemiology, Erasmus MC University Medical Center, Rotterdam, Netherlands
[12] National Institute for Health and Welfare, Helsinki, Finland
[13] Institute of Medical Informatics and Statistics, Christian-Albrechts-Universität, Kiel, Germany
[14] Department of Clinical Genetics, University Hospital, Lund, Sweden
[15] Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland
[16] Guys and St Thomas' NHS Foundation Trust, London, United Kingdom
[17] Mailman School of Public Health, Columbia University, New York, NY, United States
[18] Division of Human Development, School of Clinical Sciences, University of Nottingham, Nottingham, United Kingdom
[19] Helmholtz Center Munich, German Research Center for Environmental Health (GmbH), Neuherberg, Germany
[20] Institute and Outpatient Clinic for Occupational, Social and Environmental Medicine, Clinical Center, Ludwig Maximilians University, Munich, Germany
[21] IBMC ― Institute for Molecular and Cell Biology, and ICBAS, University of Porto, Porto, Portugal
[22] Department of Audiology, H:S Bispebjerg Hospital and Wilhelm Johannsen Centre of Functional Genomics, University of Copenhagen, Copenhagen, Denmark
[23] Department of Genetics, University Medical Center Groningen and University of Groningen, Groningen, Netherlands
[24] GeneWatch UK, The Mill House, Tideswell, Derbyshire, United Kingdom
[25] PHG Foundation, Worts Causeway, Cambridge, United Kingdom - Issue title
- Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities
- Author (monograph)
- VAN EL, Carla G (Editor)1 ; CORNEL, Martina C (Editor)1
[1] Department of Clinical Genetics/EMGO Institute for Health and Care Research, VU University Medical Center, Amsterdam, Netherlands - Source
European journal of human genetics. 2011, Vol 19 ; S6-S44 ; SUP1 ; ref : 317 ref
- Publisher
- Nature Publishing Group, Basingstoke
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Author keyword
- common disorders genetic testing monogenic subtypes predictive value public health
- Keyword (fr)
- Conseil génétique Génétique Monogénique Recommandation Santé publique Soustype Typage Valeur prédictive
- Keyword (en)
- Genetic counseling Genetics Monogenic Recommendation Public health Subtype Typing Predictive value
- Keyword (es)
- Consejo genético Genética Monogénico Recomendación Salud pública Subtipo Tipificación Valor predictivo
- Classification
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A04 Molecular and cellular biology
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A07 Genetics of eukaryotes. Biological and molecular evolution
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23A General aspects. Genetic counseling
- Discipline
- Eukaryotes genetics. Biological and molecular evolution Medical genetics Molecular and cell biology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 24016794
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1038/ejhg.2010.249 
https://dx.doi.org/10.1038/ejhg.2010.249
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arXiv access
