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Literature DB >> 18632546

European practices of genetic information and insurance: lessons for the Genetic Information Nondiscrimination Act.

Ine Van Hoyweghen¹, Klasien Horstman.

Abstract

Mesh：

Year: 2008 PMID： 18632546 DOI： 10.1001/jama.2008.62

Source DB: PubMed Journal: JAMA ISSN： 0098-7484 Impact factor: 56.272

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12 in total

1. The Genetic Information Nondiscrimination Act (GINA): public policy and medical practice in the age of personalized medicine.

Authors: Eric A Feldman
Journal: J Gen Intern Med Date: 2012-06 Impact factor: 5.128

Review 2. Genotype-phenotype databases: challenges and solutions for the post-genomic era.

Authors: Gudmundur A Thorisson; Juha Muilu; Anthony J Brookes
Journal: Nat Rev Genet Date: 2009-01 Impact factor: 53.242

3. Risk terminology in biobanking and genetic research: what's in a name?

Authors: Gwendolyn P Quinn; Heide Castañeda; Tuya Pal; Janique L Rice; Cathy D Meade; Clement K Gwede
Journal: Am J Med Genet A Date: 2013-07-03 Impact factor: 2.802

Review 4. Molecular genetic testing and the future of clinical genomics.

Authors: Sara Huston Katsanis; Nicholas Katsanis
Journal: Nat Rev Genet Date: 2013-06 Impact factor: 53.242

5. Obtaining insurance after DNA diagnostics: a survey among hypertrophic cardiomyopathy mutation carriers.

Authors: Imke Christiaans; Tjitske M Kok; Irene M van Langen; Erwin Birnie; Gouke J Bonsel; Arthur A M Wilde; Ellen M A Smets
Journal: Eur J Hum Genet Date: 2009-08-12 Impact factor: 4.246

6. Implementation of the CDC translational informatics platform--from genetic variants to the national Swedish Rheumatology Quality Register.

Authors: Imad Abugessaisa; David Gomez-Cabrero; Omri Snir; Staffan Lindblad; Lars Klareskog; Vivianne Malmström; Jesper Tegnér
Journal: J Transl Med Date: 2013-04-02 Impact factor: 5.531

European practices of genetic information and insurance: lessons for the Genetic Information Nondiscrimination Act.

1. The Genetic Information Nondiscrimination Act (GINA): public policy and medical practice in the age of personalized medicine.

Review 2. Genotype-phenotype databases: challenges and solutions for the post-genomic era.

3. Risk terminology in biobanking and genetic research: what's in a name?

Review 4. Molecular genetic testing and the future of clinical genomics.

5. Obtaining insurance after DNA diagnostics: a survey among hypertrophic cardiomyopathy mutation carriers.

6. Implementation of the CDC translational informatics platform--from genetic variants to the national Swedish Rheumatology Quality Register.

7. Keeping the GINA in the bottle: assessing the current need for genetic non-discrimination legislation in Canada.

8. Would you want to know? Public attitudes on early diagnostic testing for Alzheimer's disease.

Review 9. If you build it, they will come: unintended future uses of organised health data collections.

10. Two cheers for GINA?