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Literature DB >> 18073580

Defining purpose: a key step in genetic test evaluation.

Wylie Burke¹, Ronald L Zimmern, Mark Kroese.

Abstract

Mesh：

Year: 2007 PMID： 18073580 DOI： 10.1097/gim.0b013e318156e45b

Source DB: PubMed Journal: Genet Med ISSN： 1098-3600 Impact factor: 8.822

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Cited

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12 in total

1. Giving and withholding of information following genomic screening: challenges identified in a study of primary care physicians in Estonia.

Authors: Liis Leitsalu; Laura Hercher; Andres Metspalu
Journal: J Genet Couns Date: 2011-12-08 Impact factor: 2.537

2. Debating clinical utility.

Authors: Wylie Burke; A-M Laberge; N Press
Journal: Public Health Genomics Date: 2010-04-15 Impact factor: 2.000

3. Usefulness of factor V Leiden mutation testing in clinical practice.

Authors: Ellen Ø Blinkenberg; Ann-Helen Kristoffersen; Sverre Sandberg; Vidar M Steen; Gunnar Houge
Journal: Eur J Hum Genet Date: 2010-03-24 Impact factor: 4.246

4. Ethical, legal, and social issues in health technology assessment for prenatal/preconceptional and newborn screening: a workshop report.

Authors: B K Potter; D Avard; V Entwistle; C Kennedy; P Chakraborty; M McGuire; B J Wilson
Journal: Public Health Genomics Date: 2008-09-03 Impact factor: 2.000

10. A formal risk-benefit framework for genomic tests: facilitating the appropriate translation of genomics into clinical practice.

Authors: David L Veenstra; Joshua A Roth; Louis P Garrison; Scott D Ramsey; Wylie Burke
Journal: Genet Med Date: 2010-11 Impact factor: 8.822

Defining purpose: a key step in genetic test evaluation.

1. Giving and withholding of information following genomic screening: challenges identified in a study of primary care physicians in Estonia.

2. Debating clinical utility.

3. Usefulness of factor V Leiden mutation testing in clinical practice.

4. Ethical, legal, and social issues in health technology assessment for prenatal/preconceptional and newborn screening: a workshop report.

5. 'Over-the-counter' genetic testing: what does it really mean for primary care?

Review 6. Ethical and social implications of genetic testing for communication disorders.

7. Conceptual issues for screening in the genomic era - time for an update?

Review 8. Integrative omics for health and disease.

9. Paediatricians underuse recommended genetic tests in children with global developmental delay.

10. A formal risk-benefit framework for genomic tests: facilitating the appropriate translation of genomics into clinical practice.