Literature DB >> 10723866

Communicating genetic risk information.

T M Marteau1.   

Abstract

It is envisaged that genetic information will be used, together with other types of information, to assess individuals' risks of developing a variety of common conditions. Such risk assessments will involve providing probabilistic information partly based upon results of genetic tests in order to facilitate behaviour change without causing excessive anxiety. The behaviours targeted for change are likely to include adherence to prescribed medication, alteration to diet, increasing levels of exercise and quitting smoking. This paper reviews research already conducted on perceptions of risk and genes, methods of facilitating behaviour change and reducing anxiety following various types of risk assessment. Although risk assessment and interventions to reduce risks have been conducted for over 20 years, very little rigorous research exists. For the investments in the new genetics to be realised, research is now needed both in how individuals respond to risk information that involves the use of genetic information and in how to facilitate and maintain behaviour change to reduce such risks.

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Year:  1999        PMID: 10723866     DOI: 10.1258/0007142991902466

Source DB:  PubMed          Journal:  Br Med Bull        ISSN: 0007-1420            Impact factor:   4.291


  12 in total

1.  Information related to prenatal genetic counseling: interpretation by adolescents, effects on risk perception and ethical implications.

Authors:  Philippe A Melas; Susanne Georgsson Öhman; Niklas Juth; The-Hung Bui
Journal:  J Genet Couns       Date:  2011-10-25       Impact factor: 2.537

2.  Risky communication: pitfalls in counseling about risk, and how to avoid them.

Authors:  K O'Doherty; G K Suthers
Journal:  J Genet Couns       Date:  2007-05-01       Impact factor: 2.537

Review 3.  Communicating genetic risk information for common disorders in the era of genomic medicine.

Authors:  Denise M Lautenbach; Kurt D Christensen; Jeffrey A Sparks; Robert C Green
Journal:  Annu Rev Genomics Hum Genet       Date:  2013       Impact factor: 8.929

4.  Families' experience of oncogenetic counselling: accounts from a heterogeneous hereditary cancer risk population.

Authors:  Álvaro Mendes; Liliana Sousa
Journal:  Fam Cancer       Date:  2012-06       Impact factor: 2.375

5.  Interest in genetic testing for modest changes in breast cancer risk: implications for SNP testing.

Authors:  K D Graves; B N Peshkin; G Luta; W Tuong; M D Schwartz
Journal:  Public Health Genomics       Date:  2011-04-02       Impact factor: 2.000

Review 6.  Genetic counseling for inherited thrombophilias.

Authors:  Elizabeth A Varga
Journal:  J Thromb Thrombolysis       Date:  2007-10-19       Impact factor: 2.300

7.  Review of Spinal Muscular Atrophy (SMA) for Prenatal and Pediatric Genetic Counselors.

Authors:  Amanda Carré; Candice Empey
Journal:  J Genet Couns       Date:  2015-08-08       Impact factor: 2.537

Review 8.  Ethical issues in psychiatric genetics research: points to consider.

Authors:  Barbara Bowles Biesecker; Holly Landrum Peay
Journal:  Psychopharmacology (Berl)       Date:  2003-09-10       Impact factor: 4.530

9.  Effect of communicating genetic and phenotypic risk for type 2 diabetes in combination with lifestyle advice on objectively measured physical activity: protocol of a randomised controlled trial.

Authors:  Job G Godino; Esther M F van Sluijs; Theresa M Marteau; Stephen Sutton; Stephen J Sharp; Simon J Griffin
Journal:  BMC Public Health       Date:  2012-06-18       Impact factor: 3.295

10.  Genetic testing of children for predisposition to mood disorders: anticipating the clinical issues.

Authors:  Jessica A Erickson; Lili Kuzmich; Kelly E Ormond; Erynn Gordon; Michael F Christman; Mildred K Cho; Douglas F Levinson
Journal:  J Genet Couns       Date:  2014-03-22       Impact factor: 2.537

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