Literature DB >> 19850180

Nursing advocacy in a postgenomic age.

Rebekah Hamilton1.   

Abstract

The Human Genome Project will change how health is defined and how disease is prevented, diagnosed, and treated. As the largest group of health care providers in contact with patients, nurses need to be competent in the science of genetics. Beyond this, nurses need to understand the complexities that arise in genomic health care. Ethical, legal, and social issues are integral to the delivery of genomic health care, and nurses must have an astute understanding of such complexities. What it means to know, to reason, and to act in this postgenomic age is explored.

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Year:  2009        PMID: 19850180      PMCID: PMC2766592          DOI: 10.1016/j.cnur.2009.07.007

Source DB:  PubMed          Journal:  Nurs Clin North Am        ISSN: 0029-6465            Impact factor:   1.208


  23 in total

Review 1.  Preparing the nursing profession for participation in a genetic paradigm in health care.

Authors:  G Anderson; R B Monsen; C A Prows; S Tinley; J Jenkins
Journal:  Nurs Outlook       Date:  2000 Jan-Feb       Impact factor: 3.250

2.  Genetics in nursing education.

Authors:  F R Lashley
Journal:  Nurs Clin North Am       Date:  2000-09       Impact factor: 1.208

3.  Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information.

Authors:  N Hallowell; C Foster; R Eeles; A Ardern-Jones; V Murday; M Watson
Journal:  J Med Ethics       Date:  2003-04       Impact factor: 2.903

Review 4.  Genomic medicine--a primer.

Authors:  Alan E Guttmacher; Francis S Collins
Journal:  N Engl J Med       Date:  2002-11-07       Impact factor: 91.245

5.  A vision for the future of genomics research.

Authors:  Francis S Collins; Eric D Green; Alan E Guttmacher; Mark S Guyer
Journal:  Nature       Date:  2003-04-14       Impact factor: 49.962

Review 6.  Medication selection by genotype: How genetics is changing drug prescribing and efficacy.

Authors:  Cynthia A Prows; Daniel R Prows
Journal:  Am J Nurs       Date:  2004-05       Impact factor: 2.220

Review 7.  Family communication about genetic risk: the little that is known.

Authors:  Brenda J Wilson; Karen Forrest; Edwin R van Teijlingen; Lorna McKee; Neva Haites; Eric Matthews; Sheila A Simpson
Journal:  Community Genet       Date:  2004

8.  Duty to warn at-risk relatives for genetic disease: genetic counselors' clinical experience.

Authors:  R Beth Dugan; Georgia L Wiesner; Eric T Juengst; Maryann O'Riordan; Anne L Matthews; Nathaniel H Robin
Journal:  Am J Med Genet C Semin Med Genet       Date:  2003-05-15       Impact factor: 3.908

9.  To tell or not to tell: barriers and facilitators in family communication about genetic risk.

Authors:  K Forrest; S A Simpson; B J Wilson; E R van Teijlingen; L McKee; N Haites; E Matthews
Journal:  Clin Genet       Date:  2003-10       Impact factor: 4.438

10.  Life trajectories, genetic testing, and risk reduction decisions in 18-39 year old women at risk for hereditary breast and ovarian cancer.

Authors:  Rebekah Hamilton; Janet K Williams; Barbara J Bowers; Kathleen Calzone
Journal:  J Genet Couns       Date:  2008-11-01       Impact factor: 2.537

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