Literature DB >> 18687790

Medical ethics for the genome world: a paper from the 2007 William Beaumont hospital symposium on molecular pathology.

Kelly E Ormond1.   

Abstract

Medical genetics, and in particular the areas of genetic testing and genetic counseling, are replete with ethical and social issues. This review provides readers with a summary of the genetic testing and counseling process, as well as the clinical challenges that can lead to ethical dilemmas during these processes. Using a clinical medical ethics approach, several hypothetical case scenarios are presented and discussed to provide examples of the ethical issues that can arise.

Mesh：

Year:  2008        PMID： 18687790      PMCID： PMC2518732          DOI： 10.2353/jmoldx.2008.070162

Source DB:  PubMed          Journal:  J Mol Diagn        ISSN： 1525-1578            Impact factor:   5.568


  19 in total

1.  Tissue donors use their influence in deal over gene patent terms.

Authors:  P Smaglik
Journal:  Nature       Date:  2000-10-19       Impact factor: 49.962

2.  Effects of patents and licenses on the provision of clinical genetic testing services.

Authors:  Mildred K Cho; Samantha Illangasekare; Meredith A Weaver; Debra G B Leonard; Jon F Merz
Journal:  J Mol Diagn       Date:  2003-02       Impact factor: 5.568

Review 3.  Ethical, legal, and social implications of genomic medicine.

Authors:  Ellen Wright Clayton
Journal:  N Engl J Med       Date:  2003-08-07       Impact factor: 91.245

4.  Genetic counselors: translating genomic science into clinical practice.

Authors:  Robin L Bennett; Heather L Hampel; Jessica B Mandell; Joan H Marks
Journal:  J Clin Invest       Date:  2003-11       Impact factor: 14.808

5.  Age at onset and life table risks in genetic counselling for Huntington's disease.

Authors:  P S Harper; R G Newcombe
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

6.  Why me? Why not me?

Authors:  Kathleen D Valverde
Journal:  J Genet Couns       Date:  2006-12       Impact factor: 2.537

7.  Genetic testing for a BRCA1 mutation: prophylactic surgery and screening behavior in women 2 years post testing.

Authors:  Jeffrey R Botkin; Ken R Smith; Robert T Croyle; Bonnie J Baty; Jean E Wylie; Debra Dutson; Anna Chan; Heidi A Hamann; Caryn Lerman; Jamie McDonald; Vickie Venne; John H Ward; Elaine Lyon
Journal:  Am J Med Genet A       Date:  2003-04-30       Impact factor: 2.802

8.  Two models of implementing informed consent.

Authors:  C W Lidz; P S Appelbaum; A Meisel
Journal:  Arch Intern Med       Date:  1988-06

9.  What do patients prefer: informed consent models for genetic carrier testing.

Authors:  K E Ormond; M Iris; S Banuvar; J Minogue; G J Annas; S Elias
Journal:  J Genet Couns       Date:  2007-05-11       Impact factor: 2.537

10.  Maternal psychological reaction to newborn genetic screening for type 1 diabetes.

Authors:  Nicola J Kerruish; Priscilla L Campbell-Stokes; Andrew Gray; Tony R Merriman; Stephen P Robertson; Barry J Taylor
Journal:  Pediatrics       Date:  2007-07-03       Impact factor: 7.124
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  1 in total

1.  Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarction.

Authors:  Aenne S Thormaehlen; Christian Schuberth; Hong-Hee Won; Peter Blattmann; Brigitte Joggerst-Thomalla; Susanne Theiss; Rosanna Asselta; Stefano Duga; Pier Angelica Merlini; Diego Ardissino; Eric S Lander; Stacey Gabriel; Daniel J Rader; Gina M Peloso; Rainer Pepperkok; Sekar Kathiresan; Heiko Runz
Journal:  PLoS Genet       Date:  2015-02-03       Impact factor: 5.917
  1 in total

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