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Literature DB >> 20823439

Exclusion of genetic information from the medical record: ethical and medical dilemmas.

Robert Klitzman¹.

Abstract

Entities: Disease Gene Species

Mesh：

Year: 2010 PMID： 20823439 PMCID： PMC3152485 DOI： 10.1001/jama.2010.1303

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

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7 in total

1. Laws restricting health insurers' use of genetic information: impact on genetic discrimination.

Authors: M A Hall; S S Rich
Journal: Am J Hum Genet Date: 2000-01 Impact factor: 11.025

2. Physician use of genetic testing for cancer susceptibility: results of a national survey.

Authors: Louise Wideroff; Andrew N Freedman; Lorayn Olson; Carrie N Klabunde; William Davis; Kadaba P Srinath; Robert T Croyle; Rachel Ballard-Barbash
Journal: Cancer Epidemiol Biomarkers Prev Date: 2003-04 Impact factor: 4.254

3. Investigating genetic discrimination in Australia: a large-scale survey of clinical genetics clients.

Authors: S Taylor; S Treloar; K Barlow-Stewart; M Stranger; M Otlowski
Journal: Clin Genet Date: 2008-05-19 Impact factor: 4.438

4. Lying for patients: physician deception of third-party payers.

Authors: V G Freeman; S S Rathore; K P Weinfurt; K A Schulman; D P Sulmasy
Journal: Arch Intern Med Date: 1999-10-25

5. Sounding Boards. Confidentiality in medicine--a decrepit concept.

Authors: M Siegler
Journal: N Engl J Med Date: 1982-12-09 Impact factor: 91.245

6. Views of discrimination among individuals confronting genetic disease.

Authors: Robert Klitzman
Journal: J Genet Couns Date: 2010-02 Impact factor: 2.537

7. Disclosures of Huntington disease risk within families: patterns of decision-making and implications.

Authors: Robert Klitzman; Deborah Thorne; Jennifer Williamson; Wendy Chung; Karen Marder
Journal: Am J Med Genet A Date: 2007-08-15 Impact factor: 2.802

7 in total

11 in total

1. Practical considerations to guide development of access controls and decision support for genetic information in electronic medical records.

Authors: Diana C Darcy; Eleanor T Lewis; Kelly E Ormond; David J Clark; Jodie A Trafton
Journal: BMC Health Serv Res Date: 2011-11-02 Impact factor: 2.655

2. Automatic Placement of Genomic Research Results in Medical Records: Do Researchers Have a Duty? Should Participants Have a Choice?

Authors: Anya E R Prince; John M Conley; Arlene M Davis; Gabriel Lázaro-Muñoz; R Jean Cadigan
Journal: J Law Med Ethics Date: 2015 Impact factor: 1.718

Review 3. Ethics and neuropsychiatric genetics: a review of major issues.

Authors: Steven K Hoge; Paul S Appelbaum
Journal: Int J Neuropsychopharmacol Date: 2012-01-25 Impact factor: 5.176

4. 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

5. Consumer awareness and attitudes about insurance discrimination post enactment of the Genetic Information Nondiscrimination Act.

Authors: Dawn C Allain; Sue Friedman; Leigha Senter
Journal: Fam Cancer Date: 2012-12 Impact factor: 2.375

6. The Alzheimer's Prevention Clinic at Weill Cornell Medical College / New York - Presbyterian Hospital: Risk Stratification and Personalized Early Intervention.

Authors: A Seifan; R Isaacson
Journal: J Prev Alzheimers Dis Date: 2015-10-01