K E Ormond

Summary

Affiliation: Stanford University
Country: USA

Publications

  1. pmc Practical considerations to guide development of access controls and decision support for genetic information in electronic medical records
    Diana C Darcy
    South Bay Regional Genetics Center, Santa Clara Valley Medical Center, San Jose, California, USA
    BMC Health Serv Res 11:294. 2011
  2. doi request reprint Medical and graduate students' attitudes toward personal genomics
    Kelly E Ormond
    Department of Genetics, Stanford Center for Biomedical Ethics, Stanford University, Stanford, California, USA
    Genet Med 13:400-8. 2011
  3. doi request reprint Assessing the understanding of biobank participants
    K E Ormond
    Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA
    Am J Med Genet A 149:188-98. 2009
  4. doi request reprint Information preferences of high literacy pregnant women regarding informed consent models for genetic carrier screening
    K E Ormond
    Department of Medicine, Center for Genetic Medicine, and Medical Humanities and Bioethics, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States
    Patient Educ Couns 75:244-50. 2009
  5. pmc Medical ethics for the genome world: a paper from the 2007 William Beaumont hospital symposium on molecular pathology
    Kelly E Ormond
    Department of Genetics, Stanford University, Stanford, California, USA
    J Mol Diagn 10:377-82. 2008
  6. ncbi request reprint What do patients prefer: informed consent models for genetic carrier testing
    K E Ormond
    Department of Medicine, Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA
    J Genet Couns 16:539-50. 2007
  7. pmc Clinical assessment incorporating a personal genome
    Euan A Ashley
    Center for Inherited Cardiovascular Disease, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, USA
    Lancet 375:1525-35. 2010
  8. pmc Best ethical practices for clinicians and laboratories in the provision of noninvasive prenatal testing
    M A Allyse
    Center for Biomedical Ethics, Stanford University, Stanford, CA, USA
    Prenat Diagn 33:656-61. 2013
  9. ncbi request reprint Knowledge and attitudes toward a free education and Ashkenazi Jewish carrier testing program
    G Hegwer
    Center for Genetic Medicine and Graduate Program in Genetic Counseling, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA
    J Genet Couns 15:61-70. 2006
  10. ncbi request reprint Attitudes of health care trainees about genetics and disability: issues of access, health care communication, and decision making
    Kelly E Ormond
    Center for Genetic Medicine, Northwestern University, 676 N St Clair 1271, Chicago, Illinois 60611, USA
    J Genet Couns 12:333-49. 2003

Collaborators

Detail Information

Publications18

  1. pmc Practical considerations to guide development of access controls and decision support for genetic information in electronic medical records
    Diana C Darcy
    South Bay Regional Genetics Center, Santa Clara Valley Medical Center, San Jose, California, USA
    BMC Health Serv Res 11:294. 2011
    ....
  2. doi request reprint Medical and graduate students' attitudes toward personal genomics
    Kelly E Ormond
    Department of Genetics, Stanford Center for Biomedical Ethics, Stanford University, Stanford, California, USA
    Genet Med 13:400-8. 2011
    ....
  3. doi request reprint Assessing the understanding of biobank participants
    K E Ormond
    Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA
    Am J Med Genet A 149:188-98. 2009
    ..These findings are informative to those establishing and implementing biobanks, and to the IRBs reviewing such studies...
  4. doi request reprint Information preferences of high literacy pregnant women regarding informed consent models for genetic carrier screening
    K E Ormond
    Department of Medicine, Center for Genetic Medicine, and Medical Humanities and Bioethics, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States
    Patient Educ Couns 75:244-50. 2009
    ..With the increasing carrier screening options being offered to pregnant women, it is critical to consider what information women want in an informed consent process, and how they make decisions regarding screening...
  5. pmc Medical ethics for the genome world: a paper from the 2007 William Beaumont hospital symposium on molecular pathology
    Kelly E Ormond
    Department of Genetics, Stanford University, Stanford, California, USA
    J Mol Diagn 10:377-82. 2008
    ..Using a clinical medical ethics approach, several hypothetical case scenarios are presented and discussed to provide examples of the ethical issues that can arise...
  6. ncbi request reprint What do patients prefer: informed consent models for genetic carrier testing
    K E Ormond
    Department of Medicine, Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA
    J Genet Couns 16:539-50. 2007
    ..It will be useful to develop model consent programs and prospectively assess their impact on informed consent and patient satisfaction, both when positive and negative results are received...
  7. pmc Clinical assessment incorporating a personal genome
    Euan A Ashley
    Center for Inherited Cardiovascular Disease, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, USA
    Lancet 375:1525-35. 2010
    ..The cost of genomic information has fallen steeply, but the clinical translation of genetic risk estimates remains unclear. We aimed to undertake an integrated analysis of a complete human genome in a clinical context...
  8. pmc Best ethical practices for clinicians and laboratories in the provision of noninvasive prenatal testing
    M A Allyse
    Center for Biomedical Ethics, Stanford University, Stanford, CA, USA
    Prenat Diagn 33:656-61. 2013
    ..The goal of this study is to provide an ethical framework for clinicians and companies providing noninvasive prenatal testing using cell-free fetal DNA or whole fetal cells...
  9. ncbi request reprint Knowledge and attitudes toward a free education and Ashkenazi Jewish carrier testing program
    G Hegwer
    Center for Genetic Medicine and Graduate Program in Genetic Counseling, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA
    J Genet Couns 15:61-70. 2006
    ..05). In conclusion, this study demonstrated that an educational carrier screening program increased knowledge about the disorders and also produced mild anxiety regarding personal and reproductive risks...
  10. ncbi request reprint Attitudes of health care trainees about genetics and disability: issues of access, health care communication, and decision making
    Kelly E Ormond
    Center for Genetic Medicine, Northwestern University, 676 N St Clair 1271, Chicago, Illinois 60611, USA
    J Genet Couns 12:333-49. 2003
    ..Therefore, it is critical to document knowledge and attitudes of various health care providers and trainees, including differences between various specialties, to improve educational interventions geared to this area...
  11. ncbi request reprint The genetic family history as a risk assessment tool in internal medicine
    Theresa M Frezzo
    Feinberg School of Medicine, Northwestern University, Department of Obstetrics and Gynecology, Section of Reproductive Genetics and Graduate Program in Genetic Counseling, Chicago, Illinois, USA
    Genet Med 5:84-91. 2003
    ....
  12. ncbi request reprint Disclosing genetic research results: examples from practice
    Kelly E Ormond
    Northwestern University, USA
    Am J Bioeth 6:30-2; author reply W10-2. 2006
  13. ncbi request reprint Effect of family history on disclosure patterns of cystic fibrosis carrier status
    Kelly E Ormond
    Department of Obstetrics and Gynecology, Section of Reproductive Genetics, Northwestern University, Chicago, Illinois, USA
    Am J Med Genet C Semin Med Genet 119:70-7. 2003
    ..Our study documents that the frequency and reasons for disclosing CF carrier status differ between individuals with and without a family history of CF despite the fact that the reproductive risks for their relatives are the same...
  14. ncbi request reprint Outcome of chromosomally abnormal pregnancies in Lebanon: obstetricians' roles during and after prenatal diagnosis
    Lama T Eldahdah
    Graduate Program in Genetic Counseling, Northwestern University, Chicago IL, USA
    Prenat Diagn 27:525-34. 2007
    ..To better understand obstetrician experiences in Lebanon when disclosing abnormal amniocentesis results...
  15. ncbi request reprint Attitudes of genetic counselors towards expanding newborn screening and offering predictive genetic testing to children
    Susan Hiraki
    Alzheimer s Disease Center, Boston University, School of Medicine, Boston, Massachusetts, USA
    Am J Med Genet A 140:2312-9. 2006
    ..Their support for NBS correlates with their interest in testing their own children and not with professional experience...
  16. ncbi request reprint Genetic risk assessment and BRCA mutation testing
    Kelly E Ormond
    Ann Intern Med 144:303-4; discussion 304. 2006
  17. ncbi request reprint Association of spinocerebellar ataxia type 3 and spinocerebellar ataxia type 8 microsatellite expansions: genetic counseling implications
    Sabrina Paganoni
    Mov Disord 23:154-5. 2008
  18. ncbi request reprint Outline of a medical genetics curriculum for internal medicine residency training programs
    Douglas L Riegert-Johnson
    McKusick Nathans Institute of Genetic Medicine, Johns Hopkins Hospital, Baltimore, Maryland, USA
    Genet Med 6:543-7. 2004
    ..Teaching should be related to clinical experiences whenever possible. The curriculum developed by the committee and presented in this article will assist in teaching residents the attitudes, knowledge, and skills they will require...