Kelly E Ormond
Biographic Data
| ID | 8210560 |
|---|---|
| NAME | Kelly E Ormond |
| GIVEN NAMES | Kelly E |
| FAMILY NAME | Ormond |
| SIGNATURE | ORMOND K E |
| AFFILIATIONS | Stanford University |
| ORCID | 0000-0002-1033-0818 |
| VERIFIED | Yes |
| TOTAL WORKS | 7 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 7 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2009 |
| LATEST PUBLICATION YEAR | 2024 |
| H-INDEX | 0 |
Talking Ethics Early in Health Data Public Private Partnerships
Data access and data sharing are vital to advance medicine. A growing number of public private partnerships are set up to facilitate data access and sharing, as private and public actors possess highly complementary health data sets and treatment development resources. However, the priorities and incentives of public and private organizations are frequently in conflict. This has complicated partnerships and sparked public concerns around ethical …
“I wouldn't want anything that would change who he is.” The relationship between perceptions of identity and attitudes towards hypothetical gene-editing in parents of children with autosomal aneuploid…
Attitudes towards hypothetical somatic and germline gene-editing technologies for those who are directly impacted by genetic conditions are of increasing importance as these potential therapeutics are developed. This study is a secondary analysis of 27 semi-structured interviews conducted with parents of children with Trisomy 13 (N = 9), Trisomy 18 (N = 8), or Trisomy 21 (N = 10) that aimed to explore the relationship between perceptions of ident…
Treatment decision-making in sickle cell disease patients
Patient and provider perspectives on the development of personalized medicine
Predictors of adverse psychological experiences surrounding genome-wide profiling for disease risk
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
What Is the Role of Nongeneticist Physicians, and Are They Prepared for It
Physicians have knowledge and skill gaps in their ability to manage the care of families with gene-related illness. Virtual Mentor is a monthly bioethics journal published by the American Medical Association
No prominent works on this page.
What Is the Role of Nongeneticist Physicians, and Are They Prepared for It
Physicians have knowledge and skill gaps in their ability to manage the care of families with gene-related illness. Virtual Mentor is a monthly bioethics journal published by the American Medical Association
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
Patient and provider perspectives on the development of personalized medicine
Predictors of adverse psychological experiences surrounding genome-wide profiling for disease risk
Treatment decision-making in sickle cell disease patients
“I wouldn't want anything that would change who he is.” The relationship between perceptions of identity and attitudes towards hypothetical gene-editing in parents of children with autosomal aneuploid…
Attitudes towards hypothetical somatic and germline gene-editing technologies for those who are directly impacted by genetic conditions are of increasing importance as these potential therapeutics are developed. This study is a secondary analysis of 27 semi-structured interviews conducted with parents of children with Trisomy 13 (N = 9), Trisomy 18 (N = 8), or Trisomy 21 (N = 10) that aimed to explore the relationship between perceptions of ident…
Talking Ethics Early in Health Data Public Private Partnerships
Data access and data sharing are vital to advance medicine. A growing number of public private partnerships are set up to facilitate data access and sharing, as private and public actors possess highly complementary health data sets and treatment development resources. However, the priorities and incentives of public and private organizations are frequently in conflict. This has complicated partnerships and sparked public concerns around ethical …
Medicine (5 works) · Biology (3 works) · BRCA gene mutations in cancer (3 works) · Genetics (3 works) · Genomics and Rare Diseases (3 works) · Internal Medicine (3 works) · Autism Spectrum Disorder Research (2 works) · CRISPR and Genetic Engineering (2 works) · Disease (2 works) · Ethics in Clinical Research (2 works)