Jill O Robinson
Biographic Data
| ID | 4423200 |
|---|---|
| NAME | Jill O Robinson |
| GIVEN NAMES | Jill |
| FAMILY NAME | O Robinson |
| SIGNATURE | ROBINSON J O |
| AFFILIATIONS | Baylor College of Medicine |
| ORCID | 0000-0002-0487-304X |
| VERIFIED | Yes |
| TOTAL WORKS | 3 |
| TOTAL CITATIONS | 4 |
| AUTHOR COUNT | 3 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2013 |
| LATEST PUBLICATION YEAR | 2022 |
| H-INDEX | 1 |
Experiences of stigma in the United States during the Covid-19 pandemic
Participants and Study Decliners’ Perspectives About the Risks of Participating in a Clinical Trial of Whole Genome Sequencing
An increasing number of individuals are being recruited to whole genome sequencing (WGS) research. When asked hypothetically, the majority of the public express willingness to participate in this type of research, yet little is known about how many individuals will actually consent to research participation or what they perceive the risks to be. The MedSeq Project is a clinical trial exploring WGS in clinical care. We documented primary reason(s)…
Participants' Recall and Understanding of Genomic Research and Large-Scale Data Sharing
As genomic researchers are urged to openly share generated sequence data with other researchers, it is important to examine the utility of informed consent documents and processes, particularly as these relate to participants' engagement with and recall of the information presented to them, their objective or subjective understanding of the key elements of genomic research (e.g., data sharing), as well as how these factors influence or mediate th…
Participants' Recall and Understanding of Genomic Research and Large-Scale Data Sharing
As genomic researchers are urged to openly share generated sequence data with other researchers, it is important to examine the utility of informed consent documents and processes, particularly as these relate to participants' engagement with and recall of the information presented to them, their objective or subjective understanding of the key elements of genomic research (e.g., data sharing), as well as how these factors influence or mediate th…
Participants' Recall and Understanding of Genomic Research and Large-Scale Data Sharing
As genomic researchers are urged to openly share generated sequence data with other researchers, it is important to examine the utility of informed consent documents and processes, particularly as these relate to participants' engagement with and recall of the information presented to them, their objective or subjective understanding of the key elements of genomic research (e.g., data sharing), as well as how these factors influence or mediate th…
Participants and Study Decliners’ Perspectives About the Risks of Participating in a Clinical Trial of Whole Genome Sequencing
An increasing number of individuals are being recruited to whole genome sequencing (WGS) research. When asked hypothetically, the majority of the public express willingness to participate in this type of research, yet little is known about how many individuals will actually consent to research participation or what they perceive the risks to be. The MedSeq Project is a clinical trial exploring WGS in clinical care. We documented primary reason(s)…
Experiences of stigma in the United States during the Covid-19 pandemic
Medicine (3 works) · Psychology (3 works) · Alternative medicine (2 works) · Ethics in Clinical Research (2 works) · Informed consent (2 works) · Patient-Provider Communication in Healthcare (2 works) · Psychiatry (2 works) · 2019-20 coronavirus outbreak (1 works) · Applied Psychology (1 works) · Applied Psychology (1 works)