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Lista de obras de Mildred Cho

"Don't Want No Risk and Don't Want No Problems": Public Understandings of the Risks and Benefits of Non-Invasive Prenatal Testing in the United States

artículo científico publicado en 2015

"I don't want to be Henrietta Lacks": diverse patient perspectives on donating biospecimens for precision medicine research

"This lifetime commitment": Public conceptions of disability and noninvasive prenatal genetic screening.

artículo científico publicado en 2015

A commentary on oocyte donation for stem cell research in South Korea

artículo científico publicado en 2006

A comparison of institutional review board professionals' and patients' views on consent for research on medical practices

artículo científico publicado en 2016

A pilot survey on the licensing of DNA inventions

artículo científico publicado en 2003

A randomized study of multimedia informational aids for research on medical practices: Implications for informed consent

artículo científico publicado en 2016

Adrift in the Gray Zone: IRB Perspectives on Research in the Learning Health System

artículo científico publicado en 2016

Anticipating uncertainty and irrevocable decisions: provider perspectives on implementing whole-genome sequencing in critically ill children with heart disease

artículo científico publicado en 2018

Are clinical trials of cell transplantation for Duchenne muscular dystrophy ethical?

artículo científico publicado en 1994

Attitudes Toward Risk and Informed Consent for Research on Medical Practices: A Cross-sectional Survey

artículo científico publicado en 2015

Awareness and Acceptable Practices: IRB and Researcher Reflections on the Havasupai Lawsuit

artículo científico publicado en 2013

Barriers to Considering Ethical and Societal Implications of Research: Perceptions of Life Scientists

artículo científico publicado en 2012

Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research

scientific article published on 01 April 2018

Biomedical scientists' perceptions of ethical and social implications: is there a role for research ethics consultation?

artículo científico publicado en 2009

Building a Central Repository for Research Ethics Consultation Data: A Proposal for a Standard Data Collection Tool

artículo científico publicado en 2015

Calculating coauthors' contributions ⬇️

artículo científico publicado el 22 de noviembre de 1997

Cell-free fetal DNA testing for fetal aneuploidy and beyond: clinical integration challenges in the US context

artículo científico publicado en 2012

Cell-free fetal DNA testing: a pilot study of obstetric healthcare provider attitudes toward clinical implementation

artículo científico publicado en 2011

Cell-free fetal nucleic acid testing: a review of the technology and its applications

artículo científico publicado en 2011

Commercial landscape of noninvasive prenatal testing in the United States

artículo científico publicado en 2013

Conflicts of interest in magnetic resonance imaging: issues in clinical practice and research

artículo científico publicado en 2002

Consent and engagement, security, and authentic living using wearable and mobile health technology

artículo científico publicado en 2017

Consent insufficient for data release

artículo científico publicado en 2019

Customers or research participants? Guidance for research practices in commercialization of personal genomics

artículo científico publicado en 2012

Data mining for health: staking out the ethical territory of digital phenotyping

scientific article published on 19 December 2018

Defining the Scope and Improving the Quality of Clinical Research Ethics Consultation: Response to Open Peer Commentaries About the National Collaborative

artículo científico publicado en 2018

Demographic and experiential correlates of public attitudes towards cell-free fetal DNA screening

artículo científico publicado en 2014

Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background

article

Diagnostic testing fails the test

artículo científico publicado en 2002

Digital Contact Tracing, Privacy, and Public Health

artículo científico publicado en 2020

Direct-to-consumer genetic tests: beyond medical regulation?

artículo científico publicado en 2009

Disposition toward privacy and information disclosure in the context of emerging health technologies

artículo científico publicado en 2019

ELSI Research and Genetics: A Co-Evolution

article

ELSI priorities for brain imaging

artículo científico publicado en 2006

Editorial policies on financial disclosure

Educational material about genetic tests: Does it provide key information for patients and practitioners? ⬇️

artículo científico publicado el 19 de diciembre de 1997

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

artículo científico publicado en 2003

Engineering Values Into Genetic Engineering: A Proposed Analytic Framework for Scientific Social Responsibility

artículo científico publicado en 2015

Ethical Considerations and Risks in Psychiatric Genetics: Preliminary Findings of a Study on Psychiatric Genetic Researchers

article

Ethical Development of Digital Phenotyping Tools for Mental Health Applications: Delphi Study

artículo científico publicado en 2021

Ethical implications of array comparative genomic hybridization in complex phenotypes: points to consider in research

artículo científico publicado en 2007

Ethical, legal, social, and policy implications of behavioral genetics.

artículo científico publicado en 2013

Ethics and empiricism in the formation of professional guidelines

artículo científico publicado en 2014

Ethics watch: the G.I. genome: ethical implications of genome sequencing in the military

artículo científico publicado en 2011

Ethics. Incidental findings in brain imaging research

artículo científico publicado en 2006

Ethics. Issues in oocyte donation for stem cell research

artículo científico publicado en 2005

Fairness and Transparency in an Expanded Access Program: Allocation of the Only Treatment for SMA1.

artículo científico publicado en 2017

Feasibility of Obtaining Measures of Lifestyle From a Smartphone App: The MyHeart Counts Cardiovascular Health Study

artículo científico publicado en 2016

Financial conflict-of-interest policies in clinical research: issues for clinical investigators

artículo científico publicado en 2003

Focusing on Cause or Cure?: Priorities and Stakeholder Presence in Childhood Psychiatry Research

scientific article published on January 2014

Forensic genetics and ethical, legal and social implications beyond the clinic

artículo científico publicado en 2004

Forensic genetics and ethical, legal and social implications beyond the clinic

article

Genetic counseling for prenatal testing: where is the discussion about disability?

artículo científico publicado en 2012

Genetic research and health disparities

artículo científico publicado en 2004

Genetic testing of children for predisposition to mood disorders: anticipating the clinical issues

artículo científico publicado en 2014

Genetics. DNA patenting and licensing

artículo científico publicado en 2002

Genetics. Toward a new vocabulary of human genetic variation

artículo científico publicado en 2002

Genomics in the clinic: ethical and policy challenges in clinical next-generation sequencing programs at early adopter USA institutions

scientific article published on 01 June 2015

How do women decide? Accepting or declining BRCA1/2 testing in a nationwide clinical sample in the United States

artículo científico publicado en 2006

Human evolutionary genomics: ethical and interpretive issues

artículo científico publicado en 2012

Impact of Psychiatric Information on Potential Jurors in Evaluating High-Functioning Autism Spectrum Disorder (hfASD).

artículo científico publicado en 2015

Improving the quality of reports on randomized controlled trials. Recommendations of the CONSORT Study Group

artículo científico publicado el 1 de enero de 1998

In support of mitochondrial replacement therapy

artículo científico publicado en 2019

In the public interest?

artículo científico publicado en 2012

Industry opposes genomic legislation

artículo científico publicado en 2002

Informational risk, institutional review, and autonomy in the proposed changes to the common rule.

artículo científico publicado en 2012

Informed Consent for Research on Medical Practices

article

Informed Consent in the Genomics Era

artículo científico publicado en 2019

Innocent fun or "microslavery"? An ethical analysis of biotic games.

artículo científico publicado en 2014

Integrating stakeholder perspectives into the translation of cell-free fetal DNA testing for aneuploidy

artículo científico publicado en 2012

Interest, rationale, and potential clinical applications of genetic testing for mood disorders: a survey of stakeholders

artículo científico publicado en 2012

Managing incidental findings and research results in genomic research involving biobanks and archived data sets

artículo científico publicado en 2012

Managing incidental findings in human subjects research: analysis and recommendations

artículo científico publicado en 2008

Medical and graduate students' attitudes toward personal genomics

artículo científico publicado en 2011

Medicine. The future of personal genomics

artículo científico publicado en 2007

Metaphors matter: from biobank to a library of medical information

artículo científico publicado en 2017

Misrepresentation conspires against potential treatment for muscular dystrophy.

artículo científico publicado en 1995

Not yet in sequence: Clinical, technical, ethical questions linger over personal genomics

artículo científico publicado en 2010

Open-Label Extension Studies: Are They Really Research?

journal article; published in The American Journal of Bioethics in 2014

Partial Entrustment in Pragmatic Clinical Trials

artículo científico publicado en 2020

Patently unpatentable: implications of the Myriad court decision on genetic diagnostics ⬇️

artículo científico publicado el 1 de noviembre de 2010

Patient Perspectives on the Learning Health System: The Importance of Trust and Shared Decision Making

artículo científico publicado en 2015

Perspectives on Precision Health Among Racial/Ethnic Minority Communities and the Physicians That Serve Them

scientific article published on 02 April 2020

Physical activity, sleep and cardiovascular health data for 50,000 individuals from the MyHeart Counts Study

article

Preventive Genomic Sequencing in the General Population: Do PGS Fly?

artículo científico publicado en 2015

Privacy issues in personalized medicine.

artículo científico publicado en 2003

Protect NIH's DNA advisory committee

scientific article published in Science

Protecting subjects' interests in genetics research

artículo científico publicado en 2002

Race and ethnicity in genetic research.

artículo científico publicado en 2007

Racial and ethnic categories in biomedical research: there is no baby in the bathwater

artículo científico publicado en 2006

Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate

artículo científico publicado en 2013

Reply to "Getting the science and the ethics right in forensic genetics"

artículo científico publicado en 2005

Reporting Race and Ethnicity in Genetics Research: Do Journal Recommendations or Resources Matter?

artículo científico publicado en 2014

Research conduct. Lessons of the stem cell scandal

artículo científico publicado en 2006

Research ethics and the challenge of whole-genome sequencing

artículo científico publicado en 2008

Research ethics consultation: ethical and professional practice challenges and recommendations

artículo científico publicado en 2015

Research ethics consultation: the Stanford experience.

artículo científico publicado en 2008

Research ethics in the era of personalized medicine: updating science's contract with society

artículo científico publicado en 2010

Research ethics recommendations for whole-genome research: consensus statement

artículo científico publicado en 2008

Research on Medical Practices (ROMP): Attitudes of IRB Personnel about Randomization and Informed Consent

article

Research on Medical Practices: Why Patients Consider Participating and the Investigational Misconception

scientific article published on 01 July 2017

Resource Allocation in COVID-19 Research: Which Trials? Which Patients?

scientific article published on 01 July 2020

Response to open peer commentaries on "Thinking about the human neuron mouse".

artículo científico publicado en 2007

Secondary researchers' duties to return incidental findings and individual research results: a partial-entrustment account

article by Henry S Richardson & Mildred Cho published April 2012 in Genetics in Medicine

Strangers at the benchside: research ethics consultation

artículo científico publicado en 2008

Synthetic "Life," Ethics, National Security, and Public Discourse

artículo científico publicado en 2010

The Emergence of Clinical Research Ethics Consultation: Insights From a National Collaborative.

artículo científico publicado en 2018

The Henrietta Lacks legacy grows

scientific article published on 13 September 2013

The OHRP and SUPPORT

artículo científico publicado en 2013

The Role of Patient Perspectives in Clinical Research Ethics and Policy: Response to Open Peer Commentaries on "Patient Perspectives on the Learning Health System".

artículo científico publicado en 2016

The ethics of characterizing difference: guiding principles on using racial categories in human genetics

artículo científico publicado en 2008

Thinking about the human neuron mouse

artículo científico publicado en 2007

Toward a Predictive Understanding of Earth's Microbiomes to Address 21st Century Challenges

artículo científico publicado en 2016

Translating cell-free fetal DNA technology: structural lessons from non-invasive RhD blood typing

artículo científico publicado en 2012

Translating genomics into the clinic: moving to the post-Mendelian world

artículo científico publicado en 2009

Translating personalized medicine using new genetic technologies in clinical practice: the ethical issues

artículo científico publicado en 2014

Triggers for research ethics consultation

artículo científico publicado en 2012

Trustworthiness in Untrustworthy Times: Response to Open Peer Commentaries on Beyond Consent

journal article; published in The American Journal of Bioethics in 2018

Understanding Ethical, Legal and Societal Issues (ELSIs) in Human Biobanking and Genomics for Research and Healthcare in Zimbabwe: The Genomics Inheritance Law Ethics and Society (GILES) initiative

scientific article published on 08 January 2019

Understanding Ethical, Legal and Societal Issues (ELSIs) in Human Biobanking and Genomics for Research and Healthcare in Zimbabwe: The Genomics Inheritance Law Ethics and Society GILES initiative

Understanding incidental findings in the context of genetics and genomics

artículo científico publicado en 2008

Using Korean Dramas as a Precision Mental Health Education Tool for Asian Americans: A Pilot Study

scientific article published on 18 June 2019

Views of genetics health professionals on the return of genomic results.

artículo científico publicado en 2013

What are gene patents and why are people worried about them?

artículo científico publicado en 2005

What is in a cause? Exploring the relationship between genetic cause and felt stigma

artículo científico publicado en 2006

Whole genome sequencing in critically ill children

artículo científico publicado en 2015

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