Wendy K. Chung

M.D., Ph.D.

Kennedy Family Professor of Pediatrics (in Medicine)

Institution(s):

Columbia University

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Methods

Qualitative Methods

Mixed Methods

Survey Research

Disciplines

Genetics/Genomics

Medicine

Areas of Expertise

Gene discovery for birth defects

Neurodevelopmental disorders

Cardiovascular Diseases

Cancer and clinical implementation of genomics

Publications

Participant choices for return of genomic results in the eMERGE Network

Ethical considerations related to return of results from genomic medicine projects: The eMERGE network (phase III) experience

Returning results in the genomic era: Initial experiences of the eMERGE Network

Clinical sequencing exploratory research consortium: Accelerating evidence-based practice of genomic medicine

Navigating the research–clinical interface in genomic medicine: Analysis from the CSER Consortium

Rethinking the “open future” argument against predictive genetic testing of children

Approaches to carrier testing and results disclosure in translational genomics research: The clinical sequencing exploratory research consortium experience

Psychological outcomes related to exome and genome sequencing result disclosure: A meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies

Impact of genetic testing for cardiomyopathy on emotional well-being and family dynamics: A study of parents and adolescents

Is there a way to reduce the inequity in variant interpretation on the basis of ancestry?

Women's thoughts on receiving and sharing genetic information: Considerations for genetic counseling

Newborn screening for neurodevelopmental diseases: Are we there yet?

ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Newborn screening for neurodevelopmental diseases: Are we there yet?

Practical considerations for reinterpretation of individual genetic variants

Individualized interventions for rare genetic ccnditions and the research-treatment spectrum: Stakeholder perspectives

Returning integrated genomic risk and clinical recommendations: The eMERGE study

Familial hypercholesterolemia in the electronic medical records and genomics network: Prevalence, penetrance, cardiovascular risk, and outcomes after return of results

Individualized interventions for rare genetic conditions and the research- treatment spectrum: Stakeholder perspectives

ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Artificial intelligence and the impact on medical genetics

Uptake of genetic research results and patient-reported outcomes with return of results incorporating web-based predisclosure education

Receiving de novo genetic diagnoses for autism with intellectual disability: Parents' views of impacts on families' reproductive decisions

Return of polygenic risk scores in research: Stakeholders' views on the eMERGE-IV Study

Understanding social, cultural, and religious factors influencing medical decision-making on BRCA1/2 genetic testing in the orthodox Jewish community

Views of genetic testing for autism among autism self-advocates: A qualitative study

Pilot study of a decision aid on BRCA1/2 genetic testing among Orthodox Jewish women

Consideration of disease penetrance in the selection of secondary findings gene- disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

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