M. Roche

发表

Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium

B. Bernhardt, J. Wynn, C. Blout, 2018, Journal of Genetic Counseling.

The who, what and why of research participants’ intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study

G. Henderson, James P Evans, J. Berg, 2017, Genetics in Medicine.

How Parents Search, Interpret, and Evaluate Genetic Information Obtained from the Internet

D. Skinner, M. Roche, 2009, Journal of Genetic Counseling.

Development and Validation of a Genomic Knowledge Scale to Advance Informed Decision-Making Research in Genomic Sequencing

J. Berg, N. Brewer, C. Rini, 2017, MDM policy & practice.

Parental preferences toward genomic sequencing for non-medically actionable conditions in children: a discrete choice experiment

J. Berg, D. Bailey, C. Powell, 2017, Genetics in Medicine.

Psychological adaptation to diagnostic genomic sequencing results: The role of hope fulfillment.

G. Henderson, C. Rini, M. Roche, 2019, Health psychology : official journal of the Division of Health Psychology, American Psychological Association.

Parental Views on Newborn Next Generation Sequencing: Implications for Decision Support

J. Berg, C. Powell, C. Rini, 2020, Maternal and Child Health Journal.

Values clarification and parental decision making about newborn genomic sequencing.

J. Berg, D. Bailey, C. Powell, 2019, Health psychology : official journal of the Division of Health Psychology, American Psychological Association.

“Possibly positive or certainly uncertain?”: Participants’ responses to uncertain diagnostic results from exome sequencing

G. Henderson, James P Evans, J. Berg, 2017, Genetics in Medicine.

Factors influencing NCGENES research participants’ requests for non-medically actionable secondary findings

G. Henderson, James P Evans, J. Berg, 2018, Genetics in Medicine.

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

Seema M Jamal, K. Ormond, L. Hudgins, 2018, Genetics in Medicine.

Evaluating the clinical utility of early exome sequencing in diverse pediatric outpatient populations in the North Carolina Clinical Genomic Evaluation of Next-generation Exome Sequencing (NCGENES) 2 study: a randomized controlled trial

Tamara S. Roman, J. Berg, Julianne M. O’Daniel, 2021, Trials.

Erratum: Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716301069) (10.1016/j.ajhg.2016.04.011))

Sara Chandros Hull, Robert C. Green, Sean D. Mooney, 2016 .

It’s time to ramp up genetic counseling training

M. Roche, A. Greb, 2016, Genetics in Medicine.

Emerging dilemmas in newborn screening.

D. Skinner, C. Powell, M. Roche, 2009, The virtual mentor : VM.

Genetic Library: Genetics and Public Health

Julianne M. O’Daniel, Barbara Lerner, M. Roche, 2004, Journal of Genetic Counseling.

Evaluating parents’ decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol

J. Berg, D. Bailey, C. Powell, 2018, Trials.

Genomic Knowledge in the Context of Diagnostic Exome Sequencing: Changes over Time, Persistent Subgroup Differences, and Associations with Psychological Sequencing Outcomes

G. Henderson, J. Berg, Julianne M. O’Daniel, 2019, Genetics in Medicine.

Is Incidental Finding the Best Term? A Study of Patients’ Preferences

B. Wilfond, G. Henderson, Julianne M. O’Daniel, 2016, Genetics in Medicine.

A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

J. Berg, Julianne M. O’Daniel, Kristy Lee, 2015, Genetics in Medicine.

Newborn Sequencing in Genomic Medicine and Public Health

Tiina K. Urv, N. Risch, P. Kwok, 2017, Pediatrics.

Maternal Consequences of the Detection of Fragile X Carriers in Newborn Screening

J. Sideris, D. Bailey, C. Powell, 2015, Pediatrics.

Supporting Parental Decisions About Genomic Sequencing for Newborn Screening: The NC NEXUS Decision Aid

J. Berg, R. Furberg, D. Bailey, 2016, Pediatrics.

Incidental Findings with Genomic Testing: Implications for Genetic Counseling Practice

J. Berg, M. Roche, 2015, Current Genetic Medicine Reports.

Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project.

Tamara S. Roman, J. Berg, Julianne M. O’Daniel, 2020, American journal of human genetics.

Family Relations in the Genomic Era: Communicating about Intergenerational Transmission of Risk for Disability

D. Bailey, C. Powell, Megan A. Lewis, 2014 .

Genetic Counseling Considerations in Molecular Diagnosis

M. Roche, 2006 .

“Not Tied Up Neatly with a Bow”: Professionals’ Challenging Cases in Informed Consent for Genomic Sequencing

Debra Skinner, Denise L. Perry, Barbara A. Bernhardt, 2016, Journal of Genetic Counseling.

Experiences with obtaining informed consent for genomic sequencing

Denise L. Perry, D. Skinner, B. Bernhardt, 2015, American journal of medical genetics. Part A.

How Can Psychological Science Inform Research About Genetic Counseling for Clinical Genomic Sequencing?

J. Roberts, G. Henderson, J. Berg, 2015, Journal of Genetic Counseling.

An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening.

J. Berg, Julianne M. O’Daniel, C. Powell, 2019, The Journal of pediatrics.

Genetic Information, Non-Discrimination, and Privacy Protections in Genetic Counseling Practice

Anya E. R. Prince, M. Roche, A. Prince, 2014, Journal of Genetic Counseling.

Can a decision aid enable informed decisions in neonatal nursery recruitment for a fragile X newborn screening study?

D. Bailey, E. Bishop, C. Bann, 2012, Genetics in Medicine.

Design and Evaluation of a Decision Aid for Inviting Parents to Participate in a Fragile X Newborn Screening Pilot Study

D. Bailey, C. Powell, Megan A. Lewis, 2013, Journal of Genetic Counseling.

Burden or benefit? Effects of providing education about and the option to request additional genomic findings from diagnostic exome sequencing: A randomized controlled trial.

G. Henderson, J. Berg, Julianne M. O’Daniel, 2021, Patient education and counseling.

The who, what and why of research participants’ intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study

G. Henderson, J. Berg, Julianne M. O’Daniel, 2017, Genetics in Medicine.

Examining the Cascade of Participant Attrition in a Genomic Medicine Research Study: Barriers and Facilitators to Achieving Diversity

G. Henderson, J. Berg, Julianne M. O’Daniel, 2018, Public Health Genomics.

Next Generation Genetic Counseling: Introduction to the Special Issue

C. Palmer, M. Roche, 2014, Journal of Genetic Counseling.

The phenotype of multiple congenital anomalies‐hypotonia‐seizures syndrome 1: Report and review

J. Berg, K. Wilhelmsen, C. Powell, 2015, American journal of medical genetics. Part A.

GCH1 heterozygous mutation identified by whole-exome sequencing as a treatable condition in a patient presenting with progressive spastic paraplegia

J. Berg, K. Wilhelmsen, Zheng Fan, 2014, Journal of Neurology.

Developing a Conceptual, Reproducible, Rubric-Based Approach to Consent and Result Disclosure for Genetic Testing by Clinicians with Minimal Genetics Background

K. Ormond, L. Hudgins, M. Cho, 2018, Genetics in Medicine.

Factors influencing NCGENES research participants’ requests for non-medically actionable secondary findings

G. Henderson, J. Berg, Julianne M. O’Daniel, 2018, Genetics in Medicine.

Parents' Decisions to Screen Newborns for FMR1 Gene Expansions in a Pilot Research Project

J. Sideris, C. Powell, M. Roche, 2011, Pediatrics.

A behavior-theoretic evaluation of values clarification on parental beliefs and intentions toward genomic sequencing for newborns.

J. Berg, D. Bailey, C. Powell, 2018, Social science & medicine.

Moving toward NextGenetic Counseling

M. Roche, 2012, Genetics in Medicine.

Values clarification exercises improved parental decision making about newborn genomic sequencing

J. Berg, D. Bailey, C. Powell, 2018 .

Genomic knowledge in the contextstic exome sequencing : changes over time , persistent subgroup differences , and associations with psychological sequencing outcomes

G. Henderson, J. Berg, C. Rini, 2019 .

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Matthew S. Lebo, Victoria A. Miller, Jeffrey W. Pennington, 2016, American journal of human genetics.

How Can Psychological Science Inform Research About Genetic Counseling for Clinical Genomic Sequencing?

G. Henderson, J. Berg, B. Bernhardt, 2015, Journal of Genetic Counseling.