Search filters

Authors whose works are in public domain in at least one jurisdiction

List of works by Barbara A Bernhardt

"Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing

scientific article published on 26 April 2015

"Set in Stone" or "Ray of Hope": Parents' Beliefs About Cause and Prognosis After Genomic Testing of Children Diagnosed with ASD.

scientific article published on 22 February 2017

"Something Extra on Chromosome 5": Parents' Understanding of Positive Prenatal Chromosomal Microarray Analysis (CMA) Results

scientific article published on 4 March 2016

"They Can't Find Anything Wrong with Him, Yet": Mothers' experiences of parenting an infant with a prenatally diagnosed copy number variant (CNV).

scientific article published on 7 November 2016

A qualitative study of healthcare providers' perspectives on the implications of genome-wide testing in pediatric clinical practice

scientific article published on 14 September 2013

Active recruitment increased enrollment in a hereditary cancer registry

scientific article

Adolescents' transition to self-management of a chronic genetic disorder

scientific article published in April 2008

An Observational Study of Children's Involvement in Informed Consent for Exome Sequencing Research

scientific article published on 20 October 2016

An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing

scientific article

Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings

scientific article published in February 2018

Are Practicing and Future Physicians Prepared to Obtain Informed Consent? The Case of Genetic Testing forSusceptibility to Breast Cancer ⬇️

scientific article published on January 1, 1998

Balancing Genetics (Science) and Counseling (Art) in Prenatal Chromosomal Microarray Testing

scientific article published on 21 May 2016

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

scientific article

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

article

Clinical providers' experiences with returning results from genomic sequencing: an interview study.

scientific article

Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing

scientific article

Cost savings through molecular diagnosis for hereditary hemorrhagic telangiectasia

scientific article published on 26 January 2012

Direct‐to‐Consumer Genetic Testing: Introduction to the Special Issue ⬇️

scientific article published on March 23, 2012

Distress and burnout among genetic service providers

scientific article published on July 2009

Experiences with obtaining informed consent for genomic sequencing.

scientific article

Genetic risk perception and reproductive decision making among people with epilepsy

scientific article published in September 2010

Genomic decision support needs in pediatric primary care

scientific article published on 19 February 2017

Genomic variation: what does it mean?

scientific article published in February 2013

Gratitude, protective buffering, and cognitive dissonance: How families respond to pediatric whole exome sequencing in the absence of actionable results

scientific article published in March 2018

Health screening behaviors among adults with hereditary hemorrhagic telangiectasia in North America

scientific article

Houseofficers' reactions to media coverage about the sequencing of the human genome

scientific article published on May 2003

How do providers discuss the results of pediatric exome sequencing with families?

scientific article published on 4 September 2017

Incorporating direct-to-consumer genomic information into patient care: attitudes and experiences of primary care physicians

scientific article published on September 2012

Informed consent for enrolling minors in genetic susceptibility research: a qualitative study of at-risk children's and parents' views about children's role in decision-making

scientific article published on April 2003

Mapping the human genome: an assessment of media coverage and public reaction

scientific article published in January 2002

National Society Of Genetic Counselors Natalie Weissberger Paul National Leadership Award Address: "Patients and Research: Paths to Personal and Professional Growth".

scientific article published on 19 February 2016

Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing

scientific article published on 19 February 2018

Parents' and children's attitudes toward the enrollment of minors in genetic susceptibility research: implications for informed consent

scientific article published in February 2003

Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disorders

scientific article

Pre- and post-test genetic counseling for chromosomal and Mendelian disorders

scientific article published on 21 December 2015

Pregnancy as a proclamation of faith: Ultra-Orthodox Jewish women navigating the uncertainty of pregnancy and prenatal diagnosis

scientific article

Recommendations for the integration of genomics into clinical practice

scientific article published on 12 May 2016

Scientists' and science writers' experiences reporting genetic discoveries: toward an ethic of trust in science journalism

scientific article

Self-surveillance by adolescents and young adults transitioning to self-management of a chronic genetic disorder

scientific article published on 6 April 2009

Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group

scientific article

Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consent

scientific article published on 12 July 2013

The IGNITE network: a model for genomic medicine implementation and research

scientific article published on 5 January 2016

The adolescent research participant: strategies for productive and ethical interviewing

scientific article published on 14 May 2009

The decision to continue: the experiences and needs of parents who receive a prenatal diagnosis of holoprosencephaly

scientific article published in November 2002

The role and impact of personal faith and religion among genetic service providers

scientific article published on February 2009

Toward a Model Informed Consent Process for BRCA1 Testing: A Qualitative Assessment of Women's Attitudes ⬇️

scientific article published on June 1, 1997

What do clinicians derive from partnering with their patients? A reliable and valid measure of "personal meaning in patient care"

scientific article published on 15 May 2008

What keeps you up at night? Genetics professionals' distressing experiences in patient care

scientific article published in May 2010

When Participants in Genomic Research Grow Up: Contact and Consent at the Age of Majority

scientific article published on 15 October 2015

When genetic screening is useful, but not used

scientific article published on July 2011

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

scientific article published in March 2018

Why is genetic screening for autosomal dominant disorders underused in families? The case of hereditary hemorrhagic telangiectasia ⬇️

scientific article published on September 1, 2011

Women’s experiences receiving abnormal prenatal chromosomal microarray testing results ⬇️

scientific article published on 06 September 2012

“It's Not Like Judgment Day”: Public Understanding of and Reactions to Personalized Genomic Risk Information ⬇️

scientific article published on December 17, 2011

“What does it mean?”: Uncertainties in understanding results of chromosomal microarray testing ⬇️

scientific article published on January 5, 2012

Paulina is supported by:

About Paulina

Help