K. Lewis

发表

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

Marian J. Gilmore, B. Bernhardt, J. Wynn, 2018, Journal of Genetic Counseling.

Research participants’ attitudes towards the confidentiality of genomic sequence information

Leslie G Biesecker, Katie Lewis, Flavia M Facio, 2013, European Journal of Human Genetics.

PUGS: A novel scale to assess perceptions of uncertainties in genome sequencing

S. Woolford, W. Klein, L. Biesecker, 2017, Clinical genetics.

Perceived ambiguity as a barrier to intentions to learn genome sequencing results

Jennifer M. Taber, W. Klein, L. Biesecker, 2015, Journal of Behavioral Medicine.

Knowledge, motivations, expectations, and traits of an African, African-American, and Afro-Caribbean sequencing cohort and comparisons to the original ClinSeq® cohort

W. Klein, L. Biesecker, B. Biesecker, 2018, Genetics in Medicine.

Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutations.

Larry N. Singh, J. Mullikin, H. Kong, 2015, American journal of human genetics.

Information Avoidance Tendencies, Threat Management Resources, and Interest in Genetic Sequencing Feedback

Jennifer M. Taber, W. Klein, L. Biesecker, 2015, Annals of behavioral medicine : a publication of the Society of Behavioral Medicine.

Dispositional optimism and perceived risk interact to predict intentions to learn genome sequencing results.

Jennifer M. Taber, W. Klein, L. Biesecker, 2015, Health psychology : official journal of the Division of Health Psychology, American Psychological Association.

Web Platform vs In-Person Genetic Counselor for Return of Carrier Results From Exome Sequencing: A Randomized Clinical Trial

L. Biesecker, J. Johnston, B. Biesecker, 2018, JAMA internal medicine.

Associations of Perceived Norms With Intentions to Learn Genomic Sequencing Results: Roles for Attitudes and Ambivalence

Jennifer M. Taber, W. Klein, L. Biesecker, 2018, Health psychology : official journal of the Division of Health Psychology, American Psychological Association.

Perceptions of uncertainties about carrier results identified by exome sequencing in a randomized controlled trial.

T. Wolfsberg, L. Biesecker, A. Nguyen, 2019, Translational behavioral medicine.

Outcomes of Counseling after Education about Carrier Results: A Randomized Controlled Trial.

L. Biesecker, J. Johnston, B. Biesecker, 2018, American journal of human genetics.

A common haplotype containing functional CACNA1H variants is frequently coinherited with increased TPSAB1 copy number

L. Biesecker, J. Lyons, K. Stone, 2017, Genetics in Medicine.

Ability of Patients to Distinguish Among Cardiac Genomic Variant Subclassifications

W. Klein, L. Biesecker, B. Biesecker, 2018, Circulation Genomic and Precision Medicine.

Preferences for and acceptability of receiving pharmacogenomic results by mail: A focus group study with a primarily African‐American cohort

L. Biesecker, B. Biesecker, G. Fasaye, 2021, Journal of genetic counseling.

Preferences for results delivery from Exome Sequencing/Genome Sequencing

L. Biesecker, B. Biesecker, G. Hooker, 2013, Genetics in Medicine.

How do research participants perceive “uncertainty” in genomic sequencing?

W. Klein, L. Biesecker, B. Biesecker, 2014, Genetics in Medicine.

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

Yaping Yang, Katrina A B Goddard, Kathryn M Porter, 2018, Molecular genetics & genomic medicine.

Engagement and communication among participants in the ClinSeq Genomic Sequencing Study

L. Biesecker, B. Biesecker, G. Hooker, 2016, Genetics in Medicine.

Disclosure of cardiac variants of uncertain significance results in an exome cohort

W. Klein, L. Biesecker, J. Johnston, 2018, Clinical genetics.

The Dynamics of a Genetic Counseling Peer Supervision Group

Meredith A. Weaver, K. Lewis, L. Erby, 2017, Journal of Genetic Counseling.

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 .

Interpreting Secondary Cardiac Disease Variants in an Exome Cohort

Larry N. Singh, J. Mullikin, P. Stenson, 2013, Circulation. Cardiovascular genetics.

Future-oriented Emotions and Decisions to Receive Genomic Testing Results Among U.S. Adults of African Ancestry.

W. Klein, L. Biesecker, B. Biesecker, 2022, Annals of behavioral medicine : a publication of the Society of Behavioral Medicine.

Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number

Andrew J. Oler, Ryan J. Carlson, J. Hughes, 2016, Nature Genetics.

Increased Burden of Rare Sequence Variants in GnRH-Associated Genes in Women with Hypothalamic Amenorrhea.

Christopher A. Lavender, L. Biesecker, R. Quinton, 2020, The Journal of clinical endocrinology and metabolism.

Elective genomic testing: Practice resource of the National Society of Genetic Counselors

Matthew S. Lebo, E. Orlova, D. Bick, 2023, Journal of genetic counseling.

The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.

N. Risch, P. Kwok, S. Fullerton, 2018, American journal of human genetics.

Participant use and communication of findings from exome sequencing: A mixed methods study

L. Biesecker, B. Biesecker, G. Hooker, 2015, Genetics in Medicine.

Characterizing Participants in the ClinSeq Genome Sequencing Cohort as Early Adopters of a New Health Technology

W. Klein, L. Biesecker, B. Biesecker, 2015, PloS one.

Defining personal utility in genomics: A Delphi study

B. Wilfond, L. Biesecker, J. Kohler, 2017, Clinical genetics.

Health Behaviors Amongst Unaffected Participants Following Receipt of Variants of Uncertain Significance in Cardiomyopathy-Associated Genes

L. Biesecker, J. Johnston, B. Biesecker, 2018, Genetics in Medicine.

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

N. Spinner, H. Rehm, K. Goddard, 2018, Genetics in Medicine.

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

B. Bernhardt, J. Wynn, C. McMullen, 2018, BMC Medical Genomics.

A systematic literature review of disclosure practices and reported outcomes for medically-actionable genomic secondary findings

Julie C. Sapp, L. Biesecker, P. J. van der Wees, 2021, Genetics in Medicine.

Roles of attitudes and injunctive norms in decisional conflict and disclosure following receipt of genome sequencing results.

W. Klein, L. Biesecker, B. Biesecker, 2020, Social science & medicine.

Intentions to share exome sequencing results with family members: exploring spousal beliefs and attitudes

Jennifer M. Taber, W. Klein, L. Biesecker, 2018, European Journal of Human Genetics.

Examining access to care in clinical genomic research and medicine: Experiences from the CSER Consortium

L. Hindorff, B. Wilfond, Julianne M. O’Daniel, 2021, Journal of Clinical and Translational Science.

Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

N. Spinner, H. Rehm, K. Goddard, 2019, Genetics in Medicine.

Cardiff sciSCREEN: A model for using film screenings to engage publics in University research

K. Lewis, Jamie Lewis, Luis Reyes-Galindo, 2017 .

The role of future-oriented affect in engagement with genomic testing results

W. Klein, L. Biesecker, B. Biesecker, 2021, Journal of Behavioral Medicine.

The role of current affect, anticipated affect and spontaneous self-affirmation in decisions to receive self-threatening genetic risk information

Jennifer M. Taber, W. Klein, L. Biesecker, 2015, Cognition & emotion.

Web-Based Platform vs Genetic Counselors in Educating Patients About Carrier Results From Exome Sequencing-Reply.

L. Biesecker, B. Biesecker, K. Lewis, 2018, JAMA internal medicine.

Engagement and return of results preferences among a primarily African American genomic sequencing research cohort.

L. Biesecker, B. Biesecker, G. Fasaye, 2021, American journal of human genetics.

Using the diffusion of innovations model to guide participant engagement in the genomics era

Katie L Lewis, Flavia M Facio, Courtney D Berrios, 2019, Journal of genetic counseling.

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

B. Bernhardt, J. Wynn, C. McMullen, 2018, BMC Medical Genomics.

Ethnic identity and engagement with genome sequencing research

Brittany M. Hollister, W. Klein, L. Biesecker, 2018, Genetics in Medicine.

The PrU: development and validation of a measure to assess personal utility of genomic results.

K. Goddard, B. Wilfond, M. Leo, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Reactions to clinical reinterpretation of a gene variant by participants in a sequencing study

Jennifer M. Taber, W. Klein, L. Biesecker, 2017, Genetics in Medicine.

An open‐source python library for detection of known and novel Kell, Duffy and Kidd variants from exome sequencing

Oscar A. Montemayor, L. Biesecker, S. Adams, 2021, Vox sanguinis.

Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

N. Spinner, H. Rehm, K. Goddard, 2019, Genetics in Medicine.

Adaptation of the working alliance inventory for the assessment of the therapeutic alliance in genetic counseling

L. Biesecker, B. Biesecker, K. Lewis, 2021, Journal of genetic counseling.

Ethnic identity and engagement with genome sequencing research

Brittany M. Hollister, W. Klein, L. Biesecker, 2018, Genetics in Medicine.

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

N. Spinner, K. Goddard, L. Hindorff, 2018, Genetics in Medicine.

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.

Knowledge, motivations, expectations, and traits of an African, African-American, and Afro-Caribbean sequencing cohort and comparisons to the original ClinSeq® cohort

W. Klein, L. Biesecker, B. Biesecker, 2018, Genetics in Medicine.

Dyadic concordance and associations of beliefs with intentions to learn carrier results from genomic sequencing

Jennifer M. Taber, W. Klein, L. Biesecker, 2021, Journal of Behavioral Medicine.

Feasibility of Coping Effectiveness Training for Caregivers of Children with Autism Spectrum Disorder: a Genetic Counseling Intervention

J. Muschelli, B. Biesecker, K. Lewis, 2018, Journal of Genetic Counseling.