K. East

发表

The Therapeutic Odyssey: Positioning Genomic Sequencing in the Search for a Child’s Best Possible Life

R. Myers, G. Barsh, G. Cooper, 2021, AJOB empirical bioethics.

Genomic sequencing identifies secondary findings in a cohort of parent study participants

R. Myers, G. Barsh, G. Cooper, 2017, Genetics in Medicine.

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

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

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

Nikhil Wagle, Peter Tarczy-Hornoch, Richard M Myers, 2016, American journal of human genetics.

A review and definition of ‘usual care’ in genetic counseling trials to standardize use in research

Sarah E Lillie, Marian J. Gilmore, Julianne M. O’Daniel, 2020, Journal of genetic counseling.

Understanding the present and preparing for the future: Exploring the needs of diagnostic and elective genomic medicine patients

D. Bick, M. Cochran, K. East, 2019, 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 .

Systematic reanalysis of genomic data improves quality of variant interpretation

R. Myers, G. Barsh, G. Cooper, 2018, Clinical genetics.

Genomic diagnosis for children with intellectual disability and/or developmental delay

G. Barsh, G. Cooper, K. Bowling, 2017, Genome Medicine.

Genomic diagnosis for children with intellectual disability and/or developmental delay

R. Myers, G. Barsh, G. Cooper, 2016, bioRxiv.

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.

A study of elective genome sequencing and pharmacogenetic testing in an unselected population

R. Myers, D. Bick, M. Cochran, 2021, Molecular genetics & genomic medicine.

Genome sequencing as a first-line diagnostic test for hospitalized newborns

G. Barsh, G. Cooper, S. Knight, 2021, medRxiv.

Illustrative case studies in the return of exome and genome sequencing results

B. Bernhardt, G. Jarvik, J. Wynn, 2015, Personalized medicine.

Characteristics and experiences of patients from a community-based and consumer-directed hereditary cancer population screening initiative

K. East, N. Lamb, V. Greve, 2021, HGG advances.

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.

Eliciting Preferences on Secondary Findings: The Preferences Instrument for Genomic Secondary Results (PIGSR)

R. Myers, G. Barsh, E. Clayton, 2016, Genetics in Medicine.

Identifying rare, medically-relevant genetic variation in a diverse population: opportunities and pitfalls

D. Absher, G. Barsh, G. Cooper, 2020, bioRxiv.

Genome sequencing as a first-line diagnostic test for hospitalized infants.

G. Barsh, G. Cooper, B. Korf, 2021, Genetics in medicine : official journal of the American College of Medical Genetics.

Identifying rare, medically relevant variation via population-based genomic screening in Alabama: opportunities and pitfalls

D. Absher, G. Barsh, G. Cooper, 2020, Genetics in Medicine.

Education and Training of Non-Genetics Providers on the Return of Genome Sequencing Results in a NICU Setting

M. Danila, M. Cochran, B. Korf, 2022, Journal of personalized medicine.

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.

A state-based approach to genomics for rare disease and population screening

G. Barsh, J. Cimino, G. Cooper, 2020, Genetics in Medicine.

Biotech 101: An Educational Outreach Program in Genetics and Biotechnology

K. East, N. Lamb, N. Callanan, 2012, Journal of Genetic Counseling.

Lessons learned about harmonizing survey measures for the CSER consortium

K. Goddard, L. Hindorff, A. McGuire, 2020, Journal of clinical and translational science.

Genomic sequencing identifies secondary findings in a cohort of parent study participants

R. Myers, G. Barsh, G. Cooper, 2017, bioRxiv.

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.

Recruiting diversity where it exists: The Alabama Genomic Health Initiative

J. Cimino, B. Korf, M. Fouad, 2020, Journal of genetic counseling.

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.

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

Joseph S. Salama, W. Chung, I. Krantz, 2016, American journal of human genetics.

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.

“Touching Triton”: Building Student Understanding of Complex Disease Risk

K. East, N. Lamb, Adam M. Hott, 2016, The American biology teacher.