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K. East · SciRah

Researcher profile · Semantic Scholar

K. East

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K. East — researcher profile on SciRah

h-index: 17
Works: 52
Citations: 1,225

Most-cited papers

Genomic diagnosis for children with intellectual disability and/or developmental delay
Kevin M. Bowling, M. L. Thompson, Michelle D. Amaral, Candice R. Finnila +18 more
2016bioRxiv274 citations Open access
Semantic Scholar
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
R. Green, K. Goddard, G. Jarvik, L. Amendola +60 more
2016American Journal of Human Genetics157 citations Open access
Semantic Scholar
Secondary findings from clinical genomic sequencing: Prevalence, patient perspectives, family history assessment, and healthcare costs from a multi-site study
M. R. Hart, B. Biesecker, C. Blout, Kurt D. Christensen +38 more
2018Genetics in Medicine139 citations Open access
Semantic Scholar
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.
L. Amendola, J. Berg, C. Horowitz, Frank A Angelo +34 more
2018American Journal of Human Genetics130 citations Open access
Semantic Scholar
Systematic reanalysis of genomic data improves quality of variant interpretation
S. Hiatt, Michelle D. Amaral, Kevin M. Bowling, C. Finnila +17 more
2018Clinical Genetics52 citations Open access
Semantic Scholar
Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium
L. Amendola, J. Robinson, Ragan Hart, Sawona Biswas +10 more
2018Journal of Genetic Counseling44 citations Open access
Semantic Scholar
Genome sequencing as a first-line diagnostic test for hospitalized infants
K. Bowling, M. Thompson, C. Finnila, S. Hiatt +35 more
2021Genetics in Medicine41 citations Open access
Semantic Scholar
Eliciting Preferences on Secondary Findings: The Preferences Instrument for Genomic Secondary Results (PIGSR)
K. Brothers, K. East, Whitley V. Kelley, M. F. Wright +13 more
2016Genetics in Medicine40 citations Open access
Semantic Scholar
Illustrative case studies in the return of exome and genome sequencing results
L. Amendola, Denise M. Lautenbach, S. Scollon, B. Bernhardt +9 more
2015Personalized Medicine38 citations Open access
Semantic Scholar
Genomic sequencing identifies secondary findings in a cohort of parent study participants
M. Thompson, C. Finnila, K. Bowling, Kyle B. Brothers +15 more
2017Genetics in Medicine29 citations Open access
Semantic Scholar
The Therapeutic Odyssey: Positioning genomic sequencing in the search for a child’s best possible life
Janet E. Childerhose, Carla A. Rich, K. East, Whitley V. Kelley +14 more
2021AJOB Empirical Bioethics27 citations Open access
Semantic Scholar
A State-Based Approach to Genomics for Rare Disease and Population Screening
K. East, Whitley V. Kelley, A. Cannon, M. Cochran +17 more
2020Genetics in Medicine25 citations Open access
Semantic Scholar
A Review and Definition of “Usual Care” in Genetic Counseling Trials to Standardize Use in Research
B. Biesecker, Sarah E Lillie, L. Amendola, Katherine E. Donohue +13 more
2020Journal of Genetic Counseling23 citations Open access
Semantic Scholar
Lessons learned about harmonizing survey measures for the CSER consortium
K. Goddard, Frank A Angelo, Sara L. Ackerman, J. Berg +19 more
2020Journal of Clinical and Translational Science23 citations Open access
Semantic Scholar
Education and Training of Non-Genetics Providers on the Return of Genome Sequencing Results in a NICU Setting
K. East, M. Cochran, Whitley V. Kelley, V. Greve +9 more
2022Journal of Personalized Medicine22 citations Open access
Semantic Scholar
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
R. Green, Katrina A. B. Goddard, G. Jarvik, L. Amendola +237 more
2016American Journal of Human Genetics20 citations Open access
Semantic Scholar
Recruiting diversity where it exists: The Alabama Genomic Health Initiative
Thomas May, A. Cannon, Irene P. Moss, Mariko Nakano-Okuno +14 more
2020Journal of Genetic Counseling14 citations Open access
Semantic Scholar
Understanding the present and preparing for the future: Exploring the needs of diagnostic and elective genomic medicine patients
K. East, M. Cochran, Whitley V. Kelley, V. Greve +5 more
2019Journal of Genetic Counseling14 citations
Semantic Scholar
Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
M. R. Hart, B. Biesecker, C. Blout, Kurt D. Christensen +38 more
2019Genetics in Medicine14 citations Open access
Semantic Scholar
A study of elective genome sequencing and pharmacogenetic testing in an unselected population
M. Cochran, K. East, V. Greve, M. Kelly +6 more
2021Molecular Genetics & Genomic Medicine11 citations Open access
Semantic Scholar
Identifying rare, medically relevant variation via population-based genomic screening in Alabama: opportunities and pitfalls
Kevin M. Bowling, M. L. Thompson, David E. Gray, James M. J. Lawlor +11 more
2020Genetics in Medicine11 citations Open access
Semantic Scholar
Parents’ Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit
A. Lemke, M. Thompson, Emily C. Gimpel, K. McNamara +37 more
2023Journal of Personalized Medicine9 citations Open access
Semantic Scholar
Genomic sequencing in diverse and underserved pediatric populations: parent perspectives on understanding, uncertainty, psychosocial impact, and personal utility of results
Barbara Biesecker, Sara L. Ackerman, Kyle B. Brothers, K. East +15 more
2025Genetics in Medicine6 citations Open access
Semantic Scholar
Experiences and attitudes of hereditary cancer screening patients in a consumer directed testing model.
V. Greve, M. Garner, K. Odom, Sara J. Cooper +1 more
2021Patient Education and Counseling6 citations
Semantic Scholar
“Touching Triton”: Building Student Understanding of Complex Disease Risk
Madelene Loftin, K. East, A. Hott, N. Lamb
2016The American history teacher6 citations Open access
Semantic Scholar
Errors in Genome Sequencing Result Disclosures: A Randomized Controlled Trial Comparing Neonatology Non-Genetics Healthcare Professionals and Genetic Counselors.
Tanner F. Coleman, Jada Pugh, Whitley V. Kelley, K. East +7 more
2024Genetics in Medicine4 citations
Semantic Scholar
Does genetic testing offer utility as a supplement to traditional family health history intake for inherited disease risk?
Thomas May, C. Smith, Whitley V. Kelley, K. East +7 more
2023Family Practice4 citations
Semantic Scholar
Biotech 101: An Educational Outreach Program in Genetics and Biotechnology
K. East, A. Hott, N. Callanan, N. Lamb
2012Journal of Genetic Counseling4 citations Open access
Semantic Scholar
Medical and psychosocial outcomes of state-funded population genomic screening
A. Cannon, Olivia McMillan, Whitley V. Kelley, K. East +8 more
2023Clinical Genetics3 citations Open access
Semantic Scholar
Return of raw data in genomic testing and research: ownership, partnership, and risk–benefit
Thomas May, Mariko Nakano-Okuno, Whitley V. Kelley, K. East +4 more
2019Genetics in Medicine3 citations Open access
Semantic Scholar
A study of the cross-hatched gold foils from Sutton Hoo
K. East
19853 citations
Semantic Scholar
338 The Alabama Genomic Health Initiative: Integrating Genomic Medicine into Primary Care
N. Limdi, D. Absher, I. Asif, Lori Bateman +21 more
2023Journal of Clinical and Translational Science2 citations Open access
Semantic Scholar
eP494: Integration of genomics into primary care via the Alabama Genomic Health Initiative
Bruce Korf, D. Absher, I. Asif, Lori Bateman +20 more
2022Genetics in Medicine2 citations Open access
Semantic Scholar
Characteristics and experiences of patients from a community-based and consumer-directed hereditary cancer population screening initiative
V. Greve, K. Odom, S. Pudner, N. Lamb +2 more
2021HGG advances2 citations Open access
Semantic Scholar
Integrating genomic medicine into primary care –examining perceptions of community advisory board members
P. Das, Whitley V. Kelley, Catanya G. Stager, Tiffany Osborne +6 more
2026Journal of Community Genetics1 citations Open access
Semantic Scholar
eP425: Parental impact of genome sequencing during the neonatal period
K. Brothers, Carla A. Rich, E. Gimpel, K. East +37 more
2022Genetics in Medicine1 citations Open access
Semantic Scholar
OP055: Comparing error rates in disclosure of genome sequencing results between non-genetics providers and genetic counselors
M. Cochran, K. East, Whitley V. Kelley, V. Greve +12 more
2022Genetics in Medicine1 citations Open access
Semantic Scholar
Review for "Longitudinal outcomes with cancer multigene panel testing in previously tested BRCA1/2 negative patients"
K. East
20191 citations
Semantic Scholar
Implementing Genomic Medicine in Primary Care: A Convergent Mixed Method Case Study
Emory W Heffernan, K. Hearld, Irene P. Moss, K. East +7 more
2026Journal of Evaluation In Clinical Practice0 citations Open access
Semantic Scholar
P362: Long-read genome sequencing to diagnose rare disease in a state-funded study
Whitley V. Kelley, S. Hiatt, Irene P. Moss, Gregory Cooper +13 more
2025Genetics in Medicine Open0 citations Open access
Semantic Scholar
FILTERED: A puzzle-based introduction to bioinformatics
Michèle R. Morris, Madelene Loftin, M. Parker, K. East +1 more
2025The American history teacher0 citations Open access
Semantic Scholar
P522: Personalized prescriptions: Potential clinical impact of pharmacogenetic screening
Jada Pugh, Madison Thomas, M. Cochran, K. East
2024Genetics in Medicine Open0 citations Open access
Semantic Scholar
P392: Genomic medicine and primary care: The Alabama Genomic Health Initiative*
Whitley V. Kelley, K. East, I. Asif, Lori Bateman +18 more
2023Genetics in Medicine Open0 citations Open access
Semantic Scholar
Ethical Issues in Clinical Genetics
T. May, K. East, Whitley V. Kelley, J. Craig
2022Guidance for Healthcare Ethics Committees0 citations
Semantic Scholar
eP370: SouthSeq: Genome sequencing for a diverse population of hospitalized infants
Donald R. Latner, K. Bowling, M. Thompson, C. Finnila +35 more
2022Genetics in Medicine0 citations Open access
Semantic Scholar
SouthSeq: genome sequencing as a frontline genetic test in the NICU
Michelle D. Amaral, M. Thompson, K. Bowling, C. Finnila +30 more
20210 citations
Semantic Scholar
Relief, empowerment, and uncertainty: Perspectives of clinical hereditary cancer population screening participants
V. Greve, K. Odom, S. Pudner, M. Cochran +4 more
20210 citations
Semantic Scholar
Genome sequencing as a first-line diagnostic test for hospitalized newborns
K. Bowling, M. L. Thompson, Candice R. Finnila, S. Hiatt +35 more
2021medRxiv0 citations Open access
Semantic Scholar
Identifying rare, medically-relevant genetic variation in a diverse population: opportunities and pitfalls
Kevin M. Bowling, M. L. Thompson, David E. Gray, James M. J. Lawlor +11 more
2020bioRxiv0 citations Open access
Semantic Scholar
Genomic diagnosis for children with intellectual disability and/or developmental delay
K. Bowling, M. Thompson, Michelle D. Amaral, C. Finnila +18 more
2017Genome Medicine0 citations Open access
Semantic Scholar

Frequent co-authors

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Whitley V. Kelley×34
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Whitley V. Kelley — researcher profile on SciRah
C. Finnila×18
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C. Finnila — researcher profile on SciRah
M. Cochran×17
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M. Cochran — researcher profile on SciRah
Gregory M. Cooper×16
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×15

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K. Bowling — researcher profile on SciRah

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S. Hiatt — researcher profile on SciRah

David E. Gray×14

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David E. Gray — researcher profile on SciRah

James M. J. Lawlor×14

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V. Greve — researcher profile on SciRah

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Irene P. Moss×13

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Irene P. Moss — researcher profile on SciRah

Michelle D. Amaral×12

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Michelle D. Amaral — researcher profile on SciRah