A citation-based method for searching scientific literature

Flavia M Facio, Haley Eidem, Tyler Fisher, Stephanie Brooks, Amy Linn, Kimberly A Kaphingst, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2013
Times Cited: 122

Katie L Lewis, Paul K J Han, Gillian W Hooker, William M P Klein, Leslie G Biesecker, Barbara B Biesecker. PLoS One 2015
Times Cited: 33

List of shared articles

Times cited

A survey of aortic disease biorepository participants' preferences for return of research genetic results.
Jamie Love-Nichols, Wendy R Uhlmann, Patricia Arscott, Cristen Willer, Whitney Hornsby, J Scott Roberts. J Genet Couns 2021

Dyadic concordance and associations of beliefs with intentions to learn carrier results from genomic sequencing.
Chloe O Huelsnitz, Erin Turbitt, Jennifer M Taber, Katie L Lewis, Leslie G Biesecker, Barbara B Biesecker, William M P Klein. J Behav Med 2021

Using the diffusion of innovations model to guide participant engagement in the genomics era.
Katie L Lewis, Flavia M Facio, Courtney D Berrios. J Genet Couns 2019

Development of patient "profiles" to tailor counseling for incidental genomic sequencing results.
Chloe Mighton, Lindsay Carlsson, Marc Clausen, Selina Casalino, Salma Shickh, Laura McCuaig, Esha Joshi, Seema Panchal, Tracy Graham, Melyssa Aronson,[...]. Eur J Hum Genet 2019

Mind the gap: resources required to receive, process and interpret research-returned whole genome data.
Dana C Crawford, Jessica N Cooke Bailey, Farren B S Briggs. Hum Genet 2019

Web Platform vs In-Person Genetic Counselor for Return of Carrier Results From Exome Sequencing: A Randomized Clinical Trial.
Barbara B Biesecker, Katie L Lewis, Kendall L Umstead, Jennifer J Johnston, Erin Turbitt, Kristen P Fishler, John H Patton, Ilana M Miller, Alexis R Heidlebaugh, Leslie G Biesecker. JAMA Intern Med 2018

Disclosure of cardiac variants of uncertain significance results in an exome cohort.
T A Lawal, K L Lewis, J J Johnston, A R Heidlebaugh, D Ng, F G Gaston-Johansson, W M P Klein, B B Biesecker, L G Biesecker. Clin Genet 2018

A randomized controlled study of a consent intervention for participating in an NIH genome sequencing study.
Erin Turbitt, Paola P Chrysostomou, Holly L Peay, Alexis R Heidlebaugh, Lawrence M Nelson, Barbara B Biesecker. Eur J Hum Genet 2018

Intentions to share exome sequencing results with family members: exploring spousal beliefs and attitudes.
Erin Turbitt, Megan C Roberts, Rebecca A Ferrer, Jennifer M Taber, Katie L Lewis, Leslie G Biesecker, Barbara B Biesecker, William Mp Klein. Eur J Hum Genet 2018

Ability of Patients to Distinguish Among Cardiac Genomic Variant Subclassifications.
Lydia D Hellwig, Barbara B Biesecker, Katie L Lewis, Leslie G Biesecker, Cynthia A James, William M P Klein. Circ Genom Precis Med 2018

Engagement and communication among participants in the ClinSeq Genomic Sequencing Study.
Gillian W Hooker, Kendall L Umstead, Katie L Lewis, Laura K Koehly, Leslie G Biesecker, Barbara B Biesecker. Genet Med 2017

Defining personal utility in genomics: A Delphi study.
J N Kohler, E Turbitt, K L Lewis, B S Wilfond, L Jamal, H L Peay, L G Biesecker, B B Biesecker. Clin Genet 2017

Known unknowns: buildingĀ an ethics of uncertainty into genomic medicine.
Ainsley J Newson, Samantha J Leonard, Alison Hall, Clara L Gaff. BMC Med Genomics 2016

Information Avoidance Tendencies, Threat Management Resources, and Interest in Genetic Sequencing Feedback.
Jennifer M Taber, William M P Klein, Rebecca A Ferrer, Katie L Lewis, Peter R Harris, James A Shepperd, Leslie G Biesecker. Ann Behav Med 2015

Perceived ambiguity as a barrier to intentions to learn genome sequencing results.
Jennifer M Taber, William M P Klein, Rebecca A Ferrer, Paul K J Han, Katie L Lewis, Leslie G Biesecker, Barbara B Biesecker. J Behav Med 2015