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

Martha F Wright, Katie L Lewis, Tyler C Fisher, Gillian W Hooker, Toby E Emanuel, Leslie G Biesecker, Barbara B Biesecker. Genet Med 2014
Times Cited: 43

List of shared articles

Times cited

Views on genomic research result delivery methods and informed consent: a review.
Danya F Vears, Joel T Minion, Stephanie J Roberts, James Cummings, Mavis Machirori, Madeleine J Murtagh. Per Med 2021

Exploring the motivations of research participants who chose not to learn medically actionable secondary genetic findings about themselves.
Will Schupmann, Skye A Miner, Haley K Sullivan, Jamie R Glover, Janet E Hall, Shepherd H Schurman, Benjamin E Berkman. Genet Med 2021

Factors influencing NCGENES research participants' requests for non-medically actionable secondary findings.
Myra I Roche, Ida Griesemer, Cynthia M Khan, Elizabeth Moore, Feng-Chang Lin, Julianne M O'Daniel, Ann Katherine M Foreman, Kristy Lee, Bradford C Powell, Jonathan S Berg,[...]. Genet Med 2019

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

Cancer patients' intentions towards receiving unsolicited genetic information obtained using next-generation sequencing.
Rhodé M Bijlsma, Hester Wessels, Roel H P Wouters, Anne M May, Margreet G E M Ausems, Emile E Voest, Annelien L Bredenoord. Fam Cancer 2018

"I would like to discuss it further with an expert": a focus group study of Finnish adults' perspectives on genetic secondary findings.
M Vornanen, K Aktan-Collan, N Hallowell, H Konttinen, H Kääriäinen, A Haukkala. J Community Genet 2018

Managing unsolicited findings in genomics: A qualitative interview study with cancer patients.
R M Bijlsma, R H P Wouters, H Wessels, A M May, M G E M Ausems, E E Voest, A L Bredenoord. Psychooncology 2018

A comparison of Australian and French families affected by sarcoma: perceptions of genetics and incidental findings.
Victoria Rasmussen, Laura E Forrest, Muriel Rogasik, Magali Girodet, Pierre Meeus, Marie-Pierre Sunyach, Jean-Yves Blay, Olivia Bally, Mehdi Brahmi, Mandy L Ballinger,[...]. Per Med 2018

What People Want to Know About Their Genes: A Critical Review of the Literature on Large-Scale Genome Sequencing Studies.
Courtney L Scherr, Sharon Aufox, Amy A Ross, Sanjana Ramesh, Catherine A Wicklund, Maureen Smith. Healthcare (Basel) 2018

Acceptability of Electronic Visits for Return of Research Results in the Mayo Clinic Biobank.
Janet E Olson, Euijung Ryu, Kelly J Lyke, Suzette J Bielinski, Erin M Winkler, Matthew A Hathcock, Joshua T Bublitz, Paul Y Takahashi, James R Cerhan. Mayo Clin Proc Innov Qual Outcomes 2018

Choices for return of primary and secondary genomic research results of 790 members of families with Mendelian disease.
Katie Fiallos, Carolyn Applegate, Debra Jh Mathews, Juli Bollinger, Amanda L Bergner, Cynthia A James. Eur J Hum Genet 2017

Personal utility in genomic testing: a systematic literature review.
Jennefer N Kohler, Erin Turbitt, Barbara B Biesecker. Eur J Hum Genet 2017

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Robert C Green, Katrina A B Goddard, Gail P Jarvik, Laura M Amendola, Paul S Appelbaum, Jonathan S Berg, Barbara A Bernhardt, Leslie G Biesecker, Sawona Biswas, Carrie L Blout,[...]. Am J Hum Genet 2016

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

Characterizing Participants in the ClinSeq Genome Sequencing Cohort as Early Adopters of a New Health Technology.
Katie L Lewis, Paul K J Han, Gillian W Hooker, William M P Klein, Leslie G Biesecker, Barbara B Biesecker. PLoS One 2015