A citation-based method for searching scientific literature

Layla Shahmirzadi, Elizabeth C Chao, Erika Palmaer, Melissa C Parra, Sha Tang, Kelly D Farwell Gonzalez. Genet Med 2014
Times Cited: 74



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




List of shared articles



Times cited

Exome sequencing in clinical settings: preferences and experiences of parents of children with rare diseases (SEQUAPRE study).
Aline Chassagne, Aurore Pélissier, Françoise Houdayer, Elodie Cretin, Elodie Gautier, Dominique Salvi, Sarah Kidri, Aurélie Godard, Christel Thauvin-Robinet, Alice Masurel,[...]. Eur J Hum Genet 2019
5

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
5


Participant choices for return of genomic results in the eMERGE Network.
Christin Hoell, Julia Wynn, Luke V Rasmussen, Keith Marsolo, Sharon A Aufox, Wendy K Chung, John J Connolly, Robert R Freimuth, David Kochan, Hakon Hakonarson,[...]. Genet Med 2020
4

A new approach to assessing affect and the emotional implications of personal genomic testing for common disease risk.
Suzanne C O'Neill, Kenneth P Tercyak, Chanza Baytop, Sharon Hensley Alford, Colleen M McBride. Public Health Genomics 2015
9

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
9

Acceptability of, and Information Needs Regarding, Next-Generation Sequencing in People Tested for Hereditary Cancer: A Qualitative Study.
Bettina Meiser, Ben Storey, Veronica Quinn, Belinda Rahman, Lesley Andrews. J Genet Couns 2016
10

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
0

Much ado about nothing: A qualitative study of the experiences of an average-risk population receiving results of exome sequencing.
Shannon Rego, Orit Dagan-Rosenfeld, Stephanie A Bivona, Michael P Snyder, Kelly E Ormond. J Genet Couns 2019
6

Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial.
Salma Shickh, Marc Clausen, Chloe Mighton, Mariana Gutierrez Salazar, Kathleen-Rose Zakoor, Rita Kodida, Emma Reble, Christine Elser, Andrea Eisen, Seema Panchal,[...]. BMJ Open 2019
4

Parents, their children, whole exome sequencing and unsolicited findings: growing towards the child's future autonomy.
Aad Tibben, Wybo Dondorp, Candice Cornelis, Nine Knoers, Eva Brilstra, Marieke van Summeren, Ineke Bolt. Eur J Hum Genet 2021
3


Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
Michael P Mackley, Benjamin Fletcher, Michael Parker, Hugh Watkins, Elizabeth Ormondroyd. Genet Med 2017
71

The who, what, and why of research participants' intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study.
Christine Rini, Cynthia M Khan, Elizabeth Moore, Myra I Roche, James P Evans, Jonathan S Berg, Bradford C Powell, Giselle Corbie-Smith, Ann Katherine M Foreman, Ida Griesemer,[...]. Genet Med 2018
13

Great expectations: patient perspectives and anticipated utility of non-diagnostic genomic-sequencing results.
Robyn Hylind, Maureen Smith, Laura Rasmussen-Torvik, Sharon Aufox. J Community Genet 2018
10

Research participant interest in primary, secondary, and incidental genomic findings.
Jennifer T Loud, Renee C Bremer, Phuong L Mai, June A Peters, Neelam Giri, Douglas R Stewart, Mark H Greene, Blanche P Alter, Sharon A Savage. Genet Med 2016
14

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
20

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
9

Research participants in NGS studies want to know about incidental findings.
Anne Marie Jelsig, Niels Qvist, Klaus Brusgaard, Lilian Bomme Ousager. Eur J Hum Genet 2015
21