A citation-based method for searching scientific literature

Yvonne Bombard, Marc Clausen, Salma Shickh, Chloe Mighton, Selina Casalino, Theresa H M Kim, Sarah M Muir, Lindsay Carlsson, Nancy Baxter, Adena Scheer, Christine Elser, Andrea Eisen, Seema Panchal, Tracy Graham, Melyssa Aronson, Carolyn Piccinin, Talia Mancuso, Kara Semotiuk, Michael Evans, June C Carroll, Kenneth Offit, Mark Robson, Jada G Hamilton, Emily Glogowski, Kasmintan Schrader, Raymond H Kim, Jordan Lerner-Ellis, Kevin E Thorpe, Andreas Laupacis. Genet Med 2020
Times Cited: 11







List of co-cited articles
37 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
902
54

The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results.
Yvonne Bombard, Marc Clausen, Chloe Mighton, Lindsay Carlsson, Selina Casalino, Emily Glogowski, Kasmintan Schrader, Michael Evans, Adena Scheer, Nancy Baxter,[...]. Eur J Hum Genet 2018
22
54

Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial.
Salma Shickh, Marc Clausen, Chloe Mighton, Selina Casalino, Esha Joshi, Emily Glogowski, Kasmintan A Schrader, Adena Scheer, Christine Elser, Seema Panchal,[...]. BMJ Open 2018
14
27


The past, present and future of service delivery in genetic counseling: Keeping up in the era of precision medicine.
Katie Stoll, Shobana Kubendran, Stephanie A Cohen. Am J Med Genet C Semin Med Genet 2018
76
27

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
73
27

How digital tools can advance quality and equity in genomic medicine.
Yvonne Bombard, Robin Z Hayeems. Nat Rev Genet 2020
10
30

The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.
Jason L Vassy, Kurt D Christensen, Erica F Schonman, Carrie L Blout, Jill O Robinson, Joel B Krier, Pamela M Diamond, Matthew Lebo, Kalotina Machini, Danielle R Azzariti,[...]. Ann Intern Med 2017
107
27


Clinical application of whole-exome sequencing across clinical indications.
Kyle Retterer, Jane Juusola, Megan T Cho, Patrik Vitazka, Francisca Millan, Federica Gibellini, Annette Vertino-Bell, Nizar Smaoui, Julie Neidich, Kristin G Monaghan,[...]. Genet Med 2016
498
27

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
8
25

Saturation in qualitative research: exploring its conceptualization and operationalization.
Benjamin Saunders, Julius Sim, Tom Kingstone, Shula Baker, Jackie Waterfield, Bernadette Bartlam, Heather Burroughs, Clare Jinks. Qual Quant 2018
18

Outcomes of interest in evidence-based evaluations of genetic tests.
Jeffrey R Botkin, Steven M Teutsch, Celia I Kaye, Maxine Hayes, James E Haddow, Linda A Bradley, Kathleen Szegda, W David Dotson. Genet Med 2010
64
18

Personal utility in genomic testing: a systematic literature review.
Jennefer N Kohler, Erin Turbitt, Barbara B Biesecker. Eur J Hum Genet 2017
64
18

Genetic Misdiagnoses and the Potential for Health Disparities.
Arjun K Manrai, Birgit H Funke, Heidi L Rehm, Morten S Olesen, Bradley A Maron, Peter Szolovits, David M Margulies, Joseph Loscalzo, Isaac S Kohane. N Engl J Med 2016
344
18

Current conditions in medical genetics practice.
Deborah R Maiese, Alisha Keehn, Megan Lyon, David Flannery, Michael Watson. Genet Med 2019
53
18

DECIDE: a Decision Support Tool to Facilitate Parents' Choices Regarding Genome-Wide Sequencing.
Patricia Birch, S Adam, N Bansback, R R Coe, J Hicklin, A Lehman, K C Li, J M Friedman. J Genet Couns 2016
24
18

Societal preferences for the return of incidental findings from clinical genomic sequencing: a discrete-choice experiment.
Dean A Regier, Stuart J Peacock, Reka Pataky, Kimberly van der Hoek, Gail P Jarvik, Jeffrey Hoch, David Veenstra. CMAJ 2015
54
18

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
18

Projecting the Supply and Demand for Certified Genetic Counselors: a Workforce Study.
Jennifer M Hoskovec, R L Bennett, M E Carey, J E DaVanzo, M Dougherty, S E Hahn, B S LeRoy, S O'Neal, J G Richardson, C A Wicklund. J Genet Couns 2018
131
18

A systematic development process for patient decision aids.
Angela Coulter, Diana Stilwell, Jennifer Kryworuchko, Patricia Dolan Mullen, Chirk Jenn Ng, Trudy van der Weijden. BMC Med Inform Decis Mak 2013
243
18


The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists.
Kym Boycott, Taila Hartley, Shelin Adam, Francois Bernier, Karen Chong, Bridget A Fernandez, Jan M Friedman, Michael T Geraghty, Stacey Hume, Bartha M Knoppers,[...]. J Med Genet 2015
126
18

Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing.
Tara Schmidlen, Amy C Sturm, Shelly Hovick, Laura Scheinfeldt, J Scott Roberts, Lindsey Morr, Joseph McElroy, Amanda E Toland, Michael Christman, Julianne M O'Daniel,[...]. J Genet Couns 2018
16
18

Assessing an Interactive Online Tool to Support Parents' Genomic Testing Decisions.
Shelin Adam, Patricia H Birch, Rachel R Coe, Nick Bansback, Adrian L Jones, Mary B Connolly, Michelle K Demos, Eric B Toyota, Matthew J Farrer, Jan M Friedman. J Genet Couns 2018
10
20

Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
626
18


Diagnostic and cost utility of whole exome sequencing in peripheral neuropathy.
Maie Walsh, Katrina M Bell, Belinda Chong, Emma Creed, Gemma R Brett, Kate Pope, Natalie P Thorne, Simon Sadedin, Peter Georgeson, Dean G Phelan,[...]. Ann Clin Transl Neurol 2017
23
18

Diagnostic Utility of Exome Sequencing for Kidney Disease.
Emily E Groopman, Maddalena Marasa, Sophia Cameron-Christie, Slavé Petrovski, Vimla S Aggarwal, Hila Milo-Rasouly, Yifu Li, Junying Zhang, Jordan Nestor, Priya Krithivasan,[...]. N Engl J Med 2019
199
18

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
50

Quality of life drives patients' preferences for secondary findings from genomic sequencing.
Chloe Mighton, Lindsay Carlsson, Marc Clausen, Selina Casalino, Salma Shickh, Laura McCuaig, Esha Joshi, Seema Panchal, Kara Semotiuk, Karen Ott,[...]. Eur J Hum Genet 2020
9
22

Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings.
Emma Reble, Mariana Gutierrez Salazar, Kathleen-Rose Zakoor, Sam Khalouei, Marc Clausen, Rita Kodida, Salma Shickh, Chloe Mighton, Iris Cohn, Kasmintan A Schrader,[...]. Hum Genet 2021
3
66

Informing Integration of Genomic Medicine Into Primary Care: An Assessment of Current Practice, Attitudes, and Desired Resources.
June C Carroll, Judith Allanson, Shawna Morrison, Fiona A Miller, Brenda J Wilson, Joanne A Permaul, Deanna Telner. Front Genet 2019
22
18

Re-analysis of whole-exome sequencing data uncovers novel diagnostic variants and improves molecular diagnostic yields for sudden death and idiopathic diseases.
Elias L Salfati, Emily G Spencer, Sarah E Topol, Evan D Muse, Manuel Rueda, Jonathan R Lucas, Glenn N Wagner, Steven Campman, Eric J Topol, Ali Torkamani. Genome Med 2019
20
18

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.
Anath C Lionel, Gregory Costain, Nasim Monfared, Susan Walker, Miriam S Reuter, S Mohsen Hosseini, Bhooma Thiruvahindrapuram, Daniele Merico, Rebekah Jobling, Thomas Nalpathamkalam,[...]. Genet Med 2018
218
18

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
18

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG).
David T Miller, Kristy Lee, Adam S Gordon, Laura M Amendola, Kathy Adelman, Sherri J Bale, Wendy K Chung, Michael H Gollob, Steven M Harrison, Gail E Herman,[...]. Genet Med 2021
27
18


Improving the efficiency and relevance of evidence-based recommendations in the era of whole-genome sequencing: an EGAPP methods update.
David L Veenstra, Margaret Piper, James E Haddow, Stephen G Pauker, Roger Klein, Carolyn Sue Richards, Sean R Tunis, Benjamin Djulbegovic, Michael Marrone, Jennifer S Lin,[...]. Genet Med 2013
39
9


Making genomic medicine evidence-based and patient-centered: a structured review and landscape analysis of comparative effectiveness research.
Kathryn A Phillips, Patricia A Deverka, Harold C Sox, Muin J Khoury, Lewis G Sandy, Geoffrey S Ginsburg, Sean R Tunis, Lori A Orlando, Michael P Douglas. Genet Med 2017
38
9

Psychometric assessment of the Quality of Life Index.
C E Ferrans, M J Powers. Res Nurs Health 1992
445
9


Interest and Attitudes of Patients With Advanced Cancer With Regard to Secondary Germline Findings From Tumor Genomic Profiling.
Jada G Hamilton, Elyse Shuk, Margaux C Genoff, Vivian M Rodríguez, Jennifer L Hay, Kenneth Offit, Mark E Robson. J Oncol Pract 2017
20
9

Patients' perceived utility of whole-genome sequencing for their healthcare: findings from the MedSeq project.
Philip J Lupo, Jill O Robinson, Pamela M Diamond, Leila Jamal, Heather E Danysh, Jennifer Blumenthal-Barby, Lisa Soleymani Lehmann, Jason L Vassy, Kurt D Christensen, Robert C Green,[...]. Per Med 2016
25
9

How is genetic testing evaluated? A systematic review of the literature.
Erica Pitini, Corrado De Vito, Carolina Marzuillo, Elvira D'Andrea, Annalisa Rosso, Antonio Federici, Emilio Di Maria, Paolo Villari. Eur J Hum Genet 2018
38
9

Health Technology Assessment for Molecular Diagnostics: Practices, Challenges, and Recommendations from the Medical Devices and Diagnostics Special Interest Group.
Susan Garfield, Julie Polisena, Daryl S Spinner, Anne Postulka, Christine Y Lu, Simrandeep K Tiwana, Eric Faulkner, Nick Poulios, Vladimir Zah, Michael Longacre. Value Health 2016
19
9

Translating genomics in cancer care.
Yvonne Bombard, Peter B Bach, Kenneth Offit. J Natl Compr Canc Netw 2013
49
9

Preferences for results delivery from exome sequencing/genome sequencing.
Martha F Wright, Katie L Lewis, Tyler C Fisher, Gillian W Hooker, Toby E Emanuel, Leslie G Biesecker, Barbara B Biesecker. Genet Med 2014
46
9



Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.