A citation-based method for searching scientific literature

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, Erynn S Gordon, Barbara A Bernhardt, Kelly E Ormond, Kevin Sweet. J Genet Couns 2018
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


Coming full circle: a reciprocal-engagement model of genetic counseling practice.
Patricia McCarthy Veach, Dianne M Bartels, Bonnie S Leroy. J Genet Couns 2007
121
40

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
720
30


Genetic counseling globally: Where are we now?
Kelly E Ormond, Mercy Ygoña Laurino, Kristine Barlow-Stewart, Tina-Marié Wessels, Shelley Macaulay, Jehannine Austin, Anna Middleton. Am J Med Genet C Semin Med Genet 2018
37
20

Defining Our Clinical Practice: The Identification of Genetic Counseling Outcomes Utilizing the Reciprocal Engagement Model.
Krista Redlinger-Grosse, Patricia McCarthy Veach, Stephanie Cohen, Bonnie S LeRoy, Ian M MacFarlane, Heather Zierhut. J Genet Couns 2016
21
20

Direct-to-Consumer Genetic Testing: User Motivations, Decision Making, and Perceived Utility of Results.
J Scott Roberts, Michele C Gornick, Deanna Alexis Carere, Wendy R Uhlmann, Mack T Ruffin, Robert C Green. Public Health Genomics 2017
49
20

Characteristics of users of online personalized genomic risk assessments: implications for physician-patient interactions.
Colleen M McBride, Sharon Hensley Alford, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody. Genet Med 2009
85
20

Personalized genomic results: analysis of informational needs.
Tara J Schmidlen, Lisa Wawak, Rachel Kasper, J Felipe García-España, Michael F Christman, Erynn S Gordon. J Genet Couns 2014
24
20

"I want to know what's in Pandora's Box": comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing.
Anne Townsend, Shelin Adam, Patricia H Birch, Zoe Lohn, Francois Rousseau, Jan M Friedman. Am J Med Genet A 2012
116
20

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
20

Randomized Noninferiority Trial of Telephone Delivery of BRCA1/2 Genetic Counseling Compared With In-Person Counseling: 1-Year Follow-Up.
Anita Y Kinney, Laurie E Steffen, Barbara H Brumbach, Wendy Kohlmann, Ruofei Du, Ji-Hyun Lee, Amanda Gammon, Karin Butler, Saundra S Buys, Antoinette M Stroup,[...]. J Clin Oncol 2016
55
20


A Rapid Systematic Review of Outcomes Studies in Genetic Counseling.
Lisa Madlensky, Angela M Trepanier, Deborah Cragun, Barbara Lerner, Kristen M Shannon, Heather Zierhut. J Genet Couns 2017
34
20


A Systematic Review of Randomized Controlled Trials to Assess Outcomes of Genetic Counseling.
Barbara A Athens, Samantha L Caldwell, Kendall L Umstead, Philip D Connors, Ethan Brenna, Barbara B Biesecker. J Genet Couns 2017
32
20

A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.
Robert Resta, Barbara Bowles Biesecker, Robin L Bennett, Sandra Blum, Susan Estabrooks Hahn, Michelle N Strecker, Janet L Williams. J Genet Couns 2006
334
20

Effects of informed consent for individual genome sequencing on relevant knowledge.
K A Kaphingst, F M Facio, M-R Cheng, S Brooks, H Eidem, A Linn, B B Biesecker, L G Biesecker. Clin Genet 2012
74
20

Focusing on patient needs and preferences may improve genetic counseling for colorectal cancer.
Simone Salemink, Nicky Dekker, Carolien M Kets, Erica van der Looij, Wendy A G van Zelst-Stams, Nicoline Hoogerbrugge. J Genet Couns 2013
10
20

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
107
20

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
16
20

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
20

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
19
20

Genetic Counseling in Portugal: Education, Practice and a Developing Profession.
Milena Paneque, Álvaro Mendes, Jorge Saraiva, Jorge Sequeiros. J Genet Couns 2015
7
14





Commentary on Genetic Counseling-A Profession in Search of Itself.
Patricia McCarthy Veach, Dianne M Bartels, Bonnie S LeRoy. J Genet Couns 2002
14
10


Genetic counselor perceptions of genetic counseling session goals: a validation study of the reciprocal-engagement model.
Julianne E Hartmann, Patricia McCarthy Veach, Ian M MacFarlane, Bonnie S LeRoy. J Genet Couns 2015
25
10



[Proposal of a Portuguese Tool for Quality Assessment of Genetic Counselling: a New Tool for Healthcare Professionals].
Milena Paneque, Catarina Costa, Carolina Lemos, Miguel Alves-Ferreira, Jorge Sequeiros, Marina Serra Lemos. Acta Med Port 2018
2
50

Design and implementation of a randomized controlled trial of genomic counseling for patients with chronic disease.
Kevin Sweet, Erynn S Gordon, Amy C Sturm, Tara J Schmidlen, Kandamurugu Manickam, Amanda Ewart Toland, Margaret A Keller, Catharine B Stack, J Felipe García-España, Mark Bellafante,[...]. J Pers Med 2014
16
10

My46: a Web-based tool for self-guided management of genomic test results in research and clinical settings.
Holly K Tabor, Seema M Jamal, Joon-Ho Yu, Julia M Crouch, Aditi G Shankar, Karin M Dent, Nick Anderson, Damon A Miller, Brett T Futral, Michael J Bamshad. Genet Med 2017
17
10

"It's not like judgment day": public understanding of and reactions to personalized genomic risk information.
Erynn S Gordon, Georgia Griffin, Lisa Wawak, Hauchie Pang, Sarah E Gollust, Barbara A Bernhardt. J Genet Couns 2012
41
10

Outcomes of a Randomized Controlled Trial of Genomic Counseling for Patients Receiving Personalized and Actionable Complex Disease Reports.
Kevin Sweet, Amy C Sturm, Tara Schmidlen, Joseph McElroy, Laura Scheinfeldt, Kandamurugu Manickam, Erynn S Gordon, Shelly Hovick, J Scott Roberts, Amanda Ewart Toland,[...]. J Genet Couns 2017
11
10

Patient Perceptions of Telephone vs. In-Person BRCA1/BRCA2 Genetic Counseling.
Beth N Peshkin, Scott Kelly, Rachel H Nusbaum, Morgan Similuk, Tiffani A DeMarco, Gillian W Hooker, Heiddis B Valdimarsdottir, Andrea D Forman, Jessica Rispoli Joines, Claire Davis,[...]. J Genet Couns 2016
24
10

Clinically relevant lessons from Family HealthLink: a cancer and coronary heart disease familial risk assessment tool.
Kevin Sweet, Amy C Sturm, Amy Rettig, Joseph McElroy, Doreen Agnese. Genet Med 2015
5
20

Analysis of Advantages, Limitations, and Barriers of Genetic Counseling Service Delivery Models.
Stephanie A Cohen, Rachelle C Huziak, Shanna Gustafson, Robin E Grubs. J Genet Couns 2016
24
10

mHealth plus community health worker interventions: the future research agenda.
Shiva Raj Mishra, Dinesh Neupane, Tom G Briffa, Per Kallestrup. Lancet Diabetes Endocrinol 2016
6
16

Models of service delivery for cancer genetic risk assessment and counseling.
Angela M Trepanier, Dawn C Allain. J Genet Couns 2014
41
10

Preferences for genetic and behavioral health information: the impact of risk factors and disease attributions.
Suzanne C O'Neill, Colleen M McBride, Sharon Hensley Alford, Kimberly A Kaphingst. Ann Behav Med 2010
26
10

Interactive Health Communication Applications for people with chronic disease.
E Murray, J Burns, Tai S See, R Lai, I Nazareth. Cochrane Database Syst Rev 2005
391
10

Identification of genetic counseling service delivery models in practice: a report from the NSGC Service Delivery Model Task Force.
Stephanie A Cohen, Monica L Marvin, Bronson D Riley, Hetal S Vig, Julie A Rousseau, Shanna L Gustafson. J Genet Couns 2013
71
10

Participant use and communication of findings from exome sequencing: a mixed-methods study.
Katie L Lewis, Gillian W Hooker, Philip D Connors, Travis C Hyams, Martha F Wright, Samantha Caldwell, Leslie G Biesecker, Barbara B Biesecker. Genet Med 2016
39
10


Delivery of Internet-based cancer genetic counselling services to patients' homes: a feasibility study.
Neal J Meropol, Mary B Daly, Hetal S Vig, Frank J Manion, Sharon L Manne, Carla Mazar, Camara Murphy, Nicholas Solarino, Vadim Zubarev. J Telemed Telecare 2011
31
10

Effect of Lifestyle-Focused Text Messaging on Risk Factor Modification in Patients With Coronary Heart Disease: A Randomized Clinical Trial.
Clara K Chow, Julie Redfern, Graham S Hillis, Jay Thakkar, Karla Santo, Maree L Hackett, Stephen Jan, Nicholas Graves, Laura de Keizer, Tony Barry,[...]. JAMA 2015
290
10

Coriell Personalized Medicine Collaborative®: a prospective study of the utility of personalized medicine.
Margaret A Keller, Erynn S Gordon, Catharine B Stack, Neda Gharani, Courtney J Sill, Tara J Schmidlen, Mintzer Joseph, John Pallies, Norman P Gerry, Michael F Christman. Per Med 2010
41
10


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.