A citation-based method for searching scientific literature

France Légaré, Hubert Robitaille, Claire Gane, Jessica Hébert, Michel Labrecque, François Rousseau. PLoS One 2016
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


Genetic testing and cancer risk management recommendations by physicians for at-risk relatives.
Sharon E Plon, H Paul Cooper, Bethany Parks, Shweta U Dhar, P Adam Kelly, Armin D Weinberg, Stephanie Staggs, Tao Wang, Susan Hilsenbeck. Genet Med 2011
77
16

Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement.
Douglas K Owens, Karina W Davidson, Alex H Krist, Michael J Barry, Michael Cabana, Aaron B Caughey, Chyke A Doubeni, John W Epling, Martha Kubik, C Seth Landefeld,[...]. JAMA 2019
121
16

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
11

Personalised medicine in Canada: a survey of adoption and practice in oncology, cardiology and family medicine.
Katherine Bonter, Clarissa Desjardins, Nathan Currier, Jason Pun, Fredrick D Ashbury. BMJ Open 2011
59
11

Supporting Parental Decisions About Genomic Sequencing for Newborn Screening: The NC NEXUS Decision Aid.
Megan A Lewis, Ryan S Paquin, Myra I Roche, Robert D Furberg, Christine Rini, Jonathan S Berg, Cynthia M Powell, Donald B Bailey. Pediatrics 2016
26
11

Physicians' preparedness for integration of genomic and pharmacogenetic testing into practice within a major healthcare system.
Christina G Selkirk, Scott M Weissman, Andy Anderson, Peter J Hulick. Genet Test Mol Biomarkers 2013
80
11

Use of genetic tests among neurologists and psychiatrists: knowledge, attitudes, behaviors, and needs for training.
Melissa Salm, Kristopher Abbate, Paul Appelbaum, Ruth Ottman, Wendy Chung, Karen Marder, Cheng-Shiun Leu, Roy Alcalay, Jill Goldman, Alexander Malik Curtis,[...]. J Genet Couns 2014
55
11

A statewide survey of practitioners to assess knowledge and clinical practices regarding hereditary breast and ovarian cancer.
Tuya Pal, Deborah Cragun, Courtney Lewis, Andrea Doty, Maria Rodriguez, Cristi Radford, Zachary Thompson, Jongphil Kim, Susan T Vadaparampil. Genet Test Mol Biomarkers 2013
41
11

The current state of implementation science in genomic medicine: opportunities for improvement.
Megan C Roberts, Amy E Kennedy, David A Chambers, Muin J Khoury. Genet Med 2017
70
11

Attitudes and practices among internists concerning genetic testing.
Robert Klitzman, Wendy Chung, Karen Marder, Anita Shanmugham, Lisa J Chin, Meredith Stark, Cheng-Shiun Leu, Paul S Appelbaum. J Genet Couns 2013
105
11

US physicians' attitudes toward genetic testing for cancer susceptibility.
A N Freedman, L Wideroff, L Olson, W Davis, C Klabunde, K P Srinath, B B Reeve, R T Croyle, R Ballard-Barbash. Am J Med Genet A 2003
133
11

Physicians' opinions following pharmacogenetic testing for psychotropic medication.
Lucas M Walden, Eva J Brandl, Amtul Changasi, Jessica E Sturgess, Alexander Soibel, Janna Fe D Notario, Sheraz Cheema, Nicole Braganza, Victoria S Marshe, Natalie Freeman,[...]. Psychiatry Res 2015
32
11


Analyzing communication in genetic consultations--a systematic review.
Jean Paul, Sylvia Metcalfe, Lesley Stirling, Brenda Wilson, Jan Hodgson. Patient Educ Couns 2015
27
11

What does it mean to be genomically literate?: National Human Genome Research Institute Meeting Report.
Belen Hurle, Toby Citrin, Jean F Jenkins, Kimberly A Kaphingst, Neil Lamb, Jo Ellen Roseman, Vence L Bonham. Genet Med 2013
60
11

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.
Omri Gottesman, Helena Kuivaniemi, Gerard Tromp, W Andrew Faucett, Rongling Li, Teri A Manolio, Saskia C Sanderson, Joseph Kannry, Randi Zinberg, Melissa A Basford,[...]. Genet Med 2013
404
11

General performance on a numeracy scale among highly educated samples.
I M Lipkus, G Samsa, B K Rimer. Med Decis Making 2001
693
11

Barriers and Facilitators to Patient-Provider Communication When Discussing Breast Cancer Risk to Aid in the Development of Decision Support Tools.
Haeseung Yi, Tong Xiao, Parijatham S Thomas, Alejandra N Aguirre, Cindy Smalletz, Jill Dimond, Joseph Finkelstein, Katherine Infante, Meghna Trivedi, Raven David,[...]. AMIA Annu Symp Proc 2015
12
16

Usability Testing of a Web-Based Decision Aid for Breast Cancer Risk Assessment Among Multi-Ethnic Women.
Austin M Coe, William Ueng, Jennifer M Vargas, Raven David, Alejandro Vanegas, Katherine Infante, Meghna Trivedi, Haeseung Yi, Jill Dimond, Katherine D Crew,[...]. AMIA Annu Symp Proc 2017
10
20

Why Breast Cancer Risk by the Numbers Is Not Enough: Evaluation of a Decision Aid in Multi-Ethnic, Low-Numerate Women.
Rita Kukafka, Haeseung Yi, Tong Xiao, Parijatham Thomas, Alejandra Aguirre, Cindy Smalletz, Raven David, Katherine Crew. J Med Internet Res 2015
20
11

Uptake rates for breast cancer genetic testing: a systematic review.
Mary E Ropka, Jennifer Wenzel, Elayne K Phillips, Mir Siadaty, John T Philbrick. Cancer Epidemiol Biomarkers Prev 2006
114
11


Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers.
Karoline B Kuchenbaecker, John L Hopper, Daniel R Barnes, Kelly-Anne Phillips, Thea M Mooij, Marie-José Roos-Blom, Sarah Jervis, Flora E van Leeuwen, Roger L Milne, Nadine Andrieu,[...]. JAMA 2017
867
11


Primary care providers' experiences with and perceptions of personalized genomic medicine.
June C Carroll, Tutsirai Makuwaza, Donna P Manca, Nicolette Sopcak, Joanne A Permaul, Mary Ann O'Brien, Ruth Heisey, Elizabeth A Eisenhauer, Julie Easley, Monika K Krzyzanowska,[...]. Can Fam Physician 2016
51
11

Family Communication, Risk Perception and Cancer Knowledge of Young Adults from BRCA1/2 Families: a Systematic Review.
Alison L Young, Phyllis N Butow, Janine Vetsch, Veronica F Quinn, Andrea F Patenaude, Katherine M Tucker, Claire E Wakefield. J Genet Couns 2017
23
11

Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.
Mary B Daly, Robert Pilarski, Jennifer E Axilbund, Michael Berry, Saundra S Buys, Beth Crawford, Meagan Farmer, Susan Friedman, Judy E Garber, Seema Khan,[...]. J Natl Compr Canc Netw 2016
112
11

Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group.
Stacy W Gray, Yolanda Martins, Lindsay Z Feuerman, Barbara A Bernhardt, Barbara B Biesecker, Kurt D Christensen, Steven Joffe, Christine Rini, David Veenstra, Amy L McGuire. Genet Med 2014
46
11

Effect of a computer-based decision aid on knowledge, perceptions, and intentions about genetic testing for breast cancer susceptibility: a randomized controlled trial.
Michael J Green, Susan K Peterson, Maria Wagner Baker, Gregory R Harper, Lois C Friedman, Wendy S Rubinstein, David T Mauger. JAMA 2004
218
11


Genetic susceptibility testing from a stress and coping perspective.
Holly C Gooding, Kurt Organista, Jeffrey Burack, Barbara Bowles Biesecker. Soc Sci Med 2006
64
11

Delivery Of Cascade Screening For Hereditary Conditions: A Scoping Review Of The Literature.
Megan C Roberts, W David Dotson, Christopher S DeVore, Erica M Bednar, Deborah J Bowen, Theodore G Ganiats, Ridgely Fisk Green, Georgia M Hurst, Alisdair R Philp, Charité N Ricker,[...]. Health Aff (Millwood) 2018
57
11

Expanded carrier screening: what determines intended participation and can this be influenced by message framing and narrative information?
Jan S Voorwinden, Anne H Buitenhuis, Erwin Birnie, Anneke M Lucassen, Marian A Verkerk, Irene M van Langen, Mirjam Plantinga, Adelita V Ranchor. Eur J Hum Genet 2017
11
18

Factors determining dissemination of results and uptake of genetic testing in families with known BRCA1/2 mutations.
Esme Finlay, Jill E Stopfer, Eric Burlingame, Katherine Goldfeder Evans, Katherine L Nathanson, Barbara L Weber, Katrina Armstrong, Timothy R Rebbeck, Susan M Domchek. Genet Test 2008
102
11

Considering medical risk information and communicating values: A mixed-method study of women's choice in prenatal testing.
An Chen, Henni Tenhunen, Paulus Torkki, Seppo Heinonen, Paul Lillrank, Vedran Stefanovic. PLoS One 2017
12
16

Points to consider for laboratories reporting results from diagnostic genomic sequencing.
D F Vears, K Sénécal, A J Clarke, L Jackson, A M Laberge, L Lovrecic, A Piton, K L I Van Gassen, H G Yntema, B M Knoppers,[...]. Eur J Hum Genet 2018
31
5

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
5

Decision aids for people facing health treatment or screening decisions.
Dawn Stacey, France Légaré, Nananda F Col, Carol L Bennett, Michael J Barry, Karen B Eden, Margaret Holmes-Rovner, Hilary Llewellyn-Thomas, Anne Lyddiatt, Richard Thomson,[...]. Cochrane Database Syst Rev 2014
5

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur J Hum Genet 2013
206
5


Three approaches to qualitative content analysis.
Hsiu-Fang Hsieh, Sarah E Shannon. Qual Health Res 2005
5

A secondary benefit: the reproductive impact of carrier results from newborn screening for cystic fibrosis.
Yvonne Bombard, Fiona A Miller, Carolyn J Barg, Sarah J Patton, June C Carroll, Pranesh Chakraborty, Beth K Potter, Karen Tam, Louise Taylor, Elizabeth Kerr,[...]. Genet Med 2017
6
16

Decision aids for people facing health treatment or screening decisions.
Dawn Stacey, France Légaré, Krystina Lewis, Michael J Barry, Carol L Bennett, Karen B Eden, Margaret Holmes-Rovner, Hilary Llewellyn-Thomas, Anne Lyddiatt, Richard Thomson,[...]. Cochrane Database Syst Rev 2017
5


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
842
5


Development and usability testing of a web-based decision support for users and health professionals in psychiatric services.
Katarina Grim, David Rosenberg, Petra Svedberg, Ulla-Karin Schön. Psychiatr Rehabil J 2017
8
12

A decision aid for women considering hormone therapy after menopause: decision support framework and evaluation.
A M O'Connor, P Tugwell, G A Wells, T Elmslie, E Jolly, G Hollingworth, R McPherson, H Bunn, I Graham, E Drake. Patient Educ Couns 1998
414
5

Development and testing of a decision aid for breast cancer prevention for women with a BRCA1 or BRCA2 mutation.
K A Metcalfe, A Poll, A O'Connor, S Gershman, S Armel, A Finch, R Demsky, B Rosen, S A Narod. Clin Genet 2007
51
5



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.