A citation-based method for searching scientific literature

Kimberly A Kaphingst, Jennifer Ivanovich, Sarah Lyons, Barbara Biesecker, Rebecca Dresser, Ashley Elrick, Cindy Matsen, Melody Goodman. Transl Behav Med 2018
Times Cited: 11







List of co-cited articles
25 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
550
27

Patient communication of cancer genetic test results in a diverse population.
Charité N Ricker, Rachel B Koff, Chenxu Qu, Julie Culver, Duveen Sturgeon, Kerry E Kingham, Katrina Lowstuter, Nicolette M Chun, Courtney Rowe-Teeter, Alexandra Lebensohn,[...]. Transl Behav Med 2018
6
33

Genetic test reporting of CDKN2A provides informational and motivational benefits for managing melanoma risk.
Lisa G Aspinwall, Tammy K Stump, Jennifer M Taber, Danielle M Drummond, Wendy Kohlmann, Marjan Champine, Sancy A Leachman. Transl Behav Med 2018
8
25



Measuring numeracy without a math test: development of the Subjective Numeracy Scale.
Angela Fagerlin, Brian J Zikmund-Fisher, Peter A Ubel, Aleksandra Jankovic, Holly A Derry, Dylan M Smith. Med Decis Making 2007
343
18

Behavioral health outcomes associated with religious faith and media exposure about human genetics.
Roxanne Parrott, Kami Silk, Janice Raup Krieger, Tina Harris, Celeste Condit. Health Commun 2004
18
18

Shared decision making: a model for clinical practice.
Glyn Elwyn, Dominick Frosch, Richard Thomson, Natalie Joseph-Williams, Amy Lloyd, Paul Kinnersley, Emma Cording, Dave Tomson, Carole Dodd, Stephen Rollnick,[...]. J Gen Intern Med 2012
979
18

How, who, and when: preferences for delivery of genome sequencing results among women diagnosed with breast cancer at a young age.
Kimberly A Kaphingst, Jennifer Ivanovich, Ashley Elrick, Rebecca Dresser, Cindy Matsen, Melody S Goodman. Mol Genet Genomic Med 2016
3
66

Age differences in genetic knowledge, health literacy and causal beliefs for health conditions.
S Ashida, M Goodman, C Pandya, L M Koehly, C Lachance, J Stafford, K A Kaphingst. Public Health Genomics 2011
49
18

Coming full circle: a reciprocal-engagement model of genetic counseling practice.
Patricia McCarthy Veach, Dianne M Bartels, Bonnie S Leroy. J Genet Couns 2007
113
18

Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
661
18

Preparing for genomic medicine: a real world demonstration of health system change.
Clara L Gaff, Ingrid M Winship, Susan M Forrest, David P Hansen, Julian Clark, Paul M Waring, Mike South, Andrew H Sinclair.  2017
35
18

Attitudes of African Americans toward return of results from exome and whole genome sequencing.
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am. J. Med. Genet. A 2013
50
18

Diversity and inclusion in genomic research: why the uneven progress?
Amy R Bentley, Shawneequa Callier, Charles N Rotimi.  2017
49
18

Attitudes of non-African American focus group participants toward return of results from exome and whole genome sequencing.
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Michael J Bamshad, Holly K Tabor. Am. J. Med. Genet. A 2014
33
18


BRCA1 and BRCA2 genetic testing-pitfalls and recommendations for managing variants of uncertain clinical significance.
D M Eccles, G Mitchell, A N A Monteiro, R Schmutzler, F J Couch, A B Spurdle, E B Gómez-García. Ann. Oncol. 2015
89
18

Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.
Saskia C Sanderson, Michael D Linderman, Sabrina A Suckiel, George A Diaz, Randi E Zinberg, Kadija Ferryman, Melissa Wasserstein, Andrew Kasarskis, Eric E Schadt. Eur. J. Hum. Genet. 2016
34
18

Assessment of Survivor Concerns (ASC): a newly proposed brief questionnaire.
Carolyn C Gotay, Ian S Pagano. Health Qual Life Outcomes 2007
76
18

Retention and use of breast cancer recurrence risk information from genomic tests: the role of health literacy.
Sarah E Lillie, Noel T Brewer, Suzanne C O'Neill, Edward F Morrill, E Claire Dees, Lisa A Carey, Barbara K Rimer. Cancer Epidemiol. Biomarkers Prev. 2007
59
18

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N. Engl. J. Med. 2015
18

Patients' understanding of and responses to multiplex genetic susceptibility test results.
Kimberly A Kaphingst, Colleen M McBride, Christopher Wade, Sharon Hensley Alford, Robert Reid, Eric Larson, Andreas D Baxevanis, Lawrence C Brody. Genet. Med. 2012
71
18

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N. Engl. J. Med. 2014
306
18

BRCA genetic counseling among at-risk Latinas in New York City: new beliefs shape new generation.
Katarina M Sussner, Tiffany Edwards, Cristina Villagra, M Carina Rodriguez, Hayley S Thompson, Lina Jandorf, Heiddis B Valdimarsdottir. J Genet Couns 2015
23
18

Will Precision Medicine Improve Population Health?
Muin J Khoury, Sandro Galea. JAMA 2016
76
9


Heart disease risk information, encouragement, and physical activity among Mexican-origin couples: Self- or spouse-driven change?
Kaley F Skapinsky, Susan Persky, Megan Lewis, Andrea Goergen, Sato Ashida, Hendrik D de Heer, Donald Hadley, Anna V Wilkinson, Laura M Koehly. Transl Behav Med 2018
5
20

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
32
9

Introduction to the special series on health disparities in genomic medicine.
Kristi D Graves, Kenneth P Tercyak. Health Psychol 2015
2
50

The impact of raw DNA availability and corresponding online interpretation services: A mixed-methods study.
Caitlin G Allen, Jazmine Gabriel, Maureen Flynn, Tricia N Cunningham, Catharine Wang. Transl Behav Med 2018
10
10

Factors influencing the impact of pharmacogenomic prescribing on adherence to nicotine replacement therapy: A qualitative study of participants from a randomized controlled trial.
Alison J Wright, Stephen Sutton, David Armstrong, Paul Aveyard, Ann Louise Kinmonth, Theresa M Marteau. Transl Behav Med 2018
2
50

Potentially Preventable Deaths Among the Five Leading Causes of Death - United States, 2010 and 2014.
Macarena C García, Brigham Bastian, Lauren M Rossen, Robert Anderson, Arialdi Miniño, Paula W Yoon, Mark Faul, Greta Massetti, Cheryll C Thomas, Yuling Hong,[...]. MMWR Morb. Mortal. Wkly. Rep. 2016
19
9

Communication of cancer-related genetic and genomic information: A landscape analysis of reviews.
Emily B Peterson, Wen-Ying Sylvia Chou, Anna Gaysynsky, Melinda Krakow, Ashley Elrick, Muin J Khoury, Kimberly A Kaphingst. Transl Behav Med 2018
10
10

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
50
9

Parental attitudes and expectations towards receiving genomic test results in healthy children.
Alanna Kulchak Rahm, Lindsay Bailey, Kara Fultz, Audrey Fan, Janet L Williams, Adam Buchanan, F Daniel Davis, Michael F Murray, Marc S Williams. Transl Behav Med 2018
3
33

Social and behavioral science priorities for genomic translation.
Laura M Koehly, Susan Persky, Erica Spotts, Gillian Acca. Transl Behav Med 2018
2
50

Toward the implementation of genomic applications for smoking cessation and smoking-related diseases.
Alex T Ramsey, Li-Shiun Chen, Sarah M Hartz, Nancy L Saccone, Sherri L Fisher, Enola K Proctor, Laura J Bierut. Transl Behav Med 2018
3
33

Effect of co-payment on behavioral response to consumer genomic testing.
Wendy Liu, Jessica J Outlaw, Nathan Wineinger, Debra Boeldt, Cinnamon S Bloss. Transl Behav Med 2018
2
50

A comparison of views regarding the use of de-identified data.
Deborah Goodman, Catherine O Johnson, Deborah Bowen, Megan Smith, Lari Wenzel, Karen L Edwards. Transl Behav Med 2018
2
50

The research participant perspective related to the conduct of genomic cohort studies: A systematic review of the quantitative literature.
Deborah Goodman, Deborah Bowen, Lari Wenzel, Paris Tehrani, Francis Fernando, Araksi Khacheryan, Farihah Chowdhury, Catherine O Johnson, Karen Edwards. Transl Behav Med 2018
5
20


Models of consent to return of incidental findings in genomic research.
Paul S Appelbaum, Erik Parens, Cameron R Waldman, Robert Klitzman, Abby Fyer, Josue Martinez, W Nicholson Price, Wendy K Chung. Hastings Cent Rep 2014
43
9

Stakeholder views on returning research results.
Susanne B Haga, Jennifer Q Zhao. Adv. Genet. 2013
10
10




Effects of racial and ethnic group and health literacy on responses to genomic risk information in a medically underserved population.
Kimberly A Kaphingst, Jewel D Stafford, Lucy D'Agostino McGowan, Joann Seo, Christina R Lachance, Melody S Goodman. Health Psychol 2015
16
9

Latina patient perspectives about informed treatment decision making for breast cancer.
Sarah T Hawley, Nancy K Janz, Ann Hamilton, Jennifer J Griggs, Amy K Alderman, Mahasin Mujahid, Steven J Katz. Patient Educ Couns 2008
79
9

Clinical interpretation and implications of whole-genome sequencing.
Frederick E Dewey, Megan E Grove, Cuiping Pan, Benjamin A Goldstein, Jonathan A Bernstein, Hassan Chaib, Jason D Merker, Rachel L Goldfeder, Gregory M Enns, Sean P David,[...]. JAMA 2014
256
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.