A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Will Precision Medicine Improve Population Health?
Muin J Khoury, Sandro Galea. JAMA 2016
105
40

Preferences for learning different types of genome sequencing results among young breast cancer patients: Role of psychological and clinical factors.
Kimberly A Kaphingst, Jennifer Ivanovich, Sarah Lyons, Barbara Biesecker, Rebecca Dresser, Ashley Elrick, Cindy Matsen, Melody Goodman. Transl Behav Med 2018
13
40

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
8
40

"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
47
40

Melanoma genetic testing, counseling, and adherence to skin cancer prevention and detection behaviors.
Karen Glanz, Kathryn Volpicelli, Peter A Kanetsky, Michael E Ming, Lynn M Schuchter, Christopher Jepson, Susan M Domchek, Katrina Armstrong. Cancer Epidemiol Biomarkers Prev 2013
24
40

Does personalized melanoma genomic risk information trigger conversations about skin cancer prevention and skin examination with family, friends and health professionals?
A K Smit, L A Keogh, A J Newson, P N Butow, K Dunlop, R L Morton, J Kirk, D Espinoza, A E Cust. Br J Dermatol 2017
13
40

Public preferences for communicating personal genomic risk information: a focus group study.
Amelia K Smit, Louise A Keogh, Jolyn Hersch, Ainsley J Newson, Phyllis Butow, Gabrielle Williams, Anne E Cust. Health Expect 2016
23
40

The impact of communicating genetic risks of disease on risk-reducing health behaviour: systematic review with meta-analysis.
Gareth J Hollands, David P French, Simon J Griffin, A Toby Prevost, Stephen Sutton, Sarah King, Theresa M Marteau. BMJ 2016
228
40

From public health genomics to precision public health: a 20-year journey.
Muin J Khoury, M Scott Bowen, Mindy Clyne, W David Dotson, Marta L Gwinn, Ridgely Fisk Green, Katherine Kolor, Juan L Rodriguez, Anja Wulf, Wei Yu. Genet Med 2018
50
40

Future health applications of genomics: priorities for communication, behavioral, and social sciences research.
Colleen M McBride, Deborah Bowen, Lawrence C Brody, Celeste M Condit, Robert T Croyle, Marta Gwinn, Muin J Khoury, Laura M Koehly, Bruce R Korf, Theresa M Marteau,[...]. Am J Prev Med 2010
102
40

Research and practice opportunities at the intersection of health education, health behavior, and genomics.
Catharine Wang, Deborah J Bowen, Sharon L R Kardia. Health Educ Behav 2005
35
40

Using a Historical Lens to Envision the Next Generation of Genomic Translation Research.
Colleen M McBride, Leah R Abrams, Laura M Koehly. Public Health Genomics 2015
5
40

Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) network.
Nina R Sperber, Janet S Carpenter, Larisa H Cavallari, Laura J Damschroder, Rhonda M Cooper-DeHoff, Joshua C Denny, Geoffrey S Ginsburg, Yue Guan, Carol R Horowitz, Kenneth D Levy,[...]. BMC Med Genomics 2017
49
40


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

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
13
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
37
20

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
9
20

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
14
20

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
3
33

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
25
20

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
17
20

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
63
20

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
8
20


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

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
12
20


Reduced melanoma after regular sunscreen use: randomized trial follow-up.
Adèle C Green, Gail M Williams, Valerie Logan, Geoffrey M Strutton. J Clin Oncol 2011
378
20

Making numbers matter: present and future research in risk communication.
Angela Fagerlin, Peter A Ubel, Dylan M Smith, Brian J Zikmund-Fisher. Am J Health Behav 2007
118
20

Reducing death from melanoma and standards of evidence.
Martin A Weinstock. J Invest Dermatol 2012
12
20

Primary care patients' views and decisions about, experience of and reactions to direct-to-consumer genetic testing: a longitudinal study.
Katherine Wasson, Tonya Nashay Sanders, Nancy S Hogan, Sara Cherny, Kathy J Helzlsouer. J Community Genet 2013
21
20

Methods for the synthesis of qualitative research: a critical review.
Elaine Barnett-Page, James Thomas. BMC Med Res Methodol 2009
596
20

Standards for reporting qualitative research: a synthesis of recommendations.
Bridget C O'Brien, Ilene B Harris, Thomas J Beckman, Darcy A Reed, David A Cook. Acad Med 2014
20

The impact of the format of graphical presentation on health-related knowledge and treatment choices.
Sarah T Hawley, Brian Zikmund-Fisher, Peter Ubel, Aleksandra Jancovic, Todd Lucas, Angela Fagerlin. Patient Educ Couns 2008
213
20

Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project.
Saskia C Sanderson, Michael D Linderman, Sabrina A Suckiel, Randi Zinberg, Melissa Wasserstein, Andrew Kasarskis, George A Diaz, Eric E Schadt. Eur J Hum Genet 2017
32
20

Psychological Distress, Anxiety, and Depression of Cancer-Affected BRCA1/2 Mutation Carriers: a Systematic Review.
Johanna Ringwald, Christina Wochnowski, Kristin Bosse, Katrin Elisabeth Giel, Norbert Schäffeler, Stephan Zipfel, Martin Teufel. J Genet Couns 2016
39
20


A Pilot Randomized Controlled Trial of the Feasibility, Acceptability, and Impact of Giving Information on Personalized Genomic Risk of Melanoma to the Public.
Amelia K Smit, David Espinoza, Ainsley J Newson, Rachael L Morton, Georgina Fenton, Lucinda Freeman, Kate Dunlop, Phyllis N Butow, Matthew H Law, Michael G Kimlin,[...]. Cancer Epidemiol Biomarkers Prev 2017
27
20

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
20

The melanoma genomics managing your risk study: A protocol for a randomized controlled trial evaluating the impact of personal genomic risk information on skin cancer prevention behaviors.
Amelia K Smit, Ainsley J Newson, Rachael L Morton, Michael Kimlin, Louise Keogh, Matthew H Law, Judy Kirk, Suzanne Dobbinson, Peter A Kanetsky, Georgina Fenton,[...]. Contemp Clin Trials 2018
10
20

Development and Evaluation of a Telephone Communication Protocol for the Delivery of Personalized Melanoma Genomic Risk to the General Population.
Georgina L Fenton, Amelia K Smit, Lucinda Freeman, Caro Badcock, Kate Dunlop, Phyllis N Butow, Judy Kirk, Anne E Cust. J Genet Couns 2018
11
20

Psychosocial and behavioral outcomes of genomic testing in cancer: a systematic review.
Tatiane Yanes, Amanda M Willis, Bettina Meiser, Katherine M Tucker, Megan Best. Eur J Hum Genet 2019
26
20

Communicating genetic risk information for common disorders in the era of genomic medicine.
Denise M Lautenbach, Kurt D Christensen, Jeffrey A Sparks, Robert C Green. Annu Rev Genomics Hum Genet 2013
83
20

Population genetic testing for cancer susceptibility: founder mutations to genomes.
William D Foulkes, Bartha Maria Knoppers, Clare Turnbull. Nat Rev Clin Oncol 2016
61
20


How much melanoma is caused by sun exposure?
B K Armstrong, A Kricker. Melanoma Res 1993
326
20


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.