A citation-based method for searching scientific literature

Beth N Peshkin, Mary Kate Ladd, Claudine Isaacs, Hannah Segal, Aryana Jacobs, Kathryn L Taylor, Kristi D Graves, Suzanne C O'Neill, Marc D Schwartz. J Cancer Educ 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Outcomes of a randomised controlled trial of a complex genetic counselling intervention to improve family communication.
Jan Hodgson, Sylvia Metcalfe, Clara Gaff, Susan Donath, Martin B Delatycki, Ingrid Winship, Loane Skene, MaryAnne Aitken, Jane Halliday. Eur J Hum Genet 2016
38
66

A Research Agenda for Communication Scholars in the Precision Medicine Era.
Courtney L Scherr, Marleah Dean, Margaret F Clayton, Bradford W Hesse, Kami Silk, Richard L Street, Janice Krieger. J Health Commun 2017
9
33


Communication of Information about Genetic Risks: Putting Families at the Center.
Álvaro Mendes, Alison Metcalfe, Milena Paneque, Liliana Sousa, Angus J Clarke, Jorge Sequeiros. Fam Process 2018
14
33

Stigmatization and male identity: Norwegian males' experience after identification as BRCA1/2 mutation carriers.
Nina Strømsvik, Målfrid Råheim, Nina Oyen, Lars Fredrik Engebretsen, Eva Gjengedal. J Genet Couns 2010
19
33

Three approaches to qualitative content analysis.
Hsiu-Fang Hsieh, Sarah E Shannon. Qual Health Res 2005
33



Negotiating jurisdictional boundaries in response to new genetic possibilities in breast cancer care: The creation of an 'oncogenetic taskscape'.
Sarah Wright, Mary Porteous, Diane Stirling, Oliver Young, Charlie Gourley, Nina Hallowell. Soc Sci Med 2019
6
33

Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information.
N Hallowell, C Foster, R Eeles, A Ardern-Jones, V Murday, M Watson. J Med Ethics 2003
119
33

To tell or not to tell: barriers and facilitators in family communication about genetic risk.
K Forrest, S A Simpson, B J Wilson, E R van Teijlingen, L McKee, N Haites, E Matthews. Clin Genet 2003
237
33

An Internet intervention for management of uncertainty during active surveillance for prostate cancer.
Meredith Wallace Kazer, Donald E Bailey, Martin Sanda, John Colberg, William Kevin Kelly. Oncol Nurs Forum 2011
31
33



Barriers and facilitators to BRCA genetic counseling among at-risk Latinas in New York City.
Katarina M Sussner, Lina Jandorf, Hayley S Thompson, Heiddis B Valdimarsdottir. Psychooncology 2013
45
33


Life events may contribute to family communication about cancer risk following BRCA1/2 testing.
Julie Lapointe, Claudia Côté, Karine Bouchard, Béatrice Godard, Jacques Simard, Michel Dorval. J Genet Couns 2013
12
33

Physician trust moderates the relationship between intolerance of uncertainty and cancer worry interference among women with Lynch syndrome.
Lindsey A Torbit, Jenna J Albiani, Melyssa Aronson, Spring Holter, Kara Semotiuk, Zane Cohen, Tae L Hart. J Behav Med 2016
5
33

Uncertainty in illness.
M H Mishel. Image J Nurs Sch 1988
552
33

Diversity and inclusion in genomic research: why the uneven progress?
Amy R Bentley, Shawneequa Callier, Charles N Rotimi. J Community Genet 2017
83
33

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
783
33



Understanding health decision making: An exploration of homophily.
Donna L Berry, Traci M Blonquist, Rachel Pozzar, Manan M Nayak. Soc Sci Med 2018
1
100

Cancer risks for men with BRCA1/2 mutations
Suzanne M Mahon. Oncol Nurs Forum 2014
7
33

The nature of communication work during cancer: advancing the theory of illness trajectories.
Erin Donovan-Kicken, Andrew C Tollison, Elizabeth S Goins. Health Commun 2012
21
33

Family communication between children and their parents about inherited genetic conditions: a meta-synthesis of the research.
Alison Metcalfe, Jane Coad, Gill M Plumridge, Paramjit Gill, Peter Farndon. Eur J Hum Genet 2008
87
33


How to inform at-risk relatives? Attitudes of 1379 Dutch patients, relatives, and members of the general population.
Lieke Marleen van den Heuvel, Daphne Stemkens, Wendy A G van Zelst-Stams, Floor Willeboordse, Imke Christiaans. J Genet Couns 2020
4
33


Interventions to improve risk communication in clinical genetics: systematic review.
A Edwards, J Gray, A Clarke, J Dundon, G Elwyn, C Gaff, K Hood, R Iredale, S Sivell, C Shaw,[...]. Patient Educ Couns 2008
73
33

Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2.
Sigurdis Haraldsdottir, Thorunn Rafnar, Wendy L Frankel, Sylvia Einarsdottir, Asgeir Sigurdsson, Heather Hampel, Petur Snaebjornsson, Gisli Masson, Daniel Weng, Reynir Arngrimsson,[...]. Nat Commun 2017
46
33

Cascade Genetic Testing of Relatives for Hereditary Cancer Risk: Results of an Online Initiative.
Jennifer L Caswell-Jin, Anjali D Zimmer, Will Stedden, Kerry E Kingham, Alicia Y Zhou, Allison W Kurian. J Natl Cancer Inst 2019
37
33

Feasibility of screening for Lynch syndrome among patients with colorectal cancer.
Heather Hampel, Wendy L Frankel, Edward Martin, Mark Arnold, Karamjit Khanduja, Philip Kuebler, Mark Clendenning, Kaisa Sotamaa, Thomas Prior, Judith A Westman,[...]. J Clin Oncol 2008
529
33

Availability and payer coverage of BRCA1/2 tests and gene panels.
Elizabeth Clain, Julia R Trosman, Michael P Douglas, Christine B Weldon, Kathryn A Phillips. Nat Biotechnol 2015
17
33

Cancer risks for BRCA1 and BRCA2 mutation carriers: results from prospective analysis of EMBRACE.
Nasim Mavaddat, Susan Peock, Debra Frost, Steve Ellis, Radka Platte, Elena Fineberg, D Gareth Evans, Louise Izatt, Rosalind A Eeles, Julian Adlard,[...]. J Natl Cancer Inst 2013
482
33

A Population-Based Study of Genes Previously Implicated in Breast Cancer.
Chunling Hu, Steven N Hart, Rohan Gnanaolivu, Hongyan Huang, Kun Y Lee, Jie Na, Chi Gao, Jenna Lilyquist, Siddhartha Yadav, Nicholas J Boddicker,[...]. N Engl J Med 2021
39
33

Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012.
Jacques Ferlay, Isabelle Soerjomataram, Rajesh Dikshit, Sultan Eser, Colin Mathers, Marise Rebelo, Donald Maxwell Parkin, David Forman, Freddie Bray. Int J Cancer 2015
33

Preparing individuals to communicate genetic test results to their relatives: report of a randomized control trial.
Susan V Montgomery, Andrea M Barsevick, Brian L Egleston, Ruth Bingler, Karen Ruth, Suzanne M Miller, John Malick, Terrence P Cescon, Mary B Daly. Fam Cancer 2013
44
33

What motivates interest in attending a familial cancer genetics clinic?
L Fraser, S Bramald, C Chapman, C Chu, V Cornelius, F Douglas, A Lucassen, A Nehammer, S Sutton, M Trivella,[...]. Fam Cancer 2003
26
33

Development of a Web-based Family Intervention for BRCA Carriers and Their Biological Relatives: Acceptability, Feasibility, and Usability Study.
Maria C Katapodi, Miyeon Jung, Ann M Schafenacker, Kara J Milliron, Kari E Mendelsohn-Victor, Sofia D Merajver, Laurel L Northouse. JMIR Cancer 2018
10
33

Health-care professionals' responsibility to patients' relatives in genetic medicine: a systematic review and synthesis of empirical research.
Sandi Dheensa, Angela Fenwick, Shiri Shkedi-Rafid, Gillian Crawford, Anneke Lucassen. Genet Med 2016
44
33

Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.
David Moher, Alessandro Liberati, Jennifer Tetzlaff, Douglas G Altman. PLoS Med 2009
33

Low rates of cascade genetic testing among families with hereditary gynecologic cancer: An opportunity to improve cancer prevention.
Natalie E Griffin, Tommy R Buchanan, Stephanie H Smith, Andrea A Leon, Melissa F Meyer, Jingxia Liu, Rachel G Tabak, Katherine C Fuh, Premal H Thaker, Matthew A Powell,[...]. Gynecol Oncol 2020
6
33


Screening for Colorectal Cancer: US Preventive Services Task Force Recommendation Statement.
Kirsten Bibbins-Domingo, David C Grossman, Susan J Curry, Karina W Davidson, John W Epling, Francisco A R García, Matthew W Gillman, Diane M Harper, Alex R Kemper, Alex H Krist,[...]. JAMA 2016
970
33


A Pilot study of the Sharing Risk Information Tool (ShaRIT) for Families with Hereditary Breast and Ovarian Cancer Syndrome.
Ani Kardashian, Julia Fehniger, Jennifer Creasman, Eleanor Cheung, Mary Stanley Beattie. Hered Cancer Clin Pract 2012
21
33

De-duplication of database search results for systematic reviews in EndNote.
Wichor M Bramer, Dean Giustini, Gerdien B de Jonge, Leslie Holland, Tanja Bekhuis. J Med Libr Assoc 2016
248
33

How to support cancer genetics counselees in informing at-risk relatives? Lessons from a randomized controlled trial.
Willem Eijzenga, Eveline de Geus, Cora M Aalfs, Fred H Menko, Rolf H Sijmons, Hanneke C J M de Haes, Ellen M A Smets. Patient Educ Couns 2018
8
33


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.