A citation-based method for searching scientific literature

Deborah O Himes, Sarah H Davis, Jane H Lassetter, Neil E Peterson, Margaret F Clayton, Wendy C Birmingham, Anita Y Kinney. J Community Genet 2019
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Challenges and strategies proposed by genetic health professionals to assist with family communication.
Alison L Young, Phyllis N Butow, Katherine M Tucker, Claire E Wakefield, Emma Healey, Rachel Williams. Eur J Hum Genet 2019
9
100

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
100

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
20
100

Development and evaluation of a breast cancer prevention decision aid for higher-risk women.
Dawn Stacey, Annette M O'Connor, Cathy DeGrasse, Shailendra Verma. Health Expect 2003
56
100

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
100

Systematic methodological review: developing a framework for a qualitative semi-structured interview guide.
Hanna Kallio, Anna-Maija Pietilä, Martin Johnson, Mari Kangasniemi. J Adv Nurs 2016
153
100

Learning of your parent's BRCA mutation during adolescence or early adulthood: a study of offspring experiences.
Angela R Bradbury, Linda Patrick-Miller, Kimberly Pawlowski, Comfort N Ibe, Shelly A Cummings, Fay Hlubocky, Olufunmilayo I Olopade, Christopher K Daugherty. Psychooncology 2009
36
100

How communication of genetic information within the family is addressed in genetic counselling: a systematic review of research evidence.
Álvaro Mendes, Milena Paneque, Liliana Sousa, Angus Clarke, Jorge Sequeiros. Eur J Hum Genet 2016
34
100

Stakeholder perspectives on implementing a universal Lynch syndrome screening program: a qualitative study of early barriers and facilitators.
Jennifer L Schneider, James Davis, Tia L Kauffman, Jacob A Reiss, Cheryl McGinley, Kathleen Arnold, Jamilyn Zepp, Marian Gilmore, Kristin R Muessig, Sapna Syngal,[...]. Genet Med 2016
25
100


Examining intrafamilial communication of colorectal cancer risk status to family members and kin responses to colonoscopy: a qualitative study.
Kaitlin M McGarragle, Crystal Hare, Spring Holter, Dorian Anglin Facey, Kelly McShane, Steven Gallinger, Tae L Hart. Hered Cancer Clin Pract 2019
5
100

Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery.
Ivan Eisler, Matthew Ellison, Frances Flinter, Jo Grey, Suzanne Hutchison, Carole Jackson, Louise Longworth, Rhona MacLeod, Marion McAllister, Alison Metcalfe,[...]. Eur J Hum Genet 2016
21
100

Communicating genetic risk information within families: a review.
Mel Wiseman, Caroline Dancyger, Susan Michie. Fam Cancer 2010
72
100


Intrafamilial disclosure of risk for hereditary breast and ovarian cancer: points to consider.
Lee Black, Kelly A McClellan, Denise Avard, Bartha Maria Knoppers. J Community Genet 2013
15
100

Estimating the efficacy and efficiency of cascade genetic screening.
M Krawczak, D N Cooper, J Schmidtke. Am J Hum Genet 2001
52
100

Family communication about positive BRCA1 and BRCA2 genetic test results.
Bobbi McGivern, Jessica Everett, Geoffrey G Yager, Robert C Baumiller, Amanda Hafertepen, Howard M Saal. Genet Med 2004
88
100

Cascade Screening for Familial Hypercholesterolemia and the Use of Genetic Testing.
Joshua W Knowles, Daniel J Rader, Muin J Khoury. JAMA 2017
74
100

Genetic Testing and Counseling Among Patients With Newly Diagnosed Breast Cancer .
Allison W Kurian, Kent A Griffith, Ann S Hamilton, Kevin C Ward, Monica Morrow, Steven J Katz, Reshma Jagsi. JAMA 2017
68
100

Developing distress protocols for research on sensitive topics.
Claire Burke Draucker, Donna S Martsolf, Candice Poole. Arch Psychiatr Nurs 2009
50
100

Genetic health professionals and the communication of genetic information in families: Practice during and after a genetic consultation.
Laura E Forrest, Martin B Delatycki, Lisette Curnow, Loane Skene, Maryanne Aitken. Am J Med Genet A 2010
31
100

Development and Testing of a Decision Aid for Unaffected Women with a BRCA1 or BRCA2 Mutation.
Terri Jabaley, Meghan L Underhill-Blazey, Donna L Berry. J Cancer Educ 2020
4
100

Shared decision making in patients at risk of cancer: the role of domain and numeracy.
Yaniv Hanoch, Talya Miron-Shatz, Jonathan J Rolison, Zehra Omer, Elisa Ozanne. Health Expect 2015
9
100

Family communication about genetic risk: the little that is known.
Brenda J Wilson, Karen Forrest, Edwin R van Teijlingen, Lorna McKee, Neva Haites, Eric Matthews, Sheila A Simpson. Community Genet 2004
114
100

Acceptability of, and Information Needs Regarding, Next-Generation Sequencing in People Tested for Hereditary Cancer: A Qualitative Study.
Bettina Meiser, Ben Storey, Veronica Quinn, Belinda Rahman, Lesley Andrews. J Genet Couns 2016
9
100

The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice.
Fred H Menko, Jacqueline A Ter Stege, Lizet E van der Kolk, Kiki N Jeanson, Winnie Schats, Daoud Ait Moha, Eveline M A Bleiker. Fam Cancer 2019
37
100

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
17
100

Informing relatives at risk of inherited cardiac conditions: experiences and attitudes of healthcare professionals and counselees.
Lieke M van den Heuvel, Mette J Huisinga, Yvonne M Hoedemaekers, Annette F Baas, Mirjam Plantinga, Lidewij Henneman, J Peter van Tintelen, Ellen M A Smets, Imke Christiaans. Eur J Hum Genet 2019
6
100

Psychosocial and Clinical Factors Associated with Family Communication of Cancer Genetic Test Results among Women Diagnosed with Breast Cancer at a Young Age.
Ashley Elrick, Sato Ashida, Jennifer Ivanovich, Sarah Lyons, Barbara B Biesecker, Melody S Goodman, Kimberly A Kaphingst. J Genet Couns 2017
22
100



A randomized trial of a breast/ovarian cancer genetic testing decision aid used as a communication aid during genetic counseling.
Claire E Wakefield, Bettina Meiser, Judi Homewood, Alan Taylor, Margaret Gleeson, Rachel Williams, Kathy Tucker. Psychooncology 2008
33
100

Familial communication and cascade testing among relatives of BRCA population screening participants.
Sari Lieberman, Amnon Lahad, Ariela Tomer, Sivan Koka, Malka BenUziyahu, Aviad Raz, Ephrat Levy-Lahad. Genet Med 2018
24
100

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
100

Genetic testing for hereditary cancer syndromes: patient recommendations for improved risk communication.
Samantha Pollard, Steve Kalloger, Deirdre Weymann, Sophie Sun, Jennifer Nuk, Kasmintan A Schrader, Dean A Regier. Health Expect 2020
3
100

Assessing relatives' readiness for hereditary cancer cascade genetic testing.
Erica M Bednar, Charlotte C Sun, Sheryl McCurdy, Sally W Vernon. Genet Med 2020
5
100

Information and support needs of young women regarding breast cancer risk and genetic testing: adapting effective interventions for a novel population.
Suzanne C O'Neill, Chalanda Evans, Rebekah J Hamilton, Beth N Peshkin, Claudine Isaacs, Sue Friedman, Kenneth P Tercyak. Fam Cancer 2018
6
100

A patient decision aid for risk-reducing surgery in premenopausal BRCA1/2 mutation carriers: Development process and pilot testing.
Marline G Harmsen, Miranda P Steenbeek, Nicoline Hoogerbrugge, Helena C van Doorn, Katja N Gaarenstroom, M Caroline Vos, Leon F A G Massuger, Joanne A de Hullu, Rosella P M G Hermens. Health Expect 2018
10
100


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.