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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Communicating genetic risk information within families: a review
Mel Wiseman, Caroline Dancyger, Susan Michie
Familial Cancer (2010) Vol. 9, Iss. 4, pp. 691-703
Closed Access | Times Cited: 144

Showing 1-25 of 144 citing articles:

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, et al.
European Journal of Human Genetics (2015) Vol. 24, Iss. 3, pp. 315-325
Open Access | Times Cited: 77
Limitations and Pitfalls of Using Family Letters to Communicate Genetic Risk: a Qualitative Study with Patients and Healthcare Professionals
Sandi Dheensa, Anneke Lucassen, Angela Fenwick
Journal of Genetic Counseling (2017) Vol. 27, Iss. 3, pp. 689-701
Open Access | Times Cited: 74
Psychosocial and behavioral outcomes of genomic testing in cancer: a systematic review
Tatiane Yanes, Amanda Willis, Bettina Meiser, et al.
European Journal of Human Genetics (2018) Vol. 27, Iss. 1, pp. 28-35
Open Access | Times Cited: 61
Quantifying family dissemination and identifying barriers to communication of risk information in Australian BRCA families
Emma Healey, Natalie Taylor, Sian Greening, et al.
Genetics in Medicine (2017) Vol. 19, Iss. 12, pp. 1323-1331
Open Access | Times Cited: 46
Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists
Fred H. Menko, Cora M. Aalfs, Lidewij Henneman, et al.
Familial Cancer (2013) Vol. 12, Iss. 2, pp. 319-324
Closed Access | Times Cited: 45
Development of FOCUS‐GC: Framework for Outcomes of Clinical Communication Services in Genetic Counseling
Deborah Cragun, Heather Zierhut
Journal of Genetic Counseling (2017) Vol. 27, Iss. 1, pp. 33-58
Open Access | Times Cited: 45
Family Communication, Risk Perception and Cancer Knowledge of Young Adults from BRCA1/2 Families: a Systematic Review
Alison L. Young, Phyllis Butow, Janine Vetsch, et al.
Journal of Genetic Counseling (2017) Vol. 26, Iss. 6, pp. 1179-1196
Open Access | Times Cited: 43
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, et al.
Journal of Genetic Counseling (2016) Vol. 26, Iss. 1, pp. 173-181
Open Access | Times Cited: 41
The Communication Chain of Genetic Risk: Analyses of Narrative Data Exploring Proband–Provider and Proband–Family Communication in Hereditary Breast and Ovarian Cancer
Carla Pedrazzani, Mónica Aceti, Reka Schweighoffer, et al.
Journal of Personalized Medicine (2022) Vol. 12, Iss. 8, pp. 1249-1249
Open Access | Times Cited: 19
Communicating Genetic Information in Families with Inherited Late-Onset Neurodegenerative Diseases: A Scoping Review
Sofia Fontoura Dias, Maria das Graças Vale Barbosa, Filipa Júlio, et al.
Health Communication (2025), pp. 1-23
Closed Access
Facilitators and Barriers to Uptake of Genetic and Cascade Testing in Familial Hypercholesterolemia: a Systematic Review
Chaitanyasre Lenin, Phoebe X. H. Lim, Ashna Nastar, et al.
International Journal of Behavioral Medicine (2025)
Open Access
A family genetic risk communication framework: guiding tool development in genetics health services
Miriam Wiens, Brenda J. Wilson, Christina Honeywell, et al.
Journal of Community Genetics (2013) Vol. 4, Iss. 2, pp. 233-242
Open Access | Times Cited: 43
Evaluating the utilization of educational materials in communicating about Lynch syndrome to at-risk relatives
Kristen Dilzell, Kerry Kingham, Kelly E. Ormond, et al.
Familial Cancer (2014) Vol. 13, Iss. 3, pp. 381-389
Closed Access | Times Cited: 37
Unsolicited information letters to increase awareness of Lynch syndrome and familial colorectal cancer: reactions and attitudes
Helle Vendel Petersen, Birgitte Frederiksen, Charlotte Kvist Lautrup, et al.
Familial Cancer (2018) Vol. 18, Iss. 1, pp. 43-51
Closed Access | Times Cited: 34
Family Ties: The Role of Family Context in Family Health History Communication About Cancer
Vivian M. Rodríguez, Rosalie Corona, Joann Bodurtha, et al.
Journal of Health Communication (2016) Vol. 21, Iss. 3, pp. 346-355
Open Access | Times Cited: 33
Care delivery considerations for widespread and equitable implementation of inherited cancer predisposition testing
Deborah Cragun, Anita Y. Kinney, Tuya Pal
Expert Review of Molecular Diagnostics (2016) Vol. 17, Iss. 1, pp. 57-70
Open Access | Times Cited: 33
Talking across generations: Family communication aboutBRCA1andBRCA2genetic cancer risk
Alison L. Young, Phyllis Butow, Paul Rhodes, et al.
Journal of Genetic Counseling (2019) Vol. 28, Iss. 3, pp. 516-532
Closed Access | Times Cited: 30
Family Communication Following BRCA1/2 Genetic Testing: A Close Look at the Process
Darquise Lafrenière, Karine Bouchard, Béatrice Godard, et al.
Journal of Genetic Counseling (2012) Vol. 22, Iss. 3, pp. 323-335
Open Access | Times Cited: 33
Looking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice
Gabriel Lázaro‐Muñoz, John M. Conley, Arlene M. Davis, et al.
The American Journal of Bioethics (2015) Vol. 15, Iss. 7, pp. 3-14
Open Access | Times Cited: 32
The KinFact Intervention – A Randomized Controlled Trial to Increase Family Communication About Cancer History
Joann Bodurtha, Donna K. McClish, Maria Gyure, et al.
Journal of Women s Health (2014) Vol. 23, Iss. 10, pp. 806-816
Open Access | Times Cited: 32
Family Communication About Genetic Risk of Hereditary Cardiomyopathies and Arrhythmias: an Integrative Review
Lisa Shah, Sandra Daack‐Hirsch
Journal of Genetic Counseling (2018) Vol. 27, Iss. 5, pp. 1022-1039
Open Access | Times Cited: 30
How to inform at‐risk relatives? Attitudes of 1379 Dutch patients, relatives, and members of the general population
Lieke M. van den Heuvel, Daphne Stemkens, Wendy A.G. van Zelst–Stams, et al.
Journal of Genetic Counseling (2019) Vol. 29, Iss. 5, pp. 786-799
Open Access | Times Cited: 28
How to inform relatives at risk of hereditary diseases? A mixed‐methods systematic review on patient attitudes
Lieke M. van den Heuvel, Ellen M.A. Smets, J. Peter van Tintelen, et al.
Journal of Genetic Counseling (2019) Vol. 28, Iss. 5, pp. 1042-1058
Closed Access | Times Cited: 27
A systematic literature review of disclosure practices and reported outcomes for medically actionable genomic secondary findings
Julie C. Sapp, Flavia M. Facio, Diane Cooper, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 12, pp. 2260-2269
Open Access | Times Cited: 22
When does precision matter? Personalized medicine from the perspective of public health
James Wilson
Oxford University Press eBooks (2022), pp. 173-186
Closed Access | Times Cited: 15
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