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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:

To tell or not to tell: barriers and facilitators in family communication about genetic risk
Karen Forrest, SA Simpson, Wilson Bj, et al.
Clinical Genetics (2003) Vol. 64, Iss. 4, pp. 317-326
Closed Access | Times Cited: 365

Showing 1-25 of 365 citing articles:

Beyond individualism: Is there a place for relational autonomy in clinical practice and research?
Edward S. Dove, Susan Kelly, Federica Lucivero, et al.
Clinical Ethics (2017) Vol. 12, Iss. 3, pp. 150-165
Open Access | Times Cited: 204
Young-onset colorectal cancer
Manon C.W. Spaander, Ann G. Zauber, Sapna Syngal, et al.
Nature Reviews Disease Primers (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 134
Process and outcome in communication of genetic information within families: a systematic review
Clara Gaff, Angus Clarke, Paul Atkinson, et al.
European Journal of Human Genetics (2007) Vol. 15, Iss. 10, pp. 999-1011
Open Access | Times Cited: 241
What Facilitates or Impedes Family Communication Following Genetic Testing for Cancer Risk? A Systematic Review and Meta‐Synthesis of Primary Qualitative Research
Kim Chivers Seymour, Julia Addington‐Hall, Anneke Lucassen, et al.
Journal of Genetic Counseling (2010) Vol. 19, Iss. 4, pp. 330-342
Closed Access | Times Cited: 178
Letting the family know: balancing ethics and effectiveness when notifying relatives about genetic testing for a familial disorder
Graeme Suthers
Journal of Medical Genetics (2005) Vol. 43, Iss. 8, pp. 665-670
Open Access | Times Cited: 177
Genetic testing in asymptomatic minors
Pascal Borry, Gerry Evers‐Kiebooms, Martina C. Cornel, et al.
European Journal of Human Genetics (2009) Vol. 17, Iss. 6, pp. 711-719
Open Access | Times Cited: 173
Factors Determining Dissemination of Results and Uptake of Genetic Testing in Families with Known BRCA1/2 Mutations
Esmé Finlay, Jill E. Stopfer, E. Burlingame, et al.
Genetic Testing (2008) Vol. 12, Iss. 1, pp. 81-91
Open Access | Times Cited: 151
Family communication between children and their parents about inherited genetic conditions: a meta-synthesis of the research
Alison Metcalfe, Jane Coad, Gill Plumridge, et al.
European Journal of Human Genetics (2008) Vol. 16, Iss. 10, pp. 1193-1200
Open Access | Times Cited: 146
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
Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care
Fiona A. Miller, Robin Z. Hayeems, Jessica Bytautas, et al.
European Journal of Human Genetics (2013) Vol. 22, Iss. 3, pp. 391-395
Open Access | Times Cited: 107
Family Communication about Genetic Risk: The Little That Is Known
Brenda J. Wilson, Karen Forrest, Edwin van Teijlingen, et al.
Public Health Genomics (2004) Vol. 7, Iss. 1, pp. 15-24
Closed Access | Times Cited: 169
Uptake Rates for Breast Cancer Genetic Testing: A Systematic Review
Mary E. Ropka, Jennifer Wenzel, Elayne Kornblatt Phillips, et al.
Cancer Epidemiology Biomarkers & Prevention (2006) Vol. 15, Iss. 5, pp. 840-855
Open Access | Times Cited: 154
Communicating genetic information in families – a review of guidelines and position papers
Laura Forrest, Martin B. Delatycki, Loane Skene, et al.
European Journal of Human Genetics (2007) Vol. 15, Iss. 6, pp. 612-618
Open Access | Times Cited: 127
Genetic professionals' reports of nondisclosure of genetic risk information within families
Angus Clarke, Martin Richards, L Kerzin-Storrar, et al.
European Journal of Human Genetics (2005) Vol. 13, Iss. 5, pp. 556-562
Open Access | Times Cited: 123
Facilitating Family Communication About Predictive Genetic Testing: Probands’ Perceptions
Clara Gaff, Veronica Collins, Tiffany Symes, et al.
Journal of Genetic Counseling (2005) Vol. 14, Iss. 2, pp. 133-140
Closed Access | Times Cited: 123
Communication about genetic testing in families of male BRCA1/2 carriers and non‐carriers: patterns, priorities and problems
Nina Hallowell, Audrey Ardern‐Jones, Rosalind A. Eeles, et al.
Clinical Genetics (2005) Vol. 67, Iss. 6, pp. 492-502
Closed Access | Times Cited: 119
Ethical, Legal, and Social Concerns About Expanded Newborn Screening: Fragile X Syndrome as a Prototype for Emerging Issues
Donald B. Bailey, Debra Skinner, Arlene M. Davis, et al.
PEDIATRICS (2008) Vol. 121, Iss. 3, pp. e693-e704
Closed Access | Times Cited: 115
Increased genetic counseling support improves communication of genetic information in families
Laura Forrest, Jo Burke, Sonya Bacic, et al.
Genetics in Medicine (2008) Vol. 10, Iss. 3, pp. 167-172
Closed Access | Times Cited: 98
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, et al.
Genetics in Medicine (2015) Vol. 18, Iss. 4, pp. 290-301
Open Access | Times Cited: 78
Familial communication and cascade testing among relatives of BRCA population screening participants
Sari Lieberman, Amnon Lahad, Ariela Tomer, et al.
Genetics in Medicine (2018) Vol. 20, Iss. 11, pp. 1446-1454
Open Access | Times Cited: 78
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
Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications
Elizabeth Ormondroyd, Stephanie Oates, Michael Parker, et al.
European Journal of Human Genetics (2013) Vol. 22, Iss. 1, pp. 88-93
Open Access | Times Cited: 75
Patients’ perceptions and practices of informing relatives: a qualitative study within a randomised trial on healthcare-assisted risk disclosure
Charlotta Nääs, Jenny von Salomé, Anna Rosén
European Journal of Human Genetics (2024) Vol. 32, Iss. 4, pp. 448-455
Open Access | Times Cited: 6
Measures of familial aggregation depend on definition of family history: meta-analysis for colorectal cancer
Laura Baglietto, Mark A. Jenkins, Gianluca Severi, et al.
Journal of Clinical Epidemiology (2006) Vol. 59, Iss. 2, pp. 114-124
Closed Access | Times Cited: 104
Disclosing Genetic Test Results to Family Members
Rebekah Hamilton, Barbara J. Bowers, Janet K. Williams
Journal of Nursing Scholarship (2005) Vol. 37, Iss. 1, pp. 18-24
Closed Access | Times Cited: 102
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