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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:

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

Showing 1-25 of 123 citing articles:

Technical report: ethical and policy issues in genetic testing and screening of children
L. F. Ross, Howard M. Saal, Karen L. David, et al.
Genetics in Medicine (2013) Vol. 15, Iss. 3, pp. 234-245
Open Access | Times Cited: 421
Ethical and Policy Issues in Genetic Testing and Screening of Children
Mary E. Fallat, Aviva L. Katz, Mark R. Mercurio, et al.
PEDIATRICS (2013) Vol. 131, Iss. 3, pp. 620-622
Closed Access | Times Cited: 365
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
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
Familial hypercholesterolaemia: A model of care for Australasia
Gerald F. Watts, David Sullivan, Nicola Poplawski, et al.
Atherosclerosis Supplements (2011) Vol. 12, Iss. 2, pp. 221-263
Closed Access | Times Cited: 196
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
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
Parents’ and children's communication about genetic risk: a qualitative study, learning from families’ experiences
Alison Metcalfe, Gill Plumridge, Jane Coad, et al.
European Journal of Human Genetics (2011) Vol. 19, Iss. 6, pp. 640-646
Open Access | Times Cited: 111
2012 European Thyroid Association Guidelines for Genetic Testing and Its Clinical Consequences in Medullary Thyroid Cancer
Rossella Elisei, Maria Alevizaki, B. Conte‐Devolx, et al.
European Thyroid Journal (2012) Vol. 1, Iss. 4, pp. 216-231
Open Access | Times Cited: 106
Uptake of Huntington disease predictive testing in a complete population
PJ Morrison, S Harding-Lester, Aoife Bradley
Clinical Genetics (2010) Vol. 80, Iss. 3, pp. 281-286
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
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
‘Is this knowledge mine and nobody else's? I don't feel that.’ Patient views about consent, confidentiality and information-sharing in genetic medicine: Table 1
Sandi Dheensa, Angela Fenwick, Anneke Lucassen
Journal of Medical Ethics (2016) Vol. 42, Iss. 3, pp. 174-179
Open Access | Times Cited: 66
Guidelines for Disclosing Genetic Information to Family Members: From Development to Use
Béatrice Godard, Thierry Hurlimann, Martin Letendre, et al.
Familial Cancer (2006) Vol. 5, Iss. 1, pp. 103-116
Open Access | Times Cited: 87
Ethics in genetic counselling
Angus Clarke, Carina Wallgren‐Pettersson
Journal of Community Genetics (2018) Vol. 10, Iss. 1, pp. 3-33
Open Access | Times Cited: 55
Ethical concerns relating to genetic risk scores for suicide
Anna R. Docherty, Brent M. Kious, Teneille R. Brown, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2021) Vol. 186, Iss. 8, pp. 433-444
Open Access | Times Cited: 35
The role of disease perceptions and results sharing in psychological adaptation after genetic susceptibility testing: the REVEAL Study
Sato Ashida, Laura M. Koehly, J. Scott Roberts, et al.
European Journal of Human Genetics (2010) Vol. 18, Iss. 12, pp. 1296-1301
Open Access | Times Cited: 55
Ethical Problems and Genetics Practice
Michael Parker
(2012)
Closed Access | Times Cited: 47
Healthy citizenship beyond autonomy and discipline: Tactical engagements with genetic testing
Tamar Sharon
BioSocieties (2014) Vol. 10, Iss. 3, pp. 295-316
Closed Access | Times Cited: 47
Communication of Information about Genetic Risks: Putting Families at the Center
Álvaro Mendes, Alison Metcalfe, Milena Paneque, et al.
Family Process (2017) Vol. 57, Iss. 3, pp. 836-846
Open Access | Times Cited: 44
Approaching confidentiality at a familial level in genomic medicine: a focus group study with healthcare professionals
Sandi Dheensa, Angela Fenwick, Anneke Lucassen
BMJ Open (2017) Vol. 7, Iss. 2, pp. e012443-e012443
Open Access | Times Cited: 42
Genomic findings with familial implications: agenda setting in light of mainstreaming
Amicia Phillips, Eva Van Steijvoort, Maria Siermann, et al.
Open Research Europe (2025) Vol. 5, pp. 4-4
Open Access
Controversies and ethical issues in cancer-genetics clinics
Marion Harris, Ingrid Winship, Merle Spriggs
The Lancet Oncology (2005) Vol. 6, Iss. 5, pp. 301-310
Closed Access | Times Cited: 71
Improving Service Evaluation in Clinical Genetics: Identifying Effects of Genetic Diseases on Individuals and Families
Marion McAllister, Katherine Payne, Stuart G. Nicholls, et al.
Journal of Genetic Counseling (2007) Vol. 16, Iss. 1, pp. 71-83
Open Access | Times Cited: 56
How young people find out about their family history of Huntington's disease
Karen Forrest Keenan, Edwin van Teijlingen, Martin McKee, et al.
Social Science & Medicine (2009) Vol. 68, Iss. 10, pp. 1892-1900
Closed Access | Times Cited: 53
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