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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:

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

Showing 1-25 of 123 citing articles:

Genetics, genomics, and cancer risk assessment
Jeffrey N. Weitzel, Kathleen R. Blazer, Deborah J. MacDonald, et al.
CA A Cancer Journal for Clinicians (2011) Vol. 61, Iss. 5, pp. 327-359
Open Access | Times Cited: 240
Cascade Testing for Hereditary Cancer Syndromes: Should We Move Toward Direct Relative Contact? A Systematic Review and Meta-Analysis
Melissa K. Frey, Muhammad Danyal Ahsan, Hannah Bergeron, et al.
Journal of Clinical Oncology (2022) Vol. 40, Iss. 35, pp. 4129-4143
Open Access | Times Cited: 76
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
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
Sharing Genetic Test Results in Lynch Syndrome: Communication With Close and Distant Relatives
Elena M. Stoffel, Beth Ford, Rowena Mercado, et al.
Clinical Gastroenterology and Hepatology (2008) Vol. 6, Iss. 3, pp. 333-338
Open Access | Times Cited: 121
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
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
Do people with hereditary cancer syndromes inform their at-risk relatives? A systematic review and meta-analysis
Muhammad Danyal Ahsan, Sarah R. Levi, Emily Webster, et al.
PEC Innovation (2023) Vol. 2, pp. 100138-100138
Open Access | Times Cited: 21
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
Cascade genetic testing for hereditary cancer syndromes: a review of barriers and breakthroughs
Rachel M. Levine, Ryan Kahn, Luiza Perez, et al.
Familial Cancer (2024) Vol. 23, Iss. 2, pp. 111-120
Closed Access | Times Cited: 6
Assessment of Psychosocial Outcomes in Genetic Counseling Research: An Overview of Available Measurement Scales
Nadine A. Kasparian, Claire E. Wakefield, Bettina Meiser
Journal of Genetic Counseling (2007) Vol. 16, Iss. 6, pp. 693-712
Open Access | Times Cited: 79
Outcomes of a randomised controlled trial of a complex genetic counselling intervention to improve family communication
Jan Hodgson, Sylvia A. Metcalfe, Clara Gaff, et al.
European Journal of Human Genetics (2015) Vol. 24, Iss. 3, pp. 356-360
Open Access | Times Cited: 58
Hereditary nonpolyposis colorectal cancer: diagnostic strategies and their implications.
Peter A Bonis, Thomas A Trikalinos, Mei Chung, et al.
PubMed (2007), Iss. 150, pp. 1-180
Closed Access | Times Cited: 70
Colorectal cancer survivors undergoing genetic testing for hereditary non‐polyposis colorectal cancer: motivational factors and psychosocial functioning
M. J. Esplen, Lisa Madlensky, Melyssa Aronson, et al.
Clinical Genetics (2007) Vol. 72, Iss. 5, pp. 394-401
Open Access | Times Cited: 69
Communicating BRCA1/2 genetic test results within the family: A qualitative analysis
Caroline Dancyger, Mel Wiseman, Chris Jacobs, et al.
Psychology and Health (2011) Vol. 26, Iss. 8, pp. 1018-1035
Closed Access | Times Cited: 53
Patient communication of cancer genetic test results in a diverse population
Charité Ricker, Rachel Koff, Chenxu Qu, et al.
Translational Behavioral Medicine (2018) Vol. 8, Iss. 1, pp. 85-94
Open Access | Times Cited: 40
Assessing relatives’ readiness for hereditary cancer cascade genetic testing
Erica M. Bednar, Charlotte C. Sun, Sheryl McCurdy, et al.
Genetics in Medicine (2019) Vol. 22, Iss. 4, pp. 719-726
Open Access | Times Cited: 36
Family communication regarding inherited high cholesterol: Why and how do patients disclose genetic risk?
Hélène W.P. van den Nieuwenhoff, Ilse Mesters, Caroline Gielen, et al.
Social Science & Medicine (2007) Vol. 65, Iss. 5, pp. 1025-1037
Closed Access | Times Cited: 59
Risk Reduction and Health Promotion Behaviors Following Genetic Testing for Adult-Onset Disorders
Theresa A. Beery, Janet K. Williams
Genetic Testing (2007) Vol. 11, Iss. 2, pp. 111-123
Closed Access | Times Cited: 56
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
Development and Pilot Testing of Two Decision Aids for Individuals Considering Genetic Testing for Cancer Risk
Claire E. Wakefield, Bettina Meiser, Judi Homewood, et al.
Journal of Genetic Counseling (2007) Vol. 16, Iss. 3, pp. 325-339
Closed Access | Times Cited: 52
Sharing genetic risk with next generation: mutation-positive parents’ communication with their offspring in Lynch Syndrome
Katja Aktan–Collan, H Kääriäinen, Eeva M. Kolttola, et al.
Familial Cancer (2010) Vol. 10, Iss. 1, pp. 43-50
Closed Access | Times Cited: 52
Formal and Informal Support Needs of Young Women withBRCAMutations
Allison Werner‐Lin
Journal of Psychosocial Oncology (2008) Vol. 26, Iss. 4, pp. 111-133
Closed Access | Times Cited: 50
Why is genetic screening for autosomal dominant disorders underused in families? The case of hereditary hemorrhagic telangiectasia
Barbara A. Bernhardt, Cara Zayac, Reed E. Pyeritz
Genetics in Medicine (2011) Vol. 13, Iss. 9, pp. 812-820
Open Access | Times Cited: 44
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