Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

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

Showing 1-25 of 178 citing articles:

Critical research gaps and translational priorities for the successful prevention and treatment of breast cancer
Suzanne A. Eccles, Eric O. Aboagye, Simak Ali, et al.
Breast Cancer Research (2013) Vol. 15, Iss. 5
Open Access | Times Cited: 405
Using framework-based synthesis for conducting reviews of qualitative studies
Mary Dixon‐Woods
BMC Medicine (2011) Vol. 9, Iss. 1
Open Access | Times Cited: 398
Essential Elements of Genetic Cancer Risk Assessment, Counseling, and Testing: Updated Recommendations of the National Society of Genetic Counselors
Bronson D. Riley, Julie O. Culver, Cécile Skrzynia, et al.
Journal of Genetic Counseling (2011) Vol. 21, Iss. 2, pp. 151-161
Closed Access | Times Cited: 318
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
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
What are the barriers and facilitators to exercise and physical activity uptake and adherence among South Asian older adults: A systematic review of qualitative studies
Maria Horne, Stephanie Tierney
Preventive Medicine (2012) Vol. 55, Iss. 4, pp. 276-284
Closed Access | Times Cited: 122
Cascading After Peridiagnostic Cancer Genetic Testing: An Alternative to Population-Based Screening
Kenneth Offit, Kaitlyn Tkachuk, Zsofia K. Stadler, et al.
Journal of Clinical Oncology (2020) Vol. 38, Iss. 13, pp. 1398-1408
Open Access | Times Cited: 85
Use of a chatbot to increase uptake of cascade genetic testing
Tara Schmidlen, Claire L. Jones, Gemme Campbell‐Salome, et al.
Journal of Genetic Counseling (2022) Vol. 31, Iss. 5, pp. 1219-1230
Closed Access | Times Cited: 48
Aligning Policy to Promote Cascade Genetic Screening for Prevention and Early Diagnosis of Heritable Diseases
Rani Mary George, Karen Kovak, Summer L. Cox
Journal of Genetic Counseling (2015) Vol. 24, Iss. 3, pp. 388-399
Open Access | Times Cited: 87
Dealing with the unexpected: consumer responses to direct-accessBRCAmutation testing
Uta Francke, Cheri Dijamco, Amy K. Kiefer, et al.
PeerJ (2013) Vol. 1, pp. e8-e8
Open Access | Times Cited: 82
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
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
Sociodemographic, psychosocial and clinical factors associated with uptake of genetic counselling for hereditary cancer: a systematic review
Amanda Willis, Sian K. Smith, Bettina Meiser, et al.
Clinical Genetics (2016) Vol. 92, Iss. 2, pp. 121-133
Open Access | Times Cited: 57
Exploring broad consent in the context of the 100,000 Genomes Project: a mixed methods study
Lisa Ballard, Rachel Horton, Sandi Dheensa, et al.
European Journal of Human Genetics (2020) Vol. 28, Iss. 6, pp. 732-741
Open Access | Times Cited: 41
Cascade Genetic Testing for Hereditary Cancer Risk: An Underutilized Tool for Cancer Prevention
Kristen Whitaker, Elias Obeid, Mary B. Daly, et al.
JCO Precision Oncology (2021), Iss. 5, pp. 1387-1396
Open Access | Times Cited: 39
Interventions to support patients with sharing genetic test results with at-risk relatives: a synthesis without meta-analysis (SWiM)
Lisa Ballard, Rebecca Band, Anneke Lucassen
European Journal of Human Genetics (2023) Vol. 31, Iss. 9, pp. 988-1002
Open Access | Times Cited: 14
The structural basis for cancer treatment decisions
Ruth Nussinov, Hyunbum Jang, Chung‐Jung Tsai
Oncotarget (2014) Vol. 5, Iss. 17, pp. 7285-7302
Open Access | Times Cited: 48
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
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
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
Sharing genetic test results with family members of BRCA, PALB2, CHEK2, and ATM carriers
Marleah Dean, Ann Tezak, Sabrina Johnson, et al.
Patient Education and Counseling (2021) Vol. 104, Iss. 4, pp. 720-725
Open Access | Times Cited: 32
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
Page 1 - Next Page

Scroll to top