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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:

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

Showing 1-25 of 151 citing articles:

Randomized Noninferiority Trial of Telephone Versus In-Person Genetic Counseling for Hereditary Breast and Ovarian Cancer
Mark D. Schwartz, Heiðdís Valdimarsdóttir, Beth N. Peshkin, et al.
Journal of Clinical Oncology (2014) Vol. 32, Iss. 7, pp. 618-626
Open Access | Times Cited: 241
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
CYP2C19 Genetic Testing for Oral P2Y12 Inhibitor Therapy: A Scientific Statement From the American Heart Association
Naveen L. Pereira, Sharon Cresci, Dominick J. Angiolillo, et al.
Circulation (2024) Vol. 150, Iss. 6
Closed Access | Times Cited: 23
Delivery Of Cascade Screening For Hereditary Conditions: A Scoping Review Of The Literature
Megan C. Roberts, W. David Dotson, Christopher S. DeVore, et al.
Health Affairs (2018) Vol. 37, Iss. 5, pp. 801-808
Open Access | Times Cited: 145
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
Barriers and facilitators for cascade testing in genetic conditions: a systematic review
Swetha Srinivasan, Nae Won, W. David Dotson, et al.
European Journal of Human Genetics (2020) Vol. 28, Iss. 12, pp. 1631-1644
Open Access | Times Cited: 113
Communicating genetic test results within the family: Is it lost in translation? A survey of relatives in the randomized six-step study
Mary B. Daly, Susan Montgomery, Ruth Bingler, et al.
Familial Cancer (2016) Vol. 15, Iss. 4, pp. 697-706
Open Access | Times Cited: 93
The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice
Fred H. Menko, Jacqueline A. ter Stege, Lizet E. van der Kolk, et al.
Familial Cancer (2018) Vol. 18, Iss. 1, pp. 127-135
Closed Access | Times Cited: 92
Communication of BRCA Results and Family Testing in 1,103 High-Risk Women
Eleanor Cheung, Ashley Olson, Tina M. Yu, et al.
Cancer Epidemiology Biomarkers & Prevention (2010) Vol. 19, Iss. 9, pp. 2211-2219
Open Access | Times Cited: 89
Family Communication of BRCA1/2 Results and Family Uptake of BRCA1/2 Testing in a Diverse Population of BRCA1/2 Carriers
Julia Fehniger, Feng Lin, Mary Beattie, et al.
Journal of Genetic Counseling (2013) Vol. 22, Iss. 5, pp. 603-612
Open Access | Times Cited: 88
Preparing individuals to communicate genetic test results to their relatives: report of a randomized control trial
Susan Montgomery, Andrea M. Barsevick, Brian L. Egleston, et al.
Familial Cancer (2013) Vol. 12, Iss. 3, pp. 537-546
Open Access | Times Cited: 87
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
Disparities in gynecologic cancer genetics evaluation
Emily Hinchcliff, Erica M. Bednar, Karen H. Lu, et al.
Gynecologic Oncology (2019) Vol. 153, Iss. 1, pp. 184-191
Open Access | Times Cited: 72
New Case Detection by Cascade Testing in Familial Hypercholesterolemia
Christopher Lee, Miriannie Rivera-Valerio, Hana Bangash, et al.
Circulation Genomic and Precision Medicine (2019) Vol. 12, Iss. 11
Open Access | Times Cited: 56
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
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
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
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
Genetic counseling for patients and families with hereditary breast and ovarian cancer in a developing Asian country: an observational descriptive study
Sook‐Yee Yoon, Meow‐Keong Thong, Nur Aishah Mohd Taib, et al.
Familial Cancer (2011) Vol. 10, Iss. 2, pp. 199-205
Closed Access | Times Cited: 52
Factors influencing uptake of familial long QT syndrome genetic testing
Charlotte Burns, Julie McGaughran, Andrew M. Davis, et al.
American Journal of Medical Genetics Part A (2015) Vol. 170, Iss. 2, pp. 418-425
Closed Access | Times Cited: 47
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
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 effect of a celebrity health disclosure on demand for health care: trends in BRCA testing and subsequent health services use
Megan C. Roberts, Stacie B. Dusetzina
Journal of Community Genetics (2017) Vol. 8, Iss. 2, pp. 141-146
Open Access | Times Cited: 40
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
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