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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:

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

Showing 1-25 of 93 citing articles:

2023 ESC Guidelines for the management of cardiomyopathies
Elena Arbelo, Alexandros Protonotarios, Juan R. Gimeno, et al.
European Heart Journal (2023) Vol. 44, Iss. 37, pp. 3503-3626
Open Access | Times Cited: 1021
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
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: 84
Psychosocial barriers and facilitators for cascade genetic testing in hereditary breast and ovarian cancer: a scoping review
Agani Afaya, Sung‐Won Kim, Hyung Seok Park, et al.
Familial Cancer (2024) Vol. 23, Iss. 2, pp. 121-132
Closed Access | Times Cited: 8
Public perspectives on healthcare professional-directed communication of hereditary genetic risks: a mixed-method systematic review
Lea Godino, Daniela Turchetti, Valentina Gentili, et al.
European Journal of Human Genetics (2025)
Closed Access | Times Cited: 1
Interventions Facilitating Family Communication of Genetic Testing Results and Cascade Screening in Hereditary Breast/Ovarian Cancer or Lynch Syndrome: A Systematic Review and Meta-Analysis
Vasiliki Baroutsou, Meghan Underhill‐Blazey, Christian Appenzeller‐Herzog, et al.
Cancers (2021) Vol. 13, Iss. 4, pp. 925-925
Open Access | Times Cited: 46
The challenges of the expanded availability of genomic information: an agenda-setting paper
Pascal Borry, Heidi Beate Bentzen, Isabelle Budin‐Ljøsne, et al.
Journal of Community Genetics (2017) Vol. 9, Iss. 2, pp. 103-116
Open Access | Times Cited: 60
Germline Genetic Testing for Breast Cancer Risk: The Past, Present, and Future
Siddhartha Yadav, Fergus J. Couch
American Society of Clinical Oncology Educational Book (2019), Iss. 39, pp. 61-74
Closed Access | Times Cited: 53
Does a proactive procedure lead to a higher uptake of predictive testing in families with a pathogenic BRCA1/BRCA2 variant? A family cancer clinic evaluation
Fred H. Menko, Sophie L. van der Velden, Diana N. Griffioen, et al.
Journal of Genetic Counseling (2023) Vol. 33, Iss. 3, pp. 615-622
Closed Access | Times Cited: 14
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
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
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
Uptake of Risk-Reducing Measures, Cascade Testing, and Related Challenges Among Carriers of Breast Cancer–Associated Germline Pathogenic Variants in Mexico
Fernanda Mesa-Chavez, Yanin Chávarri-Guerra, Dione Aguilar, et al.
JCO Global Oncology (2024), Iss. 10
Open Access | Times Cited: 4
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
Healthcare provider-mediated cascade testing of Lynch syndrome to at-risk family members: an interview study
Serene Ong, Zi Yang Chua, Jeanette Yuen, et al.
Familial Cancer (2025) Vol. 24, Iss. 1
Closed Access
Hypertrophic Cardiomyopathy: Genes and Mechanisms
Jinli Chen, Yang Xing, Jie Sun, et al.
Frontiers in Bioscience-Landmark (2025) Vol. 30, Iss. 2
Open Access
Perceptions and Use of Germline Genetic Testing Among Patients With Prostate Cancer
Laura B. Beidler, Kimberly Zayhowski, Mary Nahorniak, et al.
JCO Oncology Practice (2025)
Closed Access
Attitudes, knowledge and consequences of uncertain genetic findings in hypertrophic cardiomyopathy
Charlotte Burns, Laura Yeates, Catherine Spinks, et al.
European Journal of Human Genetics (2017) Vol. 25, Iss. 7, pp. 809-815
Open Access | Times Cited: 34
Communication of genetic information to families with inherited rhythm disorders
Charlotte Burns, Cynthia A. James, Jodie Ingles
Heart Rhythm (2017) Vol. 15, Iss. 5, pp. 780-786
Closed Access | Times Cited: 34
The big reveal: Family disclosure patterns of BRCA genetic test results among young Black women with invasive breast cancer
Claire C. Conley, Dana Ketcher, Maija Reblin, et al.
Journal of Genetic Counseling (2020) Vol. 29, Iss. 3, pp. 410-422
Open Access | Times Cited: 32
Talking with Children About Adult‐Onset Hereditary Cancer Risk: A Developmental Approach for Parents
Allison Werner‐Lin, Shana L. Merrill, Amanda Brandt
Journal of Genetic Counseling (2018) Vol. 27, Iss. 3, pp. 533-548
Closed Access | Times Cited: 31
The uptake of predictive DNA testing in 40 families with a pathogenic BRCA1/BRCA2 variant. An evaluation of the proband-mediated procedure
Fred H. Menko, Kiki N. Jeanson, Eveline M. A. Bleiker, et al.
European Journal of Human Genetics (2020) Vol. 28, Iss. 8, pp. 1020-1027
Open Access | Times Cited: 26
What guidance does HIPAA offer to providers considering familial risk notification and cascade genetic testing?
Nora B. Henrikson, Jennifer K. Wagner, Heather Hampel, et al.
Journal of Law and the Biosciences (2020) Vol. 7, Iss. 1
Open Access | Times Cited: 25
Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in Sweden
Andréas Andersson, Carolina Hawranek, Anna Öfverholm, et al.
Hereditary Cancer in Clinical Practice (2020) Vol. 18, Iss. 1
Open Access | Times Cited: 24
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