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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:

All in the family: Evaluation of the process and content of sisters' communication about BRCA1 and BRCA2 genetic test results
Chanita Hughes, Caryn Lerman, Marc D. Schwartz, et al.
American Journal of Medical Genetics (2001) Vol. 107, Iss. 2, pp. 143-150
Closed Access | Times Cited: 206

Showing 1-25 of 206 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
To tell or not to tell: barriers and facilitators in family communication about genetic risk
Karen Forrest, SA Simpson, Wilson Bj, et al.
Clinical Genetics (2003) Vol. 64, Iss. 4, pp. 317-326
Closed Access | Times Cited: 365
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
Letting the family know: balancing ethics and effectiveness when notifying relatives about genetic testing for a familial disorder
Graeme Suthers
Journal of Medical Genetics (2005) Vol. 43, Iss. 8, pp. 665-670
Open Access | Times Cited: 177
Randomized Trial of Telegenetics vs. In‐Person Cancer Genetic Counseling: Cost, Patient Satisfaction and Attendance
Adam H. Buchanan, Santanu Datta, Celette Sugg Skinner, et al.
Journal of Genetic Counseling (2015) Vol. 24, Iss. 6, pp. 961-970
Open Access | Times Cited: 174
Sharing BRCA1/2 Test Results With First-Degree Relatives: Factors Predicting Who Women Tell
Andrea Farkas Patenaude, Michel Dorval, Lisa S. DiGianni, et al.
Journal of Clinical Oncology (2006) Vol. 24, Iss. 4, pp. 700-706
Open Access | Times Cited: 168
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
Characteristics of Health Information Gatherers, Disseminators, and Blockers Within Families at Risk of Hereditary Cancer: Implications for Family Health Communication Interventions
Laura M. Koehly, June A. Peters, Regina H. Kenen, et al.
American Journal of Public Health (2009) Vol. 99, Iss. 12, pp. 2203-2209
Open Access | Times Cited: 150
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
Medical Mistrust Influences Black Women’s Level of Engagement in BRCA1/2 Genetic Counseling and Testing
Vanessa B. Sheppard, Darren Mays, Kenneth P. Tercyak, et al.
Journal of the National Medical Association (2013) Vol. 105, Iss. 1, pp. 17-22
Open Access | Times Cited: 120
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
Family Communication about Genetic Risk: The Little That Is Known
Brenda J. Wilson, Karen Forrest, Edwin van Teijlingen, et al.
Public Health Genomics (2004) Vol. 7, Iss. 1, pp. 15-24
Closed Access | Times Cited: 169
A social network analysis of communication about hereditary nonpolyposis colorectal cancer genetic testing and family functioning.
Laura M. Koehly, Susan K. Peterson, Beatty G. Watts, et al.
PubMed (2003) Vol. 12, Iss. 4, pp. 304-13
Closed Access | Times Cited: 160
Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11
X. Jiao, Abeda Sultana, Prashant Garg, et al.
Journal of Medical Genetics (2006) Vol. 44, Iss. 1, pp. 64-68
Open Access | Times Cited: 151
Family communication about positive BRCA1 and BRCA2 genetic test results
Bobbi McGivern, Jessica N. Everett, Geoffrey G. Yager, et al.
Genetics in Medicine (2004) Vol. 6, Iss. 6, pp. 503-509
Open Access | Times Cited: 136
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
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
Known unknowns: building an ethics of uncertainty into genomic medicine
Ainsley J. Newson, Samantha Leonard, Alison Hall, et al.
BMC Medical Genomics (2016) Vol. 9, Iss. 1
Open Access | Times Cited: 81
Risk of Pancreatic Cancer in the Long-Term Prospective Follow-Up of Familial Pancreatic Cancer Kindreds
Nancy Porter, Daniel A. Laheru, Bryan Lau, et al.
JNCI Journal of the National Cancer Institute (2022) Vol. 114, Iss. 12, pp. 1681-1688
Open Access | Times Cited: 28
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
The Role of the Family in Genetic Testing: Theoretical Perspectives, Current Knowledge, and Future Directions
Susan K. Peterson
Health Education & Behavior (2005) Vol. 32, Iss. 5, pp. 627-639
Closed Access | Times Cited: 110
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