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:

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

Showing 1-25 of 168 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
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 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
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
Distress among women receiving uninformativeBRCA1/2results: 12-month outcomes
Suzanne C. O’Neill, Christine Rini, Rachel E. Goldsmith, et al.
Psycho-Oncology (2009) Vol. 18, Iss. 10, pp. 1088-1096
Open Access | Times Cited: 104
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
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
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
How Often Do BRCA Mutation Carriers Tell Their Young Children of the Family's Risk for Cancer? A Study of Parental Disclosure of BRCA Mutations to Minors and Young Adults
Angela R. Bradbury, James J. Dignam, Comfort N. Ibe, et al.
Journal of Clinical Oncology (2007) Vol. 25, Iss. 24, pp. 3705-3711
Closed Access | Times Cited: 82
The Effect of BRCA Gene Testing on Family Relationships: A Thematic Analysis of Qualitative Interviews
Heather Douglas, Robert J. Hamilton, Robin E. Grubs
Journal of Genetic Counseling (2009) Vol. 18, Iss. 5, pp. 418-435
Open Access | Times Cited: 82
Sisters in hereditary breast and ovarian cancer families: communal coping, social integration, and psychological well‐being
Laura M. Koehly, June A. Peters, Natalia Kuhn, et al.
Psycho-Oncology (2008) Vol. 17, Iss. 8, pp. 812-821
Open Access | Times Cited: 77
Selection of family members for communication of cancer risk and barriers to this communication before and after genetic cancer risk assessment
Deborah J. MacDonald, Linda Sarna, Gwen van Servellen, et al.
Genetics in Medicine (2007) Vol. 9, Iss. 5, pp. 275-282
Open Access | Times Cited: 74
Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information
Gillian Nycum, Denise Avard, Bartha Maria Knoppers
European Journal of Human Genetics (2009) Vol. 17, Iss. 7, pp. 872-880
Open Access | Times Cited: 68
A whisper-game perspective on the family communication of DNA-test results: a retrospective study on the communication process of BRCA1/2-test results between proband and relatives
Joël Vos, Fred H. Menko, Anna M. Jansen, et al.
Familial Cancer (2010) Vol. 10, Iss. 1, pp. 87-96
Open Access | Times Cited: 54
Young adult daughters of BRCA1/2 positive mothers: What do they know about hereditary cancer and how much do they worry?
Andrea Farkas Patenaude, Nadine Tung, Paula D. Ryan, et al.
Psycho-Oncology (2013) Vol. 22, Iss. 9, pp. 2024-2031
Closed Access | Times Cited: 53
When parents disclose BRCA1/2 test results: Their communication and perceptions of offspring response
Angela R. Bradbury, Linda Patrick‐Miller, Brian L. Egleston, et al.
Cancer (2012) Vol. 118, Iss. 13, pp. 3417-3425
Open Access | Times Cited: 52
Specific Psychosocial Issues of Individuals Undergoing Genetic Counseling for Cancer – A Literature Review
Willem Eijzenga, Daniela Hahn, Neil K. Aaronson, et al.
Journal of Genetic Counseling (2013) Vol. 23, Iss. 2, pp. 133-146
Closed Access | Times Cited: 48
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
Page 1 - Next Page

Scroll to top