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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:

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

Showing 1-25 of 241 citing articles:

Strategies to Identify the Lynch Syndrome Among Patients With Colorectal Cancer
Uri Ladabaum, Grace Wang, Jonathan P. Terdiman, et al.
Annals of Internal Medicine (2011) Vol. 155, Iss. 2, pp. 69-69
Open Access | Times Cited: 330
Effects of communicating DNA-based disease risk estimates on risk-reducing behaviours
Theresa M. Marteau, David French, Simon J. Griffin, et al.
Cochrane library (2010)
Closed Access | Times Cited: 255
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
Uptake of Genetic Testing by Relatives of Lynch Syndrome Probands: A Systematic Review
Ravi Sharaf, Parvathi A. Myer, Christopher D Stave, et al.
Clinical Gastroenterology and Hepatology (2013) Vol. 11, Iss. 9, pp. 1093-1100
Closed Access | Times Cited: 130
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
Parents’ and children's communication about genetic risk: a qualitative study, learning from families’ experiences
Alison Metcalfe, Gill Plumridge, Jane Coad, et al.
European Journal of Human Genetics (2011) Vol. 19, Iss. 6, pp. 640-646
Open Access | Times Cited: 110
Uptake of genetic counselling and predictive DNA testing in hypertrophic cardiomyopathy
Imke Christiaans, Erwin Birnie, Gouke J. Bonsel, et al.
European Journal of Human Genetics (2008) Vol. 16, Iss. 10, pp. 1201-1207
Open Access | Times Cited: 104
Efficacy of a Web-Based Intelligent Tutoring System for Communicating Genetic Risk of Breast Cancer
Christopher R. Wolfe, Valerie F. Reyna, Colin L. Widmer, et al.
Medical Decision Making (2014) Vol. 35, Iss. 1, pp. 46-59
Open Access | Times Cited: 93
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
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
Patients’ perceptions and practices of informing relatives: a qualitative study within a randomised trial on healthcare-assisted risk disclosure
Charlotta Nääs, Jenny von Salomé, Anna Rosén
European Journal of Human Genetics (2024) Vol. 32, Iss. 4, pp. 448-455
Open Access | Times Cited: 6
Family letters are an effective way to inform relatives about inherited cardiac disease
Wilma P. van der Roest, José M. Pennings, Marian K. Bakker, et al.
American Journal of Medical Genetics Part A (2009) Vol. 149A, Iss. 3, pp. 357-363
Closed Access | Times Cited: 83
Genomic Inheritances: Disclosing Individual Research Results From Whole-Exome Sequencing to Deceased Participants’ Relatives
Ben Chan, Flavia M. Facio, Haley Eidem, et al.
The American Journal of Bioethics (2012) Vol. 12, Iss. 10, pp. 1-8
Open Access | Times Cited: 63
Outcomes of a randomised controlled trial of a complex genetic counselling intervention to improve family communication
Jan Hodgson, Sylvia A. Metcalfe, Clara Gaff, et al.
European Journal of Human Genetics (2015) Vol. 24, Iss. 3, pp. 356-360
Open Access | Times Cited: 58
The role of genetic testing in dyslipidaemia
Amanda J. Berberich, Robert A. Hegele
Pathology (2018) Vol. 51, Iss. 2, pp. 184-192
Open Access | Times Cited: 58
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
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
Family communication, genetic testing and colonoscopy screening in hereditary non‐polyposis colon cancer: a qualitative study
Siobhan McCann, Domhnall MacAuley, Yvonne Barnett, et al.
Psycho-Oncology (2009) Vol. 18, Iss. 11, pp. 1208-1215
Closed Access | Times Cited: 57
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
Sources of Uncertainty About Daughters’ Breast Cancer Risk that Emerge During Genetic Counseling Consultations
Carma L. Bylund, Carla L. Fisher, Dale E. Brashers, et al.
Journal of Genetic Counseling (2011) Vol. 21, Iss. 2, pp. 292-304
Open Access | Times Cited: 53
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
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
Addressing key issues in the consanguinity-related risk of autosomal recessive disorders in consanguineous communities: lessons from a qualitative study of British Pakistanis
Aliya Darr, Neil Small, Waqar Ahmad, et al.
Journal of Community Genetics (2015) Vol. 7, Iss. 1, pp. 65-79
Open Access | Times Cited: 41
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