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:

Communicating genetic information in families – a review of guidelines and position papers
Laura Forrest, Martin B. Delatycki, Loane Skene, et al.
European Journal of Human Genetics (2007) Vol. 15, Iss. 6, pp. 612-618
Open Access | Times Cited: 127

Showing 1-25 of 127 citing articles:

Defeating Alzheimer's disease and other dementias: a priority for European science and society
Bengt Winblad, Philippe Amouyel, Sandrine Andrieu, et al.
The Lancet Neurology (2016) Vol. 15, Iss. 5, pp. 455-532
Open Access | Times Cited: 1497
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
Familial hypercholesterolaemia: A model of care for Australasia
Gerald F. Watts, David Sullivan, Nicola Poplawski, et al.
Atherosclerosis Supplements (2011) Vol. 12, Iss. 2, pp. 221-263
Closed Access | Times Cited: 196
Role of Genetic Testing in Inherited Cardiovascular Disease
Allison L. Cirino, Stephanie Harris, Neal K. Lakdawala, et al.
JAMA Cardiology (2017) Vol. 2, Iss. 10, pp. 1153-1153
Open Access | Times Cited: 96
Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations
Susan M. Wolf, Rebecca Branum, Barbara A. Koenig, et al.
The Journal of Law Medicine & Ethics (2015) Vol. 43, Iss. 3, pp. 440-463
Open Access | Times Cited: 94
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
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
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
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
Highly prevalent TP53 mutation predisposing to many cancers in the Brazilian population: a case for newborn screening?
Maria Isabel Achatz, Pierre Hainaut, Patrícia Ashton‐Prolla
The Lancet Oncology (2009) Vol. 10, Iss. 9, pp. 920-925
Closed Access | Times Cited: 73
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
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
Recommendations for neonatologists and pediatricians working in first level birthing centers on the first communication of genetic disease and malformation syndrome diagnosis: consensus issued by 6 Italian scientific societies and 4 parents’ associations
Gregorio Serra, Luigi Memo, Alessandra Coscia, et al.
˜The œItalian Journal of Pediatrics/Italian journal of pediatrics (2021) Vol. 47, Iss. 1
Open Access | Times Cited: 34
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
Disclosure of Genetic Information Within Families
Agatha M. Gallo, Denise B. Angst, Kathleen A. Knafl
AJN American Journal of Nursing (2009) Vol. 109, Iss. 4, pp. 65-69
Open Access | Times Cited: 60
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
Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists
Fred H. Menko, Cora M. Aalfs, Lidewij Henneman, et al.
Familial Cancer (2013) Vol. 12, Iss. 2, pp. 319-324
Closed Access | Times Cited: 45
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
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
Ethical challenges in nephrology: a call for action
Dominique Martin, David C.H. Harris, Vivekanand Jha, et al.
Nature Reviews Nephrology (2020) Vol. 16, Iss. 10, pp. 603-613
Open Access | Times Cited: 33
Disclosure of genetic information to family members: a systematic review of normative documents
Amicia Phillips, Pascal Borry, Ine Van Hoyweghen, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 11, pp. 2038-2046
Open Access | Times Cited: 29
National Experiences from 30 Years of Provider-Mediated Cascade Testing in Lynch Syndrome Families—The Danish Model
Lars Joachim Lindberg, Karin Wadt, Christina Therkildsen, et al.
Cancers (2024) Vol. 16, Iss. 8, pp. 1577-1577
Open Access | Times Cited: 4
How young people find out about their family history of Huntington's disease
Karen Forrest Keenan, Edwin van Teijlingen, Martin McKee, et al.
Social Science & Medicine (2009) Vol. 68, Iss. 10, pp. 1892-1900
Closed Access | Times Cited: 53
Page 1 - Next Page

Scroll to top