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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:

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

Showing 1-25 of 81 citing articles:

Towards a genomics-informed, real-time, global pathogen surveillance system
Jennifer L. Gardy, Nicholas J. Loman
Nature Reviews Genetics (2017) Vol. 19, Iss. 1, pp. 9-20
Open Access | Times Cited: 646
Genetic counselling in the era of genomic medicine
Christine Patch, Anna Middleton
British Medical Bulletin (2018) Vol. 126, Iss. 1, pp. 27-36
Open Access | Times Cited: 123
Patients’ views on variants of uncertain significance across indications
Kristin Clift, Sarah Macklin, Colin Halverson, et al.
Journal of Community Genetics (2019) Vol. 11, Iss. 2, pp. 139-145
Open Access | Times Cited: 70
Clinical and psychological outcomes of receiving a variant of uncertain significance from multigene panel testing or genomic sequencing: a systematic review and meta-analysis
Chloe Mighton, Salma Shickh, Elizabeth Uleryk, et al.
Genetics in Medicine (2020) Vol. 23, Iss. 1, pp. 22-33
Open Access | Times Cited: 61
A scoping review of practice recommendations for clinicians’ communication of uncertainty
Niki M. Medendorp, Anne M. Stiggelbout, Cora M. Aalfs, et al.
Health Expectations (2021) Vol. 24, Iss. 4, pp. 1025-1043
Open Access | Times Cited: 43
Understanding communication between patients and healthcare professionals regarding comprehensive biomarker testing in precision oncology: A scoping review
Theresia Pichler, Friederike Mumm, Navdeep Dehar, et al.
Cancer Medicine (2024) Vol. 13, Iss. 3
Open Access | Times Cited: 6
Ethics in genetic counselling
Angus Clarke, Carina Wallgren‐Pettersson
Journal of Community Genetics (2018) Vol. 10, Iss. 1, pp. 3-33
Open Access | Times Cited: 55
“Possibly positive or certainly uncertain?”: participants’ responses to uncertain diagnostic results from exome sequencing
Debra Skinner, Myra I. Roche, Karen E. Weck, et al.
Genetics in Medicine (2018) Vol. 20, Iss. 3, pp. 313-319
Open Access | Times Cited: 47
Reconceptualizing Autonomy for Bioethics
Lisa Dive, Ainsley J. Newson
Kennedy Institute of Ethics journal (2018) Vol. 28, Iss. 2, pp. 171-203
Open Access | Times Cited: 46
Ethical considerations in prenatal testing: Genomic testing and medical uncertainty
Anastasia Richardson, Kelly E. Ormond
Seminars in Fetal and Neonatal Medicine (2017) Vol. 23, Iss. 1, pp. 1-6
Closed Access | Times Cited: 45
Receiving results of uncertain clinical relevance from population genetic screening: systematic review & meta-synthesis of qualitative research
Faye Johnson, Fiona Ulph, Rhona MacLeod, et al.
European Journal of Human Genetics (2022) Vol. 30, Iss. 5, pp. 520-531
Open Access | Times Cited: 21
Is It Just for a Screening Program to Give People All the Information They Want?
Lisa Dive, Isabella Holmes, Ainsley J. Newson
The American Journal of Bioethics (2023) Vol. 23, Iss. 7, pp. 34-42
Closed Access | Times Cited: 12
Clinical metagenomics: ethical issues
Tess Johnson, Euzebiusz Jamrozik, Prashanth Ramachandran, et al.
Journal of Medical Microbiology (2025) Vol. 74, Iss. 2
Closed Access
Children and young people's understanding of inherited conditions and their attitudes towards genetic testing: A systematic review
Brittany C. McGill, Claire E. Wakefield, Janine Vetsch, et al.
Clinical Genetics (2018) Vol. 95, Iss. 1, pp. 10-22
Open Access | Times Cited: 36
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
Ethical issues in reproductive genetic carrier screening
Lisa Dive, Ainsley J. Newson
The Medical Journal of Australia (2020) Vol. 214, Iss. 4, pp. 165-165
Open Access | Times Cited: 30
Ethical considerations in gene selection for reproductive carrier screening
Lisa Dive, Alison D. Archibald, Ainsley J. Newson
Human Genetics (2021) Vol. 141, Iss. 5, pp. 1003-1012
Open Access | Times Cited: 25
Addressing ethical issues related to prenatal diagnostic procedures
Dan K. Kaye
Maternal Health Neonatology and Perinatology (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 9
Exome sequencing in clinical settings: preferences and experiences of parents of children with rare diseases (SEQUAPRE study)
Aline Chassagne, Aurore Pélissier, Françoise Houdayer, et al.
European Journal of Human Genetics (2019) Vol. 27, Iss. 5, pp. 701-710
Open Access | Times Cited: 26
Application of a framework to guide genetic testing communication across clinical indications
Miranda L. G. Hallquist, Eric P. Tricou, Kelly E. Ormond, et al.
Genome Medicine (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 22
Advanced genomic testing may aid in counseling of isolated agenesis of the corpus callosum on prenatal ultrasound
M. C. de Wit, Ferry Boekhorst, Grazia M.S. Mancini, et al.
Prenatal Diagnosis (2017) Vol. 37, Iss. 12, pp. 1191-1197
Closed Access | Times Cited: 28
The ethical plausibility of the ‘Right To Try’ laws
Daniele Carrieri, Fedro A. Peccatori, Giovanni Boniolo
Critical Reviews in Oncology/Hematology (2017) Vol. 122, pp. 64-71
Open Access | Times Cited: 25
Hope versus reality: Parent expectations of genomic testing
Katherine E. Donohue, Siobhan M. Dolan, Dana Watnick, et al.
Patient Education and Counseling (2021) Vol. 104, Iss. 8, pp. 2073-2079
Open Access | Times Cited: 20
Investigating the Adoption of Clinical Genomics in Australia. An Implementation Science Case Study
Stephanie Best, Janet C. Long, Clara Gaff, et al.
Genes (2021) Vol. 12, Iss. 2, pp. 317-317
Open Access | Times Cited: 18
Patient decision support resources inform decisions about cancer susceptibility genetic testing and risk management: a systematic review of patient impact and experience
Kelly Kohut, Katherine Morton, Lesley Turner, et al.
Frontiers in Health Services (2023) Vol. 3
Open Access | Times Cited: 7
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