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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:

Patient-facing digital tools for delivering genetic services: a systematic review
Whiwon Lee, Salma Shickh, Daniel Assamad, et al.
Journal of Medical Genetics (2022) Vol. 60, Iss. 1, pp. 1-10
Open Access | Times Cited: 35

Showing 1-25 of 35 citing articles:

Shared Decision Making in the Care of Patients With Cancer
Salma Shickh, Konstantinos Leventakos, Mark A. Lewis, et al.
American Society of Clinical Oncology Educational Book (2023), Iss. 43
Open Access | Times Cited: 22
Finding the sweet spot: a qualitative study exploring patients’ acceptability of chatbots in genetic service delivery
Stephanie Luca, Marc Clausen, Angela Shaw, et al.
Human Genetics (2023) Vol. 142, Iss. 3, pp. 321-330
Open Access | Times Cited: 16
Genetic counseling workforce diversity, inclusion, and capacity in Australia and New Zealand
Anaita Kanga‐Parabia, Lucas Mitchell, Renee Smyth, et al.
Genetics in Medicine Open (2024) Vol. 2, pp. 101848-101848
Open Access | Times Cited: 7
Evaluation of the Rosa Chatbot Providing Genetic Information to Patients at Risk of Hereditary Breast and Ovarian Cancer: Qualitative Interview Study
Elen Siglen, Hildegunn Høberg‐Vetti, Mirjam Tonheim Augestad, et al.
Journal of Medical Internet Research (2023) Vol. 25, pp. e46571-e46571
Open Access | Times Cited: 13
BRCA genetic testing and counseling in breast cancer: how do we meet our patients’ needs?
Peter Dubsky, Christian Jackisch, Seock‐Ah Im, et al.
npj Breast Cancer (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 5
DNA-poli: design and development of a digital platform for family communication support and predictive genetic counseling on inherited diseases
Tessa Beinema, Marlies N. van Lingen, Lieke M. van den Heuvel, et al.
Patient Education and Counseling (2025), pp. 108746-108746
Closed Access
Clinician and Patient Perspectives on a Patient-Facing Online Breast Cancer Symptom Visualization Tool
Gillian Gresham, Michael Luu, N. Lynn Henry, et al.
JCO Clinical Cancer Informatics (2025), Iss. 9
Closed Access
Transforming neonatal care: a position paper on the potential of augmented and mixed reality
Pedro M. S. M. Rodrigues, Danieli Mayumi Kimura Leandro, Samuel Azevedo, et al.
Frontiers in Digital Health (2025) Vol. 7
Open Access
Genetics Adviser: The development and usability testing of a new patient digital health application to support clinical genomic testing
Marc Clausen, Suvetha Krishnapillai, Daena Hirjikaka, et al.
Genetics in Medicine Open (2024) Vol. 2, pp. 101814-101814
Open Access | Times Cited: 4
Experiences of perinatal genetic screening for people from migrant and refugee backgrounds: a scoping review
Anaita Kanga‐Parabia, Alison D. Archibald, Laura Biggs, et al.
European Journal of Human Genetics (2025)
Open Access
Uptake, utility and resource requirements of a genetic counselling telephone helpline within the BRCA-DIRECT digital pathway for mainstreamed BRCA testing in patients with breast cancer
Bethany Torr, Grace Kavanaugh, Monica Hamill, et al.
Journal of Medical Genetics (2025), pp. jmg-110428
Closed Access
Evolving cardiovascular genetic counseling needs in the era of precision medicine
Ana Morales, Jessica Goehringer, Despina Sanoudou
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 8
BRCA-DIRECT digital pathway for diagnostic germline genetic testing within a UK breast oncology setting: a randomised, non-inferiority trial
Bethany Torr, Christopher I. Jones, Grace Kavanaugh, et al.
British Journal of Cancer (2024)
Open Access | Times Cited: 2
From the patient to the population: Use of genomics for population screening
Chloe Mighton, Salma Shickh, Vernie Aguda, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 11
Workforce Implications of Increased Referrals to Hereditary Cancer Services in Canada: A Scenario-Based Analysis
Nick Dragojlovic, Kennedy Borle, Nicola Kopac, et al.
Current Oncology (2023) Vol. 30, Iss. 8, pp. 7241-7251
Open Access | Times Cited: 4
The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic results disclosure in diverse families
Sabrina A. Suckiel, Nicole Kelly, Jacqueline A. Odgis, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 12, pp. 2029-2041
Open Access | Times Cited: 4
Genetics providers’ perspectives on the use of digital tools in clinical practice
Whiwon Lee, Daena Hirjikaka, Sonya Grewal, et al.
Genetics in Medicine (2024) Vol. 26, Iss. 6, pp. 101122-101122
Closed Access | Times Cited: 1
Innovative Implementation Strategies for Familial Hypercholesterolemia Cascade Testing: The Impact of Genetic Counseling
Kelly Morgan, Gemme Campbell‐Salome, Nicole L. Walters, et al.
Journal of Personalized Medicine (2024) Vol. 14, Iss. 8, pp. 841-841
Open Access | Times Cited: 1
Genetic Predisposition to Myelodysplastic Syndrome: Genetic Counseling and Transplant Implications
Yi Liu, Kathleen A. Calzone, Lisa J. McReynolds
Seminars in Hematology (2024)
Closed Access | Times Cited: 1
Rectifying or Reinforcing? The (In)Equity Implications of Recontacting Practices in Genomic Medicine
Michael P. Mackley, Hanna Faghfoury, Lauren Chad
The Hastings Center Report (2024) Vol. 54, Iss. S2
Open Access | Times Cited: 1
A model for the return and referral of all clinically significant secondary findings of genomic sequencing
Rita Kodida, Emma Reble, Marc Clausen, et al.
Journal of Medical Genetics (2023) Vol. 60, Iss. 8, pp. 733-739
Closed Access | Times Cited: 3
BRCA-DIRECT digital pathway for diagnostic germline genetic testing within a UK breast oncology setting: a randomised, non-inferiority trial
Bethany Torr, Christopher I. Jones, Grace Kavanaugh, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Validation of a guidelines-based digital tool to assess the need for germline cancer genetic testing
Callan D. Russell, Ashley Daley, Durand R. Van Arnem, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Satisfaction with mode of delivery of genomic sequencing results in a diverse national sample of research participants through the Clinical Sequencing Evidence-Generating Research Consortium
Sarah Scollon, Jill O. Robinson, Eunji Jo, et al.
Genetics in Medicine (2024) Vol. 26, Iss. 9, pp. 101176-101176
Closed Access
Integrating ARAS with PyFWZIC to evaluate and benchmark patient-facing genetic services digital tools
Ghazala Bilquise, Samar Ibrahim
Neural Computing and Applications (2024) Vol. 36, Iss. 29, pp. 18201-18222
Closed Access
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