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:

Uptake of Genetic Testing Among Patients with Cancer At Risk for Lynch Syndrome in the National Health Interview Survey
Ky’Era V. Actkins, Swetha Srinivasan, Lisa P. Spees, et al.
Cancer Prevention Research (2021) Vol. 14, Iss. 10, pp. 927-932
Open Access | Times Cited: 10

Showing 10 citing articles:

Psychosocial factors impacting barriers and motivators to cancer genetic testing
Erika Hanson, Emerson Delacroix, Sarah Austin, et al.
Cancer Medicine (2023) Vol. 12, Iss. 8, pp. 9945-9955
Open Access | Times Cited: 14
Modifiable risk factors for cancer among people with lynch syndrome: an international, cross-sectional survey
Robert Power, Damien Doherty, Roberta Horgan, et al.
Hereditary Cancer in Clinical Practice (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 2
Sociodemographic and Clinical Characteristics Associated with Genetic Testing among Cancer Survivors: Evidence from Three Cancer Registries
Young‐Rock Hong, Ruixuan Wang, Guanming Chen, et al.
Public Health Genomics (2024) Vol. 27, Iss. 1, pp. 124-135
Open Access | Times Cited: 2
Incomplete Penetrance of Population-Based Genetic Screening Results in Electronic Health Record
Gai Elhanan, Daniel Kiser, Iva Neveux, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 6
A Canadian Provincial Screening Program for Lynch Syndrome
James Stone, Remington Winter, Deirdre Khan, et al.
The American Journal of Gastroenterology (2022) Vol. 118, Iss. 2, pp. 345-353
Closed Access | Times Cited: 4
Genetic Testing and/or Counseling for Colorectal Cancer by Health Insurance Type
Arian Mansur, Fang Zhang, Christine Y. Lu
Journal of Personalized Medicine (2022) Vol. 12, Iss. 7, pp. 1146-1146
Open Access | Times Cited: 3
Delivery of hereditary cancer genetics services to patients newly diagnosed with ovarian and endometrial cancers at three gynecologic oncology clinics in the USA, Brazil, and Mexico
Erica M. Bednar, Keiry A Paiz, Karen H. Lu, et al.
International Journal of Gynecological Cancer (2024) Vol. 34, Iss. 7, pp. 1020-1026
Closed Access
Poor compliance with germline testing recommendations in colorectal cancer patients undergoing molecular residual disease testing
Suzanne Schrock-Kelley, Vivienne Souter, Michael J. Hall, et al.
Communications Medicine (2024) Vol. 4, Iss. 1
Open Access
Identifying the psychosocial barriers and facilitators associated with the uptake of genetic services for hereditary cancer syndromes: a systematic review of qualitative studies
Sara Tasnim, Phoebe X. H. Lim, Konstadina Griva, et al.
Health Psychology Review (2024), pp. 1-28
Closed Access
A Scoring Model and Protocol to Adapt Universal Screening for Lynch Syndrome to Identify Germline Pathogenic Variants by Next Generation Sequencing from Colorectal Cancer Patients and Cascade Screening
Ramadhani Chambuso, Barbara Robertson, Raj Ramesar
Cancers (2022) Vol. 14, Iss. 12, pp. 2901-2901
Open Access | Times Cited: 2
Page 1

Scroll to top