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:
“A very big challenge”: a qualitative study to explore the early barriers and enablers to implementing a national genomic medicine service in England
Bettina Friedrich, Cecilia Vindrola‐Padros, Anneke Lucassen, et al.
Frontiers in Genetics (2024) Vol. 14
Open Access | Times Cited: 6
Bettina Friedrich, Cecilia Vindrola‐Padros, Anneke Lucassen, et al.
Frontiers in Genetics (2024) Vol. 14
Open Access | Times Cited: 6
Showing 6 citing articles:
Bridging the Divide: A Review on the Implementation of Personalized Cancer Medicine
Michele Masucci, Claes Karlsson, Lennart Blomqvist, et al.
Journal of Personalized Medicine (2024) Vol. 14, Iss. 6, pp. 561-561
Open Access | Times Cited: 5
Michele Masucci, Claes Karlsson, Lennart Blomqvist, et al.
Journal of Personalized Medicine (2024) Vol. 14, Iss. 6, pp. 561-561
Open Access | Times Cited: 5
The expanding global genomics landscape: Converging priorities from national genomics programs
Caitlin Howley, Matilda Haas, Wadha A. Al Muftah, et al.
The American Journal of Human Genetics (2025)
Open Access
Caitlin Howley, Matilda Haas, Wadha A. Al Muftah, et al.
The American Journal of Human Genetics (2025)
Open Access
Delivery of a national prenatal exome sequencing service in England: a mixed methods study exploring healthcare professionals’ views and experiences
Michelle Peter, Rhiannon Mellis, Hannah McInnes‐Dean, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 4
Michelle Peter, Rhiannon Mellis, Hannah McInnes‐Dean, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 4
Parental knowledge, attitudes, satisfaction and decisional conflict regarding whole genome sequencing in the Genomic Medicine Service: a multisite survey study in England
Ria Patel, Bettina Friedrich, Saskia C. Sanderson, et al.
Journal of Medical Genetics (2025), pp. jmg-110458
Closed Access
Ria Patel, Bettina Friedrich, Saskia C. Sanderson, et al.
Journal of Medical Genetics (2025), pp. jmg-110458
Closed Access
What does a consent conversation for whole genome sequencing look like in the NHS Genomic Medicine Service? An observational study
Holly Ellard, Huda Alfardus, Saskia C. Sanderson, et al.
European Journal of Human Genetics (2024)
Open Access | Times Cited: 2
Holly Ellard, Huda Alfardus, Saskia C. Sanderson, et al.
European Journal of Human Genetics (2024)
Open Access | Times Cited: 2
“I’m quite proud of how we’ve handled it”: health professionals’ experiences of returning additional findings from the 100,000 genomes project
Bethany Stafford‐Smith, Jana Gurasashvili, Michelle Peter, et al.
European Journal of Human Genetics (2024)
Open Access | Times Cited: 1
Bethany Stafford‐Smith, Jana Gurasashvili, Michelle Peter, et al.
European Journal of Human Genetics (2024)
Open Access | Times Cited: 1
