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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:

Exome/Genome-Wide Testing in Newborn Screening: A Proportionate Path Forward
Vasiliki Rahimzadeh, Jan M. Friedman, Guido de Wert, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 11

Showing 11 citing articles:

Are We Ready for Whole Population Genomic Sequencing of Asymptomatic Newborns?
Danya F. Vears, Julian Savulescu, John Christodoulou, et al.
Pharmacogenomics and Personalized Medicine (2023) Vol. Volume 16, pp. 681-691
Open Access | Times Cited: 14
Genomic sequencing in newborn screening: balancing consent with the right of the asymptomatic at-risk child to be found
Bartha Maria Knoppers, Ana Eliza Bonilha, Anne‐Marie Laberge, et al.
European Journal of Human Genetics (2024)
Open Access | Times Cited: 3
Parents' and childrens’ views of wider genomic testing when used as part of newborn screening to identify cystic fibrosis
Jane Chudleigh, Pru Holder, C. C. Clark, et al.
SSM - Qualitative Research in Health (2024) Vol. 6, pp. 100455-100455
Closed Access | Times Cited: 3
The Australian landscape of newborn screening in the genomics era
Charli Ji, Michelle A. Farrar, Sarah Norris, et al.
Rare Disease and Orphan Drugs Journal (2023) Vol. 2, Iss. 4
Open Access | Times Cited: 8
Call to Action for Advancing Equitable Genomic Newborn Screening
Anne L. Ersig, Cheedy Jaja, Audrey Tluczek
Public Health Genomics (2023) Vol. 26, Iss. 1, pp. 188-193
Open Access | Times Cited: 5
Feasibility of Targeted Next-Generation DNA Sequencing for Expanding Population Newborn Screening
Bennett Oh Vic Shum, Carel Pretorius, Letitia M. F. Sng, et al.
Clinical Chemistry (2023) Vol. 69, Iss. 8, pp. 890-900
Closed Access | Times Cited: 4
Genetic Screening—Emerging Issues
Martina C. Cornel, Karuna R. M. van der Meij, Carla van El, et al.
Genes (2024) Vol. 15, Iss. 5, pp. 581-581
Open Access | Times Cited: 1
Non-Genetic Healthcare Providers’ Experiences and Perspectives with Rapid Genome-Wide Sequencing in Canadian Neonatal Intensive Care Units
Lauren Piers, Tasha Wainstein, Gustavo Pelligra, et al.
Children (2024) Vol. 11, Iss. 8, pp. 910-910
Open Access | Times Cited: 1
Prospects for Expansion of Universal Newborn Screening in Bulgaria: A Survey among Medical Professionals
Георги Искров, Vyara Angelova, Boyan Bochev, et al.
International Journal of Neonatal Screening (2023) Vol. 9, Iss. 4, pp. 57-57
Open Access | Times Cited: 2
Genomic newborn screening - ethical questions and practical challenges
Věra Franková, Pavel Ješina
Česko-slovenská pediatrie (2024) Vol. 79, Iss. 6, pp. 349-352
Open Access
Implementing genomic newborn screening as an effective public health intervention: sidestepping the hype and criticism
Jan M. Friedman
npj Genomic Medicine (2024) Vol. 9, Iss. 1
Open Access
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