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:
Expanded Newborn Screening Using Genome Sequencing for Early Actionable Conditions
Alban Ziegler, Carrie Koval‐Burt, Denise M. Kay, et al.
JAMA (2024)
Closed Access | Times Cited: 12
Alban Ziegler, Carrie Koval‐Burt, Denise M. Kay, et al.
JAMA (2024)
Closed Access | Times Cited: 12
Showing 12 citing articles:
Newborn Screening Using Genome Sequencing for Early Actionable Conditions—Reply
Alban Ziegler, Wendy K. Chung
JAMA (2025)
Closed Access | Times Cited: 1
Alban Ziegler, Wendy K. Chung
JAMA (2025)
Closed Access | Times Cited: 1
Newborn Screening Using Genome Sequencing for Early Actionable Conditions
Gujie Wu, Lin Cheng, Caiyun Lei
JAMA (2025)
Closed Access | Times Cited: 1
Gujie Wu, Lin Cheng, Caiyun Lei
JAMA (2025)
Closed Access | Times Cited: 1
DNA Sequencing in Newborn Screening: Opportunities, Challenges, and Future Directions
Médéric Jeanne, Wendy K. Chung
Clinical Chemistry (2025) Vol. 71, Iss. 1, pp. 77-86
Closed Access
Médéric Jeanne, Wendy K. Chung
Clinical Chemistry (2025) Vol. 71, Iss. 1, pp. 77-86
Closed Access
Situación actual y nuevos pasos en el cribado neonatal en España
María L. Couce, María Cernada, Héctor Boix, et al.
Anales de Pediatría (2025), pp. 503775-503775
Open Access
María L. Couce, María Cernada, Héctor Boix, et al.
Anales de Pediatría (2025), pp. 503775-503775
Open Access
Current situation and new steps in newborn screening in Spain
María L. Couce, María Cernada, Héctor Boix, et al.
Anales de Pediatría (English Edition) (2025), pp. 503775-503775
Open Access
María L. Couce, María Cernada, Héctor Boix, et al.
Anales de Pediatría (English Edition) (2025), pp. 503775-503775
Open Access
The new newborn screening
Wendy K. Chung
Nature Medicine (2025) Vol. 31, Iss. 4, pp. 1075-1076
Closed Access
Wendy K. Chung
Nature Medicine (2025) Vol. 31, Iss. 4, pp. 1075-1076
Closed Access
Rapid Whole-Genome Sequencing in Critically Ill Infants and Children with Suspected, Undiagnosed Genetic Diseases: Evolution to a First-Tier Clinical Laboratory Test in the Era of Precision Medicine
Rina Kansal
Children (2025) Vol. 12, Iss. 4, pp. 429-429
Open Access
Rina Kansal
Children (2025) Vol. 12, Iss. 4, pp. 429-429
Open Access
Erweitertes Neugeborenen- Screening mit Hilfe der Genomsequenzierung
Das Gesundheitswesen (2025) Vol. 87, Iss. 04, pp. 238-238
Closed Access
Das Gesundheitswesen (2025) Vol. 87, Iss. 04, pp. 238-238
Closed Access
The Path to Genomic Screening—Far From Simple, but the Journey Has Begun
Jonathan S. Berg
JAMA (2024)
Closed Access | Times Cited: 1
Jonathan S. Berg
JAMA (2024)
Closed Access | Times Cited: 1
Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trial
Stephen F. Kingsmore, Meredith S. Wright, L. Olsen, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 12, pp. 2643-2667
Closed Access | Times Cited: 1
Stephen F. Kingsmore, Meredith S. Wright, L. Olsen, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 12, pp. 2643-2667
Closed Access | Times Cited: 1
Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselection
Stephen F. Kingsmore, Meredith S. Wright, Laurie D. Smith, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 12, pp. 2618-2642
Closed Access | Times Cited: 1
Stephen F. Kingsmore, Meredith S. Wright, Laurie D. Smith, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 12, pp. 2618-2642
Closed Access | Times Cited: 1
Newborn Screening by DNA-First: Systematic Evaluation of the Eligibility of Inherited Metabolic Disorders Based on Treatability
Abigail Veldman, Birgit Sikkema‐Raddatz, Terry G. J. Derks, et al.
International Journal of Neonatal Screening (2024) Vol. 11, Iss. 1, pp. 1-1
Open Access
Abigail Veldman, Birgit Sikkema‐Raddatz, Terry G. J. Derks, et al.
International Journal of Neonatal Screening (2024) Vol. 11, Iss. 1, pp. 1-1
Open Access
