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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:

Current Status of Newborn Bloodspot Screening Worldwide 2024: A Comprehensive Review of Recent Activities (2020–2023)
Bradford L. Therrell, Carmencita D. Padilla, Gustavo Borrajo, et al.
International Journal of Neonatal Screening (2024) Vol. 10, Iss. 2, pp. 38-38
Open Access | Times Cited: 27

Showing 1-25 of 27 citing articles:

Current Advances and Challenges in Gene Therapies for Neurologic Disorders
Giulia Porcari, J. Collyer, Laura Adang, et al.
Neurology Genetics (2025) Vol. 11, Iss. 1
Closed Access | Times Cited: 1
Lessons of screening two million newborns for congenital adrenal hyperplasia: 10-year experience of the Minas Gerais Public Health Program
Cristina Botelho Barra, Gabrielly Souza Sena, Helena Pereira Oliveira, et al.
Jornal de Pediatria (2025)
Open Access | Times Cited: 1
Non-Uptake of Newborn Screening in Planned Homebirth Is Associated with Preventive Health Practices for Infants: A Retrospective Case-Control Study
Chen Stein‐Zamir, Hanna Shoob, Sandra Katan, et al.
International Journal of Neonatal Screening (2025) Vol. 11, Iss. 1, pp. 15-15
Open Access | Times Cited: 1
CFTR haplotype phasing using long-read genome sequencing from ultra-low input DNA
Neeru Gandotra, Antariksh Tyagi, Irina G. Tikhonova, et al.
Genetics in Medicine Open (2025), pp. 101962-101962
Open Access
Barriers to the Management of Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Kelsey B. Eitel, Patricia Y. Fechner
The Journal of Clinical Endocrinology & Metabolism (2025) Vol. 110, Iss. Supplement_1, pp. S67-S73
Open Access
Premarital spinal muscular atrophy screening program results from a province in the Black Sea region of Turkiye: Two years of experience
Feyza Nur Topcu Yenercag, Günay Kaya Tarhan
Research Square (Research Square) (2025)
Open Access
Optimizing Biotinidase Activity Assays: Insights From Clinical and Laboratory Evaluation From a Low-Middle Income Country
Hafsa Majid, Muhammad Umer Naeem Effendi, Lena Jafri, et al.
Cureus (2025)
Open Access
Evaluation of primary health care nurses’ knowledge and neonatal screening performance for phenylketonuria in Alexandria
Esraa Ismail, Wafaa Elarousy, Shaymaa Saeed Mohamed Badawe, et al.
BMC Nursing (2025) Vol. 24, Iss. 1
Open Access
Emergency Management of Intoxication‐Type Inherited Metabolic Disorders
James Dexter Tarr, Andrew A. M. Morris
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access
Tandem mass spectrometry in screening for inborn errors of metabolism: comprehensive bibliometric analysis
Victoria Kononets, Gulmira Zharmakhanova, Saule Balmagambetova, et al.
Frontiers in Pediatrics (2025) Vol. 13
Open Access
A public health success: newborn screening for congenital adrenal hyperplasia in a middle-income Brazilian state
Scott D Grosses
Jornal de Pediatria (2025)
Open Access
Perspective Chapter: Next-Generation Sequencing and Variant Cataloging for Screening and Diagnosis of Sphingolipidoses and Mucopolysaccharidoses
Irina Vlasova-St. Louis, Uri Barak, Svetlana F. Khaiboullina
IntechOpen eBooks (2025)
Closed Access
The Genomic Essential Competencies Expected for all Registered Nurses
Kathleen A. Calzone, Laurie Badzek
Nursing Clinics of North America (2025)
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
Early-Onset Inherited Metabolic Diseases: When Clinical Symptoms Precede Newborn Screening—Insights from Emilia-Romagna (Italy)
Giulia Montanari, Egidio Candela, Federico Baronio, et al.
Children (2025) Vol. 12, Iss. 4, pp. 464-464
Open Access
The value of large-scale programmes in human genomics
Ruth Horn, Angeliki Kerasidou, Jennifer Merchant
European Journal of Human Genetics (2025)
Open Access
The Establishment of Expanded Newborn Screening in Rural Areas of a Developing Country: A Model from Health Regions 7 and 8 in Thailand
Khunton Wichajarn, Nopporn Sawatjui, Prinya Prasongdee, et al.
International Journal of Neonatal Screening (2025) Vol. 11, Iss. 2, pp. 26-26
Open Access
Dried blood spots analysis for targeted and non-targeted exposomics
Vinicius Verri Hernandes, Maximilian Zeyda, Lukas Wisgrill, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Newborn screening for neuro-metabolic disorders: Strategies, clinical benefits, and prerequisites for program expansion
Ulrike Mütze, Svenja Scharré, Elena Schnabel, et al.
European Journal of Paediatric Neurology (2025)
Open Access
Urgent need for newborn targeted sequencing screening technology in Shandong Province, China
Jie Mu, Meng Sun, Yulin Li, et al.
World Journal of Pediatrics (2025)
Open Access
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
Wilson and Jungner Revisited: Are Screening Criteria Fit for the 21st Century?
Elena Schnabel, Ulrike Mütze, Nicola Dikow, et al.
International Journal of Neonatal Screening (2024) Vol. 10, Iss. 3, pp. 62-62
Open Access | Times Cited: 2
Adeno-associated Virus Serotype 9 Antibodies in Neonates and Young Children: Seroprevalence and Kinetics
Rudolf W. van Olden, Christophe Lo Bianco, Keith W. Dilly, et al.
Molecular Therapy — Methods & Clinical Development (2024) Vol. 32, Iss. 4, pp. 101344-101344
Open Access | Times Cited: 1
Consolidated Newborn Bloodspot Screening Efforts in Developing Countries in the Asia Pacific—2024
Bradford L. Therrell, Carmencita D. Padilla, Michelle E. Abadingo, et al.
International Journal of Neonatal Screening (2024) Vol. 11, Iss. 1, pp. 2-2
Open Access | Times Cited: 1
Patient organizations: advocating for timely newborn screening & improved quality of life
Helen Malherbe, Ritu Jain, Victoria Antoniadou, et al.
Rare Disease and Orphan Drugs Journal (2024) Vol. 3, Iss. 3
Open Access
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