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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:

Newborn screening for neurodevelopmental diseases: Are we there yet?
Wendy K. Chung, Jonathan S. Berg, Jeffrey R. Botkin, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 2, pp. 222-230
Open Access | Times Cited: 23

Showing 23 citing articles:

Genomic newborn screening for rare diseases
Zornitza Stark, Richard H. Scott
Nature Reviews Genetics (2023) Vol. 24, Iss. 11, pp. 755-766
Closed Access | Times Cited: 90
Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation
Fiona Lynch, Stephanie Best, Clara Gaff, et al.
International Journal of Neonatal Screening (2024) Vol. 10, Iss. 1, pp. 6-6
Open Access | Times Cited: 18
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
Unraveling Lifelong Brain Morphometric Dynamics: A Protocol for Systematic Review and Meta-Analysis in Healthy Neurodevelopment and Ageing
Yauhen Statsenko, Tetiana Habuza, Darya Smetanina, et al.
Biomedicines (2023) Vol. 11, Iss. 7, pp. 1999-1999
Open Access | Times Cited: 14
Prenatal gene editing for neurodevelopmental diseases: Ethical considerations
Rami Major, Eric T. Juengst
The American Journal of Human Genetics (2025)
Open Access
Newborn Screening for Duchenne Muscular Dystrophy: First Year Results of a Population-Based Pilot
M. J. Hartnett, Michele A. Lloyd-Puryear, Norma P. Tavakoli, et al.
International Journal of Neonatal Screening (2022) Vol. 8, Iss. 4, pp. 50-50
Open Access | Times Cited: 16
Newborn screening for Duchenne muscular dystrophy‐early detection and diagnostic algorithm for female carriers of Duchenne muscular dystrophy
Dorota Gruber, Michele A. Lloyd-Puryear, Niki Armstrong, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 2, pp. 197-205
Open Access | Times Cited: 16
An Opportunity to Fill a Gap for Newborn Screening of Neurodevelopmental Disorders
Wendy K. Chung, Stephen M. Kanne, Zhanzhi Hu
International Journal of Neonatal Screening (2024) Vol. 10, Iss. 2, pp. 33-33
Open Access | Times Cited: 3
The Multi-Omic Approach to Newborn Screening: Opportunities and Challenges
Alex Ashenden, Ayesha Chowdhury, Lucy T. Anastasi, et al.
International Journal of Neonatal Screening (2024) Vol. 10, Iss. 3, pp. 42-42
Open Access | Times Cited: 3
Integrative genetic analysis: cornerstone of precision psychiatry
Jacob Vorstman, Jonathan Sebat, Vincent-Raphaël Bourque, et al.
Molecular Psychiatry (2024)
Closed Access | Times Cited: 3
Newborn Screening for Neurodevelopmental Disorders May Exacerbate Health Disparities
Sarah A. Sobotka, Lainie Friedman Ross
PEDIATRICS (2023) Vol. 152, Iss. 4
Closed Access | Times Cited: 7
Parents' preferences for receiving and discussing prognostic genetic information regarding their children's neurodevelopmental condition: A qualitative study
Erin Turbitt, Meg Bourne, Alison McEwen, et al.
Developmental Medicine & Child Neurology (2023) Vol. 66, Iss. 7, pp. 872-881
Open Access | Times Cited: 4
Assessing the Benefits and Harms Associated with Early Diagnosis from the Perspective of Parents with Multiple Children Diagnosed with Duchenne Muscular Dystrophy
Oindrila Bhattacharyya, Nicola B. Campoamor, Niki Armstrong, et al.
International Journal of Neonatal Screening (2024) Vol. 10, Iss. 2, pp. 32-32
Open Access | Times Cited: 1
A Systematic Review of Methods and Practice for Integrating Maternal, Fetal, and Child Health Outcomes, and Family Spillover Effects into Cost-Utility Analyses
Ramesh Lamsal, E. Ann Yeh, Eleanor Pullenayegum, et al.
PharmacoEconomics (2024) Vol. 42, Iss. 8, pp. 843-863
Open Access | Times Cited: 1
Early Intervention services in the era of genomic medicine: setting a research agenda
Katherine E. MacDuffie, Betty Cohn, Paul S. Appelbaum, et al.
Pediatric Research (2024)
Open Access | Times Cited: 1
25 years of evolution and hurdles in electronic health records and interoperability in medical research: a comprehensive review (Preprint)
Yun Shen, Jiamin Yu, Jian Zhou, et al.
Journal of Medical Internet Research (2024) Vol. 27, pp. e59024-e59024
Open Access | Times Cited: 1
GENE TARGET: A framework for evaluating Mendelian neurodevelopmental disorders for gene therapy
Maya Chopra, Meera E. Modi, Kira A. Dies, et al.
Molecular Therapy — Methods & Clinical Development (2022) Vol. 27, pp. 32-46
Open Access | Times Cited: 7
25 Years of Evolution and Hurdles in Electronic Health Records and Interoperability in Medical Research: A Comprehensive Review (Preprint)
Yun Shen, Jiamin Yu, Jian Zhou, et al.
(2024)
Open Access
Discordant Prenatal Cell-Free DNA Screening vs. Diagnostic Results of Sex Chromosome Aneuploidies: Implications for Newborn Screening and Genetic Counseling
Susan Howell, Shanlee Davis, Billie Carstens, et al.
International Journal of Neonatal Screening (2024) Vol. 10, Iss. 3, pp. 48-48
Open Access
Further laboratory-based investigations for possible gene- or genome-based disorders
Moyra Smith
Elsevier eBooks (2024), pp. 41-77
Closed Access
Arguments for and against the whole-genome sequencing of newborns.
Csaba Szalai
PubMed (2023) Vol. 15, Iss. 10, pp. 6255-6263
Closed Access | Times Cited: 1
Spotted around the web: Chromosomal hot spots, parental stress, autism guidelines in Australia
Jill Adams, Peter Hess
The Transmitter (2022)
Closed Access
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