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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:

Molecular Diagnostic Yield of Exome Sequencing and Chromosomal Microarray in Cerebral Palsy
Siddharth Srivastava, Sara A. Lewis, Julie S. Cohen, et al.
JAMA Neurology (2022) Vol. 79, Iss. 12, pp. 1287-1287
Open Access | Times Cited: 53

Showing 1-25 of 53 citing articles:

Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy
Darcy Fehlings, Mehdi Zarrei, Worrawat Engchuan, et al.
Nature Genetics (2024) Vol. 56, Iss. 4, pp. 585-594
Closed Access | Times Cited: 17
Association of Social Determinants of Health With Genetic Test Request and Completion Rates in Children With Neurologic Disorders
Jordan J. Cole, Jonathan Williams, Angela D. Sellitto, et al.
Neurology (2025) Vol. 104, Iss. 5
Closed Access | Times Cited: 2
Redefining cerebral palsies as a diverse group of neurodevelopmental disorders with genetic aetiology
Clare L. van Eyk, Michael Fahey, Jozef Gécz
Nature Reviews Neurology (2023) Vol. 19, Iss. 9, pp. 542-555
Closed Access | Times Cited: 28
Exome sequencing reveals genetic heterogeneity and clinically actionable findings in children with cerebral palsy
Yangong Wang, Yiran Xu, Chongchen Zhou, et al.
Nature Medicine (2024) Vol. 30, Iss. 5, pp. 1395-1405
Closed Access | Times Cited: 11
Genetic investigations in cerebral palsy
Anna Basu, Karen Low, Thiloka Ratnaike, et al.
Developmental Medicine & Child Neurology (2024) Vol. 67, Iss. 2, pp. 177-185
Open Access | Times Cited: 7
Uncertainties Regarding Cerebral Palsy Diagnosis
Bhooma R. Aravamuthan, Darcy Fehlings, Iona Novak, et al.
Neurology Clinical Practice (2024) Vol. 14, Iss. 6
Closed Access | Times Cited: 6
All Patients With a Cerebral Palsy Diagnosis Merit Genomic Sequencing
Clare L. van Eyk, Suzanna C. MacLennan, Alastair H. MacLennan
JAMA Pediatrics (2023) Vol. 177, Iss. 5, pp. 455-455
Closed Access | Times Cited: 15
The Brain Gene Registry: a data snapshot
Dustin Baldridge, Levi Kaster, Catherine Sancimino, et al.
Journal of Neurodevelopmental Disorders (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 5
Bi-allelic variants in the ESAM tight-junction gene cause a neurodevelopmental disorder associated with fetal intracranial hemorrhage
Mauro Lecca, Davut Pehli̇van, Damián Heine‐Suñer, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 4, pp. 681-690
Open Access | Times Cited: 12
Advances in Chromosomal Microarray Analysis: Transforming Neurology and Neurosurgery
Wireko Andrew Awuah, Muhammad Hamza Shah, Vivek Sanker, et al.
Brain and Spine (2025), pp. 104197-104197
Open Access
Social Determinants of Genetics Referral and Completion Rates Among Pediatric Neurology Patients
Jordan J. Cole, Angela D. Sellitto, Laura Rosa Baratta, et al.
Pediatric Neurology (2025)
Closed Access
The Genetics of Cerebral Palsy
Marije Meuwissen, Katrien Janssens
(2025), pp. 75-86
Closed Access
Movement Disorders in Children
Elizabeth Pickup, Jordan Garris, Alonso Zea Vera
Physical Medicine and Rehabilitation Clinics of North America (2025)
Closed Access
Molecular Diagnostic Yield of Exome Sequencing and Chromosomal Microarray in Short Stature
Qing Li, Zefu Chen, Jie Wang, et al.
JAMA Pediatrics (2023) Vol. 177, Iss. 11, pp. 1149-1149
Closed Access | Times Cited: 10
Use of Computational Phenotypes for Predicting Genetic Subgroups of Cerebral Palsy
Imen F. Alkuraya, Alexandra Santana Almansa, Azubuike Eleonu, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
The Need to Standardize the Diagnosis of Cerebral Palsy
Bhooma R. Aravamuthan, Michael Fahey, Darcy Fehlings, et al.
PEDIATRICS (2025)
Closed Access
Clinical utility of a genetic diagnosis in individuals with cerebral palsy and related motor disorders
Alexandra Santana Almansa, Dustin L. Gable, Zoë Frazier, et al.
Annals of Clinical and Translational Neurology (2024) Vol. 11, Iss. 2, pp. 251-262
Open Access | Times Cited: 3
Diagnostic findings and yield of investigations for children with developmental regression
Kirsten Furley, Matthew F. Hunter, Michael Fahey, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 8
Open Access | Times Cited: 3
Inhibition of GSK3α,β rescues cognitive phenotypes in a preclinical mouse model of CTNNB1 syndrome
Jonathan Alexander, Leeanne Vazquez-Ramirez, Crystal Lin, et al.
EMBO Molecular Medicine (2024) Vol. 16, Iss. 9, pp. 2109-2131
Closed Access | Times Cited: 2
Genetic pathways in cerebral palsy: a review of the implications for precision diagnosis and understanding disease mechanisms
Yiran Xu, Yifei Li, Seidu A. Richard, et al.
Neural Regeneration Research (2023) Vol. 19, Iss. 7, pp. 1499-1508
Open Access | Times Cited: 4
Etiology and Ontogeny of Cerebral Palsy: Implications for Practice and Research
Mark I. Evans, David W. Britt, Lawrence D. Devoe
Reproductive Sciences (2023) Vol. 31, Iss. 5, pp. 1179-1189
Closed Access | Times Cited: 4
A bibliometric analysis of cerebral palsy from 2003 to 2022
Yue Hu, Yadan Zheng, Yue Yang, et al.
Frontiers in Neurology (2024) Vol. 15
Open Access | Times Cited: 1
Cerebral Palsy Heterogeneity: Clinical Characteristics and Diagnostic Significance from a Large-Sample Analysis
Junying Yuan, Mengli Cui, Qiongqiong Liang, et al.
Neuroepidemiology (2024), pp. 1-11
Open Access | Times Cited: 1
Potential clinical applications of advanced genomic analysis in cerebral palsy
Sara A. Lewis, Andrew Ruttenberg, Tuğçe Iyiyol, et al.
EBioMedicine (2024) Vol. 106, pp. 105229-105229
Open Access | Times Cited: 1
Survey of the Landscape of Society Practice Guidelines for Genetic Testing of Neurodevelopmental Disorders
Siddharth Srivastava, Jordan J. Cole, Julie S. Cohen, et al.
Annals of Neurology (2024) Vol. 96, Iss. 5, pp. 900-913
Open Access | Times Cited: 1
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