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:
Opposing white matter microstructure abnormalities in 22q11.2 deletion and duplication carriers
Johanna Seitz‐Holland, M Lyons, Leila Kushan, et al.
Translational Psychiatry (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 7
Johanna Seitz‐Holland, M Lyons, Leila Kushan, et al.
Translational Psychiatry (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 7
Showing 7 citing articles:
Matrix metalloproteinase 9 (MMP-9) activity, hippocampal extracellular free water, and cognitive deficits are associated with each other in early phase psychosis
Johanna Seitz‐Holland, Yasser Alemán‐Gómez, Kang Ik K. Cho, et al.
Neuropsychopharmacology (2024) Vol. 49, Iss. 7, pp. 1140-1150
Open Access | Times Cited: 6
Johanna Seitz‐Holland, Yasser Alemán‐Gómez, Kang Ik K. Cho, et al.
Neuropsychopharmacology (2024) Vol. 49, Iss. 7, pp. 1140-1150
Open Access | Times Cited: 6
Source‐based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome
Ruiyang Ge, Christopher R. K. Ching, Anne S. Bassett, et al.
Human Brain Mapping (2024) Vol. 45, Iss. 1
Open Access | Times Cited: 5
Ruiyang Ge, Christopher R. K. Ching, Anne S. Bassett, et al.
Human Brain Mapping (2024) Vol. 45, Iss. 1
Open Access | Times Cited: 5
Comparison of autism domains across thirty rare variant genotypes
Nabila M.H. Ali, Samuel J. R. A. Chawner, Leila Kushan, et al.
EBioMedicine (2025) Vol. 112, pp. 105521-105521
Open Access
Nabila M.H. Ali, Samuel J. R. A. Chawner, Leila Kushan, et al.
EBioMedicine (2025) Vol. 112, pp. 105521-105521
Open Access
An exploratory fetal MRI study examining the impact of 22q11.2 microdeletion syndrome on early brain growth
Daniel Cromb, Tom Finck, Alexandra F. Bonthrone, et al.
Journal of Neurodevelopmental Disorders (2025) Vol. 17, Iss. 1
Open Access
Daniel Cromb, Tom Finck, Alexandra F. Bonthrone, et al.
Journal of Neurodevelopmental Disorders (2025) Vol. 17, Iss. 1
Open Access
Neuroimaging Findings in Neurodevelopmental Copy Number Variants: Identifying Molecular Pathways to Convergent Phenotypes
Ana Isabel Silva, Friederike Ehrhart, Magnús Ö. Úlfarsson, et al.
Biological Psychiatry (2022) Vol. 92, Iss. 5, pp. 341-361
Open Access | Times Cited: 14
Ana Isabel Silva, Friederike Ehrhart, Magnús Ö. Úlfarsson, et al.
Biological Psychiatry (2022) Vol. 92, Iss. 5, pp. 341-361
Open Access | Times Cited: 14
Lifespan Normative Modeling of Brain Microstructure
Julio E. Villalón‐Reina, Alyssa H. Zhu, Sebastian M. Benavidez, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Julio E. Villalón‐Reina, Alyssa H. Zhu, Sebastian M. Benavidez, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
White matter microstructure alterations in idiopathic restless legs syndrome: a study combining crossing fiber-based and tensor-based approaches
Yibo Xue, Sangma Xie, Xun‐Heng Wang, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 3
Yibo Xue, Sangma Xie, Xun‐Heng Wang, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 3
