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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:

All for one and one for all: heterogeneity of genetic etiologies in neurodevelopmental psychiatric disorders
Daniel Moreno‐De‐Luca, Christa Lese Martin
Current Opinion in Genetics & Development (2021) Vol. 68, pp. 71-78
Open Access | Times Cited: 21

Showing 21 citing articles:

Contrastive machine learning reveals the structure of neuroanatomical variation within autism
Aidas Aglinskas, Joshua K. Hartshorne, Stefano Anzellotti
Science (2022) Vol. 376, Iss. 6597, pp. 1070-1074
Open Access | Times Cited: 63
Schizophrenia genomics: genetic complexity and functional insights
Patrick F. Sullivan, Shuyang Yao, Jens Hjerling‐Leffler
Nature reviews. Neuroscience (2024) Vol. 25, Iss. 9, pp. 611-624
Closed Access | Times Cited: 11
Machine Learning algorithm unveils glutamatergic alterations in the post-mortem schizophrenia brain
Arianna De Rosa, Andrea Fontana, Tommaso Nuzzo, et al.
Schizophrenia (2022) Vol. 8, Iss. 1
Open Access | Times Cited: 33
Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence
Jakub Kopál, Kuldeep Kumar, Karin Saltoun, et al.
Nature Human Behaviour (2023) Vol. 7, Iss. 6, pp. 1001-1017
Open Access | Times Cited: 14
Subcortical Brain Alterations in Carriers of Genomic Copy Number Variants
Kuldeep Kumar, Claudia Modenato, Clara Moreau, et al.
American Journal of Psychiatry (2023) Vol. 180, Iss. 9, pp. 685-698
Open Access | Times Cited: 12
Neural cell-types and circuits linking thermoregulation and social behavior
Joseph F. Rogers, Morgane Vandendoren, Jonathan F. Prather, et al.
Neuroscience & Biobehavioral Reviews (2024) Vol. 161, pp. 105667-105667
Open Access | Times Cited: 4
Shared Etiology in Autism Spectrum Disorder and Epilepsy with Functional Disability
Aqeela Zahra, Yunfu Wang, Qun Wang, et al.
Behavioural Neurology (2022) Vol. 2022, pp. 1-13
Open Access | Times Cited: 15
The future of disentangling the heterogeneity of autism with neuroimaging studies
Xujun Duan, Xiaolong Shan, Lucina Q. Uddin, et al.
Biological Psychiatry (2024)
Closed Access | Times Cited: 2
A Genetic Bridge Between Medicine and Neurodiversity for Autism
Claire S. Leblond, Thomas Rolland, Eli Barthome, et al.
Annual Review of Genetics (2024) Vol. 58, Iss. 1, pp. 487-512
Open Access | Times Cited: 2
Sex Differences in the Broad Autism Phenotype: Insights from the Australian Biobank
Blaise Di Mento, James Rufus John, Antonio Mendoza Diaz, et al.
Journal of Autism and Developmental Disorders (2024)
Open Access | Times Cited: 1
Advanced paternal age diversifies individual trajectories of vocalization patterns in neonatal mice
Lingling Mai, Hitoshi Inada, Ryuichi Kimura, et al.
iScience (2022) Vol. 25, Iss. 8, pp. 104834-104834
Open Access | Times Cited: 5
From Genes to Therapy in Autism Spectrum Disorder
Jacob Vorstman, Christine M. Freitag, Antonio M. Persico
Genes (2022) Vol. 13, Iss. 8, pp. 1377-1377
Open Access | Times Cited: 5
Genome-wide CNV analysis uncovers novel pathogenic regions in cohort of five multiplex families with neurodevelopmental disorders
Behjat Ul Mudassir, Mashael Alhumaidi Alotaibi, Nadeem Kizilbash, et al.
Heliyon (2023) Vol. 9, Iss. 9, pp. e19718-e19718
Open Access | Times Cited: 2
Rare CNVs and phenome-wide profiling: a tale of brain-structural divergence and phenotypical convergence
Jakub Kopál, Kuldeep Kumar, Karin Saltoun, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Closed Access | Times Cited: 3
Disentangling disorder-specific variation is key for precision psychiatry in autism
Aidas Aglinskas, Emily Schwartz, Stefano Anzellotti
Frontiers in Behavioral Neuroscience (2023) Vol. 17
Open Access | Times Cited: 1
Unlocking disease associations during prefrontal cortex development with scRNAseq
Kathryn Olivia Farley, Kevin G. Chen, Timo Lassmann
Research Square (Research Square) (2024)
Closed Access
Importance of copy number variants in childhood apraxia of speech and other speech sound disorders
E. Ricky Chan, Penelope Benchek, Gabrielle Miller, et al.
Communications Biology (2024) Vol. 7, Iss. 1
Open Access
Advanced paternal age diversifies individual trajectories of vocalization patterns in neonatal mice
Lingling Mai, Hitoshi Inada, Ryuichi Kimura, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access | Times Cited: 2
Psychiatry is the flagship of personalized and precision medicine: proposing an epistemic horizon to biological psychiatry
Ridha Joober
Journal of Psychiatry and Neuroscience (2022) Vol. 47, Iss. 6, pp. E447-E454
Open Access | Times Cited: 2
Subcortical brain alterations in carriers of genomic copy number variants
Kuldeep Kumar, Claudia Modenato, Clara Moreau, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Structural variation in families with speech and language disorder provides a deeper understanding of the genetic basis for naturally acquired speech
E. Ricky Chan, Penelope Benchek, Gabrielle Miller, et al.
Research Square (Research Square) (2023)
Closed Access
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