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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:

Genomic architecture of autism from comprehensive whole-genome sequence annotation
Brett Trost, Bhooma Thiruvahindrapuram, Ada J. S. Chan, et al.
Cell (2022) Vol. 185, Iss. 23, pp. 4409-4427.e18
Open Access | Times Cited: 152

Showing 1-25 of 152 citing articles:

The microbiota–gut–brain axis and neurodevelopmental disorders
Qinwen Wang, Qianyue Yang, Xingyin Liu
Protein & Cell (2023) Vol. 14, Iss. 10, pp. 762-775
Open Access | Times Cited: 101
Single-cell genomics meets human genetics
Anna Cuomo, Aparna Nathan, Soumya Raychaudhuri, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 8, pp. 535-549
Closed Access | Times Cited: 72
The contributions of rare inherited and polygenic risk to ASD in multiplex families
Matilde Cirnigliaro, Timothy S. Chang, Stephanie A. Arteaga, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 31
Open Access | Times Cited: 50
Sequence composition changes in short tandem repeats: heterogeneity, detection, mechanisms and clinical implications
Indhu‐Shree Rajan‐Babu, Egor Dolzhenko, Michael A. Eberle, et al.
Nature Reviews Genetics (2024) Vol. 25, Iss. 7, pp. 476-499
Closed Access | Times Cited: 26
Autism-Associated Genes and Neighboring lncRNAs Converge on Key Gene Regulatory Networks
Rebecca Andersen, Maya Talukdar, T. Sakamoto, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access | Times Cited: 2
A full semantic toolbox is essential for autism research and practice to thrive
Alison Singer, Amy S. F. Lutz, Jill Escher, et al.
Autism Research (2022) Vol. 16, Iss. 3, pp. 497-501
Open Access | Times Cited: 54
CTNNB1 in neurodevelopmental disorders
Wenting Zhuang, Tong Ye, Wei Wang, et al.
Frontiers in Psychiatry (2023) Vol. 14
Open Access | Times Cited: 37
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: 14
Focusing on mitochondria in the brain: from biology to therapeutics
Nanshan Song, Shuyuan Mei, Xiang-Xu Wang, et al.
Translational Neurodegeneration (2024) Vol. 13, Iss. 1
Open Access | Times Cited: 13
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates
Marta Viggiano, Fabiola Ceroni, Paola Visconti, et al.
npj Genomic Medicine (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 9
Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations
Marina Natividad Avila, Seulgi Jung, F. Kyle Satterstrom, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access | Times Cited: 1
The emergence of artificial intelligence in autism spectrum disorder research: A review of neuro imaging and behavioral applications
i b, P. M. Durai Raj Vincent
Computer Science Review (2025) Vol. 56, pp. 100718-100718
Closed Access | Times Cited: 1
Longitudinal Analysis of Cancer Risk in Children and Adults With Germline PTEN Variants
Lamis Yehia, Gilman Plitt, Ann M. Tushar, et al.
JAMA Network Open (2023) Vol. 6, Iss. 4, pp. e239705-e239705
Open Access | Times Cited: 21
Gene copy number variation and pediatric mental health/neurodevelopment in a general population
Mehdi Zarrei, Christie L. Burton, Worrawat Engchuan, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 15, pp. 2411-2421
Open Access | Times Cited: 17
Genome-wide association study between copy number variation and feeding behavior, feed efficiency, and growth traits in Nellore cattle
Lorena Ferreira Benfica, Luiz F. Brito, Djalma Rabelo Ricardo, et al.
BMC Genomics (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 7
Compensation between FOXP transcription factors maintains proper striatal function
Newaz Ahmed, Nitin Khandelwal, Ashley G. Anderson, et al.
Cell Reports (2024) Vol. 43, Iss. 5, pp. 114257-114257
Open Access | Times Cited: 7
Microbiome–Gut–Mucosal–Immune–Brain Axis and Autism Spectrum Disorder (ASD): A Novel Proposal of the Role of the Gut Microbiome in ASD Aetiology
Amapola De Sales-Millán, José Felix Aguirre‐Garrido, Rina María González-Cervantes, et al.
Behavioral Sciences (2023) Vol. 13, Iss. 7, pp. 548-548
Open Access | Times Cited: 14
Modeling Autism Spectrum Disorders with Induced Pluripotent Stem Cell-Derived Brain Organoids
John Lenon de Souza Santos, Cecília de Almeida Araújo, Clarissa Araújo Gurgel Rocha, et al.
Biomolecules (2023) Vol. 13, Iss. 2, pp. 260-260
Open Access | Times Cited: 13
Synergistic hyperactivation of both mTORC1 and mTORC2 underlies the neural abnormalities of PTEN-deficient human neurons and cortical organoids
Navroop K. Dhaliwal, Octavia Yifang Weng, Xiaoxue Dong, et al.
Cell Reports (2024) Vol. 43, Iss. 5, pp. 114173-114173
Open Access | Times Cited: 5
Metabolic network analysis of pre-ASD newborns and 5-year-old children with autism spectrum disorder
Sai Sachin Lingampelly, Jane C. Naviaux, Luke S. Heuer, et al.
Communications Biology (2024) Vol. 7, Iss. 1
Open Access | Times Cited: 5
Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes
Dmitrijs Rots, Sanaa Choufani, Víctor Faùndes, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 8, pp. 1626-1642
Closed Access | Times Cited: 5
Whole genome sequencing analysis identifies sex differences of familial pattern contributing to phenotypic diversity in autism
Soo-Whee Kim, Hyeji Lee, Da Yea Song, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 5
Genome-wide association testing beyond SNPs
Laura Harris, Ellen M. McDonagh, Xiaolei Zhang, et al.
Nature Reviews Genetics (2024)
Closed Access | Times Cited: 5
Association Analysis of Rare CNTN5 Variants With Autism Spectrum Disorder in a Japanese Population
Abdul Fuad Hadi, Reza K. Arta, Itaru Kushima, et al.
Neuropsychopharmacology Reports (2025) Vol. 45, Iss. 1
Open Access
m6A‐mRNA Reader YTHDF2 Identified as a Potential Risk Gene in Autism With Disproportionate Megalencephaly
Sierra S. Nishizaki, Nicholas K. Haghani, Gabriana N. La, et al.
Autism Research (2025)
Open Access
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