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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:

Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders
Zhonghua Hu, Xiao Xiao, Zhuohua Zhang, et al.
Molecular Psychiatry (2019) Vol. 24, Iss. 10, pp. 1400-1414
Closed Access | Times Cited: 76

Showing 1-25 of 76 citing articles:

The cell biology of synapse formation
Thomas C. Südhof
The Journal of Cell Biology (2021) Vol. 220, Iss. 7
Open Access | Times Cited: 249
Neurexins: molecular codes for shaping neuronal synapses
Andrea M. Gomez, Lisa Traunmüller, Peter Scheiffele
Nature reviews. Neuroscience (2021) Vol. 22, Iss. 3, pp. 137-151
Open Access | Times Cited: 156
Pleiotropy and Cross-Disorder Genetics Among Psychiatric Disorders
Phil H. Lee, Yen‐Chen Anne Feng, Jordan W. Smoller
Biological Psychiatry (2020) Vol. 89, Iss. 1, pp. 20-31
Open Access | Times Cited: 121
Autism spectrum disorder and schizophrenia: An updated conceptual review
Amandeep Jutla, Jennifer H. Foss‐Feig, Jeremy Veenstra‐VanderWeele
Autism Research (2021) Vol. 15, Iss. 3, pp. 384-412
Open Access | Times Cited: 85
Copy number variation and neuropsychiatric illness
Elliott Rees, George Kirov
Current Opinion in Genetics & Development (2021) Vol. 68, pp. 57-63
Open Access | Times Cited: 72
Autism Spectrum Disorder: Focus on Glutamatergic Neurotransmission
Martina Montanari, Giuseppina Martella, Paola Bonsi, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 7, pp. 3861-3861
Open Access | Times Cited: 64
GluD1 is a signal transduction device disguised as an ionotropic receptor
Jinye Dai, Christopher Patzke, Kifayathullah Liakath‐Ali, et al.
Nature (2021) Vol. 595, Iss. 7866, pp. 261-265
Open Access | Times Cited: 63
Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derivedNRXN1-mutant neurons
ChangHui Pak, Tamás Dankó, Vincent R. Mirabella, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 22
Open Access | Times Cited: 59
A sex-specific genome-wide association study of depression phenotypes in UK Biobank
Patrícia Pelufo Silveira, Irina Pokhvisneva, David M. Howard, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 6, pp. 2469-2479
Open Access | Times Cited: 32
Neurexin-2: An inhibitory neurexin that restricts excitatory synapse formation in the hippocampus
Pei-Yi Lin, Lulu Y. Chen, Man Jiang, et al.
Science Advances (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 29
Synapse organizers as molecular codes for synaptic plasticity
Steven A. Connor, Tabrez J. Siddiqui
Trends in Neurosciences (2023) Vol. 46, Iss. 11, pp. 971-985
Closed Access | Times Cited: 24
The genome-wide risk alleles for psychiatric disorders at 3p21.1 show convergent effects on mRNA expression, cognitive function, and mushroom dendritic spine
Zhihui Yang, Danyang Zhou, Huijuan Li, et al.
Molecular Psychiatry (2019) Vol. 25, Iss. 1, pp. 48-66
Closed Access | Times Cited: 72
Neurexins in autism and schizophrenia—a review of patient mutations, mouse models and potential future directions
Alisha Tromp, Bryan Mowry, Jean Giacomotto
Molecular Psychiatry (2020) Vol. 26, Iss. 3, pp. 747-760
Open Access | Times Cited: 69
Analyses of the autism-associated neuroligin-3 R451C mutation in human neurons reveal a gain-of-function synaptic mechanism
Le Wang, Vincent R. Mirabella, Rujia Dai, et al.
Molecular Psychiatry (2022) Vol. 29, Iss. 6, pp. 1620-1635
Open Access | Times Cited: 23
Chromosome-Level Genome Assembly of the Meishan Pig and Insights into Its Domestication Mechanisms
Hui-Peng Du, Jianchao Hu, Zhiyan Zhang, et al.
Animals (2025) Vol. 15, Iss. 4, pp. 603-603
Open Access
A Complex Network of Obesity‐Risk Genes Revealed by Systematic Bioinformatics and Single‐Cell Transcriptomic Analyses
Y. Liu, Honglei Yuan, Junhui Hu, et al.
Journal of Obesity (2025) Vol. 2025, Iss. 1
Open Access
Antioxidant-Effective Quercetin Through Modulation of Brain Interleukin-13 Mitigates Autistic-Like Behaviors in the Propionic Acid-Induced Autism Model in Rats
Kubilay Doğan Kılıç, Gökçen Garipoğlu, Burak Çakar, et al.
Journal of Neuroimmune Pharmacology (2025) Vol. 20, Iss. 1
Open Access
Landscape of NRXN1 Gene Variants in Phenotypic Manifestations of Autism Spectrum Disorder: A Systematic Review
Jaimee Cooper, Jeenu Mittal, Akhila Sangadi, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 7, pp. 2067-2067
Open Access | Times Cited: 4
Chronic stress induces depression through MDGA1-Neuroligin2 mediated suppression of inhibitory synapses in the lateral habenula
Xuehui Wang, Wei Hao, Zhe Hu, et al.
Theranostics (2025) Vol. 15, Iss. 5, pp. 1842-1863
Open Access
Identification and characterization of mitochondrial autophagy-related genes in osteosarcoma and predicting clinical prognosis
Hongliang Zhang, Jingyu Zhang, Kai Zhu, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Disrupted synaptic gene expression in Fabry disease: Findings from RNA sequencing
Laura López-Valverde, M.E. Vázquez-Mosquera, Cristóbal Colón, et al.
Neurobiology of Disease (2025) Vol. 209, pp. 106908-106908
Open Access
Targeted splicing approach for alleviation of a neurexin 1 haploinsufficiency model
H. Peter Lu, Kyle M. Roddick, Yuan Ge, et al.
Molecular Psychiatry (2025)
Closed Access
Maternal immune activation targeted to a window of parvalbumin interneuron development improves spatial working memory: Implications for autism
Jay Nakamura, Brendan Gillespie, Andrew S. Gibbons, et al.
Brain Behavior and Immunity (2020) Vol. 91, pp. 339-349
Closed Access | Times Cited: 28
Analyzing schizophrenia-related phenotypes in mice caused by autoantibodies against NRXN1α in schizophrenia
Hiroki Shiwaku, Shingo Katayama, Mengxuan Gao, et al.
Brain Behavior and Immunity (2023) Vol. 111, pp. 32-45
Open Access | Times Cited: 9
SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsy
Delnaz Roshandel, Eric J. Sanders, Amy Shakeshaft, et al.
npj Genomic Medicine (2023) Vol. 8, Iss. 1
Open Access | Times Cited: 9
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