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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:

De Novo Synonymous Mutations in Regulatory Elements Contribute to the Genetic Etiology of Autism and Schizophrenia
Atsushi Takata, Iuliana Ionita‐Laza, Joseph A. Gogos, et al.
Neuron (2016) Vol. 89, Iss. 5, pp. 940-947
Open Access | Times Cited: 137

Showing 26-50 of 137 citing articles:

Sequential Defects in Cardiac Lineage Commitment and Maturation Cause Hypoplastic Left Heart Syndrome
Markus Krane, Martina Dreßen, Gianluca Santamaria, et al.
Circulation (2021) Vol. 144, Iss. 17, pp. 1409-1428
Open Access | Times Cited: 42
Epigenetic Targets in Schizophrenia Development and Therapy
Agnieszka Wawrzczak‐Bargieła, Wiktor Bilecki, Marzena Maćkowiak
Brain Sciences (2023) Vol. 13, Iss. 3, pp. 426-426
Open Access | Times Cited: 17
Histone Lysine Methylation and Neurodevelopmental Disorders
Jeong‐Hoon Kim, Jang Yong Lee, Im‐Soon Lee, et al.
International Journal of Molecular Sciences (2017) Vol. 18, Iss. 7, pp. 1404-1404
Open Access | Times Cited: 60
Integrating evolutionary and regulatory information with a multispecies approach implicates genes and pathways in obsessive-compulsive disorder
Hyun Ji Noh, Ruqi Tang, Jason Flannick, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 60
The Yin and Yang of Autism Genetics: How Rare De Novo and Common Variations Affect Liability
Pauline Chaste, Kathryn Roeder, Bernie Devlin
Annual Review of Genomics and Human Genetics (2017) Vol. 18, Iss. 1, pp. 167-187
Open Access | Times Cited: 49
Neuronal Deletion of Kmt2a/Mll1 Histone Methyltransferase in Ventral Striatum is Associated with Defective Spike-Timing-Dependent Striatal Synaptic Plasticity, Altered Response to Dopaminergic Drugs, and Increased Anxiety
Erica Shen, Yan Jiang, Behnam Javidfar, et al.
Neuropsychopharmacology (2016) Vol. 41, Iss. 13, pp. 3103-3113
Open Access | Times Cited: 48
ARNT2 Tunes Activity-Dependent Gene Expression through NCoR2-Mediated Repression and NPAS4-Mediated Activation
Nikhil Sharma, Elizabeth A. Pollina, M. Aurel Nagy, et al.
Neuron (2019) Vol. 102, Iss. 2, pp. 390-406.e9
Open Access | Times Cited: 48
Molecular mechanisms underlying noncoding risk variations in psychiatric genetic studies
Xue Xiao, Hong Chang, Ming Li
Molecular Psychiatry (2017) Vol. 22, Iss. 4, pp. 497-511
Open Access | Times Cited: 46
Principles and methods of in-silico prioritization of non-coding regulatory variants
Phil H. Lee, Christian Lee, Xihao Li, et al.
Human Genetics (2017) Vol. 137, Iss. 1, pp. 15-30
Open Access | Times Cited: 45
Exonic splice regulation imposes strong selection at synonymous sites
Rosina Savisaar, Laurence D. Hurst
Genome Research (2018) Vol. 28, Iss. 10, pp. 1442-1454
Open Access | Times Cited: 44
Dysregulated Translation in Neurodevelopmental Disorders: An Overview of Autism‐Risk Genes Involved in Translation
Yan‐Chu Chen, Yu‐Wei Chang, Yi‐Shuian Huang
Developmental Neurobiology (2018) Vol. 79, Iss. 1, pp. 60-74
Open Access | Times Cited: 41
Advances in Biomarker Studies in Autism Spectrum Disorders
Liming Shen, Yuxi Zhao, Huajie Zhang, et al.
Advances in experimental medicine and biology (2019), pp. 207-233
Closed Access | Times Cited: 41
Regional Variation of Splicing QTLs in Human Brain
Yida Zhang, Harry Taegyun Yang, Kathryn E. Kadash-Edmondson, et al.
The American Journal of Human Genetics (2020) Vol. 107, Iss. 2, pp. 196-210
Open Access | Times Cited: 38
Rab2 drives axonal transport of dense core vesicles and lysosomal organelles
Viktor K. Lund, Matthew D. Lycas, Anders Schack, et al.
Cell Reports (2021) Vol. 35, Iss. 2, pp. 108973-108973
Open Access | Times Cited: 31
Decreased DNA methylation at promoters and gene-specific neuronal hypermethylation in the prefrontal cortex of patients with bipolar disorder
Miki Bundo, Junko Ueda, Yutaka Nakachi, et al.
Molecular Psychiatry (2021) Vol. 26, Iss. 7, pp. 3407-3418
Open Access | Times Cited: 29
FDPSM: Feature-Driven Prediction Modeling of Pathogenic Synonymous Mutations
Fangfang Jin, Na Cheng, Lihua Wang, et al.
Journal of Chemical Information and Modeling (2025)
Closed Access
Progress in Genetic Studies of Tourette’s Syndrome
Yan‐Jie Qi, Yi Zheng, Zhanjiang Li, et al.
Brain Sciences (2017) Vol. 7, Iss. 10, pp. 134-134
Open Access | Times Cited: 37
Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection
Antonio F. Pardiñas, Peter Holmans, Andrew Pocklington, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2016)
Open Access | Times Cited: 36
Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families
Andreas J. Forstner, Sascha B. Fischer, Lorena M. Schenk, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 32
Cell-Type-Specific Analysis of Molecular Pathology in Autism Identifies Common Genes and Pathways Affected Across Neocortical Regions
Dmitry Velmeshev, Marco Magistri, Emilia Maria Cristina Mazza, et al.
Molecular Neurobiology (2020) Vol. 57, Iss. 5, pp. 2279-2289
Closed Access | Times Cited: 29
Somatic synonymous mutations in regulatory elements contribute to the genetic aetiology of melanoma
Di Zhang, Junfeng Xia
BMC Medical Genomics (2020) Vol. 13, Iss. S5
Open Access | Times Cited: 26
Rab2 regulates presynaptic precursor vesicle biogenesis at the trans-Golgi
Torsten Götz, Dmytro Puchkov, Veronika Lysiuk, et al.
The Journal of Cell Biology (2021) Vol. 220, Iss. 5
Open Access | Times Cited: 23
Histone–lysine N-methyltransferase 2 (KMT2) complexes – a new perspective
Elżbieta Poręba, Krzysztof Leśniewicz, Julia Durzyńska
Mutation Research/Reviews in Mutation Research (2022) Vol. 790, pp. 108443-108443
Open Access | Times Cited: 16
Distorted neurocomputation by a small number of extra-large spines in psychiatric disorders
Kisho Obi-Nagata, Norimitsu Suzuki, Ryuhei Miyake, et al.
Science Advances (2023) Vol. 9, Iss. 23
Open Access | Times Cited: 8
A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility
Hiroki Kimura, Yuki Fujita, Takeshi Kawabata, et al.
Translational Psychiatry (2017) Vol. 7, Iss. 8, pp. e1214-e1214
Open Access | Times Cited: 28

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