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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:

Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases
Niek de Klein, Ellen Tsai, Martijn Vochteloo, et al.
Nature Genetics (2023) Vol. 55, Iss. 3, pp. 377-388
Open Access | Times Cited: 143

Showing 1-25 of 143 citing articles:

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Wouter van Rheenen, Rick A. A. van der Spek, Mark K. Bakker, et al.
Nature Genetics (2021) Vol. 53, Iss. 12, pp. 1636-1648
Open Access | Times Cited: 385
Heart-brain connections: Phenotypic and genetic insights from magnetic resonance images
Bingxin Zhao, Tengfei Li, Zirui Fan, et al.
Science (2023) Vol. 380, Iss. 6648
Closed Access | Times Cited: 119
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
Remi Stevelink, Ciarán Campbell, Siwei Chen, et al.
Nature Genetics (2023) Vol. 55, Iss. 9, pp. 1471-1482
Open Access | Times Cited: 88
Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
Jonggeol Jeffrey Kim, Dan Vitale, Diego Véliz Otani, et al.
Nature Genetics (2023) Vol. 56, Iss. 1, pp. 27-36
Open Access | Times Cited: 79
GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors
Anna R. Docherty, Niamh Mullins, Allison E. Ashley‐Koch, et al.
American Journal of Psychiatry (2023) Vol. 180, Iss. 10, pp. 723-738
Open Access | Times Cited: 63
Proteo-genomics of soluble TREM2 in cerebrospinal fluid provides novel insights and identifies novel modulators for Alzheimer’s disease
Lihua Wang, Niko-Petteri Nykänen, Daniel Western, et al.
Molecular Neurodegeneration (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 22
Eye-brain connections revealed by multimodal retinal and brain imaging genetics
Bingxin Zhao, Yujue Li, Zirui Fan, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 17
Cell state-dependent allelic effects and contextual Mendelian randomization analysis for human brain phenotypes
Alexander Haglund, Verena Zuber, Maya Abouzeid, et al.
Nature Genetics (2025)
Open Access | Times Cited: 3
Massively parallel reporter assay investigates shared genetic variants of eight psychiatric disorders
Sool Lee, Jessica C. McAfee, Jiseok Lee, et al.
Cell (2025)
Closed Access | Times Cited: 2
A genetic link between risk for Alzheimer's disease and severe COVID-19 outcomes via the OAS1 gene
Naciye Magusali, Andrew Graham, Thomas M. Piers, et al.
Brain (2021) Vol. 144, Iss. 12, pp. 3727-3741
Open Access | Times Cited: 87
Evaluating the efficacy and mechanism of metformin targets on reducing Alzheimer’s disease risk in the general population: a Mendelian randomisation study
Jie Zheng, Min Xu, Venexia Walker, et al.
Diabetologia (2022) Vol. 65, Iss. 10, pp. 1664-1675
Open Access | Times Cited: 65
Proteogenomic analysis of human cerebrospinal fluid identifies neurologically relevant regulation and informs causal proteins for Alzheimer’s disease
Carlos Cruchaga, Daniel Western, Jigyasha Timsina, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 26
From genetic associations to genes: methods, applications, and challenges
Ting Qi, Liyang Song, Yazhou Guo, et al.
Trends in Genetics (2024) Vol. 40, Iss. 8, pp. 642-667
Open Access | Times Cited: 15
Genome-wide association study identifies 30 obsessive-compulsive disorder associated loci
Nora I. Strom, Zachary F. Gerring, Marco Galimberti, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 12
Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects
Silva Kasela, François Aguet, Sarah Kim-Hellmuth, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 1, pp. 133-149
Open Access | Times Cited: 10
omicSynth: An open multi-omic community resource for identifying druggable targets across neurodegenerative diseases
Chelsea X. Alvarado, Mary B. Makarious, Cory A. Weller, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 1, pp. 150-164
Open Access | Times Cited: 9
Proteogenomic analysis of human cerebrospinal fluid identifies neurologically relevant regulation and implicates causal proteins for Alzheimer’s disease
Daniel Western, Jigyasha Timsina, Lihua Wang, et al.
Nature Genetics (2024) Vol. 56, Iss. 12, pp. 2672-2684
Open Access | Times Cited: 9
Brain cell-type shifts in Alzheimer’s disease, autism, and schizophrenia interrogated using methylomics and genetics
Chloe X. Yap, Daniel Vo, Matthew G. Heffel, et al.
Science Advances (2024) Vol. 10, Iss. 21
Open Access | Times Cited: 8
Spatially resolved mapping of cells associated with human complex traits
Liyang Song, Wenhao Chen, Junren Hou, et al.
Nature (2025)
Open Access | Times Cited: 1
Brain-trait-associated variants impact cell-type-specific gene regulation during neurogenesis
Nil Aygün, Angela L. Elwell, Dan Liang, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 9, pp. 1647-1668
Open Access | Times Cited: 49
Identification of genetic variants that impact gene co-expression relationships using large-scale single-cell data
Shuang Li, Katharina T. Schmid, Dylan H. de Vries, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 17
The ChickenGTEx pilot analysis: a reference of regulatory variants across 28 chicken tissues
Dailu Guan, Zhonghao Bai, Xiaoning Zhu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 17
Mendelian Randomization Using the Druggable Genome Reveals Genetically Supported Drug Targets for Psychiatric Disorders
Xiaoyan Li, Aotian Shen, Yiran Zhao, et al.
Schizophrenia Bulletin (2023) Vol. 49, Iss. 5, pp. 1305-1315
Open Access | Times Cited: 15
Inferring cell-type-specific causal gene regulatory networks during human neurogenesis
Nil Aygün, Dan Liang, Wesley L. Crouse, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 14
Genetic map of regional sulcal morphology in the human brain from UK biobank data
Benjamin B. Sun, Stephanie Loomis, Fabrizio Pizzagalli, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 19
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