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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:

A computational tool (H-MAGMA) for improved prediction of brain-disorder risk genes by incorporating brain chromatin interaction profiles
Nancy Y. A. Sey, Benxia Hu, Won Mah, et al.
Nature Neuroscience (2020) Vol. 23, Iss. 4, pp. 583-593
Open Access | Times Cited: 262

Showing 1-25 of 262 citing articles:

A mechanistic model and therapeutic interventions for COVID-19 involving a RAS-mediated bradykinin storm
Michael R. Garvin, Christiane Alvarez, J Izaak Miller, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 370
Stroke genetics informs drug discovery and risk prediction across ancestries
Aniket Mishra, Rainer Malik, Tsuyoshi Hachiya, et al.
Nature (2022) Vol. 611, Iss. 7934, pp. 115-123
Open Access | Times Cited: 338
A large-scale genome-wide association study meta-analysis of cannabis use disorder
Emma C. Johnson, Ditte Demontis, Thorgeir E. Thorgeirsson, et al.
The Lancet Psychiatry (2020) Vol. 7, Iss. 12, pp. 1032-1045
Open Access | Times Cited: 297
Single-cell epigenomic analyses implicate candidate causal variants at inherited risk loci for Alzheimer’s and Parkinson’s diseases
M. Ryan Corces, Anna Shcherbina, Soumya Kundu, et al.
Nature Genetics (2020) Vol. 52, Iss. 11, pp. 1158-1168
Open Access | Times Cited: 296
Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction
Richard Karlsson Linnér, Travis T. Mallard, Peter B. Barr, et al.
Nature Neuroscience (2021) Vol. 24, Iss. 10, pp. 1367-1376
Open Access | Times Cited: 245
A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex
Danny Antaki, James P. Guevara, Adam X. Maihofer, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1284-1292
Open Access | Times Cited: 137
Natural Variation in Crops: Realized Understanding, Continuing Promise
Yameng Liang, Haijun Liu, Jianbing Yan, et al.
Annual Review of Plant Biology (2021) Vol. 72, Iss. 1, pp. 357-385
Open Access | Times Cited: 110
Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders
Weiming Gong, Ping Guo, Yuanming Li, et al.
JAMA Psychiatry (2023) Vol. 80, Iss. 4, pp. 360-360
Open Access | Times Cited: 107
Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals
Hang Zhou, Rachel L. Kember, Joseph D. Deak, et al.
Nature Medicine (2023) Vol. 29, Iss. 12, pp. 3184-3192
Open Access | Times Cited: 76
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
Xiangrui Meng, Georgina Navoly, Olga Giannakopoulou, et al.
Nature Genetics (2024) Vol. 56, Iss. 2, pp. 222-233
Open Access | Times Cited: 64
Genetic insights into human cortical organization and development through genome-wide analyses of 2,347 neuroimaging phenotypes
Varun Warrier, Eva-Maria Stauffer, Qin Qin Huang, et al.
Nature Genetics (2023) Vol. 55, Iss. 9, pp. 1483-1493
Open Access | Times Cited: 44
Single-cell multi-cohort dissection of the schizophrenia transcriptome
W. Brad Ruzicka, Shahin Mohammadi, John F. Fullard, et al.
Science (2024) Vol. 384, Iss. 6698
Open Access | Times Cited: 38
Cortical gene expression architecture links healthy neurodevelopment to the imaging, transcriptomics and genetics of autism and schizophrenia
Richard Dear, Konrad Wagstyl, Jakob Seidlitz, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 6, pp. 1075-1086
Open Access | Times Cited: 20
Multi-ancestry meta-analysis of tobacco use disorder identifies 461 potential risk genes and reveals associations with multiple health outcomes
Sylvanus Toikumo, Mariela Jennings, Benjamin K. Pham, et al.
Nature Human Behaviour (2024) Vol. 8, Iss. 6, pp. 1177-1193
Open Access | Times Cited: 18
Cross-ancestry atlas of gene, isoform, and splicing regulation in the developing human brain
Cindy Wen, Michael Margolis, Rujia Dai, et al.
Science (2024) Vol. 384, Iss. 6698
Open Access | Times Cited: 18
Trans-ancestry genome-wide study of depression identifies 697 associations implicating cell types and pharmacotherapies
Mark J. Adams, Fabian Streit, Xiangrui Meng, et al.
Cell (2025)
Open Access | Times Cited: 5
Mapping the cellular etiology of schizophrenia and complex brain phenotypes
Laramie E. Duncan, Tayden Li, Madeleine Salem, et al.
Nature Neuroscience (2025)
Open Access | Times Cited: 2
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
Cell-type-specific 3D epigenomes in the developing human cortex
Michael Song, Mark-Phillip Pebworth, Xiaoyu Yang, et al.
Nature (2020) Vol. 587, Iss. 7835, pp. 644-649
Open Access | Times Cited: 136
Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits
Bryan C. Quach, Michael J. Bray, Nathan Gaddis, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 110
Item-Level Genome-Wide Association Study of the Alcohol Use Disorders Identification Test in Three Population-Based Cohorts
Travis T. Mallard, Jeanne E. Savage, Emma C. Johnson, et al.
American Journal of Psychiatry (2021) Vol. 179, Iss. 1, pp. 58-70
Open Access | Times Cited: 89
Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders
Benxia Hu, Hyejung Won, Won Mah, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 86
Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism
Nana Matoba, Dan Liang, Huaigu Sun, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 82
MOSTWAS: Multi-Omic Strategies for Transcriptome-Wide Association Studies
Arjun Bhattacharya, Yun Li, Michael I. Love
PLoS Genetics (2021) Vol. 17, Iss. 3, pp. e1009398-e1009398
Open Access | Times Cited: 66
The functional and evolutionary impacts of human-specific deletions in conserved elements
James R. Xue, Ava Mackay-Smith, Kousuke Mouri, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 41
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