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:

Mapping cis-regulatory chromatin contacts in neural cells links neuropsychiatric disorder risk variants to target genes
Michael Song, Xiaoyu Yang, Xingjie Ren, et al.
Nature Genetics (2019) Vol. 51, Iss. 8, pp. 1252-1262
Open Access | Times Cited: 170

Showing 1-25 of 170 citing articles:

A single-cell atlas of chromatin accessibility in the human genome
Kai Zhang, James D. Hocker, Michael Miller, et al.
Cell (2021) Vol. 184, Iss. 24, pp. 5985-6001.e19
Open Access | Times Cited: 327

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

Neuronal enhancers are hotspots for DNA single-strand break repair
Wei Wu, Sarah E. Hill, William J. Nathan, et al.
Nature (2021) Vol. 593, Iss. 7859, pp. 440-444
Open Access | Times Cited: 176

3D Genome of macaque fetal brain reveals evolutionary innovations during primate corticogenesis
Xin Luo, Yuting Liu, Dachang Dang, et al.
Cell (2021) Vol. 184, Iss. 3, pp. 723-740.e21
Open Access | Times Cited: 111

Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis
Sai Zhang, Johnathan Cooper‐Knock, Annika K. Weimer, et al.
Neuron (2022) Vol. 110, Iss. 6, pp. 992-1008.e11
Open Access | Times Cited: 97

Common variants contribute to intrinsic human brain functional networks
Bingxin Zhao, Tengfei Li, Stephen M. Smith, et al.
Nature Genetics (2022) Vol. 54, Iss. 4, pp. 508-517
Open Access | Times Cited: 89

Three-dimensional genome rewiring in loci with human accelerated regions
Kathleen C. Keough, Sean Whalen, Fumitaka Inoue, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 61

Machine learning dissection of human accelerated regions in primate neurodevelopment
Sean Whalen, Fumitaka Inoue, Hane Ryu, et al.
Neuron (2023) Vol. 111, Iss. 6, pp. 857-873.e8
Open Access | Times Cited: 60

Single-cell genomics and regulatory networks for 388 human brains
Prashant S. Emani, Jason Liu, Declan Clarke, et al.
Science (2024) Vol. 384, Iss. 6698
Open Access | Times Cited: 42

Massively parallel characterization of regulatory elements in the developing human cortex
Chengyu Deng, Sean Whalen, Marilyn Steyert, et al.
Science (2024) Vol. 384, Iss. 6698
Closed Access | Times Cited: 23

Allele-specific open chromatin in human iPSC neurons elucidates functional disease variants
Siwei Zhang, Hanwen Zhang, Yifan Zhou, et al.
Science (2020) Vol. 369, Iss. 6503, pp. 561-565
Open Access | Times Cited: 96

Context-Specific Striatal Astrocyte Molecular Responses Are Phenotypically Exploitable
Xinzhu Yu, Jun Nagai, Maria Martí-Solano, et al.
Neuron (2020) Vol. 108, Iss. 6, pp. 1146-1162.e10
Open Access | Times Cited: 93

Enhancer RNAs predict enhancer–gene regulatory links and are critical for enhancer function in neuronal systems
Nancy V. N. Carullo, Robert A. Phillips, Rhiana C. Simon, et al.
Nucleic Acids Research (2020) Vol. 48, Iss. 17, pp. 9550-9570
Open Access | Times Cited: 87

ANANSE: an enhancer network-based computational approach for predicting key transcription factors in cell fate determination
Quan Xu, Γεώργιος Γεωργίου, Siebren Frölich, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 14, pp. 7966-7985
Open Access | Times Cited: 61

The threat of programmed DNA damage to neuronal genome integrity and plasticity
Keith W. Caldecott, Michael E. Ward, André Nussenzweig
Nature Genetics (2022) Vol. 54, Iss. 2, pp. 115-120
Closed Access | Times Cited: 52

HiCAR is a robust and sensitive method to analyze open-chromatin-associated genome organization
Xiaolin Wei, Yu Xiang, Derek T Peters, et al.
Molecular Cell (2022) Vol. 82, Iss. 6, pp. 1225-1238.e6
Open Access | Times Cited: 43

Functional characterization of Alzheimer’s disease genetic variants in microglia
Xiaoyu Yang, Jia Wen, Han Yang, et al.
Nature Genetics (2023) Vol. 55, Iss. 10, pp. 1735-1744
Open Access | Times Cited: 38

Multiplex, single-cell CRISPRa screening for cell type specific regulatory elements
Florence M. Chardon, Troy A. McDiarmid, Nicholas F. Page, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 13

Towards understanding sex differences in autism spectrum disorders
Karen Q. Leow, Mary A. Tonta, Jing Lü, et al.
Brain Research (2024) Vol. 1833, pp. 148877-148877
Open Access | Times Cited: 10

Relationship between sex biases in gene expression and sex biases in autism and Alzheimer’s disease
Stuart B. Fass, Bernard Mulvey, Rebecca Chase, et al.
Biology of Sex Differences (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 9

Comparative characterization of human accelerated regions in neurons
Xiekui Cui, Han Yang, Charles Q. Cai, et al.
Nature (2025)
Closed Access | Times Cited: 1

Transcription factors: building hubs in the 3D space
Dafne Campigli Di Giammartino, Alexander Polyzos, Effie Apostolou
Cell Cycle (2020) Vol. 19, Iss. 19, pp. 2395-2410
Open Access | Times Cited: 63

Hemispheric asymmetry in the human brain and in Parkinson’s disease is linked to divergent epigenetic patterns in neurons
Peipei Li, Elizabeth Ensink, Seán Lang, et al.
Genome biology (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 59

ABCA7 and the altered lipidostasis hypothesis of Alzheimer's disease
Nicholas N. Lyssenko, Domenico Praticò
Alzheimer s & Dementia (2020) Vol. 17, Iss. 2, pp. 164-174
Open Access | Times Cited: 55

Interpreting the impact of noncoding structural variation in neurodevelopmental disorders
Eva D’haene, Sarah Vergult
Genetics in Medicine (2020) Vol. 23, Iss. 1, pp. 34-46
Open Access | Times Cited: 53

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