Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

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

Showing 1-25 of 96 citing articles:

Integrated profiling of human pancreatic cancer organoids reveals chromatin accessibility features associated with drug sensitivity
Xiaohan Shi, Yunguang Li, Qiuyue Yuan, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 66
Global discovery of lupus genetic risk variant allelic enhancer activity
Xiaoming Lu, Xiaoting Chen, Carmy Forney, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 65
BIN1 is a key regulator of proinflammatory and neurodegeneration-related activation in microglia
Ari Sudwarts, Supriya Ramesha, Tianwen Gao, et al.
Molecular Neurodegeneration (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 61
Modeling gene × environment interactions in PTSD using human neurons reveals diagnosis-specific glucocorticoid-induced gene expression
Carina Seah, Michael S. Breen, Tom Rusielewicz, et al.
Nature Neuroscience (2022) Vol. 25, Iss. 11, pp. 1434-1445
Open Access | Times Cited: 41
Systematic investigation of allelic regulatory activity of schizophrenia-associated common variants
Jessica C. McAfee, Sool Lee, Jiseok Lee, et al.
Cell Genomics (2023) Vol. 3, Iss. 10, pp. 100404-100404
Open Access | Times Cited: 24
Brain Lipids and Lipid Droplet Dysregulation in Alzheimer’s Disease and Neuropsychiatric Disorders
Xiaojie Zhao, Siwei Zhang, Alan R. Sanders, et al.
Complex Psychiatry (2023) Vol. 9, Iss. 1-4, pp. 154-171
Open Access | Times Cited: 24
Genetic regulation of cell type–specific chromatin accessibility shapes brain disease etiology
Biao Zeng, Jaroslav Bendl, Chengyu Deng, et al.
Science (2024) Vol. 384, Iss. 6698
Closed Access | Times Cited: 14
Schizophrenia genomics: genetic complexity and functional insights
Patrick F. Sullivan, Shuyang Yao, Jens Hjerling‐Leffler
Nature reviews. Neuroscience (2024) Vol. 25, Iss. 9, pp. 611-624
Closed Access | Times Cited: 11
Perspectives on Allele-Specific Expression
Siobhán Cleary, Cathal Seoighe
Annual Review of Biomedical Data Science (2021) Vol. 4, Iss. 1, pp. 101-122
Closed Access | Times Cited: 41
Functional characterization of human genomic variation linked to polygenic diseases
Tania Fabo, Paul A. Khavari
Trends in Genetics (2023) Vol. 39, Iss. 6, pp. 462-490
Open Access | Times Cited: 19
Massively parallel functional dissection of schizophrenia-associated noncoding genetic variants
Christine K. Rummel, Miriam Gagliardi, Ruhel Ahmad, et al.
Cell (2023) Vol. 186, Iss. 23, pp. 5165-5182.e33
Open Access | Times Cited: 19
Multiple genes in a single GWAS risk locus synergistically mediate aberrant synaptic development and function in human neurons
Siwei Zhang, Hanwen Zhang, Marc P. Forrest, et al.
Cell Genomics (2023) Vol. 3, Iss. 9, pp. 100399-100399
Open Access | Times Cited: 17
Systematic identification of genotype-dependent enhancer variants in eosinophilic esophagitis
Molly Shook, Xiaoming Lu, Xiaoting Chen, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 2, pp. 280-294
Open Access | Times Cited: 6
Massively parallel techniques for cataloguing the regulome of the human brain
Kayla G. Townsley, Kristen Brennand, Laura M. Huckins
Nature Neuroscience (2020) Vol. 23, Iss. 12, pp. 1509-1521
Open Access | Times Cited: 49
Chromatin architecture in addiction circuitry identifies risk genes and potential biological mechanisms underlying cigarette smoking and alcohol use traits
Nancy Y. A. Sey, Benxia Hu, Marina Iskhakova, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 7, pp. 3085-3094
Open Access | Times Cited: 27
Focus on your locus with a massively parallel reporter assay
Jessica C. McAfee, Jessica Bell, Oleh Krupa, et al.
Journal of Neurodevelopmental Disorders (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 24
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: 24
Examining the biological mechanisms of human mental disorders resulting from gene-environment interdependence using novel functional genomic approaches
Patrícia Pelufo Silveira, Michael J. Meaney
Neurobiology of Disease (2023) Vol. 178, pp. 106008-106008
Open Access | Times Cited: 13
Genome-wide DNA methylation analysis of peripheral blood cells derived from patients with first-episode schizophrenia in the Chinese Han population
Mingrui Li, Yanli Li, Haide Qin, et al.
Molecular Psychiatry (2020) Vol. 26, Iss. 8, pp. 4475-4485
Closed Access | Times Cited: 38
Integrative analyses highlight functional regulatory variants associated with neuropsychiatric diseases
Margaret Guo, David L. Reynolds, Cheen Euong Ang, et al.
Nature Genetics (2023) Vol. 55, Iss. 11, pp. 1876-1891
Closed Access | Times Cited: 12
Scaled and efficient derivation of loss-of-function alleles in risk genes for neurodevelopmental and psychiatric disorders in human iPSCs
Hanwen Zhang, Ada McCarroll, Lilia Peyton, et al.
Stem Cell Reports (2024)
Open Access | Times Cited: 4
Single-cell multiomics of neuronal activation reveals context-dependent genetic control of brain disorders
Lifan Liang, Siwei Zhang, Zicheng Wang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Implications of gene × environment interactions in post-traumatic stress disorder risk and treatment
Carina Seah, Anne Elizabeth Sidamon‐Eristoff, Laura M. Huckins, et al.
Journal of Clinical Investigation (2025) Vol. 135, Iss. 5
Open Access
Contrasting genetic predisposition and diagnosis in psychiatric disorders: A multi-omic single-nucleus analysis of the human OFC
Nathalie Gerstner, Anna S. Fröhlich, Natalie Matosin, et al.
Science Advances (2025) Vol. 11, Iss. 10
Open Access
Evaluating brain structure traits as endophenotypes using polygenicity and discoverability
Nana Matoba, Michael I. Love, Jason L. Stein
Human Brain Mapping (2020) Vol. 43, Iss. 1, pp. 329-340
Open Access | Times Cited: 29
Page 1 - Next Page

Scroll to top