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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:

Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus
Herbert Schulz, Ann‐Kathrin Ruppert, Stefan Herms, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 76

Showing 26-50 of 76 citing articles:

Methylation quantitative loci analysis in nonsyndromic orofacial clefts
Ligiane Alves Machado‐Paula, Julia Romanowska, Rolv T. Lie, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Edge-induced Selective Etching of bilayer MoS2 Kirigami Structure via Space-Confined method
Weijie Ma, Andrew Keong Ng, Jie Zhu, et al.
Nanoscale Horizons (2025)
Closed Access
Characterizing somatic mutations in ovarian cancer germline risk regions
P K Lai, Jonathan P. Tyrer, Paul D.P. Pharoah, et al.
Communications Biology (2025) Vol. 8, Iss. 1
Open Access
Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performance
Hao Mei, Jeannette Simino, Lianna Li, et al.
Alzheimer s Research & Therapy (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 2
Treating the “E” in “G × E”: Trauma-Informed Approaches and Psychological Therapy Interventions in Psychosis
Olympia Gianfrancesco, Vivien J. Bubb, John P. Quinn
Frontiers in Psychiatry (2019) Vol. 10
Open Access | Times Cited: 18
Genetic and Epigenetic Analysis Revealing Variants in the NCAM1–TTC12–ANKK1–DRD2 Cluster Associated Significantly With Nicotine Dependence in Chinese Han Smokers
Qiang Liu, Yi Xu, Ying Mao, et al.
Nicotine & Tobacco Research (2019) Vol. 22, Iss. 8, pp. 1301-1309
Closed Access | Times Cited: 18
Identification of 34 genes conferring genetic and pharmacological risk for the comorbidity of schizophrenia and smoking behaviors
Yunlong Ma, Jinɡjinɡ Li, Yi Xu, et al.
Aging (2020) Vol. 12, Iss. 3, pp. 2169-2225
Open Access | Times Cited: 17
Investigation of Schizophrenia with Human Induced Pluripotent Stem Cells
Samuel K. Powell, Callan O’Shea, Sara Rose Shannon, et al.
Advances in neurobiology (2020), pp. 155-206
Open Access | Times Cited: 17
Cell-type-specific meQTLs extend melanoma GWAS annotation beyond eQTLs and inform melanocyte gene-regulatory mechanisms
Tongwu Zhang, Jiyeon Choi, Ramile Dilshat, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 9, pp. 1631-1646
Open Access | Times Cited: 16
2017 WONOEP appraisal: Studying epilepsy as a network disease using systems biology approaches
John Matthew Mahoney, James D. Mills, Angelika Mühlebner, et al.
Epilepsia (2019) Vol. 60, Iss. 6, pp. 1045-1053
Closed Access | Times Cited: 16
Profiling the DNA methylation patterns of imprinted genes in abnormal semen samples by next-generation bisulfite sequencing
Wanhong He, Υuhua Sun, Sufen Zhang, et al.
Journal of Assisted Reproduction and Genetics (2020) Vol. 37, Iss. 9, pp. 2211-2221
Open Access | Times Cited: 16
Multi-omic association study identifies DNA methylation-mediated genotype and smoking exposure effects on lung function in children living in urban settings
Matthew Dapas, Emma E. Thompson, William Wentworth-Sheilds, et al.
PLoS Genetics (2023) Vol. 19, Iss. 1, pp. e1010594-e1010594
Open Access | Times Cited: 5
Derivation of poly-methylomic profile scores for schizophrenia
Oliver J. Watkeys, Sarah Cohen‐Woods, Yann Quidé, et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry (2020) Vol. 101, pp. 109925-109925
Open Access | Times Cited: 13
Relationships between neurotransmitter receptor densities and expression levels of their corresponding genes in the human hippocampus
Ling Zhao, Thomas W. Mühleisen, Dominique I. Pelzer, et al.
NeuroImage (2023) Vol. 273, pp. 120095-120095
Open Access | Times Cited: 5
Genome-wide DNA methylation sequencing identifies epigenetic perturbations in the upper airways under long-term exposure to moderate levels of ambient air pollution
Marey Messingschlager, Martina Bartel-Steinbach, Sebastian D. Mackowiak, et al.
Environmental Research (2023) Vol. 233, pp. 116413-116413
Open Access | Times Cited: 5
Integrating brain methylome with GWAS for psychiatric risk gene discovery
Shizhong Han, Ying Lin, Minghui Wang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2018)
Open Access | Times Cited: 14
Durchbrüche im Verständnis der molekularen Ursachen psychiatrischer Störungen
Markus M. Nöthen, Franziska Degenhardt, Andreas J. Forstner
Der Nervenarzt (2019) Vol. 90, Iss. 2, pp. 99-106
Open Access | Times Cited: 11
Genetic association study of a novel indel polymorphism in HSPA1B with the risk of sudden cardiac death in the Chinese populations
Zhenzhen Yang, Qing Zhang, Huan Yu, et al.
Forensic Science International (2020) Vol. 318, pp. 110637-110637
Closed Access | Times Cited: 11
Identifying causal models between genetically regulated methylation patterns and gene expression in healthy colon tissue
Anna Díez-Villanueva, Mireia Jordà, Robert Carreras‐Torres, et al.
Clinical Epigenetics (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 10
HBI: a hierarchical Bayesian interaction model to estimate cell-type-specific methylation quantitative trait loci incorporating priors from cell-sorted bisulfite sequencing data
Youshu Cheng, Biao Cai, Hongyu Li, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 1
ME-Class2 reveals context dependent regulatory roles for 5-hydroxymethylcytosine
Christopher Schlosberg, Dennis Y. Wu, Harrison W. Gabel, et al.
Nucleic Acids Research (2019) Vol. 47, Iss. 5, pp. e28-e28
Open Access | Times Cited: 9
A causal association of ANKRD37 with human hippocampal volume
Jiayuan Xu, Xianyou Xia, Qiaojun Li, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 11, pp. 4432-4445
Closed Access | Times Cited: 6
Iterative integrated imputation for missing data and pathway models with applications to breast cancer subtypes
Henry Linder, Yuping Zhang
Communications for Statistical Applications and Methods (2019) Vol. 26, Iss. 4, pp. 411-430
Open Access | Times Cited: 7
mir152hypomethylation as a mechanism for non-syndromic cleft lip and palate
Lucas Alvizi, Luciano Abreu Brito, Gerson Shigeru Kobayashi, et al.
Epigenetics (2022) Vol. 17, Iss. 13, pp. 2278-2295
Open Access | Times Cited: 5
Dichotomy in redundant enhancers points to presence of initiators of gene regulation
Wei Song, Ivan Ovcharenko
BMC Genomics (2018) Vol. 19, Iss. 1
Open Access | Times Cited: 6

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