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:

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 1-25 of 76 citing articles:

Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
Bassel Abou‐Khalil, Pauls Auce, Andreja Avberšek, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 420
Genetic impacts on DNA methylation: research findings and future perspectives
Sergio Villicaña, Jordana T. Bell
Genome biology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 170
DNA methylation QTL mapping across diverse human tissues provides molecular links between genetic variation and complex traits
Meritxell Oliva, Kathryn Demanelis, Yihao Lu, et al.
Nature Genetics (2022) Vol. 55, Iss. 1, pp. 112-122
Open Access | Times Cited: 117
Modern Mars' geomorphological activity, driven by wind, frost, and gravity
S. Diniega, A. M. Bramson, B. J. Buratti, et al.
Geomorphology (2021) Vol. 380, pp. 107627-107627
Open Access | Times Cited: 60
Genetic impacts on DNA methylation help elucidate regulatory genomic processes
Sergio Villicaña, Juan Castillo‐Fernandez, Eilís Hannon, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 30
Deep learning predicts DNA methylation regulatory variants in specific brain cell types and enhances fine mapping for brain disorders
Jiyun Zhou, Daniel R. Weinberger, Shizhong Han
Science Advances (2025) Vol. 11, Iss. 1
Open Access | Times Cited: 1
CancerSplicingQTL: a database for genome-wide identification of splicing QTLs in human cancer
Jianbo Tian, Zhihua Wang, Shufang Mei, et al.
Nucleic Acids Research (2018) Vol. 47, Iss. D1, pp. D909-D916
Open Access | Times Cited: 76
Functional genetic variants can mediate their regulatory effects through alteration of transcription factor binding
Andrew D. Johnston, Cláudia A. Simões‐Pires, Taylor V. Thompson, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 60
Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidney
James Eales, Xiao Jiang, Xiaoguang Xu, et al.
Nature Genetics (2021) Vol. 53, Iss. 5, pp. 630-637
Open Access | Times Cited: 53
Genome-wide sequencing-based identification of methylation quantitative trait loci and their role in schizophrenia risk
Kira A. Perzel Mandell, Nicholas J. Eagles, Richard Wilton, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 51
Heritability of DNA methylation in threespine stickleback (Gasterosteus aculeatus)
Juntao Hu, Sara J. Smith, Tegan N. Barry, et al.
Genetics (2021) Vol. 217, Iss. 1
Open Access | Times Cited: 46
Global DNA methylation changes spanning puberty are near predicted estrogen-responsive genes and enriched for genes involved in endocrine and immune processes
Emma E. Thompson, Jessie Nicodemus‐Johnson, Kyung Won Kim, et al.
Clinical Epigenetics (2018) Vol. 10, Iss. 1
Open Access | Times Cited: 59
Pancan-meQTL: a database to systematically evaluate the effects of genetic variants on methylation in human cancer
Jing Gong, Hao Wan, Shufang Mei, et al.
Nucleic Acids Research (2018) Vol. 47, Iss. D1, pp. D1066-D1072
Open Access | Times Cited: 56
Identification of expression quantitative trait loci associated with schizophrenia and affective disorders in normal brain tissue
Oneil G. Bhalala, Artika P. Nath, Michael Inouye, et al.
PLoS Genetics (2018) Vol. 14, Iss. 8, pp. e1007607-e1007607
Open Access | Times Cited: 47
SNP2APA: a database for evaluating effects of genetic variants on alternative polyadenylation in human cancers
Yanbo Yang, Qiong Zhang, Ya‐Ru Miao, et al.
Nucleic Acids Research (2019) Vol. 48, Iss. D1, pp. D226-D232
Open Access | Times Cited: 46
Genome-wide analysis of pseudogenes reveals HBBP1’s human-specific essentiality in erythropoiesis and implication in β-thalassemia
Yanni Ma, Siqi Liu, Jie Gao, et al.
Developmental Cell (2021) Vol. 56, Iss. 4, pp. 478-493.e11
Open Access | Times Cited: 36
The importance of enhancer methylation for epigenetic regulation of tumorigenesis in squamous lung cancer
Jae-Won Cho, Hyo Sup Shim, Chang Young Lee, et al.
Experimental & Molecular Medicine (2022) Vol. 54, Iss. 1, pp. 12-22
Open Access | Times Cited: 26
NERD-seq: a novel approach of Nanopore direct RNA sequencing that expands representation of non-coding RNAs
Luke Saville, Li Wu, Jemaneh Habtewold, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 6
DNA Methylation-Mediated Modulation of Endocytosis as Potential Mechanism for Synaptic Function Regulation in Murine Inhibitory Cortical Interneurons
Daniel Pensold, Julia Reichard, Karen M. J. van Loo, et al.
Cerebral Cortex (2020) Vol. 30, Iss. 7, pp. 3921-3937
Open Access | Times Cited: 36
Integrative analysis of genetics, epigenetics and RNA expression data reveal three susceptibility loci for smoking behavior in Chinese Han population
Ming D. Li, Qiang Liu, Xiaoqiang Shi, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 11, pp. 3516-3526
Closed Access | Times Cited: 4
Multiomics analyses identified epigenetic modulation of the S100A gene family in Kawasaki disease and their significant involvement in neutrophil transendothelial migration
Lien‐Hung Huang, Ho‐Chang Kuo, Cheng-Tsung Pan, et al.
Clinical Epigenetics (2018) Vol. 10, Iss. 1
Open Access | Times Cited: 35
CancerImmunityQTL: a database to systematically evaluate the impact of genetic variants on immune infiltration in human cancer
Jianbo Tian, Yimin Cai, Yue Li, et al.
Nucleic Acids Research (2020) Vol. 49, Iss. D1, pp. D1065-D1073
Open Access | Times Cited: 32
Multi-omics in mesial temporal lobe epilepsy with hippocampal sclerosis: Clues into the underlying mechanisms leading to disease
Estela M. Bruxel, Danielle Bruno, Amanda M. do Canto, et al.
Seizure (2021) Vol. 90, pp. 34-50
Open Access | Times Cited: 27
Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
Lindsay F. Rizzardi, Peter F. Hickey, Adrian Idrizi, et al.
Genome biology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 27
Deep learning predicts DNA methylation regulatory variants in the human brain and elucidates the genetics of psychiatric disorders
Jiyun Zhou, Qiang Chen, Patricia Braun, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 34
Open Access | Times Cited: 18
Page 1 - Next Page

Scroll to top