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:

Allele-specific DNA methylation reinforces PEAR1 enhancer activity
Benedetta Izzi, Mariaelena Pistoni, Katrien Cludts, et al.
Blood (2016) Vol. 128, Iss. 7, pp. 1003-1012
Open Access | Times Cited: 53

Showing 1-25 of 53 citing articles:

Integrative analysis of drug response and clinical outcome in acute myeloid leukemia
Daniel Bottomly, Nicola Long, Anna Reister Schultz, et al.
Cancer Cell (2022) Vol. 40, Iss. 8, pp. 850-864.e9
Open Access | Times Cited: 203

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: 169

QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes
Zhanye Zheng, Dandan Huang, Jianhua Wang, et al.
Nucleic Acids Research (2019) Vol. 48, Iss. D1, pp. D983-D991
Open Access | Times Cited: 115

Pharmacogenomic polygenic response score predicts ischaemic events and cardiovascular mortality in clopidogrel-treated patients
Joshua P. Lewis, Joshua Backman, Jean‐Luc Reny, et al.
European Heart Journal - Cardiovascular Pharmacotherapy (2019) Vol. 6, Iss. 4, pp. 203-210
Open Access | Times Cited: 87

Dynamic Enhancer DNA Methylation as Basis for Transcriptional and Cellular Heterogeneity of ESCs
Yuelin Song, Patrick R. van den Berg, Styliani Markoulaki, et al.
Molecular Cell (2019) Vol. 75, Iss. 5, pp. 905-920.e6
Open Access | Times Cited: 83

Crosstalk of Genetic Variants, Allele-Specific DNA Methylation, and Environmental Factors for Complex Disease Risk
Huishan Wang, Dan Lou, Zhibin Wang
Frontiers in Genetics (2019) Vol. 9
Open Access | Times Cited: 73

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

The genetics of platelet count and volume in humans
John D. Eicher, Guillaume Lettre, Andrew D. Johnson
Platelets (2017) Vol. 29, Iss. 2, pp. 125-130
Open Access | Times Cited: 52

Genome sequencing unveils a regulatory landscape of platelet reactivity
Ali R. Keramati, Ming‐Huei Chen, Benjamin A.T. Rodriguez, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 40

Establishment of regulatory elements during erythro-megakaryopoiesis identifies hematopoietic lineage-commitment points
Elisabeth F. Heuston, Cheryl A. Keller, Jens Lichtenberg, et al.
Epigenetics & Chromatin (2018) Vol. 11, Iss. 1
Open Access | Times Cited: 44

EnhancerDB: a resource of transcriptional regulation in the context of enhancers
Ran Kang, Yiming Zhang, Qingqing Huang, et al.
Database (2018) Vol. 2019
Open Access | Times Cited: 38

Epigenetic Regulation of F2RL3 Associates With Myocardial Infarction and Platelet Function
Laura J. Corbin, Stephen J. White, Amy E. Taylor, et al.
Circulation Research (2022) Vol. 130, Iss. 3, pp. 384-400
Open Access | Times Cited: 21

Decoding the Therapeutic Target SVEP1: Harnessing Molecular Trait GWASs to Unravel Mechanisms of Human Disease
Jared S. Elenbaas, Paul C. Lee, Ved Patel, et al.
The Annual Review of Pharmacology and Toxicology (2025) Vol. 65, Iss. 1, pp. 131-148
Closed Access

QTLbase2: an enhanced catalog of human quantitative trait loci on extensive molecular phenotypes
Dandan Huang, Xiangling Feng, Hongxi Yang, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D1122-D1128
Open Access | Times Cited: 18

Variation of PEAR1 DNA methylation influences platelet and leukocyte function
Benedetta Izzi, Francesco Gianfagna, Wen‐Yi Yang, et al.
Clinical Epigenetics (2019) Vol. 11, Iss. 1
Open Access | Times Cited: 28

Non-coding DNA in IBD: from sequence variation in DNA regulatory elements to novel therapeutic potential
Claartje Meddens, Amy C. J. van der List, Edward E. S. Nieuwenhuis, et al.
Gut (2019) Vol. 68, Iss. 5, pp. 928-941
Open Access | Times Cited: 26

Genetic basis of pregnancy-associated decreased platelet counts and gestational thrombocytopenia
Zijing Yang, Liang Hu, Jianxin Zhen, et al.
Blood (2023) Vol. 143, Iss. 15, pp. 1528-1538
Open Access | Times Cited: 8

The Mutagenic Consequences of DNA Methylation within and across Generations
Haley E. Hanson, Andrea L. Liebl
Epigenomes (2022) Vol. 6, Iss. 4, pp. 33-33
Open Access | Times Cited: 13

Targeted deep sequencing of the PEAR1 locus for platelet aggregation in European and African American families
Ali R. Keramati, Lisa R. Yanek, Kruthika Iyer, et al.
Platelets (2018) Vol. 30, Iss. 3, pp. 380-386
Open Access | Times Cited: 21

Epigenetic regulation of megakaryopoiesis and platelet formation
Baichuan Xu, Xianpeng Ye, Zhaoyang Wen, et al.
Haematologica (2024)
Open Access | Times Cited: 2

LOXL2-induced PEAR1 Ser891 phosphorylation suppresses CD44 degradation and promotes triple-negative breast cancer metastasis
Yingzhi Shen, Jie Yan, Lin Li, et al.
Journal of Clinical Investigation (2024) Vol. 134, Iss. 16
Open Access | Times Cited: 2

Convergence of evidence from a methylome-wide CpG-SNP association study and GWAS of major depressive disorder
Karolina A. Åberg, Andrey A. Shabalin, Robin F. Chan, et al.
Translational Psychiatry (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 20

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