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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:

Using long-read sequencing to detect imprinted DNA methylation
Scott Gigante, Quentin Gouil, Alexis Lucattini, et al.
Nucleic Acids Research (2019) Vol. 47, Iss. 8, pp. e46-e46
Open Access | Times Cited: 109

Showing 1-25 of 109 citing articles:

Opportunities and challenges in long-read sequencing data analysis
Shanika L. Amarasinghe, Shian Su, Xueyi Dong, et al.
Genome biology (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 2043
A guide for the diagnosis of rare and undiagnosed disease: beyond the exome
Shruti Marwaha, Joshua W. Knowles, Euan A. Ashley
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 228
Simultaneous profiling of chromatin accessibility and methylation on human cell lines with nanopore sequencing
Isac Lee, Roham Razaghi, Timothy Gilpatrick, et al.
Nature Methods (2020) Vol. 17, Iss. 12, pp. 1191-1199
Open Access | Times Cited: 185
Nanopore Sequencing Enables Comprehensive Transposable Element Epigenomic Profiling
Adam D. Ewing, Nathan Smits, Francisco J. Sánchez‐Luque, et al.
Molecular Cell (2020) Vol. 80, Iss. 5, pp. 915-928.e5
Open Access | Times Cited: 162
Third-Generation Sequencing: The Spearhead towards the Radical Transformation of Modern Genomics
Konstantina Athanasopoulou, Michaela A. Boti, Panagiotis G. Adamopoulos, et al.
Life (2021) Vol. 12, Iss. 1, pp. 30-30
Open Access | Times Cited: 157
Multi-omics data integration considerations and study design for biological systems and disease
Stefan Graw, Kevin Chappell, Charity L. Washam, et al.
Molecular Omics (2020) Vol. 17, Iss. 2, pp. 170-185
Open Access | Times Cited: 156
Latest techniques to study DNA methylation
Quentin Gouil, Andrew Keniry
Essays in Biochemistry (2019) Vol. 63, Iss. 6, pp. 639-648
Open Access | Times Cited: 154
Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes
Wei Wei, Katherine Schon, Greg Elgar, et al.
Nature (2022) Vol. 611, Iss. 7934, pp. 105-114
Open Access | Times Cited: 146
Multi-omics approaches for understanding gene-environment interactions in noncommunicable diseases: techniques, translation, and equity issues
Robel Alemu, Nigussie Tadesse Sharew, Yodit Y. Arsano, et al.
Human Genomics (2025) Vol. 19, Iss. 1
Open Access | Times Cited: 2
New Twists in Detecting mRNA Modification Dynamics
Ina Anreiter, Quoseena Mir, Jared T. Simpson, et al.
Trends in biotechnology (2020) Vol. 39, Iss. 1, pp. 72-89
Open Access | Times Cited: 134
Recent advances in the detection of base modifications using the Nanopore sequencer
Liu Xu, Masahide Seki
Journal of Human Genetics (2019) Vol. 65, Iss. 1, pp. 25-33
Open Access | Times Cited: 132
Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies
Xuefang Zhao, Ryan L. Collins, Wan‐Ping Lee, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 5, pp. 919-928
Open Access | Times Cited: 100
Allelic H3K27me3 to allelic DNA methylation switch maintains noncanonical imprinting in extraembryonic cells
Zhiyuan Chen, Qiangzong Yin, Azusa Inoue, et al.
Science Advances (2019) Vol. 5, Iss. 12
Open Access | Times Cited: 98
A new era of long-read sequencing for cancer genomics
Yoshitaka Sakamoto, Sarun Sereewattanawoot, Ayako Suzuki
Journal of Human Genetics (2019) Vol. 65, Iss. 1, pp. 3-10
Open Access | Times Cited: 93
Accurate targeted long-read DNA methylation and hydroxymethylation sequencing with TAPS
Yibin Liu, Jingfei Cheng, Paulina Siejka-Zielińska, et al.
Genome biology (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 72
Regulatory T cell differentiation is controlled by αKG-induced alterations in mitochondrial metabolism and lipid homeostasis
Maria I. Matias, Carmen S. Yong, Amir Foroushani, et al.
Cell Reports (2021) Vol. 37, Iss. 5, pp. 109911-109911
Open Access | Times Cited: 67
Megabase-scale methylation phasing using nanopore long reads and NanoMethPhase
Vahid Akbari, Jean‐Michel Garant, Kieran O’Neill, et al.
Genome biology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 59
Genome-wide detection of imprinted differentially methylated regions using nanopore sequencing
Vahid Akbari, Jean‐Michel Garant, Kieran O’Neill, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 42
MethPhaser: methylation-based long-read haplotype phasing of human genomes
Yilei Fu, Sergey Aganezov, Medhat Mahmoud, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 9
A Hitchhiker's Guide to long-read genomic analysis
Medhat Mahmoud, Daniel Paiva Agustinho, Fritz J. Sedlazeck
Genome Research (2025) Vol. 35, Iss. 4, pp. 545-558
Closed Access | Times Cited: 1
Evolution of genome-wide methylation profiling technologies
Carolina Montaño, Winston Timp
Genome Research (2025) Vol. 35, Iss. 4, pp. 572-582
Closed Access | Times Cited: 1
A call for direct sequencing of full-length RNAs to identify all modifications
Juan Alfonzo, Jessica A. Brown, Peter H. Byers, et al.
Nature Genetics (2021) Vol. 53, Iss. 8, pp. 1113-1116
Open Access | Times Cited: 54
Genomic imprinting in mouse blastocysts is predominantly associated with H3K27me3
Laura Santini, Florian Halbritter, Fabian Titz‐Teixeira, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 43
Glioma Stem Cells: Novel Data Obtained by Single-Cell Sequencing
A. M. Gisina, И. В. Холоденко, Yan Kim, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 22, pp. 14224-14224
Open Access | Times Cited: 34
Modification mapping by nanopore sequencing
Laura K. White, Jay R. Hesselberth
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 32
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