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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:

Semi-automated assembly of high-quality diploid human reference genomes
Erich D. Jarvis, Giulio Formenti, Arang Rhie, et al.
Nature (2022) Vol. 611, Iss. 7936, pp. 519-531
Open Access | Times Cited: 140

Showing 1-25 of 140 citing articles:

A draft human pangenome reference
Wen‐Wei Liao, Mobin Asri, Jana Ebler, et al.
Nature (2023) Vol. 617, Iss. 7960, pp. 312-324
Open Access | Times Cited: 577
Gfastats: conversion, evaluation and manipulation of genome sequences using assembly graphs
Giulio Formenti, Linelle Abueg, Angelo Brajuka, et al.
Bioinformatics (2022) Vol. 38, Iss. 17, pp. 4214-4216
Open Access | Times Cited: 432
The complete sequence of a human Y chromosome
Arang Rhie, Sergey Nurk, Monika Čechová, et al.
Nature (2023) Vol. 621, Iss. 7978, pp. 344-354
Open Access | Times Cited: 234
Telomere-to-telomere assembly of diploid chromosomes with Verkko
Mikko Rautiainen, Sergey Nurk, Brian P. Walenz, et al.
Nature Biotechnology (2023) Vol. 41, Iss. 10, pp. 1474-1482
Open Access | Times Cited: 212
Method of the year: long-read sequencing
Vivien Marx
Nature Methods (2023) Vol. 20, Iss. 1, pp. 6-11
Open Access | Times Cited: 199
plotsr: visualizing structural similarities and rearrangements between multiple genomes
Manish Goel, Korbinian Schneeberger
Bioinformatics (2022) Vol. 38, Iss. 10, pp. 2922-2926
Open Access | Times Cited: 165
ODGI: understanding pangenome graphs
Andrea Guarracino, Simon Heumos, Sven Nahnsen, et al.
Bioinformatics (2022) Vol. 38, Iss. 13, pp. 3319-3326
Open Access | Times Cited: 97
Evolutionary analysis of a complete chicken genome
Zhen Huang, Zaoxu Xu, Hao Bai, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 8
Open Access | Times Cited: 87
A pangenome reference of 36 Chinese populations
Yang Gao, Xiaofei Yang, Hao Chen, et al.
Nature (2023) Vol. 619, Iss. 7968, pp. 112-121
Open Access | Times Cited: 84
Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation
Mikhail Kolmogorov, Kimberley Billingsley, Mira Mastoras, et al.
Nature Methods (2023) Vol. 20, Iss. 10, pp. 1483-1492
Open Access | Times Cited: 80
Variant calling and benchmarking in an era of complete human genome sequences
Nathan D. Olson, Justin Wagner, Nathan Dwarshuis, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 7, pp. 464-483
Closed Access | Times Cited: 77
Genomics in the long-read sequencing era
Erwin L. van Dijk, Delphine Naquin, Kévin Gorrichon, et al.
Trends in Genetics (2023) Vol. 39, Iss. 9, pp. 649-671
Closed Access | Times Cited: 73
Increased mutation and gene conversion within human segmental duplications
Mitchell R. Vollger, Philip C. Dishuck, William T. Harvey, et al.
Nature (2023) Vol. 617, Iss. 7960, pp. 325-334
Open Access | Times Cited: 65
Genome assembly in the telomere-to-telomere era
Heng Li, Richard Durbin
Nature Reviews Genetics (2024) Vol. 25, Iss. 9, pp. 658-670
Closed Access | Times Cited: 64
Long-Read DNA Sequencing: Recent Advances and Remaining Challenges
Peter E. Warburton, Robert Sebra
Annual Review of Genomics and Human Genetics (2023) Vol. 24, Iss. 1, pp. 109-132
Open Access | Times Cited: 63
Applications of long-read sequencing to Mendelian genetics
Francesco Mastrorosa, Danny E. Miller, Evan E. Eichler
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 56
A 25-year odyssey of genomic technology advances and structural variant discovery
David Porubský, Evan E. Eichler
Cell (2024) Vol. 187, Iss. 5, pp. 1024-1037
Closed Access | Times Cited: 26
Analysis and benchmarking of small and large genomic variants across tandem repeats
Adam C. English, Egor Dolzhenko, Helyaneh Ziaei Jam, et al.
Nature Biotechnology (2024)
Closed Access | Times Cited: 26
Leveraging a phased pangenome for haplotype design of hybrid potato
Lin Cheng, Nan Wang, Zhigui Bao, et al.
Nature (2025)
Open Access | Times Cited: 4
Structural polymorphism and diversity of human segmental duplications
Hyeonsoo Jeong, Philip C. Dishuck, DongAhn Yoo, et al.
Nature Genetics (2025)
Open Access | Times Cited: 2
The complete and fully-phased diploid genome of a male Han Chinese
Chentao Yang, Yang Zhou, Yanni Song, et al.
Cell Research (2023) Vol. 33, Iss. 10, pp. 745-761
Open Access | Times Cited: 37
Gaps and complex structurally variant loci in phased genome assemblies
David Porubský, Mitchell R. Vollger, William T. Harvey, et al.
Genome Research (2023) Vol. 33, Iss. 4, pp. 496-510
Open Access | Times Cited: 31
Current advances in primate genomics: novel approaches for understanding evolution and disease
David Juan, Gabriel Santpere, Joanna L. Kelley, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 5, pp. 314-331
Closed Access | Times Cited: 30
Graph construction method impacts variation representation and analyses in a bovine super-pangenome
Alexander S. Leonard, Danang Crysnanto, Xena Marie Mapel, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 28
Multiscale analysis of pangenomes enables improved representation of genomic diversity for repetitive and clinically relevant genes
Chen-Shan Chin, Sairam Behera, Asif Khalak, et al.
Nature Methods (2023) Vol. 20, Iss. 8, pp. 1213-1221
Open Access | Times Cited: 28
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