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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:

A complete reference genome improves analysis of human genetic variation
Sergey Aganezov, Stephanie M. Yan, Daniela C. Soto, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 47

Showing 1-25 of 47 citing articles:

The Human Pangenome Project: a global resource to map genomic diversity
Ting Wang, Lucinda Antonacci-Fulton, Kerstin Howe, et al.
Nature (2022) Vol. 604, Iss. 7906, pp. 437-446
Open Access | Times Cited: 350
Curated variation benchmarks for challenging medically relevant autosomal genes
Justin Wagner, Nathan D. Olson, Lindsay Harris, et al.
Nature Biotechnology (2022) Vol. 40, Iss. 5, pp. 672-680
Open Access | Times Cited: 146
Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-space
Michael C. Schatz, Anthony Philippakis, Enis Afgan, et al.
Cell Genomics (2022) Vol. 2, Iss. 1, pp. 100085-100085
Open Access | Times Cited: 99
Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing
Sneha D. Goenka, John E. Gorzynski, Kishwar Shafin, et al.
Nature Biotechnology (2022) Vol. 40, Iss. 7, pp. 1035-1041
Open Access | Times Cited: 71
Systematic benchmark of state-of-the-art variant calling pipelines identifies major factors affecting accuracy of coding sequence variant discovery
Yury A. Barbitoff, Ruslan Abasov, Varvara E. Tvorogova, et al.
BMC Genomics (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 55
Homozygous might be hemizygous: CRISPR/Cas9 editing in iPSCs results in detrimental on-target defects that escape standard quality controls
Dina Simkin, Vasileios Papakis, Bernabé I. Bustos, et al.
Stem Cell Reports (2022) Vol. 17, Iss. 4, pp. 993-1008
Open Access | Times Cited: 46
Local adaptation and archaic introgression shape global diversity at human structural variant loci
Stephanie M. Yan, Rachel M. Sherman, Dylan J. Taylor, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 44
Benchmarking challenging small variants with linked and long reads
Justin Wagner, Nathan D. Olson, Lindsay Harris, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 40
Towards a Comprehensive Variation Benchmark for Challenging Medically-Relevant Autosomal Genes
Justin Wagner, Nathan D. Olson, Lindsay Harris, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 27
Automated assembly of high-quality diploid human reference genomes
Erich D. Jarvis, Giulio Formenti, Arang Rhie, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 19
Tutankhamun and the Tomb that Changed the World
Bob Brier
Oxford University Press eBooks (2022)
Closed Access | Times Cited: 16
Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex Lipoprotein(a) KIV-2 VNTR
Stephan Amstler, Gertraud Streiter, Cathrin Pfurtscheller, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Complete genomic and epigenetic maps of human centromeres
Nicolas Altemose, Glennis A. Logsdon, Andrey V. Bzikadze, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 13
Human Pangenomics: Promises and Challenges of a Distributed Genomic Reference
Paolo Abondio, Elisabetta Cilli, Donata Luiselli
Life (2023) Vol. 13, Iss. 6, pp. 1360-1360
Open Access | Times Cited: 5
Improved sequence mapping using a complete reference genome and lift-over
Nae-Chyun Chen, Luis F. Paulin, Fritz J. Sedlazeck, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 6
Genozip Dual-Coordinate VCF format enables efficient genomic analyses and alleviates liftover limitations
Divon Lan, Gludhug A. Purnomo, Raymond Tobler, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 3
Quality control of large genome datasets
Max Robinson, Arpita Joshi, Ansh Vidyarthi, et al.
Human Genetics and Genomics Advances (2022) Vol. 3, Iss. 3, pp. 100123-100123
Open Access | Times Cited: 1
Whole-genome sequencing across 449 samples spanning 47 ethnolinguistic groups provides insights into genetic diversity in Nigeria
Esha Joshi, Arjun Biddanda, Olajumoke Adeniji-Popoola, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 1
Quality control of large genome datasets using genome fingerprints
Max Robinson, Arpita Joshi, Ansh Vidyarthi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access
Is Nefertiti in Tut’s Tomb?
Bob Brier
Oxford University Press eBooks (2022), pp. 207-216
Closed Access
Wonderful Things
Bob Brier
Oxford University Press eBooks (2022), pp. 57-73
Closed Access
CSI Thebes: The Case of the Missing Pectoral
Bob Brier
Oxford University Press eBooks (2022), pp. 227-236
Closed Access
Tutankhamun as Activist
Bob Brier
Oxford University Press eBooks (2022), pp. 239-256
Closed Access
Tutankhamun as Warrior
Bob Brier
Oxford University Press eBooks (2022), pp. 177-191
Closed Access
Final Clearance
Bob Brier
Oxford University Press eBooks (2022), pp. 101-120
Closed Access
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