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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:

High coverage whole genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios
Marta Byrska-Bishop, Uday S. Evani, Xuefang Zhao, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 147

Showing 1-25 of 147 citing articles:

The complete sequence of a human genome
Sergey Nurk, Sergey Koren, Arang Rhie, et al.
Science (2022) Vol. 376, Iss. 6588, pp. 44-53
Open Access | Times Cited: 2127
Haplotype-resolved diverse human genomes and integrated analysis of structural variation
Peter Ebert, Peter A. Audano, Qihui Zhu, et al.
Science (2021) Vol. 372, Iss. 6537
Open Access | Times Cited: 534
Complete genomic and epigenetic maps of human centromeres
Nicolas Altemose, Glennis A. Logsdon, Andrey V. Bzikadze, et al.
Science (2022) Vol. 376, Iss. 6588
Open Access | Times Cited: 366
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Jack Fu, F. Kyle Satterstrom, Minshi Peng, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1320-1331
Open Access | Times Cited: 358
A complete reference genome improves analysis of human genetic variation
Sergey Aganezov, Stephanie M. Yan, Daniela C. Soto, et al.
Science (2022) Vol. 376, Iss. 6588
Open Access | Times Cited: 269
Pangenomics enables genotyping of known structural variants in 5202 diverse genomes
Jouni Sirén, Jean Monlong, Xian Chang, et al.
Science (2021) Vol. 374, Iss. 6574
Open Access | Times Cited: 232
Pangenome-based genome inference allows efficient and accurate genotyping across a wide spectrum of variant classes
Jana Ebler, Peter Ebert, Wayne E. Clarke, et al.
Nature Genetics (2022) Vol. 54, Iss. 4, pp. 518-525
Open Access | Times Cited: 157
Protein-coding repeat polymorphisms strongly shape diverse human phenotypes
Ronen E. Mukamel, Robert E. Handsaker, Maxwell A. Sherman, et al.
Science (2021) Vol. 373, Iss. 6562, pp. 1499-1505
Open Access | Times Cited: 135
A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases
Stephen F. Kingsmore, Laurie D. Smith, Chris M. Kunard, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 9, pp. 1605-1619
Open Access | Times Cited: 110
A Draft Human Pangenome Reference
Wen‐Wei Liao, Mobin Asri, Jana Ebler, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 73
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: 99
Cost-efficient whole genome-sequencing using novel mostly natural sequencing-by-synthesis chemistry and open fluidics platform
Gilad Almogy, Mark Pratt, Florian C. Oberstrass, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 53
Integrating whole-genome sequencing with multi-omic data reveals the impact of structural variants on gene regulation in the human brain
Ricardo A. Vialle, Kátia de Paiva Lopes, David A. Bennett, et al.
Nature Neuroscience (2022) Vol. 25, Iss. 4, pp. 504-514
Open Access | Times Cited: 51
PharmVar GeneFocus: SLCO1B1
Laura B. Ramsey, Li Gong, Seung‐been Lee, et al.
Clinical Pharmacology & Therapeutics (2022) Vol. 113, Iss. 4, pp. 782-793
Open Access | Times Cited: 38
Cas9 targeted enrichment of mobile elements using nanopore sequencing
T. L. McDonald, Weichen Zhou, Christopher P. Castro, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 52
Nonparametric coalescent inference of mutation spectrum history and demography
William S. DeWitt, Kameron Decker Harris, Aaron P. Ragsdale, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 21
Open Access | Times Cited: 51
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
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
Jasmine: Population-scale structural variant comparison and analysis
Melanie Kirsche, G. G. Prabhu, Rachel M. Sherman, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 36
Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism
Jack Fu, F. Kyle Satterstrom, Minshi Peng, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 34
Including diverse and admixed populations in genetic epidemiology research
Amke Caliebe, Fasil Tekola‐Ayele, Burcu F. Darst, et al.
Genetic Epidemiology (2022) Vol. 46, Iss. 7, pp. 347-371
Open Access | Times Cited: 26
Characterization of CYP2D6 Pharmacogenetic Variation in Sub‐Saharan African Populations
David Twesigomwe, Britt I. Drögemöller, Galen E.B. Wright, et al.
Clinical Pharmacology & Therapeutics (2022) Vol. 113, Iss. 3, pp. 643-659
Open Access | Times Cited: 26
Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seq
Vahid Akbari, Vincent C. T. Hanlon, Kieran O’Neill, et al.
Cell Genomics (2022) Vol. 3, Iss. 1, pp. 100233-100233
Open Access | Times Cited: 26
Truvari: Refined Structural Variant Comparison Preserves Allelic Diversity
Adam C. English, Vipin K. Menon, Richard A. Gibbs, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 25
Widespread genetic heterogeneity of human ribosomal RNA genes
Wenjun Fan, Eetu Eklund, Rachel M. Sherman, et al.
RNA (2022) Vol. 28, Iss. 4, pp. 478-492
Open Access | Times Cited: 23
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