
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:
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: 538
Peter Ebert, Peter A. Audano, Qihui Zhu, et al.
Science (2021) Vol. 372, Iss. 6537
Open Access | Times Cited: 538
Showing 1-25 of 538 citing articles:
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.
Cell (2022) Vol. 185, Iss. 18, pp. 3426-3440.e19
Open Access | Times Cited: 632
Marta Byrska-Bishop, Uday S. Evani, Xuefang Zhao, et al.
Cell (2022) Vol. 185, Iss. 18, pp. 3426-3440.e19
Open Access | Times Cited: 632
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
Wen‐Wei Liao, Mobin Asri, Jana Ebler, et al.
Nature (2023) Vol. 617, Iss. 7960, pp. 312-324
Open Access | Times Cited: 577
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: 360
Jack Fu, F. Kyle Satterstrom, Minshi Peng, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1320-1331
Open Access | Times Cited: 360
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: 352
Ting Wang, Lucinda Antonacci-Fulton, Kerstin Howe, et al.
Nature (2022) Vol. 604, Iss. 7906, pp. 437-446
Open Access | Times Cited: 352
The structure, function and evolution of a complete human chromosome 8
Glennis A. Logsdon, Mitchell R. Vollger, PingHsun Hsieh, et al.
Nature (2021) Vol. 593, Iss. 7857, pp. 101-107
Open Access | Times Cited: 284
Glennis A. Logsdon, Mitchell R. Vollger, PingHsun Hsieh, et al.
Nature (2021) Vol. 593, Iss. 7857, pp. 101-107
Open Access | Times Cited: 284
Graph pangenome captures missing heritability and empowers tomato breeding
Yao Zhou, Zhiyang Zhang, Zhigui Bao, et al.
Nature (2022) Vol. 606, Iss. 7914, pp. 527-534
Open Access | Times Cited: 277
Yao Zhou, Zhiyang Zhang, Zhigui Bao, et al.
Nature (2022) Vol. 606, Iss. 7914, pp. 527-534
Open Access | Times Cited: 277
From telomere to telomere: The transcriptional and epigenetic state of human repeat elements
Savannah J. Hoyt, Jessica M. Storer, Gabrielle A. Hartley, et al.
Science (2022) Vol. 376, Iss. 6588
Open Access | Times Cited: 258
Savannah J. Hoyt, Jessica M. Storer, Gabrielle A. Hartley, et al.
Science (2022) Vol. 376, Iss. 6588
Open Access | Times Cited: 258
Towards population-scale long-read sequencing
Wouter De Coster, Matthias H. Weissensteiner, Fritz J. Sedlazeck
Nature Reviews Genetics (2021) Vol. 22, Iss. 9, pp. 572-587
Open Access | Times Cited: 254
Wouter De Coster, Matthias H. Weissensteiner, Fritz J. Sedlazeck
Nature Reviews Genetics (2021) Vol. 22, Iss. 9, pp. 572-587
Open Access | Times Cited: 254
Segmental duplications and their variation in a complete human genome
Mitchell R. Vollger, Xavi Guitart, Philip C. Dishuck, et al.
Science (2022) Vol. 376, Iss. 6588
Open Access | Times Cited: 248
Mitchell R. Vollger, Xavi Guitart, Philip C. Dishuck, et al.
Science (2022) Vol. 376, Iss. 6588
Open Access | Times Cited: 248
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: 238
Jouni Sirén, Jean Monlong, Xian Chang, et al.
Science (2021) Vol. 374, Iss. 6574
Open Access | Times Cited: 238
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
Arang Rhie, Sergey Nurk, Monika Čechová, et al.
Nature (2023) Vol. 621, Iss. 7978, pp. 344-354
Open Access | Times Cited: 234
Targeted long-read sequencing identifies missing disease-causing variation
Danny E. Miller, Arvis Sulovari, Tianyun Wang, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 8, pp. 1436-1449
Open Access | Times Cited: 166
Danny E. Miller, Arvis Sulovari, Tianyun Wang, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 8, pp. 1436-1449
Open Access | Times Cited: 166
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: 162
Jana Ebler, Peter Ebert, Wayne E. Clarke, et al.
Nature Genetics (2022) Vol. 54, Iss. 4, pp. 518-525
Open Access | Times Cited: 162
The complete sequence of a human genome
Sergey Nurk, Sergey Koren, Arang Rhie, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 160
Sergey Nurk, Sergey Koren, Arang Rhie, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 160
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
Marta Byrska-Bishop, Uday S. Evani, Xuefang Zhao, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 147
Next-generation cytogenetics: Comprehensive assessment of 52 hematological malignancy genomes by optical genome mapping
Kornelia Neveling, Tuomo Mantere, Susan Vermeulen, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 8, pp. 1423-1435
Open Access | Times Cited: 147
Kornelia Neveling, Tuomo Mantere, Susan Vermeulen, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 8, pp. 1423-1435
Open Access | Times Cited: 147
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
Erich D. Jarvis, Giulio Formenti, Arang Rhie, et al.
Nature (2022) Vol. 611, Iss. 7936, pp. 519-531
Open Access | Times Cited: 140
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
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
Pangenome graph construction from genome alignments with Minigraph-Cactus
Glenn Hickey, Jean Monlong, Jana Ebler, et al.
Nature Biotechnology (2023) Vol. 42, Iss. 4, pp. 663-673
Open Access | Times Cited: 130
Glenn Hickey, Jean Monlong, Jana Ebler, et al.
Nature Biotechnology (2023) Vol. 42, Iss. 4, pp. 663-673
Open Access | Times Cited: 130
Detection of mosaic and population-level structural variants with Sniffles2
Moritz Smolka, Luis F. Paulin, Christopher M. Grochowski, et al.
Nature Biotechnology (2024) Vol. 42, Iss. 10, pp. 1571-1580
Open Access | Times Cited: 129
Moritz Smolka, Luis F. Paulin, Christopher M. Grochowski, et al.
Nature Biotechnology (2024) Vol. 42, Iss. 10, pp. 1571-1580
Open Access | Times Cited: 129
Recurrent inversion polymorphisms in humans associate with genetic instability and genomic disorders
David Porubský, Wolfram Höps, Hufsah Ashraf, et al.
Cell (2022) Vol. 185, Iss. 11, pp. 1986-2005.e26
Open Access | Times Cited: 110
David Porubský, Wolfram Höps, Hufsah Ashraf, et al.
Cell (2022) Vol. 185, Iss. 11, pp. 1986-2005.e26
Open Access | Times Cited: 110
Truvari: refined structural variant comparison preserves allelic diversity
Adam C. English, Vipin K. Menon, Richard A. Gibbs, et al.
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 107
Adam C. English, Vipin K. Menon, Richard A. Gibbs, et al.
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 107
StainedGlass: interactive visualization of massive tandem repeat structures with identity heatmaps
Mitchell R. Vollger, Peter Kerpedjiev, Adam M. Phillippy, et al.
Bioinformatics (2022) Vol. 38, Iss. 7, pp. 2049-2051
Open Access | Times Cited: 103
Mitchell R. Vollger, Peter Kerpedjiev, Adam M. Phillippy, et al.
Bioinformatics (2022) Vol. 38, Iss. 7, pp. 2049-2051
Open Access | Times Cited: 103
Human-specific genetics: new tools to explore the molecular and cellular basis of human evolution
Alex A. Pollen, Umut Kilik, Craig B. Lowe, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 10, pp. 687-711
Open Access | Times Cited: 96
Alex A. Pollen, Umut Kilik, Craig B. Lowe, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 10, pp. 687-711
Open Access | Times Cited: 96
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
Yang Gao, Xiaofei Yang, Hao Chen, et al.
Nature (2023) Vol. 619, Iss. 7968, pp. 112-121
Open Access | Times Cited: 84