
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:
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: 54
Gilad Almogy, Mark Pratt, Florian C. Oberstrass, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 54
Showing 1-25 of 54 citing articles:
Climate change impacts on plant pathogens, food security and paths forward
Brajesh K. Singh, Manuel Delgado‐Baquerizo, Eleonora Egidi, et al.
Nature Reviews Microbiology (2023) Vol. 21, Iss. 10, pp. 640-656
Open Access | Times Cited: 561
Brajesh K. Singh, Manuel Delgado‐Baquerizo, Eleonora Egidi, et al.
Nature Reviews Microbiology (2023) Vol. 21, Iss. 10, pp. 640-656
Open Access | Times Cited: 561
Spatial profiling technologies illuminate the tumor microenvironment
Ofer Elhanani, Raz Ben-Uri, Leeat Keren
Cancer Cell (2023) Vol. 41, Iss. 3, pp. 404-420
Open Access | Times Cited: 198
Ofer Elhanani, Raz Ben-Uri, Leeat Keren
Cancer Cell (2023) Vol. 41, Iss. 3, pp. 404-420
Open Access | Times Cited: 198
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
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
Beyond the exome: What’s next in diagnostic testing for Mendelian conditions
Monica H. Wojcik, Chloe M. Reuter, Shruti Marwaha, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 8, pp. 1229-1248
Open Access | Times Cited: 65
Monica H. Wojcik, Chloe M. Reuter, Shruti Marwaha, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 8, pp. 1229-1248
Open Access | Times Cited: 65
Splicing neoantigen discovery with SNAF reveals shared targets for cancer immunotherapy
Guangyuan Li, Shweta Mahajan, Siyuan Ma, et al.
Science Translational Medicine (2024) Vol. 16, Iss. 730
Open Access | Times Cited: 28
Guangyuan Li, Shweta Mahajan, Siyuan Ma, et al.
Science Translational Medicine (2024) Vol. 16, Iss. 730
Open Access | Times Cited: 28
Ultrasensitive plasma-based monitoring of tumor burden using machine-learning-guided signal enrichment
Adam J. Widman, Minita Shah, Amanda Frydendahl, et al.
Nature Medicine (2024) Vol. 30, Iss. 6, pp. 1655-1666
Open Access | Times Cited: 24
Adam J. Widman, Minita Shah, Amanda Frydendahl, et al.
Nature Medicine (2024) Vol. 30, Iss. 6, pp. 1655-1666
Open Access | Times Cited: 24
A genome-wide atlas of human cell morphology
Meraj Ramezani, Erin Weisbart, Julia Bauman, et al.
Nature Methods (2025)
Open Access | Times Cited: 5
Meraj Ramezani, Erin Weisbart, Julia Bauman, et al.
Nature Methods (2025)
Open Access | Times Cited: 5
Systematic reconstruction of molecular pathway signatures using scalable single-cell perturbation screens
Longda Jiang, Carol Dalgarno, Efthymia Papalexi, et al.
Nature Cell Biology (2025)
Closed Access | Times Cited: 2
Longda Jiang, Carol Dalgarno, Efthymia Papalexi, et al.
Nature Cell Biology (2025)
Closed Access | Times Cited: 2
Single-molecule genome-wide mutation profiles of cell-free DNA for non-invasive detection of cancer
Daniel C. Bruhm, Dimitrios Mathios, Zachariah H. Foda, et al.
Nature Genetics (2023) Vol. 55, Iss. 8, pp. 1301-1310
Open Access | Times Cited: 32
Daniel C. Bruhm, Dimitrios Mathios, Zachariah H. Foda, et al.
Nature Genetics (2023) Vol. 55, Iss. 8, pp. 1301-1310
Open Access | Times Cited: 32
A genome-wide atlas of human cell morphology
Meraj Ramezani, Julia Bauman, Avtar Singh, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 26
Meraj Ramezani, Julia Bauman, Avtar Singh, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 26
Systematic reconstruction of molecular pathway signatures using scalable single-cell perturbation screens
Longda Jiang, Carol Dalgarno, Efthymia Papalexi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 9
Longda Jiang, Carol Dalgarno, Efthymia Papalexi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 9
Mostly natural sequencing-by-synthesis for scRNA-seq using Ultima sequencing
Sean Simmons, Gila Lithwick‐Yanai, Xian Adiconis, et al.
Nature Biotechnology (2022) Vol. 41, Iss. 2, pp. 204-211
Open Access | Times Cited: 33
Sean Simmons, Gila Lithwick‐Yanai, Xian Adiconis, et al.
Nature Biotechnology (2022) Vol. 41, Iss. 2, pp. 204-211
Open Access | Times Cited: 33
Comparison of tumor‐informed and tumor‐naïve sequencing assays for ctDNA detection in breast cancer
Ángela Santonja, Wendy N. Cooper, Matthew Eldridge, et al.
EMBO Molecular Medicine (2023) Vol. 15, Iss. 6
Open Access | Times Cited: 20
Ángela Santonja, Wendy N. Cooper, Matthew Eldridge, et al.
EMBO Molecular Medicine (2023) Vol. 15, Iss. 6
Open Access | Times Cited: 20
Genomic variant benchmark: if you cannot measure it, you cannot improve it
Sina Majidian, Daniel Paiva Agustinho, Chen-Shan Chin, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 20
Sina Majidian, Daniel Paiva Agustinho, Chen-Shan Chin, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 20
Most large structural variants in cancer genomes can be detected without long reads
Zi-Ning Choo, Julie M. Behr, Aditya Deshpande, et al.
Nature Genetics (2023) Vol. 55, Iss. 12, pp. 2139-2148
Open Access | Times Cited: 20
Zi-Ning Choo, Julie M. Behr, Aditya Deshpande, et al.
Nature Genetics (2023) Vol. 55, Iss. 12, pp. 2139-2148
Open Access | Times Cited: 20
Innovative technologies crowd the short-read sequencing market
Michael Eisenstein
Nature (2023) Vol. 614, Iss. 7949, pp. 798-800
Closed Access | Times Cited: 13
Michael Eisenstein
Nature (2023) Vol. 614, Iss. 7949, pp. 798-800
Closed Access | Times Cited: 13
Chasing Sequencing Perfection: Marching Toward Higher Accuracy and Lower Costs
Hangxing Jia, Shengjun Tan, Yong E. Zhang
Genomics Proteomics & Bioinformatics (2024) Vol. 22, Iss. 2
Open Access | Times Cited: 5
Hangxing Jia, Shengjun Tan, Yong E. Zhang
Genomics Proteomics & Bioinformatics (2024) Vol. 22, Iss. 2
Open Access | Times Cited: 5
Innovations in Short-Read Sequencing Technologies and Their Applications to Clinical Genomics
Katarzyna Polonis, Joseph H. Blommel, Andrew Hughes, et al.
Clinical Chemistry (2025) Vol. 71, Iss. 1, pp. 97-108
Closed Access
Katarzyna Polonis, Joseph H. Blommel, Andrew Hughes, et al.
Clinical Chemistry (2025) Vol. 71, Iss. 1, pp. 97-108
Closed Access
Next-generation sequencing: principles and technical considerations
Lars Paulín
Elsevier eBooks (2025), pp. 31-52
Closed Access
Lars Paulín
Elsevier eBooks (2025), pp. 31-52
Closed Access
Error-corrected flow-based sequencing at whole-genome scale and its application to circulating cell-free DNA profiling
Alexandre Pellan Cheng, Adam J. Widman, Anushri Arora, et al.
Nature Methods (2025)
Closed Access
Alexandre Pellan Cheng, Adam J. Widman, Anushri Arora, et al.
Nature Methods (2025)
Closed Access
Next-generation forward genetic screens: uniting high-throughput perturbations with single-cell analysis
John Morris, Jennifer S. Sun, Neville E. Sanjana
Trends in Genetics (2023) Vol. 40, Iss. 2, pp. 118-133
Closed Access | Times Cited: 10
John Morris, Jennifer S. Sun, Neville E. Sanjana
Trends in Genetics (2023) Vol. 40, Iss. 2, pp. 118-133
Closed Access | Times Cited: 10
Omics Approaches to Investigate the Pathogenesis of Suicide
Maura Boldrini, Yang Xiao, Tarjinder Singh, et al.
Biological Psychiatry (2024) Vol. 96, Iss. 12, pp. 919-928
Closed Access | Times Cited: 3
Maura Boldrini, Yang Xiao, Tarjinder Singh, et al.
Biological Psychiatry (2024) Vol. 96, Iss. 12, pp. 919-928
Closed Access | Times Cited: 3
Next-generation sequencing in dermatology
Andrew King, Hany Deirawan, Paytra A. Klein, et al.
Frontiers in Medicine (2023) Vol. 10
Open Access | Times Cited: 8
Andrew King, Hany Deirawan, Paytra A. Klein, et al.
Frontiers in Medicine (2023) Vol. 10
Open Access | Times Cited: 8
A cost–benefit analysis for use of large SNP panels and high throughput typing for forensic investigative genetic genealogy
Bruce Budowle, Andrew N. Arnette, Antti Sajantila
International Journal of Legal Medicine (2023) Vol. 137, Iss. 5, pp. 1595-1614
Open Access | Times Cited: 7
Bruce Budowle, Andrew N. Arnette, Antti Sajantila
International Journal of Legal Medicine (2023) Vol. 137, Iss. 5, pp. 1595-1614
Open Access | Times Cited: 7
A comprehensive adsorption and desorption study on the interaction of DNA oligonucleotides with TiO2 nanolayer
Jin Yang, Qiong Su, Chongyang Song, et al.
Physical Chemistry Chemical Physics (2024) Vol. 26, Iss. 34, pp. 22681-22695
Closed Access | Times Cited: 2
Jin Yang, Qiong Su, Chongyang Song, et al.
Physical Chemistry Chemical Physics (2024) Vol. 26, Iss. 34, pp. 22681-22695
Closed Access | Times Cited: 2