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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:

Comprehensive and accurate genome analysis at scale using DRAGEN accelerated algorithms
Sairam Behera, Severine Catreux, Massimiliano Rossi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 16

Showing 16 citing articles:

A framework for sharing of clinical and genetic data for precision medicine applications
Ahmed El‐Hussein, Ulugbek K. Baymuradov, Noémie Elhadad, et al.
Nature Medicine (2024)
Open Access | Times Cited: 5
Genome-wide association testing beyond SNPs
Laura Harris, Ellen M. McDonagh, Xiaolei Zhang, et al.
Nature Reviews Genetics (2024)
Closed Access | Times Cited: 5
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
Rare disease genomics and precision medicine
Juhyeon Hong, D. Lee, A. Hwang, et al.
Genomics & Informatics (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 2
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.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 1
Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomes
Courtney E. French, Nancy C. Andrews, Alan H. Beggs, et al.
npj Genomic Medicine (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 1
SurVIndel2: improving copy number variant calling from next-generation sequencing using hidden split reads
Ramesh Rajaby, Wing‐Kin Sung
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 1
Generative Haplotype Prediction Outperforms Statistical Methods for Small Variant Detection in NGS Data
Brendan O’Fallon, Ashini Bolia, Jacob Durtschi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Benchmarking of Germline Copy Number Variant Callers from Whole Genome Sequencing Data for Clinical Applications
Francisco M. De La Vega, Sean A. Irvine, Pavana Anur, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Whole‐genome sequencing study in Koreans identifies novel loci for Alzheimer's disease
Moon-Il Kang, John Farrell, Congcong Zhu, et al.
Alzheimer s & Dementia (2024)
Open Access
A consensus-based classification workflow to determine genetically inferred ancestry from comprehensive genomic profiling of patients with solid tumors
Zachary D. Wallen, Mary Nesline, Sarabjot Pabla, et al.
Briefings in Bioinformatics (2024) Vol. 25, Iss. 6
Open Access
Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications
Judith Arres, Santosh Elavalli, Shalini Behl, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Disease Biomarker Discovery
Tikam Chand Dakal, Alisha Kumar, Alisha Parveen
Elsevier eBooks (2024)
Closed Access
A systematic benchmark of copy number variation detection tools for high density SNP genotyping arrays
M N van Baardwijk, Leo Heijnen, Hui Zhao, et al.
Genomics (2024) Vol. 116, Iss. 6, pp. 110962-110962
Open Access
Whole-Genome Sequencing Data Analysis
Chadi Saad
Elsevier eBooks (2024)
Closed Access
Whole-Exome Sequencing Data Analysis
Chadi Saad
Elsevier eBooks (2024)
Closed Access
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