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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:

Accurate rare variant phasing of whole-genome and whole-exome sequencing data in the UK Biobank
Robin J. Hofmeister, Diogo M. Ribeiro, Simone Rubinacci, et al.
Nature Genetics (2023) Vol. 55, Iss. 7, pp. 1243-1249
Open Access | Times Cited: 93

Showing 1-25 of 93 citing articles:

Imputation of low-coverage sequencing data from 150,119 UK Biobank genomes
Simone Rubinacci, Robin J. Hofmeister, Bárbara Sousa da Mota, et al.
Nature Genetics (2023) Vol. 55, Iss. 7, pp. 1088-1090
Open Access | Times Cited: 63
Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture
Jennifer R. S. Meadows, Jeffrey M. Kidd, Guodong Wang, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 46
A harmonized public resource of deeply sequenced diverse human genomes
Zan Koenig, Mary T. Yohannes, Lethukuthula L. Nkambule, et al.
Genome Research (2024) Vol. 34, Iss. 5, pp. 796-809
Open Access | Times Cited: 41
Genetic variation across and within individuals
Zhi Yu, Tim H. H. Coorens, Md Mesbah Uddin, et al.
Nature Reviews Genetics (2024) Vol. 25, Iss. 8, pp. 548-562
Closed Access | Times Cited: 22
A harmonized public resource of deeply sequenced diverse human genomes
Zan Koenig, Mary T. Yohannes, Lethukuthula L. Nkambule, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 38
Long-read sequencing and structural variant characterization in 1,019 samples from the 1000 Genomes Project
Siegfried Schloissnig, Samarendra Pani, Bernardo Rodríguez–Martín, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 15
A metabolomic profile of biological aging in 250,341 individuals from the UK Biobank
Shiyu Zhang, Zheng Wang, Yijing Wang, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 10
A scalable approach for genome-wide inference of ancestral recombination graphs
Arni F. Gunnarsson, Jiazheng Zhu, Brian C. Zhang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 8
The effects of runs-of-homozygosity on pig domestication and breeding
Lin Tao, Hang Liu, Adeniyi C. Adeola, et al.
BMC Genomics (2025) Vol. 26, Iss. 1
Open Access | Times Cited: 1
Genome-wide association testing beyond SNPs
Laura Harris, Ellen M. McDonagh, Xiaolei Zhang, et al.
Nature Reviews Genetics (2024)
Closed Access | Times Cited: 6
Inferring compound heterozygosity from large-scale exome sequencing data
Michael H. Guo, Laurent C. Francioli, Sarah L. Stenton, et al.
Nature Genetics (2023) Vol. 56, Iss. 1, pp. 152-161
Open Access | Times Cited: 16
Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank
Frederik H. Lassen, Samvida S. Venkatesh, Nikolas Baya, et al.
Cell Genomics (2024) Vol. 4, Iss. 7, pp. 100602-100602
Open Access | Times Cited: 5
Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies
Alex Lipov, Sean J. Jurgens, Francesco Mazzarotto, et al.
Nature Cardiovascular Research (2023) Vol. 2, Iss. 11, pp. 1078-1094
Open Access | Times Cited: 11
St. Jude Survivorship Portal: Sharing and Analyzing Large Clinical and Genomic Datasets from Pediatric Cancer Survivors
Gavriel Y. Matt, Edgar Sioson, Kyla Shelton, et al.
Cancer Discovery (2024) Vol. 14, Iss. 8, pp. 1403-1417
Open Access | Times Cited: 4
Enabling efficient analysis of biobank-scale data with genotype representation graphs
Drew DeHaas, Ziqing Pan, Xinzhu Wei
Nature Computational Science (2024)
Closed Access | Times Cited: 4
Population Genomics of Japanese Macaques (Macaca fuscata): Insights into Deep Population Divergence and Multiple Merging Histories
Atsunori Higashino, Katsuki Nakamura, Naoki Osada
Genome Biology and Evolution (2025) Vol. 17, Iss. 1
Open Access
The impact of a secondary, rare, non-pathogenic PKD1 variant on disease progression in autosomal dominant polycystic kidney disease
Elhussein A. Elhassan, Kane E. Collins, Sophia Heneghan, et al.
Journal of Nephrology (2025)
Open Access
STICI: Split-Transformer with integrated convolutions for genotype imputation
Mohammad Erfan Mowlaei, Chong Li, Oveis Jamialahmadi, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Genetics and Population Analysis
Prachi Balyan, Nismabi A Nisamudheen, Jan Zainab, et al.
Elsevier eBooks (2025)
Closed Access
Haplotype-based Parallel PBWT for Biobank Scale Data
Kecong Tang, Ahsan Sanaullah, Degui Zhi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
IGD: A simple, efficient genotype data format
Drew DeHaas, Xinzhu Wei
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
A refined analysis of Neanderthal-introgressed sequences in modern humans with a complete reference genome
Shen-Ao Liang, Tianxin Ren, Jiayu Zhang, et al.
Genome biology (2025) Vol. 26, Iss. 1
Open Access
Elevated Plasma Complement Factors in CRB1-Associated Inherited Retinal Dystrophies
Lude Moekotte, Joke de Boer, Sanne Hiddingh, et al.
Investigative Ophthalmology & Visual Science (2025) Vol. 66, Iss. 2, pp. 55-55
Open Access
Divergent adaptation to highland and tropical environments in Bolivian Creole cattle
Olivia Marcuzzi, Paulo Álvarez Cecco, Leónidas H. Olivera, et al.
Gene (2025), pp. 149354-149354
Closed Access
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