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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:

Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
Anna V. Mikhaylova, Caitlin McHugh, Linda M. Polfus, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 10, pp. 1836-1851
Open Access | Times Cited: 20

Showing 20 citing articles:

Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI
Quan Sun, Bryce Rowland, Jiawen Chen, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 28
ImmuneLENS characterizes systemic immune dysregulation in aging and cancer
Robert Bentham, Thomas P. Jones, James R. Black, et al.
Nature Genetics (2025)
Open Access | Times Cited: 2
TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data
Le Huang, Jonathan D. Rosen, Quan Sun, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 6, pp. 1175-1181
Open Access | Times Cited: 60
Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations
Elena V. Feofanova, Michael R. Brown, Taryn Alkis, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 27
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: 9
Major sex differences in allele frequencies for X chromosomal variants in both the 1000 Genomes Project and gnomAD
Zhong Wang, Lei Sun, Andrew D. Paterson
PLoS Genetics (2022) Vol. 18, Iss. 5, pp. e1010231-e1010231
Open Access | Times Cited: 19
Determinants of mosaic chromosomal alteration fitness
Yash Pershad, Taralynn Mack, Hannah Poisner, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 3
Intrinsic Effects of Exposome in Atopic Dermatitis: Genomics, Epigenomics and Regulatory Layers
Katerina Grafanaki, Charalabos Antonatos, Alexandros Maniatis, et al.
Journal of Clinical Medicine (2023) Vol. 12, Iss. 12, pp. 4000-4000
Open Access | Times Cited: 8
Building a collaborative cloud platform to accelerate heart, lung, blood, and sleep research
Stanley C. Ahalt, Paul Avillach, Rebecca Boyles, et al.
Journal of the American Medical Informatics Association (2023) Vol. 30, Iss. 7, pp. 1293-1300
Open Access | Times Cited: 6
MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric
Quan Sun, Yingxi Yang, Jonathan D. Rosen, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 5, pp. 990-995
Closed Access | Times Cited: 2
Differences in the Circulating Proteome in Individuals with versus without Sickle Cell Trait
Yanwei Cai, Nora Franceschini, Aditya Surapaneni, et al.
Clinical Journal of the American Society of Nephrology (2023) Vol. 18, Iss. 11, pp. 1416-1425
Closed Access | Times Cited: 5
Genetic determinants and phenotypic consequences of blood T-cell proportions in 207,000 diverse individuals
Hannah Poisner, Annika Faucon, Nancy R. Cox, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 1
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program
Marsha M. Wheeler, Adrienne M. Stilp, Shuquan Rao, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 6
Whole genome sequencing identifies common and rare structural variants contributing to hematologic traits in the NHLBI TOPMed program
Marsha M. Wheeler, Adrienne M. Stilp, Shuquan Rao, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 6
Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program
Nicole D. Armstrong, Vinodh Srinivasasainagendra, Farah Ammous, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 2
StocSum: stochastic summary statistics for whole genome sequencing studies
Nannan Wang, Bing Yu, Goo Jun, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium
Min-Zhi Jiang, Sheila Gaynor, Xihao Li, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Determinants of mosaic chromosomal alteration fitness
Yash Pershad, Taralynn Mack, Hannah Poisner, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Whole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium.
Min-Zhi Jiang, Sheila Gaynor, Xihao Li, et al.
PubMed (2024) Vol. 33, Iss. 16, pp. 1429-1441
Closed Access
Genetic Determinants in Airways Obstructive Diseases: The Case of Asthma Chronic Obstructive Pulmonary Disease Overlap
Aabida Saferali, Craig P. Hersh
Immunology and Allergy Clinics of North America (2022) Vol. 42, Iss. 3, pp. 559-573
Open Access | Times Cited: 2
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