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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:

Rare variant contribution to human disease in 281,104 UK Biobank exomes
Quanli Wang, Ryan S. Dhindsa, Keren Carss, et al.
Nature (2021) Vol. 597, Iss. 7877, pp. 527-532
Open Access | Times Cited: 368

Showing 1-25 of 368 citing articles:

The sequences of 150,119 genomes in the UK Biobank
Bjarni V. Halldórsson, Hannes P. Eggertsson, Kristjan H. S. Moore, et al.
Nature (2022) Vol. 607, Iss. 7920, pp. 732-740
Open Access | Times Cited: 329
The next-generation Open Targets Platform: reimagined, redesigned, rebuilt
David Ochoa, Andrew Hercules, Miguel Carmona, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D1353-D1359
Open Access | Times Cited: 261
Genome-wide analyses of 200,453 individuals yield new insights into the causes and consequences of clonal hematopoiesis
Siddhartha Kar, Pedro M. Quirós, Muxin Gu, et al.
Nature Genetics (2022) Vol. 54, Iss. 8, pp. 1155-1166
Open Access | Times Cited: 220
Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes
Konrad J. Karczewski, Matthew Solomonson, Katherine R. Chao, et al.
Cell Genomics (2022) Vol. 2, Iss. 9, pp. 100168-100168
Open Access | Times Cited: 192
Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank
Sean J. Jurgens, Seung Hoan Choi, Valerie N. Morrill, et al.
Nature Genetics (2022) Vol. 54, Iss. 3, pp. 240-250
Open Access | Times Cited: 126
Targeting the CCL2–CCR2 axis for atheroprotection
Marios K. Georgakis, Jürgen Bernhagen, Laura H. Heitman, et al.
European Heart Journal (2022) Vol. 43, Iss. 19, pp. 1799-1808
Open Access | Times Cited: 116
Genetic associations of protein-coding variants in human disease
Benjamin B. Sun, Mitja Kurki, Christopher N. Foley, et al.
Nature (2022) Vol. 603, Iss. 7899, pp. 95-102
Open Access | Times Cited: 112
Polygenic architecture of rare coding variation across 394,783 exomes
Daniel J. Weiner, Ajay Nadig, Karthik A. Jagadeesh, et al.
Nature (2023) Vol. 614, Iss. 7948, pp. 492-499
Open Access | Times Cited: 111
Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype
Sarah R. Senum, Ying Li, Katherine A. Benson, et al.
The American Journal of Human Genetics (2021) Vol. 109, Iss. 1, pp. 136-156
Open Access | Times Cited: 104
Using genetic association data to guide drug discovery and development: Review of methods and applications
Stephen Burgess, Amy M. Mason, Andrew J. Grant, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 2, pp. 195-214
Open Access | Times Cited: 101
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
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Nick Shrine, Abril G. Izquierdo, Jing Chen, et al.
Nature Genetics (2023) Vol. 55, Iss. 3, pp. 410-422
Open Access | Times Cited: 88
Germline Mutations in CIDEB and Protection against Liver Disease
Niek Verweij, Mary E. Haas, Jonas B. Nielsen, et al.
New England Journal of Medicine (2022) Vol. 387, Iss. 4, pp. 332-344
Open Access | Times Cited: 78
Rare variant associations with plasma protein levels in the UK Biobank
Ryan S. Dhindsa, Oliver S. Burren, Benjamin B. Sun, et al.
Nature (2023) Vol. 622, Iss. 7982, pp. 339-347
Open Access | Times Cited: 78
Updated benchmarking of variant effect predictors using deep mutational scanning
Benjamin Livesey, Joseph A. Marsh
Molecular Systems Biology (2023) Vol. 19, Iss. 8
Open Access | Times Cited: 63
Genetic association analysis of 77,539 genomes reveals rare disease etiologies
Daniel Greene, Daniela Pirri, Karen Frudd, et al.
Nature Medicine (2023) Vol. 29, Iss. 3, pp. 679-688
Open Access | Times Cited: 52
The contribution of copy number variants to psychiatric symptoms and cognitive ability
Josephine Mollon, Laura Almasy, Sébastien Jacquemont, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 4, pp. 1480-1493
Open Access | Times Cited: 47
Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine
Pascal Schlosser, Nora Scherer, Franziska Grundner-Culemann, et al.
Nature Genetics (2023) Vol. 55, Iss. 6, pp. 995-1008
Open Access | Times Cited: 47
Whole genome sequencing in clinical practice
Frederik Otzen Bagger, Line Borgwardt, Andreas Sand Jespersen, et al.
BMC Medical Genomics (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 36
High-dimensional phenotyping to define the genetic basis of cellular morphology
Matthew Tegtmeyer, Jatin Arora, Samira Asgari, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 29
A deep catalogue of protein-coding variation in 983,578 individuals
Kathie Sun, Xiaodong Bai, Siying Chen, et al.
Nature (2024) Vol. 631, Iss. 8021, pp. 583-592
Open Access | Times Cited: 22
Haemoglobin thresholds to define anaemia from age 6 months to 65 years: estimates from international data sources
Sabine Braat, Katherine Fielding, Ji-Ru Han, et al.
The Lancet Haematology (2024) Vol. 11, Iss. 4, pp. e253-e264
Open Access | Times Cited: 19
Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver disease
Yajie Zhao, Maria Chukanova, Katherine A. Kentistou, et al.
Nature Genetics (2024) Vol. 56, Iss. 4, pp. 579-584
Open Access | Times Cited: 18
Disease prediction with multi-omics and biomarkers empowers case–control genetic discoveries in the UK Biobank
Manik Garg, Marcin Karpiński, Dorota Matelska, et al.
Nature Genetics (2024) Vol. 56, Iss. 9, pp. 1821-1831
Open Access | Times Cited: 17
Atlas of the plasma proteome in health and disease in 53,026 adults
Yue‐Ting Deng, Jia You, Yu He, et al.
Cell (2024)
Open Access | Times Cited: 16
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