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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:

The Polygenic and Monogenic Basis of Blood Traits and Diseases
Dragana Vuckovic, Erik L. Bao, Parsa Akbari, et al.
Cell (2020) Vol. 182, Iss. 5, pp. 1214-1231.e11
Open Access | Times Cited: 556

Showing 1-25 of 556 citing articles:

Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Ming‐Huei Chen, Laura M. Raffield, Abdou Mousas, et al.
Cell (2020) Vol. 182, Iss. 5, pp. 1198-1213.e14
Open Access | Times Cited: 523
Plasma proteomic associations with genetics and health in the UK Biobank
Benjamin B. Sun, Joshua Chiou, Matthew Traylor, et al.
Nature (2023) Vol. 622, Iss. 7982, pp. 329-338
Open Access | Times Cited: 507
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Wouter van Rheenen, Rick A. A. van der Spek, Mark K. Bakker, et al.
Nature Genetics (2021) Vol. 53, Iss. 12, pp. 1636-1648
Open Access | Times Cited: 385
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
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses
Alison R. Barton, Maxwell A. Sherman, Ronen E. Mukamel, et al.
Nature Genetics (2021) Vol. 53, Iss. 8, pp. 1260-1269
Open Access | Times Cited: 208
Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores
Omer Weissbrod, Masahiro Kanai, Huwenbo Shi, et al.
Nature Genetics (2022) Vol. 54, Iss. 4, pp. 450-458
Open Access | Times Cited: 199
Incomplete Penetrance and Variable Expressivity: From Clinical Studies to Population Cohorts
Rebecca Kingdom, Caroline F. Wright
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 141
GWAS of three molecular traits highlights core genes and pathways alongside a highly polygenic background
Nasa Sinnott-Armstrong, Sahin Naqvi, Manuel A. Rivas, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 131
Human immune diversity: from evolution to modernity
Adrian Liston, Stéphanie Humblet‐Baron, Darragh Duffy, et al.
Nature Immunology (2021) Vol. 22, Iss. 12, pp. 1479-1489
Open Access | Times Cited: 127
Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screens
John Morris, Christina M. Caragine, Zharko Daniloski, et al.
Science (2023) Vol. 380, Iss. 6646
Open Access | Times Cited: 110
Genetic regulation of the human plasma proteome in 54,306 UK Biobank participants
Benjamin B. Sun, Joshua Chiou, Matthew Traylor, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 105
The missing link between genetic association and regulatory function
Noah J Connally, Sumaiya Nazeen, Daniel Lee, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 100
GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia
Michael Chong, Pedrum Mohammadi‐Shemirani, Nicolas Perrot, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 83
Massively parallel base editing to map variant effects in human hematopoiesis
Jorge D. Martin-Rufino, Nicole Castano, Michael Pang, et al.
Cell (2023) Vol. 186, Iss. 11, pp. 2456-2474.e24
Open Access | Times Cited: 77
Genetic estimates of correlation and causality between blood-based biomarkers and psychiatric disorders
William R. Reay, Dylan J. Kiltschewskij, Michael P. Geaghan, et al.
Science Advances (2022) Vol. 8, Iss. 14
Open Access | Times Cited: 70
Neutrophil counts and cardiovascular disease
Jiao Luo, Jesper Qvist Thomassen, Børge G. Nordestgaard, et al.
European Heart Journal (2023) Vol. 44, Iss. 47, pp. 4953-4964
Open Access | Times Cited: 70
The Michigan Genomics Initiative: A biobank linking genotypes and electronic clinical records in Michigan Medicine patients
Matthew Zawistowski, Lars G. Fritsche, Anita Pandit, et al.
Cell Genomics (2023) Vol. 3, Iss. 2, pp. 100257-100257
Open Access | Times Cited: 69
Leveraging base-pair mammalian constraint to understand genetic variation and human disease
Patrick F. Sullivan, Jennifer R. S. Meadows, Steven Gazal, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 69
Human germline heterozygous gain-of-functionSTAT6variants cause severe allergic disease
Mehul Sharma, Daniel Leung, Mana Momenilandi, et al.
The Journal of Experimental Medicine (2023) Vol. 220, Iss. 5
Open Access | Times Cited: 63
HOCOMOCO in 2024: a rebuild of the curated collection of binding models for human and mouse transcription factors
Ilya E. Vorontsov, Irina A. Eliseeva, Arsenii Zinkevich, et al.
Nucleic Acids Research (2023) Vol. 52, Iss. D1, pp. D154-D163
Open Access | Times Cited: 53
Microvascular and macrovascular complications of type 2 diabetes mellitus: Exome wide association analyses
Afnan Mansour, Mira Mousa, Dima Abdelmannan, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 52
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: 26
Proteo-genomics of soluble TREM2 in cerebrospinal fluid provides novel insights and identifies novel modulators for Alzheimer’s disease
Lihua Wang, Niko-Petteri Nykänen, Daniel Western, et al.
Molecular Neurodegeneration (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 22
Proteomic signatures improve risk prediction for common and rare diseases
Julia Carrasco-Zanini, Maik Pietzner, Jonathan Davitte, et al.
Nature Medicine (2024) Vol. 30, Iss. 9, pp. 2489-2498
Open Access | Times Cited: 20
Position-dependent function of human sequence-specific transcription factors
Sascha H. Duttke, Carlos Guzman, Max W. Chang, et al.
Nature (2024) Vol. 631, Iss. 8022, pp. 891-898
Open Access | Times Cited: 17
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