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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:

Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
Urmo Võsa, Annique Claringbould, Harm-Jan Westra, et al.
Nature Genetics (2021) Vol. 53, Iss. 9, pp. 1300-1310
Open Access | Times Cited: 1177

Showing 1-25 of 1177 citing articles:

Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Vassily Trubetskoy, Antonio F. Pardiñas, Ting Qi, et al.
Nature (2022) Vol. 604, Iss. 7906, pp. 502-508
Open Access | Times Cited: 1822
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: 386
Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets
Jing Hua Zhao, David Stacey, Niclas Eriksson, et al.
Nature Immunology (2023) Vol. 24, Iss. 9, pp. 1540-1551
Open Access | Times Cited: 370
Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation
Josine L. Min, Gibran Hemani, Eilís Hannon, et al.
Nature Genetics (2021) Vol. 53, Iss. 9, pp. 1311-1321
Open Access | Times Cited: 349
Single-cell eQTL mapping identifies cell type–specific genetic control of autoimmune disease
Seyhan Yazar, José Alquicira-Hernández, Kristof Wing, et al.
Science (2022) Vol. 376, Iss. 6589
Closed Access | Times Cited: 342
Whole-genome sequencing reveals host factors underlying critical COVID-19
Athanasios Kousathanas, Erola Pairo‐Castineira, Konrad Rawlik, et al.
Nature (2022) Vol. 607, Iss. 7917, pp. 97-103
Open Access | Times Cited: 277
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Heidi Hautakangas, Bendik S. Winsvold, Sanni Ruotsalainen, et al.
Nature Genetics (2022) Vol. 54, Iss. 2, pp. 152-160
Open Access | Times Cited: 258
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: 227
Common and rare variant associations with clonal haematopoiesis phenotypes
Michael D. Kessler, Amy Damask, Sean O’Keeffe, et al.
Nature (2022) Vol. 612, Iss. 7939, pp. 301-309
Open Access | Times Cited: 189
Systematic differences in discovery of genetic effects on gene expression and complex traits
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
Nature Genetics (2023) Vol. 55, Iss. 11, pp. 1866-1875
Closed Access | Times Cited: 157
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
Nilüfer Rahmioğlu, Sally Mortlock, Marzieh Ghiasi, et al.
Nature Genetics (2023) Vol. 55, Iss. 3, pp. 423-436
Open Access | Times Cited: 153
Multi-Omics Profiling for Health
Mohan Babu, M Snyder
Molecular & Cellular Proteomics (2023) Vol. 22, Iss. 6, pp. 100561-100561
Open Access | Times Cited: 148
Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases
Niek de Klein, Ellen Tsai, Martijn Vochteloo, et al.
Nature Genetics (2023) Vol. 55, Iss. 3, pp. 377-388
Open Access | Times Cited: 145
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Zhe Wang, Andrew Emmerich, Nicolas J. Pillon, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1332-1344
Open Access | Times Cited: 133
Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome
Catherine S. Storm, Demis A. Kia, Mona Mohammad Almramhi, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 129
Genetic control of RNA splicing and its distinct role in complex trait variation
Ting Qi, Yang Wu, Hailing Fang, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1355-1363
Open Access | Times Cited: 126
Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity
Steven Gazal, Omer Weissbrod, Farhad Hormozdiari, et al.
Nature Genetics (2022) Vol. 54, Iss. 6, pp. 827-836
Open Access | Times Cited: 125
Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways
Kyoko Watanabe, Philip R. Jansen, Jeanne E. Savage, et al.
Nature Genetics (2022) Vol. 54, Iss. 8, pp. 1125-1132
Open Access | Times Cited: 125
Epigenome-wide association studies: current knowledge, strategies and recommendations
Maria Pia Campagna, Alexandre Xavier, Jeannette Lechner‐Scott, et al.
Clinical Epigenetics (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 121
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
Erola Pairo‐Castineira, Konrad Rawlik, Andrew D. Bretherick, et al.
Nature (2023) Vol. 617, Iss. 7962, pp. 764-768
Open Access | Times Cited: 121
Heart-brain connections: Phenotypic and genetic insights from magnetic resonance images
Bingxin Zhao, Tengfei Li, Zirui Fan, et al.
Science (2023) Vol. 380, Iss. 6648
Closed Access | Times Cited: 121
DNA methylation QTL mapping across diverse human tissues provides molecular links between genetic variation and complex traits
Meritxell Oliva, Kathryn Demanelis, Yihao Lu, et al.
Nature Genetics (2022) Vol. 55, Iss. 1, pp. 112-122
Open Access | Times Cited: 117
Oxidative stress gene expression, DNA methylation, and gut microbiota interaction trigger Crohn’s disease: a multi-omics Mendelian randomization study
Shu Xu, Xiaozhi Li, Shenghong Zhang, et al.
BMC Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 108
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: 107
The Nucleotide Transformer: Building and Evaluating Robust Foundation Models for Human Genomics
Hugo Dalla-Torre, Liam Gonzalez, Javier Mendoza‐Revilla, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 107
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