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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:

Eliciting priors and relaxing the single causal variant assumption in colocalisation analyses
Chris Wallace
PLoS Genetics (2020) Vol. 16, Iss. 4, pp. e1008720-e1008720
Open Access | Times Cited: 317

Showing 1-25 of 317 citing articles:

Mendelian randomization
Eleanor Sanderson, M. Maria Glymour, Michael V. Holmes, et al.
Nature Reviews Methods Primers (2022) Vol. 2, Iss. 1
Open Access | Times Cited: 1215
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease
Douglas P. Wightman, Iris E. Jansen, Jeanne E. Savage, et al.
Nature Genetics (2021) Vol. 53, Iss. 9, pp. 1276-1282
Open Access | Times Cited: 722
A fast and efficient colocalization algorithm for identifying shared genetic risk factors across multiple traits
Christopher N. Foley, James R Staley, Philip G. Breen, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 361
A more accurate method for colocalisation analysis allowing for multiple causal variants
Chris Wallace
PLoS Genetics (2021) Vol. 17, Iss. 9, pp. e1009440-e1009440
Open Access | Times Cited: 314
A compendium of uniformly processed human gene expression and splicing quantitative trait loci
Nurlan Kerimov, James Hayhurst, Kateryna Peikova, et al.
Nature Genetics (2021) Vol. 53, Iss. 9, pp. 1290-1299
Open Access | Times Cited: 313
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
Ruth Chia, Marya S. Sabir, Sara Bandrés‐Ciga, et al.
Nature Genetics (2021) Vol. 53, Iss. 3, pp. 294-303
Open Access | Times Cited: 307
Combining evidence from Mendelian randomization and colocalization: Review and comparison of approaches
Verena Zuber, Nastasiya F. Grinberg, Dipender Gill, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 5, pp. 767-782
Open Access | Times Cited: 306
Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity
Parsa Akbari, Ankit Gilani, Olukayode Sosina, et al.
Science (2021) Vol. 373, Iss. 6550
Open Access | Times Cited: 209
Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19
Liam Gaziano, Claudia Giambartolomei, Alexandre C. Pereira, et al.
Nature Medicine (2021) Vol. 27, Iss. 4, pp. 668-676
Open Access | Times Cited: 194
A genome-wide association study of serum proteins reveals shared loci with common diseases
Alexander Guðjónsson, Valborg Guðmundsdóttir, G. Axelsson, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 170
Identification of LZTFL1 as a candidate effector gene at a COVID-19 risk locus
Damien J. Downes, Amy Cross, Hua Peng, et al.
Nature Genetics (2021) Vol. 53, Iss. 11, pp. 1606-1615
Open Access | Times Cited: 150
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
Immune disease risk variants regulate gene expression dynamics during CD4+ T cell activation
Blagoje Soskic, Eddie Cano-Gamez, Deborah J. Smyth, et al.
Nature Genetics (2022) Vol. 54, Iss. 6, pp. 817-826
Open Access | Times Cited: 111
GPNMB confers risk for Parkinson’s disease through interaction with α-synuclein
Maria E. Diaz‐Ortiz, Yunji Seo, Marijan Posavi, et al.
Science (2022) Vol. 377, Iss. 6608
Open Access | Times Cited: 101
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism
Jonas Ghouse, Vinicius Tragante, Gustav Ahlberg, et al.
Nature Genetics (2023) Vol. 55, Iss. 3, pp. 399-409
Closed Access | Times Cited: 91
Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers
Iris E. Jansen, Sven J. van der Lee, Duber Gomez‐Fonseca, et al.
Acta Neuropathologica (2022) Vol. 144, Iss. 5, pp. 821-842
Open Access | Times Cited: 85
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer
Jinyoung Byun, Younghun Han, Yafang Li, et al.
Nature Genetics (2022) Vol. 54, Iss. 8, pp. 1167-1177
Open Access | Times Cited: 71
Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architecture
Linda Kachuri, Angel C. Y. Mak, Donglei Hu, et al.
Nature Genetics (2023) Vol. 55, Iss. 6, pp. 952-963
Open Access | Times Cited: 58
Impact of the gut microbiota and associated metabolites on cardiometabolic traits, chronic diseases and human longevity: a Mendelian randomization study
Éloi Gagnon, Patricia L. Mitchell, Hasanga D. Manikpurage, et al.
Journal of Translational Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 49
Genetic effects on the timing of parturition and links to fetal birth weight
Pol Solé-Navais, Christopher Flatley, Valgerður Steinthórsdóttir, et al.
Nature Genetics (2023) Vol. 55, Iss. 4, pp. 559-567
Open Access | Times Cited: 49
Proteome-Wide Mendelian Randomization Identifies Causal Links Between Blood Proteins and Acute Pancreatitis
Jérôme Bourgault, Erik Abner, Hasanga D. Manikpurage, et al.
Gastroenterology (2023) Vol. 164, Iss. 6, pp. 953-965.e3
Open Access | Times Cited: 43
Integrating genetic regulation and single-cell expression with GWAS prioritizes causal genes and cell types for glaucoma
Andrew R. Hamel, Wenjun Yan, John M. Rouhana, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 31
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
Jonas Ghouse, Garðar Sveinbjörnsson, Marijana Vujković, et al.
Nature Genetics (2024) Vol. 56, Iss. 5, pp. 827-837
Open Access | Times Cited: 19
Epigenetic variation impacts individual differences in the transcriptional response to influenza infection
Katherine A Aracena, Yen‐Lung Lin, Kaixuan Luo, et al.
Nature Genetics (2024) Vol. 56, Iss. 3, pp. 408-419
Closed Access | Times Cited: 17
Genetic factors shaping the plasma lipidome and the relations to cardiometabolic risk in children and adolescents
Yun Huang, Sara Stinson, Malte Thodberg, et al.
EBioMedicine (2025) Vol. 112, pp. 105537-105537
Open Access | Times Cited: 2
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