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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:

Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits
Farhad Hormozdiari, Steven Gazal, Bryce van de Geijn, et al.
Nature Genetics (2018) Vol. 50, Iss. 7, pp. 1041-1047
Open Access | Times Cited: 189

Showing 1-25 of 189 citing articles:

The GTEx Consortium atlas of genetic regulatory effects across human tissues
François Aguet, Shankara Anand, Kristin Ardlie, et al.
Science (2020) Vol. 369, Iss. 6509, pp. 1318-1330
Open Access | Times Cited: 3765
Leveraging Polygenic Functional Enrichment to Improve GWAS Power
Gleb Kichaev, Gaurav Bhatia, Po−Ru Loh, et al.
The American Journal of Human Genetics (2018) Vol. 104, Iss. 1, pp. 65-75
Open Access | Times Cited: 884
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
Genomics of disease risk in globally diverse populations
Deepti Gurdasani, Inês Barroso, Eleftheria Zeggini, et al.
Nature Reviews Genetics (2019) Vol. 20, Iss. 9, pp. 520-535
Closed Access | Times Cited: 273
Quantifying genetic effects on disease mediated by assayed gene expression levels
Douglas Yao, Luke J. O’Connor, Alkes L. Price, et al.
Nature Genetics (2020) Vol. 52, Iss. 6, pp. 626-633
Open Access | Times Cited: 272
Genomic Analysis in the Age of Human Genome Sequencing
Tuuli Lappalainen, Alexandra J. Scott, Margot Brandt, et al.
Cell (2019) Vol. 177, Iss. 1, pp. 70-84
Open Access | Times Cited: 269
Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration
Rinki Ratnapriya, Olukayode Sosina, Margaret R. Starostik, et al.
Nature Genetics (2019) Vol. 51, Iss. 4, pp. 606-610
Open Access | Times Cited: 266
Where Are the Disease-Associated eQTLs?
Benjamin D. Umans, Alexis Battle, Yoav Gilad
Trends in Genetics (2020) Vol. 37, Iss. 2, pp. 109-124
Open Access | Times Cited: 257
Extreme Polygenicity of Complex Traits Is Explained by Negative Selection
Luke J. O’Connor, Armin Schoech, Farhad Hormozdiari, et al.
The American Journal of Human Genetics (2019) Vol. 105, Iss. 3, pp. 456-476
Open Access | Times Cited: 245
Plasma proteome analyses in individuals of European and African ancestry identify cis-pQTLs and models for proteome-wide association studies
Jingning Zhang, Diptavo Dutta, Anna Köttgen, et al.
Nature Genetics (2022) Vol. 54, Iss. 5, pp. 593-602
Open Access | Times Cited: 231
Dynamic landscape of immune cell-specific gene regulation in immune-mediated diseases
Mineto Ota, Yasuo Nagafuchi, Hiroaki Hatano, et al.
Cell (2021) Vol. 184, Iss. 11, pp. 3006-3021.e17
Open Access | Times Cited: 227
The GTEx Consortium atlas of genetic regulatory effects across human tissues
François Aguet, Alvaro Barbeira, Rodrigo Bonazzola, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access | Times Cited: 207
Statistical methods for Mendelian randomization in genome-wide association studies: A review
Frederick J. Boehm, Xiang Zhou
Computational and Structural Biotechnology Journal (2022) Vol. 20, pp. 2338-2351
Open Access | Times Cited: 194
Interrogation of human hematopoiesis at single-cell and single-variant resolution
Jacob C. Ulirsch, Caleb A. Lareau, Erik L. Bao, et al.
Nature Genetics (2019) Vol. 51, Iss. 4, pp. 683-693
Open Access | Times Cited: 190
The single-cell eQTLGen consortium
Monique G.P. van der Wijst, DH de Vries, Hilde E. Groot, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 190
Topologically associating domain boundaries that are stable across diverse cell types are evolutionarily constrained and enriched for heritability
Evonne McArthur, John A. Capra
The American Journal of Human Genetics (2021) Vol. 108, Iss. 2, pp. 269-283
Open Access | Times Cited: 170
Genetic analyses support the contribution of mRNA N6-methyladenosine (m6A) modification to human disease heritability
Zijie Zhang, Kaixuan Luo, Zhongyu Zou, et al.
Nature Genetics (2020) Vol. 52, Iss. 9, pp. 939-949
Open Access | Times Cited: 147
Identifying disease-critical cell types and cellular processes by integrating single-cell RNA-sequencing and human genetics
Karthik A. Jagadeesh, Kushal K. Dey, Daniel T. Montoro, et al.
Nature Genetics (2022) Vol. 54, Iss. 10, pp. 1479-1492
Open Access | Times Cited: 147
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
RNA editing underlies genetic risk of common inflammatory diseases
Qin Li, Michael J. Gloudemans, Jonathan M. Geisinger, et al.
Nature (2022) Vol. 608, Iss. 7923, pp. 569-577
Open Access | Times Cited: 119
Multi-ancestry eQTL meta-analysis of human brain identifies candidate causal variants for brain-related traits
Biao Zeng, Jaroslav Bendl, Roman Kosoy, et al.
Nature Genetics (2022) Vol. 54, Iss. 2, pp. 161-169
Open Access | Times Cited: 74
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: 72
Pleiotropy, epistasis and the genetic architecture of quantitative traits
Trudy F. C. Mackay, Robert R. H. Anholt
Nature Reviews Genetics (2024) Vol. 25, Iss. 9, pp. 639-657
Closed Access | Times Cited: 28
Genetic and molecular architecture of complex traits
Tuuli Lappalainen, Yang Li, Sohini Ramachandran, et al.
Cell (2024) Vol. 187, Iss. 5, pp. 1059-1075
Open Access | Times Cited: 21
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