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:
Multiple causal variants underlie genetic associations in humans
Nathan S. Abell, Marianne K. DeGorter, Michael J. Gloudemans, et al.
Science (2022) Vol. 375, Iss. 6586, pp. 1247-1254
Open Access | Times Cited: 136
Nathan S. Abell, Marianne K. DeGorter, Michael J. Gloudemans, et al.
Science (2022) Vol. 375, Iss. 6586, pp. 1247-1254
Open Access | Times Cited: 136
Showing 1-25 of 136 citing articles:
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: 155
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
Nature Genetics (2023) Vol. 55, Iss. 11, pp. 1866-1875
Closed Access | Times Cited: 155
AI-powered therapeutic target discovery
Frank W. Pun, Ivan V. Ozerov, Alex Zhavoronkov
Trends in Pharmacological Sciences (2023) Vol. 44, Iss. 9, pp. 561-572
Open Access | Times Cited: 140
Frank W. Pun, Ivan V. Ozerov, Alex Zhavoronkov
Trends in Pharmacological Sciences (2023) Vol. 44, Iss. 9, pp. 561-572
Open Access | Times Cited: 140
Limited overlap of eQTLs and GWAS hits due to systematic differences in discovery
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 91
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 91
geneHapR: an R package for gene haplotypic statistics and visualization
Renliang Zhang, Guanqing Jia, Xianmin Diao
BMC Bioinformatics (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 54
Renliang Zhang, Guanqing Jia, Xianmin Diao
BMC Bioinformatics (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 54
Molecular quantitative trait loci
François Aguet, Kaur Alasoo, Yang Li, et al.
Nature Reviews Methods Primers (2023) Vol. 3, Iss. 1
Closed Access | Times Cited: 50
François Aguet, Kaur Alasoo, Yang Li, et al.
Nature Reviews Methods Primers (2023) Vol. 3, Iss. 1
Closed Access | Times Cited: 50
Common genetic factors among autoimmune diseases
Adil Harroud, David A. Hafler
Science (2023) Vol. 380, Iss. 6644, pp. 485-490
Closed Access | Times Cited: 47
Adil Harroud, David A. Hafler
Science (2023) Vol. 380, Iss. 6644, pp. 485-490
Closed Access | Times Cited: 47
Massively parallel characterization of regulatory elements in the developing human cortex
Chengyu Deng, Sean Whalen, Marilyn Steyert, et al.
Science (2024) Vol. 384, Iss. 6698
Closed Access | Times Cited: 21
Chengyu Deng, Sean Whalen, Marilyn Steyert, et al.
Science (2024) Vol. 384, Iss. 6698
Closed Access | Times Cited: 21
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
Yue‐Ting Deng, Jia You, Yu He, et al.
Cell (2024)
Open Access | Times Cited: 16
A single genetic locus controls both expression of DPEP1/CHMP1A and kidney disease development via ferroptosis
Yuting Guan, Xiujie Liang, Ziyuan Ma, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 65
Yuting Guan, Xiujie Liang, Ziyuan Ma, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 65
Genetics of multiple sclerosis: lessons from polygenicity
An Goris, Marijne Vandebergh, Jacob L. McCauley, et al.
The Lancet Neurology (2022) Vol. 21, Iss. 9, pp. 830-842
Closed Access | Times Cited: 62
An Goris, Marijne Vandebergh, Jacob L. McCauley, et al.
The Lancet Neurology (2022) Vol. 21, Iss. 9, pp. 830-842
Closed Access | Times Cited: 62
Redefining tissue specificity of genetic regulation of gene expression in the presence of allelic heterogeneity
Marios Arvanitis, Karl Tayeb, Benjamin J. Strober, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 2, pp. 223-239
Open Access | Times Cited: 52
Marios Arvanitis, Karl Tayeb, Benjamin J. Strober, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 2, pp. 223-239
Open Access | Times Cited: 52
Current challenges in understanding the role of enhancers in disease
Judith B. Zaugg, Pelin Sahlén, Robin Andersson, et al.
Nature Structural & Molecular Biology (2022) Vol. 29, Iss. 12, pp. 1148-1158
Open Access | Times Cited: 48
Judith B. Zaugg, Pelin Sahlén, Robin Andersson, et al.
Nature Structural & Molecular Biology (2022) Vol. 29, Iss. 12, pp. 1148-1158
Open Access | Times Cited: 48
Alternative polyadenylation transcriptome-wide association study identifies APA-linked susceptibility genes in brain disorders
Ya Cui, Frederick J. Arnold, Fanglue Peng, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 33
Ya Cui, Frederick J. Arnold, Fanglue Peng, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 33
eQTL studies: from bulk tissues to single cells
Jingfei Zhang, Hongyu Zhao
Journal of genetics and genomics/Journal of Genetics and Genomics (2023) Vol. 50, Iss. 12, pp. 925-933
Open Access | Times Cited: 27
Jingfei Zhang, Hongyu Zhao
Journal of genetics and genomics/Journal of Genetics and Genomics (2023) Vol. 50, Iss. 12, pp. 925-933
Open Access | Times Cited: 27
mBAT-combo: A more powerful test to detect gene-trait associations from GWAS data
Ang Li, Shouye Liu, Andrew Bakshi, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 1, pp. 30-43
Open Access | Times Cited: 26
Ang Li, Shouye Liu, Andrew Bakshi, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 1, pp. 30-43
Open Access | Times Cited: 26
Proteogenomic links to human metabolic diseases
Mine Koprulu, Julia Carrasco-Zanini, Eleanor Wheeler, et al.
Nature Metabolism (2023) Vol. 5, Iss. 3, pp. 516-528
Open Access | Times Cited: 26
Mine Koprulu, Julia Carrasco-Zanini, Eleanor Wheeler, et al.
Nature Metabolism (2023) Vol. 5, Iss. 3, pp. 516-528
Open Access | Times Cited: 26
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases
Kai Yuan, Ryan J. Longchamps, Antonio F. Pardiñas, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 23
Kai Yuan, Ryan J. Longchamps, Antonio F. Pardiñas, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 23
Systematic investigation of allelic regulatory activity of schizophrenia-associated common variants
Jessica C. McAfee, Sool Lee, Jiseok Lee, et al.
Cell Genomics (2023) Vol. 3, Iss. 10, pp. 100404-100404
Open Access | Times Cited: 23
Jessica C. McAfee, Sool Lee, Jiseok Lee, et al.
Cell Genomics (2023) Vol. 3, Iss. 10, pp. 100404-100404
Open Access | Times Cited: 23
Early intermittent hyperlipidaemia alters tissue macrophages to fuel atherosclerosis
Minoru Takaoka, Xiaohui Zhao, Hwee Ying Lim, et al.
Nature (2024) Vol. 634, Iss. 8033, pp. 457-465
Open Access | Times Cited: 15
Minoru Takaoka, Xiaohui Zhao, Hwee Ying Lim, et al.
Nature (2024) Vol. 634, Iss. 8033, pp. 457-465
Open Access | Times Cited: 15
Genetic regulation of cell type–specific chromatin accessibility shapes brain disease etiology
Biao Zeng, Jaroslav Bendl, Chengyu Deng, et al.
Science (2024) Vol. 384, Iss. 6698
Closed Access | Times Cited: 14
Biao Zeng, Jaroslav Bendl, Chengyu Deng, et al.
Science (2024) Vol. 384, Iss. 6698
Closed Access | Times Cited: 14
Functional dissection of complex and molecular trait variants at single nucleotide resolution
Layla Siraj, Rodrigo Castro, Hannah B. Dewey, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 9
Layla Siraj, Rodrigo Castro, Hannah B. Dewey, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 9
An evolving understanding of multiple causal variants underlying genetic association signals
Erping Long, Jacob Williams, Haoyu Zhang, et al.
The American Journal of Human Genetics (2025)
Closed Access | Times Cited: 1
Erping Long, Jacob Williams, Haoyu Zhang, et al.
The American Journal of Human Genetics (2025)
Closed Access | Times Cited: 1
GWAS Atlas: an updated knowledgebase integrating more curated associations in plants and animals
Xiaonan Liu, Dongmei Tian, Cuiping Li, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D969-D976
Open Access | Times Cited: 33
Xiaonan Liu, Dongmei Tian, Cuiping Li, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D969-D976
Open Access | Times Cited: 33
SNPs in 3′UTR miRNA Target Sequences Associated with Individual Drug Susceptibility
Elena Y. Rykova, Nikita Ershov, Igor S. Damarov, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 22, pp. 13725-13725
Open Access | Times Cited: 30
Elena Y. Rykova, Nikita Ershov, Igor S. Damarov, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 22, pp. 13725-13725
Open Access | Times Cited: 30
Research progress and applications of genome‐wide association study in farm animals
Xiaodong Tan, Zhengxiao He, Alan G. Fahey, et al.
Animal Research and One Health (2023) Vol. 1, Iss. 1, pp. 56-77
Open Access | Times Cited: 20
Xiaodong Tan, Zhengxiao He, Alan G. Fahey, et al.
Animal Research and One Health (2023) Vol. 1, Iss. 1, pp. 56-77
Open Access | Times Cited: 20
