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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:

Integrative analysis of 3604 GWAS reveals multiple novel cell type-specific regulatory associations
Charles E. Breeze, Eric Haugen, Alex Reynolds, et al.
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 30

Showing 1-25 of 30 citing articles:

Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries
Zhili Zheng, Shouye Liu, Julia Sidorenko, et al.
Nature Genetics (2024) Vol. 56, Iss. 5, pp. 767-777
Open Access | Times Cited: 34
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population
Jianxin Shi, Kouya Shiraishi, Jiyeon Choi, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 37
FORGEdb: a tool for identifying candidate functional variants and uncovering target genes and mechanisms for complex diseases
Charles E. Breeze, Eric Haugen, María Gutiérrez‐Arcelus, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 16
Causal role of immune cells in generalized anxiety disorder: Mendelian randomization study
Zhen Ma, Min Zhao, Huanghong Zhao, et al.
Frontiers in Immunology (2024) Vol. 14
Open Access | Times Cited: 16
Epigenomic insights into common human disease pathology
Christopher G. Bell
Cellular and Molecular Life Sciences (2024) Vol. 81, Iss. 1
Open Access | Times Cited: 11
Genetic insights into immune mechanisms of Alzheimer’s and Parkinson’s disease
Alexi Nott, Inge R. Holtman
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 20
Pulmonary Function and Blood DNA Methylation: A Multiancestry Epigenome-Wide Association Meta-analysis
Mi Kyeong Lee, Tianxiao Huan, Daniel L. McCartney, et al.
American Journal of Respiratory and Critical Care Medicine (2022) Vol. 206, Iss. 3, pp. 321-336
Open Access | Times Cited: 24
Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries
Zhili Zheng, Shouye Liu, Julia Sidorenko, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 21
Joint analysis of genome‐wide cross‐trait and multi‐omics reveals molecular mechanisms of inflammatory bowel disease and nominates its novel therapeutic genes
Zhu Zi-jun, Rongxing Wei, Hailong Li, et al.
The FASEB Journal (2025) Vol. 39, Iss. 1
Closed Access
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes
Sonja I. Berndt, Joseph Vijai, Yolanda Benavente, et al.
Leukemia (2022) Vol. 36, Iss. 12, pp. 2835-2844
Open Access | Times Cited: 16
Ancestry-driven metabolite variation provides insights into disease states in admixed populations
Kaylia M. Reynolds, Andréa R. V. R. Horimoto, Bridget M. Lin, et al.
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 8
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas
Odessica N. Hughes, Amy R. Bentley, Charles E. Breeze, et al.
Cell Genomics (2023) Vol. 4, Iss. 1, pp. 100468-100468
Open Access | Times Cited: 7
Non-coding variants impact cis-regulatory coordination in a cell type-specific manner
Olga Pushkarev, Guido van Mierlo, Judith F. Kribelbauer, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 2
Causal relationship between plasma lipidome and four types of pancreatitis: a bidirectional Mendelian randomization study
Runzhou Ma, Cheng-Ming Chen, Ziyi Wang, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 2
Distinct genome-wide DNA methylation and gene expression signatures in classical monocytes from African American patients with systemic sclerosis
Peter C. Allen, Sarah E. Smith, Robert C. Wilson, et al.
Clinical Epigenetics (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 4
Identification of Candidate Genes Associated with Yak Body Size Using a Genome-Wide Association Study and Multiple Populations of Information
Xinrui Liu, Mingxiu Wang, Jie Qin, et al.
Animals (2023) Vol. 13, Iss. 9, pp. 1470-1470
Open Access | Times Cited: 4
Admixture Mapping of Chronic Kidney Disease and Risk Factors in Hispanic/Latino Individuals From Central America Country of Origin
Andréa R. V. R. Horimoto, Quan Sun, James P. Lash, et al.
Circulation Genomic and Precision Medicine (2024) Vol. 17, Iss. 4
Closed Access | Times Cited: 1
DNA-binding factor footprints and enhancer RNAs identify functional non-coding genetic variants
Simon C. Biddie, Giovanna Weykopf, Elizabeth F Hird, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 1
Associations between the New DNA-Methylation-Based Telomere Length Estimator, the Mediterranean Diet and Genetics in a Spanish Population at High Cardiovascular Risk
Óscar Coltell, Eva M. Asensio, José V. Sorlí, et al.
Antioxidants (2023) Vol. 12, Iss. 11, pp. 2004-2004
Open Access | Times Cited: 3
The RNA editing landscape in acute myeloid leukemia reveals associations with disease mutations and clinical outcome
Eshwar Meduri, Charles E. Breeze, Ludovica Marando, et al.
iScience (2022) Vol. 25, Iss. 12, pp. 105622-105622
Open Access | Times Cited: 5
FORGEdb: a tool for identifying candidate functional variants and uncovering target genes and mechanisms for complex diseases
Charles E. Breeze, Eric Haugen, María Gutiérrez‐Arcelus, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 4
PALM: a powerful and adaptive latent model for prioritizing risk variants with functional annotations
Xinyi Yu, Jiashun Xiao, Mingxuan Cai, et al.
Bioinformatics (2023) Vol. 39, Iss. 2
Open Access | Times Cited: 2
DNA-binding factor footprints and enhancer RNAs identify functional non-coding genetic variants
Simon C. Biddie, Giovanna Weykopf, Elizabeth F Hird, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Enhancer RNA transcriptome-wide association study reveals an atlas of pan-cancer susceptibility eRNAs
Wenyan Chen, Zeyang Wang, Jianxiang Lin, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Causality between immunocytes and polymyositis: A Mendelian randomization analysis
Ni Yang, Chang Li, Ruhui Liu, et al.
Medicine (2024) Vol. 103, Iss. 43, pp. e40254-e40254
Open Access
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