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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:

Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs
Seong Kyu Han, Michelle Mcnulty, Christopher J. Benway, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 19

Showing 19 citing articles:

Rationale and design of the Nephrotic Syndrome Study Network (NEPTUNE) Match in glomerular diseases: designing the right trial for the right patient, today
Howard Trachtman, Hailey Desmond, Amanda Williams, et al.
Kidney International (2024) Vol. 105, Iss. 2, pp. 218-230
Open Access | Times Cited: 13
Large-scale cross-ancestry genome-wide meta-analysis of serum urate
Chamlee Cho, Beomsu Kim, Dan Say Kim, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 11
The Omics‐Driven Machine Learning Path to Cost‐Effective Precision Medicine in Chronic Kidney Disease
Marta B. Lopes, Roberta Coletti, Flore Duranton, et al.
PROTEOMICS (2025)
Open Access | Times Cited: 1
PPDPF preserves integrity of proximal tubule by modulating NMNAT activity in chronic kidney diseases
Xiaoliang Fang, Yi Zhong, Rui Zheng, et al.
Science Advances (2025) Vol. 11, Iss. 12
Open Access | Times Cited: 1
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome
Alexandra Barry, Michelle Mcnulty, Xiaoyuan Jia, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 21
Integrated multi-omics with machine learning to uncover the intricacies of kidney disease
Xinze Liu, Jingxuan Shi, Yuanyuan Jiao, et al.
Briefings in Bioinformatics (2024) Vol. 25, Iss. 5
Open Access | Times Cited: 8
Genetic imputation of kidney transcriptome, proteome and multi-omics illuminates new blood pressure and hypertension targets
Xiaoguang Xu, Chachrit Khunsriraksakul, James Eales, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 6
Multivariate canonical correlation analysis identifies additional genetic variants for chronic kidney disease
Amy J. Osborne, Agnieszka Bierżyńska, Elizabeth Colby, et al.
npj Systems Biology and Applications (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 2
Genetic association and transferability for urinary albumin-creatinine ratio as a marker of kidney disease in four Sub-Saharan African populations and non-continental individuals of African ancestry
Jean‐Tristan Brandenburg, Wenlong Carl Chen, Palwendé Romuald Boua, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 2
Genome-wide association study of hospitalized patients and acute kidney injury
Edward D. Siew, Jacklyn N. Hellwege, Adriana M. Hung, et al.
Kidney International (2024) Vol. 106, Iss. 2, pp. 291-301
Closed Access | Times Cited: 2
Kidney 'pathway-orphan' genes as a potential overlooked source of novel insights into kidney health and disease
Dianne Acoba, Sophie Gunnarsson, Anna Reznichenko
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Genetic Association and Transferability for Urinary Albumin-Creatinine Ratio as a Marker of Kidney Disease in four Sub-Saharan African Populations and non-continental Individuals of African Ancestry
Jean‐Tristan Brandenburg, Wenlong Carl Chen, Palwendé Romuald Boua, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Spatial Multi-Omics Connect SHROOM3 and COL18A1 in Chronic Kidney Disease
Pukhraj S. Gaheer, Nikhil Uppal, A. Paul, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Phenotypic spectrum of FAM47E-SHROOM3 haplotype composition in a general population sample
Dariush Ghasemi-Semeskandeh, Eva König, Luisa Foco, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Genetically-proxied lower PAR1 and renal phenotypes: a drug-target Mendelian Randomization study
Haotian Tang, Tom R. Gaunt, Venexia Walker
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Rare heterozygous variants in paediatric steroid resistant nephrotic syndrome – a population-based analysis of their significance
Christopher Platt, Agnieszka Bierżyńska, Weimao Ding, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access
Multimodal predictions of end stage chronic kidney disease from asymptomatic individuals for discovery of genomic biomarkers
Simona Rabinovici‐Cohen, Daniel E. Platt, Toshiya Iwamori, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Uncovering causal gene-tissue pairs and variants: A multivariable TWAS method controlling for infinitesimal effects
Yihe Yang, Noah Lorincz‐Comi, Xiaofeng Zhu
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Distinct pathway-based effects of blood pressure and body mass index on cardiovascular traits: comparison of novel Mendelian Randomization approaches
Maria K. Sobczyk, Tom G. Richardson, Genevieve M Leyden, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
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