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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:

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

Showing 1-25 of 26 citing articles:

Interpreting population- and family-based genome-wide association studies in the presence of confounding
Carl Veller, Graham Coop
PLoS Biology (2024) Vol. 22, Iss. 4, pp. e3002511-e3002511
Open Access | Times Cited: 31
From genetic associations to genes: methods, applications, and challenges
Ting Qi, Liyang Song, Yazhou Guo, et al.
Trends in Genetics (2024) Vol. 40, Iss. 8, pp. 642-667
Open Access | Times Cited: 15
Genome-wide association study identifies 30 obsessive-compulsive disorder associated loci
Nora I. Strom, Zachary F. Gerring, Marco Galimberti, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 12
Gene-based Hardy–Weinberg equilibrium test using genotype count data: application to six types of cancers
Jo Nishino, Fuyuki Miya, Mamoru Kato
BMC Genomics (2025) Vol. 26, Iss. 1
Open Access | Times Cited: 1
Interpreting population and family-based genome-wide association studies in the presence of confounding
Carl Veller, Graham Coop
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 20
Genetic associations of protein-coding variants in venous thromboembolism
Xiao‐Yu He, Bang‐Sheng Wu, Yang Liu, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
An integrative approach to identifying NPC1 as a susceptibility gene for gestational diabetes mellitus
Yuping Shan, Hong Hu, Anning Yang, et al.
The Journal of Maternal-Fetal & Neonatal Medicine (2025) Vol. 38, Iss. 1
Open Access
Genomic Characterisation of the Relationship and Causal Links Between Vascular Calcification, Alzheimer’s Disease, and Cognitive Traits
Emmanuel O Adewuyi, Simon M. Laws
Biomedicines (2025) Vol. 13, Iss. 3, pp. 618-618
Open Access
Cross-ancestry genome-wide association study identifies new susceptibility genes for preeclampsia
Yuping Shan, Hong Hu, Yijing Chu
BMC Pregnancy and Childbirth (2025) Vol. 25, Iss. 1
Open Access
Characterizing the Genetic Landscape of Major Depression through Multiple-trait and Cross-ancestry GWAS Meta-Analysis of 1,396,021 Individuals
Yu Feng, Xiaolong Ji, Peng Huang, et al.
Research Square (Research Square) (2025)
Closed Access
Genome‐wide meta‐analysis identifies ancestry‐specific loci for Alzheimer's disease
Yi‐Jun Ge, Shi‐Dong Chen, Bang‐Sheng Wu, et al.
Alzheimer s & Dementia (2024) Vol. 20, Iss. 9, pp. 6243-6256
Open Access | Times Cited: 2
Incorporating genetic similarity of auxiliary samples into eGene identification under the transfer learning framework
Shuo Zhang, Zhou Jiang, Ping Zeng
Journal of Translational Medicine (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 2
Macular structural integrity estimates are associated with Parkinson’s disease genetic risk
Santiago Diaz‐Torres, Samantha Sze‐Yee Lee, Natalia Ogonowski, et al.
Acta Neuropathologica Communications (2024) Vol. 12, Iss. 1
Open Access | Times Cited: 2
Shared genetic architecture and bidirectional clinical risks within the psycho-metabolic nexus
Xiaonan Guo, Yu Feng, Xiaolong Ji, et al.
EBioMedicine (2024) Vol. 111, pp. 105530-105530
Open Access | Times Cited: 1
Genome-wide multi-ethnic meta-analysis identifies 22 independent risk loci for normal tension glaucoma and predominantly overlaps with high tension glaucoma.
Santiago Diaz‐Torres, Weixiong He, Regina Yu, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 3
Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selection
Martin Jinye Zhang, Alkes L. Price, Arun Durvasula, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 2
Gene-based Hardy-Weinberg equilibrium test using genotype count data identifies novel cancer-related genes
Jo Nishino, Fuyuki Miya, Mamoru Kato
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Unraveling the Genetic Interplay and Therapeutic Potentials between Major Depressive Disorder and Metabolic Syndrome: Multi-Ancestry and Multi-Trait Genome-Wide Association Analyses
Yu Feng, Ningning Jia, Xiaochu Gu, et al.
Research Square (Research Square) (2024)
Open Access
Genome-wide fine-mapping improves identification of causal variants
Yang‐Chang Wu, Zhili Zheng, L Thibaut, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Genome-wide assessment of shared genetic landscape of idiopathic pulmonary fibrosis and its comorbidities
Yuanhao Yang, Yonghua Sheng, Patrícia Carreira, et al.
Human Genetics (2024) Vol. 143, Iss. 9-10, pp. 1223-1239
Open Access
Genome-wide fine-mapping improves identification of causal variants
Yang Wu, Zhili Zheng, L Thibaut, et al.
Research Square (Research Square) (2024)
Open Access
DINGO: increasing the power of locus discovery in maternal and fetal genome-wide association studies of perinatal traits
Liang‐Dar Hwang, Gabriel Cuéllar-Partida, Loïc Yengo, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access
Assessing shared genetic and causal links between vascular calcification, Alzheimer's disease, and cognitive traits
Emmanuel O Adewuyi, Simon M. Laws
Research Square (Research Square) (2024)
Open Access
Genome-wide meta-analysis identifies 22 loci for normal tension glaucoma with significant overlap with high tension glaucoma
Santiago Diaz‐Torres, Weixiong He, Regina Yu, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access
Direct and INdirect effects analysis of Genetic lOci (DINGO): A software package to increase the power of locus discovery in GWAS meta-analyses of perinatal phenotypes and traits influenced by indirect genetic effects
Liang‐Dar Hwang, Gabriel Cuéllar-Partida, Loïc Yengo, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
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