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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:

Rare coding variants in CHRNB2 reduce the likelihood of smoking
Veera M. Rajagopal, Kyoko Watanabe, Joelle Mbatchou, et al.
Nature Genetics (2023) Vol. 55, Iss. 7, pp. 1138-1148
Open Access | Times Cited: 12

Showing 12 citing articles:

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
Drug development advances in human genetics‐based targets
X. Zhang, Wenjun Yu, Yan Li, et al.
MedComm (2024) Vol. 5, Iss. 2
Open Access | Times Cited: 7
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
Smoking during pregnancy and its effect on placental weight: a Mendelian randomization study
Annika Jaitner, Marc Vaudel, Krasimira Tsaneva‐Atanasova, et al.
BMC Pregnancy and Childbirth (2024) Vol. 24, Iss. 1
Open Access | Times Cited: 5
Deep representation learning for clustering longitudinal survival data from electronic health records
Jiajun Qiu, Yao Hu, Li Li, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
The genetic landscape of substance use disorders
Zachary F. Gerring, Jackson G. Thorp, Jorien L. Treur, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 11, pp. 3694-3705
Open Access | Times Cited: 2
Whole-exome sequencing study of opioid dependence offers novel insights into the contributions of exome variants
Lu Wang, Yaira Z. Nuñez, Henry R. Kranzler, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access | Times Cited: 2
Implementing Core Genes and an Omnigenic Model for Behaviour Traits Prediction in Genomics
Tautvydas Rančelis, Ingrida Domarkienė, Laima Ambrozaitytė, et al.
Genes (2023) Vol. 14, Iss. 8, pp. 1630-1630
Open Access | Times Cited: 3
Deep representation learning for clustering longitudinal survival data from electronic health records
Jiajun Qiu, Yao Hu, Li Li, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Deep sequencing of candidate genes identified 14 variants associated with smoking abstinence in an ethnically diverse sample
Paul M. Cinciripini, David W. Wetter, Jian Wang, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access
Exploring and accounting for genetically driven effect heterogeneity in Mendelian Randomization
Annika Jaitner, Krasimira Tsaneva‐Atanasova, Rachel M. Freathy, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Exploring and Accounting for Genetically Driven Effect Heterogeneity in Mendelian Randomization
Annika Jaitner, Krasimira Tsaneva‐Atanasova, Rachel M. Freathy, et al.
Genetic Epidemiology (2024)
Open Access
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