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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:

GWAS of three molecular traits highlights core genes and pathways alongside a highly polygenic background
Nasa Sinnott-Armstrong, Sahin Naqvi, Manuel A. Rivas, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 131

Showing 26-50 of 131 citing articles:

Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits
Andrew Brown, Juan Fernández‐Tajes, Mun‐Gwan Hong, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 16
Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK Biobank
Abhishek Nag, Ryan S. Dhindsa, Lawrence Middleton, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 3, pp. 487-498
Open Access | Times Cited: 15
Genetic determinants of sex hormone levels in endometriosis patients [Ссылка на источник: Golovchenko IO. Genetic determinants of sex hormone levels in endometriosis patients. Research Results in Biomedicine
Ilya O. Golovchenko
RESEARCH RESULTS IN BIOMEDICINE (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 11
Sex-Hormone-Binding Globulin Gene Polymorphisms and Breast Cancer Risk in Caucasian Women of Russia
Irina Ponomarenko, Konstantin N. Pasenov, Maria Churnosova, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 4, pp. 2182-2182
Open Access | Times Cited: 4
Functional genomics of human skeletal development and the patterning of height heritability
Daniel Richard, Pushpanathan Muthuirulan, Mariel Young, et al.
Cell (2024)
Open Access | Times Cited: 4
Causal modeling of gene effects from regulators to programs to traits: integration of genetic associations and Perturb-seq
Mineto Ota, Jeffrey P. Spence, Tony Zeng, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Prioritizing effector genes at trait-associated loci using multimodal evidence
Marijn Schipper, Christiaan de Leeuw, Bernardo de A.P.C. Maciel, et al.
Nature Genetics (2025)
Closed Access
Comparison of the multivariate genetic architecture of eight major psychiatric disorders across sex
Ted Schwaba, Travis T. Mallard, Adam X. Maihofer, et al.
Nature Genetics (2025)
Open Access
Tradeoffs in Modeling Context Dependency in Complex Trait Genetics
Eric Weine, Samuel Pattillo Smith, Rebecca Kathryn Knowlton, et al.
(2025)
Open Access
Pathway-Specific Polygenic Scores for Predicting Clinical Lithium Treatment Response in Patients with Bipolar Disorder
Nigussie Tadesse Sharew, Scott Clark, Sergi Papiol, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Trade-offs in modeling context dependency in complex trait genetics
Eric Weine, Samuel Pattillo Smith, Rebecca Kathryn Knowlton, et al.
eLife (2025) Vol. 13
Open Access
Discovery of novel ancestry specific genes for androgens and hypogonadism in Million Veteran Program Men
Meghana S. Pagadala, Craig C. Teerlink, Guneet K. Jasuja, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Computational Genomics in the Era of Precision Medicine: Applications to Variant Analysis and Gene Therapy
Yung-Chun Wang, Yuchang Wu, Julie Choi, et al.
Journal of Personalized Medicine (2022) Vol. 12, Iss. 2, pp. 175-175
Open Access | Times Cited: 17
Sex Hormone Candidate Gene Polymorphisms Are Associated with Endometriosis
I.O. Golovchenko, Boris Aizikovich, Oleg Golovchenko, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 22, pp. 13691-13691
Open Access | Times Cited: 17
Speos: an ensemble graph representation learning framework to predict core gene candidates for complex diseases
Florin Ratajczak, Mitchell Joblin, Marcel Hildebrandt, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 10
Polygenic risk score phenome-wide association study reveals an association between endometriosis and testosterone
Isabelle M. McGrath, Grant W. Montgomery, Sally Mortlock
BMC Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 10
Fathers and sons, mothers and daughters: Sex-specific genetic architecture for fetal testosterone in a wild mammal
Ruth Fishman, Simona Kralj‐Fišer, Sivan Marglit, et al.
Hormones and Behavior (2024) Vol. 161, pp. 105525-105525
Closed Access | Times Cited: 3
A scalable and robust variance components method reveals insights into the architecture of gene-environment interactions underlying complex traits
Ali Pazokitoroudi, Zhengtong Liu, Andrew Dahl, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 7, pp. 1462-1480
Open Access | Times Cited: 3
Methylome-wide association analyses of lipids and modifying effects of behavioral factors in diverse race and ethnicity participants
Yao Hu, Jeff Haessler, Jessica I. Lundin, et al.
Clinical Epigenetics (2025) Vol. 17, Iss. 1
Open Access
Purine metabolites and complex diseases: role of genes and nutrients
Kendra L Nelson, V. Saroja Voruganti
Current Opinion in Clinical Nutrition & Metabolic Care (2021) Vol. 24, Iss. 4, pp. 296-302
Closed Access | Times Cited: 22
Integrated analysis of direct and proxy genome wide association studies highlights polygenicity of Alzheimer’s disease outside of the APOE region
Javier de la Fuente, Andrew D. Grotzinger, Riccardo E. Marioni, et al.
PLoS Genetics (2022) Vol. 18, Iss. 6, pp. e1010208-e1010208
Open Access | Times Cited: 16
Singling out motor neurons in the age of single-cell transcriptomics
Jacob A. Blum, Aaron D. Gitler
Trends in Genetics (2022) Vol. 38, Iss. 9, pp. 904-919
Open Access | Times Cited: 15
Dissecting the loci underlying maturation timing in Atlantic salmon using haplotype and multi-SNP based association methods
Marion Sinclair‐Waters, Torfinn Nome, Jing Wang, et al.
Heredity (2022) Vol. 129, Iss. 6, pp. 356-365
Open Access | Times Cited: 15
Taking quantitative genomics into the wild
Susan E. Johnston, Nancy Chen, Emily B. Josephs
Proceedings of the Royal Society B Biological Sciences (2022) Vol. 289, Iss. 1989
Open Access | Times Cited: 15
Sex-Specific Features of the Correlation between GWAS-Noticeable Polymorphisms and Hypertension in Europeans of Russia
Т. И. Иванова, Maria Churnosova, Maria Abramova, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 9, pp. 7799-7799
Open Access | Times Cited: 9

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