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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:

Genetic analyses identify widespread sex-differential participation bias
Nicola Pirastu, Mattia Cordioli, Priyanka Nandakumar, et al.
Nature Genetics (2021) Vol. 53, Iss. 5, pp. 663-671
Open Access | Times Cited: 185

Showing 26-50 of 185 citing articles:

Strategies to investigate and mitigate collider bias in genetic and Mendelian randomisation studies of disease progression
Ruth E. Mitchell, April Hartley, Venexia Walker, et al.
PLoS Genetics (2023) Vol. 19, Iss. 2, pp. e1010596-e1010596
Open Access | Times Cited: 40
Guidelines on the use of sex and gender in cardiovascular research
Charlotte W. Usselman, Merry L. Lindsey, Austin T. Robinson, et al.
AJP Heart and Circulatory Physiology (2023) Vol. 326, Iss. 1, pp. H238-H255
Open Access | Times Cited: 34
Quantification of race/ethnicity representation in Alzheimer’s disease neuroimaging research in the USA: a systematic review
Aaron C. Lim, Lisa L. Barnes, Gali H. Weissberger, et al.
Communications Medicine (2023) Vol. 3, Iss. 1
Open Access | Times Cited: 33
Penetrance of pathogenic genetic variants associated with premature ovarian insufficiency
Saleh Shekari, Stasa Stankovic, Eugene J. Gardner, et al.
Nature Medicine (2023) Vol. 29, Iss. 7, pp. 1692-1699
Open Access | Times Cited: 32
Obesity and risk of gestational diabetes mellitus: A two-sample Mendelian randomization study
Xinli Song, Cheng Wang, Tingting Wang, et al.
Diabetes Research and Clinical Practice (2023) Vol. 197, pp. 110561-110561
Closed Access | Times Cited: 30
Quality control and analytic best practices for testing genetic models of sex differences in large populations
Ekaterina Khramtsova, Melissa A. Wilson, Joanna Martin, et al.
Cell (2023) Vol. 186, Iss. 10, pp. 2044-2061
Open Access | Times Cited: 26
Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity
Veera M. Rajagopal, Andrea Ganna, Jonathan R. I. Coleman, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 23
Sex-specific genetic architecture of blood pressure
Min‐Lee Yang, Chang Xu, Trisha Gupte, et al.
Nature Medicine (2024) Vol. 30, Iss. 3, pp. 818-828
Closed Access | Times Cited: 11
Genetic and Phenotypic Features of Schizophrenia in the UK Biobank
Sophie E. Legge, Antonio F. Pardiñas, Grace Woolway, et al.
JAMA Psychiatry (2024) Vol. 81, Iss. 7, pp. 681-681
Open Access | Times Cited: 11
Screening embryos for polygenic disease risk: a review of epidemiological, clinical, and ethical considerations
Antonio Capalbo, G. de Wert, Heidi Mertes, et al.
Human Reproduction Update (2024) Vol. 30, Iss. 5, pp. 529-557
Open Access | Times Cited: 11
A unified framework for estimating country-specific cumulative incidence for 18 diseases stratified by polygenic risk
Bradley Jermy, Kristi Läll, Brooke N. Wolford, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 9
A scalable variational inference approach for increased mixed-model association power
Hrushikesh Loya, Georgios Kalantzis, Fergus Cooper, et al.
Nature Genetics (2025)
Open Access | Times Cited: 1
Interactions between Polygenic Scores and Environments: Methodological and Conceptual Challenges
Benjamin W. Domingue, Sam Trejo, Emma Armstrong‐Carter, et al.
Sociological Science (2020) Vol. 7, pp. 365-386
Open Access | Times Cited: 63
The search for sexually antagonistic genes: Practical insights from studies of local adaptation and statistical genomics
Filip Ruzicka, Ludovic Dutoit, Peter Czuppon, et al.
Evolution Letters (2020) Vol. 4, Iss. 5, pp. 398-415
Open Access | Times Cited: 57
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Stavroula Kanoni, Sarah E. Graham, Yuxuan Wang, et al.
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 35
Ten challenges for clinical translation in psychiatric genetics
Eske M. Derks, Jackson G. Thorp, Zachary F. Gerring
Nature Genetics (2022) Vol. 54, Iss. 10, pp. 1457-1465
Closed Access | Times Cited: 31
Effects of general and central adiposity on circulating lipoprotein, lipid, and metabolite levels in UK Biobank: A multivariable Mendelian randomization study
Joshua A. Bell, Tom G. Richardson, Qin Wang, et al.
The Lancet Regional Health - Europe (2022) Vol. 21, pp. 100457-100457
Open Access | Times Cited: 30
Dimensional and transdiagnostic phenotypes in psychiatric genome-wide association studies
Monika A. Waszczuk, Katherine Jonas, Marina A. Bornovalova, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 12, pp. 4943-4953
Open Access | Times Cited: 21
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
Genetics implicates overactive osteogenesis in the development of diffuse idiopathic skeletal hyperostosis
Anurag Sethi, J. Graham Ruby, Matthew A. Veras, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 19
Examining the shared etiology of psychopathology with genome-wide association studies
Travis T. Mallard, Andrew D. Grotzinger, Jordan W. Smoller
Physiological Reviews (2023) Vol. 103, Iss. 2, pp. 1645-1665
Open Access | Times Cited: 17
Studying the genetics of participation using footprints left on the ascertained genotypes
Stefania Benónísdóttir, Augustine Kong
Nature Genetics (2023) Vol. 55, Iss. 8, pp. 1413-1420
Open Access | Times Cited: 17
Patterns of item nonresponse behaviour to survey questionnaires are systematic and associated with genetic loci
Gianmarco Mignogna, Caitlin E. Carey, Robbee Wedow, et al.
Nature Human Behaviour (2023) Vol. 7, Iss. 8, pp. 1371-1387
Open Access | Times Cited: 16
The impact of assortative mating, participation bias and socioeconomic status on the polygenic risk of behavioural and psychiatric traits
Brenda Cabrera‐Mendoza, Frank R. Wendt, Gita A. Pathak, et al.
Nature Human Behaviour (2024) Vol. 8, Iss. 5, pp. 976-987
Closed Access | Times Cited: 7
Breaking down causes, consequences, and mediating effects of telomere length variation on human health
Samuel Moix, Marie C. Sadler, Zoltán Kutalik, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 7

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