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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:

Signatures of negative selection in the genetic architecture of human complex traits
Jian Zeng, Ronald de Vlaming, Yang Wu, et al.
Nature Genetics (2018) Vol. 50, Iss. 5, pp. 746-753
Open Access | Times Cited: 382

Showing 26-50 of 382 citing articles:

Missing heritability of complex diseases: case solved?
Emmanuelle Génin
Human Genetics (2019) Vol. 139, Iss. 1, pp. 103-113
Closed Access | Times Cited: 181
Evaluating and improving heritability models using summary statistics
Doug Speed, John Bradley Holmes, David J. Balding
Nature Genetics (2020) Vol. 52, Iss. 4, pp. 458-462
Open Access | Times Cited: 167
Beyond SNP heritability: Polygenicity and discoverability of phenotypes estimated with a univariate Gaussian mixture model
Dominic Holland, Oleksandr Frei, Rahul S. Desikan, et al.
PLoS Genetics (2020) Vol. 16, Iss. 5, pp. e1008612-e1008612
Open Access | Times Cited: 167
The polygenic architecture of schizophrenia — rethinking pathogenesis and nosology
Olav B. Smeland, Oleksandr Frei, Anders M. Dale, et al.
Nature Reviews Neurology (2020) Vol. 16, Iss. 7, pp. 366-379
Closed Access | Times Cited: 163
Genomics of hypertension: the road to precision medicine
Sandosh Padmanabhan, Anna F. Dominiczak
Nature Reviews Cardiology (2020) Vol. 18, Iss. 4, pp. 235-250
Open Access | Times Cited: 158
Systematic differences in discovery of genetic effects on gene expression and complex traits
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
Nature Genetics (2023) Vol. 55, Iss. 11, pp. 1866-1875
Closed Access | Times Cited: 158
Evaluation of polygenic prediction methodology within a reference-standardized framework
Oliver Pain, Kylie P. Glanville, Saskia P. Hagenaars, et al.
PLoS Genetics (2021) Vol. 17, Iss. 5, pp. e1009021-e1009021
Open Access | Times Cited: 155
Enhancers in disease: molecular basis and emerging treatment strategies
Annique Claringbould, Judith B. Zaugg
Trends in Molecular Medicine (2021) Vol. 27, Iss. 11, pp. 1060-1073
Open Access | Times Cited: 146
Twelve years of GWAS discoveries for osteoporosis and related traits: advances, challenges and applications
Xiaowei Zhu, Wei-Yang Bai, Hou‐Feng Zheng
Bone Research (2021) Vol. 9, Iss. 1
Open Access | Times Cited: 145
New insights from the last decade of research in psychiatric genetics: discoveries, challenges and clinical implications
Ole A. Andreassen, Guy Hindley, Oleksandr Frei, et al.
World Psychiatry (2023) Vol. 22, Iss. 1, pp. 4-24
Open Access | Times Cited: 133
Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets
Carla Márquez‐Luna, Steven Gazal, Po−Ru Loh, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 122
Population-specific causal disease effect sizes in functionally important regions impacted by selection
Huwenbo Shi, Steven Gazal, Masahiro Kanai, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 115
Polygenic architecture of rare coding variation across 394,783 exomes
Daniel J. Weiner, Ajay Nadig, Karthik A. Jagadeesh, et al.
Nature (2023) Vol. 614, Iss. 7948, pp. 492-499
Open Access | Times Cited: 112
A unified framework for cross-population trait prediction by leveraging the genetic correlation of polygenic traits
Mingxuan Cai, Jiashun Xiao, Shunkang Zhang, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 4, pp. 632-655
Open Access | Times Cited: 107
Large uncertainty in individual polygenic risk score estimation impacts PRS-based risk stratification
Yi Ding, Kangcheng Hou, Kathryn S. Burch, et al.
Nature Genetics (2021) Vol. 54, Iss. 1, pp. 30-39
Open Access | Times Cited: 107
Limited overlap of eQTLs and GWAS hits due to systematic differences in discovery
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 91
Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals
Kangcheng Hou, Yi Ding, Ziqi Xu, et al.
Nature Genetics (2023) Vol. 55, Iss. 4, pp. 549-558
Closed Access | Times Cited: 75
Leveraging base-pair mammalian constraint to understand genetic variation and human disease
Patrick F. Sullivan, Jennifer R. S. Meadows, Steven Gazal, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 72
A meta-analysis of genetic effects associated with neurodevelopmental disorders and co-occurring conditions
Agnieszka Gidziela, Yasmin I. Ahmadzadeh, Giorgia Michelini, et al.
Nature Human Behaviour (2023) Vol. 7, Iss. 4, pp. 642-656
Open Access | Times Cited: 51
Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries
Zhili Zheng, Shouye Liu, Julia Sidorenko, et al.
Nature Genetics (2024) Vol. 56, Iss. 5, pp. 767-777
Open Access | Times Cited: 33
Pleiotropy, epistasis and the genetic architecture of quantitative traits
Trudy F. C. Mackay, Robert R. H. Anholt
Nature Reviews Genetics (2024) Vol. 25, Iss. 9, pp. 639-657
Closed Access | Times Cited: 29
Heritable polygenic editing: the next frontier in genomic medicine?
Peter M. Visscher, Christopher Gyngell, Loïc Yengo, et al.
Nature (2025) Vol. 637, Iss. 8046, pp. 637-645
Open Access | Times Cited: 4
Functional architecture of low-frequency variants highlights strength of negative selection across coding and non-coding annotations
Steven Gazal, Po−Ru Loh, Hilary K. Finucane, et al.
Nature Genetics (2018) Vol. 50, Iss. 11, pp. 1600-1607
Open Access | Times Cited: 161
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk
Mitja Mitrovič, Nikolaos A. Patsopoulos, Ashley Beecham, et al.
Cell (2018) Vol. 175, Iss. 6, pp. 1679-1687.e7
Open Access | Times Cited: 140
Quantification of frequency-dependent genetic architectures in 25 UK Biobank traits reveals action of negative selection
Armin Schoech, Daniel M. Jordan, Po−Ru Loh, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 132

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