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:

Common Disease Is More Complex Than Implied by the Core Gene Omnigenic Model
Naomi R. Wray, Cisca Wijmenga, Patrick F. Sullivan, et al.
Cell (2018) Vol. 173, Iss. 7, pp. 1573-1580
Open Access | Times Cited: 292

Showing 1-25 of 292 citing articles:

Benefits and limitations of genome-wide association studies
Vivian Tam, Nikunj Patel, Michelle Turcotte, et al.
Nature Reviews Genetics (2019) Vol. 20, Iss. 8, pp. 467-484
Closed Access | Times Cited: 1692

A global overview of pleiotropy and genetic architecture in complex traits
Kyoko Watanabe, Sven Stringer, Oleksandr Frei, et al.
Nature Genetics (2019) Vol. 51, Iss. 9, pp. 1339-1348
Open Access | Times Cited: 1094

The Polygenic and Monogenic Basis of Blood Traits and Diseases
Dragana Vuckovic, Erik L. Bao, Parsa Akbari, et al.
Cell (2020) Vol. 182, Iss. 5, pp. 1214-1231.e11
Open Access | Times Cited: 560

Update on NAFLD genetics: From new variants to the clinic
Eric Trépo, Luca Valenti
Journal of Hepatology (2020) Vol. 72, Iss. 6, pp. 1196-1209
Open Access | Times Cited: 318

Extreme Polygenicity of Complex Traits Is Explained by Negative Selection
Luke J. O’Connor, Armin Schoech, Farhad Hormozdiari, et al.
The American Journal of Human Genetics (2019) Vol. 105, Iss. 3, pp. 456-476
Open Access | Times Cited: 245

Getting to the Cores of Autism
Lilia M. Iakoucheva, Alysson R. Muotri, Jonathan Sebat
Cell (2019) Vol. 178, Iss. 6, pp. 1287-1298
Open Access | Times Cited: 231

Synergistic effects of common schizophrenia risk variants
Nadine Schrode, Seok‐Man Ho, Kazuhiko Yamamuro, et al.
Nature Genetics (2019) Vol. 51, Iss. 10, pp. 1475-1485
Open Access | Times Cited: 226

The future of rodent models in depression research
Anand Gururajan, Andreas Reif, John F. Cryan, et al.
Nature reviews. Neuroscience (2019) Vol. 20, Iss. 11, pp. 686-701
Closed Access | Times Cited: 226

Systems biology in cardiovascular disease: a multiomics approach
Abhishek Joshi, Marieke Rienks, Konstantinos Theofilatos, et al.
Nature Reviews Cardiology (2020) Vol. 18, Iss. 5, pp. 313-330
Closed Access | Times Cited: 200

Distinct subtypes of polycystic ovary syndrome with novel genetic associations: An unsupervised, phenotypic clustering analysis
Matthew Dapas, Frederick T. J. Lin, Girish N. Nadkarni, et al.
PLoS Medicine (2020) Vol. 17, Iss. 6, pp. e1003132-e1003132
Open Access | Times Cited: 199

Meaningful associations in the adolescent brain cognitive development study
Anthony Steven Dick, Daniel A. Lopez, Ashley L. Watts, et al.
NeuroImage (2021) Vol. 239, pp. 118262-118262
Open Access | Times Cited: 183

Missing heritability of complex diseases: case solved?
Emmanuelle Génin
Human Genetics (2019) Vol. 139, Iss. 1, pp. 103-113
Closed Access | Times Cited: 181

Deconstructing a Syndrome: Genomic Insights Into PCOS Causal Mechanisms and Classification
Matthew Dapas, Andrea Dunaif
Endocrine Reviews (2022) Vol. 43, Iss. 6, pp. 927-965
Open Access | Times Cited: 176

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

Convergent molecular, cellular, and cortical neuroimaging signatures of major depressive disorder
Kevin Anderson, Meghan A. Collins, Ru Kong, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 117, Iss. 40, pp. 25138-25149
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

Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity
Steven Gazal, Omer Weissbrod, Farhad Hormozdiari, et al.
Nature Genetics (2022) Vol. 54, Iss. 6, pp. 827-836
Open Access | Times Cited: 125

Functional regulatory variants implicate distinct transcriptional networks in dementia
Yonatan A. Cooper, Noam Teyssier, Nina M. Dräger, et al.
Science (2022) Vol. 377, Iss. 6608
Open Access | Times Cited: 87

The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits
Maria C. Costanzo, Marcin von Grotthuss, Jeffrey Massung, et al.
Cell Metabolism (2023) Vol. 35, Iss. 4, pp. 695-710.e6
Open Access | Times Cited: 82

Evolution of polygenic traits under global vs local adaptation
Sam Yeaman
Genetics (2022) Vol. 220, Iss. 1
Open Access | Times Cited: 76

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

Pleiotropy and Cross-Disorder Genetics Among Psychiatric Disorders
Phil H. Lee, Yen‐Chen Anne Feng, Jordan W. Smoller
Biological Psychiatry (2020) Vol. 89, Iss. 1, pp. 20-31
Open Access | Times Cited: 125

Into the Wild: GWAS Exploration of Non-coding RNAs
Héctor Giral, Ulf Landmesser, Adelheid Kratzer
Frontiers in Cardiovascular Medicine (2018) Vol. 5
Open Access | Times Cited: 115

Development of ADHD: Etiology, Heterogeneity, and Early Life Course
Joel T. Nigg, Margaret H. Sibley, Anita Thapar, et al.
Annual Review of Developmental Psychology (2020) Vol. 2, Iss. 1, pp. 559-583
Open Access | Times Cited: 115

The genetics of depression: successful genome-wide association studies introduce new challenges
Johan Ormel, Catharina A. Hartman, Harold Snieder
Translational Psychiatry (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 106

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